[CAS NO. 914913-88-5]  Palomid 529 (P529)

Ships within Stock Price Qty Total
$0.00
$0.00
Please click "REQUEST A QUOTE" button if you need other sizes or custom synthesis
request a quote
If there is no stock, or you need other sizes or custom synthesis, please:

PRODUCTS SPECIFICATIONS [914913-88-5]

Store
Catalog
SLK-S2238
Brand
Selleck
CAS
914913-88-5

DESCRIPTION [914913-88-5]

Overview

MDLMFCD18633224
Molecular Weight406.43
Molecular FormulaC24H22O6
SMILESO(C)C=1C=C2C=3C(C(=O)OC2=CC1OCC4=CC=C(OC)C=C4)=CC(C(C)O)=CC3

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 mM2.4604 mL12.3022 mL24.6045 mL
5 mM0.4921 mL2.4604 mL4.9209 mL
10 mM0.2460 mL1.2302 mL2.4604 mL
50 mM0.0492 mL0.2460 mL0.4921 mL

Description

Palomid 529 (P529, SG 00529) inhibits both the and complexes, reduces phosphorylation of pAktS473, pGSK3βS9, and pS6. Phase 1.

Targets

mTORC1 [1]mTORC2 [1]

In vitro

Palomid 529 inhibits proliferation and increases apoptosis of endothelial cells. Palomid 529 inhibits both VEGF-driven and bFGF-driven endothelial cell proliferation with IC50 of 20 nM and 30 nM, respectively. Palomid 529 retains the ability to induce endothelial cell apoptosis. Palomid 529 decreases VEGF-A–driven phosphorylation of pAktS473, pGSK3βS9, and pS6. However, Palomid 529 prevents neither phosphorylated mitogen-activated protein kinase (pMAPK) nor pAktT308 as potently as pAktS473. Palomid 529 not only reduces the proliferative response in the ischemic retina but also improves the organization and structure of the vessels that form. Palomid 529 shows a potent antiproliferative activity in the NCI-60 cell lines panel, with growth inhibitory 50 (GI50) <35 μM. In addition, Palomid 529 significantly enhances the antiproliferative effect of radiation in prostate cancer cells (PC-3). Palomid 529 gives rise to a concentration dependent growth inhibition on PC-3 cells. Doses of 2 and 7μM resulted in 30 and 60% growth inhibition, respectively. Palomid 529 inhibits the radiation-induced p-Akt activation and decreases Bcl-2/Bax ratio in PC-3. Palomid 529 not only inhibits radiation-induced overexpression of Id-1 and VEGF but also down-regulates radiation-induced MMP-2 and MMP-9.


Synonyms

6H-Dibenzo[b,d]pyran-6-one, 8-(1-hydroxyethyl)-2-methoxy-3-[(4-methoxyphenyl)methoxy]-
8-(1-Hydroxyethyl)-2-methoxy-3-[(4-methoxyphenyl)methoxy]-6H-dibenzo[b,d]pyran-6-one
SG 00529
Palomid 529
P 529
8-(1-hydroxyethyl)-2-methoxy-3-(4-methoxybenzyloxy)-benzo[c]chromen-6-one