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You search for a phrase ""Carbonic Anhydrase IX"" according to the criterion: Subject Terms


Title:
Affinity fine-tuning anti-CAIX CAR-T cells mitigate on-target off-tumor side effects.
Authors:
Wang Y; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.; Harvard Medical School, Boston, MA, 02115, USA.
Buck A; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Piel B; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Zerefa L; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Murugan N; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Coherd CD; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Miklosi AG; ONI (Oxford Nanoimaging Ltd.), Oxford, UK.
Johal H; ONI (Oxford Nanoimaging Ltd.), Oxford, UK.
Bastos RN; ONI (Oxford Nanoimaging Ltd.), Oxford, UK.
Huang K; Molecular Imaging Core, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Ficial M; Department of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Laimon YN; Department of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Signoretti S; Harvard Medical School, Boston, MA, 02115, USA.; Department of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.; Department of Oncologic Pathology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Zhong Z; LUMICKS, Waltham, MA, 02453, USA.
Hoang SM; LUMICKS, Waltham, MA, 02453, USA.
Kastrunes GM; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Grimaud M; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Fayed A; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Yuan HC; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Nguyen QD; Lurie Family Imaging Center, Center for Biomedical Imaging in Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Thai T; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Ivanova EV; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.; Belfer Center of Applied Cancer Science, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Paweletz CP; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.; Belfer Center of Applied Cancer Science, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Wu MR; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.; Harvard Medical School, Boston, MA, 02115, USA.
Choueiri TK; Harvard Medical School, Boston, MA, 02115, USA.; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Wee JO; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Freeman GJ; Harvard Medical School, Boston, MA, 02115, USA.; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Barbie DA; Harvard Medical School, Boston, MA, 02115, USA.; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.; Belfer Center of Applied Cancer Science, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Marasco WA; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA. wayne_.; Harvard Medical School, Boston, MA, 02115, USA. wayne_.
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Source:
Molecular cancer [Mol Cancer] 2024 Mar 16; Vol. 23 (1), pp. 56. Date of Electronic Publication: 2024 Mar 16.
Publication Type:
Journal Article
MeSH Terms:
Carcinoma, Renal Cell*/metabolism
Kidney Neoplasms*/pathology
Receptors, Chimeric Antigen*/genetics
Carbonic Anhydrases*/metabolism
Carbonic Anhydrases*/therapeutic use
Animals ; Mice ; Humans ; Carbonic Anhydrase IX/genetics ; Antigens, Neoplasm ; Antibodies ; T-Lymphocytes/metabolism
Academic Journal
Title:
Benzothiadiazinone-1,1-Dioxide Carbonic Anhydrase Inhibitors Suppress the Growth of Drug-Resistant Mycobacterium tuberculosis Strains.
Authors:
Bua S; Research Institute of the University of Bucharest (ICUB), University of Bucharest, 050095 Bucharest, Romania.
Bonardi A; Pharmaceutical and Nutraceutical Section, Laboratory of Molecular Modeling Cheminformatics & QSA, Neurofarba Department, University of Florence, Via U. Schiff 6, Sesto Fiorentino, 50019 Florence, Italy.
Mük GR; Faculty of Biology, University of Bucharest, Splaiul Independenței 91-95, 050095 Bucharest, Romania.; St. Stephen's Pneumoftiziology Hospital, Șoseaua Ștefan cel Mare 11, 020122 Bucharest, Romania.
Nocentini A; Pharmaceutical and Nutraceutical Section, Laboratory of Molecular Modeling Cheminformatics & QSA, Neurofarba Department, University of Florence, Via U. Schiff 6, Sesto Fiorentino, 50019 Florence, Italy.
Gratteri P; Pharmaceutical and Nutraceutical Section, Laboratory of Molecular Modeling Cheminformatics & QSA, Neurofarba Department, University of Florence, Via U. Schiff 6, Sesto Fiorentino, 50019 Florence, Italy.
Supuran CT; Pharmaceutical and Nutraceutical Section, Laboratory of Molecular Modeling Cheminformatics & QSA, Neurofarba Department, University of Florence, Via U. Schiff 6, Sesto Fiorentino, 50019 Florence, Italy.
