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Abemaciclib D8

CAS No.
2088650-53-5
Chemical Name:
Abemaciclib D8
Synonyms
Abemaciclib D8
CBNumber:
CB98019751
Molecular Formula:
C27H32F2N8
Molecular Weight:
506.61
MDL Number:
MOL File:
2088650-53-5.mol
MSDS File:
SDS
Last updated:2026-07-27 17:00:41

Abemaciclib D8 Properties

storage temp. Store at -20°C
form Solid
color White to yellow

Abemaciclib D8 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0374427 Abemaciclib-d8 99.96% 2088650-53-5 1mg $455 2026-06-04 Buy
ChemScene CS-0374427 Abemaciclib-d8 99.96% 2088650-53-5 5mg $1192 2026-06-04 Buy
Arctom HY-16297AS Abemaciclib-d8 99.96% 2088650-53-5 1mg $399 2026-05-26 Buy
Arctom HY-16297AS Abemaciclib-d8 99.96% 2088650-53-5 5mg $1045 2026-05-26 Buy
Product number Packaging Price Buy
CS-0374427 1mg $455 Buy
CS-0374427 5mg $1192 Buy
HY-16297AS 1mg $399 Buy
HY-16297AS 5mg $1045 Buy

Abemaciclib D8 Chemical Properties, Uses, Production

Uses

Isotope labelled Abemaciclib is a potent and selective inhibitor of cyclin-dependent kinases, CDK4 and CDK6, as a method to inhibit the proliferation of cancer cells.

Biological Activity

Abemaciclib-d8 (LY2835219-d8) is the deuterium labeled Abemaciclib. Abemaciclib (LY2835219) is a selective CDK4/6 inhibitor with IC50 values of 2 nM and 10 nM for CDK4 and CDK6, respectively. Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [2]. Ku BM, et al. The CDK4/6 inhibitor LY2835219 has potent activity in combination with mTOR inhibitor in head and neck squamous cell carcinoma. Oncotarget.2016 Mar 22;7(12):14803-13. [3]. Yadav V, et al. The CDK4/6 inhibitor LY2835219 overcomes PLX4032 resistance resulting from MAPK reactivation and cyclin D1 upregulation. Mol Cancer Ther. 2014 Oct;13(10):2253-63. [4]. Gelbert LM, et al. Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with NSC 613327. Invest New Drugs. 2014 Oct;32(5):825-37.

Abemaciclib D8 Preparation Products And Raw materials

Raw materials

Preparation Products

Abemaciclib D8 Suppliers

Global Suppliers ( 12)
Supplier Tel Email Country ProdList Advantage
BOC Sciences +1-631-485-4226 inquiry@bocsci.com United States 19935 58
Guangzhou Younan Technology Co., Ltd 020-82000279 18988941452 YN_research@163.com China 2984 58
SHENZHEN PHYSTANDARD BIO-TECH CO.,LTD 0755-83725350 13380397412 3001280422@qq.com China 10000 58
Manhag Testing Technology Co., Ltd 400-818 0104 18918165978 yanyan.guo@bestown.net.cn China 7770 58
LGC Science (Shanghai) Ltd. 17717235263 offer.de@lgcgroup.com China 19036 58
Shanghai Haohong Scientific Co., Ltd. 400-8210725 4008210725 malulu@leyan.com China 39319 58
Cato Research Chemicals Inc. 81960175 18933936954 2853283383@qq.com China 11418 58
Hubei YoungXin Pharmaceutical Tech Co.,Ltd. 0714-3999001 19171453112 2881391661@qq.com China 10000 58
Aladdin Scientific tp@aladdinsci.com United States 50089 58
Abemaciclib D8 2088650-53-5