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TargetCOUP transcription factor 2
LigandBDBM36871
Substrate/Competitorn/a
IC50 3111±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:
BDBM36871
n/a
NameBDBM36871
Synonyms:MLS000027766 | N-[4-(1-Methanesulfonyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-thiazol-2-yl]-2-thiophen-2-yl-acetamide | N-[4-(1-mesyl-2-methyl-indolin-5-yl)thiazol-2-yl]-2-(2-thienyl)acetamide | N-[4-(2-methyl-1-methylsulfonyl-2,3-dihydroindol-5-yl)-1,3-thiazol-2-yl]-2-thiophen-2-yl-ethanamide | N-[4-(2-methyl-1-methylsulfonyl-2,3-dihydroindol-5-yl)-1,3-thiazol-2-yl]-2-thiophen-2-ylacetamide | N-[4-(2-methyl-1-methylsulfonyl-2,3-dihydroindol-5-yl)-2-thiazolyl]-2-thiophen-2-ylacetamide | SMR000007522 | cid_654842
TypeSmall organic molecule
Emp. Form.C19H19N3O3S3
Mol. Mass.433.567
SMILESCC1Cc2cc(ccc2N1S(C)(=O)=O)-c1csc(NC(=O)Cc2cccs2)n1
Structure
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