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Thieno derivative and / or Furobeta pyridines and pyrimidines of Potassium Channel inhibitors
专利权人:
XENTION LIMITED
发明人:
FIONA CHAN,DEREK EDWARD JOHN,SIMON D. EDWARDS,LINDSAY BROWN,BASIL HARTZOULAKIS,DAVID MADGE,RICHARD BLUNT
申请号:
ARP120104296
公开号:
AR090037A1
申请日:
2012.11.14
申请国别(地区):
AR
年份:
2014
代理人:
摘要:
Claim 1: a compound characterized by formula (1) or a pharmaceutically acceptable derivative, characterized by: A is or s; X is n or Cr * II; V is n or Cr * III; Z is n or Cr * IV; wherein 1 or 2 is V, X and Z are n; R1 is selected from the optional alternative asphalt and optionally replaces cycloarmour. R2 was selected from h, halo, - CN, trifluometyl, alternative, alcox alternative, - nr8308; - r83099;-No. 8310; (c) r8311;-No. 8310; (s (o) 8322; r831181;-S (o) 8322; - 8308; - r83099;-CONR⁴R⁵,-CO₂R⁷,Substituted oxazolinilo, - sr8308;-S (O) R y -S (O) RR3: I from h, halo CN, trifluometilo, optional replacement asphalt, optional replacement alcox, optional replacement heterocyclic hyperoxia, - No. 8310;; C (o) r8311;-No. 8310; (s (o) 8322; r831181;-S (o) 8322; - 8308; - r83099;-CONR⁴R⁵,-CO₂R⁷,-8312; 8313;-C ° C-J, optionally substituted cycloalkyl-J and - (NRᵃRᵇ) -J; each of R³II, R³III, and R³IV is independently selected from H, halo, -CN, trifluoromethyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted heterocycloalkoxy, optionally substituted heterocycloalkylalkyl, -NR⁶C (O) R⁷,-No. 8310; (s (o) 8322; r831181;-S (o) 8322; - 8308; - r83099;-CONR⁴R⁵,-Lessor - conr8308; - No. 83099 optional replacement, - No. co8322; - No. 831181;-No. 830404; R1,-C CJ cicloalquil-J opcionalmente sustituido y - (NR R) -J con la condici n de que R es -C CJ cicloalquil-J opcionalmente sustituido o - (NR R) -J y 2Fo al menos uno de R II R III - that is...That's it, that's it.wherein the optionally substituted heterocycloalkyl ring that optionally forms a bridge is selected from the group consisting of azetidinyl, pyrrolidinyl, piperidinyl, morpholinyl, tetrahydro-1,3-oxazinyl, hexahydropyrimidinyl, 1,4-thiazanyl, azepanyl, 1,4-oxaazepanyl , and 1,4-tieazepanyl; where Rᶜ and Rᵈ join to form an optionally substituted 4- and 7-membered heterocycloalkyl ring, which is optionally linked to form a bridge, optionally substituted C₁₋₂ alkylene, -NR⁶-,- that i
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