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LY2603618

CAS No.
911222-45-2
Chemical Name:
LY2603618
Synonyms
IC-83;CS-508;LY2603618;Rabusertib;LY2603618, >=99%;ly2603618 IC-83;RABUSERTIB;IC-83;Rabusertib (LY2603618);ly2603618 IC-83 USP/EP/BP;IC-83; LY 2603618; LY-2603618
CBNumber:
CB92538917
Molecular Formula:
C18H22BrN5O3
Molecular Weight:
436.3
MDL Number:
MFCD18633253
MOL File:
911222-45-2.mol
Last updated:2023-06-30 15:45:59

LY2603618 Properties

Boiling point 503.1±50.0 °C(Predicted)
Density 1.461
storage temp. -20°C
solubility Soluble in DMSO (up to 10 mg/ml)
form solid
pka 12.06±0.70(Predicted)
color Off-white
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
FDA UNII 3S9L1NU6U7
NCI Drug Dictionary rabusertib

SAFETY

Risk and Safety Statements

HS Code  29349990

LY2603618 price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 20351 LY2603618 ≥98% 911222-45-2 5mg $40 2024-03-01 Buy
Cayman Chemical 20351 LY2603618 ≥95% 911222-45-2 50 mg $236 2024-03-01 Buy
Cayman Chemical 20351 LY2603618 ≥98% 911222-45-2 1mg $32 2022-04-27 Buy
Cayman Chemical 20351 LY2603618 ≥98% 911222-45-2 10mg $72 2024-03-01 Buy
Cayman Chemical 20351 LY2603618 ≥98% 911222-45-2 25mg $158 2024-03-01 Buy
Product number Packaging Price Buy
20351 5mg $40 Buy
20351 50 mg $236 Buy
20351 1mg $32 Buy
20351 10mg $72 Buy
20351 25mg $158 Buy

LY2603618 Chemical Properties,Uses,Production

Description

LY2603618 is a highly selective Chk1 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.

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.

In vivo

In xenograft models, LY2603618 delays tumor growth when given in combination with pemetrexed.

Description

LY2603618 (911222-45-2) is a potent (IC50?= 7nM) and selective (>1000x over Chk2) Checkpoint kinase 1 (Chk1) inhibitor.1?Chk1 is an important regulator of the DNA damage response – combination treatment of LY2603618 with other chemotherapeutic agents significantly increased tumor growth inhibition when compared to chemotherapeutic alone.2,3,4?LY2603618 caused a dramatic suppression of cell growth in MCF-7 and MDA-MB-231 human breast cancer cells?via?Chk1 inhibition induced upregulation of replication stress caused by oncogenes.5

Uses

LY2603618 is a selective Chk1 inhibitor that can treat idiopathic pulmonary fibrosis.

Definition

ChEBI: 1-[5-bromo-4-methyl-2-[[(2S)-2-morpholinyl]methoxy]phenyl]-3-(5-methyl-2-pyrazinyl)urea is a member of ureas.

Biological Activity

Rabusertib (LY2603618, IC-83) is a highly selective inhibitor of Chk1 with potential antitumor activity in cell-free assays, IC50=7 nM, potency against Chk1 versus multiple other protein kinases tested 100 times higher. Rabusertib (LY2603618) induces cell cycle arrest, DNA damage response and autophagy in cancer cells. Rabusertib (LY2603618) induces bak-dependent apoptosis in AML cell lines.

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].

storage

Store at -20°C

References

1) King?et al.?(2014),?Characterization and preclinical development of LY2603618: a selective and potent Chk1 inhibitor; Invest. New Drugs,?32?213 2) Calvo?et al.?(2014),?Preclinical analyses and phase I evaluation of LY2603618 administered in combination with pemetrexed and cisplatin in patients with advanced cancer; Invest. New Drugs,?32?955 3) Calvo?et al. (2016),?Phase I Study of CHK1 Inhibitor LY2603618 in Combination with Gemcitabine in Patients with Solid Tumors; Oncology,?91?251 4) Zhao?et al.?(2016),?Inhibition of CHK1 enhances cell death induced by the Bcl-1-selective inhibitor ABT-199 in acute myeloid leukemia cells; Oncotarget,?7?34785 5) Zhang?et al.?(2016),?Targeting radioresistant breast cancer cells by single agent CHK1 inhibitor via enhancing replication stress; Oncotarget,?7?34688

LY2603618 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 117)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49390 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29220 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24738 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054 trendseenbio@gmail.com China 11681 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8474 58

View Lastest Price from LY2603618 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
ly2603618 IC-83 pictures 2019-12-26 ly2603618 IC-83
911222-45-2
US $9.80 / KG 1g ≥99% 100kg Career Henan Chemical Co

LY2603618 Spectrum

IC-83 ly2603618 IC-83 LY2603618 N-[5-Bromo-4-methyl-2-[(2S)-2-morpholinylmethoxy]phenyl]-N'-(5-methyl-2-pyrazinyl)urea 3-(5-BroMo-4-Methyl-2-[(2s)-Morpholin-2- 1-[5-broMo-4-Methyl-2-[[(2S)-Morpholin-2-yl]Methoxy]phenyl]-3-(5-Methylpyrazin-2-yl)urea (S)-1-(5-bromo-4-methyl-2-(morpholin-2-ylmethoxy)phenyl)-3-(5-methylpyrazin-2-yl)urea N-[5-Bromo-4-methyl-2-[(2S)-2-morpholinylmethoxy]phenyl]-N'-(5-methyl-2-pyrazinyl)urea LY 2603618 LY2603618, >=99% Rabusertib CS-508 IC-83; LY 2603618; LY-2603618 RABUSERTIB;IC-83 Rabusertib (LY2603618) Urea, N-[5-bromo-4-methyl-2-[(2S)-2-morpholinylmethoxy]phenyl]-N'-(5-methyl-2-pyrazinyl)- ly2603618 IC-83 USP/EP/BP 911222-45-2 Inhibitors