Reaction Details |
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Target | 5-hydroxytryptamine receptor 5B |
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Ligand | BDBM85330 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_225803 |
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Ki | >10000±n/a nM |
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Citation | van Wijngaarden, I; Hamminga, D; van Hes, R; Standaar, PJ; Tipker, J; Tulp, MT; Mol, F; Olivier, B; de Jonge, A Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1,7-annelated indole derivatives. J Med Chem36:3693-9 (1994) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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5-hydroxytryptamine receptor 5B |
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Name: | 5-hydroxytryptamine receptor 5B |
Synonyms: | 5-HT5B | 5-hydroxytryptamine receptor 5B | 5HT5B_RAT | 5ht5b | Htr5b | Serotonin (5-HT) receptor | Serotonin 5b (5-HT5b) receptor |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 41141.95 |
Organism: | RAT |
Description: | 5-HT5B 0 RAT::P35365 |
Residue: | 370 |
Sequence: | MEVSNLSGATPGIAFPPGPESCSDSPSSGRSMGSTPGGLILSGREPPFSAFTVLVVTLLV
LLIAATFLWNLLVLVTILRVRAFHRVPHNLVASTAVSDVLVAALVMPLSLVSELSAGRRW
QLGRSLCHVWISFDVLCCTASIWNVAAIALDRYWTITRHLQYTLRTRRRASALMIAITWA
LSALIALAPLLFGWGEAYDARLQRCQVSQEPSYAVFSTCGAFYVPLAVVLFVYWKIYKAA
KFRFGRRRRAVVPLPATTQAKEAPQESETVFTARCRATVAFQTSGDSWREQKEKRAAMMV
GILIGVFVLCWIPFFLTELVSPLCACSLPPIWKSIFLWLGYSNSFFNPLIYTAFNKNYNN
AFKSLFTKQR
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BDBM85330 |
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n/a |
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Name | BDBM85330 |
Synonyms: | CAS_68647 | NSC_68647 | ONDANSETRON | Ondansetron hydrochloride |
Type | Small organic molecule |
Emp. Form. | C18H19N3O |
Mol. Mass. | 293.363 |
SMILES | Cc1nccn1CC1CCc2c(C1=O)c1ccccc1n2C |
Structure |
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