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TargetIsocitrate dehydrogenase [NADP] cytoplasmic [R132H]
LigandBDBM278620
Substrate/Competitorn/a
Meas. Tech.Inhibitory Activity Against IDH1R132H and IDH1R132C Enzymes
pH7.5±n/a
Temperature298.15±n/a K
IC50 13±n/a nM
Commentsextracted
Citation Saito, SItoh, MFujisawa, TSaito, HKiyotsuka, YWatanabe, HMatsunaga, HKagoshima, YSuzuki, TOgawara, YKitabayashi, K Isoxazole derivative as mutant isocitrate dehydrogenase 1 inhibitor US Patent US10040791 Publication Date 8/7/2018
More Info.:Get all data from this article,  Assay Method
 
Isocitrate dehydrogenase [NADP] cytoplasmic [R132H]
Name:Isocitrate dehydrogenase [NADP] cytoplasmic [R132H]
Synonyms:Cytosolic NADP-isocitrate dehydrogenase (IDH1)(R132H) | IDH1 | IDH1 R132H | IDH1(R132H) | IDHC_HUMAN | Isocitrate dehydrogenase (IDH1)(R132H) | Isocitrate dehydrogenase 1 mutant (R132H) | Isocitrate dehydrogenase [NADP] cytoplasmic (IDH)(R132H) | Isocitrate dehydrogenase [NADP] cytoplasmic (IDH1)(R132H) | Isocitrate dehydrogenase [NADP] cytoplasmic (R132H) | PICD
Type:Protein
Mol. Mass.:46641.74
Organism:Homo sapiens (Human)
Description:Human IDH1 R132H (SEQ ID No. 2 in patent). First three are removed. Google patent parsed wrong.
Residue:414
Sequence:
MSKKISGGSVVEMQGDEMTRIIWELIKEKLIFPYVELDLHSYDLGIENRDATNDQVTKDA
AEAIKKHNVGVKCATITPDEKRVEEFKLKQMWKSPNGTIRNILGGTVFREAIICKNIPRL
VSGWVKPIIIGHHAYGDQYRATDFVVPGPGKVEITYTPSDGTQKVTYLVHNFEEGGGVAM
GMYNQDKSIEDFAHSSFQMALSKGWPLYLSTKNTILKKYDGRFKDIFQEIYDKQYKSQFE
AQKIWYEHRLIDDMVAQAMKSEGGFIWACKNYDGDVQSDSVAQGYGSLGMMTSVLVCPDG
KTVEAEAAHGTVTRHYRMYQKGQETSTNPIASIFAWTRGLAHRAKLDNNKELAFFANALE
EVSIETIEAGFMTKDLAACIKGLPNVQRSDYLNTFEFMDKLGENLKIKLAQAKL
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  Blast E-value cutoff:
BDBM278620
n/a
NameBDBM278620
Synonyms:(2E)-3-(1-{[5-[1- (Dimethylamino)cyclopropyl]- 3-(2,4,6-trichlorophenyl)-1,2- oxazol-4-yl]carbonyl}-3- methyl-1H-indol-4-yl)prop-2- enoic acid | US10040791, Example 82
TypeSmall organic molecule
Emp. Form.C27H22Cl3N3O4
Mol. Mass.558.84
SMILESCN(C)C1(CC1)c1onc(c1C(=O)n1cc(C)c2c(\C=C\C(O)=O)cccc12)-c1c(Cl)cc(Cl)cc1Cl |(-.89,4.78,;.2,3.69,;1.69,4.09,;-.2,2.2,;.2,.71,;1.29,1.8,;-1.69,1.8,;-2.93,2.71,;-4.18,1.8,;-3.7,.34,;-2.16,.34,;-1.39,-1,;-2.16,-2.33,;.15,-1,;1.05,.25,;2.52,-.23,;3.85,.54,;2.52,-1.77,;3.66,-2.8,;5.13,-2.32,;5.45,-.81,;6.91,-.34,;8.06,-1.37,;7.23,1.17,;3.34,-4.3,;1.88,-4.78,;.73,-3.75,;1.05,-2.24,;-4.79,-.75,;-6.28,-.35,;-6.68,1.14,;-7.37,-1.44,;-6.97,-2.93,;-8.06,-4.02,;-5.48,-3.33,;-4.39,-2.24,;-2.9,-2.64,)|
Structure
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