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107534-93-0

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107534-93-0 Usage

Description

Anwulignan, a bioactive chemical compound, is a member of the lignan class and is naturally found in Schisandra fruit. It is characterized by a chemical structure with two benzene rings connected by an aliphatic chain and has the molecular formula C18H16O8. Anwulignan exhibits a range of therapeutic properties, including cytotoxic, antimicrobial, and anti-inflammatory activities, which make it valuable for medical and pharmaceutical applications. However, more research is required to fully understand its metabolic pathways and pharmacological potential.

Uses

Used in Pharmaceutical Applications:
Anwulignan is used as a therapeutic agent for its cytotoxic, antimicrobial, and anti-inflammatory properties, making it beneficial in the development of new drugs and treatments.
Used in Medical Applications:
Anwulignan is used as a potential treatment option for various medical conditions due to its demonstrated therapeutic effects, such as its ability to combat infections and reduce inflammation.
Used in Antimicrobial Applications:
Anwulignan is used as an antimicrobial agent to combat bacterial and fungal infections, given its natural ability to inhibit the growth of these microorganisms.
Used in Anti-inflammatory Applications:
Anwulignan is used as an anti-inflammatory agent to reduce inflammation and alleviate pain, making it a potential candidate for the treatment of inflammatory conditions.
Used in Cancer Research:
Anwulignan is used as a cytotoxic agent in cancer research, as its ability to inhibit the growth of cancer cells could lead to the development of new cancer therapies.
Used in Drug Delivery Systems:
Anwulignan is used in the development of drug delivery systems to improve the bioavailability and therapeutic outcomes of medications, taking advantage of its natural properties to enhance drug efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 107534-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,3 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107534-93:
(8*1)+(7*0)+(6*7)+(5*5)+(4*3)+(3*4)+(2*9)+(1*3)=120
120 % 10 = 0
So 107534-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O4/c1-13(8-15-4-6-17(21)19(10-15)22-3)14(2)9-16-5-7-18-20(11-16)24-12-23-18/h4-7,10-11,13-14,21H,8-9,12H2,1-3H3/t13-,14+/m0/s1

107534-93-0 Well-known Company Product Price

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  • Sigma

  • (SML1519)  Macelignan  ≥98% (HPLC)

  • 107534-93-0

  • SML1519-5MG

  • 983.97CNY

  • Detail
  • Sigma

  • (SML1519)  Macelignan  ≥98% (HPLC)

  • 107534-93-0

  • SML1519-25MG

  • 3,970.98CNY

  • Detail

107534-93-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(2S,3R)-4-(1,3-benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol

1.2 Other means of identification

Product number -
Other names HMS2219A18

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107534-93-0 SDS

107534-93-0Downstream Products

107534-93-0Relevant articles and documents

Synthesis of Lignans Based on a Borate-mediated One-pot Sequential Suzuki-Miyaura Coupling of Cyclic Boranes

Sato, Ko,Tanaka, Hiroshi

supporting information, p. 9422 - 9428 (2021/05/26)

Lignans are a group of polyphenolic phytochemicals that possess a large spectrum of chemical structures and biological activities. Here the syntheses of lignans – anwulignan, burseran, dehydroxycubebin, ruburisandrin B, and sesamin – are achieved based on a borate-mediated one-pot sequential Suzuki-Miyaura coupling of cis- and trans-fused bicyclic boranes, which were prepared by diastereoselective cyclic hydroboration of exo-cyclic diene with cyclopentyl- and thexylboranes, respectively. A one-pot sequential Suzuki-Miyaura coupling of each cyclic borate with various aryl bromides initiated by activation of the cyclic borane with the carbon nucleophile provided 2,3-dibenzylbutane derivatives with different aromatic substituents. Finally, the syntheses of naturally occurring lignans were accomplished in several steps from the products of Suzuki-Miyaura coupling.

The structure of chicanine, a new lignan from Schisandra sp.

Liu, Jia-Sen,Huang, Mei-Fen,Gao, Yao-Liang,Findlay, John A.

, p. 1680 - 1684 (2007/10/02)

A new lignan, chicanine, isolated from the fruit of Schisandra sp., is shown to possess structure 1, 2S-(3-methoxy-4-hydroxyphenyl)-3R,4S-dimethyl-5S-(3,4-methylenedioxyphenyl)tetrahydrofuran, from spectra analysis and chemical conversions.The tetrahydrof

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