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Cat. No. Product Name Target Signaling Pathways
T15551 IDH889

Dehydrogenase Metabolism
IDH889 是可口服有效的,脑渗透性的,变构和突变特异性的异柠檬酸脱氢酶抑制剂,对 IDH1 R132* 突变型具有高效选择性。它高效抑制细胞内 2-HG 水平,IC50为 0.014 μM。
T15550 IDH-305

Dehydrogenase Metabolism
IDH-305 是突变选择性的、口服性的、脑渗透性的 IDH1抑制剂,靶向 IDH1 (R132) 突变。它对突变体 IDH1 亚型的选择性比野生型高 200 倍 (IC50= 27 nM (IDH1R132H), 28 nM (IDH1R132C), 6.14 µM (IDH1WT))。
T2104 AGI-5198

IDH-C35

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
AGI-5198 (IDH-C35) 是一种选择性的突变体 IDH1R132H 抑制剂,IC50=0.07 μM。
T16161 Mutant IDH1 inhibitor

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
Mutant IDH1 inhibitor 是一种突变型IDH1 R132H 的抑制剂,IC50<72 nM。
T7741 DS-1001b

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
DS-1001b 是IDH-1(异柠檬酸脱氢酶-1) 突变体抑制剂。
T12128 Mutant IDH1-IN-2

Isocitrate Dehydrogenase (IDH) Metabolism
Mutant IDH1-IN-2是突变型异柠檬酸脱氢酶蛋白抑制剂, 在荧光生物化学检测中IC50为16.6 nM,LS-MS 生物化学检测中IC50为<22 nM,。
TQ0042 BAY-1436032

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
BAY-1436032 是一种选择性泛突变异柠檬酸脱氢酶 1 新型口服抑制剂。
T1809 AGI-6780

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
AGI6780 能够选择性抑制肿瘤相关突变体IDH2R140Q,IC50=23±1.7 nM。它对IDH2WT 的作用效果微弱,IC50=190±8.1 nM。
T2346 Enasidenib

恩西地平,AG-221

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
Enasidenib (AG-221) 是口服具有活力的、可逆的、选择性IDH2突变酶抑制剂,抑制IDH2R140Q 和 IDH2R172K 的IC50分别为100 和 400 nM。
T2043 Mutant IDH1-IN-1

IDH1-IN-1

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
Mutant IDH1-IN-1 是 IDH1突变体的选择性抑制剂,能够作用于突变体 IDH1 R132C/R132C (IC50:4 nM) ,IDH1 R132H/R132H (IC50:42 nM) ,IDH1 R132H/WT (IC50:80 nM) 和野生型 IDH1 (IC50:143 nM)。
T16384 Olutasidenib

FT-2102

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
Olutasidenib (FT-2102) 是一种可透过血脑屏障的、具有口服活性的、突变型异柠檬酸脱氢酶(IDH)1的选择性有效抑制剂,对IDH1- R132H 和 IDH1- R132C 的IC50分别为 21.2 nM 和 114 nM,可用于急性髓性白血病或骨髓增生异常综合征的研究。
T3617 Ivosidenib

艾伏尼布,AG-120

Dehydrogenase; Isocitrate Dehydrogenase (IDH) Metabolism
Ivosidenib (AG-120) 是一种口服具有活力的异柠檬酸脱氢酶 1 的突变体酶 (mIDH1 enzyme) 抑制剂,能够使 d-2- hydroxyglutatrate (2-HG) 在体内降低。它具有良好的的安全性和临床活性,具有研究 AML 的潜力。
T7307 Vorasidenib

PVM/MA,PVM/MA共聚物,AG-881

Isocitrate Dehydrogenase (IDH) Metabolism
Vorasidenib (PVM/MA) 是口服具有活力的、脑渗透的突变体异柠檬酸脱氢酶 1 和 2 双重抑制剂。
T12129 Mutant IDH1-IN-4

Others Others
Mutant IDH1-IN-4 is an mutant Isocitrate dehydrogenase 1 (IDH 1) inhibitor.
T39716 Mutant IDH1-IN-6

Mutant IDH1-IN-6

Mutant IDH1-IN-6 is an orally active compound that effectively inhibits mutant isocitrate dehydrogenase (IDH) enzymes. It demonstrates potency and selectivity, with IC50 values of 6.27, 3.71, 36.9, and 11.5 nM for IDH1 R132H, IDH1 R132C, IDH2 R140Q, and IDH2 R172K mutants, respectively. Notably, Mutant IDH1-IN-6 exhibits lower activity in inhibiting wild-type IDH enzymes.

化合物

IDH889
Cat.No: T15551
Synonym:
Target: Dehydrogenase
IDH-305
Cat.No: T15550
Synonym:
Target: Dehydrogenase
AGI-5198
Cat.No: T2104
Synonym: IDH-C35
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
Mutant IDH1 inhibitor
Cat.No: T16161
Synonym:
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
DS-1001b
Cat.No: T7741
Synonym:
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
Mutant IDH1-IN-2
Cat.No: T12128
Synonym:
Target: Isocitrate Dehydrogenase (IDH)
BAY-1436032
Cat.No: TQ0042
Synonym:
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
AGI-6780
Cat.No: T1809
Synonym:
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
Enasidenib
Cat.No: T2346
Synonym: 恩西地平,AG-221
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
Mutant IDH1-IN-1
Cat.No: T2043
Synonym: IDH1-IN-1
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
Olutasidenib
Cat.No: T16384
Synonym: FT-2102
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
Ivosidenib
Cat.No: T3617
Synonym: 艾伏尼布,AG-120
Target: Dehydrogenase, Isocitrate Dehydrogenase (IDH)
Vorasidenib
Cat.No: T7307
Synonym: PVM/MA,PVM/MA共聚物,AG-881
Target: Isocitrate Dehydrogenase (IDH)
Mutant IDH1-IN-4
Cat.No: T12129
Synonym:
Target: Others
Mutant IDH1-IN-6
Cat.No: T39716
Synonym: Mutant IDH1-IN-6
Target:
TargetMol Loading
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