Articles - 3p5a mentioned but not cited (3)
- Dithiocarbamates strongly inhibit carbonic anhydrases and show antiglaucoma action in vivo. Carta F, Aggarwal M, Maresca A, Scozzafava A, McKenna R, Masini E, Supuran CT. J. Med. Chem. 55 1721-1730 (2012)
- Explainable Deep Relational Networks for Predicting Compound-Protein Affinities and Contacts. Karimi M, Wu D, Wang Z, Shen Y. J Chem Inf Model 61 46-66 (2021)
- Dithiocarbamates effectively inhibit the α-carbonic anhydrase from Neisseria gonorrhoeae. Giovannuzzi S, Abutaleb NS, Hewitt CS, Carta F, Nocentini A, Seleem MN, Flaherty DP, Supuran CT. J Enzyme Inhib Med Chem 37 1-8 (2022)
Reviews citing this publication (17)
- Structure-based drug discovery of carbonic anhydrase inhibitors. Supuran CT. J Enzyme Inhib Med Chem 27 759-772 (2012)
- How many carbonic anhydrase inhibition mechanisms exist? Supuran CT. J Enzyme Inhib Med Chem 31 345-360 (2016)
- Antiglaucoma carbonic anhydrase inhibitors: a patent review. Masini E, Carta F, Scozzafava A, Supuran CT. Expert Opin Ther Pat 23 705-716 (2013)
- Advances in structure-based drug discovery of carbonic anhydrase inhibitors. Supuran CT. Expert Opin Drug Discov 12 61-88 (2017)
- Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors. De Simone G, Alterio V, Supuran CT. Expert Opin Drug Discov 8 793-810 (2013)
- Bacterial, fungal and protozoan carbonic anhydrases as drug targets. Capasso C, Supuran CT. Expert Opin. Ther. Targets 19 1689-1704 (2015)
- Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids. Nepali K, Sharma S, Sharma M, Bedi PM, Dhar KL. Eur J Med Chem 77 422-487 (2014)
- Recent advances in the discovery of zinc-binding motifs for the development of carbonic anhydrase inhibitors. Winum JY, Supuran CT. J Enzyme Inhib Med Chem 30 321-324 (2015)
- Targeting tumour hypoxia to prevent cancer metastasis. From biology, biosensing and technology to drug development: the METOXIA consortium. Pettersen EO, Ebbesen P, Gieling RG, Williams KJ, Dubois L, Lambin P, Ward C, Meehan J, Kunkler IH, Langdon SP, Ree AH, Flatmark K, Lyng H, Calzada MJ, Peso LD, Landazuri MO, Görlach A, Flamm H, Kieninger J, Urban G, Weltin A, Singleton DC, Haider S, Buffa FM, Harris AL, Scozzafava A, Supuran CT, Moser I, Jobst G, Busk M, Toustrup K, Overgaard J, Alsner J, Pouyssegur J, Chiche J, Mazure N, Marchiq I, Parks S, Ahmed A, Ashcroft M, Pastorekova S, Cao Y, Rouschop KM, Wouters BG, Koritzinsky M, Mujcic H, Cojocari D. J Enzyme Inhib Med Chem 30 689-721 (2015)
- Probing the surface of human carbonic anhydrase for clues towards the design of isoform specific inhibitors. Pinard MA, Mahon B, McKenna R. Biomed Res Int 2015 453543 (2015)
- Carbonic Anhydrases: New Perspectives on Protein Functional Role and Inhibition in Helicobacter pylori. Campestre C, De Luca V, Carradori S, Grande R, Carginale V, Scaloni A, Supuran CT, Capasso C. Front Microbiol 12 629163 (2021)
- A Highlight on the Inhibition of Fungal Carbonic Anhydrases as Drug Targets for the Antifungal Armamentarium. Supuran CT, Capasso C. Int J Mol Sci 22 4324 (2021)
