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Adonirubin, a member of the anthraquinone family, is a red pigment naturally occurring in the fungus Aspergillus ochraceus. It is recognized for its anti-tumor and anti-inflammatory properties, making it a subject of interest for pharmaceutical research and development. Its unique structure and biological activities position it as a potential candidate for the creation of new drugs and dyes.

4418-72-8

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4418-72-8 Usage

Uses

Used in Pharmaceutical Industry:
Adonirubin is used as an anti-tumor agent for its potential in treating cancer due to its inherent anti-tumor properties. It is being investigated for its efficacy in targeting and managing various types of cancer.
Used in Inflammation-Related Disease Treatment:
Adonirubin is utilized as an anti-inflammatory agent, leveraging its properties to alleviate inflammation and potentially treat inflammation-related diseases.
Used in Dye Industry:
Adonirubin is employed as a natural dye due to its vibrant red pigmentation, offering an alternative to synthetic dyes in various applications.
Used in Drug Development:
Adonirubin is used as a starting point for the development of new drugs, capitalizing on its biological activities to create novel therapeutics for cancer and inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 4418-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4418-72:
(6*4)+(5*4)+(4*1)+(3*8)+(2*7)+(1*2)=88
88 % 10 = 8
So 4418-72-8 is a valid CAS Registry Number.

4418-72-8Relevant academic research and scientific papers

Synthese von optisch aktiven, natuerlichen Carotinoiden und strukturell verwandten Naturprodukten. IX. Synthese von (3R)-Hydroxyechinenon, (3R,3'R)- und (3R,3'S)-Adonixanthin, (3R)-Adonirubin, deren optischen Antipoden und verwandten Verbindungen

Bernhard, Kurt,Englert, Gerhard,Mayer, Hans,Mueller, Robert K.,Ruettimann, August,et al.

, p. 2469 - 2484 (2007/10/02)

The synthesis of racemic and optically active hydroxyechinenone (12-14), adonixanthin (16-19), adonirubin (22-24), meso-astaxanthin (26) and their corresponding diosphenols (15, 20, 21, 25, 27, 28, and 29) by Wittig reaction is reported, starting from suitable C15-phosphonium salts and C10-aldehydes.

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