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ZS34

ZS34 is a potent, orally active, and selective MAT2A inhibitor with an IC50 of 13.7 nM, displaying minimal hERG and UGT1A1 liabilities. ZS34 selectively suppresses the growth of methylthioadenosine phosphorylase (MTAP) -deficient cancer cells by inhibiting SAM synthesis, reducing SDMA levels, and inducing DNA damage. ZS34 exhibits antitumor efficacy in a HCT116 MTAP-/- xenograft mouse model. ZS34 can be used for the research of MTAP-deficient cancer[1].

Product Specifications

CAS Number

[3106086-17-0]

UNSPSC

12352005

Target

Methionine Adenosyltransferase (MAT)

Related Pathways

Epigenetics; Metabolic Enzyme/Protease

Field of Research

Cancer

Smiles

O=C1N(C2=C(C(NC)=N1)C3=C(C(Cl)=C2)C=CO3)C4=CC=CC=C4C

Molecular Formula

C18H14ClN3O2

Molecular Weight

339.78

References & Citations

[1]Zihan Shi, et al. Furo[2,3-f]quinazolin-7 (6H) -one Derivatives as Potent, Selective, and Orally Bioavailable MAT2A Inhibitors for MTAP-Deficient Cancer Therapy. J. Med. Chem. 2025, 68, 24213-24231

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Curated Selection

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