- Thermodynamic, kinetic, and structural parameterization of human carbonic anhydrase interactions toward enhanced inhibitor design. Linkuvienė V, Zubrienė A, Manakova E, Petrauskas V, Baranauskienė L, Zakšauskas A, Smirnov A, Gražulis S, Ladbury JE, Matulis D. Q Rev Biophys 51 e10 (2018)
- New Developments in Carbonic Anhydrase IX-Targeted Fluorescence and Nuclear Imaging Agents. Chen KT, Seimbille Y. Int J Mol Sci 23 6125 (2022)
- Carbonic Anhydrase Sensitivity to Pesticides: Perspectives for Biomarker Development. Lionetto MG, Caricato R, Giordano ME. Int J Mol Sci 21 (2020)
- Emerging trends in environmental and industrial applications of marine carbonic anhydrase: a review. Iraninasab S, Sharifian S, Homaei A, Homaee MB, Sharma T, Nadda AK, Kennedy JF, Bilal M, Iqbal HMN. Bioprocess Biosyst Eng 45 431-451 (2022)
- The revival of dithiocarbamates: from pesticides to innovative medical treatments. Kaul L, Süss R, Zannettino A, Richter K. iScience 24 102092 (2021)
Articles citing this publication (77)
- Introductory Journal Article Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnological use for CO(2) capture. Supuran CT. J Enzyme Inhib Med Chem 28 229-230 (2013)
- Discovery of a new family of carbonic anhydrases in the malaria pathogen Plasmodium falciparum--the η-carbonic anhydrases. Del Prete S, Vullo D, Fisher GM, Andrews KT, Poulsen SA, Capasso C, Supuran CT. Bioorg. Med. Chem. Lett. 24 4389-4396 (2014)
- Editorial Carbonic anhydrases. Supuran CT. Bioorg. Med. Chem. 21 1377-1378 (2013)
- Anion inhibition studies of an α-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1. De Luca V, Vullo D, Scozzafava A, Carginale V, Rossi M, Supuran CT, Capasso C. Bioorg. Med. Chem. Lett. 22 5630-5634 (2012)
- Insights towards sulfonamide drug specificity in α-carbonic anhydrases. Aggarwal M, Kondeti B, McKenna R. Bioorg. Med. Chem. 21 1526-1533 (2013)
- An α-carbonic anhydrase from the thermophilic bacterium Sulphurihydrogenibium azorense is the fastest enzyme known for the CO2 hydration reaction. Luca VD, Vullo D, Scozzafava A, Carginale V, Rossi M, Supuran CT, Capasso C. Bioorg. Med. Chem. 21 1465-1469 (2013)
- Anion inhibition studies of the α-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae. Vullo D, Isik S, Del Prete S, De Luca V, Carginale V, Scozzafava A, Supuran CT, Capasso C. Bioorg. Med. Chem. Lett. 23 1636-1638 (2013)
- Out of the active site binding pocket for carbonic anhydrase inhibitors. D'Ambrosio K, Carradori S, Monti SM, Buonanno M, Secci D, Vullo D, Supuran CT, De Simone G. Chem. Commun. (Camb.) 51 302-305 (2015)
- Anion inhibition studies of two new β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila. Nishimori I, Vullo D, Minakuchi T, Scozzafava A, Osman SM, AlOthman Z, Capasso C, Supuran CT. Bioorg. Med. Chem. Lett. 24 1127-1132 (2014)
- Anion inhibition studies of the α-carbonic anhydrase from the protozoan pathogen Trypanosoma cruzi, the causative agent of Chagas disease. Pan P, Vermelho AB, Scozzafava A, Parkkila S, Capasso C, Supuran CT. Bioorg. Med. Chem. 21 4472-4476 (2013)