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Source:
International journal of molecular sciences [Int J Mol Sci] 2024 Feb 23; Vol. 25 (5). Date of Electronic Publication: 2024 Feb 23.
Publication Type:
Journal Article
MeSH Terms:
Mycobacterium tuberculosis*
Carbonic Anhydrases*/metabolism
Tuberculosis*
Humans ; Molecular Structure ; Carbonic Anhydrase Inhibitors/pharmacology ; Isoenzymes/metabolism ; Structure-Activity Relationship ; Antitubercular Agents/pharmacology ; Carbonic Anhydrase IX
Academic Journal
Title:
Diffuse Carbonic Anhydrase 9 and GATA3 Expression in Fumarate Hydratase Deficient Renal Cell Carcinoma - A Case Report and Immunoprofile Review.
Authors:
Pacheco RR; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY, USA.
Pacheco R; Department of Radiology, Albany Medical Center, Albany, NY, USA.
Cooley C; Department of Radiology, Albany Medical Center, Albany, NY, USA.
Kaufman R; Department of Urology, Albany Medical Center, Albany, NY, USA.
Akgul M; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY, USA.
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Source:
International journal of surgical pathology [Int J Surg Pathol] 2024 Feb; Vol. 32 (1), pp. 145-149. Date of Electronic Publication: 2023 Apr 12.
Publication Type:
Case Reports; Journal Article
MeSH Terms:
Carcinoma, Renal Cell*/diagnosis
Carcinoma, Renal Cell*/pathology
Kidney Neoplasms*/diagnosis
Kidney Neoplasms*/pathology
Carcinoma, Transitional Cell*
Urinary Bladder Neoplasms*
Humans ; Fumarate Hydratase/genetics ; Carbonic Anhydrase IX ; GATA3 Transcription Factor
Academic Journal
Title:
2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms.
Authors:
Sequeira L; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.; CIQUP-IMS/Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Porto, Portugal.
Distinto S; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.
Meleddu R; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.
Gaspari M; Department of Experimental and Clinical Medicine, Research Centre for Advanced Biochemistry and Molecular Biology, 'Magna Græcia' University of Catanzaro, Catanzaro, Italy.
Angeli A; Department of NEUROFARBA, Section of Pharmaceutical Sciences, University of Florence, Florence, Italy.
Cottiglia F; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.
Secci D; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.
Onali A; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.
Sanna E; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.
Borges F; CIQUP-IMS/Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Porto, Portugal.
Uriarte E; Department of Organic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, Santiago de Compostela, Spain.
Alcaro S; Department of Health Sciences, 'Magna Græcia' University of Catanzaro, Catanzaro, Italy.
Supuran CT; Department of NEUROFARBA, Section of Pharmaceutical Sciences, University of Florence, Florence, Italy.
Maccioni E; Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2270183. Date of Electronic Publication: 2023 Oct 23.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Neoplasms*/drug therapy
Neoplasms*/pathology
Humans ; Carbonic Anhydrase IX ; Carbonic Anhydrase I ; Carbonic Anhydrase II ; Structure-Activity Relationship ; Carbonic Anhydrase Inhibitors/pharmacology ; Carbonic Anhydrase Inhibitors/chemistry ; Antigens, Neoplasm/chemistry ; Benzopyrans/pharmacology ; Isoenzymes/metabolism ; Molecular Structure
Academic Journal
Title:
Discovery of new 6-ureido/amidocoumarins as highly potent and selective inhibitors for the tumour-relevant carbonic anhydrases IX and XII.
Authors:
El-Damasy AK; Center for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, South Korea.; Department of Medicinal Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
Kim HJ; Center for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, South Korea.
Nocentini A; Section of Pharmaceutical and Nutraceutical Sciences, Department of NEUROFARBA, University of Florence, Florence, Italy.; Laboratory of Molecular Modeling Cheminformatics & QSAR, Department of NEUROFARBA-Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.
Seo SH; Center for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, South Korea.
Eldehna WM; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafr El Sheikh, Egypt.
Bang EK; Center for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, South Korea.
Supuran CT; Section of Pharmaceutical and Nutraceutical Sciences, Department of NEUROFARBA, University of Florence, Florence, Italy.
