09 - Appareils et instruments scientifiques et électriques
42 - Services scientifiques, technologiques et industriels, recherche et conception
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
Safes; locks of metal; safety boxes; strongboxes; electronic
safes. Software and application software; software and application
software, all for use in enabling the operation of and
interaction and interface between mobile devices and
electronic safes; authentication software; digital locks;
biometric locks; electric locks; electronic locking
mechanisms for safes; electronic locks and access control
apparatus; electronic locking systems and apparatus for
safes; computer programs for controlling electric locks;
software and application software for mobile devices,
namely, software for use in mental health and well-being
support. Software as a service [SaaS]; software as a service [SaaS]
featuring software for use in enabling the operation of and
interaction and interface between mobile devices and
electronic safes; user authentication services for online
software applications; user authentication services using
sign-on technology for online software applications;
authentication services of data transmitted via
telecommunications; application service provider featuring a
software application for use in connection with electric and
electronic safes; design and development of software. Rental of safes.
The disclosure concerns use of a compound for treating a lysosomal storage disorder, increasing lysosomal clearance, reducing a neurological pathology or reducing seizures. The disclosure further concerns a method for treating a lysosomal storage disorder, increasing lysosomal clearance, reducing a neurological pathology or reducing seizures, which comprises administering a compound to a subject. The disclosure also concerns use of a compound in the manufacture of a medicament for use in treating one or more symptoms of a lysosomal storage disorder, increasing lysosomal clearance, reducing a neurological pathology or reducing seizures. In any case, the compound is steroid, a GABA receptor ligand, a Sigma-1 receptor ligand, a cannabinoid receptor ligand, a TRP channel ligand and/or a microtubule modulator.
A61K 31/573 - Composés contenant des systèmes cycliques du cyclopenta[a]hydrophénanthrèneLeurs dérivés, p. ex. stéroïdes substitués en position 17 bêta par une chaîne à deux atomes de carbone, p. ex. prégnane ou progestérone substitués en position 21, p. ex. cortisone, dexaméthasone, prednisone ou aldostérone
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
C12Q 1/6893 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour la détection ou l’identification d’organismes pour les protozoaires
The present disclosure relates to a method of treating or preventing a disease in an individual, the method comprising reducing pyroptosis by administering to the individual a composition comprising an agent whose administration reduces TSPO signalling in the individual. The method of the disclosure can thus be used to treat or prevent diseases associated with pyroptosis such as inflammatory disease, cancer, neurodegenerative disease, cardiovascular disease, kidney disease and sepsis. The disclosure also relates to use of TSPO expression as a biomarker for pyroptosis, a method of assessing the degree of pyroptosis in an individual based on TSPO expression, an in vitro model of pyroptosis, a method of producing the in vitro model and associated vector, and a method for determining the ability of an agent to inhibit pyroptosis.
C12N 15/113 - Acides nucléiques non codants modulant l'expression des gènes, p. ex. oligonucléotides anti-sens
A61K 31/4045 - Indole-alkylaminesLeurs amides, p. ex. sérotonine, mélatonine
A61K 31/472 - Isoquinoléines non condensées, p. ex. papavérine
A61K 31/5025 - PyridazinesPyridazines hydrogénées condensées en ortho ou en péri avec des systèmes hétérocycliques
A61K 31/522 - Purines, p. ex. adénine ayant des groupes oxo liés directement à l'hétérocycle, p. ex. hypoxanthine, guanine, acyclovir
A61K 31/536 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec au moins un azote et au moins un oxygène comme hétéro-atomes d'un cycle, p. ex. 1,2-oxazines condensées en ortho ou en péri avec des systèmes carbocycliques
A61P 29/00 - Agents analgésiques, antipyrétiques ou anti-inflammatoires non centraux, p. ex. agents antirhumatismauxMédicaments anti-inflammatoires non stéroïdiens [AINS]
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
5.
COMPOUNDS FOR TREATING DISEASES ASSOCIATED WITH HYALURONAN OVERPRODUCTION
There are provided compounds of formula (I): [hyaluronan production inhibitor]-[labile linker]-X (I), which compounds are useful in the treatment of diseases associated with hyaluronan overproduction.
A61K 31/24 - Esters, p. ex. nitroglycérine, sélénocyanates d'acides carboxyliques ayant un noyau aromatique lié au groupe carboxyle ayant un groupe amino ou nitro
The disclosure concerns a method for detecting the presence or absence of mycobacteria in a sample and a method for diagnosing the presence or absence of a mycobacterial infection in a subject. The disclosure also concerns a lysis agent comprising bacteriophage capable of lysing viable mycobacteria and use of the lysis agent in the methods of the disclosure.
09 - Appareils et instruments scientifiques et électriques
42 - Services scientifiques, technologiques et industriels, recherche et conception
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
(1) Safes; locks of metal; safety boxes; strongboxes; electronic safes.
(2) Software and application software; software and application software, all for use in enabling the operation of and interaction and interface between mobile devices and electronic safes; authentication software; digital locks; biometric locks; electric locks; electronic locking mechanisms for safes; electronic locks and access control apparatus; electronic locking systems and apparatus for safes; computer programs for controlling electric locks; software and application software for mobile devices, namely, software for use in mental health and well-being support. (1) Software as a service [SaaS]; software as a service [SaaS] featuring software for use in enabling the operation of and interaction and interface between mobile devices and electronic safes; user authentication services for online software applications; user authentication services using sign-on technology for online software applications; authentication services of data transmitted via telecommunications; application service provider featuring a software application for use in connection with electric and electronic safes; design and development of software.
(2) Rental of safes.