- 7-Substituted-sulfocoumarins are isoform-selective, potent carbonic anhydrase II inhibitors. Tanc M, Carta F, Bozdag M, Scozzafava A, Supuran CT. Bioorg. Med. Chem. 21 4502-4510 (2013)
- Restoring catalytic activity to the human carbonic anhydrase (CA) related proteins VIII, X and XI affords isoforms with high catalytic efficiency and susceptibility to anion inhibition. Nishimori I, Vullo D, Minakuchi T, Scozzafava A, Capasso C, Supuran CT. Bioorg. Med. Chem. Lett. 23 256-260 (2013)
- A class of carbonic anhydrase I - selective activators. Licsandru E, Tanc M, Kocsis I, Barboiu M, Supuran CT. J Enzyme Inhib Med Chem 32 37-46 (2017)
- 7-Aryl-triazolyl-substituted sulfocoumarins are potent, selective inhibitors of the tumor-associated carbonic anhydrase IX and XII. Nocentini A, Ceruso M, Carta F, Supuran CT. J Enzyme Inhib Med Chem 31 1226-1233 (2016)
- In vitro anti-proliferative and anti-angiogenic activities of thalidomide dithiocarbamate analogs. El-Aarag BY, Kasai T, Zahran MA, Zakhary NI, Shigehiro T, Sekhar SC, Agwa HS, Mizutani A, Murakami H, Kakuta H, Seno M. Int. Immunopharmacol. 21 283-292 (2014)
- Mono-/dihydroxybenzoic acid esters and phenol pyridinium derivatives as inhibitors of the mammalian carbonic anhydrase isoforms I, II, VII, IX, XII and XIV. Carta F, Vullo D, Maresca A, Scozzafava A, Supuran CT. Bioorg. Med. Chem. 21 1564-1569 (2013)
- Dipotassium-trioxohydroxytetrafluorotriborate, K₂[B₃O₃F₄OH], is a potent inhibitor of human carbonic anhydrases. Vullo D, Milos M, Galic B, Scozzafava A, Supuran CT. J Enzyme Inhib Med Chem 30 341-344 (2015)
- Inhibition of the β-carbonic anhydrase from the dandruff-producing fungus Malassezia globosa with monothiocarbamates. Nocentini A, Vullo D, Del Prete S, Osman SM, Alasmary FAS, AlOthman Z, Capasso C, Carta F, Gratteri P, Supuran CT. J Enzyme Inhib Med Chem 32 1064-1070 (2017)
- Synthesis of a new series of dithiocarbamates with effective human carbonic anhydrase inhibitory activity and antiglaucoma action. Bozdag M, Carta F, Vullo D, Akdemir A, Isik S, Lanzi C, Scozzafava A, Masini E, Supuran CT. Bioorg. Med. Chem. 23 2368-2376 (2015)
- X-ray crystallography-promoted drug design of carbonic anhydrase inhibitors. Ivanova J, Leitans J, Tanc M, Kazaks A, Zalubovskis R, Supuran CT, Tars K. Chem. Commun. (Camb.) 51 7108-7111 (2015)
- 5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: solution and X-ray crystallographic studies. Leitans J, Sprudza A, Tanc M, Vozny I, Zalubovskis R, Tars K, Supuran CT. Bioorg. Med. Chem. 21 5130-5138 (2013)
- 6-Substituted 1,2-benzoxathiine-2,2-dioxides are isoform-selective inhibitors of human carbonic anhydrases IX, XII and VA. Tanc M, Carta F, Scozzafava A, Supuran CT. Org. Biomol. Chem. 13 77-80 (2015)
- Novel Sulfamide-Containing Compounds as Selective Carbonic Anhydrase I Inhibitors. Berrino E, Bua S, Mori M, Botta M, Murthy VS, Vijayakumar V, Tamboli Y, Bartolucci G, Mugelli A, Cerbai E, Supuran CT, Carta F. Molecules 22 (2017)
- Synthesis and carbonic anhydrase I, II, VII, and IX inhibition studies with a series of benzo[d]thiazole-5- and 6-sulfonamides. Abdoli M, Angeli A, Bozdag M, Carta F, Kakanejadifard A, Saeidian H, Supuran CT. J Enzyme Inhib Med Chem 32 1071-1078 (2017)