Keum G; Center for Brain Technology, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, South Korea.; Division of Bio-Medical Science & Technology, KIST School, Korea University of Science and Technology (UST), Seoul, South Korea.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2154603.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Humans ; Structure-Activity Relationship ; Carbonic Anhydrase Inhibitors/pharmacology ; Carbonic Anhydrase IX ; Antigens, Neoplasm ; MCF-7 Cells ; Coumarins/pharmacology ; Molecular Structure
Academic Journal
Title:
Discovery of 2,4-thiazolidinedione-tethered coumarins as novel selective inhibitors for carbonic anhydrase IX and XII isoforms.
Authors:
Eldehna WM; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.
Taghour MS; Pharmaceutical Medicinal Chemistry & Drug Design Department, Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.
Al-Warhi T; Department of Chemistry, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Nocentini A; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Firenze, Italy.
Elbadawi MM; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.
Mahdy HA; Pharmaceutical Medicinal Chemistry & Drug Design Department, Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.
Abdelrahman MA; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Egyptian Russian University, Cairo, Egypt.
Alotaibi OJ; Department of Chemistry, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Aljaeed N; Department of Chemistry, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Elimam DM; Department of Pharmacognosy, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.; School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom.
Afarinkia K; Institute of Cancer Therapeutics, University of Bradford, Bradford, United Kingdom.
Abdel-Aziz HA; Department of Applied Organic Chemistry, National Research Center, Giza, Egypt.
Supuran CT; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Firenze, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2022 Dec; Vol. 37 (1), pp. 531-541.
Publication Type:
Journal Article
MeSH Terms:
Drug Discovery*
Carbonic Anhydrase IX/*antagonists & inhibitors
Carbonic Anhydrase Inhibitors/*pharmacology
Carbonic Anhydrases/*metabolism
Coumarins/*pharmacology
Thiazolidinediones/*pharmacology
Antigens, Neoplasm/metabolism ; Apoptosis/drug effects ; Carbonic Anhydrase IX/metabolism ; Carbonic Anhydrase Inhibitors/chemical synthesis ; Carbonic Anhydrase Inhibitors/chemistry ; Cell Cycle/drug effects ; Cell Proliferation/drug effects ; Cell Survival/drug effects ; Coumarins/chemical synthesis ; Coumarins/chemistry ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Humans ; MCF-7 Cells ; Molecular Structure ; Structure-Activity Relationship ; Thiazolidinediones/chemical synthesis ; Thiazolidinediones/chemistry
Academic Journal
Title:
Isocoumarins: a new class of selective carbonic anhydrase IX and XII inhibitors.
Authors:
Onyılmaz M; Faculty of Science and Arts, Department of Chemistry, Harran University, Şanlıurfa, Turkey.
Koca M; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Adıyaman University, Adıyaman, Turkey.
Bonardi A; Department of Neurofarba, Sezione di Scienze Farmaceutiche, Università degli Studi di Firenze, Sesto Fiorentino, Italy.
Degirmenci M; Faculty of Science and Arts, Department of Chemistry, Harran University, Şanlıurfa, Turkey.
Supuran CT; Department of Neurofarba, Sezione di Scienze Farmaceutiche, Università degli Studi di Firenze, Sesto Fiorentino, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2022 Dec; Vol. 37 (1), pp. 743-748.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrase IX/*antagonists & inhibitors
Carbonic Anhydrase Inhibitors/*pharmacology
Carbonic Anhydrases/*metabolism
Isocoumarins/*pharmacology
Antigens, Neoplasm/metabolism ; Carbonic Anhydrase IX/metabolism ; Carbonic Anhydrase Inhibitors/chemical synthesis ; Carbonic Anhydrase Inhibitors/chemistry ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Humans ; Isocoumarins/chemical synthesis ; Isocoumarins/chemistry ; Molecular Structure ; Structure-Activity Relationship
Academic Journal
Title:
The three-tails approach as a new strategy to improve selectivity of action of sulphonamide inhibitors against tumour-associated carbonic anhydrase IX and XII.
Authors:
Bonardi A; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, Laboratory of Molecular Modeling Cheminformatics & QSAR, University of Firenze, Florence, Italy.
Bua S; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.
Combs J; Department of Biochemistry and Molecular Biology, College of Medicine, University of Florida, Gainesville, FL, USA.
