Synthesis and evaluation of new benzodioxole-based dithiocarbamate derivatives as potential anticancer agents and hCA-I and hCA-II inhibitors.

[1]  C. Supuran,et al.  Synthesis of a new series of dithiocarbamates with effective human carbonic anhydrase inhibitory activity and antiglaucoma action. , 2015, Bioorganic & medicinal chemistry.

[2]  Yingbo Li,et al.  Discovery and optimization of novel dual dithiocarbamates as potent anticancer agents. , 2015, European journal of medicinal chemistry.

[3]  Z. Kaplancıklı,et al.  Synthesis and evaluation of new thiadiazole derivatives as potential inhibitors of human carbonic anhydrase isozymes (hCA-I and hCA-II) , 2015, Journal of enzyme inhibition and medicinal chemistry.

[4]  Krishna Bisetty,et al.  Dithiocarbamates as hazardous remediation agent: A critical review on progress in environmental chemistry for inorganic species studies of 20th century , 2014 .

[5]  Z. Kaplancıklı,et al.  Synthesis and Biological Evaluation of a Series of Dithiocarbamates as New Cholinesterase Inhibitors , 2013, Archiv der Pharmazie.

[6]  G. Çiftçi,et al.  Synthesis and Biological Evaluation of Some Pyrazoline Derivatives Bearing a Dithiocarbamate Moiety as New Cholinesterase Inhibitors , 2013, Archiv der Pharmazie.

[7]  Man Xing,et al.  Synthesis, molecular docking and evaluation of thiazolyl-pyrazoline derivatives containing benzodioxole as potential anticancer agents. , 2013, Bioorganic & medicinal chemistry.

[8]  C. Supuran,et al.  Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms? , 2012, Chemical reviews.

[9]  C. Supuran,et al.  Dithiocarbamates strongly inhibit carbonic anhydrases and show antiglaucoma action in vivo. , 2012, Journal of medicinal chemistry.

[10]  C. Supuran,et al.  Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations. , 2012, Chemical communications.

[11]  C. Supuran,et al.  Dithiocarbamates are strong inhibitors of the beta-class fungal carbonic anhydrases from Cryptococcus neoformans, Candida albicans and Candida glabrata. , 2012, Bioorganic & medicinal chemistry letters.

[12]  S. Sahoo,et al.  Carbonic anhydrase I and II inhibition with natural products: caffeine and piperine , 2012, Journal of enzyme inhibition and medicinal chemistry.

[13]  Claudiu T. Supuran,et al.  Recent Developments in Targeting Carbonic Anhydrase IX for Cancer Therapeutics , 2012, Oncotarget.

[14]  Claudiu T. Supuran,et al.  Interfering with pH regulation in tumours as a therapeutic strategy , 2011, Nature Reviews Drug Discovery.

[15]  J. Pastorek,et al.  Carbonic anhydrase IX as an anticancer therapy target: preclinical evaluation of internalizing monoclonal antibody directed to catalytic domain. , 2010, Current pharmaceutical design.

[16]  S. Poulsen Carbonic anhydrase inhibition as a cancer therapy: a review of patent literature, 2007 – 2009 , 2010, Expert opinion on therapeutic patents.

[17]  C. Supuran,et al.  Carbonic anhydrase inhibitors. Inhibition of transmembrane isoforms IX, XII, and XIV with less investigated anions including trithiocarbonate and dithiocarbamate. , 2010, Bioorganic & medicinal chemistry letters.

[18]  Claudiu T Supuran,et al.  Carbonic anhydrase inhibitors. , 2003, Bioorganic & medicinal chemistry letters.

[19]  C. Supuran,et al.  Design, synthesis, and docking studies of new 1,3,4-thiadiazole-2-thione derivatives with carbonic anhydrase inhibitory activity. , 2007, Bioorganic & medicinal chemistry.

[20]  C. Supuran,et al.  Targeting tumor-associated carbonic anhydrase IX in cancer therapy. , 2006, Trends in pharmacological sciences.

[21]  C. Supuran,et al.  Carbonic anhydrase inhibitors. Inhibition of the cytosolic and tumor-associated carbonic anhydrase isozymes I, II, and IX with a series of 1,3,4-thiadiazole- and 1,2,4-triazole-thiols. , 2005, Bioorganic & medicinal chemistry letters.

[22]  C. Supuran,et al.  Modulation of carbonic anhydrase activity and its applications in therapy , 2004 .

[23]  O. Arslan,et al.  A New Method for Purification of Carbonic Anhydrase Isozymes by Affinity Chromatography , 1996, Biochemistry (Moscow).

[24]  Y. Demir,et al.  THE ACTIVITIES OF CARBONIC ANHYDRASE AND ALKALINE PHOSPHATASE IN ANCIENT HUMAN BONES. PURIFICATION AND CHARACTERIZATION OF OUTER PERIPHERAL, CYTOSOLIC, INNER PERIPHERAL, AND INTEGRAL CA , 2001, Preparative biochemistry & biotechnology.

[25]  Claudiu T. Supuran,et al.  Carbonic anhydrase inhibitors - Part 94. 1,3,4-Thiadiazole-2-sulfonamide derivatives as antitumor agents? , 2000 .

[26]  D. Tipton,et al.  Cytotoxicity of mineral trioxide aggregate using human periodontal ligament fibroblasts. , 2000, Journal of endodontics.

[27]  E. Bakan,et al.  Purification and Characterization of Carbonic Anhydrase from Bovine Erythrocyte Plasma Membrane , 2000, Preparative biochemistry & biotechnology.

[28]  T. Mosmann Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. , 1983, Journal of immunological methods.

[29]  J. Edsall,et al.  CARBONIC ANHYDRASES FROM HUMAN ERYTHROCYTES. PREPARATION AND PROPERTIES OF TWO ENZYMES. , 1964, The Journal of biological chemistry.

[30]  N. Anderson,et al.  Electrometric and colorimetric determination of carbonic anhydrase. , 1948, The Anatomical record.