- Synthesis and carbonic anhydrase inhibitory properties of novel 1,4-dihydropyrimidinone substituted diarylureas. Celik F, Arslan M, Yavuz E, Demir D, Gençer N. J Enzyme Inhib Med Chem 29 18-22 (2014)
- Dithiocarbamates with potent inhibitory activity against the Saccharomyces cerevisiae β-carbonic anhydrase. Bozdag M, Carta F, Vullo D, Isik S, AlOthman Z, Osman SM, Scozzafava A, Supuran CT. J Enzyme Inhib Med Chem 31 132-136 (2016)
- Evaluation of selenide, diselenide and selenoheterocycle derivatives as carbonic anhydrase I, II, IV, VII and IX inhibitors. Angeli A, Tanini D, Viglianisi C, Panzella L, Capperucci A, Menichetti S, Supuran CT. Bioorg. Med. Chem. 25 2518-2523 (2017)
- Inhibition of the α-carbonic anhydrase from Vibrio cholerae with amides and sulfonamides incorporating imidazole moieties. De Vita D, Angeli A, Pandolfi F, Bortolami M, Costi R, Di Santo R, Suffredini E, Ceruso M, Del Prete S, Capasso C, Scipione L, Supuran CT. J Enzyme Inhib Med Chem 32 798-804 (2017)
- Sulfonamide inhibition studies of the β carbonic anhydrase from Drosophila melanogaster. Syrjänen L, Parkkila S, Scozzafava A, Supuran CT. Bioorg. Med. Chem. Lett. 24 2797-2801 (2014)
- Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors. Ramya PVS, Angapelly S, Angeli A, Digwal CS, Arifuddin M, Babu BN, Supuran CT, Kamal A. J Enzyme Inhib Med Chem 32 1274-1281 (2017)
- Dithiocarbamates effectively inhibit the β-carbonic anhydrase from the dandruff-producing fungus Malassezia globosa. Vullo D, Del Prete S, Nocentini A, Osman SM, AlOthman Z, Capasso C, Bozdag M, Carta F, Gratteri P, Supuran CT. Bioorg. Med. Chem. 25 1260-1265 (2017)
- More effective dithiocarbamate derivatives inhibiting carbonic anhydrases, generated by QSAR and computational design. Avram S, Milac AL, Carta F, Supuran CT. J Enzyme Inhib Med Chem 28 350-359 (2013)
- Sulfonamide inhibition profiles of the β-carbonic anhydrase from the pathogenic bacterium Francisella tularensis responsible of the febrile illness tularemia. Del Prete S, Vullo D, Osman SM, AlOthman Z, Supuran CT, Capasso C. Bioorg. Med. Chem. 25 3555-3561 (2017)
- Sulphonamide inhibition studies of the β-carbonic anhydrase from the bacterial pathogen Clostridium perfringens. Vullo D, Kumar RSS, Scozzafava A, Ferry JG, Supuran CT. J Enzyme Inhib Med Chem 33 31-36 (2018)
- Synthesis and biological evaluation of novel aromatic and heterocyclic bis-sulfonamide Schiff bases as carbonic anhydrase I, II, VII and IX inhibitors. Akocak S, Lolak N, Nocentini A, Karakoc G, Tufan A, Supuran CT. Bioorg. Med. Chem. 25 3093-3097 (2017)
- Carbonic anhydrases activation with 3-amino-1H-1,2,4-triazole-1-carboxamides: Discovery of subnanomolar isoform II activators. Le Duc Y, Licsandru E, Vullo D, Barboiu M, Supuran CT. Bioorg. Med. Chem. 25 1681-1686 (2017)
- Synthesis of an acridine orange sulfonamide derivative with potent carbonic anhydrase IX inhibitory action. Bragagni M, Carta F, Osman SM, AlOthman Z, Supuran CT. J Enzyme Inhib Med Chem 32 701-706 (2017)
