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2,6-dimethyl-4-[(E)-2-(2-phenylmethoxyphenyl)ethenyl]phenol, commonly known as bis-resveratrol, is a chemical compound derived from resveratrol, a natural compound found in grapes and other plants. It is characterized by its molecular structure, which includes two methyl groups and a phenol ring with a phenylmethoxyphenyl ethenyl substituent. Bis-resveratrol possesses potential antioxidant and anti-inflammatory properties, making it a compound of interest for various therapeutic applications.

142115-52-4

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142115-52-4 Usage

Uses

Used in Pharmaceutical Applications:
2,6-dimethyl-4-[(E)-2-(2-phenylmethoxyphenyl)ethenyl]phenol is used as a potential therapeutic agent for various conditions, such as cancer, cardiovascular disease, and neurodegenerative disorders. Its antioxidant and anti-inflammatory properties, as well as its ability to modulate various cellular signaling pathways, contribute to its potential efficacy in these areas.
Used in Cancer Treatment:
In the field of oncology, 2,6-dimethyl-4-[(E)-2-(2-phenylmethoxyphenyl)ethenyl]phenol is used as a potential anticancer agent. Research suggests that it may modulate oncological signaling pathways, exerting inhibitory effects on tumor growth and progression. Additionally, it may demonstrate synergistic anticancer effects when combined with conventional chemotherapeutic drugs, enhancing chemo-sensitivity and efficacy in resistant cases.
Used in Cardiovascular Disease Prevention:
2,6-dimethyl-4-[(E)-2-(2-phenylmethoxyphenyl)ethenyl]phenol is used as a potential agent for the prevention and treatment of cardiovascular diseases. Its antioxidant properties may help protect against oxidative stress, a key factor in the development of cardiovascular conditions.
Used in Neurodegenerative Disorder Management:
In the context of neurodegenerative disorders, 2,6-dimethyl-4-[(E)-2-(2-phenylmethoxyphenyl)ethenyl]phenol is used as a potential therapeutic agent. Its anti-inflammatory and antioxidant properties may help mitigate the effects of neuroinflammation and oxidative stress, which are common in conditions such as Alzheimer's disease and Parkinson's disease.
Used in Drug Delivery Systems:
To enhance the bioavailability and stability of 2,6-dimethyl-4-[(E)-2-(2-phenylmethoxyphenyl)ethenyl]phenol, various drug delivery systems have been developed. These systems, which may include organic and metallic nanoparticles, aim to improve the compound's delivery, bioavailability, and therapeutic outcomes in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 142115-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,1,1 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 142115-52:
(8*1)+(7*4)+(6*2)+(5*1)+(4*1)+(3*5)+(2*5)+(1*2)=84
84 % 10 = 4
So 142115-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C23H22O2/c1-17-14-20(15-18(2)23(17)24)12-13-21-10-6-7-11-22(21)25-16-19-8-4-3-5-9-19/h3-15,24H,16H2,1-2H3/b13-12+

142115-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-4-[2-(2-phenylmethoxyphenyl)ethenyl]phenol

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:142115-52-4 SDS

142115-52-4Downstream Products

142115-52-4Relevant academic research and scientific papers

Effect of structure on potency and selectivity in 2,6-disubstituted 4-(2-arylethenyl)phenol lipoxygenase inhibitors

Lazer,Wong,Wegner,Graham,Farina

, p. 1892 - 1898 (2007/10/02)

A series of 2,6-disubstituted 4-(2-arylethenyl)phenols with potent human neutrophil 5-lipoxygenase (5-LO) inhibiting activity (IC50s in the 10-7 M range) and weaker human platelet cyclooxygenase (CO) inhibiting activity (IC50/s

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