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TargetCOUP transcription factor 2
LigandBDBM100245
Substrate/Competitorn/a
IC50 2538±n/a nM
Citation PubChem, PC Luminescence-based cell-based high throughput dose response assay to identify inhibitors of COUP-TFII (NR2F2) PubChem Bioassay(2013)[AID]
More Info.:Get all data from this article
 
COUP transcription factor 2
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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  Blast E-value cutoff:
BDBM100245
n/a
NameBDBM100245
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
TypeSmall organic molecule
Emp. Form.C22H25NO8
Mol. Mass.431.4358
SMILESCOc1cc(NC(=O)COc2cc(O)c3C(=O)CC(C)(C)Oc3c2)cc(OC)c1OC
Structure
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