http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-534990-A

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filingDate 2003-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fb352b1d14977a57ef48a05141fa379
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6380a621eeb31e882a9f78badc450a6
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publicationDate 2006-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-534990-A
titleOfInvention Heterocyclic amide derivatives as inhibitors of glycogen phosphorylase
abstract Heterocyclic amide derivatives of formula 1 having glycogen phosphorylase inhibitory activity are described wherein: --- is a single or double bond; X is N or CH; R4 and R5 together are either -S-C(R6)=C(R7)- or -C(R7)=C(R6)-S-; R6 and R7 are independently selected from hydrogen, halo, nitro, cyano, hydroxy, fluoromethyl, difluoromethyl, trifluoromethyl, trifluoromethoxy, carboxy, carbamoyl, C1-4alkyl, C2-4alkenyl, C2-4alkynyl, C1-4alkoxy and C1-4alkanoyl; A is phenylene or heteroarylene; n is 0, 1 or 2; R1 is independently selected from halo, nitro, cyano, hydroxy, carboxy, carbamoyl, N-C1-4alkylcarbamoyl, N,N-(C1-4alkyl)2carbamoyl, sulphamoyl, N-C1-4alkylsulphamoyl, N,N-(C1-4alkyl)2sulphamoyl, -S(O)bC1-4alkyl (wherein b is 0, 1, or 2), C1-4alkyl, C2-4alkenyl, C2- 4alkynyl, C1-4alkoxy, C1-4alkanoyl, C1-4alkanoyloxy, hydroxyC1-4alkyl, fluoromethyl, difluoromethyl, trifluoromethyl and trifluoromethoxy ; or when n is 2, the two R1 groups, together with the carbon atoms of A to which they are attached, may form a 4 to 7 membered ring, optionally containing 1 or 2 heteroatoms independently selected from O, S and N, and optionally being substituted by one or two methyl groups; R2 is hydrogen, hydroxy or carboxy; R3 is selected from hydrogen, hydroxy, C1-4alkoxy, C1-4alkanoyl, carbamoyl, C3-7cycloalkyl (optionally substituted with 1 or 2 hydroxy groups), cyano(C1-4)alkyl, aryl, heterocyclyl, C1- 4alkyl (optionally substituted), and groups of the formulae B and B' wherein y is 0 or 1, t is 0, 1,2 or 3 and u is 1 or 2; provided that the hydroxy group is not a substituent on the ring carbon adjacent to the ring oxygen; with the proviso that the compound of formula (1) is not: (i) 2,3-dichloro-5-[N-2-oxo-1,2,3,4-tetrahydroquinol-3-yl)carbamoyl]-4H-thieno[3,4-b]pyrrole; (ii) 2-chloro-5-[N-(2-oxo-1,2,3,4-tetrahydroquinol-3-yl)carbamoyl]-6H-thieno[2,3- b]pyrrole; (iii) 2-chloro-5-[N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinol-3-yl)carbamoyl]-6H- thieno [2, 3-b]pyrrole. Pharmaceutical compositions comprising the compounds are useful for treating type 2 diabetes, insulin resistance, syndrome X, hyperinsulinaemia, hyperglucagonaemia, cardiac ischemia and obesity
priorityDate 2002-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 451.