Reaction Details |
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Target | Retinoic acid receptor alpha |
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Ligand | BDBM50032221 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_195316 (CHEMBL799871) |
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IC50 | 638±n/a nM |
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Citation | Boehm, MF; McClurg, MR; Pathirana, C; Mangelsdorf, D; White, SK; Hebert, J; Winn, D; Goldman, ME; Heyman, RA Synthesis of high specific activity [3H]-9-cis-retinoic acid and its application for identifying retinoids with unusual binding properties. J Med Chem37:408-14 (1994) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Retinoic acid receptor alpha |
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Name: | Retinoic acid receptor alpha |
Synonyms: | NR1B1 | Nuclear receptor subfamily 1 group B member 1 | RAR-alpha | RARA | RARA_HUMAN | Retinoic acid receptor alpha | Retinoic acid receptor alpha/Retinoid X receptor alpha | Retinoid X receptor gamma/retinoic acid receptor alpha | Retinoid receptor |
Type: | PROTEIN |
Mol. Mass.: | 50778.87 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1466191 |
Residue: | 462 |
Sequence: | MASNSSSCPTPGGGHLNGYPVPPYAFFFPPMLGGLSPPGALTTLQHQLPVSGYSTPSPAT
IETQSSSSEEIVPSPPSPPPLPRIYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNM
VYTCHRDKNCIINKVTRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKEVPKPECSESYTL
TPEVGELIEKVRKAHQETFPALCQLGKYTTNNSSEQRVSLDIDLWDKFSELSTKCIIKTV
EFAKQLPGFTTLTIADQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHNA
GFGPLTDLVFAFANQLLPLEMDDAETGLLSAICLICGDRQDLEQPDRVDMLQEPLLEALK
VYVRKRRPSRPHMFPKMLMKITDLRSISAKGAERVITLKMEIPGSMPPLIQEMLENSEGL
DTLSGQPGGGGRDGGGLAPPPGSCSPSLSPSSNRSSPATHSP
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BDBM50032221 |
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n/a |
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Name | BDBM50032221 |
Synonyms: | 4-[(E)-2-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-propenyl]-benzoic acid | CHEMBL32505 |
Type | Small organic molecule |
Emp. Form. | C25H30O2 |
Mol. Mass. | 362.5045 |
SMILES | C\C(=C/c1ccc(cc1)C(O)=O)c1cc2c(cc1C)C(C)(C)CCC2(C)C |
Structure |
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