Ginkgetin
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Ginkgetin
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CAS No:
481-46-9
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Formula:
C32H22O10
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Chemical Name:
Ginkgetin
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Synonyms:
4H-1-Benzopyran-4-one,5,7-dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl]-2-(4-hydroxyphenyl)-;3′′′,8-Biflavone,4′,5,5′′,7-tetrahydroxy-4′′′,7′′-dimethoxy-;5,7-Dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl]-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Ginkgetin;Amentoflavone 7′′,4′′′-dimethyl ether;7,4′-Dimethylamentoflavone;Ginkgotin
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CAS No:
Description
Ginkgetin is a natural biflavonoid isolated from leaves of Ginkgo biloba L; effects of anti-inflammation and anticancer have been reported.IC50 value:Target:in vitro: Ginkgetin inhibits COX-2 dependent phases of prostaglandin D(2) (PGD(2)) generation in bone marrow-derived mast cells (BMMC) in a concentration-dependent manner with IC(50) values of 0.75 microM. Ginkgetin consistently inhibited the production of leukotriene C(4) (LTC(4)) in a dose dependent manner, with an IC(50) value of
Solid
Ginkgetin is a biflavonoid that is the 7,4'-dimethyl ether derivative of amentoflavone. Isolated from Ginkgo biloba and Dioon, it exhibits anti-HSV-1, antineoplastic and inhibitory activities towards arachidonate 5-lipoxygenase and cyclooxygenase 2. It has a role as an anti-HSV-1 agent, a cyclooxygenase 2 inhibitor, an EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor, an antineoplastic agent and a metabolite. It is a biflavonoid, a hydroxyflavone, a methoxyflavone and a ring assembly. It derives from an amentoflavone.
Characteristics
152
4.45
Solid
1.5±0.1 g/cm3
297 °C @ Solvent: Acetone
863.7±65.0 °C at 760 mmHg
287.2±27.8 °C
1.714
0.002419 mg/L @ 25 °C (est)
2.28E-31mmHg at 25°C
Ginkgetin Use and Manufacturing
Polyketides [PK] -> Flavonoids [PK12] -> Biflavonoids and polyflavonoids [PK1204]
Computed Properties
Molecular Weight:566.5
XLogP3:5.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:5
Exact Mass:566.12129689
Monoisotopic Mass:566.12129689
Topological Polar Surface Area:152
Heavy Atom Count:42
Complexity:1080
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Regulation of the circulatory system: It produces arterial relaxation by stimulating the release of catecholamines and inhibiting their degradation, as well as stimulating the production of prostacyclin and endothelial relaxing factor, thereby maintaining the tension of arteries and veins.
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