Reaction Details |
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Target | Protachykinin-1 |
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Ligand | BDBM22913 |
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Substrate/Competitor | n/a |
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Ki | >10000±n/a nM |
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Comments | PDSP_2292 |
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Citation | Leurs, R; Tulp, MT; Menge, WM; Adolfs, MJ; Zuiderveld, OP; Timmerman, H Evaluation of the receptor selectivity of the H3 receptor antagonists, iodophenpropit and thioperamide: an interaction with the 5-HT3 receptor revealed. Br J Pharmacol116:2315-21 (1995) [PubMed] Article |
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More Info.: | Get all data from this article |
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Protachykinin-1 |
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Name: | Protachykinin-1 |
Synonyms: | NKA | NKNA | Protachykinin-1 | Substance P | TAC1 | TAC2 | TKN1_HUMAN |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 15006.99 |
Organism: | Homo sapiens (Human) |
Description: | Substance P 0 HUMAN::P20366 |
Residue: | 129 |
Sequence: | MKILVALAVFFLVSTQLFAEEIGANDDLNYWSDWYDSDQIKEELPEPFEHLLQRIARRPK
PQQFFGLMGKRDADSSIEKQVALLKALYGHGQISHKRHKTDSFVGLMGKRALNSVAYERS
AMQNYERRR
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BDBM22913 |
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n/a |
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Name | BDBM22913 |
Synonyms: | CHEMBL1237146 | CHEMBL498770 | Iodophenpropit | {[3-(1H-imidazol-5-yl)propyl]sulfanyl}-N''-[2-(4-iodophenyl)ethyl]methanimidamide |
Type | Small organic molecule |
Emp. Form. | C15H19IN4S |
Mol. Mass. | 414.308 |
SMILES | NC(SCCCc1cnc[nH]1)=NCCc1ccc(I)cc1 |w:11.12| |
Structure |
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