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62949-79-5

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62949-79-5 Usage

Description

KUWANONC, also known as Mulberrin, is a natural compound derived from the roots of the Morus alba tree. It possesses a variety of biological activities, including hepatoprotective, antiviral, antibacterial, and anti-inflammatory properties. Its unique structure and functional groups enable it to interact with various biological targets, making it a promising candidate for pharmaceutical and nutraceutical applications.

Uses

Used in Pharmaceutical Industry:
KUWANONC is used as a hepatoprotective agent for its ability to protect and repair liver cells from damage caused by various factors, such as toxins, diseases, and oxidative stress. It modulates several signaling pathways and enzymes involved in liver regeneration and detoxification processes, promoting liver health and function.
Used in Antiviral Applications:
KUWANONC is used as an antiviral agent for its ability to inhibit the replication and infectivity of various viruses. It targets viral proteins and enzymes, preventing viral entry, assembly, and release, thereby reducing viral load and transmission.
Used in Antibacterial Applications:
KUWANONC is used as an antibacterial agent for its ability to inhibit the growth and proliferation of various bacteria. It targets bacterial cell walls and membrane functions, disrupting their structural integrity and metabolic processes, thereby reducing bacterial load and preventing infections.
Used in Anti-inflammatory Applications:
KUWANONC is used as an anti-inflammatory agent for its ability to modulate the production and activity of various inflammatory mediators, such as cytokines, prostaglandins, and leukotrienes. It reduces inflammation, swelling, and pain, promoting tissue repair and recovery.
Used in Nutraceutical Industry:
KUWANONC is used as a nutraceutical compound for its potential health benefits and therapeutic properties. It can be incorporated into dietary supplements, functional foods, and beverages to promote overall health and well-being, as well as to prevent and treat various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 62949-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,4 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62949-79:
(7*6)+(6*2)+(5*9)+(4*4)+(3*9)+(2*7)+(1*9)=165
165 % 10 = 5
So 62949-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C25H26O6/c1-13(2)5-8-17-20(28)12-21(29)22-23(30)18(9-6-14(3)4)24(31-25(17)22)16-10-7-15(26)11-19(16)27/h5-7,10-12,26-29H,8-9H2,1-4H3

62949-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-3,8-bis(3-methylbut-2-enyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names Kuwanon C

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:62949-79-5 SDS

62949-79-5Downstream Products

62949-79-5Relevant articles and documents

Total syntheses of Nigrasin i and Kuwanon C

Tang, Fei,Wang, Yang,Hou, Ai-Jun

, p. 3963 - 3970 (2014/06/09)

The efficient total syntheses of Nigrasin I and Kuwanon C, two biologically interesting natural flavonoids with two regioisomeric isoprenyl side chains, were realized for the first time starting from commercially available 1-(2,4,6-trihydroxyphenyl)ethano

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