09 - Appareils et instruments scientifiques et électriques
42 - Services scientifiques, technologiques et industriels, recherche et conception
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
Safes; locks of metal; safety boxes; strongboxes; electronic safes. Software and application software; software and application software, all for use in enabling the operation of and interaction and interface between mobile devices and electronic safes; authentication software; digital locks; biometric locks; electric locks; electronic locking mechanisms for safes; electronic locks and access control apparatus; electronic locking systems and apparatus for safes; computer programs for controlling electric locks; software and application software for mobile devices, namely, software for use in mental health and well-being support. Software as a service [SaaS]; software as a service [SaaS] featuring software for use in enabling the operation of and interaction and interface between mobile devices and electronic safes; user authentication services for online software applications; user authentication services using sign-on technology for online software applications; authentication services of data transmitted via telecommunications; application service provider featuring a software application for use in connection with electric and electronic safes; design and development of software. Rental of safes.
C12Q 1/6883 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique
The disclosure relates to a method of screening a dog for a predisposition to diabetes mellitus, and a method of determining the potential of a dog to produce progeny that are genetically predisposed to diabetes mellitus. The disclosure also relates to a method of selecting a treatment for diabetes mellitus in a dog, a method of preventing, delaying or treating diabetes mellitus in a dog using an oral hypoglycaemic drug, and a composition comprising an oral hypoglycaemic drug for use in a method of preventing, delaying or treating diabetes mellitus in a dog. The disclosure further concerns a method of preventing or delaying diabetes mellitus in a dog using an anti-hyperglycaemic diet or by means of neutering, and an anti-hyperglycaemic diet for use in a method of preventing or delaying diabetes mellitus in a dog.
C12Q 1/6883 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique
11.
METHOD AND TREATMENT FOR OSTEOARTHRITIS AND DISEASES OF CHONDROCYTE HYPERTROPHY
The disclosure concerns a method of treating a disorder characterised by chondrocyte hypertrophy e.g. osteoarthritis, and a composition for use in such a method. The disclosure also concerns a method of producing a miniaturised model of endochondral ossification, and a miniaturised model of endochondral ossification producible by such method. The disclosure further provides a method of screening for compositions for use in treating a disorder characterised by chondrocyte hypertrophy, and a composition identified by such method.
A61K 31/4353 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle condensés en ortho ou en péri avec des systèmes hétérocycliques
A61K 31/44 - Pyridines non condenséesLeurs dérivés hydrogénés
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
C12Q 1/00 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions
12.
METHOD AND TREATMENT FOR OSTEOARTHRITIS AND DISEASES OF CHONDROCYTE HYPERTROPHY
A61K 31/4353 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle condensés en ortho ou en péri avec des systèmes hétérocycliques
A61K 31/44 - Pyridines non condenséesLeurs dérivés hydrogénés
A61P 19/02 - Médicaments pour le traitement des troubles du squelette des troubles articulaires, p. ex. arthrites, arthroses
A61P 19/04 - Médicaments pour le traitement des troubles du squelette des troubles non-spécifiques du tissu conjonctif
A61P 19/08 - Médicaments pour le traitement des troubles du squelette des maladies osseuses, p. ex. rachitisme, maladie de Paget
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
The invention relates to method of diagnosing stage B2 degenerative mitral valve disease (DMVD) in a dog, a method of determining the probability of a dog having stage B2 DMVD, a method of training a model to predict stage B2 DMVD in a dog, and a related computer program and system.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
14.
METHODS FOR THE NON-INVASIVE DIAGNOSIS OF INTESTINAL INFECTION IN BIRDS
C12Q 1/6888 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour la détection ou l’identification d’organismes
15.
METHODS FOR THE NON-INVASIVE DIAGNOSIS OF INTESTINAL INFECTION IN BIRDS
C12Q 1/6888 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour la détection ou l’identification d’organismes
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
A61K 31/536 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec au moins un azote et au moins un oxygène comme hétéro-atomes d'un cycle, p. ex. 1,2-oxazines condensées en ortho ou en péri avec des systèmes carbocycliques
A61K 31/137 - Arylalkylamines, p. ex. amphétamine, épinéphrine, salbutamol, éphédrine
A61K 31/5513 - 1,4-Benzodiazépines, p. ex. diazépam
A61K 31/713 - Acides nucléiques ou oligonucléotides à structure en double-hélice
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
A61P 9/00 - Médicaments pour le traitement des troubles du système cardiovasculaire
A61P 11/00 - Médicaments pour le traitement des troubles du système respiratoire
A61P 13/12 - Médicaments pour le traitement des troubles du système urinaire des reins
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
A61P 29/00 - Agents analgésiques, antipyrétiques ou anti-inflammatoires non centraux, p. ex. agents antirhumatismauxMédicaments anti-inflammatoires non stéroïdiens [AINS]
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/48 - Matériau biologique, p. ex. sang, urineHémocytomètres
C12Q 3/00 - Procédés de commande sensible aux conditions du milieu
C12Q 1/00 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions
C40B 30/00 - Procédés de criblage des bibliothèques
17.
COMPOUNDS FOR TREATING DISEASES ASSOCIATED WITH HYALURONAN OVERPRODUCTION
There are provided compounds of formula (I): [hyaluronan production inhibitor][labile linker]X (I), which compounds are useful in the treatment of diseases associated with hyaluronan overproduction.
