A2A receptor ligands: past, present and future trends.

Abstract:

:The adenosine A(2A) receptor is a member of the G protein-coupled receptor family and mediates multiple physiological effects of adenosine, both at the central nervous system and at peripheral tissues. Increasing evidence relates the A(2A) receptor with several pathological conditions such as neurodegenerative disorders, inflammation, pharmacological stress, and wound healing renewing the interest in A(2A) receptor agonists and antagonists as promising leads for drugs. However some of them initially tested in clinical trials presented several side effects, short half-life, lower solubility, and in some cases a lack of effects, perhaps attributable to receptor desensitization or to low receptor density in the targeted tissue. For these reasons it is evident that additional rational chemical modifications of the existing A(2A) receptor ligands to improve their affinity/selectivity and bioavailability as well as further studies to get new template for A(2A)AR ligands are necessary. The purpose of this review is to analyze and summarize the past and the present aspects related to the medicinal chemistry of A(2A) receptor ligands. Moreover their current and possible therapeutic applications have been also highlighted.

journal_name

Curr Top Med Chem

authors

Clementina M,Giuseppe S

doi

10.2174/156802610791268765

subject

Has Abstract

pub_date

2010-01-01 00:00:00

pages

902-22

issue

9

eissn

1568-0266

issn

1873-4294

pii

BSP/ CTMC /E-Pub/-0054-10-9

journal_volume

10

pub_type

杂志文章,评审
  • Computational Study of Nanosized Drug Delivery from Cyclodextrins, Crown Ethers and Hyaluronan in Pharmaceutical Formulations.

    abstract::The problem in this work is the computational characterization of cyclodextrins, crown ethers and hyaluronan (HA) as hosts of inclusion complexes for nanosized drug delivery vehicles in pharmaceutical formulations. The difficulty is addressed through a computational study of some thermodynamic, geometric and topologic...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026615666150506145619

    authors: Torrens F,Castellano G

    更新日期:2015-01-01 00:00:00

  • (6-bromo-1,4-dimethyl-9H-carbazol-3-yl-methylene)-hydrazine (carbhydraz) acts as a GPER agonist in breast cancer cells.

    abstract::Estrogens control a wide number of aspects of human physiology and play a key role in multiple diseases, including cancer. Estrogens act by binding to and activating the cognate receptor (ER), however numerous studies have revealed that the G protein-coupled receptor named GPR30/GPER mediates also estrogen signals. As...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026615666150317221549

    authors: Sinicropi MS,Lappano R,Caruso A,Santolla MF,Pisano A,Rosano C,Capasso A,Panno A,Lancelot JC,Rault S,Saturnino C,Maggiolini M

    更新日期:2015-01-01 00:00:00

  • Ascidians: An Emerging Marine Model for Drug Discovery and Screening.

    abstract::Ascidians (tunicates; sea squirts) are marine animals which provide a source of diverse, bioactive natural products, and a model for toxicity screenings. Compounds isolated from ascidians comprise an approved anti-tumor drug and many others are potent drug leads. Furthermore, the use of invertebrate embryos for toxico...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026617666170130104922

    authors: Dumollard R,Gazo I,Gomes IDL,Besnardeau L,McDougall A

    更新日期:2017-01-01 00:00:00

  • Connecting small molecules to nuclear receptor pathways.

    abstract::Many efforts are currently being made to connect small molecules to target proteins by extracting pharmacological data from bibliographic sources and storing them in annotated chemical libraries. Here, small molecules are further connected to biological pathways, with particular focus to pathways involving members of ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/156802607782194671

    authors: Hettne K,Cases M,Boyer S,Mestres J

    更新日期:2007-01-01 00:00:00

  • Protective effect of schizolobium parahyba flavonoids against snake venoms and isolated toxins.

    abstract::Four compounds (isoquercitrin, myricetin-3-O-glucoside, catechin and gallocatechin) were isolated from lyophilized aqueous extract of Schizolobium parahyba leaves by chromatography on Sephadex LH-20, followed by semipreparative HPLC using a C-18 column, and identified by 1H and 13C NMR. The compounds were then, tested...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/156802611797633438

    authors: F Vale LH,Mendes MM,Fernandes RS,Costa TR,S Hage-Melim LI,A Sousa M,Hamaguchi A,Homsi-Brandeburgo MI,Franca SC,Silva CH,Pereira PS,Soares AM,Rodrigues VM

