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(4E)-3-(2-deoxypentofuranosyl)-5-(diaminomethylidene)-3,5-dihydro-4H-imidazol-4-imine is a nucleoside chemical compound that features a pentofuranosyl group, a diaminomethylidene group, and an imidazol-imine group. The pentofuranosyl group is a five-carbon sugar derivative, and the diaminomethylidene and imidazol-imine groups contain nitrogen atoms. As a nucleoside, it is composed of a nitrogenous base (imidazol-imine group) and a five-carbon sugar (pentofuranosyl group), which are essential components of nucleic acids like DNA and RNA, playing a vital role in genetic information storage and transmission. The unique structure of (4E)-3-(2-deoxypentofuranosyl)-5-(diaminomethylidene)-3,5-dihydro-4H-imidazol-4-imine indicates its potential involvement in nucleic acid synthesis or function.

35966-91-7

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35966-91-7 Usage

Uses

Used in Pharmaceutical Industry:
(4E)-3-(2-deoxypentofuranosyl)-5-(diaminomethylidene)-3,5-dihydro-4H-imidazol-4-imine is used as a potential therapeutic agent for the development of new drugs targeting nucleic acid-related diseases. Its unique structure may allow it to interact with nucleic acids or enzymes involved in their synthesis and function, offering novel treatment options for various conditions.
Used in Research and Development:
In the field of molecular biology and genetics, (4E)-3-(2-deoxypentofuranosyl)-5-(diaminomethylidene)-3,5-dihydro-4H-imidazol-4-imine serves as a valuable research tool for studying the mechanisms of nucleic acid synthesis, replication, and repair. It can be utilized in experiments to investigate the interactions between nucleosides and other biomolecules, contributing to a deeper understanding of genetic processes and the development of targeted therapies.
Used in Diagnostic Applications:
(4E)-3-(2-deoxypentofuranosyl)-5-(diaminomethylidene)-3,5-dihydro-4H-imidazol-4-imine can be employed in the development of diagnostic assays and tests aimed at detecting and monitoring nucleic acid-related disorders. Its specific interactions with nucleic acids or their metabolizing enzymes may enable the design of sensitive and accurate diagnostic tools for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 35966-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35966-91:
(7*3)+(6*5)+(5*9)+(4*6)+(3*6)+(2*9)+(1*1)=157
157 % 10 = 7
So 35966-91-7 is a valid CAS Registry Number.

35966-91-7Downstream Products

35966-91-7Relevant academic research and scientific papers

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