Reaction Details |
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Target | COUP transcription factor 2 |
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Ligand | BDBM100241 |
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Substrate/Competitor | n/a |
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IC50 | 3662±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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BDBM100241 |
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n/a |
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Name | BDBM100241 |
Synonyms: | MLS001072485 | N-[1-(2,4-difluorophenyl)-4,5,6,7-tetrahydroindazol-4-yl]-6-methyl-3-pyridinecarboxamide | N-[1-(2,4-difluorophenyl)-4,5,6,7-tetrahydroindazol-4-yl]-6-methyl-nicotinamide | N-[1-(2,4-difluorophenyl)-4,5,6,7-tetrahydroindazol-4-yl]-6-methylpyridine-3-carboxamide | N-[1-[2,4-bis(fluoranyl)phenyl]-4,5,6,7-tetrahydroindazol-4-yl]-6-methyl-pyridine-3-carboxamide | SMR000658115 | cid_24790171 |
Type | Small organic molecule |
Emp. Form. | C20H18F2N4O |
Mol. Mass. | 368.3799 |
SMILES | Cc1ccc(cn1)C(=O)NC1CCCc2c1cnn2-c1ccc(F)cc1F |
Structure |
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