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9-(2,3,5-tri-O-benzoylpentofuranosyl)-3,9-dihydro-1H-purine-2,6-dione is a synthetic chemical compound derived from purine, featuring a purine base attached to a modified sugar molecule with benzoyl groups. 9-(2,3,5-tri-O-benzoylpentofuranosyl)-3,9-dihydro-1H-purine-2,6-dione has been synthesized for its potential pharmaceutical applications, particularly in medicinal chemistry research and drug development. Its unique structure allows for specific interactions with biological systems, making it a promising candidate for further studies in drug discovery and development.

73024-64-3

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73024-64-3 Usage

Uses

Used in Pharmaceutical Research:
9-(2,3,5-tri-O-benzoylpentofuranosyl)-3,9-dihydro-1H-purine-2,6-dione is used as a research compound for investigating its potential antiviral and anticancer properties. As a nucleoside analog, it may exhibit therapeutic effects against various viral infections and cancer cells.
Used in Drug Development:
In the field of drug development, 9-(2,3,5-tri-O-benzoylpentofuranosyl)-3,9-dihydro-1H-purine-2,6-dione is utilized as a candidate molecule for the design and synthesis of new drugs. Its unique structure and potential to interact with biological systems in a targeted manner make it a valuable asset in the development of novel therapeutic agents.
Used in Medicinal Chemistry:
9-(2,3,5-tri-O-benzoylpentofuranosyl)-3,9-dihydro-1H-purine-2,6-dione serves as a key component in medicinal chemistry, where it is studied for its potential to modulate biological processes and target specific pathways. Its synthesis and modification can lead to the discovery of new drugs with improved efficacy and selectivity.
Used in Antiviral Applications:
9-(2,3,5-tri-O-benzoylpentofuranosyl)-3,9-dihydro-1H-purine-2,6-dione is used as an antiviral agent, where it may inhibit viral replication and reduce the severity of viral infections. Its specific interactions with biological systems can potentially lead to the development of effective antiviral therapies.
Used in Anticancer Applications:
In the field of oncology, 9-(2,3,5-tri-O-benzoylpentofuranosyl)-3,9-dihydro-1H-purine-2,6-dione is employed as an anticancer agent, targeting cancer cells and inhibiting their growth and proliferation. Its potential to modulate oncological signaling pathways and exhibit synergistic effects with conventional chemotherapeutic drugs makes it a promising candidate for cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 73024-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,2 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73024-64:
(7*7)+(6*3)+(5*0)+(4*2)+(3*4)+(2*6)+(1*4)=103
103 % 10 = 3
So 73024-64-3 is a valid CAS Registry Number.

73024-64-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,5S,9R,10S,13R,15S,17R)-14-ethyl-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,5,6,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,15-diol

1.2 Other means of identification

Product number -
Other names 4-Amino-tetrafluor-benzamid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73024-64-3 SDS

73024-64-3Downstream Products

73024-64-3Relevant academic research and scientific papers

Nucleoside Syntheses, XXII. Nucleoside Synthesis with Trimethylsilyl Triflate and Perchlorate as Catalysts

Vorbrueggen, Helmut,Krolikiewicz, Konrad,Bennua, Baerbel

, p. 1234 - 1255 (2007/10/02)

The novel Lewis acids (CH3)3SiOSO2CF3 (5), (CH3)3SiOSO2C4F9 (6), and (CH3)3SiClO4 (4) are highly selective and efficient Friedel-Crafts catalysts for nucleoside formation from silylated heterocycles and peracylated sugars as well as for rearrangements of persilylated protected nucleosides.With basic silylated heterocycles these new catalysts give much higher yields of the natural N-1-nucleosides than with SnCl4.

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