Welcome to LookChem.com Sign In|Join Free
  • or
Licochalcone E is a natural chemical compound derived from the roots of the Chinese licorice plant, known for its potential medicinal properties such as anti-inflammatory, antioxidant, and anti-cancer effects. It has demonstrated the ability to inhibit the growth of various cancer cells and possesses antimicrobial activity against a range of pathogens, positioning it as a promising candidate for therapeutic applications.

864232-34-8

Post Buying Request

864232-34-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

864232-34-8 Usage

Uses

Used in Pharmaceutical Industry:
Licochalcone E is used as an anti-inflammatory agent for its ability to reduce inflammation and oxidative stress, which are associated with various chronic diseases.
Used in Oncology:
Licochalcone E is used as an anti-cancer agent for its capacity to inhibit the growth of cancer cells, particularly those of the breast, prostate, and colon.
Used in Antimicrobial Applications:
Licochalcone E is used as an antimicrobial agent due to its demonstrated activity against various pathogens, making it a potential candidate for the development of new antimicrobial agents.

Check Digit Verification of cas no

The CAS Registry Mumber 864232-34-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,2,3 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 864232-34:
(8*8)+(7*6)+(6*4)+(5*2)+(4*3)+(3*2)+(2*3)+(1*4)=168
168 % 10 = 8
So 864232-34-8 is a valid CAS Registry Number.

864232-34-8Downstream Products

864232-34-8Relevant academic research and scientific papers

An enantioselective total synthesis of (S)-(-)-licochalcone E: determination of the absolute configuration

Liu, Zhiguo,Yoon, Goo,Cheon, Seung Hoon

experimental part, p. 3165 - 3172 (2010/05/19)

The absolute configuration of (-)-licochalcone E (1) was determined to be (S) via the first enantioselective total synthesis of the compound. The chirality in (S)-(-)-licochalcone E (1) was installed by asymmetric methylation of the Evans' oxazolidinone d

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 864232-34-8