145904-69-4

Basic information

• Product Name: (+)-Myristinin A
• Synonyms: (+)-Myristinin A
• CAS NO: 145904-69-4
• Molecular Formula: C33H40O7
• Molecular Weight: 548.672
• Product Categories: Flavaniods
• Mol File: 145904-69-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (+)-Myristinin A(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-Myristinin A(145904-69-4)
• EPA Substance Registry System: (+)-Myristinin A(145904-69-4)

Safety Data

• Hazardous Substances Data: 145904-69-4(Hazardous Substances Data)

Usage

Description

(+)-Myristinin A is a natural compound isolated from the seeds of Myristica fragrans, also known as nutmeg. It belongs to the neolignan family of compounds and exhibits various biological activities, such as anti-inflammatory, antioxidant, and antimicrobial properties. (+)-Myristinin A has demonstrated potential as a therapeutic agent for treating various diseases and conditions, with ongoing research exploring its pharmacological properties and potential medical uses.
Used in Pharmaceutical Industry:
(+)-Myristinin A is used as a therapeutic agent for its potential in treating various diseases and conditions due to its diverse biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties.
Used in Hepatoprotective Applications:
(+)-Myristinin A is used as a hepatoprotective agent for its potential in developing new treatments for liver disorders, given its demonstrated hepatoprotective effects.
Used in Antimicrobial Applications:
(+)-Myristinin A is used as an antimicrobial agent for its ability to combat various microorganisms, contributing to the development of treatments for infectious diseases.
Used in Antioxidant Applications:
(+)-Myristinin A is used as an antioxidant agent for its potential in reducing oxidative stress and contributing to the prevention and treatment of conditions associated with oxidative damage.
Used in Anti-inflammatory Applications:
(+)-Myristinin A is used as an anti-inflammatory agent for its potential in reducing inflammation and alleviating symptoms associated with inflammatory conditions.

Upstream product

• 888026-39-9 1-(2,4,6-trimethoxyphenyl)dodecan-1-one 
• 621-23-8 1,2,3-trimethoxybenzene 
• 112-16-3 n-dodecanoyl chloride 
• 888026-48-0 (2R,3S,4S)-2-(4-benzoxyphenyl)-7-benzoxy-4-(2,4,6-trimethoxy-3-(dodecanoyl)phenyl)chroman-3-yl O-phenylcarbonothioate 
• 888026-40-2 (2R,3S,4S)-7-(benzoxy)-2-(4-(benzoxy)phenyl)-4-(3-dodecanoyl-2,4,6-trimethoxyphenyl)chroman-3-yl acetate 
• 888026-41-3 (2R,3S,4S)-2-(4-benzoxyphenyl)-7-benzoxy-4-(2,4,6-trimethoxy-3-(dodecanoyl)phenyl)chroman-3-ol 
• 888026-38-8 (2R,3S)-2-(4-benzoxyphenyl)-7-benzoxy-4-(2-hydroxyethoxy)chroman-3-yl acetate 
• 888026-43-5 (2R,3S)-7-(benzoxy)-2-(4-(benzoxy)phenyl)chroman-3-yl acetate 
• 850816-16-9 (2R,3S)-2-(4-benzyloxyphenyl)-7-benzyloxychroman-3-ol 
• 888026-42-4 (2S,4S)-2-(4-benzoxyphenyl)-7-benzoxy-4-(2,4,6-trimethoxy-3-(dodecanoyl)phenyl)chroman 
• 850816-10-3 (2R,3R,4R)-2-(4-benzyloxyphenyl)-7-benzyloxy-4-(2,4,6-tribenzyloxy-3-(dodecanoyl)phenyl)chroman-3-yl acetate 
• 850816-18-1 (2R,3R,4R)-2-(4-benzyloxyphenyl)-7-benzyloxy-4-(2,4,6-tribenzyloxy-3-(dodecanoyl)phenyl)chroman-3-ol 
• 850816-19-2 1-(2,4,6-tribenzyloxyphenyl)dodecan-1-one 
• 850816-14-7 (4S,5S)-4-(4-benzyloxyphenyl)-5-(4-benzyloxy-2-(tert-butyldimethylsilyloxy)benzyl)-2-ethoxy-1,3-dioxolane 

Relevant articles and documents

Stereoselective synthesis of the atropisomers of myristinin B/C

The first stereoselective synthesis of a potent DNA damaging agent, (-)-myristinin B/C, has been accomplished. This efficient synthesis allowed for unambiguous confirmation of the structure and absolute stereochemistry of the atropisomeric natural product