A61K 31/427 - Thiazoles non condensés et contenant d'autres hétérocycles
A61P 19/02 - Médicaments pour le traitement des troubles du squelette des troubles articulaires, p. ex. arthrites, arthroses
A61P 29/00 - Agents analgésiques, antipyrétiques ou anti-inflammatoires non centraux, p. ex. agents antirhumatismauxMédicaments anti-inflammatoires non stéroïdiens [AINS]
C07C 229/12 - Composés contenant des groupes amino et carboxyle liés au même squelette carboné ayant des groupes amino et carboxyle liés à des atomes de carbone acycliques du même squelette carboné le squelette carboné étant acyclique et saturé ayant un seul groupe amino et un seul groupe carboxyle liés au squelette carboné l'atome d'azote du groupe amino étant lié de plus à des atomes de carbone acycliques ou à des atomes de carbone de cycles autres que des cycles aromatiques à six chaînons à des atomes de carbone de squelettes carbonés acycliques
C07C 327/30 - Esters d'acides monothiocarboxyliques ayant des atomes de soufre de groupes thiocarboxyle estérifiés liés à des atomes de carbone de radicaux hydrocarbonés substitués par des atomes d'azote, ne faisant pas partie de groupes nitro ou nitroso
C07D 277/22 - Composés hétérocycliques contenant des cycles thiazole-1, 3 ou thiazole-1, 3 hydrogénés non condensés avec d'autres cycles comportant deux ou trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle
C07D 311/30 - Benzo [b] pyrannes non hydrogénés dans le carbocycle avec des atomes d'oxygène ou de soufre liés directement en position 4 avec des cycles aromatiques liés en position 2 ou 3 avec des cycles aromatiques liés uniquement en position 2 non hydrogénés dans l'hétérocycle, p. ex. flavones
C07D 417/12 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre et d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
18.
COMPOUNDS FOR TREATING DISEASES ASSOCIATED WITH HYALURONAN OVERPRODUCTION
There are provided compounds of formula (I): [hyaluronan production inhibitor]—[labile linker]—X (I), which compounds are useful in the treatment of diseases associated with hyaluronan overproduction.
C07C 229/12 - Composés contenant des groupes amino et carboxyle liés au même squelette carboné ayant des groupes amino et carboxyle liés à des atomes de carbone acycliques du même squelette carboné le squelette carboné étant acyclique et saturé ayant un seul groupe amino et un seul groupe carboxyle liés au squelette carboné l'atome d'azote du groupe amino étant lié de plus à des atomes de carbone acycliques ou à des atomes de carbone de cycles autres que des cycles aromatiques à six chaînons à des atomes de carbone de squelettes carbonés acycliques
C07C 327/30 - Esters d'acides monothiocarboxyliques ayant des atomes de soufre de groupes thiocarboxyle estérifiés liés à des atomes de carbone de radicaux hydrocarbonés substitués par des atomes d'azote, ne faisant pas partie de groupes nitro ou nitroso
C07D 311/30 - Benzo [b] pyrannes non hydrogénés dans le carbocycle avec des atomes d'oxygène ou de soufre liés directement en position 4 avec des cycles aromatiques liés en position 2 ou 3 avec des cycles aromatiques liés uniquement en position 2 non hydrogénés dans l'hétérocycle, p. ex. flavones
C07D 277/22 - Composés hétérocycliques contenant des cycles thiazole-1, 3 ou thiazole-1, 3 hydrogénés non condensés avec d'autres cycles comportant deux ou trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle
C07D 417/12 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre et d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
A61K 31/223 - Esters, p. ex. nitroglycérine, sélénocyanates d'acides carboxyliques d'acides acycliques, p. ex. pravastatine d'alpha-amino-acides
A61P 29/00 - Agents analgésiques, antipyrétiques ou anti-inflammatoires non centraux, p. ex. agents antirhumatismauxMédicaments anti-inflammatoires non stéroïdiens [AINS]
A61P 19/02 - Médicaments pour le traitement des troubles du squelette des troubles articulaires, p. ex. arthrites, arthroses
The present disclosure provides an aircraft (10) for flying in a forward direction (F). The aircraft (10) comprises an aircraft body (20), and a wing comprising a first wing portion (30A) and a second wing portion (30B). The first wing portion (30A) and the second wing portion (30B) extend away from the aircraft body (20). The first wing portion (30A) and the second wing portion (30B) are configured to generate a first lift value during level flight of the aircraft (10) in the forward direction (F) when the first wing portion (30A) and the second wing portion (30B) are in an equilibrium position. Each of the first wing portion (30A) and the second wing portion (30B) is flexibly mounted relative to the aircraft body (20) such that when a lift force generated by the first wing portion (30A) changes from the first lift value to a second lift value, the first wing portion (30A) is deflected substantially vertically away from an equilibrium position. The aircraft (10) is configured to provide a further force to the first wing portion (30A) to substantially prevent further deflection of the first wing portion (30A) away from the equilibrium position.
The invention relates to method of diagnosing stage B2 degenerative mitral valve disease (DMVD) in a dog, a method of determining the probability of a dog having stage B2 DMVD, a method of training a model to predict stage B2 DMVD in a dog, and a related computer program and system.
G01N 33/48 - Matériau biologique, p. ex. sang, urineHémocytomètres
G16B 5/00 - TIC spécialement adaptées à la modélisation ou aux simulations dans la biologie des systèmes, p. ex. réseaux de régulation génétique, réseaux d’interaction entre protéines ou réseaux métaboliques
G16B 40/00 - TIC spécialement adaptées aux biostatistiquesTIC spécialement adaptées à l’apprentissage automatique ou à l’exploration de données liées à la bio-informatique, p. ex. extraction de connaissances ou détection de motifs
The invention relates to method of diagnosing stage B2 degenerative mitral valve disease (DMVD) in a dog, a method of determining the probability of a dog having stage B2 DMVD, a method of training a model to predict stage B2 DMVD in a dog, and a related computer program and system.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
22.
