8-(1-hydroxyethyl)-2-methoxy-3-[(4-methoxyphenyl)methoxy]-6H-benzo[c]chromen-6-one

• ChemBase编号: 72722
• 分子式: C24H22O6
• 平均质量: 406.42788
• 单一同位素质量: 406.14163842
• SMILES: c1c(ccc(c1)COc1c(cc2c(c1)oc(=O)c1c2ccc(c1)C(C)O)OC)OC
• Canonical SMILES: COc1ccc(cc1)COc1cc2oc(=O)c3c(c2cc1OC)ccc(c3)C(O)C
• InChI: 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
• InChIKey: YEAHTLOYHVWAKW-UHFFFAOYSA-N

名称和登记号

名称

• IUPAC标准名: 8-(1-hydroxyethyl)-2-methoxy-3-[(4-methoxyphenyl)methoxy]-6H-benzo[c]chromen-6-one
• IUPAC传统名: 8-(1-hydroxyethyl)-2-methoxy-3-[(4-methoxyphenyl)methoxy]benzo[c]chromen-6-one
• 别名: P529; Palomid 529

登记号

• CAS号: 914913-88-5
• PubChem SID: 162037643
• PubChem CID: 11998575

理论计算性质

• Acid pKa: 14.5892935
• 质子受体: 5
• 质子供体: 1
• LogD (pH = 5.5): 3.8260121
• LogD (pH = 7.4): 3.826012
• Log P: 3.8260121
• 摩尔折射率: 112.176 cm^3
• 极化性: 44.543434 Å^3
• 极化表面积: 74.22 Å^2
• 可自由旋转的化学键: 6
• 里宾斯基五规则: true

分子性质

安全信息

• 保存条件: -20°C

药理学性质

• 作用靶点: Akt; mTOR

产品相关信息

• 成盐信息: Free Base

详细说明

Selleck Chemicals - S2238

Biological Activity

• Description: Palomid 529 (P529) is a PI3K/Akt/mTOR inhibitor for VEGF-A and bFGF with IC50 of 10 nM and 30 nM, respectively.
• Targets: VEGF-A; bFGF
• IC50: 10 nM; 30 nM ^[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. ^[1] 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.="">^[2]
• In Vivo: Palomid 529 shows a dose-dependent inhibition of the Ad-VEGF-A–driven angiogenesis following Palomid 529 treatment. Palomid 529 inhibits C6V10 glioma tumor growth in nude mice following i.p. dosing. Palomid 529 decreases AktS473 but not AktT308 signaling. Palomid 529 inhibits C6V10 glioma tumor growth in nude mice following i.p. dosing. Palomid 529 decreases AktS473 but not AktT308 signaling. Palomid 529 inhibits tumor growth, angiogenesis, and vascular permeability. ^[1] Treatment of PC-3 tumour-bearing mice with Palomid 529 reduced tumour growth to 57.1% compared with controls. ^[2] Palomid 529 is an effective suppressor of Müller cell proliferation, glial scar formation, and photoreceptor cell death in a rabbit model of retinal detachment (RD). ^[3] Palomid 529 significantly suppresses Brca1-deficient tumor growth in mice through inhibition of both Akt and mTOR signaling. ^[4]
• Clinical Trials: Palomid 529 has entered in a Phase I clinical trial in the treatment of age-related macular degeneration.

Combination Therapy

• Description: Palomid 529 synergizes with Docetaxel and Cisplatin. The strongest synergism is achieved when prostate cancer (PCa) cells are sequentially exposed to Cisplatin or Docetaxel followed by treatment with Palomid 529. Treatment with Palomid 529 before the exposure to chemotherapeutic drugs results in a moderate synergism, whereas intermediated values of combination index are found when drugs are administered simultaneously. In vivo treatment of a combination of Palomid 529 with Docetaxel or Cisplatin increases the percentage of complete responses and reduced the number of mice with tumor progression. ^[5]

Protocol

• Protocol: Kinase Assay ^[1]
• Estrogen receptor binding assays: The proteins are produced with rabbit reticulocyte lysates. The amount of template used in each reaction is determined empirically and expression is monitored in parallel reactions where [^35S]methionine is incorporated into the receptor followed by gel electrophoresis and exposure to film. Binding reactions of the estrogen receptors (ER) and Palomid 529 are carried out in 100 mL final volumes in TEG buffer [10 mM Tris (pH 7.5), 1.5 mM EDTA, 10% glycerol]. In vitro transcribed-translated receptor (5 μL) is used in each binding reaction in the presence of 0.5 nM [^3H]estradiol (E2). Palomid 529 is routinely tested from 10^?11 to 10^?6 M and diluted in ethanol. The reactions are incubated at 4 °C overnight and bound E2 is quantified by adding 200 mL dextran-coated charcoal. After a 15-minutes rotation at 4 °C, the tubes are centrifuged for 10 minutes and 150 mL of the supernatant are added to 5 mL scintillation mixture for determination of cpm by liquid scintillation counting. The maximum binding is determined by competing bound E2 with only the ethanol vehicle. Controls for background are included in each experiment using 5 mL unprogrammed rabbit reticulocyte lysate. This value, typically 10% to 15% of the maximal counts, is subtracted from all values. The data are plotted and K_i values are calculated. Experiments are conducted at least thrice in duplicate.
• Protocol: Cell Assay ^[1]
• Cell Lines: Human umbilical vascular endothelial cells (HUVEC)
• Concentrations: ~20 μM
• Incubation Time: 48 hours
• Methods: Human umbilical vascular endothelial cells (HUVEC) are used. The proliferation assay is carried out by seeding the HUVECs in 96-well plates at a density of 1,000 per well in complete medium. Following a 24-hour plating period, the cells are starved for 24 hours in 0.5% serum before being treated with Palomid 529 in the presence of 10 ng/mL basic fibroblast growth factor (bFGF) or VEGF in complete medium. After 48 hours, cell number is determined using a colorimetric method. The results are expressed as the percentage of the maximal bFGF or VEGF response in the absence of Palomid 529. Nonproliferating endothelial cells are assayed by growing HUVECs to quiescence in 96-well plates and treating with Palomid 529 for 48 hours. Initially, 5,000 cells per well are seeded and confluence is achieved the next day. The plates are incubated for another 24 hours to ensure growth arrest before treatment with Palomid 529.
• Protocol: Animal Study ^[1]
• Animal Models: Female nude mice with C6V10 rat glioma cells or U87 cells
• Doses: 50 mg/kg/2 d, 25 mg/kg/2 d and 200 mg/kg/2 d
• Administration: Administered via i.p.

References

• References: [1] Xue Q, et al. Cancer Res, 2008, 68(22), 9551-9557.
• References: [2] Diaz R, et al. Br J Cancer 2009, 100(6), 932-940.
• References: [3] Lewis GP, et al. Invest Ophthalmol Vis Sci, 2009, 50(9), 4429-4435.
• References: [4] Xiang T, et al. Oncogene, 2011, 30(21), 2443-2450.
• References: [5] Gravina GL, et al. Endocr Relat Cancer, 2011, 18(4), 385-400.

参考文献

• Xue Q, et al. Cancer Res, 2008, 68(22), 9551-9557.
• Diaz R, et al. Br J Cancer 2009, 100(6), 932-940.
• Lewis GP, et al. Invest Ophthalmol Vis Sci, 2009, 50(9), 4429-4435.
• Xiang T, et al. Oncogene, 2011, 30(21), 2443-2450.
• Gravina GL, et al. Endocr Relat Cancer, 2011, 18(4), 385-400.