A8638-5mg | LY2603618 [911222-45-2] Biotrend USA

LY2603618

Catalog No.

A8638

Chk1 inhibitor,highly selective

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Background
Product Citation
Chemical Properties
Protocol
Biological Activity
Quality Control

Background

LY2603618 is a novel small molecular checkpoint kinase 1 (Chk1) inhibitor that has direct anti-tumour effect [1], as well as desensitizing tumour cell against DNA-damaging chemotherapy treatment [2].

Checkpoint kinase 1 (Chk1) is a type of kinase that coordinates damaged-DNA repair [1]. Some tumour cells have been found to possess over-regulated populations of Chk1 that desensitize the cell from DNA-targeting chemotherapy, promoting tumour proliferation [3].

LY2603618 inhibits Chk1 by competing with ATP molecules [2]. In A549 and H1299 non-small cancer cell lines, lethal concentration of LY2603618 (10 /M phase from 13% to 38%) but also directly DNA damage, the latter of which was indicated by the increasing occurrence of H2AX phosphorylation[1].

In vivo, experiment was carried out to determine the combining effect of LY2603618 with other chemotherapy[2] . In mice xenograft model that inculated with Calu-6 lung cancer cell, combining administration of injected gemcitabine 150 mg/kg and orally uptake LY2603618 (200 mg/kg) resulted in increased DNA damage of tumour, as was demonstrated by a 2-fold increase in Chk1 s345 phosphorylation in comparison with mice treated with gemcitabine alone[2].

References:
[1]. kinase inhibitor LY2603618 induces cell cycle arrest, DNA damage response and autophagy in cancer cells. Apoptosis, 2014,19:1389-1398.
[2].: a selective and potent Chk1 inhibitor. Invest New Drugs, 2014, 32: 213-26.
[3]. in cell biology and cancer therapy. Int J Cancer, 2014. 134: 1013-23.

Product Citation

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Chemical Properties

Storage	Store at -20
Cas No.	911222-45-2
Formula	C₁₈H₂₂BrN₅O₃
Solubility	mg/mL in DMSO with gentle warming; insoluble in H2O; insoluble in EtOH
Chemical Name	1-[5-bromo-4-methyl-2-[[(2S)-morpholin-2-yl]methoxy]phenyl]-3-(5-methylpyrazin-2-yl)urea
SDF	Download SDF
Canonical SMILES	CC1=CC(=C(C=C1Br)NC(=O)NC2=NC=C(N=C2)C)OCC3CNCCO3
Shipping Condition	Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips	We do not recommend long-term storage for the solution, please use it up soon.

Protocol

Cell experiment [1]:
Cell lines	HeLa cervical cancer cells, Calu-6 non-small cell lung cancer cells, HT29 and HCT-116 colon cancer cells
Preparation method	The solubility of this compound in DMSO is >21.8mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20 nM, 2500 nM, 24 h
Applications	Treatment with 1250 nM LY2603618 resulted in a clear decrease in the G1 population and an increase in late S-phase cells. Cells treated with 5000 nM LY2603618 were predominantly found in the S-phase peak with a DNA content intermediate between 2 and 4N. LY2603618 induced DNA damage and arrested DNA synthesis while increasing the number of cells expressing an early marker of mitosis. LY2603618 treated cells lacked normal mitotic cells. An increased proportion of LY2603618 treated cells stained for pH3(S10) and were arrested in an abnormal prometaphase relative to the control cells. LY2603618 increased the potency of gemcitabine in p53-mutant HT-29 cells, but not in p53 WT HCT-116 cells
Animal experiment [1]:
Animal models	Female Harlan athymic nude mice bearing Calu-6 xenografts
Dosage form	Oral administration, 200 mg/kg
Application	LY2603618 effectively inhibited the activation of Chk1 but not ATR by gemcitabine in Calu-6 tumor xenografts.
Other notes	Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.
References: [1]. King C, Diaz H, Barnard D, et al. Characterization and preclinical development of LY2603618: a selective and potent Chk1 inhibitor[J]. Investigational new drugs, 2014, 32(2): 213-226.