VE-821


Catalog No. Size PriceQuantity
M10888-2 Solid 2 mg $85
M10888-10 Solid 10 mg $255

Description

VE-821 is the first highly selective and potent ATR inhibitor. VE-821 inhibited radiation- and gemcitabine-induced phosphorylation of Chk1, confirming inhibition of ATR signaling. Consistently, VE-821 significantly enhanced the sensitivity of PSN-1, MiaPaCa-2 and primary PancM pancreatic cancer cells to radiation and gemcitabine under both normoxic and hypoxic conditions. ATR inhibition by VE-821 led to inhibition of radiation-induced G 2/M arrest in cancer cells.

Product information

CAS Number: 1232410-49-9

Molecular Weight: 368.41

Formula: C18H16N4O3S

Chemical Name: 3-amino-6-(4-methanesulfonylphenyl)-N-phenylpyrazine-2-carboxamide

Smiles: CS(=O)(=O)C1C=CC(=CC=1)C1=CN=C(N)C(=N1)C(=O)NC1C=CC=CC=1

InChiKey: DUIHHZKTCSNTGM-UHFFFAOYSA-N

InChi: InChI=1S/C18H16N4O3S/c1-26(24,25)14-9-7-12(8-10-14)15-11-20-17(19)16(22-15)18(23)21-13-5-3-2-4-6-13/h2-11H,1H3,(H2,19,20)(H,21,23)

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥360 days if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

Products are for research use only. Not for human use.

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