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97534-21-9

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97534-21-9 Usage

Uses

Merbarone has been used to study its effect on the occurrence of DNA lesions.

General Description

A cell-permeable anticancer drug that inhibits the catalytic activity of topoisomerase II (topo II) without damaging DNA or stabilizing DNA-topo II cleavable complexes (IC50 = 20 μM for purified mammalian topo II versus IC50 = ~ 200 μM for topo I). Also induces apoptosis in human leukemic CEM cells through a caspase-3-like protease-dependent mechanism.

Biochem/physiol Actions

Cell permeable: yes

Check Digit Verification of cas no

The CAS Registry Mumber 97534-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,3 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97534-21:
(7*9)+(6*7)+(5*5)+(4*3)+(3*4)+(2*2)+(1*1)=159
159 % 10 = 9
So 97534-21-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H9N3O3S/c15-8(12-6-4-2-1-3-5-6)7-9(16)13-11(18)14-10(7)17/h1-5,7H,(H,12,15)(H2,13,14,16,17,18)

97534-21-9 Well-known Company Product Price

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  • Sigma

  • (M2070)  Merbarone  ≥98% (HPLC), solid

  • 97534-21-9

  • M2070-25MG

  • 1,325.61CNY

  • Detail

97534-21-9SDS

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 6-hydroxy-4-oxo-N-phenyl-2-sulfanylidene-1H-pyrimidine-5-carboxamide

1.2 Other means of identification

Product number -
Other names CC-PMLSC-PW-kmcmerbarone

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:97534-21-9 SDS

97534-21-9Downstream Products

97534-21-9Relevant articles and documents

Pharmacophore Hybridization to Discover Novel Topoisomerase II Poisons with Promising Antiproliferative Activity

Ortega, Jose Antonio,Riccardi, Laura,Minniti, Elirosa,Borgogno, Marco,Arencibia, Jose M.,Greco, Maria L.,Minarini, Anna,Sissi, Claudia,De Vivo, Marco

, p. 1375 - 1379 (2018)

We used a pharmacophore hybridization strategy to combine key structural elements of merbarone and etoposide and generated new type II topoisomerase (topoII) poisons. This first set of hybrid topoII poisons shows promising antiproliferative activity on hu

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