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Tupichilignan A, a biphenyl compound derived from the bark of T. tupidanthus, exhibits a range of biological activities. It is characterized by its potent cytotoxic activity against various cancer cell lines, such as lung, breast, and colon cancer cells, as well as its inhibitory effects on nitric oxide production, suggesting potential anti-inflammatory properties. The unique chemical structure and promising pharmacological activities of Tupichilignan A position it as a potential candidate for the development of novel anticancer and anti-inflammatory drugs. Further research is required to elucidate its mechanisms of action and explore its potential therapeutic applications.

69586-96-5

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69586-96-5 Usage

Uses

Used in Pharmaceutical Industry:
Tupichilignan A is used as a cytotoxic agent for its potent activity against various cancer cell lines, including lung, breast, and colon cancer cells. Its ability to inhibit tumor growth and progression makes it a promising candidate for the development of anticancer drugs.
Used in Anti-inflammatory Applications:
Tupichilignan A is used as an anti-inflammatory agent due to its inhibitory effects on nitric oxide production. This property suggests its potential use in treating inflammatory conditions and diseases.
Further research is necessary to fully understand the mechanisms of action of Tupichilignan A and to explore its potential therapeutic applications in various fields, including oncology and inflammation management.

Check Digit Verification of cas no

The CAS Registry Mumber 69586-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,8 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69586-96:
(7*6)+(6*9)+(5*5)+(4*8)+(3*6)+(2*9)+(1*6)=195
195 % 10 = 5
So 69586-96-5 is a valid CAS Registry Number.

69586-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,4R)-3-(3,4-Dimethoxybenzyl)-4-[(R)-(3,4-dimethoxyphenyl)(hydr oxy)methyl]dihydro-2(3H)-furanone

1.2 Other means of identification

Product number -
Other names 5-Hydroxylaminopyridin-2-carbonsaeure

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:69586-96-5 SDS

69586-96-5Relevant academic research and scientific papers

Introduction of an Alcoholic Hydroxyl Group into 2,3-Dibenzylbutyrolactone Lignans with Oxidizing Agents and Carbon-13 Nuclear Magnetic Resonance Spectra of the Oxidation Products

Nishibe, Sansei,Chiba, Mariko,Sakushima, Akiyo,Hisada, Sueo,Yamanouchi, Sakae,et al.

, p. 850 - 860 (2007/10/02)

Attempts were made to introduce an alcoholic hydroxyl group stereospecifically at the C-5 or C-6 position of 2,3-dibenzylbutyrolactone lignans with lead tetraacetate and osmic acid as oxidizing agents. 5-Acetoxyarctigenin monoacetate (III) was obtained from arctigenin monoacetate (II), 5-acetoxyisoarctigenin monoacetate (XIII) from isoarctigenin monoacetate (XII) and 5-acetoxytrachelogenin diacetate (XXIII) from trachelogenin diacetate (XXII) by oxidation with lead tetraacetate in acetic acid. 6-Hydroxyisomethyltrachelogenin (XXXII) was obtained from 3-(3,4-dimethoxybenzyl)-2-(3,4-dimethoxybenzylidene)butyrolactone (XXXI) by oxidation with osmic acid.The 13C-NMR spectra of these oxidation products and analogs are discussed with regard to the differences of the chemical shifts resulting from changes in the substituents and the stereochemistry of the 2,3-dibenzylbutyrolactone skeleton.Keywords - 2,3-dibenzylbutyrolactone lignans; reaction with oxidizing agents; introduction of an alcoholic hydroxyl group; 5-hydroxy-2,3-dibenzylbutyrolactone lignans; 2,5-dihydroxy-2,3-dibenzylbutyrolactone lignans; 2,6-dihydroxy-2,3-dibenzylbutyrolactone lignans; 13C-NMR

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