AZD-8055
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


AZD-8055
Description :
AZD-8055 is a potent, selective, and orally bioavailable ATP-competitive mTOR kinase inhibitor with an IC50 of 0.8 nM. AZD-8055 inhibits both mTORC1 and mTORC2[1].UNSPSC :
12352005Hazard Statement :
H302, H315, H319, H335Target :
Apoptosis; Autophagy; mTORType :
Reference compoundRelated Pathways :
Apoptosis; Autophagy; PI3K/Akt/mTORApplications :
Cancer-Kinase/proteaseField of Research :
CancerAssay Protocol :
https://www.medchemexpress.com/AZD-8055.htmlPurity :
99.60Solubility :
DMSO : 33.33 mg/mL (ultrasonic)Smiles :
OCC1=CC(C2=NC3=NC(N4CCOC[C@@H]4C)=NC(N5[C@@H](C)COCC5)=C3C=C2)=CC=C1OCMolecular Formula :
C25H31N5O4Molecular Weight :
465.54Precautions :
H302, H315, H319, H335References & Citations :
[1]Chresta CM, et al. AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity. Cancer Res, 2010, 70 (1), 288-298.|[2]You W, et al. Inhibition of mammalian target of rapamycin attenuates early brain injury through modulating microglial polarization after experimental subarachnoid hemorrhage in rats. J Neurol Sci. 2016 Aug 15;367:224-31.|[3]Kawata T, et al. Dual inhibition of the mTORC1 and mTORC2 signaling pathways is a promising therapeutic target for adult T-cell leukemia. Cancer Sci. 2017 Oct 27.Shipping Conditions :
Room TemperatureStorage Conditions :
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category :
Reference compound1Clinical Information :
Phase 1Isoform :
MTOR; mTORC1; mTORC2CAS Number :
[1009298-09-2]

