Reaction Details |
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Target | Retinoic acid receptor beta |
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Ligand | BDBM50082042 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_195482 (CHEMBL798904) |
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EC50 | 1004±n/a nM |
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Citation | Zacheis, D; Dhar, A; Lu, S; Madler, MM; Klucik, J; Brown, CW; Liu, S; Clement, F; Subramanian, S; Weerasekare, GM; Berlin, KD; Gold, MA; Houck, JR; Fountain, KR; Benbrook, DM Heteroarotinoids inhibit head and neck cancer cell lines in vitro and in vivo through both RAR and RXR retinoic acid receptors. J Med Chem42:4434-45 (1999) [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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BDBM50082042 |
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n/a |
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Name | BDBM50082042 |
Synonyms: | CHEMBL139536 | N-(2,2,4,4-Tetramethyl-thiochroman-6-yl)-terephthalamic acid methyl ester |
Type | Small organic molecule |
Emp. Form. | C22H25NO3S |
Mol. Mass. | 383.504 |
SMILES | COC(=O)c1ccc(cc1)C(=O)Nc1ccc2SC(C)(C)CC(C)(C)c2c1 |
Structure |
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