COLLISION AVOIDANCE SYSTEM FOR A MOBILE DEVICE CAPABLE OF AUTONOMOUS TRAVEL
A mobile device (10) capable of autonomous travel comprises drive means (12, 13) to provide movement of the device over a surface and an obstacle detecting and movement influencing system (15, 16, 17) to detect an obstacle (20) in the path of the device and in response to detection of an obstacle to control the drive means to influence movement of the device. The obstacle detecting and movement influencing system comprises a pneumatic element (15) which is positioned on a body (11) of the device to face in the forward direction of movement of the device and which is resiliently compressible on contact with an obstacle (20). The device (10) includes a control unit (18) responsive to sensing by a sensor (17) of the contact to then control the drive means (12, 13) so as to cause travel of the device in the direction of forward movement to be arrested and subsequently resumed in that direction after a delay, during which the device may remain stationary, execute reverse travel and/or execute a bypass routine.
The present disclosure provides an aircraft (10) for flying in a forward direction (F). The aircraft (10) comprises an aircraft body (20), and a wing comprising a first wing portion (30A) and a second wing portion (30B). The first wing portion (30A) and the second wing portion (30B) extend away from the aircraft body (20). The first wing portion (30A) and the second wing portion (30B) are configured to generate a first lift value during level flight of the aircraft (10) in the forward direction (F) when the first wing portion (30A) and the second wing portion (30B) are in an equilibrium position. Each of the first wing portion (30A) and the second wing portion (30B) is flexibly mounted relative to the aircraft body (20) such that when a lift force generated by the first wing portion (30A) changes from the first lift value to a second lift value, the first wing portion (30A) is deflected substantially vertically away from an equilibrium position. The aircraft (10) is configured to provide a further force to the first wing portion (30A) to substantially prevent further deflection of the first wing portion (30A) away from the equilibrium position.
A vehicle includes a propulsion unit configured to move the vehicle and to change a characteristic of the environment of the vehicle. The vehicle also includes a proximity sensor configured to detect the characteristic of the environment of the vehicle. The characteristic of the environment is changed by operation of the propulsion unit. The vehicle further includes obstacle detection circuitry configured to determine a presence of an obstacle in the vicinity of the vehicle based on a comparison between the detected characteristic of the environment and a reference value.
G05D 1/00 - Commande de la position, du cap, de l'altitude ou de l'attitude des véhicules terrestres, aquatiques, aériens ou spatiaux, p. ex. utilisant des pilotes automatiques
G06V 20/58 - Reconnaissance d’objets en mouvement ou d’obstacles, p. ex. véhicules ou piétonsReconnaissance des objets de la circulation, p. ex. signalisation routière, feux de signalisation ou routes
B64C 13/16 - Dispositifs amorçant la mise en œuvre actionnés automatiquement, p. ex. répondant aux détecteurs de rafales
B64C 39/02 - Aéronefs non prévus ailleurs caractérisés par un emploi spécial
G05D 1/02 - Commande de la position ou du cap par référence à un système à deux dimensions
There is provided a vehicle (18) comprising a propulsion unit (34) configured to move the vehicle (18) and to change a characteristic of the environment of the vehicle (18). The vehicle (18) further comprises a proximity sensor (19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31) configured to detect the characteristic of the environment of the vehicle. The characteristic of the environment is changed by operation of the propulsion unit (34). The vehicle (18) further comprises obstacle detection circuitry (32) configured to determine a presence of an obstacle in the vicinity of the vehicle based on a comparison between the detected characteristic of the environment and a reference value.
There is provided a vehicle (18) comprising a propulsion unit (34) configured to move the vehicle (18) and to change a characteristic of the environment of the vehicle (18). The vehicle (18) further comprises a proximity sensor (19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31) configured to detect the characteristic of the environment of the vehicle. The characteristic of the environment is changed by operation of the propulsion unit (34). The vehicle (18) further comprises obstacle detection circuitry (32) configured to determine a presence of an obstacle in the vicinity of the vehicle based on a comparison between the detected characteristic of the environment and a reference value.
09 - Appareils et instruments scientifiques et électriques
35 - Publicité; Affaires commerciales
41 - Éducation, divertissements, activités sportives et culturelles
42 - Services scientifiques, technologiques et industriels, recherche et conception
44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.
