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294856-66-9

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294856-66-9 Usage

General Description

Cypellocarpin C is a chemical compound derived from the plant Cephalotaxus hainanensis, a member of the Cephalotaxaceae family. It is classified as a polyhydroxylated alkaloid and has shown potential pharmaceutical properties. Research has demonstrated that cypellocarpin C exhibits strong inhibitory activity against a range of human cancer cell lines, making it a promising candidate for the development of anti-cancer drugs. Additionally, it has been found to possess anti-inflammatory and anti-viral properties, further adding to its potential therapeutic applications. The unique chemical structure and bioactivity of cypellocarpin C make it an interesting compound for further study and potential pharmacological development.

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 articles and documents

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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