Lomelino C; Department of Biochemistry and Molecular Biology, College of Medicine, University of Florida, Gainesville, FL, USA.
Andring J; Department of Biochemistry and Molecular Biology, College of Medicine, University of Florida, Gainesville, FL, USA.
Osman SM; Chemistry Department, College of Science, King Saud University, Riyadh, Saudi Arabia.
Toti A; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.
Di Cesare Mannelli L; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.
Gratteri P; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, Laboratory of Molecular Modeling Cheminformatics & QSAR, University of Firenze, Florence, Italy.
Ghelardini C; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.
McKenna R; Department of Biochemistry and Molecular Biology, College of Medicine, University of Florida, Gainesville, FL, USA.
Nocentini A; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.
Supuran CT; Department NEUROFARBA - Pharmaceutical and Nutraceutical Section, University of Firenze, Florence, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2022 Dec; Vol. 37 (1), pp. 930-939.
Publication Type:
Journal Article
MeSH Terms:
Antineoplastic Agents/*pharmacology
Carbonic Anhydrase IX/*antagonists & inhibitors
Carbonic Anhydrase Inhibitors/*pharmacology
Carbonic Anhydrases/*metabolism
Sulfonamides/*pharmacology
Antigens, Neoplasm/metabolism ; Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/chemistry ; Carbonic Anhydrase IX/metabolism ; Carbonic Anhydrase Inhibitors/chemical synthesis ; Carbonic Anhydrase Inhibitors/chemistry ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Cell Survival/drug effects ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Humans ; Molecular Structure ; Structure-Activity Relationship ; Sulfonamides/chemical synthesis ; Sulfonamides/chemistry
Academic Journal
Title:
1,2,3-Benzoxathiazine-2,2-dioxides - effective inhibitors of human carbonic anhydrases.
Authors:
Ivanova J; Latvian Institute of Organic Synthesis, Riga, Latvia.
Abdoli M; Faculty of Materials Science and Applied Chemistry, Institute of Technology of Organic Chemistry, Riga Technical University, Riga, Latvia.
Nocentini A; Neurofarba Department, Università degli Studi di Firenze, Florence, Italy.
Žalubovskis R; Latvian Institute of Organic Synthesis, Riga, Latvia.; Faculty of Materials Science and Applied Chemistry, Institute of Technology of Organic Chemistry, Riga Technical University, Riga, Latvia.
Supuran CT; Neurofarba Department, Università degli Studi di Firenze, Florence, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 225-238.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Neoplasms*
Humans ; Carbonic Anhydrase Inhibitors/pharmacology ; Carbonic Anhydrase IX/metabolism ; Structure-Activity Relationship ; Antigens, Neoplasm ; Molecular Structure
Academic Journal
Title:
Design and synthesis of some new benzoylthioureido benzenesulfonamide derivatives and their analogues as carbonic anhydrase inhibitors.
Authors:
Oudah KH; Pharmaceutical Chemistry Department, College of Pharmacy, Al-Ayen University, Nasiriyah, Iraq.
Mahmoud WR; Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Awadallah FM; Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Taher AT; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt.; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, October 6 University(O6U), Giza, Egypt.
Abbas SE; Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Allam HA; Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Vullo D; Department NEUROFARBA - Pharmaceutical and Nutraceutical section, University of Firenze, Università degli Studi di Firenze, Sesto Fiorentino, Italy.
Supuran CT; Department NEUROFARBA - Pharmaceutical and Nutraceutical section, University of Firenze, Università degli Studi di Firenze, Sesto Fiorentino, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 12-23.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrase Inhibitors*/chemistry
Carbonic Anhydrases*/metabolism
Molecular Docking Simulation ; Structure-Activity Relationship ; Molecular Structure ; Acetazolamide ; Protein Isoforms ; Carbonic Anhydrase IX/metabolism ; Benzenesulfonamides
Academic Journal
Title:
Novel thiazolone-benzenesulphonamide inhibitors of human and bacterial carbonic anhydrases.
Authors:
Abdoli M; Faculty of Materials Science and Applied Chemistry, Institute of Technology of Organic Chemistry, Riga Technical University, Riga, Latvia.
