104901-06-6 Usage
Description
[2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester is a complex organic compound characterized by its naphtho[2,1-c]pyran core fused to a furan ring. This methyl ester derivative of a carboxylic acid features multiple stereocenters, predominantly at the 2nd position, and includes hydroxyl and methyl groups at various positions. [2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester's structural intricacy and functional groups indicate potential biological activity, rendering it a promising candidate for exploration in the fields of medicine and pharmaceuticals.
Uses
Used in Pharmaceutical Applications:
[2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester is used as a potential therapeutic agent for various medical conditions due to its complex molecular structure and functional groups. [2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester's stereochemistry and functional profile suggest it may interact with biological targets in ways that could lead to novel treatments or therapies.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester serves as a subject of study for understanding its interactions with biological systems. Its structural features may provide insights into the design of new drugs with improved efficacy and selectivity.
Used in Drug Delivery Systems:
Similar to other complex organic compounds, [2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester could be employed in the development of advanced drug delivery systems. These systems may enhance the compound's bioavailability, targeting, and overall therapeutic potential.
Used in Chemical Synthesis:
[2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester's unique structure and functional groups make it a valuable building block for the synthesis of other complex organic molecules. It can be used as a starting material or intermediate in the preparation of novel chemical entities with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Analytical Chemistry:
The stereochemistry and functional groups of [2S,(-)]-2β-(3-Furanyl)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-6α,9α-dihydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester make it an interesting subject for analytical chemistry studies. It can be used to develop new methods for the separation, detection, and quantification of complex mixtures, as well as to improve the understanding of molecular interactions and recognition processes.
Check Digit Verification of cas no
The CAS Registry Mumber 104901-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,0 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104901-06:
(8*1)+(7*0)+(6*4)+(5*9)+(4*0)+(3*1)+(2*0)+(1*6)=86
86 % 10 = 6
So 104901-06-6 is a valid CAS Registry Number.
104901-06-6Relevant articles and documents
STUDIES ON THE CONSTITUENTS OF THE STEMS OF TINOSPORA TUBERCULATA BEUMEE. III. NEW DITERPENOIDS, BORAPETOSIDE B AND BORAPETOL B
Fukuda, Naomichi,Yonemitsu, Michiko,Kimura, Takeatsu
, p. 2868 - 2872 (2007/10/02)
A new diterpene glucoside, borapetoside B (1), and its aglycone, borapetol B (2), were isolated from the stems of Tinospora tuberculata Beumee as the bitter principles, and their structures were elucidated.Keywords - Tinospora tuberculata; Menispermaceae; borapet; borapetoside B; borapetol B; bitter principle; diterpenoid; glycoside
