
N-Desethylsunitinib hydrochloride
CAS No. 1261432-05-6
N-Desethylsunitinib hydrochloride( —— )
Catalog No. M23434 CAS No. 1261432-05-6
N-Desethylsunitinib hydrochloride is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFRβ, and KIT inhibitor.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 272 | In Stock |
![]() ![]() |
10MG | 408 | In Stock |
![]() ![]() |
25MG | 672 | In Stock |
![]() ![]() |
50MG | 945 | In Stock |
![]() ![]() |
100MG | Get Quote | In Stock |
![]() ![]() |
200MG | Get Quote | In Stock |
![]() ![]() |
500MG | Get Quote | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameN-Desethylsunitinib hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionN-Desethylsunitinib hydrochloride is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFRβ, and KIT inhibitor.
-
DescriptionN-Desethylsunitinib hydrochloride is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFRβ, and KIT inhibitor.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayAngiogenesis
-
Targetc-Kit
-
RecptorKIT|PDGFRβ|VEGFR
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1261432-05-6
-
Formula Weight406.88
-
Molecular FormulaC20H24ClFN4O2
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESO=C1C(C2=CC(F)=CC=C2N1)=CC(NC(C)=C3C(NCCNCC)=O)=C3C.Cl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Determination of Sunitinib and Its Active Metabolite N-Desethylsunitinib in Sweat of a Patient.[J]. Journal of Analytical Toxicology, 2011.
molnova catalog



related products
-
KBP-7018
A novel potent, multikinase inhibitor with IC50 of 10, 7.6 and 25 nM for c-Kit, RET and PDGFRβ, respectively.
-
AMG-25
AMG-25 is a novel selective and potent c-Kit inhibitor.
-
Amuvatinib
A novel RTK inhibitor that effectively inhibits c-Kit, PDGFRα and Flt3 with IC50 of 10 nM, 40 nM and 81 nM, respectively.