    更新日期:2011-01-01 00:00:00

  • Quinoline-based compounds with potential activity against drug-resistant cancers.

    abstract::Drug resistance is the major cause of the failure of cancer chemotherapy, so one of the most important features in developing effective cancer therapeutic strategies is to overcome drug resistance. Quinoline moiety has become one of the most privileged structural motifs in anticancer agent discovery since its derivati...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026620666200618113957

    authors: Li HT,Zhu X

    更新日期:2020-06-18 00:00:00

  • Engineering "Antimicrobial Peptides" and Other Peptides to Modulate Protein-Protein Interactions in Cancer.

    abstract::Antimicrobial peptides (AMPs) are a class of peptides found across a wide array of organisms that play key roles in host defense. AMPs induce selective death in target cells and orchestrate specific or nonspecific immune responses. Many AMPs exhibit native anticancer activity in addition to antibacterial activity, and...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026620666201021141401

    authors: Rubin SJS,Qvit N

    更新日期:2020-01-01 00:00:00

  • On the structural basis of the hypertensive properties of angiotensin II: a solved mystery or a controversial issue?

    abstract::Angiotensin II (AII), Asp1-Arg2-Val3-Tyr4-Ile5-His6-Pro7-Phe8, the primary active hormone of the Renin-Angiotensin-System (RAS), is a major vasoconstrictor implicated in the cause of hypertension. To unravel the question of the biologically active conformation(s) of this flexible peptide hormone and to better understa...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026043451375

    authors: Tzakos AG,Gerothanassis IP,Troganis AN

    更新日期:2004-01-01 00:00:00

  • Multi-potent Natural Scaffolds Targeting Amyloid Cascade: In Search of Alzheimer's Disease Therapeutics.

    abstract::Alzheimer's Disease (AD) once considered a rare disorder emerges as a major health concern in recent times. The disease pathogenesis is very complex and yet to be understood completely. However, "Amyloid Cascade" is the central event in disease pathogenesis. Several proteins of the amyloid cascade are currently being ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026618666180116122921

    authors: Chakraborty S

    更新日期:2017-01-01 00:00:00

  • Clinical application of ropivacaine for the upper extremity.

    abstract::Ropivacaine, the S-(-)-enantiomer of N-(2,6-dimethylphenyl)-1-propyl-2-piperidinecarboxamide is a new long-acting local anesthetic. This review demonstrates that it is effective in brachial plexus anesthesia. It is at least as efficient as bupivacaine in terms of quality, duration of analgesia, anesthesia, and motor b...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026013395326

    authors: Singelyn FJ

    更新日期:2001-08-01 00:00:00

  • The histamine H₃ receptor as a therapeutic drug target for metabolic disorders: status, challenges and opportunities.

    abstract::Since the histamine-3 receptor (H₃R) was cloned in 1999, huge efforts have been made by most of the key players in the pharmaceutical industry as well as in smaller biotech companies to increase the knowledge on this peculiar receptor, with the ultimate goal of bringing new drugs to the market. This review gives a sur...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802611795860906

    authors: Plancher JM

    更新日期:2011-01-01 00:00:00

  • Aminoquinoline melanin-concentrating hormone 1-receptor (MCH1-R) antagonists.

    abstract::Structure-activity relationships of a 4-aminoquinoline MCH-1R antagonist lead series were explored by synthesis of analogs with modifications at the 2-, 4- and 6-positions of the original HTS hit. Improvements to the original screening lead were made by addition of lipophilic groups at the 2-position and biphenyl, cyc...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802607782194789

    authors: DeVita RJ

    更新日期:2007-01-01 00:00:00

  • Modulators of protein-protein interactions: novel approaches in targeting protein kinases and other pharmaceutically relevant biomolecules.

