Reaction Details |
| Report a problem with these data |
Target | Neurotensin |
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Ligand | BDBM50130880 |
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Substrate/Competitor | n/a |
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Ki | 51±n/a nM |
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Comments | PDSP_1394 |
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Citation | Betancur, C; Canton, M; Gully, D; Vela, G; Pélaprat, D; Rostène, W Characterization and distribution of binding sites for a new neurotensin receptor antagonist ligand, [3H]SR 48692, in the guinea pig brain. J Pharmacol Exp Ther273:1450-8 (1995) [PubMed] |
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More Info.: | Get all data from this article |
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Neurotensin |
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Name: | Neurotensin |
Synonyms: | NEUT_CAVPO | NT | NTS | Neurotensin |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 1681.93 |
Organism: | GUINEA PIG |
Description: | NT 0 GUINEA PIG::P32560 |
Residue: | 13 |
Sequence: | |
BDBM50130880 |
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n/a |
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Name | BDBM50130880 |
Synonyms: | CHEMBL407196 | NT(1-13) | neurotensin | pGlu-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu | pGlu-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu-OH |
Type | Small organic molecule |
Emp. Form. | C78H121N21O20 |
Mol. Mass. | 1672.924 |
SMILES | [#6]-[#6]-[#6@H](-[#6])-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccc(-[#8])cc1)-[#7]-[#6](=O)-[#6@@H]-1-[#6]-[#6]-[#6]-[#7]-1-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6](=O)-[#6@@H]-1-[#6]-[#6]-[#6]-[#7]-1-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]-[#6]-[#7])-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#7])=O)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccc(-[#8])cc1)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#6])-[#6])-[#7]-[#6](=O)-[#6@@H]-1-[#6]-[#6]-[#6](=O)-[#7]-1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#6])-[#6])-[#6](-[#8])=O |r| |
Structure |
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