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Search results for: 'research area cell cycle rock'

Search results for: 'research area cell cycle rock'

A8336 KU-60019

2 Citation

Target: ATM/ATR

Summary: ATM kinase inhibitor,potent and selective

≥27.4 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
A1402 Gemcitabine HCl

Summary: Inhibits DNA synthesis,deoxycytidine analog

≥10.1 mg/mL
A1912 Lomeguatrib

Target: O6-methylguanine-DNA-methyl-transferase (MGMT)

Summary: MGMT inhibitor

≥50 mg/mL
A8331 Bleomycin Sulfate

1 Citation

Summary: Chemotherapy agent, induces DNA strand break

≥125 mg/mL
A8183 Trichostatin A (TSA)

13 Citation

Target: Histone Deacetylases (HDACs)

Summary: HDAC inhibitor

insoluble in H2O; ≥15.12 mg/mL
A4091 PCI-34051

1 Citation

Target: Histone Deacetylases (HDACs)

Summary: HDAC8 inhibitor,potent and selective

insoluble in H2O; insoluble in EtOH; ≥14.8 mg/mL
A4090 JNJ-26481585

3 Citation

Target: Histone Deacetylases (HDACs)

Summary: Potent HDAC inhibitor

insoluble in H2O; insoluble in EtOH; ≥19.2 mg/mL
A4084 Vorinostat (SAHA, MK0683)

9 Citation

Target: Histone Deacetylases (HDACs)

Summary: HDAC inhibitor

insoluble in EtOH; insoluble in H2O; ≥4.41 mg/mL
A4096 Belinostat (PXD101)

2 Citation

Target: Histone Deacetylases (HDACs)

Summary: Hydroxamate-type HDAC inhibitor

insoluble in H2O; ≥15.92 mg/mL