- Characterization, bioinformatic analysis and dithiocarbamate inhibition studies of two new α-carbonic anhydrases, CAH1 and CAH2, from the fruit fly Drosophila melanogaster. Syrjänen L, Tolvanen ME, Hilvo M, Vullo D, Carta F, Supuran CT, Parkkila S. Bioorg. Med. Chem. 21 1516-1521 (2013)
- Sulfocoumarin-, Coumarin-, 4-Sulfamoylphenyl-Bearing Indazole-3-carboxamide Hybrids: Synthesis and Selective Inhibition of Tumor-Associated Carbonic Anhydrase Isozymes IX and XII. Angapelly S, Sri Ramya PV, Angeli A, Supuran CT, Arifuddin M. ChemMedChem 12 1578-1584 (2017)
- Comparison of the anion inhibition profiles of the β- and γ-carbonic anhydrases from the pathogenic bacterium Burkholderia pseudomallei. Del Prete S, Vullo D, di Fonzo P, Carginale V, Supuran CT, Capasso C. Bioorg. Med. Chem. 25 2010-2015 (2017)
- Crystal structure of the human carbonic anhydrase II adduct with 1-(4-sulfamoylphenyl-ethyl)-2,4,6-triphenylpyridinium perchlorate, a membrane-impermeant, isoform selective inhibitor. Alterio V, Esposito D, Monti SM, Supuran CT, De Simone G. J Enzyme Inhib Med Chem 33 151-157 (2018)
- Design, synthesis and antibacterial evaluation of novel AHL analogues. Ren JL, Zhang E, Ye XW, Wang MM, Yu B, Wang WH, Guo YZ, Liu HM. Bioorg. Med. Chem. Lett. 23 4154-4156 (2013)
- Identification of metal dithiocarbamates as a novel class of antileishmanial agents. Pal DS, Mondal DK, Datta R. Antimicrob. Agents Chemother. 59 2144-2152 (2015)
- Solid-state UV-MALDI-MS assay of transition metal dithiocarbamate fungicides. Ivanova B, Spiteller M. Environ Sci Pollut Res Int 21 1163-1177 (2014)
- Synthesis of bulky-tailed sulfonamides incorporating pyrido[2,3-d][1,2,4]triazolo[4,3-a]pyrimidin-1(5H)-yl) moieties and evaluation of their carbonic anhydrases I, II, IV and IX inhibitory effects. Fares M, Eladwy RA, Nocentini A, El Hadi SRA, Ghabbour HA, Abdel-Megeed A, Eldehna WM, Abdel-Aziz HA, Supuran CT. Bioorg. Med. Chem. 25 2210-2217 (2017)
- Synthesis of novel acyl selenoureido benzensulfonamides as carbonic anhydrase I, II, VII and IX inhibitors. Angeli A, Carta F, Bartolucci G, Supuran CT. Bioorg. Med. Chem. 25 3567-3573 (2017)
- Uncaging carbon disulfide. Delivery platforms for potential pharmacological applications: a mechanistic approach. DeMartino AW, Souza ML, Ford PC. Chem Sci 8 7186-7196 (2017)
- Anion inhibition studies of the α-carbonic anhydrases from Neisseria gonorrhoeae. Nocentini A, Hewitt CS, Mastrolorenzo MD, Flaherty DP, Supuran CT. J Enzyme Inhib Med Chem 36 1061-1066 (2021)
- Carbonic anhydrase I, II, IV and IX inhibition with a series of 7-amino-3,4-dihydroquinolin-2(1H)-one derivatives. Bozdag M, Bua S, Osman SM, AlOthman Z, Supuran CT. J Enzyme Inhib Med Chem 32 885-892 (2017)
- Coumarins and other fused bicyclic heterocycles with selective tumor-associated carbonic anhydrase isoforms inhibitory activity. Bozdag M, Alafeefy AM, Altamimi AM, Vullo D, Carta F, Supuran CT. Bioorg. Med. Chem. 25 677-683 (2017)
