An inhibitor of mTORC1 and mTORC2 formation
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Palomid 529

Item No. 22706

Technical Information
Formal Name
8-(1-hydroxyethyl)-2-methoxy-3-[(4-methoxyphenyl)methoxy]-6H-dibenzo[b,d]pyran-6-one
CAS Number
914913-88-5
Synonyms
  • P529
  • RES-529
  • SG 00529
Molecular Formula
C24H22O6
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 30 mg/mlDMF:PBS (pH 7.2)(1:3): 0.25 mg/mlDMSO: 25 mg/ml
λmax
219, 279, 315 nm
SMILES
OC(C)C1=CC=C2C(C(OC3=C2C=C(OC)C(OCC4=CC=C(OC)C=C4)=C3)=O)=C1
InChi Code
InChI=1S/C24H22O6/c1-14(25)16-6-9-18-19-11-22(28-3)23(12-21(19)30-24(26)20(18)10-16)29-13-15-4-7-17(27-2)8-5-15/h4-12,14,25H,13H2,1-3H3
InChi Key
YEAHTLOYHVWAKW-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Palomid 529 (P529) is an inhibitor of mammalian target of rapamycin complex (mTORC) formation.1 It is a derivative of a non-steroidal estrogen antagonist that has anti-angiogenic and anticancer activity but lacks estrogen receptor binding activity in estrogen binding assays in vitro. Palomid 529 inhibits VEGF-driven and bFGF-driven endothelial cell proliferation (IC50s = 20 and 30 nM, respectively) and reduces VEGF-A-driven phosphorylation of AktS473, an mTORC2 substrate. In vivo, palomid 529 inhibits retinal neovascularization in mice with oxygen-induced retinopathy, a commonly used assay for pathogenic angiogenesis, Ad-VEGF-A-driven angiogenesis, and phosphorylation of AktS473. Palomid 529 has anticancer effects in glioma cancer cells and xenografts via AktS473 signaling downtstream of mTORC.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Xue, Q., Hopkins, B., Perruzzi, C., et alPalomid 529, a novel small-molecule drug, is a TORC1/TORC2 inhibitor that reduces tumor growth, tumor angiogenesis, and vascular permeability. Cancer Res. 68(22), 9551-9557 (2008).