Literature DB >> 27188264

When alcohol is the answer: Trapping, identifying and quantifying simple alkylating species in aqueous environments.

Philip G Penketh1, Krishnamurthy Shyam2, Raymond P Baumann2, Rui Zhu2, Kimiko Ishiguro3, Alan C Sartorelli2, Elena S Ratner3.   

Abstract

Alkylating agents are a significant class of environmental carcinogens as well as commonly used anticancer therapeutics. Traditional alkylating activity assays have utilized the colorimetric reagent 4-(4-nitrobenzyl)pyridine (4NBP). However, 4NBP based assays have a relatively low sensitivity towards harder, more oxophilic alkylating species and are not well suited for the identification of the trapped alkyl moiety due to adduct instability. Herein we describe a method using water as the trapping agent which permits the trapping of simple alkylating electrophiles with a comparatively wide range of softness/hardness and permits the identification of donated simple alkyl moieties.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alkylating; Carcinogen; Chemotherapy; Laromustine; Nitrosoureas; Sulfonylhydrazines

Mesh:

Substances:

Year:  2016        PMID: 27188264      PMCID: PMC4955734          DOI: 10.1016/j.ab.2016.04.020

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  13 in total

1.  Purification and properties of alcohol oxidase from Poria contigua.

Authors:  S Bringer; B Sprey; H Sahm
Journal:  Eur J Biochem       Date:  1979-11

2.  Fluorometric assay for the determination of DNA-DNA cross-links utilizing Hoechst 33258 at neutral pH values.

Authors:  P G Penketh; K Shyam; A C Sartorelli
Journal:  Anal Biochem       Date:  1997-10-01       Impact factor: 3.365

3.  [Carcinogenic alkylating substances. I. Dimethylsulfate, carcinogenic action in rats and probable cause of occupational cancer].

Authors:  H Druckrey; R Preussmann; N Nashed; S Ivankovic
Journal:  Z Krebsforsch       Date:  1966

4.  Spectroscopic aqueous-phase assay for alkylating activity suitable for automation or multiwell plate application.

Authors:  P G Penketh; K Shyam; A C Sartorelli
Journal:  Anal Biochem       Date:  1995-11-01       Impact factor: 3.365

5.  Alkylating activity of 1,3-bis(2-chloroethyl)-1-nitrosourea and related compounds.

Authors:  G P Wheeler; S Chumley
Journal:  J Med Chem       Date:  1967-03       Impact factor: 7.446

6.  Antitumor sulfonylhydrazines: design, structure-activity relationships, resistance mechanisms, and strategies for improving therapeutic utility.

Authors:  Krishnamurthy Shyam; Philip G Penketh; Raymond P Baumann; Rick A Finch; Rui Zhu; Yong-Lian Zhu; Alan C Sartorelli
Journal:  J Med Chem       Date:  2015-02-09       Impact factor: 7.446

Review 7.  From old alkylating agents to new minor groove binders.

Authors:  Stéphane Puyo; Danièle Montaudon; Philippe Pourquier
Journal:  Crit Rev Oncol Hematol       Date:  2013-08-20       Impact factor: 6.312

8.  Influence of phosphate and phosphoesters on the decomposition pathway of 1,2-bis(methylsulfonyl)-1-(2-chloroethyhydrazine (90CE), the active anticancer moiety generated by Laromustine, KS119, and KS119W.

Authors:  Philip G Penketh; Krishnamurthy Shyam; Rui Zhu; Raymond P Baumann; Kimiko Ishiguro; Alan C Sartorelli
Journal:  Chem Res Toxicol       Date:  2014-03-24       Impact factor: 3.739

9.  Influence of glutathione and glutathione S-transferases on DNA interstrand cross-link formation by 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)hydrazine, the active anticancer moiety generated by laromustine.

Authors:  Philip G Penketh; Eric Patridge; Krishnamurthy Shyam; Raymond P Baumann; Rui Zhu; Kimiko Ishiguro; Alan C Sartorelli
Journal:  Chem Res Toxicol       Date:  2014-07-17       Impact factor: 3.739

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