- Investigations into the carbonic anhydrase inhibition of COS-releasing donor core motifs. Steiger AK, Zhao Y, Choi WJ, Crammond A, Tillotson MR, Pluth MD. Biochem. Pharmacol. 149 124-130 (2018)
- Native mass spectrometry of human carbonic anhydrase I and its inhibitor complexes. Zoppi C, Nocentini A, Supuran CT, Pratesi A, Messori L. J Biol Inorg Chem 25 979-993 (2020)
- Synthesis and antitumor activity of tetrahydrocarbazole hybridized with dithioate derivatives. El-Nassan HB. J Enzyme Inhib Med Chem 30 308-315 (2015)
- Synthesis and biological evaluation of cyclic imides incorporating benzenesulfonamide moieties as carbonic anhydrase I, II, IV and IX inhibitors. Abdel-Aziz AA, Angeli A, El-Azab AS, Abu El-Enin MA, Supuran CT. Bioorg. Med. Chem. 25 1666-1671 (2017)
- A new aspect to chaperone-like activity of bovine β-casein by protein-protein interactions study. Sharifizadeh A, Saboury AA, Moosavi-Movahedi AA, Salami M, Yousefi R. Int. J. Biol. Macromol. 51 901-907 (2012)
- Cyclodextrin complexation highly enhances efficacy of arylsulfonylureido benzenesulfonamide carbonic anhydrase inhibitors as a topical antiglaucoma agents. Bragagni M, Bozdag M, Carta F, Scozzafava A, Lanzi C, Masini E, Mura P, Supuran CT. Bioorg. Med. Chem. 23 6223-6227 (2015)
- Design, synthesis and pharmacological analysis of 5-[4'-(substituted-methyl)[1,1'-biphenyl]-2-yl]-1H-tetrazoles. Kamble A, Kamble R, Dodamani S, Jalalpure S, Rasal V, Kumbar M, Joshi S, Dixit S. Arch. Pharm. Res. 40 444-457 (2017)
- N-Substituted and ring opened saccharin derivatives selectively inhibit transmembrane, tumor-associated carbonic anhydrases IX and XII. Ivanova J, Carta F, Vullo D, Leitans J, Kazaks A, Tars K, Žalubovskis R, Supuran CT. Bioorg. Med. Chem. 25 3583-3589 (2017)
- Proteochemometric Modeling of the Interaction Space of Carbonic Anhydrase and its Inhibitors: An Assessment of Structure-based and Sequence-based Descriptors. Rasti B, Namazi M, Karimi-Jafari MH, Ghasemi JB. Mol Inform 36 (2017)
- Synthesis and Biological Evaluation of Imidazo[2 ,1-b]Thiazole based Sulfonyl Piperazines as Novel Carbonic Anhydrase II Inhibitors. Manasa KL, Pujitha S, Sethi A, Mohammed A, Alvala M, Angeli A, Supuran CT. Metabolites 10 (2020)
- Synthesis and human/bacterial carbonic anhydrase inhibition with a series of sulfonamides incorporating phthalimido moieties. Mohamed MA, Abdel-Aziz AA, Sakr HM, El-Azab AS, Bua S, Supuran CT. Bioorg. Med. Chem. 25 2524-2529 (2017)
- A novel three-component reaction between isocyanides, alcohols or thiols and elemental sulfur: a mild, catalyst-free approach towards O-thiocarbamates and dithiocarbamates. Németh AG, Keserű GM, Ábrányi-Balogh P. Beilstein J Org Chem 15 1523-1533 (2019)
- An update on anticancer drug development and delivery targeting carbonic anhydrase IX. Kazokaitė J, Aspatwar A, Parkkila S, Matulis D. PeerJ 5 e4068 (2017)
- Anion Inhibition Studies of the β-Class Carbonic Anhydrase CAS3 from the Filamentous Ascomycete Sordaria macrospora. Vullo D, Lehneck R, Donald WA, Pöggeler S, Supuran CT. Metabolites 10 (2020)
- Anion inhibition studies of a beta carbonic anhydrase from the malaria mosquito Anopheles gambiae. Vullo D, Syrjänen L, Kuuslahti M, Parkkila S, Supuran CT. J Enzyme Inhib Med Chem 33 359-363 (2018)
