SML0032
Triacetyl resveratrol
≥98% (HPLC)
동의어(들):
3,5,4′-Tri-O-acetylresveratrol, 5-[(1E)-2-[4-(acetyloxy)phenyl]ethenyl]-1,3-Benzenediol-1,3-diacetate
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C20H18O6
CAS Number:
Molecular Weight:
354.35
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.25
추천 제품
Quality Level
분석
≥98% (HPLC)
양식
powder
저장 조건
protect from light
색상
white to tan
solubility
DMSO: ≥18 mg/mL
응용 분야
metabolomics
vitamins, nutraceuticals, and natural products
저장 온도
room temp
SMILES string
CC(=O)Oc1ccc(cc1)\C=C\c2cc(OC(C)=O)cc(OC(C)=O)c2
InChI
1S/C20H18O6/c1-13(21)24-18-8-6-16(7-9-18)4-5-17-10-19(25-14(2)22)12-20(11-17)26-15(3)23/h4-12H,1-3H3/b5-4+
InChI key
PDAYUJSOJIMKIS-SNAWJCMRSA-N
일반 설명
Resveratrol (RSV) is a natural polyphenolic antioxidant.
생화학적/생리학적 작용
Resveratrol prodrug. SIRT inhibitor
Resveratrol prodrug. SIRT inhibitor
Resveratrol (RSV) plays a protective role on the nervous and cardiovascular systems. It is considered as a modulator of energetic metabolism as it controls glucose homeostasis in obese mice, improves fatty acid oxidation (FAO) and promotes the expression of genes that participate in mitochondrial biogenesis.
Resveratrol (RSV) plays a protective role on the nervous and cardiovascular systems. It is considered as a modulator of energetic metabolism as it controls glucose homeostasis in obese mice, improves fatty acid oxidation (FAO) and promotes the expression of genes that participate in mitochondrial biogenesis.
Triacetyl resveratrol displays superior bioavailability to the parent compound, resveratrol. The compound induces p53 activity and inhibits proliferation in breast and prostate tumor cell lines.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
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이미 열람한 고객
Resveratrol induces a mitochondrial complex I dependent increase in NADH oxidation responsible for sirtuin activation in liver cells.
Desquiret-Dumas V, et al.
The Journal of Biological Chemistry, 2013 (2013)
Tammy R Dugas et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 107(3), 646-651 (2018-08-10)
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Hyeanjeong Jeong et al.
International journal of molecular sciences, 20(17) (2019-09-05)
Epigenetic remodeling via histone acetylation has become a popular therapeutic strategy to treat Alzheimer's disease (AD). In particular, histone deacetylase (HDAC) inhibitors including M344 and SAHA have been elucidated to be new drug candidates for AD, improving cognitive abilities impaired
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Journal of innate immunity, 13(2), 94-106 (2020-09-17)
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