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Resveratrol

Resveratrol is a stilbene-type phytoalexin found in the skins and seeds of grapes, as well as in various other plants such as peanuts, soybeans, and mulberries. Similar to other phytoalexins, resveratrol exhibits diverse bioactivities, including antioxidant, anticancer, neuroprotective, and cardioprotective effects.

Figure 1. Chemical Structure of Resveratrol


Main Functions:

Anti-aging: Activates Sirtuin-1, a mechanism associated with its potential anti-aging and metabolic regulatory effects.

Antioxidant: Acts as a potent antioxidant that inhibits low-density lipoprotein (LDL) oxidation and alleviates oxidative stress in vitro.

Anticancer: Demonstrates broad chemopreventive and chemotherapeutic potential in various cell and animal models; also inhibits cyclooxygenase (COX) and peroxidase activities, both of which are closely linked to cancer progression.

Metabolism-promoting: Reduces hepatic fat content and cholesterol levels, and inhibits platelet aggregation.

In addition, the resveratrol derivative pterostilbene, a fully methylated analog of resveratrol, has shown greater efficacy than resveratrol in inhibiting cell and tumor growth in colorectal and prostate cancer models. Another derivative, triacetylresveratrol, is a prodrug of resveratrol with higher bioavailability and similar potential anticancer activity to the parent compound.


Related Products

Name

ID

Grade & Purity

Resveratrol

R107315

Moligand™, ≥99%

Resveratrol

R107314

Moligand™, Analytical Standard

Resveratrol

R408711

Moligand™, 10mM in DMSO

Piceatannol

P108001

≥98%

Piceatannol

P580488

10mM in DMSO

Triacetyl resveratrol

T423911

10mM in DMSO

Triacetyl resveratrol

T133704

≥98%

3,4',5-trimethoxystilbene

T422665

10mM in DMSO

3,4',5-trimethoxystilbene

T108002

≥97%

alpha,beta-Dihydroresveratrol

A424888

10mM in DMSO

alpha,beta-Dihydroresveratrol

A275297

≥98%

Pterostilbene

P424597

Moligand™, 10mM in DMSO

Pterostilbene

P108000

Moligand™, ≥97%


References

1. Das DK, Mukherjee S, Ray D. Heart Fail Rev. 2011 Jul;16(4):425-35.

2. Prasad K. Int J Angiol. 2012 Mar;21(1):7-18.

3. Yin HT, Tian QZ, Guan L, et al. Asian Pac J Cancer Prev. 2013;14(3):1703-6.

4. Pan MH, Gao JH, Lai CS, et al. Mol Carcinog. 2008 Mar;47(3):184-96.

 

Aladdin: https://www.aladdinsci.com/

Categories: 技术文章