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32754-06-6

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32754-06-6 Usage

Chemical structure

A nucleoside analog derivative of cytarabine, consisting of a 1-beta-D-arabinofuranosyl group attached to a 4-thioxo-3,4-dihydropyrimidin-2(1H)-one moiety.

Antineoplastic activity

Exhibits potential antineoplastic (anti-cancer) properties.

Mechanism of action

Inhibits the synthesis of DNA, RNA, and protein in cancer cells, leading to their destruction.

DNA incorporation

Can be incorporated into the DNA of cancer cells, causing DNA damage and eventual cell death.

Target diseases

Used in the treatment of various forms of leukemia and lymphoma.

Development status

Has sparked interest in its further development as a potential anticancer agent.

Check Digit Verification of cas no

The CAS Registry Mumber 32754-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,5 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32754-06:
(7*3)+(6*2)+(5*7)+(4*5)+(3*4)+(2*0)+(1*6)=106
106 % 10 = 6
So 32754-06-6 is a valid CAS Registry Number.

32754-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidenepyrimidin-2-one

1.2 Other means of identification

Product number -
Other names Cytosine arabinoside 5'MP

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:32754-06-6 SDS

32754-06-6Downstream Products

32754-06-6Relevant articles and documents

Growth inhibition of Mycobacterium bovis, Mycobacterium tuberculosis and Mycobacterium avium in vitro: Effect of 1-β-D-2′-arabinofuranosyl and 1-(2′-deoxy-2′-fluoro-β-D-2′-ribofuranosyl) pyrimidine nucleoside analogs

Johar, Monika,Manning, Tracey,Tse, Christopher,Desroches, Nancy,Agrawal,Kunimoto, Dennis Y.,Kumar, Rakesh

, p. 3696 - 3705 (2008/02/09)

The resurgence of tuberculosis and the emergence of multiple-drug-resistant strains of Mycobacteria necessitate the search for new classes of antimycobacterial agents. We synthesized a series of 1-β-D-2′- arabinofuranosyl and 1-(2′-deoxy-2′-fluoro-β-D-rib

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