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- Volume 19, Issue 6, 2012
Current Medicinal Chemistry - Volume 19, Issue 6, 2012
Volume 19, Issue 6, 2012
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Editorial [ Hot Topic-I: Applications of the Photodynamic Therapy to Cancer,Water- and Vector-Borne Diseases (Guest Editor: Luigi E. Xodo )]
More LessPhotodynamic therapy (PDT) is a clinically approved treatment modality for various types of diseases, including cancer, that produces a selective cytotoxic effect on the target cells. It involves the use of a photosensitizing molecule and a source of light with a wavelength that corresponds to the absorption band of the photosensitizer. After photoactivation, the photosensitizer occupies an excited triplet state from which it tran Read More
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Non Polymeric Nanoparticles for Photodynamic Therapy Applications: Recent Developments
Authors: R. Chouikrat, A. Seve, R. Vanderesse, H. Benachour, M. Barberi-Heyob, S. Richeter, L. Raehm, J.-O. Durand, M. Verelst and C. FrochotPhotodynamic therapy has emerged as an alternative to chemotherapy and radiotherapy for cancer treatment. Nanoparticles have recently been proposed as effective carriers for photosensitizers. Depending on their chemical composition, these can be used for diagnosis and therapy due to the selective accumulation of the photosensitizer in cancer cells in vitro or in tumors in vivo. Multifunctional nanoplatforms combining se Read More
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Molecular Response to Hypericin-Induced Photodamage
Authors: B. Krammer and T. VerwangerHypericin (Hyp) is used as a powerful natural photosensitizer in photodynamic therapy (PDT). After selective accumulation in tumor tissue, vessels and matrix, and activated by visible light, it destroys the tumor mainly via generation of reactive oxygen species. After photoactivation, molecular biological mechanisms lead to different cellular endpoints: “biostimulation” (increased proliferation rate), repair of the damage leading t Read More
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The Chlorophyll Catabolite Pheophorbide a as a Photosensitizer for the Photodynamic Therapy
Authors: L. E. Xodo, V. Rapozzi, M. Zacchigna, S. Drioli and S. ZorzetPheophorbide a is a clorophyll catabolite that recently has drawn the attention of several investigators for its potential in photodynamic therapy. In this review we summarize its photophysical properties, phototoxicity, cellular localization, biodistribution and PDT activity as a free or conjugated molecule.
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Porphyrin Photosensitised Processes in the Prevention and Treatment of Water- and Vector-Borne Diseases
Authors: O. Coppellotti, C. Fabris, M. Soncin, M. Magaraggia, M. Camerin, G. Jori and L. GuidolinWater- and vector-borne diseases are a global burden which is estimated to cause several million deaths and innumerable cases of sickness every year. These infectious illnesses are emerging or resurging as a result of several factors, such as changes in climate, in public health and demography policy, as well as the spread of resistance to insecticide and drug, and genetic changes in pathogens. Integrated preventio Read More
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Editorial [ Hot Topic-II: Zinc Metallo-Enzymes as Target for Drug Design (Guest Editor: Giuseppina De Simone )]
More LessStarting from the discovery in 1940 of the first zinc metalloenzyme, carbonic anhydrase II, a very large number of enzymes requiring zinc as essential cofactor has been identified in all organisms, showing a variety of important physiological functions. These enzymes have a wide range of specific biological activities residing in the intra- and extracellular environments, and are implicated in several types of pathologies, such Read More
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Carbonic Anhydrase IX as a Target for Designing Novel Anticancer Drugs
Authors: S. M. Monti, C. T. Supuran and G. De SimoneCarbonic anhydrase IX (CA IX) is a tumor associated protein, since it is highly expressed in a multitude of carcinomas, while it is present in a limited number of normal tissues. It is a multi-domain protein consisting of an N-terminal proteoglycan-like (PG) domain, a catalytic domain, a trans-membrane portion (TM) and an intracytoplasmatic (IC) segment. These domains have peculiar biochemical and physiological features. A Read More
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Inhibition of Bacterial Carbonic Anhydrases and Zinc Proteases: From Orphan Targets to Innovative New Antibiotic Drugs
More LessZinc-containing enzymes, such as carbonic anhydrases (CAs) and metalloproteases (MPs) play critical functions in bacteria, being involved in various steps of their life cycle, which are important for survival, colonization, acquisition of nutrients for growth and proliferation, facilitation of dissemination, invasion and pathogenicity. The development of resistance to many classes of clinically used antibiotics emphasizes the n Read More
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Structure Based Drug Design of Angiotensin-I Converting Enzyme Inhibitors
Authors: C. S. Anthony, G. Masuyer, E. D. Sturrock and K. R. AcharyaCardiovascular disease (CVD) is responsible for ∼27% of deaths worldwide, with 80% of these occuring in developing countries. Hypertension is one of the most important treatable factors in the prevention of CVD. Angiotensin-I converting enzyme (ACE) is a two-domain dipeptidylcarboxypeptidase that is a key regulator of blood pressure as a result of its critical role in the reninangiotensin- aldosterone an Read More
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Glutamate Carboxypeptidase II in Diagnosis and Treatment of Neurologic Disorders and Prostate Cancer
