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Supplier NameMedChemExpress (MCE)
Contactsales
Tel609-228-6898
Mobile609-228-6898
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Emailsales@medchemexpress.com; tech@medchemexpress.com
Websitehttps://www.medchemexpress.com/
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Product NameME0328
SynonymsME0328
ME 0328
ME-0328
4-Dihydro-4-oxo-3
4-Dihydro-4-oxo-N-[(1S)-1-phenylethyl]-2-quinazolinepropanamide
(S)-3,4-Dihydro-4-oxo-N-(1-phenylethyl)-2-quinazolinepropanamide
2-Quinazolinepropanamide, 3,4-dihydro-4-oxo-N-[(1S)-1-phenylethyl]-

Synonyms

ME0328
ME 0328
ME-0328
4-Dihydro-4-oxo-3
4-Dihydro-4-oxo-N-[(1S)-1-phenylethyl]-2-quinazolinepropanamide
(S)-3,4-Dihydro-4-oxo-N-(1-phenylethyl)-2-quinazolinepropanamide
2-Quinazolinepropanamide, 3,4-dihydro-4-oxo-N-[(1S)-1-phenylethyl]-
3,4-Dihydro-4-oxo-3,4-Dihydro-4-oxo-N-[(1S)-1-phenylethyl]-2-quinazolinepropanamide
CAS1445251-22-8
EINECS808-923-8
Chemical FormulaC19H19N3O2
Molecular Weight321.37
inchi
Package10 mM * 1 mL;5 mg;10 mg;25 mg;50 mg;100 mg
PriceEmail to quote
DescriptionsME0328

ME0328

MedChemExpress (MCE)

HY-100225

1445251-22-8

99.64%

Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year

Room temperature in continental US

Descriptions

ME0328

ME0328

MedChemExpress (MCE)

HY-100225

1445251-22-8

99.64%

Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year

Room temperature in continental US
may vary elsewhere.

ME0328 is a potent and selective ARTD3/PARP3 inhibitor with an IC50 of 0.89±0.28 μM.

ME0328 is a potent and selective inhibitor of ARTD3/PARP3 that is active in cells. In in vitro histone H1 modification assay, ME0328 inhibits the transferase activity of ARTD3 with an IC50 of 0.89±0.28 μM. In human A549 cells, ME0328 and ME0355 (at 10 μM) delay the resolution of γH2AX-containing foci that serve as markers for DNA double strand break repair following γ-irradiation (2 Gy). In silico and in vitro physicochemical and metabolic profiling indicated that ME0328 is soluble, cell permeable, and metabolically stable in human liver microsomes and rat hepatocytes[1].

ARTD3/PARP3 0.89 μM (IC50) ARTD1/PARP1 6.3 μM (IC50) ARTD2/PARP2 10.8 μM (IC50) ARTD6/TNKS2 34.3 μM (IC50) ARTD5/TNKS1 47.3 μM (IC50) ARTD10/PARP10 71.3 μM (IC50)

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[1]. Lindgren AE, et al. PARP inhibitor with selectivity toward ADP-ribosyltransferase ARTD3/PARP3. ACS Chem Biol. 2013 Aug 16
8(8):1698-703.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/ME0328.html
Last Update2025-05-21 16:50:25
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