[CAS NO. 1251156-08-7]  XL388

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PRODUCTS SPECIFICATIONS [1251156-08-7]

Catalog
SLK-S7035
Brand
Selleck
CAS
1251156-08-7

DESCRIPTION [1251156-08-7]

Overview

MDLMFCD24386875
Molecular Weight455.5
Molecular FormulaC23H22FN3O4S
SMILESO=C(N1CCOC2=CC=C(C3=CC=C(N)N=C3)C=C2C1)C4=CC=C(S(=O)(C)=O)C(F)=C4C

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.1954 mL10.9769 mL21.9539 mL
5 mM---
10 mM---
50 mM---

Description

XL388 is a highly potent, selective, ATP-competitive inhibitor of with of 9.9 nM, 1000-fold selectivity over the closely related PI3K kinases.

Targets

mTORC1 [1]mTOR [2]mTORC2 [1]
8 nM9.9 nM166 nM

In vitro

In MCF-7 cells, XL388 blocks mTORC1 phosphorylation of p70S6K (T389)with an IC50 value of 94 nM and blocks mTORC2 phosphorylationof AKT (S473) with an IC50 value of 350 nM. In vitro, XL388 inhibits the viability of solid and hematopoietic tumor cell lines. The proliferation IC50 is 1.37 μM in MCF-7 cell line. XL388 also synergizes with chemotherapeutics in cell-based assays to block cell viability.

In vivo

When dosed orally once daily in mice, XL388 shows robust anti-tumor activity in multiple xenograft models including > 100% tumor growth inhibition in the MCF-7 xenograft model. XL388 displays good pharmacokinetics and oral exposure in multiple species with moderate bioavailability. The mean plasma protein binding of XL388 in human, monkey, dog, rat, and mouse plasma is evaluated at 5 μM and is determined to be 86%, 90%, 89%, 85%, and 84%, respectively. Oral administration of XL388 to athymic nude mice implanted with human tumor xenografts afforded significant and dose-dependent antitumor activity. Strong inhibition of both mTORC1 and mTORC2 is achieved 4−8 h following administration orally at 100 mg/kg. Modest inhibition (39−45%) of phosphorylation of the PI3K target AKT (T308) is also observed 4−8 h post dose.