- Cloning, purification, kinetic and anion inhibition studies of a recombinant β-carbonic anhydrase from the Atlantic salmon parasite platyhelminth Gyrodactylus salaris. Aspatwar A, Barker H, Aisala H, Zueva K, Kuuslahti M, Tolvanen M, Primmer CR, Lumme J, Bonardi A, Tripathi A, Parkkila S, Supuran CT. J Enzyme Inhib Med Chem 37 1577-1586 (2022)
- Discovery of novel heteroarylmethylcarbamodithioates as potent anticancer agents: Synthesis, structure-activity relationship analysis and biological evaluation. Li YB, Yan X, Li RD, Liu P, Sun SQ, Wang X, Cui JR, Zhou DM, Ge ZM, Li RT. Eur J Med Chem 112 217-230 (2016)
- Dithiocarbamate as a Valuable Scaffold for the Inhibition of Metallo-β-Lactmases. Ge Y, Xu LW, Liu Y, Sun LY, Gao H, Li JQ, Yang K. Biomolecules 9 (2019)
- Dual-tail approach to discovery of novel carbonic anhydrase IX inhibitors by simultaneously matching the hydrophobic and hydrophilic halves of the active site. Hou Z, Lin B, Bao Y, Yan HN, Zhang M, Chang XW, Zhang XX, Wang ZJ, Wei GF, Cheng MS, Liu Y, Guo C. Eur J Med Chem 132 1-10 (2017)
- Highly efficient synthesis of alkyl and aryl primary thiocarbamates and dithiocarbamates under metal- and solvent-free conditions. Sardarian AR, Inaloo ID, Modarresi-Alam AR. Mol. Divers. 22 863-878 (2018)
- Identification of hub genes for glaucoma: a study based on bioinformatics analysis and experimental verification. Xie RL, Nie HY, Xu YX. Int J Ophthalmol 16 1015-1025 (2023)
- In vitro inhibition of Mycobacterium tuberculosis β-carbonic anhydrase 3 with Mono- and dithiocarbamates and evaluation of their toxicity using zebrafish developing embryos. Aspatwar A, Hammaren M, Parikka M, Parkkila S, Carta F, Bozdag M, Vullo D, Supuran CT. J Enzyme Inhib Med Chem 35 65-71 (2020)
- Sulfonamide-Derived Dithiocarbamate Gold(I) Complexes Induce the Apoptosis of Colon Cancer Cells by the Activation of Caspase 3 and Redox Imbalance. Quero J, Royo JC, Fodor B, Gimeno MC, Osada J, Rodríguez-Yoldi MJ, Cerrada E. Biomedicines 10 1437 (2022)
- Synthesis and biological evaluation of dithiocarbamate esters of parthenolide as potential anti-acute myelogenous leukaemia agents. Ding Y, Yang Z, Ge W, Kuang B, Xu J, Yang J, Chen Y, Zhang Q. J Enzyme Inhib Med Chem 33 1376-1391 (2018)
- Synthesis of a new series of 3-functionalised-1-phenyl-1,2,3-triazole sulfamoylbenzamides as carbonic anhydrase I, II, IV and IX inhibitors. Swain B, Angeli A, Angapelly S, Thacker PS, Singh P, Supuran CT, Arifuddin M. J Enzyme Inhib Med Chem 34 1199-1209 (2019)
- Tip60 might be a candidate for the acetylation of hepatic carbonic anhydrase I and III in mice. Gönül Baltacı N, Koçpınar EF, Budak H. Mol Biol Rep 48 7397-7404 (2021)
- Transcriptional Induction of Cystathionine γ-Lyase, a Reactive Sulfur-Producing Enzyme, by Copper Diethyldithiocarbamate in Cultured Vascular Endothelial Cells. Fujie T, Takahashi A, Takahashi M, Hara T, Soyama A, Makino K, Takahashi H, Yamamoto C, Kumagai Y, Naka H, Kaji T. Int J Mol Sci 21 (2020)