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Gusanlung B is a chemical compound with potential therapeutic properties, primarily used in traditional Chinese medicine. It is known for its anti-inflammatory and antioxidant properties, making it a promising candidate for treating various inflammatory diseases and conditions. gusanlung B has been shown to inhibit the production of pro-inflammatory cytokines and enzymes, thereby reducing inflammation and oxidative stress in the body. Additionally, gusanlung B has been studied for its potential neuroprotective effects, suggesting its potential in treating neurodegenerative disorders. Overall, gusanlung B shows promise as a natural remedy for alleviating inflammation and protecting against oxidative damage in the body.

79082-05-6

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79082-05-6 Usage

Uses

Used in Pharmaceutical Industry:
Gusanlung B is used as an anti-inflammatory agent for its ability to inhibit the production of pro-inflammatory cytokines and enzymes, reducing inflammation and oxidative stress in the body.
Used in Neuroprotective Applications:
Gusanlung B is used as a neuroprotective agent for its potential in treating neurodegenerative disorders, due to its ability to protect against oxidative damage and inflammation in the brain.
Used in Traditional Chinese Medicine:
Gusanlung B is used as a natural remedy for alleviating inflammation and protecting against oxidative damage in the body, based on its traditional use and therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 79082-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,8 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79082-05:
(7*7)+(6*9)+(5*0)+(4*8)+(3*2)+(2*0)+(1*5)=146
146 % 10 = 6
So 79082-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H19NO5/c1-23-15-4-3-12-7-14-13-9-17-16(25-10-26-17)8-11(13)5-6-21(14)20(22)18(12)19(15)24-2/h3-4,8-9,14H,5-7,10H2,1-2H3/t14-/m0/s1

79082-05-6SDS

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 (-)-2,3-(Methylenedioxy)-8-oxo-9,10-dimethoxytetrahydroprotoberberine

1.2 Other means of identification

Product number -
Other names (-)-8-oxocanadine

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:79082-05-6 SDS

79082-05-6Downstream Products

79082-05-6Relevant academic research and scientific papers

The absolute configuration of (+)-thalictricavine

Iwasa, Kinuko,Cushman, Mark

, p. 901 - 904 (2007/10/02)

(+)-Thalictricavine (7) and (+)-canadine (1) have been synthesized from an optically resolved (+)-13-carboxy-7,8,13,14-tetrahydro-8-oxoprotoberberine 15.This establishes tha absolute configuration of (+)-thalictricavine (7) as 13S, 14R

Absolute Configurations of the cis- and trans-13-Methyltetrahydroprotoberberines. Total Synthesis of (+)-Thalictricavine, (+)-Canadine, (+/-)-, (-)-, and (+)-Thalictrifoline, and (+/-)-, (-)-, and (+)-Cavidine

Iwasa, Kinuko,Gupta, Yash Pal,Cushman, Mark

, p. 4744 - 4750 (2007/10/02)

The tetrahydroprotoberberine alkaloids (+)-thalictricavine and (+)-canadine have been synthesized from an optically resolved (+)-13-carboxy-7,8,13,14-tetrahydro-9-oxoprotoberberine .This establishes the absolute configuration of (+)-thalictricavine as 13S,14R. (+)-Thalictrifoline and (+)-cavidine have also been prepared from a common intermediate, (+)-32, whose absolute configuration was established by correlation with (+)-26.This determines the absolute configuration of (+)-thalictrifoline as 13R,14R, of (+)-corydalic acid methyl ester (22) as 3R,4R, and of the protopine (+)-corycavine (20) as 13R.

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