Reaction Details |
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Target | COUP transcription factor 2 |
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Ligand | BDBM37434 |
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Substrate/Competitor | n/a |
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IC50 | 567.98±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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BDBM37434 |
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n/a |
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Name | BDBM37434 |
Synonyms: | 2-[(1-bicyclo[2.2.1]hept-2-yl-1H-tetrazol-5-yl)thio]-N-4-quinolinylacetamide | 2-[1-(3-bicyclo[2.2.1]heptanyl)tetrazol-5-yl]sulfanyl-N-quinolin-4-ylacetamide | 2-[[1-(2-norbornyl)tetrazol-5-yl]thio]-N-(4-quinolyl)acetamide | 2-[[1-(3-bicyclo[2.2.1]heptanyl)-1,2,3,4-tetrazol-5-yl]sulfanyl]-N-quinolin-4-yl-ethanamide | 2-[[1-(3-bicyclo[2.2.1]heptanyl)-5-tetrazolyl]thio]-N-(4-quinolinyl)acetamide | MLS000066069 | SMR000079553 | cid_2967368 |
Type | Small organic molecule |
Emp. Form. | C19H20N6OS |
Mol. Mass. | 380.467 |
SMILES | [H]C12CCC([H])(C1)C(C2)n1nnnc1SCC(=O)Nc1ccnc2ccccc12 |TLB:9:7:6:3.2| |
Structure |
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