sciadopitysin

amentoflavone-4',4''',7''-trimethylether

CAS: 521-34-6 C33 H24 O10 MW: 580.54628000

Identification

Namesciadopitysin
IUPAC5,7-dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)-2-methoxyphenyl]-2-(4-methoxyphenyl)chromen-4-one
CAS Number521-34-6
EINECS208-311-5
FDA UNIIWL44VY201L
Molecular FormulaC33 H24 O10
Molecular Weight580.54628000
MDL NumberMFCD00017448
Nikkaji NumberJ92.489J

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 839.60 °C. @ 760.00 mm Hg (est)
Flash Point 529.00 °F. TCC ( 276.20 °C. ) (est)
logP (o/w) 5.500 (est)
Soluble in water, 0.0006502 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for sciadopitysin usage levels up tonot for fragrance use.
Recommendation for sciadopitysin flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

amentoflavone-4',4''',7''-trimethylether amentoflavone-4',4",7-trimethyl ether amentoflavone-7,4',4'''-trimethyl ether 5,7- dihydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-1- benzopyran-2-yl)-2-methoxyphenyl)-2-(4-methoxyphenyl)-4- benzopyrone 5,7- dihydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl)-2-(4-methoxyphenyl)-4-benzopyrone 5,7- dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl]-2-(4-methoxyphenyl)-4-benzopyrone 5,7- dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2-methoxyphenyl]-2-(4-methoxyphenyl)-4H-chromen-4-one 5,7- dihydroxy-8-[5-(5-hydroxy-7-méthoxy-4-oxo-4H-chromén-2-yl)-2-méthoxyphényl]-2-(4-méthoxyphényl)-4H-chromén-4-one 5,7- dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)-2-methoxyphenyl]-2-(4-methoxyphenyl)chromen-4-one PubMed: Sciadopitysin alleviates methylglyoxal-mediated glycation in osteoblastic MC3T3-E1 cells by enhancing glyoxalase system and mitochondrial biogenesis. PubMed: Sciadopitysin: active component from Taxus chinensis for anti-Alzheimer's disease. PubMed: Sciadopitysin protects osteoblast function via its antioxidant activity in MC3T3-E1 cells. PubMed: Two new nonacosanetriols from Ginkgo biloba sarcotesta. PubMed: [Structrue identification of biflavones and determination of Taxol from Taxus Madia]. PubMed: [Non-taxoid chemical constituents from leaves of Taxus mairei]. PubMed: New constituent from Podocarpus macrophyllus var. macrophyllus shows anti-tyrosinase effect and regulates tyrosinase-related proteins and mRNA in human epidermal melanocytes. PubMed: In vitro peroxynitrite scavenging activity of 6-hydroxykynurenic acid and other flavonoids from Gingko biloba yellow leaves. PubMed: Biflavonoids inhibited phosphatase of regenerating liver-3 (PRL-3). PubMed: Osteoblast differentiation stimulating activity of biflavonoids from Cephalotaxus koreana. PubMed: Inhibition of cGMP-phosphodiesterase-5 by biflavones of Ginkgo biloba. PubMed: Biflavones from Chamaecyparis obtusa. PubMed: Chemical constituents from Amentotaxus yunnanensis and Torreyayunnanensis. PubMed: Antifungal activity of biflavones from Taxus baccata and Ginkgo biloba. PubMed: Biflavones of Ginkgo biloba stimulate lipolysis in 3T3-L1 adipocytes. PubMed: Effect of biflavones of Ginkgo biloba against UVB-induced cytotoxicity in vitro. PubMed: Inhibition of cAMP-phosphodiesterase by biflavones of Ginkgo biloba in rat adipose tissue. PubMed: [HPLC determination of six flavonoid constituents in Ginkgo biloba leaves]. PubMed: Effects of flavonoids of Ginkgo biloba on proliferation of human skin fibroblast. PubMed: Suppression of mouse lymphocyte proliferation in vitro by naturally-occurring biflavonoids. PubMed: Flavonoid-induced acute nephropathy. PubMed: Inhibition of human non-pancreatic phospholipases A2 by retinoids and flavonoids. Mechanism of action. PubMed: Flavone modulators of rat hepatic aryl hydrocarbon hydroxylase. PubMed: HPLC Separation and Quantitative Determination of Biflavones in Leaves from Ginkgo biloba.