http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RS-52711-B

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a73cee5001ad08339ae751c10d9abf71
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filingDate 2006-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93f836b99512f2719ae3e9542c22df85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a76e8bc72a90ebbf0e7e005360bcbfe
publicationDate 2013-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RS-52711-B
titleOfInvention INDOLAMIN 2,3-DIOXYGENASE MODULATORS AND PROCEDURES FOR USING THE SAME
abstract A compound of formula: or a pharmaceutically acceptable salt thereof, wherein: W, X1 and X2 are independently selected from the group consisting of (CRaRb)t, (CRaRb)uO(CRaRb)v, (CRaRb)uC(O)(CRaRb) v, (CRaRb)uC(O)NRc(CRaRb)v, (CRaRb)uC(O)O(CRaRb)v, (CRaRb)uC(S)(CRaRb)u, (CRaRb)uC(S)NRc(CRaRb )y, (CRaRb)uS(O)(CRaRb)v, (CRaRb)uS(O)NRc(CRaRb)v, (CRaRb)uS(O)2(CRaRb)v, (CRaRb)uS(O)2NRc( CRaRb)v, (CRaRb)uNRc(CRaRb)v and (CRaRb)uC(=NRd)NRC(CRaRb)v group; R2 represents H, C1-6 alkyl or C3-7 cycloalkyl group; R3a and R5a are independently selected from the group consisting of C1-8 alkyl, C2-8 alkenyl, C2-8 alkynyl, aryl, cycloalkyl, heteroaryl and heterocycloalkyl groups each of which may be optionally substituted with 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen , C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-4 haloalkyl, cyanine1, cyanide, NO2, ORe1, SRe1, C(O)Rf1, C(O)NRg1Rh1, C(O)ORe1, OC (O)Rf1, OC(O)NRg1Rh1, NRg1C(O)NRg1Rh1, NRg1Rh1, NRg1C(O)Rf1, NRg1C(O)ORe1, C(=NRi)NRg1Rh1, NRg1C(=NRi)NRg1Rh1, P(Rf1) 2, P(ORe1)2, P(O)Re1Rf1, P(O)ORe1ORf1, S(O)Rf1, S(O)NRg1Rh1, S(O)2Rf1 and S(O)2NRg1Rh1 group; R3b represents aryl or heteroaryl group each of which may be optionally substituted with 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-4 haloalkyl, C1-4 hydroxyalkyl, cyanine2, cyanide, NO2, ORe1, SRe1, C(O)Rf1, C(O)NRg1Rh1, C(O)ORe1, OC(O)Rf1, OC(O)NRg1Rh1, NRa1C(O)NRg1Rh1, NRg1Rh1, NRg1C(O)Rf1, NRg1C(O)ORe1, C(=NRi)NRg1Rh1, NRg1C(=NRi)NRg1Rh1, P(Rf1)2, P(ORe1)2, P(O)Re1Rf1, P(O)ORe1ORf1, S(O)Rf1, S(O)NRg1Rh1, S(O)2Rf1 and S(O)2NRg1Rh1 group; R5b represents H, C1-8 alkyl, C2-8 alkenyl, C2-8 alkynyl, aryl, cycloalkyl, heteroaryl or heterocycloalkyl group, characterized in that each said C1-8 alkyl, C2-8 alkenyl, C2-8 alkynyl, aryl, cycloalkyl, heteroaryl or heterocycloalkyl group may be optionally substituted with 1, 2, 3, 4 or 5 substituents independently selected from groups consisting of halogen, alkyl, C1-6 alkenyl, C 2-6 alkynyl, C2-6 haloalkyl, C1-4 hydroxyalkyl, cyanine2, cyanide, NO2, ORe1, SRe1, C(O)Rf1, C(O)NRg1Rh1, C(O)ORe1, OC(O)Rf1, OC (O)NRg1Rh1, NRg1C(O)NRg1Rh1, NRg1Rh1, NRg1C(O)Rf1, NRg1C(O)ORe1, C(=NRi)NRg1Rh1, NRg1C(=NRi)NRg1Rh1, P(Rf1)2, P(ORe1)2 , P(O)Re1Rf1, P(O)ORe1ORf1, S(O)Rf1, S(O)NRg1Rh1, S(O)2Rf1 and S(O)2NRg1Rh1 groups; cyanine1 and cyanine2 are independently selected from the group consisting of aryl, heteroaryl, cycloalkyl and heterocycloalkyl groups each of which may be optionally substituted with 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen, C1-4 alkyl, C2-4 alkenyl, C2-4 alkynyl, C1-4 haloalkyl, cyanide, NO2, ORe3, SRc3, C(O)Rf3, C(O)NRg3Rh3, C(O)ORe3, OC(O)Rf3, OC(O)NRg3Rh3, NRg3Rh3, NRg3C(O)Rh3, NRg3C( O)ORe3, C(=NRi)NRg1Rh1, NRg1C(=NRi)NRg1Rh1, P(Rf3)2, P(ORe3), P(O)Re3Rf3, P(O)ORe3ORf3, S(O)Rf3, S(O )NRg3Rh3, S(O)2Rf3 and S(O)2NRg3Rh3 groups; Ra and Rb are independently selected from the group consisting of H, halogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-4ha
priorityDate 2005-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559548
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5975

Total number of triples: 49.