Produits et services
Databases (electronic); computer databases; databases for
the collation of information relating to companion animal
epidemiology; databases for the collation of information
relating to animal livestock; databases for the collation of
information relating to medical, pharmaceutical and
veterinary practices; databases for the collation and
compilation of clinical notes, research and data. Management and operation of a computer database in the
medical, pharmaceutical and veterinary fields; management
and operation of a computer database relating to companion
animal epidemiology; management and operation of a computer
database relating to animal livestock; data input and
compilation; compilation, collation and management of
information from medical and veterinary practices;
compilation, collation and management of clinical notes and
data; compilation, collation and management of primary data
and secondary data; compilation, collation and management of
medical and veterinary information and data for use in the
medical, pharmaceutical and veterinary fields; compilation,
analysis and retrieval of information and data; compilation
and systemisation of information into computer databases;
information, advisory and consultancy services relating to
all of the aforesaid. Education and training services in the medical,
pharmaceutical and veterinary fields; education and training
services in the field of companion animal epidemiology;
education and training services in the field of animal
livestock; educational and training information provided
from a computer database; veterinary, medical and
pharmaceutical educational and training information provided
from a computer database; companion animal epidemiology
educational and training information provided from a
computer database; animal livestock educational and training
information provided from a computer database; educational
and training services relating to the veterinary,
pharmaceutical and medical professions; educational and
training services relating to clinical data and research;
educational and training services relating to the use of a
computer database and the information contained therein;
information, advisory and consultancy services relating to
all of the aforesaid services. Scientific and technological services in the medical,
pharmaceutical and veterinary fields; research and
consulting services in the medical, pharmaceutical and
veterinary fields; design and development of a computer
database for the compilation, collation, analysis and
management of information in the medical, pharmaceutical and
veterinary fields; design and development of a computer
database for assisting with research in the medical,
pharmaceutical and veterinary fields; design and development
of a computer database for clinical research; research and
analytical services in the medical, pharmaceutical and
veterinary fields; scientific and research services in the
field of companion animal epidemiology; scientific and
research services in the field of animal livestock; design
and development of a computer database in the field of
companion animal epidemiology; design and development of a
computer database in the field of animal livestock; design
and development of a computer database for collating
clinical information; design and development of a computer
database for providing the medical, pharmaceutical and
veterinary industries with information and data collated
from clinical notes and research from medical and veterinary
practices; information, advisory and consultancy services
relating to all of the aforesaid. Provision of medical, veterinary and pharmaceutical
information to others; information services relating to the
medical, veterinary and pharmaceutical industries; provision
of information relating to clinical data and research;
provision of information to the veterinary, medical and
pharmaceutical industries relating to clinical data and
research; provision of information relating to companion
animal epidemiology; provision of information relating to
animal livestock; provision of information to the
veterinary, medical and pharmaceutical industries relating
to companion animal epidemiology; provision of information
to the veterinary, medical and pharmaceutical industries
relating to animal livestock; provision of research data in
the medical, pharmaceutical and veterinary fields; provision
of research data to the veterinary, medical and
pharmaceutical industries; information, advisory and
consultancy services relating to all of the aforesaid
services.
A preparation of an inactivated or freeze-dried yeast cell (or cell-surface-containing portion thereof) expressing a porcine viral epitope, wherein the epitope is expressed on the surface of the yeast cell. The yeast is typically is non-viable. The yeast is typically from the genus Saccharomyces, and is preferably Saccharomyces cerevisiae, but may be from the genus Pichia, for example Pichia pastoris, or may be from the genus Kluyveromyces, for example K. lactis. The viral epitope may be from a Coronavirus, optionally from PEDV, TGEV, porcine hemagglutinating encephalomyelitis virus or PRCV; a porcine Rotavirus; or a virus of the Circoviridae family, optionally from PCV2.
Low molecular weight hyaluronic acid (LMWHA) or very low molecular weight hyaluronic acid (VLMWHA) or PH20 for use in the culture of an embryo, zygote, blastocyst and/or an oocyte. A composition comprising low molecular weight hyaluronic acid (LMWHA) and/or very low molecular weight hyaluronic acid (VLMWHA) and/or PH20 may be used in the culture of an embryo, zygote, blastocyst and/or an oocyte. The LMWHA may be between 15kDa and 40kDa in size. The VLMWHA may be <10kDa, optionally the VLMWHA is a tetrasaccharide or a hexasaccharide, optionally the VLMWHA is 4-8 monosaccharides or less in size. A method for selecting an embryo or blastocyst generated through assisted fertilisation, optionally in vitro fertilisation or ICSI, as suitable for implantation, wherein the method comprises determination of the level of hyal-2 in the culture medium used to culture the embryo or blastocyst.
The present invention relates to compositions and methods for the treatment of obligate or facultative intracellular microorganisms, such as bacteria, fungi or parasites such as protozoan parasites. The present invention also relates to compositions and methods for enhancing immune cell activation, for example macrophage, dendritic cell, monocytes and lymphocyte activation, which is considered to be useful in treating infection, cancer and asthma, for example.
A method for assessing whether a test substance or treatment is potentially neuroprotective or anti-oxidant, the method comprising the steps of exposing a cell to the test substance or treatment assessing the TSPO level in the cell, wherein a substance or treatment is considered to be potentially anti-oxidant and/or neuroprotective if the TSPO level is decreased. The method may comprise the step of assessing the level of mitophagy in the cell, wherein a substance or treatment is considered to be anti-oxidant or neuroprotective if the level or induction of mitophagy is increased and the TSPO level is decreased.
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques
The disclosure relates to a sole (10) for an item of footwear (12), comprising: a toe portion (14); a heel portion (16); and a kinetic energy absorbing member (18) situated between heel and toe portions and having an extended position in which the kinetic energy absorbing member protrudes further from the sole than the heel portion and a retracted position in which the kinetic energy absorbing member protrudes no further from the sole than the heel portion.
A sole for an item of footwear comprising: • a front portion; • a heel portion; and • a energy absorbing member positioned within the front portion, and having a first position in which the energy absorbing member protrudes from the sole, and a second position in which the energy absorbing member is substantially level with a surface of the sole.
A compound comprising a C-type lectin Carbohydrate Recognition Domain (CRD) and an immunoglobulin Fc domain for use in treating or preventing a pathogen infection in a non-human, non-murine subject. Preferably the non-human, non-murine subject is not considered to be an immunocompromised or immunosuppressed subject. The non- human, non-murine subject may be a ruminant; a livestock; companion or racing animal. The CRD, immunoglobulin Fc domain and the non-human, non-murine subject may be bovine. The pathogen infection typically comprises infection by a bacterium, optionally Staphylococcus aureus or Streptococcus Uberis or Streptococcus Agalactiae/dysgalactiae. The subject (for example bovine subject) may have mastitis, subclinical mastitis, actue mastitis, chronic mastitis, high somatic cell count (high SSC), metritis or endometritis. The non-human, non-murine subject may typically be further administered an antibiotic or antifungal agent. The CRD may be from bovine Mannose binding Lectin (MBL) and the immunoglobulin Fc domain may be an lgG1 Fc domain.
