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6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine, also known as 6-Cl-2-Me-Ribosyl-Purine, is a synthetic purine nucleoside analog that exhibits antiviral and antitumor activities. It is a derivative of adenosine and has been studied for its potential use in treating various viral infections and cancer types. 6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine works by inhibiting the replication of viral DNA and RNA, as well as disrupting the synthesis of DNA and RNA in cancer cells, making it a promising candidate for the development of new antiviral and anticancer therapies.

205171-05-7

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205171-05-7 Usage

Uses

Used in Antiviral Applications:
6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine is used as an antiviral agent for the treatment of various viral infections, including HIV and herpes simplex virus. It inhibits the replication of viral DNA and RNA, thereby preventing the spread of the virus in the body.
Used in Anticancer Applications:
6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine is used as an anticancer agent, particularly in the treatment of leukemia and other lymphoid malignancies. It disrupts the synthesis of DNA and RNA in cancer cells, thereby inhibiting their growth and proliferation.
Used in Pharmaceutical Industry:
6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine is used as a key intermediate in the synthesis of various antiviral and anticancer drugs. Its unique structure and biological activities make it a valuable compound for the development of new therapeutic agents.
Used in Research and Development:
6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine is used as a research tool in the study of viral replication mechanisms and cancer cell biology. Its antiviral and antitumor properties provide valuable insights into the development of novel therapeutic strategies against these diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 205171-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,1,7 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 205171-05:
(8*2)+(7*0)+(6*5)+(5*1)+(4*7)+(3*1)+(2*0)+(1*5)=87
87 % 10 = 7
So 205171-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H13ClN4O4/c1-11(19)7(18)5(2-17)20-10(11)16-4-15-6-8(12)13-3-14-9(6)16/h3-5,7,10,17-19H,2H2,1H3/t5-,7-,10-,11-/m1/s1

205171-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-9-(2-C-methyl-β-D-ribofuranosyl)-9H-purine

1.2 Other means of identification

Product number -
Other names 6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine

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:205171-05-7 SDS

205171-05-7Relevant academic research and scientific papers

2'-C-Methyl analogues of selective adenosine receptor agonists: Synthesis and binding studies

Franchetti, Palmarisa,Cappellacci, Loredana,Marchetti, Stefano,Trincavelli, Letizia,Martini, Claudia,Mazzoni, Maria R.,Lucacchini, Antonio,Grifantini, Mario

, p. 1708 - 1715 (1998)

2'-C-Methyl analogues of selective adenosine receptor agonists such as (R)-PIA, CPA, CCPA, NECA, and IB-MECA were synthesized in order to further investigate the subdomain that binds the ribose moiety. Binding affinities of these new compounds at A1

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