Reaction Details |
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Target | Cholecystokinin |
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Ligand | BDBM50007921 |
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Substrate/Competitor | n/a |
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Ki | 28.6±n/a nM |
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Comments | PDSP_2673 |
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Citation | Van Dijk, A; Richards, JG; Trzeciak, A; Gillessen, D; Möhler, H Cholecystokinin receptors: biochemical demonstration and autoradiographical localization in rat brain and pancreas using [3H] cholecystokinin8 as radioligand. J Neurosci4:1021-33 (1984) [PubMed] |
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More Info.: | Get all data from this article |
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Cholecystokinin |
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Name: | Cholecystokinin |
Synonyms: | CCKN_RAT | Cck |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 12844.29 |
Organism: | RAT |
Description: | Cholecystokinin 0 RAT::P01355 |
Residue: | 115 |
Sequence: | MKCGVCLCVVMAVLAAGALAQPVVPVEAVDPMEQRAEEAPRRQLRAVLRPDSEPRARLGA
LLARYIQQVRKAPSGRMSVLKNLQGLDPSHRISDRDYMGWMDFGRRSAEDYEYPS
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BDBM50007921 |
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n/a |
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Name | BDBM50007921 |
Synonyms: | 3-{2-[2-(2-{2-[2-(2-Amino-3-carboxy-propionylamino)-3-(4-hydroxy-phenyl)-propionylamino]-4-methylsulfanyl-butyrylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-4-methylsulfanyl-butyrylamino}-N-(1-carbamoyl-2-phenyl-ethyl)-succinamic acid | Asp-Tyr-Met-Gly-Trp-Met-Asp-Phe-NH2 | CHEMBL216166 | Desulfated CCK8 |
Type | Small organic molecule |
Emp. Form. | C49H62N10O13S2 |
Mol. Mass. | 1063.206 |
SMILES | CSCC[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CC(O)=O)C(=O)NCC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O |
Structure |
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