Product Detail
Ermanin-D3
Ermanin Stable Isotopes
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Stable Isotopes
API Family
Ermanin
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
Ermanin-D3 Product Information
Ermanin-D3 is listed under Stable Isotopes. It is associated with Ermanin and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-103306.
Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.
Technical Data
Product Name
Ermanin-D3
CAS No.
20869-95-8(unlabelled)
CAT No.
CS-T-103306
Molecular Formula
C₁₇H₁₁D₃O₆
Molecular Weight
317.29
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
O=C(C1=C(O)C=C(O)C=C1O2)C(OC)=C2C(C=C3)=CC=C3OC([2H])([2H])[2H]
IUPAC Name
5,7-Dihydroxy-3-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one-D6; 3,4'-Di-O-methylkaempferol-D6; 5,7-Dihydroxy-3,4'-dimethoxyflavone-D6; Dimethyl-3,4'-kaempferol-D6; Kaempferol 3,4'-di-O-methyl ether-D6; Kaempferol 3,4'-dimethyl ether-D6; NSC 31882-D6
Hazard Compound
Refer MSDS for complete information.
Description
Overview
Ermanin-D3 is a deuterium labelled Ermanin (E658513), which is a useful research chemical used in HIV-1 integrase inhibition. Ermanin exhibits actioxidant properties against peroxyl and hydroxyl radicals.
Synonyms
5,7-Dihydroxy-3-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one-D6; 3,4'-Di-O-methylkaempferol-D6; 5,7-Dihydroxy-3,4'-dimethoxyflavone-D6; Dimethyl-3,4'-kaempferol-D6; Kaempferol 3,4'-di-O-methyl ether-D6; Kaempferol 3,4'-dimethyl ether-D6; NSC 31882-D6
Application Notes
Ermanin-D3 is a deuterium labelled Ermanin (E658513), which is a useful research chemical used in HIV-1 integrase inhibition. Ermanin exhibits actioxidant properties against peroxyl and hydroxyl radicals.
References
Fesen, M. et al.: Biochem. Pharmacol. 48, 3, 595-608 (1994); Cao, G. et al.: Free Radic. Biol. Med. 22, 5, 749-60 (1997)