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PKI-179 - CAS# 1197160-28-3PKI 179 is a potent and orally active dual PI3K mTOR inhibitor, with IC50s of 8 nM, 24 nM, 74 nM, 77 nM, and 0. 42 nM for PI3K , PI3K , PI3K , PI3K and mTOR, respectively. PKI 179 also exhibits activity over E545K and H1047R, with IC50s of 14 nM and 11 nM, respectively. PKI 179 shows anti tumor activity in vivo. Product information CAS Number: 1197160 28 3 Molecular Weight: 488. 54 Formula: C25H28N8O3 Chemical Name: 1 {4 [4 (morpholin 4 yl) 6 {3 oxa 8
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PKI-179 is a potent and orally active dual PI3K/mTOR inhibitor, with IC50s of 8 nM, 24 nM, 74 nM, 77 nM, and 0.42 nM for PI3K-α, PI3K-β, PI3K-γ, PI3K-δ and mTOR, respectively. PKI-179 also exhibits activity over E545K and H1047R, with IC50s of 14 nM and 11 nM, respectively. PKI-179 shows anti-tumor activity in vivo.

Product information

CAS Number: 1197160-28-3

Molecular Weight: 488.54

Formula: C25H28N8O3

Chemical Name: 1-{4-[4-(morpholin-4-yl)-6-{3-oxa-8-azabicyclo[3.2.1]octan-8-yl}-1,3,5-triazin-2-yl]phenyl}-3-(pyridin-4-yl)urea

Smiles: O=C(NC1C=CN=CC=1)NC1=CC=C(C=C1)C1=NC(=NC(=N1)N1C2COCC1CC2)N1CCOCC1

InChiKey: WXUUCRLKXQMWRY-UHFFFAOYSA-N

InChi: InChI=1S/C25H28N8O3/c34-25(28-19-7-9-26-10-8-19)27-18-3-1-17(2-4-18)22-29-23(32-11-13-35-14-12-32)31-24(30-22)33-20-5-6-21(33)16-36-15-20/h1-4,7-10,20-21H,5-6,11-16H2,(H2,26,27,28,34)

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

PKI-179 inhibits the cell proliferation, with IC50s of 22 nM and 29 nM for MDA361 and PC3 cells, respectively. PKI-179 shows inhibitory activity against a panel of 361 other kinases, hERG and cytochrome P450 (CYP) isoforms at concentrations up to >30 μM, but does have activity for CYP2C8 (IC50=3 μM).

In Vivo:

PKI-179 (5-50 mg/kg; p.o. once daily for 40 days) inhibits the tumor growth and is well tolerated in nude mice bearing MDA-361 human breast cancer tumors. PKI-179 (50 mg/kg; p.o.) results in good inhibition of PI3K signaling in nude mice bearing MDA361 tumor xenografts. PKI-179 exhibits good oral bioavailability (98% in nude mouse, 46% in rat, 38% in monkey, and 61% in dog) and a high half-life (>60 min) .

Products are for research use only. Not for human use.

PKI-179 - CAS# 1197160-28-3

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