Gilteritinib
CAS No. 1254053-43-4
Gilteritinib ( ASP2215;ASP-2215 )
Catalog No. M11028 CAS No. 1254053-43-4
A potent FLT3/AXL inhibitor with IC50 of 0.73 nM/0.29 nM respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 45 | In Stock |
|
5MG | 74 | In Stock |
|
10MG | 111 | In Stock |
|
25MG | 177 | In Stock |
|
50MG | 262 | In Stock |
|
100MG | 411 | In Stock |
|
200MG | Get Quote | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameGilteritinib
-
NoteResearch use only, not for human use.
-
Brief DescriptionA potent FLT3/AXL inhibitor with IC50 of 0.73 nM/0.29 nM respectively.
-
DescriptionA potent FLT3/AXL inhibitor with IC50 of 0.73 nM/0.29 nM respectively; also inhibits LTK and ALK (IC50=0.35 nM and 1.2 nM respectively), and shows >800-fold selectivity over c-Kit; inhibits the growth of Ba/F3 cells expressing either FLT3-ITD, FLT3-D835Y, FLT3-ITD-D835Y, FLT3-ITD-F691 L, and FLT3-ITD-F691I, with IC50 of 1.8 nM, 1.6 nM, 2.1 nM, 22 nM, and 49 nM, respectively; orally bioactive.Blood Cancer Phase 3 Clinical
-
SynonymsASP2215;ASP-2215
-
PathwayTyrosine Kinase
-
TargetFLT3
-
RecptorFLT3;AXL
-
Research AreaCancer
-
IndicationBlood cancer
Chemical Information
-
CAS Number1254053-43-4
-
Formula Weight552.71
-
Molecular FormulaC29H44N8O3
-
Purity>98% (HPLC)
-
SolubilityDMSO
-
SMILESCCC1=C(N=C(C(=N1)C(=O)N)NC2=CC(=C(C=C2)N3CCC(CC3)N4CCN(CC4)C)OC)NC5CCOCC5
-
Chemical Name2-Pyrazinecarboxamide, 6-ethyl-3-[[3-methoxy-4-[4-(4-methyl-1-piperazinyl)-1-piperidinyl]phenyl]amino]-5-[(tetrahydro-2H-pyran-4-yl)amino]-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Mori M, et al. Invest New Drugs. 2017 May 17. doi: 10.1007/s10637-017-0470-z.
2. Lee LY, et al. Blood. 2017 Jan 12;129(2):257-260.
2. Lee LY, et al. Blood. 2017 Jan 12;129(2):257-260.
molnova catalog
related products
-
KW-2449
A multikinase inhibitor of FLT3/ABL/ABL-T315I/Aurora A/Aurora B with IC50 of 6.6/14/4/48/48 nM respectively.
-
Tandutinib
A potent inhibitor of FLT3, Kit and PDGFR with IC50 of 0.22, 0.17 and 0.2 uM, respectively.
-
CGS 27023A
CGS 27023A is a non-peptidic, potent, and orally active stromelysin inhibitor.