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TargetSomatostatin receptor type 3
LigandBDBM50154521
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1560970 (CHEMBL3779603)
IC50 1.8±n/a nM
Citation He, SDobbelaar, PHGuo, LYe, ZLiu, JJian, TTruong, QShah, SKDu, WQi, HBakshi, RKHong, QDellureficio, JDSherer, EPasternak, AFeng, ZReibarkh, MLin, MSamuel, KReddy, VBMitelman, STong, SXChicchi, GGTsao, KLTrusca, DWu, MShao, QTrujillo, MEFernandez, GNelson, DBunting, PKerr, JFitzgerald, PMorissette, PVolksdorf, SEiermann, GJLi, CZhang, BBHoward, ADZhou, YPNargund, RPHagmann, WK SAR exploration at the C-3 position of tetrahydro-ß-carboline sstr3 antagonists. Bioorg Med Chem Lett26:1529-35 (2016) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Somatostatin receptor type 3
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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  Blast E-value cutoff:
BDBM50154521
n/a
NameBDBM50154521
Synonyms:CHEMBL3775532
TypeSmall organic molecule
Emp. Form.C25H24F2N4O
Mol. Mass.434.4811
SMILESFc1ccc(cc1F)-c1c[nH]c(n1)[C@H]1Cc2c([nH]c3ccccc23)[C@H](N1)C1CCOCC1 |r|
Structure
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