
Miransertib
CAS No. 1313881-70-7
Miransertib( ARQ-092 )
Catalog No. M11258 CAS No. 1313881-70-7
Miransertib (ARQ-092) is a potent, selective and allosteric inhibitor of Akt1/2/3 with IC50 of 5/4.5/16 nM respectively.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 88 | In Stock |
![]() ![]() |
10MG | 155 | In Stock |
![]() ![]() |
25MG | 327 | In Stock |
![]() ![]() |
50MG | 537 | In Stock |
![]() ![]() |
100MG | 860 | In Stock |
![]() ![]() |
500MG | 1701 | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameMiransertib
-
NoteResearch use only, not for human use.
-
Brief DescriptionMiransertib (ARQ-092) is a potent, selective and allosteric inhibitor of Akt1/2/3 with IC50 of 5/4.5/16 nM respectively.
-
DescriptionMiransertib (ARQ-092) is a potent, selective and allosteric inhibitor of Akt1/2/3 with IC50 of 5/4.5/16 nM respectively; inhibits cellular AKT activation and the phosphorylation of the downstream target PRAS40; inhibits tumor growth in a human xenograft mouse model of endometrial adenocarcinoma; orally bioavailable.Blood Cancer Phase 1 Clinical(In Vitro):In a large panel of cell lines derived from various tumor types, Miransertib (ARQ-092; Compound 21a) shows potent anti-proliferative activity in cell lines containing PIK3CA/PIK3R1 mutations compared to those with wild-type (wt) PIK3CA/PIK3R1 or PTEN loss. Miransertib shows excellent inhibition of p-Akt (S473) and p-Akt (T308) in both AN3CA and A2780 cells. The inhibition of the downstream protein p-PRAS40 (T246) is observed with Miransertib (IC50=0.31 μM).Miransertib is markedly effective against intracellular amastigotes of L. donovani or L. amazonensis-infected macrophages. Miransertib also enhances mTOR dependent autophagy in Leishmania-infected macrophages(In Vivo):Miransertib (ARQ-092; Compound 21a) shows good absolute oral bioavailability in rats (5 mg/kg) and monkeys (10 mg/kg) with F values of 62% and 49%, respectively. The half-life is longer in rats compared to monkeys with t1/2 values of 17 h in rats versus 7 h in monkeys. The Cmax is 198 ng/mL and 258 ng/mL and the AUCinf was 5496 h?ng/mL and 2960 h?ng/mL in rats and monkeys, respectively.Miransertib (ARQ-092; Compound 21a) inhibits tumor growth in a human xenograft mouse model of endometrial adenocarcinoma.
-
In Vitro——
-
In Vivo——
-
SynonymsARQ-092
-
PathwayPI3K/Akt/mTOR signaling
-
TargetAkt
-
RecptorAkt
-
Research AreaCancer
-
IndicationBlood cancer
Chemical Information
-
CAS Number1313881-70-7
-
Formula Weight432.5197
-
Molecular FormulaC27H24N6
-
Purity>98% (HPLC)
-
SolubilityDMSO: ≥ 40.2 mg/mL
-
SMILESC1CC(C1)(C2=CC=C(C=C2)N3C4=C(C=CC(=N4)C5=CC=CC=C5)N=C3C6=C(N=CC=C6)N)N
-
Chemical Name2-Pyridinamine, 3-[3-[4-(1-aminocyclobutyl)phenyl]-5-phenyl-3H-imidazo[4,5-b]pyridin-2-yl]-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Lapierre JM, et al. J Med Chem. 2016 Jul 14;59(13):6455-69.
2. Kim K, et al. Haematologica. 2017 Feb;102(2):246-259.
3. Roth GS, et al. Mol Cancer Ther. 2017 May 31. pii: molcanther.0602.2016.
molnova catalog



related products
-
GSK-690693
A potent, ATP competitive, pan-AKT inhibitor with IC50 of 2, 13, and 9 nM against AKT1, 2, and 3, respectively.
-
Miransertib
Miransertib (ARQ-092) is a potent, selective and allosteric inhibitor of Akt1/2/3 with IC50 of 5/4.5/16 nM respectively.
-
Triciribine
Triciribine is a DNA synthesis inhibitor, also inhibits Akt and HIV-1 with IC50 of 130 nM and 20 nM, respectively.