Barbigerone-d3

Stable Isotopes API Family: Barbigerone CAT No. CS-T-103351 CAS No. 75425-27-3(unlabelled)
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Product Detail

Barbigerone-d3

Barbigerone Stable Isotopes
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category Stable Isotopes
API Family Barbigerone
Storage Refer MSDS for complete information.
Hazard Information Refer MSDS for complete information.

Barbigerone-d3 Product Information

Barbigerone-d3 is listed under Stable Isotopes. It is associated with Barbigerone and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-103351.

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
Barbigerone-d3
CAS No.
75425-27-3(unlabelled)
CAT No.
CS-T-103351
Molecular Formula
C₂₃H₁₉D₃O₆
Molecular Weight
397.44
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
CC1(C)C=CC2=C(C=CC3=C2OC=C(C4=CC(OC)=C(OC)C=C4OC([2H])([2H])[2H])C3=O)O1
IUPAC Name
8,8-Dimethyl-3-(2,4,5-trimethoxyphenyl)-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one-d3; Ionchocarpusone-d3; Lonchocarpusone-d3
Hazard Compound
Refer MSDS for complete information.

Description

Overview
Barbigerone-d3 is deuterium labelled Barbigerone (B118300), which is an isoflavone that exhibits antiangiogensis, antioxidant, and anti-inflammatory properties. This compound can be isolated from the seeds of Tephrosia barbigera.
Synonyms
8,8-Dimethyl-3-(2,4,5-trimethoxyphenyl)-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one-d3; Ionchocarpusone-d3; Lonchocarpusone-d3
Application Notes
Barbigerone-d3 is deuterium labelled Barbigerone (B118300), which is an isoflavone that exhibits antiangiogensis, antioxidant, and anti-inflammatory properties. This compound can be isolated from the seeds of Tephrosia barbigera.
References
Li, X. et al.:Â Cancer Chemother. Pharmacol. 70, 425 (2012); Gong, T., et al.:Â Planta Med. 75, 236 (2009)
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