
A-770041
CAS No. 869748-10-7
A-770041( —— )
Catalog No. M24879 CAS No. 869748-10-7
A-770041 is selective and orally active Src-family Lck inhibitor, and the other Src family kinase involved in T-cell signaling.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 180 | In Stock |
![]() ![]() |
5MG | 258 | In Stock |
![]() ![]() |
10MG | 432 | 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 NameA-770041
-
NoteResearch use only, not for human use.
-
Brief DescriptionA-770041 is selective and orally active Src-family Lck inhibitor, and the other Src family kinase involved in T-cell signaling.
-
DescriptionA-770041 is selective and orally active Src-family Lck inhibitor, and the other Src family kinase involved in T-cell signaling. A-770041 is a 147 nM inhibitor of Lck (1 mM ATP) and is 300-fold selective against Fyn, IC50 value: 147 nM Target: Lck.
-
In VitroA-770041 selective inhibits Lck with an IC50 value of 0.147 μM, and inhibits other Src family kinase Src, Fgr, Fyn with IC50s of 9.1, 14.1 and 44.1 μM, respectively.A-770041 (0-30 μM; 2 h) dose-dependently inhibits anti-CD3 induced IL-2 production with an EC50 value of 80 nM.
-
In VivoA-770041 (2.5 mg/kg; i.g. once) inhibits concanavalin A-induced IL-2 in vivo.A-770041 (2.5-20 mg/kg/day; for 14 days) dose-dependently increases the survival rate with doses of 5 and 10 mg/kg/day, and survives 100% of transplanted grafts until 14 days with doses of 10 and 20 mg/kg/day. Animal Model:Male Lewis rats Dosage:2.5 mg/kg Administration:Intragastric administration; 2.5 mg/kg once Result:Showed an inhibition of concanavalin A-induced IL-2 with an in vivo EC50 value of 78 nM.
-
Synonyms——
-
PathwayTyrosine Kinase
-
TargetSrc
-
RecptorLck
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number869748-10-7
-
Formula Weight621.73
-
Molecular FormulaC34H39N9O3
-
Purity>98% (HPLC)
-
SolubilityDMSO: 100 mg/mL (160.84 mM)
-
SMILESCC(N(CC1)CCN1C(CC1)CCC1n(c1ncnc(N)c11)nc1-c(cc1)cc(OC)c1NC(c1cc(cccc2)c2n1C)=O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Stachlewitz RF, et al.A-770041, a novel and selective small-molecule inhibitor of Lck, prevents heart allograft rejection.J Pharmacol Exp Ther. 2005 Oct;315(1):36-41.
molnova catalog



related products
-
DGY-06-116
DGY-06-116 is an selective and irreversible covalent inhibitor of Src and FGFR1 with IC50 value of 3nM and 8340 nM, respectively.
-
SBC-115076
SBC-115076 is a potent extracellular proprotein convertase subtilisin kexin type 9 (PCSK9) antagonist.
-
P7C3-A20
P7C3 is a drug related to latrepirdine (dimebon), which has neuroprotective and proneurogenic effects, and may be potentially useful for the treatment of Alzheimer's disease and similar neurodegenerative disorders.