    abstract::In recent years the development of small organic molecules modulating protein-protein interactions (P-PIs) has drawn major attention in both academic and industrial research. Despite the appreciable progress being made, targeting such extensive interaction areas with comparatively small, drug-like agents has proven to...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802611795589610

    authors: Rechfeld F,Gruber P,Hofmann J,Kirchmair J

    更新日期:2011-01-01 00:00:00

  • Isoindole Derivatives: Propitious Anticancer Structural Motifs.

    abstract::Isoindole derivatives constitute an important class of biologically active heterocyclic compounds and continue to attract considerable attention due to their diverse pharmacological profile such as, antimicrobial, anthelmintic, insecticidal, cyclooxygenase isoenzyme (COX-2) and thrombin inhibition with special emphasi...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026616666160530154100

    authors: Bhatia RK

    更新日期:2017-01-01 00:00:00

  • QSAR in the pharmaceutical research setting: QSAR models for broad, large problems.

    abstract::The field of quantitative structure activity relationships (QSAR) has evolved into an integral tool for pharmaceutical discovery. It is presently an accessible technology, as can be shown by the number papers which are easily found through PubMed literature searches. At one level, QSAR is used routinely and invisibly ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802610791111506

    authors: Sprous DG,Palmer RK,Swanson JT,Lawless M

    更新日期:2010-01-01 00:00:00

  • Peptidomimetic inhibitors of HIV protease.

    abstract::There are currently (July, 2002) six protease inhibitors approved for the treatment of HIV infection, each of which can be classified as peptidomimetic in structure. These agents, when used in combination with other antiretroviral agents, produce a sustained decrease in viral load, often to levels below the limits of ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026043388330

    authors: Randolph JT,DeGoey DA

    更新日期:2004-01-01 00:00:00

  • Novel HIV-1 Integrase Inhibitor Development by Virtual Screening Based on QSAR Models.

    abstract::HIV-1 integrase (IN) plays an important role in the life cycle of HIV and is responsible for integration of the virus into the human genome. We present computational approaches used to design novel HIV-1 IN inhibitors. We created an IN inhibitor database by collecting experimental data from the literature. We develope...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026615666150813150433

    authors: Guasch L,Zakharov AV,Tarasova OA,Poroikov VV,Liao C,Nicklaus MC

    更新日期:2016-01-01 00:00:00

  • PNP anticancer gene therapy.

    abstract::Escherichia coli purine nucleoside phosphorylase (PNP) catalyzes the cleavage of 9-(2-deoxy-beta-D-ribofuranosyl)-6-methylpurine (MeP-dR), while human PNP does not. MeP-dR is well tolerated while the cleavage product, 6-methylpurine (MeP), is highly cytotoxic. This clinical profile suggests an anticancer gene therapy ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802605774463105

    authors: Zhang Y,Parker WB,Sorscher EJ,Ealick SE

    更新日期:2005-01-01 00:00:00

  • Glutamatergic neurotransmission as molecular target of new anticonvulsants.

    abstract::Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system (CNS) controlling physiological processes as learning and memory. However, the overactivation of glutamatergic neurotransmission is often related to various CNS chronic and acute diseases (epilepsy, ischaemia, Parkinson, etc.). ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802612800229242

    authors: Gitto R,De Luca L,De Grazia S,Chimirri A

    更新日期:2012-01-01 00:00:00

  • Coumarins as Promising Scaffold for the Treatment of Age-related Diseases - An Overview of the Last Five Years.

    abstract::Degenerative diseases are becoming more common with increasing life expectancy of the human population. The 20th century faced a progressive demographic change in the industrialized world, followed by identical trends in population aging in Asia, Africa, and Middle and South America. A significant increase in chronic ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026618666171215094029

    authors: Delogu GL,Matos MJ

    更新日期:2017-01-01 00:00:00

  • New Drugs and Therapeutic/Diagnostic Targets for Fungal and Parasitic Diseases - Part I.

    abstract:: ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 社论

    doi:10.2174/156802661815181101110430

    authors: Dea-Ayuela MA,Serrano DR

    更新日期:2018-01-01 00:00:00

  • The chemistry of transition metals in relation to their potential role in neurodegenerative processes.

