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Merck
CN

SMB00074

Sigma-Aldrich

Viniferin

≥95% (LC/MS-ELSD)

别名:

(+)-ε-Viniferin

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About This Item

经验公式(希尔记法):
C28H22O6
分子量:
454.47
UNSPSC代码:
12352205
PubChem化学物质编号:
NACRES:
NA.25

质量水平

检测方案

≥95% (LC/MS-ELSD)

形式

solid

应用

metabolomics
vitamins, nutraceuticals, and natural products

储存温度

−20°C

InChI

1S/C28H22O6/c29-19-7-2-16(3-8-19)1-4-18-13-22(32)15-25-26(18)27(23-12-11-21(31)14-24(23)33)28(34-25)17-5-9-20(30)10-6-17/h1-15,27-33H/b4-1+/t27-,28+/m0/s1

InChI key

KQXXUMAWOUVEHD-BQYFGGCBSA-N

一般描述

Natural product derived from plant source.

应用

Viniferin has been used to study its effect on melanin production in melanocyte cultures.

生化/生理作用

Protein Huntingtin (Htt) mutation, reduces the SIRT3 (sirtuin 3) expression. Viniferin is known to offer protection against Htt mutation by reducing oxidative stress and preventing SIRT3 depletion, which is involved in energy metabolism. In vitro analysis showed that viniferin derivative could prevent amyloid β peptide aggregation.

象形图

Environment

警示用语:

Warning

危险声明

预防措施声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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trans-(−)-ε-Viniferin increases mitochondrial sirtuin 3 (SIRT3), activates AMP-activated protein kinase (AMPK), and protects cells in models of Huntington Disease
Fu J, et al.
The Journal of Biological Chemistry, 287(29) (2012)
Protective effect of varepsilon-viniferin on beta-amyloid peptide aggregation investigated by electrospray ionization mass spectrometry
Richard T, et al.
Bioorganic & Medicinal Chemistry, 19(10) (2011)
Advances in Chorea Research and Treatment (2013)
Aude Pflieger et al.
PloS one, 8(11), e81184-e81184 (2013-12-07)
Polynucleotidyl transferases are enzymes involved in several DNA mobility mechanisms in prokaryotes and eukaryotes. Some of them such as retroviral integrases are crucial for pathogenous processes and are therefore good candidates for therapeutic approaches. To identify new therapeutic compounds and
α-Viniferin Improves Facial Hyperpigmentation via Accelerating Feedback Termination of cAMP/PKA-Signaled Phosphorylation Circuit in Facultative Melanogenesis.
Yun C Y, et al.
Theranostics, 8(7), 2031-2031 (2018)

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