Reaction Details |
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Target | Somatostatin receptor type 2 |
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Ligand | BDBM50075278 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_200690 |
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Ki | 2±n/a nM |
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Citation | Pasternak, A; Pan, Y; Marino, D; Sanderson, PE; Mosley, R; Rohrer, SP; Birzin, ET; Huskey, SE; Jacks, T; Schleim, KD; Cheng, K; Schaeffer, JM; Patchett, AA; Yang, L Potent, orally bioavailable somatostatin agonists: good absorption achieved by urea backbone cyclization. Bioorg Med Chem Lett9:491-6 (1999) [PubMed] |
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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 | SSR2_MOUSE | Smstr2 | Somatostatin receptor | Somatostatin receptor 2 | Somatostatin receptor type 2 | Sst2 | Sstr2 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 41234.26 |
Organism: | MOUSE |
Description: | SOMATOSTATIN SST2 SSTR2 MOUSE::P30875 |
Residue: | 369 |
Sequence: | MEMSSEQLNGSQVWVSSPFDLNGSLGPSNGSNQTEPYYDMTSNAVLTFIYFVVCVVGLCG
NTLVIYVILRYAKMKTITNIYILNLAIADELFMLGLPFLAMQVALVHWPFGKAICRVVMT
VDGINQFTSIFCLTVMSIDRYLAVVHPIKSAKWRRPRTAKMINVAVWCVSLLVILPIMIY
AGLRSNQWGRSSCTINWPGESGAWYTGFIIYAFILGFLVPLTIICLCYLFIIIKVKSSGI
RVGSSKRKKSEKKVTRMVSIVVAVFIFCWLPFYIFNVSSVSVAISPTPALKGMFDFVVIL
TYANSCANPILYAFLSDNFKKSFQNVLCLVKVSGTEDGERSDSKQDKSRLNETTETQRTL
LNGDLQTSI
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BDBM50075278 |
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n/a |
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Name | BDBM50075278 |
Synonyms: | CHEMBL147319 | methyl 6-amino-2-[2-(1H-3-indolyl)-1-spiro[2,3-dihydro-1H-indene-1,4'-(hexahydropyridine)]-1-ylcarboxamido-(1R)-ethylcarboxamido]-(2R)-hexanoate |
Type | Small organic molecule |
Emp. Form. | C32H41N5O4 |
Mol. Mass. | 559.699 |
SMILES | COC(=O)[C@@H](CCCCN)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)N1CCC2(CCc3ccccc23)CC1 |
Structure |
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