Reaction Details |
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Target | Somatostatin receptor type 3 |
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Ligand | BDBM50400517 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1560971 (CHEMBL3779604) |
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EC50 | 0.950000±n/a nM |
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Citation | He, S; Dobbelaar, PH; Guo, L; Ye, Z; Liu, J; Jian, T; Truong, Q; Shah, SK; Du, W; Qi, H; Bakshi, RK; Hong, Q; Dellureficio, JD; Sherer, E; Pasternak, A; Feng, Z; Reibarkh, M; Lin, 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, BB; Howard, AD; Zhou, YP; Nargund, RP; Hagmann, WK SAR exploration at the C-3 position of tetrahydro-ß-carboline sstr3 antagonists. Bioorg Med Chem Lett26:1529-35 (2016) [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 | SS-3-R | SS3-R | SS3R | SSR-28 | SSR3_HUMAN | SSTR3 | Somatostatin receptor type 3 (SSTR3) |
Type: | Protein |
Mol. Mass.: | 45855.97 |
Organism: | Homo sapiens (Human) |
Description: | P32745 |
Residue: | 418 |
Sequence: | MDMLHPSSVSTTSEPENASSAWPPDATLGNVSAGPSPAGLAVSGVLIPLVYLVVCVVGLL
GNSLVIYVVLRHTASPSVTNVYILNLALADELFMLGLPFLAAQNALSYWPFGSLMCRLVM
AVDGINQFTSIFCLTVMSVDRYLAVVHPTRSARWRTAPVARTVSAAVWVASAVVVLPVVV
FSGVPRGMSTCHMQWPEPAAAWRAGFIIYTAALGFFGPLLVICLCYLLIVVKVRSAGRRV
WAPSCQRRRRSERRVTRMVVAVVALFVLCWMPFYVLNIVNVVCPLPEEPAFFGLYFLVVA
LPYANSCANPILYGFLSYRFKQGFRRVLLRPSRRVRSQEPTVGPPEKTEEEDEEEEDGEE
SREGGKGKEMNGRVSQITQPGTSGQERPPSRVASKEQQLLPQEASTGEKSSTMRISYL
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BDBM50400517 |
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n/a |
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Name | BDBM50400517 |
Synonyms: | CHEMBL2204935 |
Type | Small organic molecule |
Emp. Form. | C27H23FN8O |
Mol. Mass. | 494.5229 |
SMILES | Cc1nc(no1)[C@@]1(N[C@H](Cc2c1[nH]c1ccccc21)c1nc(c[nH]1)-c1ccc(F)cc1)c1cnn(C)c1 |r| |
Structure |
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