Authors: C. Barinka, C. Rojas, B. Slusher and M. PomperGlutamate carboxypeptidase II (GCPII) is a membrane-bound binuclear zinc metallopeptidase with the highest expression levels found in the nervous and prostatic tissue. Throughout the nervous system, glia-bound GCPII is intimately involved in the neuronneuron and neuron-glia signaling via the hydrolysis of N-acetylaspartylglutamate (NAAG), the most abundant mammalian peptidic neurotransmitter. The inhibition of the Read More
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Exploration of Chemical Space Based on 4-Anilinoquinazoline
More LessChemical space is defined as all possible small organic molecules, including those present in biological systems, which is so vast that so far only a tiny fraction of it has been explored. Indeed, a thorough examination of all “chemical space” is practically impossible. The success of three EGFR inhibitors (Gefitnib, Erlotinib, Lapatinib) suggests that 4-anilinoquinazoline scaffold is still worth developing in the future. To date hundred Read More
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Protein Degradation by the Ubiquitin-Proteasome Pathway and Organ Fibrosis
Authors: H. Fukasawa, Y. Fujigaki, T. Yamamoto, A. Hishida and M. KitagawaAbnormal and exaggerated deposition of extracellular matrix proteins is the common feature of fibrotic diseases. The resulting fibrosis disrupts the normal architecture of the affected organs and finally leads to their dysfunction and failure. At present, there are no effective therapies for fibrotic diseases. Protein degradation via the ubiquitin-proteasome system is the major pathway for non-lysosomal proteolysis and controls man Read More
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Novel Biomarkers Assessing the Calcium Deposition in Coronary Artery Disease
Authors: D. Tousoulis, G. Siasos, K. Maniatis, E. Oikonomou, K. Vlasis, A. G. Papavassiliou and C. StefanadisCoronary atherosclerosis is the pathophysiologic background of coronary artery disease. Vascular calcification is an actively regulated form of calcified tissue metabolism and a common feature of coronary atherosclerotic plaques. Interestingly, systematic research has revealed that vascular mineralization, is also a strong and independent predictor of cardiovascular morbidity and mortality. Recently, several biomarke Read More
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Modulation of Ascorbic Acid-Induced DNA Cleavage by Polyamide: Cleavage Manner, Kinetics and Mechanism
More LessManipulation of DNA presents a great interest in biotechnology and therapeutics. The molecules that damage DNA selectively offer new prospects for controlled manipulation of DNA. The conjugations of DNA-code reading molecules such as polyamides to reagents that induce DNA damages provide an approach to reach this goal. In this work, a new compound which contained polyamide and ascorbic acid conjugated by flexi Read More
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Novel Biotransformation Process of Podophyllotoxin to 4 -Sulfur-Substituted Podophyllum Derivates with Anti-Tumor Activity by Penicillium purpurogenum Y.J. Tang
Authors: J.-K. Bai, W. Zhao, H.-M. Li and Y.-J. TangAccording to the structure-function relationship of podophyllotoxin (PTOX) and its analogue of 4'- demethylepipodophyllotoxin (DMEP), the 4 β-substitution of sulfur-containing heterocyclic compounds with a carbon-sulfur bond at 4 position of PTOX or DMEP is an essential modification direction for improving the anti-tumor activity. So, four novel 4 β-sulfursubstituted podophyllum derivatives (i.e., 4β -(1,2,4-triazole-3-yl)s Read More
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Volumes & issues
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Volume 32 (2025)
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Volume 31 (2024)
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Volume 30 (2023)
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Volume 29 (2022)
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Volume 28 (2021)
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Volume 27 (2020)
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Volume 26 (2019)
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Volume 25 (2018)
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Volume 24 (2017)
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Volume 23 (2016)
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Volume 22 (2015)
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Volume 21 (2014)
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Volume 20 (2013)
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Volume 19 (2012)
- Issue 36
- Issue 35
- Issue 34
- Issue 33
- Issue 32
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- Issue 12
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- Issue 10
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- Issue 7
- Issue 6
- Issue 5
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- Issue 3
- Issue 2
- Issue 1
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Volume 18 (2011)
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Volume 17 (2010)
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Volume 16 (2009)
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Volume 15 (2008)
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Volume 14 (2007)
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Volume 13 (2006)
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Volume 12 (2005)
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Volume 11 (2004)
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Volume 10 (2003)
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Volume 9 (2002)
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Volume 8 (2001)
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Volume 7 (2000)
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