Reaction Details |
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Target | Retinoic acid receptor beta |
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Ligand | BDBM50044098 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_196661 (CHEMBL799696) |
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IC50 | 150±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 beta |
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Name: | Retinoic acid receptor beta |
Synonyms: | HAP | HBV-activated protein | NR1B2 | Nuclear receptor subfamily 1 group B member 2 | RAR-beta | RAR-epsilon | RARB | RARB_HUMAN | Retinoic acid receptor RXR-alpha/Retinoic acid receptor beta | Retinoic acid receptor beta | Retinoid receptor |
Type: | PROTEIN |
Mol. Mass.: | 50498.70 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1458015 |
Residue: | 455 |
Sequence: | MTTSGHACPVPAVNGHMTHYPATPYPLLFPPVIGGLSLPPLHGLHGHPPPSGCSTPSPAT
IETQSTSSEELVPSPPSPLPPPRVYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNM
IYTCHRDKNCVINKVTRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKETSKQECTESYEM
TAELDDLTEKIRKAHQETFPSLCQLGKYTTNSSADHRVRLDLGLWDKFSELATKCIIKIV
EFAKRLPGFTGLTIADQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHNA
GFGPLTDLVFTFANQLLPLEMDDTETGLLSAICLICGDRQDLEEPTKVDKLQEPLLEALK
IYIRKRRPSKPHMFPKILMKITDLRSISAKGAERVITLKMEIPGSMPPLIQEMLENSEGH
EPLTPSSSGNTAEHSPSISPSSVENSGVSQSPLVQ
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BDBM50044098 |
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n/a |
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Name | BDBM50044098 |
Synonyms: | 4-[(E)-2-(3-Isopropyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-propenyl]-benzoic acid | CHEMBL424636 |
Type | Small organic molecule |
Emp. Form. | C27H34O2 |
Mol. Mass. | 390.5577 |
SMILES | CC(C)c1cc2c(cc1\C(C)=C\c1ccc(cc1)C(O)=O)C(C)(C)CCC2(C)C |
Structure |
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