133164-11-1

Basic information

• Product Name: OXYPEUCEDANIN HYDRATE
• Synonyms: OXYPEUCEDANIN HYDRATE;(-)-4-[(S)-2,3-Dihydroxy-3-methylbutoxy]-7H-furo[3,2-g][1]benzopyran-7-one;(S)-(-)-Oxypeucedan hydrate;Oxypeucedan hydrate
• CAS NO: 133164-11-1
• Molecular Formula: C₁₆H₁₆O₆
• Molecular Weight: 304.29
• Mol File: 133164-11-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 544.3±50.0 °C(Predicted)
• Appearance: /
• Density: 1.386±0.06 g/cm3(Predicted)
• PKA: 13.80±0.20(Predicted)
• CAS DataBase Reference: OXYPEUCEDANIN HYDRATE(CAS DataBase Reference)
• NIST Chemistry Reference: OXYPEUCEDANIN HYDRATE(133164-11-1)
• EPA Substance Registry System: OXYPEUCEDANIN HYDRATE(133164-11-1)

Safety Data

• Hazardous Substances Data: 133164-11-1(Hazardous Substances Data)

Usage

General Description

Oxypeucedanin hydrate is a natural chemical compound derived from the plant Angelica archangelica. It is a furanocoumarin that exhibits cytotoxic and anti-inflammatory properties. Oxypeucedanin hydrate has been studied for its potential pharmacological effects, including its ability to inhibit the growth of cancer cells and reduce inflammation. It has also shown promise in the treatment of various skin conditions and as a potential agent for phototherapy. Additionally, oxypeucedanin hydrate has been investigated for its potential use in the development of new pharmaceutical drugs. Overall, this compound offers potential applications in both the fields of medicine and pharmacology.

Upstream product

• 486-60-2 bergaptol 
• 482-45-1 isoimperatorin 
• 870-63-3 prenyl bromide 
• 484-20-8 bergapten 
• 737-52-0 oxypeucedanin 

Downstream Products

• 362467-97-8 1,3,4,5-tetraacetoxy-cyclohexanecarboxylic acid 2-hydroxy-2-methyl-1-(7-oxo-7H-furo[3,2-g]chromen-4-yloxymethyl)-propyl ester 

Relevant articles and documents

Benzofuran and coumarin derivatives from the root of Angelica dahurica and their PPAR-γ ligand-binding activity

A phytochemical investigation of the root of Angelica dahurica led to the isolation of benzofuran and coumarin derivatives. This is the first report of the isolation and identification of three furanocoumarin sulfates from A. dahurica root. The structures of a total of twelve undescribed compounds were determined by extensive spectroscopic analysis, including 2D NMR data, hydrolysis, and solvolysis, followed by either physicochemical and spectroscopic data or X-ray crystallographic analysis. The isolated compounds were evaluated for their PPAR-γ ligand-binding activity, and six compounds showed significant PPAR-γ ligand-binding activity. In particular, the undescribed benzofuran derivative, 3-[6,7-furano-9-hydroxy-4-(2″,3″-dihydroxy-3″-methylbutyloxy)]-phenyl propionic acid, exhibited the most potent PPAR-γ ligand-binding activity and accumulated intracellular lipid in 3T3-L1 cells.

Nonvolatiles of commercial lime and grapefruit oils separated by high-speed countercurrent chromatography

The nonvolatile fractions of cold-pressed peel oils of Key and Persian lime as well as grapefruit were separated by high-speed countercurrent chromatography (HS-CCC). In addition to the isolation of the main coumarins, psoralens and polymethoxyflavones, a

STEROIDS, CHROMONE AND COUMARINS FROM ANGELICA OFFICINALIS

From the ethyl acetate extract of the fresh roots of Angelica officinalis var. himaliaca, besides sitosterol, pregnenolone, peucenin-7-methyl ether, osthol and 18 furanocoumarins have been characterized by spectroscopic methods, including 13C NMR, and some chemical transformations. - Keywords: Angelica officinalis; Umbelliferae; root; pregnenolone; sitosterol; osthol; peucenin-7-methyl ether; furanocoumarins.