Literature DB >> 30102448

Colorimetric Carbonyl Sulfide (COS)/Hydrogen Sulfide (H2 S) Donation from γ-Ketothiocarbamate Donor Motifs.

Yu Zhao1, Andrea K Steiger1, Michael D Pluth1.   

Abstract

Hydrogen sulfide (H2 S) is a biologically active molecule that exhibits protective effects in a variety of physiological and pathological processes. Although several H2 S-related biological effects have been discovered by using H2 S donors, knowing how much H2 S has been released from donors under different conditions remains challenging. Now, a series of γ-ketothiocarbamate (γ-KetoTCM) compounds that provide the first examples of colorimetric H2 S donors and enable direct quantification of H2 S release, were reported. These compounds are activated through a pH-dependent deprotonation/β-elimination sequence to release carbonyl sulfide (COS), which is quickly converted into H2 S by carbonic anhydrase. The p-nitroaniline released upon donor activation provides an optical readout that correlates directly to COS/H2 S release, thus enabling colorimetric measurement of H2 S donation.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  anti-inflammation; carbonyl sulfide; colorimetry; hydrogen sulfide; γ-ketothiocarbamate

Mesh:

Substances:

Year:  2018        PMID: 30102448      PMCID: PMC6504913          DOI: 10.1002/anie.201806854

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  40 in total

1.  Inhibition of Mitochondrial Bioenergetics by Esterase-Triggered COS/H2S Donors.

Authors:  Andrea K Steiger; Michela Marcatti; Csaba Szabo; Bartosz Szczesny; Michael D Pluth
Journal:  ACS Chem Biol       Date:  2017-06-30       Impact factor: 5.100

Review 2.  Emerging Roles of Carbonyl Sulfide in Chemical Biology: Sulfide Transporter or Gasotransmitter?

Authors:  Andrea K Steiger; Yu Zhao; Michael D Pluth
Journal:  Antioxid Redox Signal       Date:  2017-05-18       Impact factor: 8.401

3.  Bio-orthogonal "click-and-release" donation of caged carbonyl sulfide (COS) and hydrogen sulfide (H2S).

Authors:  Andrea K Steiger; Yang Yang; Maksim Royzen; Michael D Pluth
Journal:  Chem Commun (Camb)       Date:  2017-01-24       Impact factor: 6.222

Review 4.  Toward Hydrogen Sulfide Based Therapeutics: Critical Drug Delivery and Developability Issues.

Authors:  Yueqin Zheng; Bingchen Yu; Ladie Kimberly De La Cruz; Manjusha Roy Choudhury; Abiodun Anifowose; Binghe Wang
Journal:  Med Res Rev       Date:  2017-02-27       Impact factor: 12.944

5.  Hydrogen Sulfide Donors Activated by Reactive Oxygen Species.

Authors:  Yu Zhao; Michael D Pluth
Journal:  Angew Chem Int Ed Engl       Date:  2016-10-24       Impact factor: 15.336

6.  Cysteine-activated hydrogen sulfide (H2S) donors.

Authors:  Yu Zhao; Hua Wang; Ming Xian
Journal:  J Am Chem Soc       Date:  2010-12-10       Impact factor: 15.419

7.  S-aroylthiooximes: a facile route to hydrogen sulfide releasing compounds with structure-dependent release kinetics.

Authors:  Jeffrey C Foster; Chadwick R Powell; Scott C Radzinski; John B Matson
Journal:  Org Lett       Date:  2014-02-27       Impact factor: 6.005

Review 8.  International Union of Basic and Clinical Pharmacology. CII: Pharmacological Modulation of H2S Levels: H2S Donors and H2S Biosynthesis Inhibitors.

Authors:  Csaba Szabo; Andreas Papapetropoulos
Journal:  Pharmacol Rev       Date:  2017-10       Impact factor: 25.468

9.  Esterase-Sensitive Prodrugs with Tunable Release Rates and Direct Generation of Hydrogen Sulfide.

Authors:  Yueqin Zheng; Bingchen Yu; Kaili Ji; Zhixiang Pan; Vayou Chittavong; Binghe Wang
Journal:  Angew Chem Int Ed Engl       Date:  2016-01-28       Impact factor: 15.336

10.  Self-Immolative Thiocarbamates Provide Access to Triggered H2S Donors and Analyte Replacement Fluorescent Probes.

Authors:  Andrea K Steiger; Sibile Pardue; Christopher G Kevil; Michael D Pluth
Journal:  J Am Chem Soc       Date:  2016-06-03       Impact factor: 15.419

View more
  8 in total

1.  H2S donors with optical responses.

Authors:  Michael D Pluth; Yu Zhao; Matthew M Cerda
Journal:  Methods Enzymol       Date:  2020-06-15       Impact factor: 1.600

Review 2.  Activatable Small-Molecule Hydrogen Sulfide Donors.

Authors:  Carolyn M Levinn; Matthew M Cerda; Michael D Pluth
Journal:  Antioxid Redox Signal       Date:  2019-10-29       Impact factor: 8.401

Review 3.  Development and Application of Carbonyl Sulfide-Based Donors for H2S Delivery.

Authors:  Carolyn M Levinn; Matthew M Cerda; Michael D Pluth
Journal:  Acc Chem Res       Date:  2019-08-07       Impact factor: 22.384

4.  Cyclic Sulfenyl Thiocarbamates Release Carbonyl Sulfide and Hydrogen Sulfide Independently in Thiol-Promoted Pathways.

Authors:  Yu Zhao; Andrea K Steiger; Michael D Pluth
Journal:  J Am Chem Soc       Date:  2019-08-14       Impact factor: 15.419

5.  Fluorogenic hydrogen sulfide (H2S) donors based on sulfenyl thiocarbonates enable H2S tracking and quantification.

Authors:  Yu Zhao; Matthew M Cerda; Michael D Pluth
Journal:  Chem Sci       Date:  2018-12-10       Impact factor: 9.825

6.  Dithioesters: simple, tunable, cysteine-selective H2S donors.

Authors:  Matthew M Cerda; Turner D Newton; Yu Zhao; Brylee K Collins; Christopher H Hendon; Michael D Pluth
Journal:  Chem Sci       Date:  2018-11-30       Impact factor: 9.825

7.  Reactive oxygen species-triggered off-on fluorescence donor for imaging hydrogen sulfide delivery in living cells.

Authors:  Yiming Hu; Xiaoyi Li; Yu Fang; Wen Shi; Xiaohua Li; Wei Chen; Ming Xian; Huimin Ma
Journal:  Chem Sci       Date:  2019-07-10       Impact factor: 9.825

Review 8.  Moving Past Quinone-Methides: Recent Advances Toward Minimizing Electrophilic Byproducts from COS/H2S Donors.

Authors:  Michael D Pluth
Journal:  Curr Top Med Chem       Date:  2021       Impact factor: 3.570

  8 in total

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