Gynuramide II

Base Information

• Chemical Name: Gynuramide II
• CAS No.: 295803-03-1
• Molecular Formula: C₄₂H₈₃NO₅
• Molecular Weight: 682.125
• Mol file: 295803-03-1.mol

Synonyms:Tetracosanamide,N-[(1S,2S,3R,7E)-2,3-dihydroxy-1-(hydroxymethyl)-7-heptadecenyl]-2-hydroxy-,(2R)- (9CI); (2S,3S,4R,8E)-2-N-(2'-Hydroxytetracosanoyl)heptadecasphinga-8-ene;Gynuramide II

Chemical Property of Gynuramide II

Chemical Property:

• PSA: 110.02000
• LogP: 11.01630

Purity/Quality:

99% ^*data from raw suppliers

GynuramideII 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: Gynuramide II, a specific chemical compound derived from natural sources, has diverse applications across various fields. In the realm of medicine, it exhibits promising potential as a pharmaceutical agent, with reported anti-inflammatory and anti-cancer properties, making it valuable for drug development and potential treatments for inflammatory conditions and certain types of cancer. In agriculture, Gynuramide II may serve as a natural pesticide due to its reported insecticidal properties, contributing to pest control and crop protection. Furthermore, in the field of biotechnology, it can be used in research settings to explore its various biological activities and potential therapeutic applications. Gynuramide II's multi-faceted roles in medicine, agriculture, and biotechnology highlight its significance and versatility as a chemical compound with diverse applications.

Technology Process of Gynuramide II

There total 1 articles about Gynuramide II which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

Glc-t18:1 h24:0 → (2S,3S,4R,8E/Z)-2N-[(2'R)-2'-hydroxytetracosanoylamino]-8(E/Z)-octadecadiene-1,3,4-triol (295803-03-1)

Guidance literature:

With imiglucerase; DL-dithiothreitol; sodium taurocholate; ascorbic acid; In aq. buffer; at 37 ℃; for 14h; pH=4.5; Enzymatic reaction;

DOI:10.1021/acs.jafc.6b04275

Refernces