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61K 39/395 - AnticorpsImmunoglobulinesImmunsérum, p. ex. sérum antilymphocitaire
A plasmid for transforming Mycoplasma hyopneumoniae comprising an OriC region comprising both AT-rich regions from a predicted OriC region of M. hyopneumoniae 232, or comprising a variant thereof that retains the ability to act as an OriC region in M. hyopneumoniae and has at least 90% sequence identity with a sequence comprising both AT-rich regions from a predicted OriC region of M. hyopneumoniae 232. A M. hyopneumoniae cell transformed with a plasmid of the invention may be useful in a vaccine composition. A nucleic acid construct comprising a nucleic acid sequence encoding a transposase enzyme and a promoter sequence, wherein the promoter sequence is active in M. hyopneumoniae; optionally wherein the promoter sequence comprises a promoter sequence from M. hyopneumoniae, or spiralin gene promoter of Spiroplasma citri or tetM promoter sequence from S. aureus; optionally wherein the promoter sequence from M. hyopneumoniae is a constitutively active promoter sequence, optionally a promoter sequence from the M. hyopneumoniae ldh, P97, secD, Tuf, rpoB, P146, ATP transporter ATP binding protein, Asparagine-tRNA synthetase or Translation elongation factor gene. The transposase enzyme may be a Mariner family transposase, optionally Himar1 transposase or Himar1 C9 mutant transposase.
A method for promoting entry of an agent (introduced agent) into a cell, the method comprising the step of complexing the introduced agent in the presence of an entry- promoting agent and then exposing to cells, wherein the entry-promoting agent comprises a linear and/or branched or cyclic polymonoguanide/polyguanidine, polybiguanide, analogue or derivative thereof according to the following Formula 1a &b. The method also provides a means for formation of nanoparticles formed between the entry promoting agent and the introduced agent. wherein: "n", refers to number of repeating units in the polymer, and n can vary from 2 to 1000, for example from 2 or 5 to 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450, 500, 600, 700, 800 or 900; G1 and G2 independently represent a cationic group comprising biguanide or guanidine, wherein L1, and L2 are directly joined to a Nitrogen atom of the guanide; L1 and L2 are linking groups between the G1 and G2 cationic groups in the polymer and independently represent an aliphatic group containing C1-C40 carbon atoms, for example an alkyl group such as methylene, ethylene, propylene, C4, C5, C6, C7, C8, C9 or C10; C1-C10, -C20, - C30, -C40, -C50 -C60 -C70, -C80, -C90, -C-100, -C110, -C120, -C130 or -C140, alkyl; or a C1-C140 (for example C1 , C2,C3, C4, C5, C6, C7, C8, C9 or C10; C1-C10, -C20, -C30, -C40, -C50 -C60, -C70, -C80, - C90, -C100, -C110, -C120, -C130o or -C140), cycloaliphatic, heterocyclic, aromatic, aryl, alkylaryl, arylalkyl, or oxyalkylene radical; or a polyalkylene radical optionally interrupted by one or more, preferably one, oxygen, nitrogen or sulphur atoms, functional groups or saturated or unsaturated cyclic moiety; N and G3 are optional end groups; X can be either present or absent; L3, L4 and X are linking groups between the G4 and G5 cationic groups in the polymer and independently represent an aliphatic group containing C1-C140 carbon atoms, for example an alkyl group such as methylene, ethylene, propylene, C4, C5, C6, C7, C8, C9 or C10; C1-C10, -C20, -C30, - C40, -C50 -C60, -C70, -C80, -C90, -C100, -C110, -C120, -C130 or -C140, alkyl; or L3 and L4 and X can independently be C1-C140 (for example C1,C2, C3, C4, C5, C6, C7, C8, C9 or C10; C1-C10, -C20, -C30, -C40, -C50 -C60, -C70, -C80, -C90, -C100, -C110, -C120, -C130 or -C140), cycloaliphatic, heterocyclic, aromatic, aryl, alkylaryl, arylalkyl, oxyalkylene radicals; or a polyalkylene radical optionally interrupted by one or more, preferably one, oxygen, nitrogen or sulphur atoms, functional groups as well as saturated or unsaturated cyclic moiety; "G4" and "G5" are cationic moieties and can be same or different, and at least one of them is a biguanidine moiety or carbamoylguanidine, and the other moiety may be biguanidine or carbamoylguanidine or amine; and cationic moieties G4 and G5 do not contain single guanidine groups. The entry-promoting agent may comprise homogeneous or heterogeneous mixture of one or more of agents arising from formulae 1 a and b, for example polyhexamethylene biguanide (PHMB), polyhexamethylene monoguanide (PHMG), polyethylene biguanide (PEB), polytetramethylene biguanide (PTMB), polyethylene hexamethylene biguanide (PEHMB), polymethylene biguanides (PMB), poly(allylbiguanidnio-co-allylamine), poly(N- vinylbiguanide), polyallybiguanide.
