Pazopanib-13C,d3 hydrochloride

Modify Date: 2024-01-13 18:49:29

Pazopanib-13C,d3 hydrochloride Structure
Pazopanib-13C,d3 hydrochloride structure
Common Name Pazopanib-13C,d3 hydrochloride
CAS Number 1261398-44-0 Molecular Weight 477.990
Density N/A Boiling Point N/A
Molecular Formula C2013CH21D3ClN7O2S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Pazopanib-13C,d3 hydrochloride


Pazopanib-13C,d3 (hydrochloride) is the deuterium and 13C labeled Pazopanib hydrochloride[1]. Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with an IC50 of 10, 30, 47, 84, 74, 140 and 146 nM, respectively[2][3].

 Names

Name 5-[(4-{(2,3-Dimethyl-2H-indazol-6-yl)[(13C,2H3)methyl]amino}-2-pyrimidinyl)amino]-2-methylbenzenesulfonamide hydrochloride (1:1)
Synonym More Synonyms

 Pazopanib-13C,d3 hydrochloride Biological Activity

Description Pazopanib-13C,d3 (hydrochloride) is the deuterium and 13C labeled Pazopanib hydrochloride[1]. Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with an IC50 of 10, 30, 47, 84, 74, 140 and 146 nM, respectively[2][3].
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]. Harris PA, et al. Discovery of 5-[[4-[(2,3-dimethyl-2H-indazol-6-yl)methylamino]-2-pyrimidinyl]amino]-2-methyl-benzenesulfonamide (Pazopanib), a novel and potent vascular endothelial growth factor receptor inhibitor. J Med Chem. 2008, 51(15), 4632-4640.  

[3]. Thakur A, et al. Pazopanib, a multitargeted tyrosine kinase inhibitor, reduces diabetic retinal vascular leukostasis and leakage. Microvasc Res. 2011 Nov82(3):346-50.  

 Chemical & Physical Properties

Molecular Formula C2013CH21D3ClN7O2S
Molecular Weight 477.990
Exact Mass 477.162262

 Synonyms

Benzenesulfonamide, 5-[[4-[(2,3-dimethyl-2H-indazol-6-yl)methyl-13C-d3-amino]-2-pyrimidinyl]amino]-2-methyl-, hydrochloride (1:1)
5-[(4-{(2,3-Dimethyl-2H-indazol-6-yl)[(13C,2H3)methyl]amino}-2-pyrimidinyl)amino]-2-methylbenzenesulfonamide hydrochloride (1:1)