
BLU-263
CAS No. 2505078-08-8
BLU-263( —— )
Catalog No. M37619 CAS No. 2505078-08-8
BLU-263 is an investigational, potent, and selective oral small molecule inhibitor of KIT with sub-nanomolar potency against D816V-mutant KIT.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 91 | Get Quote |
![]() ![]() |
5MG | 141 | Get Quote |
![]() ![]() |
10MG | 226 | Get Quote |
![]() ![]() |
25MG | 420 | Get Quote |
![]() ![]() |
50MG | 550 | Get Quote |
![]() ![]() |
100MG | 772 | Get Quote |
![]() ![]() |
200MG | 1035 | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameBLU-263
-
NoteResearch use only, not for human use.
-
Brief DescriptionBLU-263 is an investigational, potent, and selective oral small molecule inhibitor of KIT with sub-nanomolar potency against D816V-mutant KIT.
-
DescriptionElenestinib (BLU-263) is a potent and orally active tyrosine kinase inhibitor. Elenestinib has the potential for the research of systemic mastocytosis (SM). Elenestinib inhibits KIT D816V with an IC50 value of 0.2 nM.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayAngiogenesis
-
Targetc-Kit
-
Recptorc-Kit
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2505078-08-8
-
Formula Weight528.58
-
Molecular FormulaC27H29FN10O
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 125 mg/mL (236.48 mM; Ultrasonic )
-
SMILESC[C@](N)(c1ccc(F)cc1)c1cnc(nc1)N1CCN(CC1)c1ncnn2cc(cc12)-c1cnn(CCO)c1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Dave N, et al. Safety and pharmacokinetics of BLU-263, a next-generation KIT inhibitor, in healthy volunteers[C]//Cancer Res (AACR Annual Meeting Abstracts). 2021, 122.
molnova catalog



related products
-
DCC-2618
DCC-2618 (Ripretinib, DCC2618) is a potent, oral inhibitor of singly and doubly mutated KIT with IC50 of WT (IC50=4 nM), V654A (8 nM), T670I (18 nM), D816H (5 nM).
-
Apatinib
Apatinib is an orally bioavailable, selective VEGFR2 inhibitor with IC50 of 1 nM.
-
CHMFL-KIT-031
CHMFL-KIT-031 is a highly selective KIT kinase primary V559D mutant inhibitor with IC50/Kd of 28/266 nM.