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TargetSomatostatin receptor type 5
LigandBDBM50065450
Substrate/Competitorn/a
Meas. Tech.ChEMBL_200863 (CHEMBL804582)
Ki 101±n/a nM
Citation Tran, TAMattern, RHAfargan, MAmitay, OZiv, OMorgan, BATaylor, JEHoyer, DGoodman, M Design, synthesis, and biological activities of potent and selective somatostatin analogues incorporating novel peptoid residues. J Med Chem41:2679-85 (1998) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Somatostatin receptor type 5
Name:Somatostatin receptor type 5
Synonyms:SOMATOSTATIN SST5 | SS-5-R | SS5-R | SS5R | SSR5_HUMAN | SSTR5 | Somatostatin receptor type 5 (SSTR5)
Type:Enzyme
Mol. Mass.:39218.02
Organism:Homo sapiens (Human)
Description:P35346
Residue:364
Sequence:
MEPLFPASTPSWNASSPGAASGGGDNRTLVGPAPSAGARAVLVPVLYLLVCAAGLGGNTL
VIYVVLRFAKMKTVTNIYILNLAVADVLYMLGLPFLATQNAASFWPFGPVLCRLVMTLDG
VNQFTSVFCLTVMSVDRYLAVVHPLSSARWRRPRVAKLASAAAWVLSLCMSLPLLVFADV
QEGGTCNASWPEPVGLWGAVFIIYTAVLGFFAPLLVICLCYLLIVVKVRAAGVRVGCVRR
RSERKVTRMVLVVVLVFAGCWLPFFTVNIVNLAVALPQEPASAGLYFFVVILSYANSCAN
PVLYGFLSDNFRQSFQKVLCLRKGSGAKDADATEPRPDRIRQQQEATPPAHRAAANGLMQ
TSKL
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  Blast E-value cutoff:
BDBM50065450
n/a
NameBDBM50065450
Synonyms:2-Amino-3-phenyl-N-{4-[(2S,5S,8S,14S,17R)-8,10,14-tribenzyl-5-((R)-1-hydroxy-ethyl)-17-(1H-indol-3-ylmethyl)-3,6,9,12,15,18-hexaoxo-1,4,7,10,13,16hexaaza-cyclooctadec-2-yl]-butyl}-propionamide | CHEMBL2370168
TypeSmall organic molecule
Emp. Form.C57H65N9O8
Mol. Mass.1004.1815
SMILES[H][C@]1(NC(=O)[C@H](CCCCNC(=O)[C@@H](N)Cc2ccccc2)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)CN(Cc2ccccc2)C(=O)[C@H](Cc2ccccc2)NC1=O)[C@@H](C)O
Structure
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