Reaction Details |
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Target | Somatostatin receptor type 3 |
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Ligand | BDBM50400524 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_879796 (CHEMBL2210524) |
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IC50 | 0.460000±n/a nM |
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Citation | He, S; Ye, Z; Truong, Q; Shah, S; Du, W; Guo, L; Dobbelaar, PH; Lai, Z; Liu, J; Jian, T; Qi, H; Bakshi, RK; Hong, Q; Dellureficio, J; Pasternak, A; Feng, Z; deJesus, R; Yang, L; Reibarkh, M; Bradley, SA; Holmes, MA; Ball, RG; Ruck, RT; Huffman, MA; Wong, F; Samuel, K; Reddy, VB; Mitelman, S; Tong, SX; Chicchi, GG; Tsao, KL; Trusca, D; Wu, M; Shao, Q; Trujillo, ME; Eiermann, GJ; Li, C; Zhang, BB; Howard, AD; Zhou, YP; Nargund, RP; Hagmann, WK The Discovery of MK-4256, a Potent SSTR3 Antagonist as a Potential Treatment of Type 2 Diabetes. ACS Med Chem Lett3:484-489 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Somatostatin receptor type 3 |
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Name: | Somatostatin receptor type 3 |
Synonyms: | SOMATOSTATIN SST3 | SS3R | SSR-28 | SSR3_MOUSE | Smstr3 | Somatostatin receptor | Somatostatin receptor 3 | Somatostatin receptor type 3 | Sstr3 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 47225.49 |
Organism: | MOUSE |
Description: | SOMATOSTATIN SST3 SSTR3 MOUSE::P30935 |
Residue: | 428 |
Sequence: | MATVTYPSSEPTTLDPGNASSTWPLDTTLGNTSAGASLTGLAVSGILISLVYLVVCVVGL
LGNSLVIYVVLRHTSSPSVTSVYILNLALADELFMLGLPFLAAQNALSYWPFGSLMCRLV
MAVDGINQFTSIFCLTVMSVDRYLAVVHPTRSARWRTAPVARTVSAAVWVASAVVVLPVV
VFSGVPRGMSTCHMQWPEPAAAWRTAFIIYTAALGFFGPLLVICLCYLLIVVKVRSTTRR
VRAPSCQWVQAPACQRRRRSERRVTRMVVAVVALFVLCWMPFYLLNIVNVVCPLPEEPAF
FGLYFLVVALPYANSCANPILYGFLSYRFKQGFRRILLRPSRRIRSQEPGSGPPEKTEEE
EDEEEEERREEEERRMQRGQEMNGRLSQIAQAGTSGQQPRPCTGTAKEQQLLPQEATAGD
KASTLSHL
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BDBM50400524 |
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n/a |
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Name | BDBM50400524 |
Synonyms: | CHEMBL2204939 |
Type | Small organic molecule |
Emp. Form. | C28H25FN8 |
Mol. Mass. | 492.5501 |
SMILES | Cn1cc(cn1)C1(N[C@H](Cc2c1[nH]c1ccccc21)c1nc(c[nH]1)-c1ccc(F)cc1)c1cnn(C)c1 |r| |
Structure |
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