Reaction Details |
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Target | Retinoic acid receptor alpha |
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Ligand | BDBM458251 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Transactivation assays |
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EC50 | 18.0±n/a nM |
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Citation | Borthwick, AD; Mills, MT; Brown, JT; Corcoran, JP; De Castro Vasconcelos Goncalves, MB; Kalindjian, SB Bicycloheteroaryl-heteroaryl-benzoic acid compounds as retinoic acid receptor beta (RARβ) agonists US Patent US10752616 Publication Date 8/25/2020 |
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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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BDBM458251 |
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n/a |
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Name | BDBM458251 |
Synonyms: | US10752616, Code No. BHBA-016 |
Type | Small organic molecule |
Emp. Form. | C18H11ClN2O4 |
Mol. Mass. | 354.744 |
SMILES | Cc1ccc(Cl)c2cc(oc12)-c1nc(no1)-c1ccc(cc1)C(O)=O |
Structure |
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