De Luca V; Department of Biology, Agriculture and Food Sciences, Institute of Biosciences and Bioresources, Napoli, Italy.
Capasso C; Department of Biology, Agriculture and Food Sciences, Institute of Biosciences and Bioresources, Napoli, Italy.
Supuran CT; NEUROFARBA Department, Pharmaceutical and Nutraceutical Section, University of Florence, Florence, Italy.
Žalubovskis R; Faculty of Materials Science and Applied Chemistry, Institute of Technology of Organic Chemistry, Riga Technical University, Riga, Latvia.; Latvian Institute of Organic Synthesis, Riga, Latvia.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2163243.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Humans ; Carbonic Anhydrase I/metabolism ; Carbonic Anhydrase II/metabolism ; Carbonic Anhydrase Inhibitors/pharmacology ; Sulfonamides/pharmacology ; Structure-Activity Relationship ; Carbonic Anhydrase IX/metabolism ; Molecular Structure ; Benzenesulfonamides
Academic Journal
Title:
3 H -1,2-Benzoxaphosphepine 2-oxides as selective inhibitors of carbonic anhydrase IX and XII.
Authors:
Pustenko A; Latvian Institute of Organic Synthesis, Riga, Latvia.
Balašova A; Latvian Institute of Organic Synthesis, Riga, Latvia.; Institute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia.
Nocentini A; Department of Neurofarba, Università degli Studi di Firenze, Florence, Italy.
Supuran CT; Department of Neurofarba, Università degli Studi di Firenze, Florence, Italy.
Žalubovskis R; Latvian Institute of Organic Synthesis, Riga, Latvia.; Institute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 216-224.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrase Inhibitors*/pharmacology
Oxides*
Humans ; Carbonic Anhydrase IX/metabolism ; Structure-Activity Relationship ; Carbonic Anhydrase I ; Antigens, Neoplasm ; Molecular Structure
Academic Journal
Title:
Synthesis, biological evaluation and theoretical studies of ( E )-1-(4-sulfamoyl-phenylethyl)-3-arylidene-5-aryl-1H-pyrrol-2(3H)-ones as human carbonic anhydrase inhibitors.
Authors:
Ramzan F; Department of Chemistry, School of Chemical and Life Sciences, New Delhi, India.
Nabi SA; Department of Chemistry, School of Chemical and Life Sciences, New Delhi, India.
Lone MS; Department of Chemistry, School of Chemical and Life Sciences, New Delhi, India.
Bonardi A; Neurofarba Department, Section of Pharmaceutical Chemistry, Università degli Studidi Firenze, Firenze, Italy.
Hamid A; Theoretical Chemistry Section, Chemistry Division, Bhabha Atomic Research Centre, Mumbai, Maharastra, India.
Bano S; Department of Computer Science and Engineering, School of Engineering Sciences and Technology, New Delhi, India.
Sharma K; Department of Pharmaceutical Chemistry, Delhi Pharmaceutical Sciences and Research University Pushpvihar, New Delhi, India.
Shafi S; Department of Chemistry, School of Chemical and Life Sciences, New Delhi, India.
Samim M; Department of Chemistry, School of Chemical and Life Sciences, New Delhi, India.
Javed K; Department of Chemistry, School of Chemical and Life Sciences, New Delhi, India.
Supuran CT; Neurofarba Department, Section of Pharmaceutical Chemistry, Università degli Studidi Firenze, Firenze, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2189126.
Publication Type:
Journal Article
MeSH Terms:
Antigens, Neoplasm*/metabolism
Carbonic Anhydrases*/metabolism
Humans ; Carbonic Anhydrase IX ; Carbonic Anhydrase Inhibitors/chemistry ; Models, Theoretical ; Structure-Activity Relationship ; Molecular Structure
Academic Journal
Title:
Discovery of sulfonamide-tethered isatin derivatives as novel anticancer agents and VEGFR-2 inhibitors.
Authors:
Shaldam MA; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.
Almahli H; Department of Chemistry, University of Cambridge, Cambridge, UK.
Angeli A; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Sesto Fiorentino, Italy.
Badi RM; Department of Medical Physiology, College of Medicine, King Khalid University, Abha, Saudi Arabia.
