Reaction Details |
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Target | COUP transcription factor 2 |
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Ligand | BDBM100245 |
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Substrate/Competitor | n/a |
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IC50 | 2538±n/a nM |
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Citation | PubChem, PC Luminescence-based cell-based high throughput dose response assay to identify inhibitors of COUP-TFII (NR2F2) PubChem Bioassay(2013)[AID] |
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More Info.: | Get all data from this article |
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COUP transcription factor 2 |
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Name: | COUP transcription factor 2 |
Synonyms: | ARP1 | COT2_HUMAN | COUP transcription factor 2 isoform a | NR2F2 | TFCOUP2 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 45583.83 |
Organism: | Homo sapiens (Human) |
Description: | gi_14149746 |
Residue: | 414 |
Sequence: | MAMVVSTWRDPQDEVPGSQGSQASQAPPVPGPPPGAPHTPQTPGQGGPASTPAQTAAGGQ
GGPGGPGSDKQQQQQHIECVVCGDKSSGKHYGQFTCEGCKSFFKRSVRRNLSYTCRANRN
CPIDQHHRNQCQYCRLKKCLKVGMRREAVQRGRMPPTQPTHGQFALTNGDPLNCHSYLSG
YISLLLRAEPYPTSRFGSQCMQPNNIMGIENICELAARMLFSAVEWARNIPFFPDLQITD
QVALLRLTWSELFVLNAAQCSMPLHVAPLLAAAGLHASPMSADRVVAFMDHIRIFQEQVE
KLKALHVDSAEYSCLKAIVLFTSDACGLSDVAHVESLQEKSQCALEEYVRSQYPNQPTRF
GKLLLRLPSLRTVSSSVIEQLFFVRLVGKTPIETLIRDMLLSGSSFNWPYMAIQ
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BDBM100245 |
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n/a |
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Name | BDBM100245 |
Synonyms: | 2-(5-hydroxy-4-keto-2,2-dimethyl-chroman-7-yl)oxy-N-(3,4,5-trimethoxyphenyl)acetamide | 2-[(2,2-dimethyl-5-oxidanyl-4-oxidanylidene-3H-chromen-7-yl)oxy]-N-(3,4,5-trimethoxyphenyl)ethanamide | 2-[(5-hydroxy-2,2-dimethyl-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl)oxy]-N-(3,4,5-trimethoxyphenyl)acetamide | 2-[(5-hydroxy-2,2-dimethyl-4-oxo-3H-chromen-7-yl)oxy]-N-(3,4,5-trimethoxyphenyl)acetamide | MLS001160243 | SMR000652740 | cid_16406758 |
Type | Small organic molecule |
Emp. Form. | C22H25NO8 |
Mol. Mass. | 431.4358 |
SMILES | COc1cc(NC(=O)COc2cc(O)c3C(=O)CC(C)(C)Oc3c2)cc(OC)c1OC |
Structure |
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