Reaction Details |
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Target | 5-hydroxytryptamine receptor 5B |
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Ligand | BDBM81498 |
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Substrate/Competitor | n/a |
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Ki | 398.1±n/a nM |
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Comments | PDSP_1643 |
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Citation | Boess, FG; Martin, IL Molecular biology of 5-HT receptors. Neuropharmacology33:275-317 (1994) [PubMed] Article |
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More Info.: | Get all data from this article |
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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_MOUSE | 5ht5b | Htr5b |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 41221.13 |
Organism: | MOUSE |
Description: | 5-HT5B 0 MOUSE::P31387 |
Residue: | 370 |
Sequence: | MEVSNLSGATPGLAFPPGPESCSDSPSSGRSMGSTPGGLILPGREPPFSAFTVLVVTLLV
LLIAATFLWNLLVLVTILRVRAFHRVPHNLVASTAVSDVLVAVLVMPLSLVSELSAGRRW
QLGRSLCHVWISFDVLCCTASIWNVAAIALDRYWTITRHLQYTLRTRSRASALMIAITWA
LSALIALAPLLFGWGEAYDARLQRCQVSQEPSYAVFSTCGAFYLPLAVVLFVYWKIYKAA
KFRFGRRRRAVVPLPATTQAKEAPPESEMVFTARRRATVTFQTSGDSWREQKEKRAAMMV
GILIGVFVLCWIPFFLTELISPLCACSLPPIWKSIFLWLGYSNSFFNPLIYTAFNKNYNN
AFKSLFTKQR
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BDBM81498 |
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n/a |
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Name | BDBM81498 |
Synonyms: | 5-Methoxy-3-(1,2,3,6-tetrahydro-pyridin-4-yl)-1H-indole(RU-24969) | CAS_108028 | CHEMBL18785 | NSC_108028 | RU 24969 |
Type | Small organic molecule |
Emp. Form. | C14H16N2O |
Mol. Mass. | 228.2896 |
SMILES | COc1ccc2[nH]cc(C3=CCNCC3)c2c1 |t:9| |
Structure |
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