ChemicalBook--->CAS DataBase List--->1431697-96-9

1431697-96-9

1431697-96-9 Structure

1431697-96-9 Structure
IdentificationBack Directory
[Name]

CCT 241533 hydrochloride
[CAS]

1431697-96-9
[Synonyms]

CCT241533 HCl
CCT 241533 hydrochloride
CCT-241533 hydrochloride
CCT241533 (hydrochloride)
CCT-241533 HYDROCHLORIDE; CCT 241533 HYDROCHLORIDE
(3R,4S)-rel-4-[[2-(5-Fluoro-2-hydroxyphenyl)-6,7-dimethoxy-4-quinazolinyl]amino]-alpha,alpha-dimethyl-3-pyrrolidinemethanol hydrochloride (1:1)
[Molecular Formula]

C23H28ClFN4O4
[MOL File]

1431697-96-9.mol
[Molecular Weight]

478.944
Chemical PropertiesBack Directory
[solubility ]

Soluble in DMSO
[form ]

A crystalline solid
[color ]

White to light yellow
Hazard InformationBack Directory
[Description]

CCT241533 is a selective inhibitor of checkpoint kinase 2 (Chk2; IC50 = 3 nM). In human cancer cell lines, CCT241533 blocks Chk2 activity and potentiates the cytotoxicity of the PARP inhibitors, rucaparib, AG-1447; and olaparib .
[Uses]

CCT241533 hydrochloride is a potent and selective CHK2 inhibitor with an IC50 of 3 nM and a Ki of 1.16 nM[1].
[in vitro]

cct241533 inhibited chk2 with an ic50 of 3 nmol/l and showed minimal cross-reactivity against a panel of kinases at 1 mmol/l. cct241533 did not potentiate the cytotoxicity of a selection of genotoxic agents in several cell lines [1]. moreover, as the most potent chk2 inhibitor identified in the series, cct241533 showed potent selectivity (63-fold) over chk1 and low herg inhibition [2].
[IC 50]

Chk2: 3 nM (IC50); Chk1: 245 nM (IC50); Chk2: 1.16 nM (Ki)
[References]

[1] anderson ve, walton mi, eve pd, boxall kj, antoni l, caldwell jj, aherne w, pearl lh, oliver aw, collins i, garrett md. cct241533 is a potent and selective inhibitor of chk2 that potentiates the cytotoxicity of parp inhibitors. cancer res. 2011;71(2):463-72.
[2] caldwell jj, welsh ej, matijssen c, anderson ve, antoni l, boxall k, urban f, hayes a, raynaud fi, rigoreau lj, raynham t, aherne gw, pearl lh, oliver aw, garrett md, collins i. structure-based design of potent and selective 2-(quinazolin-2-yl)phenol inhibitors of checkpoint kinase 2. j med chem. 2011;54(2):580-90.
Spectrum DetailBack Directory
[Spectrum Detail]

CCT 241533 hydrochloride(1431697-96-9)1HNMR
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