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TargetCOUP transcription factor 2
LigandBDBM100201
Substrate/Competitorn/a
IC50 2680±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]
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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:
BDBM100201
n/a
NameBDBM100201
Synonyms:MLS000103799 | N-([1,3]dioxolo[4,5-f][1,3]benzothiazol-6-yl)-4-[methyl(2-oxolanylmethyl)sulfamoyl]benzamide | N-([1,3]dioxolo[4,5-f][1,3]benzothiazol-6-yl)-4-[methyl(oxolan-2-ylmethyl)sulfamoyl]benzamide | N-([1,3]dioxolo[4,5-f][1,3]benzothiazol-6-yl)-4-[methyl(tetrahydrofurfuryl)sulfamoyl]benzamide | SMR000017708 | cid_5310556
TypeSmall organic molecule
Emp. Form.C21H21N3O6S2
Mol. Mass.475.538
SMILESCN(CC1CCCO1)S(=O)(=O)c1ccc(cc1)C(=O)Nc1nc2cc3OCOc3cc2s1
Structure
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