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TargetSomatostatin receptor type 3
LigandBDBM50091414
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1498170 (CHEMBL3583390)
IC50 0.600000±n/a nM
Citation Shah, SKHe, SGuo, LTruong, QQi, HDu, WLai, ZLiu, JJian, THong, QDobbelaar, PYe, ZSherer, EFeng, ZYu, YWong, FSamuel, KMadiera, MKaranam, BVReddy, VBMitelman, STong, SXChicchi, GGTsao, KLTrusca, DFeng, YWu, MShao, QTrujillo, MEEiermann, GJLi, CPachanski, MFernandez, GNelson, DBunting, PMorissette, PVolksdorf, SKerr, JZhang, BBHoward, ADZhou, YPPasternak, ANargund, RPHagmann, WK Discovery of MK-1421, a Potent, Selective sstr3 Antagonist, as a Development Candidate for Type 2 Diabetes. ACS Med Chem Lett6:513-7 (2015) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Somatostatin receptor type 3
Name:Somatostatin receptor type 3
Synonyms:SOMATOSTATIN SST3 | SSR3_RAT | Somatostatin receptor | Somatostatin receptor 3 | Somatostatin receptor type 3 | Sstr3
Type:Enzyme Catalytic Domain
Mol. Mass.:47161.54
Organism:RAT
Description:SOMATOSTATIN SST3 SSTR3 RAT::P30936
Residue:428
Sequence:
MAAVTYPSSVPTTLDPGNASSAWPLDTSLGNASAGTSLAGLAVSGILISLVYLVVCVVGL
LGNSLVIYVVLRHTSSPSVTSVYILNLALADELFMLGLPFLAAQNALSYWPFGSLMCRLV
MAVDGINQFTSIFCLTVMSVDRYLAVVHPTRSARWRTAPVARMVSAAVWVASAVVVLPVV
VFSGVPRGMSTCHMQWPEPAAAWRTAFIIYTAALGFFGPLLVICLCYLLIVVKVRSTTRR
VRAPSCQWVQAPACQRRRRSERRVTRMVVAVVALFVLCWMPFYLLNIVNVVCPLPEEPAF
FGLYFLVVALPYANSCANPILYGFLSYRFKQGFRRILLRPSRRVRSQEPGSGPPEKTEEE
EDEEEEERREEEERRMQRGQEMNGRLSQIAQPGPSGQQQRPCTGTAKEQQLLPQEATAGD
KASTLSHL
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  Blast E-value cutoff:
BDBM50091414
n/a
NameBDBM50091414
Synonyms:CHEMBL3582336
TypeSmall organic molecule
Emp. Form.C27H24FN9O2
Mol. Mass.525.537
SMILESCCn1cc(cn1)[C@]1(N[C@H](Cc2c1[nH]c1ccccc21)c1nc(c[nH]1)-c1ccc(F)cn1)c1nn(C)c(=O)o1 |r|
Structure
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