Khaleel EF; Department of Medical Physiology, College of Medicine, King Khalid University, Abha, Saudi Arabia.
Zain-Alabdeen AI; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Elsayed ZM; Scientific Research and Innovation Support Unit, Faculty of Pharmacy, Kafrelsheikh Uinversity, Kafrelsheikh, Egypt.
Elkaeed EB; Department of Pharmaceutical Sciences, College of Pharmacy, AlMaarefa University, Riyadh, Saudi Arabia.; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo, Egypt.
Salem R; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.
Supuran CT; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Sesto Fiorentino, Italy.
Eldehna WM; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.; School of Biotechnology, Badr University in Cairo, Badr City, Egypt.
Tawfik HO; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2203389.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Isatin*/pharmacology
Isatin*/chemistry
Antineoplastic Agents*/pharmacology
Antineoplastic Agents*/chemistry
Molecular Structure ; Structure-Activity Relationship ; Vascular Endothelial Growth Factor Receptor-2 ; Sulfonamides/pharmacology ; Sulfonamides/chemistry ; Carbonic Anhydrase Inhibitors/pharmacology ; Carbonic Anhydrase Inhibitors/chemistry ; Carbonic Anhydrase IX ; Antigens, Neoplasm/metabolism
Academic Journal
Title:
Design, synthesis, and biological investigation of selective human carbonic anhydrase II, IX, and XII inhibitors using 7-aryl/heteroaryl triazolopyrimidines bearing a sulfanilamide scaffold.
Authors:
Romagnoli R; Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara, Ferrara, Italy.
De Ventura T; Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara, Ferrara, Italy.
Manfredini S; Department of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
Baldini E; Department of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
Supuran CT; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Florence, Italy.
Nocentini A; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Florence, Italy.
Brancale A; Vysoká Škola Chemicko-Technologická v Praze, Prague, Czech Republic.
Bortolozzi R; Department of Woman's and Child's Health, Hemato-Oncology Lab, University of Padova, Padova, Italy.; Department of Pharmaceutical and Pharmacological Sciences, Section of Pharmacology, University of Padova, Padova, Italy.; Laboratory of Experimental Pharmacology, Istituto di Ricerca Pediatrica (IRP), Padova, Italy.
Manfreda L; Department of Woman's and Child's Health, Hemato-Oncology Lab, University of Padova, Padova, Italy.; Laboratory of Experimental Pharmacology, Istituto di Ricerca Pediatrica (IRP), Padova, Italy.
Viola G; Department of Woman's and Child's Health, Hemato-Oncology Lab, University of Padova, Padova, Italy.; Laboratory of Experimental Pharmacology, Istituto di Ricerca Pediatrica (IRP), Padova, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2270180. Date of Electronic Publication: 2023 Oct 18.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrase II*/metabolism
Antigens, Neoplasm*
Humans ; Structure-Activity Relationship ; Carbonic Anhydrase IX/metabolism ; Carbonic Anhydrase I/metabolism ; Protein Isoforms ; Sulfanilamides ; Carbonic Anhydrase Inhibitors/pharmacology ; Molecular Structure
Academic Journal
Title:
Synthesis and biological evaluation of new 3-substituted coumarin derivatives as selective inhibitors of human carbonic anhydrase IX and XII.
Authors:
Mahammad Ghouse S; Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Bahatam K; Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Angeli A; Neurofarba Deptartment, Sezione di ScienzeFarmaceutiche e Nutraceutiche, Università Degli Studi di Firenze, Florence, Italy.
Pawar G; Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Chinchilli KK; Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Yaddanapudi VM; Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Mohammed A; Department of Chemistry, Directorate of Distance Education, Maulana Azad National Urdu University, Hyderabad, India.
Supuran CT; Neurofarba Deptartment, Sezione di ScienzeFarmaceutiche e Nutraceutiche, Università Degli Studi di Firenze, Florence, Italy.
Nanduri S; Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2185760.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*
Humans ; Carbonic Anhydrase IX ; Molecular Docking Simulation ; Coumarins ; Ethers ; Hypoxia
Academic Journal
Title:
Development of novel anilinoquinazoline-based carboxylic acids as non-classical carbonic anhydrase IX and XII inhibitors.
Authors:
Elsayed ZM; Scientific Research and Innovation Support Unit, Kafrelsheikh University, Kafrelsheikh, Egypt.