    abstract::Cells rely on several transition metals to regulate a wide range of metabolic and signaling functions. The diversity and efficiency of their physiological functions are derived from atomic properties that are specific to transition metals, most notably an incomplete inner valence subshell. These properties impart upon...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026013394796

    authors: Hamai D,Bondy SC,Becaria A,Campbell A

    更新日期:2001-12-01 00:00:00

  • Synthetic and natural products as iron chelators.

    abstract::An evaluation of existing and proposed Fe chelators, both synthetic and natural products, for the treatment of Fe-overload disease must address a number of issues. There are fundamental parameters that determine the efficacy of a drug: absorption, distribution, metabolism, clearance and toxicity. However, the administ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802611794785163

    authors: Sharpe PC,Richardson DR,Kalinowski DS,Bernhardt PV

    更新日期:2011-01-01 00:00:00

  • Antibacterial Activity of Cissus incisa Extracts against Multidrug- Resistant Bacteria.

    abstract:AIMS:The need to find new antimicrobial agents to cope with this phenomenon increases. BACKGROUND:Infection diseases are illness caused by different microorganisms, such as bacteria, among those caused by resistant bacteria are associated with greater morbidity, mortality and cost of the treatment than those caused by...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026619666191121123926

    authors: Nocedo-Mena D,Garza-González E,González-Ferrara M,Del Rayo Camacho-Corona M

    更新日期:2020-01-01 00:00:00

  • Telomere-related Markers for Cancer.

    abstract::Telomeres are structurally nucleoprotein complexes at termini of linear chromosomes and essential to chromosome stability/integrity. In normal human cells, telomere length erodes progressively with each round of cell divisions, which serves as an important barrier to uncontrolled proliferation and malignant transforma...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026620666200106145340

    authors: Yuan X,Dai M,Xu D

    更新日期:2020-01-01 00:00:00

  • Immunophilins and coupled gating of ryanodine receptors.

    abstract::The ryanodine receptor (RyR) is the major calcium (Ca(2+)) release channel in the sarcoplasmic reticulum (SR) of skeletal and cardiac muscle and is required for excitation-contraction (EC) coupling. The 565 kDa RyR protein forms a tetrameric channel that is part of a macromolecular signaling complex that also includes...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026033451907

    authors: Lehnart SE,Huang F,Marx SO,Marks AR

    更新日期:2003-01-01 00:00:00

  • Farnesyl protein transferase inhibitor ZARNESTRA R115777 - history of a discovery.

    abstract::R115777 (R)-6-amino[(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone is a potent and selective inhibitor of farnesyl protein transferase with significant antitumor effects in vivo subsequent to oral administration in mice. Taking its roots into Janssen's ketoconazole and...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026033452050

    authors: Venet M,End D,Angibaud P

    更新日期:2003-01-01 00:00:00

  • Trypanocidal activity of nitroaromatic prodrugs: current treatments and future perspectives.

    abstract::Chagas disease and African sleeping sickness are trypanosomal infections that represent important public health problems in Latin America and Africa, respectively. The restriction of these diseases to the poorer parts of the world has meant that they have been largely neglected and limited progress has been made in th...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802611796575894

    authors: Wilkinson SR,Bot C,Kelly JM,Hall BS

    更新日期:2011-01-01 00:00:00

  • Template dependent human DNA polymerases.

    abstract::The genetic material in humans contains approximately 6 billion base pairs in the nuclear genome and 16,569 base pairs in the mitochondrial genome [1-3]. In some cases the difference between a healthy and a sick individual consists in only one nucleotide. Thus, it is evident that the pristine replication of the genome...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802608786141098

    authors: Brieba LG

    更新日期:2008-01-01 00:00:00

  • A survey of quantitative descriptions of molecular structure.

    abstract::Numerical characterization of molecular structure is a first step in many computational analysis of chemical structure data. These numerical representations, termed descriptors, come in many forms, ranging from simple atom counts and invariants of the molecular graph to distribution of properties, such as charge, acro...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/156802612804910278

    authors: Guha R,Willighagen E

    更新日期:2012-01-01 00:00:00