Erlotinib-13C6 hydrochloride

Modify Date: 2024-01-16 18:46:27

Erlotinib-13C6 hydrochloride Structure
Erlotinib-13C6 hydrochloride structure
Common Name Erlotinib-13C6 hydrochloride
CAS Number 1210610-07-3 Molecular Weight 435.85300
Density N/A Boiling Point N/A
Molecular Formula C22H24ClN3O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Erlotinib-13C6 hydrochloride


Erlotinib-13C6 (hydrochloride) is the 13C labeled Erlotinib Hydrochloride[1]. Erlotinib Hydrochloride (CP-358774 Hydrochloride) inhibits purified EGFR kinase with an IC50 of 2 nM[2].

 Names

Name N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine,hydrochloride

 Erlotinib-13C6 hydrochloride Biological Activity

Description Erlotinib-13C6 (hydrochloride) is the 13C labeled Erlotinib Hydrochloride[1]. Erlotinib Hydrochloride (CP-358774 Hydrochloride) inhibits purified EGFR kinase with an IC50 of 2 nM[2].
Related Catalog
In Vitro 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 Feb;53(2):211-216.  

[2]. Moyer JD, et al. Induction of apoptosis and cell cycle arrest by CP-358,774, an inhibitor of epidermal growth factor receptor tyrosine kinase. Cancer Res. 1997 Nov 1;57(21):4838-48.  

 Chemical & Physical Properties

Molecular Formula C22H24ClN3O4
Molecular Weight 435.85300
Exact Mass 435.16600
PSA 74.73000
LogP 4.28010