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HUMAN PROTEIN TYROSINE PHOSPHATASE INHIBITORS AND METHODS OF USING SAID INHIBITORS
专利权人:
DZE PROKTER EHND GEHMBL KOMPANI
发明人:
GREhJ Dzheffri Lajl (US),ГРЭЙ Джеффри Лайл (US),AMARASINGE Kande (US),АМАРАСИНГЕ Канде (US),KLARK Sintija Moneza (US),КЛАРК Синтия Монеза (US),MAJER Meht'ju Brajan (US),МАЙЕР Мэтью Брайан (US),NIKOLS,GREHJ DZHEFFRI LAJL,AMARASINGE KANDE,KLARK SINTIJA MONEZA,MAJER MEHTJU BRAJAN,NIKOLS RAJAN,НИКОЛС Райан (U
申请号:
RU2009102516/04
公开号:
RU0002447065C2
申请日:
2007.06.27
申请国别(地区):
RU
年份:
2012
代理人:
摘要:
FIELD: chemistry.SUBSTANCE: invention relates to a compound of formula,where R denotes a substituted or unsubstituted thiazolyl group of formula or ; R4 and R5, each independently, are selected from i) hydrogen; ii) a substituted or unsubstituted C1-C6 linear, C3-C6 branched or C3-C6 cyclic alkyl; iii) a substituted or unsubstituted phenyl; iv) a substituted or unsubstituted heteroaryl containing 5 or 6 ring atoms and 1 or 2 heteratoms, where the heteroatoms are selected from nitrogen, oxygen, sulphur and combination thereof; or R4 and R5 can be taken together to form a saturated or unsaturated ring, having 5-7 atoms; said substitutes are independently selected from one or more groups, selected from C1-C6 linear, C3-C6 branched or C3-C6 cyclic alkyl, halogen, hydroxyl or cyano; R6 denotes a group selected from i) hydrogen; ii) a substituted or unsubstituted C1-C6 linear, C3-C6 branched or C3-C6 cyclic alkyl; iii) a substituted or unsubstituted phenyl or iv) a substituted or unsubstituted heteroaryl containing 5 or 6 ring atoms and 1 or 2 heteroatoms, where the heteroatoms are selected from nitrogen, oxygen, sulphur and combination thereof; where said substitutes are independently selected from one or more groups selected from C1-C6 linear, C3-C6 branched or C3-C6 cyclic alkyl, halogen, hydroxyl or cyano; R1 is selected from i) hydrogen; ii) C1-C6 linear or C3-C6 branched alkyl; iii) a substituted or unsubstituted phenyl or iv) a substituted or unsubstituted benzyl; where said substitutes are independently selected from one or more groups selected from C1-C6 linear, C3-C6 branched or C3-C6 cyclic alkyl, halogen, hydroxyl or cyano; R2 is selected from i) C1-C6 linear or C3-C6 branched alkyl or ii) C1-C6 linear or C3-C6 branched alkoxy; R3 denotes hydrogen or C1-C4 linear or C3-C6 branched alkyl.EFFECT: compounds of formula (I) are effective as human protein tyrosine phosphatase beta (HPTP-β) inhibitors.20 cl, 10 tbl, 8 exИзобретение относится к соединению, имеющему
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