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4680-63-1

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4680-63-1 Usage

Derived from

Adenine

Structure

Purine base connected to a sugar moiety through a glycosidic bond, thiol group at position 6 of the purine ring

Biological role

Plays a role in RNA and DNA modification

Therapeutic applications

Studied for potential anti-cancer and anti-viral treatments

Mechanisms of action

Inhibits nucleic acid synthesis, disrupts nucleoside metabolism

Potential uses

Development of new nucleoside analog drugs for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 4680-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4680-63:
(6*4)+(5*6)+(4*8)+(3*0)+(2*6)+(1*3)=101
101 % 10 = 1
So 4680-63-1 is a valid CAS Registry Number.

4680-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-9-(3,4-dihydroxy-5-methyloxolan-2-yl)-3H-purine-6-thione

1.2 Other means of identification

Product number -
Other names 5'-deoxy-6-thioguanosine

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:4680-63-1 SDS

4680-63-1Downstream Products

4680-63-1Relevant articles and documents

Facile synthesis of 5'-deoxy- and 2',5'-dideoxy-6-thiopurine nucleosides by nucleoside phosphorylases

Chae, Whi-Gun,Chan, Thomas C. K.,Chang, Ching-Jer

, p. 8661 - 8670 (1998)

5'-Deoxy-6-thioguanosine, 2',5'-dideoxy-6-thioguanosine, 5'-deoxy-6- mercaptopurine riboside and 2',5'-dideoxy-6-mercaptopurine riboside were synthesized enzymatically from thiopurine bases and corresponding ribosyl donors using nucleoside phosphorylase. This is the first report of trans-5'- deoxyribosylation to thiopurine bases by nucleoside phosphorylase. 5'-Deoxy- 6-thioguanosine selectively blocked the growth of v-ras-transformed human bronchial epithelial cells. In addition, the in vitro antitumor cytotoxicity data for 5'-deoxy- and 2',5'-dideoxy-6-thiopurine nucleosides were comparable to those for the corresponding thiopurine bases.

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