6191-46-4 Usage
Description
(6aS)-1,2,10,11-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline is a complex organic compound belonging to the dibenzoquinoline alkaloids class. It features a tetrahydro-4H-dibenzo[de,g]quinoline core, adorned with four methoxy groups and a methyl group. (6aS)-1,2,10,11-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline is derived from certain plant species and is being investigated for its potential pharmacological properties, which may include antiviral, anticancer, and anti-inflammatory activities. Its unique molecular structure indicates that it could possess valuable properties for various applications in the pharmaceutical and medical fields.
Uses
Used in Pharmaceutical Industry:
(6aS)-1,2,10,11-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline is used as a potential therapeutic agent for its possible antiviral, anticancer, and anti-inflammatory effects. (6aS)-1,2,10,11-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline's ability to target specific biological pathways makes it a candidate for further research and development in the treatment of various diseases and conditions.
Used in Research and Development:
In the field of scientific research, (6aS)-1,2,10,11-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline serves as a subject for exploring its chemical properties, potential interactions with biological systems, and its overall pharmacological profile. Understanding the compound's behavior and effects can lead to the discovery of new drugs or therapies based on its molecular structure and activity.
Used in Drug Design and Synthesis:
The unique molecular structure of (6aS)-1,2,10,11-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline makes it a valuable compound in the field of drug design and synthesis. Researchers can use its structure as a template or starting point for creating new drugs with improved properties or targeted effects. This application can lead to the development of more effective medications with fewer side effects.
Used in Natural Products Chemistry:
As a member of the dibenzoquinoline alkaloids, (6aS)-1,2,10,11-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline contributes to the study of natural products chemistry. Understanding the properties and potential applications of this compound can provide insights into the broader class of dibenzoquinoline alkaloids and their role in nature, as well as their potential for use in medicine and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6191-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6191-46:
(6*6)+(5*1)+(4*9)+(3*1)+(2*4)+(1*6)=94
94 % 10 = 4
So 6191-46-4 is a valid CAS Registry Number.
6191-46-4Relevant articles and documents
Faurine and O-methylfaurine, two novel benzyl-aporphine dimers from Thalictrum fauriei
Lee, Shoei-Sheng,Doskotch, Raymond W.
, p. 738 - 743 (2007/10/03)
Two new benzyl-aporphine dimers, faurine (1) and its O-methyl ether (2), were obtained from Thalictrum fauriei and their structures determined by spectral and chemical methods. Faurine (1), the first dimer with the diphenyl ether connection at C-1 of the aporphine, did not undergo a Hofmann degradation, yet formed a chiral phenanthrene product (6) with cyanogen bromide. Two nondimeric chiral aporphine alkaloids, O-acetylisocorydine and O-methylisocorydine, gave the corresponding phenanthrene products 7 and 8, respectively, under the same conditions, but only compound 7 was optically active.
Selective ether cleavage in the aporphine series. Conversion of (S) bulbocapnine into (S) corytuberine and (S) corydine methyl ether
Gerecke,Borer,Brossi
, p. 2551 - 2557 (2007/10/04)
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