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2-amino-8-(methylamino)-9-pentofuranosyl-3,9-dihydro-6H-purin-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13389-05-4

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13389-05-4 Usage

Classification

Purine nucleoside analog

Antineoplastic Activity

Potential antineoplastic activity as a synthetic purine nucleoside analogue.

Mechanism of Action

Potent inhibitor of adenosine deaminase, inhibits DNA synthesis and repair.

Target

Interferes with the biological activities of extracellular adenosine and deoxyadenosine in cancer cells.

Investigation

Being investigated for therapeutic potential in various cancers, including chronic lymphocytic leukemia, non-Hodgkin lymphoma, and solid tumors.

Check Digit Verification of cas no

The CAS Registry Mumber 13389-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,8 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13389-05:
(7*1)+(6*3)+(5*3)+(4*8)+(3*9)+(2*0)+(1*5)=104
104 % 10 = 4
So 13389-05-4 is a valid CAS Registry Number.

13389-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-8-(methylamino)-3H-purin-6-one

1.2 Other means of identification

Product number -
Other names 2-amino-8-(methylamino)-9-pentofuranosyl-3,9-dihydro-6h-purin-6-one

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:13389-05-4 SDS

13389-05-4Downstream Products

13389-05-4Relevant academic research and scientific papers

ADENOSINE ANALOG AND ITS USE IN REGULATING THE CIRCADIAN CLOCK

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Paragraph 0157; 0158; 0159; 0190, (2018/08/12)

Provided are a kind of nucleoside analogue compounds, and compositions comprising these compounds and pentostatin, their use for modulating circadian rhythm, preferably, for shifting circadian phase, and methods for modulating circadian rhythm, preferably, for shifting circadian phase via these compounds or the compositions.

8-Substituted guanosine and 2'-deoxyguanosine derivatives as potential inducers of the differentiation of Friend erythroleukemia cells

Lin,Cheng,Ishiguro,Sartorelli

, p. 1194 - 1198 (2007/10/02)

A variety of 8-substituted guanosine and 2'-deoxyguanosine derivatives were synthesized and tested as inducers of the differentiation of Friend murine erythroleukemia cells in culture. The most active agents in the guanosine series were 8-substituted -N(CH3)2, -NHCH3, -NH2, -OH, and -SO2CH3, which caused 68, 42, 34, 33, and 30% of erythroleukemia cells to attain benzidine positivity, a functional measure of maturation, at concentrations of 5, 1, 0.4, 5, and 5 mM, respectively. The 8-OH derivative of the 2'-deoxyguanosine series produced comparable activity, causing 62% benzidine-positive cells at a level of 0.2 mM. These findings indicate that 8-substituted analogues of guanosine and 2'-deoxyguanosine have the potential to terminate leukemia cell proliferation through conversion to end-stage differentiated cells.

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