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1080622-86-1

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1080622-86-1 Usage

Description

CP466722 is an inhibitor of ataxia-telangiectasia mutated (ATM) kinase, which plays a crucial role in the cellular response to DNA damage. It is a competitive, reversible inhibitor that effectively inhibits ionizing radiation-induced ATM autophosphorylation and phosphorylation of ATM targets such as SMC1, Chk2, and p53 in HeLa cells. CP466722 is selective for ATM over other kinases like PI3K and PIKK, making it a potential candidate for therapeutic applications in cancer treatment.

Uses

Used in Cancer Treatment:
CP466722 is used as an inhibitor of ATM kinase for its potential application in cancer treatment. By inhibiting ATM kinase, it can decrease cell survival in response to ionizing radiation in HeLa cells and exhibit cytotoxic effects on breast cancer cells, such as MCF-7 and SKBr-3, with IC50s of 16.92 and 12.78 μM, respectively. This suggests that CP466722 may have therapeutic potential in the treatment of certain types of cancer, particularly those involving ATM kinase dysregulation.
Used in Radiotherapy:
CP466722 is used as a radiosensitizer in radiotherapy to enhance the effectiveness of ionizing radiation in cancer treatment. By inhibiting ATM kinase, it can increase the sensitivity of cancer cells to radiation, potentially leading to improved treatment outcomes for patients undergoing radiotherapy.
Used in Research:
CP466722 is used as a research tool for studying the role of ATM kinase in various cellular processes, particularly those related to DNA damage response and cell cycle regulation. Its selective inhibition of ATM kinase makes it a valuable compound for investigating the molecular mechanisms underlying the cellular response to DNA damage and the development of cancer.

references

[1]. guo, k., et al., development of a cell-based, high-throughput screening assay for atm kinase inhibitors. j biomol screen, 2014. 19(4): p. 538-46.[2]. nadkarni, a., et al., atm inhibitor ku-55933 increases the tmz responsiveness of only inherently tmz sensitive gbm cells. j neurooncol, 2012. 110(3): p. 349-57. [3]. rainey, m.d., et al., transient inhibition of atm kinase is sufficient to enhance cellular sensitivity to ionizing radiation. cancer res, 2008. 68(18): p. 7466-74.

Check Digit Verification of cas no

The CAS Registry Mumber 1080622-86-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,0,6,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1080622-86:
(9*1)+(8*0)+(7*8)+(6*0)+(5*6)+(4*2)+(3*2)+(2*8)+(1*6)=131
131 % 10 = 1
So 1080622-86-1 is a valid CAS Registry Number.

1080622-86-1 Well-known Company Product Price

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  • Sigma

  • (SML1115)  CP466722  ≥98% (HPLC)

  • 1080622-86-1

  • SML1115-5MG

  • 1,979.64CNY

  • Detail
  • Sigma

  • (SML1115)  CP466722  ≥98% (HPLC)

  • 1080622-86-1

  • SML1115-25MG

  • 6,832.80CNY

  • Detail

1080622-86-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6,7-dimethoxyquinazolin-4-yl)-5-pyridin-2-yl-1,2,4-triazol-3-amine

1.2 Other means of identification

Product number -
Other names HMS3265B19

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1080622-86-1 SDS

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