A61K 47/48 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p.ex. supports, additifs inertes l'ingrédient non actif étant chimiquement lié à l'ingrédient actif, p.ex. conjugués polymère-médicament
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
C12N 15/87 - Introduction de matériel génétique étranger utilisant des procédés non prévus ailleurs, p. ex. co-transformation
A device comprising an ambulatory aid, the device comprising a distal end, a load, a first portion positioned at, or close to the distal end and adapted to allow the device to move along a surface, a second portion spaced apart from the first portion and the distal end and adapted to allow a user to be attached to, or hold the device, and a power unit operably connected to the first portion, the device having a deployed position in which the device is moveable, and is supported by the user, movement of the device being powered by the power unit.
Carriers are provided for transport of a substance across the blood-brain barrier. The carriers comprise an antibody specific for a target antigen, in particular, antibodies capable of binding to prion proteins. The antibodies are produced via methods which include adding a target antigen stabilising agent to a sample containing a target antigen, allowing the stabilising agent to stabilise the target antigen, incubating the stabilised target antigen with a conventional antibody immobilised on a solid support to form a complex, wherein the immobilised antibody is specific for the target antigen, immunising a host with the complex, and isolating antibodies specific for the target antigen from the host. Also provided are use of the carriers in treatment and diagnosis of disease, e.g. prion diseases.
Methods are provided for producing an antibody specific for a target antigen, in particular, antibodies capable of binding to prion proteins. The methods include adding a target antigen stabilising agent to a sample containing a target antigen, allowing the stabilising agent to stabilise the target antigen, incubating the stabilised target antigen with a conventional antibody immobilised on a solid support to form a complex, wherein the immobilised antibody is specific for the target antigen, immunising a host with the complex, and isolating antibodies specific for the target antigen from the host. Also provided are antibodies produced by the methods together with their use in treatment and diagnosis of disease, e.g. prion diseases.
C07K 16/28 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant d'animaux ou d'humains contre des récepteurs, des antigènes de surface cellulaire ou des déterminants de surface cellulaire
A61K 47/48 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p.ex. supports, additifs inertes l'ingrédient non actif étant chimiquement lié à l'ingrédient actif, p.ex. conjugués polymère-médicament
A61K 39/395 - AnticorpsImmunoglobulinesImmunsérum, p. ex. sérum antilymphocitaire
G01N 33/577 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet faisant intervenir des anticorps monoclonaux
40.
PROTECTION OF AN ANIMAL AGAINST PESTIVIRUS INFECTION
This invention involves compositions and methods for protecting animals from pestivirus infection and for treating animals infected with pestivirus. Pharmaceutical compositions containing E2 and NS3 from a pestivirus are used to protect animals or treat animals.
Apparatus for identifying sub-optimal performance in a race animal comprises means for measuring frequency of stride of the race animal, means for measuring speed of the animal and means for processing data. The data processing means is configured to receive and process said stride frequency and speed in a predetermined manner so as to identify a predetermined physiological condition such as fatigue in the race animal. Also disclosed are apparatus for measuring performance of a rider.
A61B 5/103 - Dispositifs de mesure pour le contrôle de la forme, du dessin, de la dimension ou du mouvement du corps ou de parties de celui-ci, à des fins de diagnostic
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
42.
DRUG DELIVERY SYSTEM COMPRISING MATRIX METALLOPROTEINASE INHIBITORS
A composition for topical application to a subjects skin comprising a matrix metalloproteinase inhibitor, more particularly an inhibitor selected from the group consisting of : TIMP-I, TIMP-2, TIMP-3, TIMP-4, Ilomastat, MMP inhibitor 111, CL82198, GM1489, and FN-439 is used for the prevention or treatment of soft skeletal tissue extracellular matrix degeneration, more particularly wherein the soft skeletal tissue is a tendon or ligament, and more particularly where the tendon is -selected from the group consisting of : superficial digital flexor tendon (SDFT), suspensory ligament, deep flexor tendon, deep digital flexor tendon (DDFT), accessory ligament of the deep digital flexor tendon, cruciate ligament, Achilles tendon, flexor tendon, quadriceps tendon, rotator cuff, and lateral or medial epichondylitis, and more particularly wherein the musculoskeletal injury or disorder is selected from superficial digital flexor tendinopathy and suspensory ligament desmitis, Achilles tendon injuries, rotator cuff injury, lateral epicondylitis, medial epicondylitis and patellar tendinopathy.
A spermatozoa diluent comprising isolated Hsc70 protein, in which the Hsc70 has sperm viability improving and/or prolonging activity. Also disclosed are compositions comprising the diluent, methods of prolonging/improving sperm viability and use of the diluent to prolong/improve sperm viability.
A method of identifying an agent which modulates at least one activity or function of the Mycobacterium tuberculosis protein Rv3574 or an orthologue thereof from another actinomycete, the method comprising providing Rv3574 or the orthologue thereof, providing double stranded DNA (dsDNA) comprising the sequence X1X2X3AACX4X5GTX6X7X8X9 (SEQ ID No: 2) under conditions which allow the Rv3574 or the orthologue to bind to the dsDNA, providing a test agent, and determining whether the test agent modulates at least one activity or function of the M. tuberculosis Rv3574 or the orthologue thereof.
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques
45.
TOPICAL APPLICATION OF FSH, LH, TSH OR CG TO THE CERVIX
A method of inducing relaxation of the cervix of a female mammal, the method comprising administering at least one pharmaceutical agent selected from follicle stimulating hormone or a beta-subunit thereof, luteinizing hormone or a beta- subunit thereof, thyroid stimulating hormone or a beta-subunit thereof, and chorionic gonadotrophin or a beta-subunit thereof, topically to the cervix of the mammal. The method can be used to facilitate artificial insemination of the female mammal. Also provided are medicinal formulations containing one or more of these hormones formulated as topical preparations or vaginal suppositories. A device comprising a sponge or foam impregnated with the hormone or hormone mixture is also provided.
