104901-05-5 Usage
Description
[2S,(-)]-2β-(3-Furanyl)-6β-(β-D-glucopyranosyloxy)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-9α-hydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester is a complex organic molecule characterized by its naphtho[2,1-c]pyran heterocyclic structure. It features a furanyl ring, a glucopyranosyloxy group, and a carboxylic acid methyl ester moiety, along with multiple functional groups and a long carbon chain. [2S,(-)]-2β-(3-Furanyl)-6β-(β-D-glucopyranosyloxy)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-9α-hydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester is a derivative of naphtho[2,1-c]pyran and exhibits a unique stereochemistry with a 2S, (-) configuration. Its intricate chemical structure suggests potential pharmacological and biological activities, making it a promising candidate for pharmaceutical or medicinal research.
Uses
Used in Pharmaceutical Research:
[2S,(-)]-2β-(3-Furanyl)-6β-(β-D-glucopyranosyloxy)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-9α-hydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester is used as a pharmaceutical research compound for its potential biological activities. The presence of various functional groups and its unique structure may contribute to its interaction with biological targets, offering opportunities for the development of new therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [2S,(-)]-2β-(3-Furanyl)-6β-(β-D-glucopyranosyloxy)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-9α-hydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester serves as a valuable molecule for the design and synthesis of novel drugs. Its structural features can be exploited to create new chemical entities with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Drug Discovery:
[2S,(-)]-2β-(3-Furanyl)-6β-(β-D-glucopyranosyloxy)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-9α-hydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester is utilized in drug discovery processes to identify potential lead compounds. Its unique chemical structure and functional groups can be further optimized through medicinal chemistry approaches to enhance its pharmacological properties and develop it into a viable drug candidate.
Used in Biochemical Studies:
In biochemical research, [2S,(-)]-2β-(3-Furanyl)-6β-(β-D-glucopyranosyloxy)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-9α-hydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester can be employed as a tool compound to study the mechanisms of action of various biological processes. Its interaction with specific targets can provide insights into the molecular basis of diseases and help in the development of targeted therapies.
Used in Chemical Synthesis:
[2S,(-)]-2β-(3-Furanyl)-6β-(β-D-glucopyranosyloxy)-1,4,4aα,5,6,6a,9,10,10aα,10b-decahydro-9α-hydroxy-6aα,10bβ-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester can also be used as a starting material or intermediate in the synthesis of other complex organic molecules. Its versatile structure allows for
Check Digit Verification of cas no
The CAS Registry Mumber 104901-05-5 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 104901-05:
(8*1)+(7*0)+(6*4)+(5*9)+(4*0)+(3*1)+(2*0)+(1*5)=85
85 % 10 = 5
So 104901-05-5 is a valid CAS Registry Number.
104901-05-5Relevant articles and documents
Studies on the Constituents of the Stems of Tinospora tuberculata, V Isolation and Structure Elucidation of the New Furanoid Diterpene Glucoside Borapetoside H
Fukuda, Naomichi,Yonemitsu, Michiko,Kimura, Takeatsu
, p. 1689 - 1692 (2007/10/02)
The new diterpene glucoside borapeptoside H (1) was isolated from the fresh stems of Tinospora tuberculata Beumee (Menispermaceae).Its structure as 2-O-β-D-glucopyranosylborapetoside B was elucidated on the basis of chemical and spectroscopic findings. - Keywords: Tinospora tuberculata / Menispermaceae / Borapetoside H / Diterpene glucosides
