
6-Methoxytricin
CAS No. 76015-42-4
6-Methoxytricin( —— )
Catalog No. M32758 CAS No. 76015-42-4
6-Methoxytricin, a flavonoid isolated from Centella asiatica, is an inhibitor of aldose reductase (AR) and advanced glycosylation end-products (AGE), and inhibits T-cell proliferation and activation in biologic cells.
Purity : >98% (HPLC)






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2MG | 99 | In Stock |
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5MG | 143 | In Stock |
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10MG | 254 | In Stock |
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Biological Information
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Product Name6-Methoxytricin
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NoteResearch use only, not for human use.
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Brief Description6-Methoxytricin, a flavonoid isolated from Centella asiatica, is an inhibitor of aldose reductase (AR) and advanced glycosylation end-products (AGE), and inhibits T-cell proliferation and activation in biologic cells.
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Description6-Methoxytricin (Compound 6) is an flavonoid isolated from Artemisia iwayomogi. 6-Methoxytricin (Compound 6) is an inhibitor on aldose reductase (AR) and advanced glycation endproduct (AGE) formation activities with IC50values of 30.29 μM and 134.88 μM, respectively. 6-Methoxytricin (Compound 6) has potential as an anti-diabetic complications agent.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetReductase
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RecptorReductase
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Research Area——
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Indication——
Chemical Information
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CAS Number76015-42-4
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Formula Weight360.31
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Molecular FormulaC18H16O8
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C1C=C(OC2=CC(O)=C(OC)C(O)=C12)C=3C=C(OC)C(O)=C(OC)C3
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference



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Ganoderic acid C2
Ganoderic acid C2 has anti-inflammatory,and anti-tumor-promoting activities. Ganoderic acid C2 can inhibit histamine release, it also has inhibitory effects on the induction of Epstein-Barr Virus early antigen.
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DL-Glyceraldehyde
Glyceraldehyde is produced from the action of the enzyme glyceraldehyde dehydrogenase which converts glycerol to glyceraldehyde using NADP as a cofactor. When present at sufficiently high levels glyceraldehyde can be a cytotoxin and a mutagen. A cytotoxin is a compound that kills cells.
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BYAKANGELICIN(b)
BYAKANGELICINa main furanocoumarin constituent isolated and characterized as an aldose reductase inhibitorand is effective for the treatment of sugar cataracts and diabetic neuropathy and hence might be useful as a lead compound for the development of new type drugs for clinical use.