Almahli H; Department of Chemistry, University of Cambridge, Cambridge, UK.
Nocentini A; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Firenze, Italy.
Ammara A; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Firenze, Italy.
Supuran CT; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Firenze, Italy.
Eldehna WM; Department of Pharmaceutical Chemistry, Kafrelsheikh University, Kafrelsheikh, Egypt.; School of Biotechnology, Badr University in Cairo, Badr City, Cairo, Egypt.
Abou-Seri SM; Department of Pharmaceutical Chemistry, Cairo University, Cairo, Egypt.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2191163.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Neoplasms*/pathology
Humans ; Carbonic Anhydrase IX ; Molecular Structure ; Structure-Activity Relationship ; Carboxylic Acids/pharmacology ; Carbonic Anhydrase Inhibitors ; Quinazolines/pharmacology ; Antigens, Neoplasm/metabolism
Academic Journal
Title:
Effect of hydrophobic extension of aryl enaminones and pyrazole-linked compounds combined with sulphonamide, sulfaguanidine, or carboxylic acid functionalities on carbonic anhydrase inhibitory potency and selectivity.
Authors:
Allam HA; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Giza, Egypt.
Albakry ME; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City, Egypt.
Mahmoud WR; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Giza, Egypt.
Bonardi A; Department of NEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Florence, Italy.
Moussa SA; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Giza, Egypt.
Mohamady S; Faculty of Pharmacy, The British University in Egypt, El Shorouk, Egypt.
Abdel-Aziz HA; Department of Applied Organic Chemistry, National Research Center, Giza, Egypt.
Supuran CT; Department of NEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Florence, Italy.
Ibrahim HS; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City, Egypt.; Department of Medicinal Chemistry, Institute of Pharmacy, Martin-Luther-University of Halle-Wittenberg, Halle (Saale), Germany.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2201403.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Antineoplastic Agents*/chemistry
Humans ; Carbonic Anhydrase IX ; Sulfaguanidine ; Structure-Activity Relationship ; Carboxylic Acids/pharmacology ; Sulfonamides/chemistry ; Carbonic Anhydrase Inhibitors/chemistry ; Pyrazoles/pharmacology ; Pyrazoles/chemistry ; Molecular Structure
Academic Journal
Title:
Investigation of novel alkyl/benzyl (4-sulphamoylphenyl)carbamimidothioates as carbonic anhydrase inhibitors.
Authors:
Abdoli M; Institute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia.
Bonardi A; Neurofarba Department, Universita Degli Studi di Firenze, Florence, Italy.
Supuran CT; Neurofarba Department, Universita Degli Studi di Firenze, Florence, Italy.
Žalubovskis R; Institute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia.; Latvian Institute of Organic Synthesis, Riga, Latvia.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2152811.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrase Inhibitors*/pharmacology
Carbonic Anhydrases*/metabolism
Humans ; Carbonic Anhydrase I ; Carbonic Anhydrase II ; Protein Isoforms ; Structure-Activity Relationship ; Carbonic Anhydrase IX
Academic Journal
Title:
Derivatives of 4-methyl-1,2,3-benzoxathiazine 2,2-dioxide as selective inhibitors of human carbonic anhydrases IX and XII over the cytosolic isoforms I and II.
Authors:
Ivanova J; Latvian Institute of Organic Synthesis, Riga, Latvia.
Abdoli M; Institute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia.
Nocentini A; Neurofarba Department, Università degli Studi di Firenze, Florence, Italy.
Žalubovskis R; Latvian Institute of Organic Synthesis, Riga, Latvia.; Institute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia.
Supuran CT; Neurofarba Department, Università degli Studi di Firenze, Florence, Italy.
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Source:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2023 Dec; Vol. 38 (1), pp. 2170370.
Publication Type:
Journal Article
MeSH Terms:
Carbonic Anhydrases*/metabolism
Neoplasms*
Humans ; Structure-Activity Relationship ; Carbonic Anhydrase Inhibitors/pharmacology ; Carbonic Anhydrase IX/metabolism ; Antigens, Neoplasm ; Isoenzymes/metabolism ; Molecular Structure
Academic Journal

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