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Name | Somatostatin receptor type 5 |
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Species | Rattus norvegicus (Rat) |
Gene | Sstr5 |
Synonym | SOMATO SS-5-R SS5-R SS5R SST5 receptor |
Disease | N/A for non-human GPCRs |
Length | 363 |
Amino acid sequence | MEPLSLASTPSWNASAASSGNHNWSLVGSASPMGARAVLVPVLYLLVCTVGLSGNTLVIYVVLRHAKMKTVTNVYILNLAVADVLFMLGLPFLATQNAVVSYWPFGSFLCRLVMTLDGINQFTSIFCLMVMSVDRYLAVVHPLRSARWRRPRVAKMASAAVWVFSLLMSLPLLVFADVQEGWGTCNLSWPEPVGLWGAAFITYTSVLGFFGPLLVICLCYLLIVVKVKAAGMRVGSSRRRRSEPKVTRMVVVVVLVFVGCWLPFFIVNIVNLAFTLPEEPTSAGLYFFVVVLSYANSCANPLLYGFLSDNFRQSFRKVLCLRRGYGMEDADAIEPRPDKSGRPQATLPTRSCEANGLMQTSRI |
UniProt | P30938 |
Protein Data Bank | N/A |
GPCR-HGmod model | N/A |
3D structure model | No available structures or models |
BioLiP | N/A |
Therapeutic Target Database | N/A |
ChEMBL | CHEMBL4318 |
IUPHAR | 359 |
DrugBank | N/A |
Name | cycloantagonist SA |
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Molecular formula | C42H55N7O5 |
IUPAC name | (3S,6S,9R,12S)-6-(4-aminobutyl)-12-benzyl-9-(1H-indol-3-ylmethyl)-3-[(1R)-1-phenoxyethyl]-1,4,7,10,13-pentazacyclononadecane-2,5,8,11-tetrone |
Molecular weight | 737.946 |
Hydrogen bond acceptor | 7 |
Hydrogen bond donor | 7 |
XlogP | 4.8 |
Synonyms | c[Aha-Phe-D-Trp-Lys-Thr(Bzl)] BDBM82471 |
Inchi Key | UYLQYUAFNNCEIJ-GGMHJNBLSA-N |
Inchi ID | InChI=1S/C42H55N7O5/c1-29(54-32-18-8-5-9-19-32)38-42(53)45-25-15-3-2-14-24-44-36(26-30-16-6-4-7-17-30)40(51)48-37(27-31-28-46-34-21-11-10-20-33(31)34)41(52)47-35(39(50)49-38)22-12-13-23-43/h4-11,16-21,28-29,35-38,44,46H,2-3,12-15,22-27,43H2,1H3,(H,45,53)(H,47,52)(H,48,51)(H,49,50)/t29-,35+,36+,37-,38+/m1/s1 |
PubChem CID | 57339675 |
ChEMBL | N/A |
IUPHAR | N/A |
BindingDB | 82471 |
DrugBank | N/A |
Structure | |
Lipinski's druglikeness | This ligand has more than 5 hydrogen bond donor. This ligand is heavier than 500 daltons. |
Parameter | Value | Reference | Database source |
---|---|---|---|
Ki | 51.28 nM | PMID7870182 | BindingDB |
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