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Machine translation
1. (WO2004094380) (PIPERIDINYLOXY)PHENYL, (PIPERIDINYLOXY)PYRIDINYL, (PIPERIDINYLSULFANYL)PHENYL AND (PIPERIDINYLSULFANYL)PYRIDINYL COMPOUNDS AS 5-HT1F AGONISTS
Latest bibliographic data on file with the International Bureau   

Pub. No.:    WO/2004/094380    International Application No.:    PCT/US2004/009283
Publication Date: 04.11.2004 International Filing Date: 14.04.2004
IPC:
C07D 211/44 (2006.01), C07D 211/54 (2006.01), C07D 401/12 (2006.01), C07D 401/14 (2006.01), C07D 409/12 (2006.01)
Applicants: ELI LILLY AND COMPANY [US/US]; Lilly Corporate Center, Indianapolis, IN 46285 (US) (For All Designated States Except US).
BLANCO-PILLADO, Maria-Jesus [ES/US]; (US) (For US Only).
BENESH, Dana, Rae [US/US]; (US) (For US Only).
FILLA, Sandra, Ann [US/US]; (US) (For US Only).
HUDZIAK, Kevin, John [US/US]; (US) (For US Only).
MATHES, Brian, Michael [US/US]; (US) (For US Only).
KOHLMAN, Daniel, Timothy [US/US]; (US) (For US Only).
YING, Bai-Ping [US/US]; (US) (For US Only).
ZHANG, Deyi [US/US]; (US) (For US Only).
XU, Yao-Chang [US/US]; (US) (For US Only)
Inventors: BLANCO-PILLADO, Maria-Jesus; (US).
BENESH, Dana, Rae; (US).
FILLA, Sandra, Ann; (US).
HUDZIAK, Kevin, John; (US).
MATHES, Brian, Michael; (US).
KOHLMAN, Daniel, Timothy; (US).
YING, Bai-Ping; (US).
ZHANG, Deyi; (US).
XU, Yao-Chang; (US)
Agent: TUCKER, Craig, R.; Patent Division, Eli Lilly and Company, P.O. Box 6288, Indianapolis, IN 46206-6288 (US)
Priority Data:
60/464,396 18.04.2003 US
Title (EN) (PIPERIDINYLOXY)PHENYL, (PIPERIDINYLOXY)PYRIDINYL, (PIPERIDINYLSULFANYL)PHENYL AND (PIPERIDINYLSULFANYL)PYRIDINYL COMPOUNDS AS 5-HT1F AGONISTS
(FR) COMPOSES (PIPERIDINYLOXY)PHENYLE, (PIPERIDINYLOXY)PYRIDINYLE, (PIPERIDINYLSULFANYL)PHENYLE ET (PIPERIDINYLSULFANYL)PYRIDINYLE UTILISES COMME AGONISTES DES RECEPTEURS 5-HT1F
Abstract: front page image
(EN)The present invention relates to compounds of formula 1: and pharmaceutically acceptable acid addition sails thereof. The compounds of the present invention are useful for activating 5-HTIF receptors, inhibiting neuronal protein extravasation, and for the treatment or preverition of migraine in mammals, particularly humans.
(FR)La présente invention concerne des composés correspondant à la formule (I), ainsi que des sels d'addition d'acide de ceux-ci pharmaceutiquement acceptables. Lesdits composés peuvent être utilisés pour l'activation des récepteurs 5-HTIF, pour l'inhibition de l'extravasion de protéine neuronale, et pour le traitement ou la prévention de la migraine chez les mammifères, en particulier chez l'homme.
Designated States: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BW, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NA, NI, NO, NZ, OM, PG, PH, PL, PT, RO, RU, SC, SD, SE, SG, SK, SL, SY, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, YU, ZA, ZM, ZW.
African Regional Intellectual Property Organization (BW, GH, GM, KE, LS, MW, MZ, SD, SL, SZ, TZ, UG, ZM, ZW)
Eurasian Patent Organization (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM)
European Patent Office (AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HU, IE, IT, LU, MC, NL, PL, PT, RO, SE, SI, SK, TR)
African Intellectual Property Organization (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, ML, MR, NE, SN, TD, TG).
Publication Language: English (EN)
Filing Language: English (EN)