Reaction Details |
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Target | Somatostatin receptor type 2 |
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Ligand | BDBM50175593 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_321350 (CHEMBL881494) |
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IC50 | 11±n/a nM |
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Citation | Moore, SB; van der Hoek, J; de Capua, A; van Koetsveld, PM; Hofland, LJ; Lamberts, SW; Goodman, M Discovery of iodinated somatostatin analogues selective for hsst2 and hsst5 with excellent inhibition of growth hormone and prolactin release from rat pituitary cells. J Med Chem48:6643-52 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Somatostatin receptor type 2 |
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Name: | Somatostatin receptor type 2 |
Synonyms: | SOMATOSTATIN SST2 | SRIF-1 | SS-2-R | SS2-R | SS2R | SSR2_HUMAN | SSTR2 | Somatostatin receptor type 2 (SSTR2) |
Type: | Enzyme |
Mol. Mass.: | 41344.94 |
Organism: | Homo sapiens (Human) |
Description: | P30874 |
Residue: | 369 |
Sequence: | MDMADEPLNGSHTWLSIPFDLNGSVVSTNTSNQTEPYYDLTSNAVLTFIYFVVCIIGLCG
NTLVIYVILRYAKMKTITNIYILNLAIADELFMLGLPFLAMQVALVHWPFGKAICRVVMT
VDGINQFTSIFCLTVMSIDRYLAVVHPIKSAKWRRPRTAKMITMAVWGVSLLVILPIMIY
AGLRSNQWGRSSCTINWPGESGAWYTGFIIYTFILGFLVPLTIICLCYLFIIIKVKSSGI
RVGSSKRKKSEKKVTRMVSIVVAVFIFCWLPFYIFNVSSVSMAISPTPALKGMFDFVVVL
TYANSCANPILYAFLSDNFKKSFQNVLCLVKVSGTDDGERSDSKQDKSRLNETTETQRTL
LNGDLQTSI
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BDBM50175593 |
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n/a |
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Name | BDBM50175593 |
Synonyms: | (4-amino)-D-Phe-c[Cys-Tyr-D-Trp-Lys-Val-Cys]-Asp-NH2 | CHEMBL414316 |
Type | Small organic molecule |
Emp. Form. | C50H66N12O11S2 |
Mol. Mass. | 1075.263 |
SMILES | CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](CC(O)=O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(N)cc1 |
Structure |
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