Anti-infective carbonic anhydrase inhibitors: a patent and literature review

被引:193
作者
Capasso, Clemente [1 ]
Supuran, Claudiu T. [2 ,3 ]
机构
[1] CNR, Ist Biochim Prot, I-80131 Naples, Italy
[2] Univ Florence, Lab Chim Bioinorgan, I-50019 Florence, Italy
[3] Univ Florence, NEUROFARBA Dept, Sez Sci Farmaceut & Nutraceut, I-50019 Florence, Italy
关键词
anti-infective; bacteria; carbonic anhydrase inhibitor; fungi; protozoa; sulfonamide; BETA-CLASS ENZYME; YEAST SACCHAROMYCES-CEREVISIAE; PATHOGENS CANDIDA-ALBICANS; CRYPTOCOCCUS-NEOFORMANS; MYCOBACTERIUM-TUBERCULOSIS; HELICOBACTER-PYLORI; MOLECULAR-CLONING; VIRULENCE FACTORS; ESCHERICHIA-COLI; ANION INHIBITION;
D O I
10.1517/13543776.2013.778245
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Introduction: All microorganisms that cause diseases or illnesses to their host are defined as pathogens. In this paper we will review the current state of the art for inhibiting parasite carbonic anhydrases (CAs, EC 4.2.1.1) with a goal of developing antibacterial, antifungal or antiprotozoan agents possessing a different mechanism of action compared with the clinically used drugs to which a considerable degree of drug resistance has been reported. Areas covered: Cloning of the genomes of many pathogenic microorganisms offered the possibility of exploring alternative pathways for inhibiting virulence factors or proteins essential for their life cycle, and such an approach was applied systematically for CAs from prokaryotic and eukaryotic microorganisms. Investigations of CAs in bacteria, fungi and protozoa domains will undoubtedly reveal novel aspects of microbial virulence, these efforts being part of a more general approach of using metalloenzyme inhibitors for designing novel classes of anti-infectives. Expert opinion: Covers an overview of the patent literature in the field of the anti-infective CA inhibitors. Most of the patents deal with sulfonamide CA inhibitors. Bacterial/fungal/protozoan CAs represent at this moment very promising targets for obtaining anti-infectives devoid of the resistance problems of the clinically used such agents but further studies are needed to validate these and other less investigated enzymes as novel drug targets.
引用
收藏
页码:693 / 704
页数:12
相关论文
共 109 条
[1]
CARBONIC-ANHYDRASE FROM NEISSERIA-SICCA, STRAIN 6021 .1. BACTERIAL GROWTH AND PURIFICATION OF ENZYME [J].
ADLER, L ;
NYMAN, PO ;
FALKBRIN.SO .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 284 (01) :298-+
[2]
Update on carbonic anhydrase inhibitors: a patent review (2008-2011) [J].
Aggarwal, Mayank ;
McKenna, Robert .
EXPERT OPINION ON THERAPEUTIC PATENTS, 2012, 22 (08) :903-915
[3]
The extremo-α-carbonic anhydrase (CA) from Sulfurihydrogenibium azorense, the fastest CA known, is highly activated by amino acids and amines [J].
Akdemir, Atilla ;
Vullo, Daniela ;
De Luca, Viviana ;
Scozzafava, Andrea ;
Carginale, Vincenzo ;
Rossi, Mose ;
Supuran, Claudiu T. ;
Capasso, Clemente .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (04) :1087-1090
[4]
A CARBONIC-ANHYDRASE FROM THE ARCHAEON METHANOSARCINA-THERMOPHILA [J].
ALBER, BE ;
FERRY, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :6909-6913
[5]
Alp Sehnaz, 2006, Mikrobiyoloji Bulteni, V40, P109
[6]
Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms? [J].
Alterio, Vincenzo ;
Di Fiore, Anna ;
D'Ambrosio, Katia ;
Supuran, Claudiu T. ;
De Simone, Giuseppina .
CHEMICAL REVIEWS, 2012, 112 (08) :4421-4468
[7]
Berkner JE, 2008, Process for the preparation of anticonvulsant derivatives of topiramate, Patent No. [HK1088336, 1088336]
[8]
Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata [J].
Bertucci, Anthony ;
Innocenti, Alessio ;
Scozzafava, Andrea ;
Tambutte, Sylvie ;
Zoccola, Didier ;
Supuran, Claudiu T. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (02) :710-714
[9]
Porphyromonas gingivalis: an invasive and evasive opportunistic oral pathogen [J].
Bostanci, Nagihan ;
Belibasakis, Georgios N. .
FEMS MICROBIOLOGY LETTERS, 2012, 333 (01) :1-9
[10]
Inhibition of the β-carbonic anhydrases from Mycobacterium tuberculosis with C-cinnamoyl glycosides: Identification of the first inhibitor with anti-mycobacterial activity [J].
Buchieri, Maria V. ;
Riafrecha, Leonardo E. ;
Rodriguez, Oscar M. ;
Vullo, Daniela ;
Morbidoni, Hector R. ;
Supuran, Claudiu T. ;
Colinas, Pedro A. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (03) :740-743