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MilliporeSigma™ Calbiochem™ p300/CBP Inhibitor VI, L002

Catalog No. 5052980001 Shop All MilliporeSigma Products
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50-529-80001 10 mg
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Catalog No. 50-529-80001 Supplier MilliporeSigma™ Supplier No. 5052980001
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A cell-permeable phenylsulfonyloxyiminocyclohexadienone compound that acts as a potent, selective, and reversible inhibitor of p300 histone acetyl transferase (IC50

A cell-permeable phenylsulfonyloxyiminocyclohexadienone compound that acts as a potent, selective, and reversible inhibitor of p300 histone acetyl transferase (IC50 = 1.98μM). Shown to occupy Ac-CoA binding pocket of p300, and less potent to CBP, PCAF, GCN5 and GNAT. Suppresses Histone H3 and H4 acetylation in triple negative breast cancer cell line MDAMB-468 as well as in HCT116 cell line and blocks p300-mediated STAT3 phosphorylation in pancreatic cancer cell line MIA Paca-2. Does neither inhibit the activities of histone deacetylases 1, 6, and 11 nor 8-diverse histone methyltransferases tested (DOT1, EZH1, G9a, PRMT1, SETD2, SET7-9, SMYD2, and SUV39H2). Reported to suppress tumor growth in mice bearing tumor xenografts of MDAMB-468 cell line (at 500μg/100μl, i.p. twice a week).
TRUSTED_SUSTAINABILITY

Specifications

Color Brown
Description 99% by HPLC
Target Proteins p300 HAT
Molecular Formula C15H15NO5S
Solubility DMSO
Content And Storage Protect from light
Form Solid
Quantity 10 mg
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