100007-56-5 Usage
Description
Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one,9-[[4,6-O-(1R)-ethylidene-b-D-glucopyranosyl]oxy]-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-,(5R,5aS,8aR,9S)is a complex organic molecule characterized by a furo naphtho dioxolone core structure. It features a sugar moiety with an ethylidene glucopyranosyl group and a phenyl ring substituted with hydroxy and dimethoxy groups. The molecule's stereochemistry is defined by the (5R,5aS,8aR,9S) configuration. This unique structure endows the compound with potential applications in medicinal chemistry and pharmaceutical research, particularly due to its possible biological activities.
Uses
Used in Medicinal Chemistry:
Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one,9-[[4,6-O-(1R)-ethylidene-b-D-glucopyranosyl]oxy]-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-,(5R,5aS,8aR,9S)is utilized as a key intermediate in the synthesis of novel pharmaceutical agents. Its unique structure and functional groups allow for the development of compounds with potential therapeutic properties, such as anti-inflammatory, analgesic, or antimicrobial activities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, this compound serves as a valuable scaffold for the design and optimization of new drug candidates. Its complex structure and diverse functional groups enable the exploration of various chemical modifications, leading to the discovery of molecules with improved pharmacological profiles, including enhanced potency, selectivity, and bioavailability.
Used in Drug Delivery Systems:
Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one,9-[[4,6-O-(1R)-ethylidene-b-D-glucopyranosyl]oxy]-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-,(5R,5aS,8aR,9S)can be employed in the development of targeted drug delivery systems. Its sugar moiety and phenyl ring can be exploited for specific interactions with biological targets, such as receptors or enzymes, enabling the selective delivery of therapeutic agents to diseased tissues or cells.
Used in Biochemical Studies:
Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one,9-[[4,6-O-(1R)-ethylidene-b-D-glucopyranosyl]oxy]-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-,(5R,5aS,8aR,9S)-'s unique structure and functional groups make it a promising tool for biochemical research. It can be used to investigate the binding properties and interactions of various biomolecules, such as proteins, enzymes, or nucleic acids. Additionally, it may serve as a starting point for the development of new probes or inhibitors for the study of biological processes and pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 100007-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,0 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100007-56:
(8*1)+(7*0)+(6*0)+(5*0)+(4*0)+(3*7)+(2*5)+(1*6)=45
45 % 10 = 5
So 100007-56-5 is a valid CAS Registry Number.
100007-56-5Relevant articles and documents
Preparation method of etoposide, teniposide and analogs of etoposide and teniposide
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Paragraph 0106; 0107; 0108, (2017/01/02)
The invention discloses a preparation method of etoposide, teniposide and analogs of etoposide and teniposide. The preparation method includes the following steps of 1, selective protection of 4'domethylpodophyllotoxin4'hydroxy; 2, introduction of 4 hydroxy hydroxyl; 3, removal of a protecting group. The method is mild in reaction condition and environmentally friendly, and the yield and purity of the products are high.
Stereoselective Glucosidation of Podophyllum Lignans. A New Simple Synthesis of Etoposide
Allevi, Pietro,Anastasia, Mario,Ciuffreda, Pierangela,Bigatti, Ettore,Macdonald, Peter
, p. 4175 - 4178 (2007/10/02)
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Epimerization and hydrolysis of etoposide analogues in aqueous solution
Aso,Hayashi,Yoshioka,Takeda,Kita,Nishimura,Arata
, p. 422 - 424 (2007/10/02)
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