A61P 15/08 - Médicaments pour le traitement des troubles génitaux ou sexuelsContraceptifs pour les troubles gonadiques ou pour augmenter la fertilité, p. ex. inducteurs d'ovulation ou de spermatogénèse
A61K 9/00 - Préparations médicinales caractérisées par un aspect particulier
46.
DETECTION OF ACETYLATION OF PROKARYOTIC PROTEINS BY MASS SPECTROMETRY
A method of identifying an N-terminally acetylated protein in a bacterium, the method comprising providing details of at least one putative translation start site (TSS) for at least one protein expressed in the bacterium, confirming the actual TSS of the at least one protein using mass spectrometry (MS), and determining whether the at least one protein is N-terminally acetylated using MS. A method of identifying an N-terminally acetylated protein in a bacterium, the method comprising providing a mutant strain of the bacterium comprising at least one protein N-acetyl transferase (pNAT) in mutant form, providing a wild-type strain of the bacterium comprising the at least one pNAT in wild-type form, and identifying a protein that is differentially N-terminal acetylated between the mutant and wild-type bacterial strains. A method of identifying a drug discovery target in a pathogenic bacterium, the method comprising determining at least one property of an N-terminally acetylated protein expressed in a pathogenic bacterium and which is relevant to the pathogenicity of the pathogenic bacterium. A method of identifying a bacterial pNAT. A method of screening for an inhibitor of a bacterial pNAT.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
47.
USE OF ANTI-VIMENTIN ANTIBODIES IN DIAGNOSIS OF HYPERTENSION OR HEART FAILURE
A method for predicting or diagnosing hypertension in a mammal, the method comprising detecting the presence and/or level of anti-vimentin antibodies in a suitable sample obtained from the mammal. A method for predicting or diagnosing heart disease in a mammal, the method 0 comprising detecting the presence and/or level of anti-vimentin antibodies in a suitable sample obtained from the mammal.
G01N 33/564 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour complexes immunologiques préexistants ou maladies auto-immunes
48.
TREATMENT OF EQUINE LAMINITIS WITH 5-HT1B/ 1D ANTAGONISTS
There is provided the use of a compound of general formula (I): in which: R1 represents hydrogen, halogen, C1-6 alkyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, C1-6 alkoxy, hydroxy C1-6 alkyl, C1-6alkylOC1-6 alkyl, acyl, aryl, acyloxy, hydroxy, nitro, trifluoromethyl, cyano, CO2R29, CONR30 R31 or NR30R31; R2 represents a phenyl group, having phenyl ring B, substituted by a group selected from i) a 5 to 7 membered heterocyclic ring containing three heteroatoms selected from oxygen, nitrogen or sulphur, optionally substituted by a substituent selected from halogen, C1-6 alkyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, C1-6 alkoxy, hydroxy C1-6 alkyl, C1-6 alkyl OC1-6 alkyl, acyl, aryl, acyloxy, hydroxy, nitro, trifluoromethyl, cyano, CO2R29, CONR30 R31 NR30 R31, or NR30R31, formula (ii): or formula (iii): and optionally further substituted by one or two auxiliary substituents selected from a halogen atom, a hydroxy group, a C1-6 alkyl group, or by an auxiliary substituent selected from C3-6 cycloalkyl, C3-6 cycloalkenyl, hydroxy C1-6 alkyl, C1-6 alkylOC1-6alkyl, acyl, aryl, acyloxy, nitro, trifluoromethyl, cyano, CO22R29, CONR30 R31, or NR30 R31; D is CONH or NHCO; E is formula (A): or G-(CR24 R25)-NR27R28 where R5 represents a hydrogen atom or a C1-6 alkyl group, G is oxygen, S(O)p where p is 0, 1, or 2, NR32 where R32 is hydrogen, C1-6 alkyl or phenyl C1-6 alkyl, or G is CR24 = CR25 or CR24 R25 where R24 and R25 are independently hydrogen or C1-6 alkyl; F is hydrogen, a halogen atom, a hydroxy group, a C1-6 alkoxy group, a C1-6 alkyl group or a halogenated C1-6 alkyl group; R27 and R28 are independently hydrogen, C1-6 alkyl, aralkyl, or together with the nitrogen atom to which they are attached form an optionally substituted 5-to 7-membered heterocyclic ring containing one or two heteroatoms selected from oxygen, nitrogen or sulphur; R29, R30 and R31 are independently hydrogen or C1-6 alkyl; m is 1 to 4; and n is 1 or 2 or a physiologically acceptable salt or solvate thereof in the manufacture of a medicament for the treatment or prophylaxis of laminitis.
A61K 31/41 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à cinq chaînons avec plusieurs hétéro-atomes cycliques, l'un au moins étant l'azote, p. ex. tétrazole
A61K 31/4402 - Pyridines non condenséesLeurs dérivés hydrogénés substituées uniquement en position 2, p. ex. phéniramine, bisacodyl
A61K 31/4406 - Pyridines non condenséesLeurs dérivés hydrogénés substituées uniquement en position 3, p. ex. zimeldine
A61K 31/4409 - Pyridines non condenséesLeurs dérivés hydrogénés substituées uniquement en position 4, p. ex. isoniazide, iproniazide
A61K 31/495 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec deux azote comme seuls hétéro-atomes d'un cycle, p. ex. pipérazine
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
A61K 31/5377 - 1,4-Oxazines, p. ex. morpholine non condensées et contenant d'autres hétérocycles, p. ex. timolol
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale