Rational understanding of nicotinic receptors drug binding.

Abstract:

:The atomic determination of the acetylcholine binding protein (AChBP), a molluscan cholinergic protein, homologous to the amino-terminal extracellular domain of nicotinic receptors (nAChRs), offers opportunities for the modeling of the acetylcholine binding site and its ligands. Recently, we constructed three-dimensional models of the N-terminal part of nAChR and docked in the putative ligand-binding pocket, different agonists (acetylcholine, nicotine and epibatidine) and antagonist (snake alpha-bungarotoxin). These hypothetical docking models offer a structural basis for rational design of drugs differentially binding to resting and active (or desensitized) conformations of the receptor site. These models thus pave the way to investigate, at the molecular level, the exciting challenge of the fast ion channel gating mechanisms by nicotinic agonists.

journal_name

Curr Top Med Chem

authors

Grutter T,Le Novère N,Changeux JP

doi

10.2174/1568026043451177

keywords:

subject

Has Abstract

pub_date

2004-01-01 00:00:00

pages

645-50

issue

6

eissn

1568-0266

issn

1873-4294

journal_volume

4

pub_type

杂志文章,评审
  • (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

  • Inhibition of BACE, a promising approach to Alzheimer's disease therapy.

    abstract::The first proteolytic step in the processing of amyloid precursor protein (APP) to amyloid-beta (Abeta) in the brain is performed by beta-site APP cleaving enzyme (BACE1). This enzyme is a membrane bound aspartic protease with high homology of the catalytic domain to renin and pepsin and of yet unknown physiologic fun...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026024607490

    authors: Roggo S

    更新日期:2002-04-01 00:00:00

  • Identification of high affinity bioactive Salbutamol conformer directed against mutated (Thr164Ile) beta 2 adrenergic receptor.

    abstract::Salbutamol forms an important and widely administered β2 agonist prescribed in the symptomatic treatment of bronchial asthma. Unfortunately, a subset of patients show refractoriness to it owing to ADRB2 gene variant (rs 1800888). The variant substitutes Thr to Ile at the position 164 in the β2 adrenergic receptor lead...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026615666150112113040

    authors: Bandaru S,Tiwari G,Akka J,Marri VK,Alvala M,Gutlapalli VR,Nayarisseri A,Mundluru HP

    更新日期:2015-01-01 00:00:00

  • Linking Biosynthetic Gene Clusters to their Metabolites via Pathway- Targeted Molecular Networking.

    abstract::The connection of microbial biosynthetic gene clusters to the small molecule metabolites they encode is central to the discovery and characterization of new metabolic pathways with ecological and pharmacological potential. With increasing microbial genome sequence information being deposited into publicly available da...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026616666151012111046

    authors: Trautman EP,Crawford JM

    更新日期:2016-01-01 00:00:00

  • Discovery and clinical development of dutasteride, a potent dual 5alpha-reductase inhibitor.

    abstract::In this review the preclinical medicinal chemistry, biochemistry and clinical results achieved in the treatment of prostatic disease with dutasteride, a dual inhibitor of type 1 and type 2,5alpha-reductase are described. During the discovery phase, dutasteride was optimized to inhibit both forms of human 5 alpha-reduc...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802606776743101

    authors: Frye SV

    更新日期:2006-01-01 00:00:00

  • Biochemical and structural investigations on kynurenine aminotransferase II: an example of conformation-driven species-specific inhibition?

    abstract::Kynurenic acid (KYNA), one of the metabolites belonging to the kynurenine pathway, has been described as an important neuroprotective compound, its unbalancing being associated with several pathological conditions. In human brain, the majority of KYNA production is sustained by kynurenine aminotransferase II (KAT II)....

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/156802611794863599

    authors: Casazza V,Rossi F,Rizzi M

    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

  • NAADP signaling revisited.

    abstract::Nicotinic acid adenine dinucleotide phosphate (NAADP) is the most potent Ca²⁺ mobilizing endogenous compound known to date. Although its Ca²⁺ releasing activity has been demonstrated in many cell types and in response to different extracellular stimuli, several aspects of NAADP signaling are unclear. This overview foc...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/15680266113136660212

    authors: Guse AH,Ernst IM,Fliegert R

    更新日期:2013-01-01 00:00:00

  • Biological Activities of Artemisinin Derivatives Beyond Malaria.

    abstract::Artemisinin is isolated from Artemisia annua L. with peroxide-containing sesquiterpene lactone structure. Because of its unique structural characteristics and promising anticancer, antivirus activities, it has recently received increasing attention. The aim of this review is to summarize recent discoveries of artemisi...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026619666190122144217

    authors: Liu X,Cao J,Huang G,Zhao Q,Shen J

    更新日期:2019-01-01 00:00:00

  • Surface chemistry influences implant biocompatibility.

    abstract::Implantable medical devices are increasingly important in the practice of modern medicine. Unfortunately, almost all medical devices suffer to a different extent from adverse reactions, including inflammation, fibrosis, thrombosis and infection. To improve the safety and function of many types of medical implants, a m...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802608783790901

    authors: Thevenot P,Hu W,Tang L

    更新日期:2008-01-01 00:00:00

  • NMR structural studies of human cellular prion proteins.

    abstract::Prion diseases or transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative disorders associated with the conformational conversion of the cellular prion protein, PrP(C), into a pathological form known as prion or PrP(Sc). They can be classified into sporadic, inherited and infectious forms. Spontan...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/15680266113136660169

    authors: Biljan I,Ilc G,Giachin G,Legname G,Plavec J

    更新日期:2013-01-01 00:00:00

  • Coumarin Compounds in Medicinal Chemistry: Some Important Examples from the Last Years.

    abstract::Coumarins are natural products characterized as 1,2 benzopyrones widely distributed in plants, as well as, in many species of fungi and bacteria. Nowadays, many synthetic procedures allow the discovery of coumarins with expanded chemical space. The ability to exert noncovalent interactions with many enzymes and recept...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026618666180329115523

    authors: Pereira TM,Franco DP,Vitorio F,Kummerle AE

    更新日期:2018-01-01 00:00:00

  • Nanophytomedicine Based Novel Therapeutic Strategies in Liver Cancer.

    abstract::Liver cancer is the fifth (6.3% of all cancers i.e., 548,000 cases/year) and ninth (2.8% of all cancers i.e., 244,000 cases/year) most prevalent cancer worldwide in men and women, respectively. Although multiple choices of therapies are offered for Hepatocellular Carcinoma (HCC) like liver resection or transplant, rad...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026619666191114113048

    authors: Kumar S,Fayaz F,Pottoo FH,Bajaj S,Manchanda S,Bansal H

    更新日期:2020-01-01 00:00:00

  • Ubiquitination in Rho signaling.

    abstract::The Rho family small GTPases of the Ras superfamily play key roles in regulating diverse signaling pathways that control a myriad of fundamental cellular processes such as cytoskeletal dynamics, cell cycle progression, gene expression, cell polarity, migration and cell transformation. The Rho GTPases cycle between an ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802611798281357

    authors: Ding F,Yin Z,Wang HR

    更新日期:2011-12-01 00:00:00

  • Collaborative development of 2-hydroxypropyl-β-cyclodextrin for the treatment of Niemann-Pick type C1 disease.

    abstract::In 2010, the National Institutes of Health (NIH) established the Therapeutics for Rare and Neglected Diseases (TRND) program within the National Center for Advancing Translational Sciences (NCATS), which was created to stimulate drug discovery and development for rare and neglected tropical diseases through a collabor...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026613666131127160118

    authors: Ottinger EA,Kao ML,Carrillo-Carrasco N,Yanjanin N,Shankar RK,Janssen M,Brewster M,Scott I,Xu X,Cradock J,Terse P,Dehdashti SJ,Marugan J,Zheng W,Portilla L,Hubbs A,Pavan WJ,Heiss J,Vite CH,Walkley SU,Ory DS,Silbe

    更新日期:2014-01-01 00:00:00

  • Dopamine transporter ligands: recent developments and therapeutic potential.

    abstract::The dopamine transporter (DAT) is a target for the development of pharmacotherapies for a number of central disorders including Parkinson's disease, Alzheimer's disease, schizophrenia, Tourette's syndrome, Lesch-Nyhan disease, attention deficit hyperactivity disorder (ADHD), obesity, depression, and stimulant abuse as...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802606778249775

    authors: Runyon SP,Carroll FI

    更新日期:2006-01-01 00:00:00

  • Stages of HIV replication and targets for therapeutic intervention.

    abstract::The replication cycle of human immunodeficiency virus (HIV) is divided into an early and a late phase. Most of the steps of the cycle have been targeted in antiviral therapy, although the drugs currently available for clinical use are only effective against two replication enzymes of the virus, either against the reve...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026033451781

    authors: Tözsér J

    更新日期:2003-01-01 00:00:00

  • Dipeptide inhibitors of thermolysin and angiotensin I-converting enzyme.

    abstract::Thermolysin (TLN) and other thermolysin-like zinc metalloproteinases (TLPs),are important virulence factors for pathogenesis of bacterial infections by suppressing the innate immune system of the host. Therapeutic inhibition ofTLPs is believed to be a novel strategy inthe development of a new generation antibiotics.In...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/156802612803989246

    authors: Khan MT,Dedachi K,Matsui T,Kurita N,Borgatti M,Gambari R,Sylte I

    更新日期:2012-01-01 00:00:00

  • Selective inhibitors of inducible nitric oxide synthase: potential agents for the treatment of inflammatory diseases?

    abstract::Nitric Oxide (NO) is widely recognized as an important messenger and effector molecule in a variety of biological systems. There is strong evidence from animal models that elevated or lowered NO levels are associated with a variety of pathological states. In nature, NO is synthesised from the amino acid l-arginine by ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802606775270297

    authors: Tinker AC,Wallace AV

    更新日期:2006-01-01 00:00:00

  • Biosensors for Screening Kinase Inhibitors.

    abstract::For successful drug discovery it is important to understand the fundamentals of the underlying causes and consequences of the diseases for which the drug is being developed. One such physiological process in eukaryotic cells is protein phosphorylation, which is the main post-translational modification of proteins resp...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026617666170531113233

    authors: Bhalla N,Estrela P

    更新日期:2017-01-01 00:00:00

  • Artificial hematopoietic stem cell niche: bioscaffolds to microfluidics to mathematical simulations.

    abstract::Due to the recent advancements in stem cell biology and engineering, scientists have been increasingly interested in creating in vitro niches for embryonic and adult stem cells, and, following induction and differentiation with the appropriate media, the production of large scale blood production. This artificially cr...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802611796117568

    authors: Didwania M,Didwania A,Mehta G,Basak GW,Yasukawa S,Takayama S,de Necochea-Campion R,Srivastava A,Carrier E

    更新日期:2011-01-01 00:00:00

  • Structure-based Virtual Screening Approaches in Kinase-directed Drug Discovery.

    abstract::Protein kinases are one of the most targeted protein families in current drug discovery pipelines. They are implicated in many oncological, inflammatory, CNS-related and other clinical indications. Virtual screening is a computational technique with a diverse set of available tools that has been shown many times to pr...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026617666170224121313

    authors: Bajusz D,Ferenczy GG,Keseru GM

    更新日期:2017-01-01 00:00:00

  • Genetic variability of matrix metalloproteinase genes in cardiovascular disease.

    abstract::It is well established that matrix metalloproteinases (MMPs) contribute to the degradation of the extracellular matrix of coronary plaque and contribute to the thinning of the fibrous cap. As a result, the atheromatous plaque becomes unstable and prone to rupture with consequent clinical manifestations including acute...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026611208011206

    authors: Papageorgiou N,Tousoulis D,Hatzis G,Briasoulis A,Androulakis E,Giolis A,Siasos G,Latsios G,Vogiatzi G,Tentolouris C,Stefanadis C

    更新日期:2012-01-01 00:00:00

  • Analysis of DNA microarray data.

    abstract::Recent advances in DNA microarray technology have great impact on many areas of biomedical research and pharmacogenomics: discovering novel targets and genes, elucidating signatures of complex diseases, transcriptional profiling of models for diseases, and the development of individually optimized drugs based on diffe...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026043387773

    authors: Hackl H,Sanchez Cabo F,Sturn A,Wolkenhauer O,Trajanoski Z

    更新日期:2004-01-01 00:00:00

  • Can selective ligands for glutamate binding proteins be rationally designed?

    abstract::A major neurotransmitter, L-Glutamate must be stored, transported and received, and these processes are mediated by proteins that bind this simple yet essential amino acid. Detailed evidence continues to emerge on the structure of Glu binding proteins, which includes both receptors and transporters. It appears that re...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802606777057535

    authors: Natale NR,Magnusson KR,Nelson JK

    更新日期:2006-01-01 00:00:00

  • Drug-likeness and increased hydrophobicity of commercially available compound libraries for drug screening.

    abstract::Most drug discovery programs today originate by selection of 'hit' molecules resulting from assays against large compound screening libraries. The chemical space in which these hits reside has implications for its biological activity in vivo and likelihood of progression to a drug candidate. We have created a database...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802612802652466

    authors: Zuegg J,Cooper MA

    更新日期:2012-01-01 00:00:00

  • Antioxidative Effects of Rhodiola Genus: Phytochemistry and Pharmacological Mechanisms against the Diseases.

    abstract::Rhodiola as one of traditional medicines has been used for clinical treatments due to its strong antioxidant properties. Phytochemical analysis revealed the presence of flavonoids, phenylpropanoids, phenylethanol/benzyl alcohol derivatives, cyanogenic glycosides and terpenoids. The bioactive compounds had been demonst...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/1568026617666161116141334

    authors: Li Y,Wu J,Shi R,Li N,Xu Z,Sun M

    更新日期:2017-01-01 00:00:00

  • Synthesis and Antifungal Activity of Coumarins Derivatives Against Sporothrix spp.

    abstract::Sporotrichosis is a serious public health problem in Brazil that affects human patients and domestic animals, mainly cats. Thus, the search for new antifungal agents is required also due to the emergence and to the lack of effective drugs available in the therapeutic arsenal. The aim of this study was to evaluate the ...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026618666180221115508

    authors: da S M Forezi L,Borba-Santos LP,Cardoso MFC,Ferreira VF,Rozental S,de C da Silva F

    更新日期:2018-01-01 00:00:00

  • Cyclo-oxygenase (COX) inhibiting nitric oxide donating (CINODs) drugs: a review of their current status.

    abstract::Non-steroidal anti-inflammatory drugs (NSAIDs) are widely used drugs but their use is hampered by gastrointestinal side effects. Cyclo-oxygenase Inhibitor Nitric Oxide Donors (CINODs) are a new class of anti-inflammatory and analgesic drugs generated by adding a nitric oxide generating moiety to the parent NSAID via a...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章,评审

    doi:10.2174/156802607779941350

    authors: Stefano F,Distrutti E

    更新日期:2007-01-01 00:00:00

  • On the Possible Relevance of Bottom-up Pathways in the Pathogenesis of Alzheimer's Disease.

    abstract::Dementia is an increasing health problem in older aged populations worldwide. Age-related changes in the brain can be observed decades before the first symptoms of cognitive decline appear. Cognitive impairment has chronic inflammatory components, which can be enhanced by systemic immune activation. There exist mutual...

    journal_title:Current topics in medicinal chemistry

    pub_type: 杂志文章

    doi:10.2174/1568026620666200514090359

    authors: Leblhuber F,Steiner K,Geisler S,Fuchs D,Gostner JM

    更新日期:2020-01-01 00:00:00