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Cypellocarpin C is a polyhydroxylated alkaloid chemical compound derived from the plant Cephalotaxus hainanensis, a member of the Cephalotaxaceae family. It has demonstrated potential pharmaceutical properties and is of interest for its unique chemical structure and bioactivity.

294856-66-9

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294856-66-9 Usage

Uses

Used in Pharmaceutical Industry:
Cypellocarpin C is used as an anti-cancer agent for its strong inhibitory activity against a range of human cancer cell lines, making it a promising candidate for the development of anti-cancer drugs.
Used in Anti-inflammatory Applications:
Cypellocarpin C is used as an anti-inflammatory agent due to its demonstrated anti-inflammatory properties, which can be beneficial in treating various inflammatory conditions.
Used in Antiviral Applications:
Cypellocarpin C is used as an anti-viral agent for its anti-viral properties, offering potential in the development of treatments for viral infections.

Check Digit Verification of cas no

The CAS Registry Mumber 294856-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,8,5 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 294856-66:
(8*2)+(7*9)+(6*4)+(5*8)+(4*5)+(3*6)+(2*6)+(1*6)=199
199 % 10 = 9
So 294856-66-9 is a valid CAS Registry Number.

294856-66-9Downstream Products

294856-66-9Relevant academic research and scientific papers

Synthesis of the monoterpenoid esters cypellocarpin C and cuniloside B and evidence for their widespread occurrence in Eucalyptus

Hakki, Zalihe,Cao, Benjamin,Heskes, Allison M.,Goodger, Jason Q.D.,Woodrow, Ian E.,Williams, Spencer J.

, p. 2079 - 2084 (2010)

Short syntheses of cuniloside B and cypellocarpin C, (+)-(R)-oleuropeic acid-containing carbohydrates, are reported. Also disclosed are syntheses of the noreugenin glycosides, undulatoside A and corymbosins K1 and K 2. Leaf extracts of 28 diverse eucalypts revealed cuniloside B to be present in all, and cypellocarpin C to be present in most, of the species examined. The widespread occurrence of these carbohydrate monoterpenoid esters supports their roles in essential oil biosynthesis or mobilization from sites of synthesis to secretory cavity lumena.

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