[CAS NO. 911222-45-2]  Rabusertib (LY2603618)

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PRODUCTS SPECIFICATIONS [911222-45-2]

Store
Catalog
SLK-S2626
Brand
Selleck
CAS
911222-45-2

DESCRIPTION [911222-45-2]

Overview

MDLMFCD18633253
Molecular Weight436.3
Molecular FormulaC18H22BrN5O3
SMILESO=C(NC1=NC=C(C)N=C1)NC2=CC(Br)=C(C)C=C2OC[C@@H]3CNCCO3

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.2920 mL11.4600 mL22.9200 mL
5 mM0.4584 mL2.2920 mL4.5840 mL
10 mM0.2292 mL1.1460 mL2.2920 mL
50 mM0.0458 mL0.2292 mL0.4584 mL

Description

Rabusertib (LY2603618, IC-83) is a highly selective inhibitor with potential anti-tumor activity in a cell-free assay. IC50=7 nM, showing approximately 100-fold more potent against Chk1 than against any of the other protein kinases evaluated. Rabusertib (LY2603618) induces cell cycle arrest, DNA damage response and in cancer cells. Rabusertib (LY2603618) induces bak-dependent in AML cell lines.

Targets

Chk1 [1]
(Cell-free assay)
7 nM

In vitro

Chk1 is an ATP-dependent serine-threonine kinase and a key component in the DNA replication-monitoring checkpoint system activated by double-stranded breaks (DSBs). Chk1 contributes to all currently defined cell cycle checkpoints, including G1/S, intra-S-phase, G2/M, and the mitotic spindle checkpoint. By inhibiting the activity of chk1, LY2603618 prevents the repair of DNA caused by DNA-damaging agents, thus potentiating the antitumor efficacies of various chemotherapeutic agents. However, preclinical data involving LY2603618 has not been published until now. Inhibition of Chk1 is predicted to enhance the effects of antimetabolites, such as gemcitabine. LY2603618 treatment impairs DNA synthesis, increases DNA damage (via mitotic defects), induces apoptosis, and has synergistic activity with pemetrexed, especially in p53 mutant tumor cells.