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Search results for: 'research area cell cycle e1 enzyme'

Search results for: 'research area cell cycle e1 enzyme'

A4102 CI994 (Tacedinaline)

1 Citation

Target: Histone Deacetylases (HDACs)

Summary: HDAC inhibitor

insoluble in H2O; insoluble in EtOH; ≥50 mg/mL
A1905 3-Deazaneplanocin,DZNep

6 Citation

Target: Hydrolase

Summary: S-adenosylhomocysteine and EZH2 inhibitor

insoluble in EtOH; ≥17.07 mg/mL
A4520 R8-T198wt

Summary: Pim-1 kinase inhibitor

Soluble to 2 mg/mL
A4501 Tubacin

3 Citation

Target: Histone Deacetylases (HDACs)

Summary: HDAC6 inhibitor,potent,selective,reversible,cell-permeable

insoluble in EtOH; insoluble in H2O; ≥7.19 mg/mL
A4105 M344

1 Citation

Target: Histone Deacetylases (HDACs)

Summary: HDAC inhibitor,potent and cell-permeable
A4506 DMOG

Target: Hypoxia-Inducible Factor Prolyl Hydroxylase Inhibitors (HIF-PHIs)

Summary: Competitive HIF-PH inhibitor, cell-permeable
C3095 N-Oxalylglycine

Summary: cell permeable inhibitor of α-ketoglutarate-dependent enzymes, including JMJD2A, JMJD2C, and JMJD2E.

insoluble in EtOH; ≥3.82 mg/mL
A8178 Panobinostat (LBH589)

10 Citation

Target: Histone Deacetylases (HDACs)

Summary: HDAC inhibitor

insoluble in H2O; insoluble in EtOH; ≥17.47 mg/mL
B4891 ML324

1 Citation

Summary: JMJD2 demethylase inhibitor, potent and cell-permeable

insoluble in H2O; ≥17.45 mg/mL
A4140 WP1066

Target: STAT|JAK

Summary: JAK2/STAT3 inhibitor,cell-permeable

insoluble in H2O; ≥17.8 mg/mL