Reaction Details |
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Target | Somatostatin receptor type 3 |
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Ligand | BDBM50054459 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1447894 (CHEMBL3378641) |
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IC50 | 0.410000±n/a nM |
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Citation | He, S; Lai, Z; Ye, Z; Dobbelaar, PH; Shah, SK; Truong, Q; Du, W; Guo, L; Liu, J; Jian, T; Qi, H; Bakshi, RK; Hong, Q; Dellureficio, J; Reibarkh, M; Samuel, K; Reddy, VB; Mitelman, S; Tong, SX; Chicchi, GG; Tsao, KL; Trusca, D; Wu, M; Shao, Q; Trujillo, ME; Fernandez, G; Nelson, D; Bunting, P; Kerr, J; Fitzgerald, P; Morissette, P; Volksdorf, S; Eiermann, GJ; Li, C; Zhang, B; Howard, AD; Zhou, YP; Nargund, RP; Hagmann, WK Investigation of Cardiovascular Effects of Tetrahydro-ß-carboline sstr3 antagonists. ACS Med Chem Lett5:748-53 (2014) [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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BDBM50054459 |
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n/a |
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Name | BDBM50054459 |
Synonyms: | CHEMBL3323074 |
Type | Small organic molecule |
Emp. Form. | C32H28FN7O2 |
Mol. Mass. | 561.6088 |
SMILES | CCOC(=O)c1ccnc(c1)[C@@]1(N[C@H](Cc2c1[nH]c1ccccc21)c1nc(c[nH]1)-c1ccc(F)cc1)c1cnn(C)c1 |r| |
Structure |
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