Reaction Details |
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Target | 5-hydroxytryptamine receptor 5A |
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Ligand | BDBM21392 |
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Substrate/Competitor | n/a |
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Ki | 12.58±n/a nM |
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Comments | PDSP_140 |
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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 5A |
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Name: | 5-hydroxytryptamine receptor 5A |
Synonyms: | 5-HT-5 | 5-HT-5A | 5-HT5 | 5-HT5a | 5-hydroxytryptamine receptor 5A | 5HT5A_MOUSE | 5ht5a | Htr5a | Serotonin 5a (5-HT5a) receptor | Serotonin receptor 5A |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 40749.33 |
Organism: | MOUSE |
Description: | 5-HT5 0 MOUSE::P30966 |
Residue: | 357 |
Sequence: | MDLPVNLTSFSLSTPSSLEPNRSLDTEVLRPSRPFLSAFRVLVLTLLGFLAAATFTWNLL
VLATILKVRTFHRVPHNLVASMAISDVLVAVLVMPLSLVHELSGRRWQLGRRLCQLWIAC
DVLCCTASIWNVTAIALDRYWSITRHLEYTLRTRKRVSNVMILLTWALSTVISLAPLLFG
WGETYSEPSEECQVSREPSYTVFSTVGAFYLPLCVVLFVYWKIYRAAKFRMGSRKTNSVS
PVPEAVEVKNATQHPQMVFTVRHATVTFQTEGDTWREQKEQRAALMVGILIGVFVLCWFP
FFVTELISPLCSWDVPAIWKSIFLWLGYSNSFFNPLIYTAFNRSYSSAFKVFFSKQQ
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BDBM21392 |
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n/a |
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Name | BDBM21392 |
Synonyms: | 3-(2-aminoethyl)-1H-indole-5-carboxamide | 5-CT | 5-CT,DP | 5-carboxamidotryptamine | CHEMBL1256863 | CHEMBL18840 | [3H]-5-CT | [3H]-5-Carboxamide tryptamine | [3H]-5-Carboxyamidotryptamine | [3H]-5-carboxamidotryptamine |
Type | Small organic molecule |
Emp. Form. | C11H13N3O |
Mol. Mass. | 203.2404 |
SMILES | NCCc1c[nH]c2ccc(cc12)C(N)=O |
Structure |
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