Reaction Details |
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Target | 5-hydroxytryptamine receptor 5B |
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Ligand | BDBM50286672 |
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Substrate/Competitor | n/a |
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Ki | 575.43±n/a nM |
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Comments | PDSP_913 |
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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_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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BDBM50286672 |
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n/a |
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Name | BDBM50286672 |
Synonyms: | (S)-2-(2-{2-[3-(2-Amino-ethyl)-1H-indol-5-yloxy]-acetylamino}-acetylamino)-3-(4-hydroxy-phenyl)-propionamide | CHEMBL159174 | GTI |
Type | Small organic molecule |
Emp. Form. | C23H27N5O5 |
Mol. Mass. | 453.491 |
SMILES | NCCc1c[nH]c2ccc(OCC(=O)NCC(=O)N[C@@H](Cc3ccc(O)cc3)C(N)=O)cc12 |
Structure |
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