HDAC inhibitor Mocetinostat, Purity ≥98%

Cat. No.: X23-10-ZQ300

HDAC inhibitor Mocetinostat, Purity ≥98%

Synonym: 726169-73-9; Mocetinostat; MGCD0103; MGCD-0103; MGCD 0103; N-(2-AMINOPHENYL)-4-([[4-(PYRIDIN-3-YL)PYRIMIDIN-2-YL]AMINO]METHYL)BENZAMIDE; HDAC inhibitor

  • MDL: MFCD10565970
  • CAS Number: 726169-73-9
  • Compound CID: 9865515
Product Size
5 mg; 10 mg; 25 mg; 50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
Mocetinostat, soluble in DMSO and insoluble in ethanol and water, induces DNA damage and the inhibition of DNA repair processes. It targets HDAC1, HDAC11, HDAC2, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, and HDAC8.
Molecular Weight
396.4
Molecular Formula
C23H20N6O
Targets
HDAC1: 0.15 μM; HDAC11: 0.59 μM; HDAC2: 0.29 μM; HDAC3: 0.15 μM; HDAC4: >10 μM; HDAC5: >10 μM; HDAC6: >10 μM; HDAC7: >10 μM; HDAC8: >10 μM
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 12 mg/mL (30.27 mM); Water: Insoluble; Ethanol: Insoluble
Identity
Confirmed by NMR/HPLC/MS.
Stability
The product is stable for three years when stored at the recommended temperature in lyophilized powder.
Applications
Mocetinostat can be used to inhibit HDACs, contributing to research on epigenetic modulation in cancer therapies.
Storage
Store at -20ºC.
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