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1. Anticholinesterase pesticides
: metabolism, neurotoxicity, and epidemiology
by Satoh, Tetsuo, Ph. D and Gupta, Ramesh C
2010, 1. Aufl., ISBN 9780470410301, xviii, 625
"This book offers an important reference source about the most common classes of pesticides for researchers engaged in the area of neurotoxicology, metabolism,... 
Cholinesterase-inhibiting insecticides | Toxicology | Chemistry | SCIENCE | Industrial & Technical
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2. Pseudocholinesterasen
: Pharmakogenetik, Biochemie, Klinik [von] H.W. Goedde, A. Doenicke [und] K. Altland
by Goedde, H. W. (H. Werner) and Altland, Klaus and Doenicke, Alfred
1967, 271
Cholinesterase
Book
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3. Anticholinesterase agents
by Karxzmar, A. G and Usdin, Earl and Wills, James Henry
1970, 1st ed., International encyclopedia of pharmacology and therapeutics, ISBN 008006633X, Volume section 13., v.
Cholinestérase, Inhibiteurs de | Cholinesterase inhibitors
Book
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4. Human cholinesterases and anticholinesterases
by Soreq, H and Zakut, Haim, 1935
1993, ISBN 9780126552904, xiv, 314
Cholinesterase genes | Cholinergic mechanisms | Cholinesterase Inhibitors | Cholinesterases | physiology | Cellular signal transduction | metabolism
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5. Novel functions of cholinesterases in development, physiology and disease
by Layer, Paul G and Willbold, Elmar
1995, Progress in histochemistry and cytochemistry, ISBN 9783437116285, Volume 29, no. 3., vi, 94
Book
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6. Cholinesterases
: structure, function, mechanism, genetics, and cell biology
by Massoulié, Jean and American Chemical Society
1991, Conference proceedings series., ISBN 9780841220089, xviii, 414
Cholinesterase genes | Congresses | Cholinesterase inhibitors | Cholinesterases
Book
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7. Toxicology of organophosphate and carbamate compounds
by Gupta, Ramesh C. 1949- (Ramesh Chandra)
2006, ISBN 9780120885237, xvi, 763
This text/reference book provides the most comprehensive coverage of anticholinesterase compounds (Organophosphates and Carbamates), which constitute the... 
Carbamates | Insecticides | Toxicology | Organophosphorus compounds | Cholinesterase inhibitors | Pesticides | Biology, life sciences
Book
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8. Full Text Crystal structures of human cholinesterases in complex with huprine W and tacrine: Elements of specificity for anti-Alzheimer's drugs targeting acetyl- and butyryl-cholinesterase
by Nachon, Florian and Carletti, Eugénie and Ronco, Cyril and Trovaslet, Marie and Nicolet, Yvain and Jean, Ludovic and Renard, Pierre-Yves
Biochemical Journal, ISSN 0264-6021, 08/2013, Volume 453, Issue 3, pp. 393 - 399
The multifunctional nature of Alzheimer's disease calls for MTDLs (multitarget-directed ligands) to act on different components of the pathology, like the... 
Huprine | Inhibitor | Acetylcholinesterase | Butyrylcholinesterase | Alzheimer's disease | X-ray structure | Tacrine | CRYSTALLIZATION | butyrylcholinesterase | tacrine | BIOCHEMISTRY & MOLECULAR BIOLOGY | ACTIVE-SITE GORGE | acetylcholinesterase | HUMAN BUTYRYLCHOLINESTERASE | INHIBITION | inhibitor | DROSOPHILA-MELANOGASTER ACETYLCHOLINESTERASE | SUBSTRATE | PURIFICATION | DERIVATIVES | EXPRESSION | huprine | INSIGHTS | Humans | Cholinesterase Inhibitors - chemistry | Acetylcholinesterase - chemistry | Alzheimer Disease - enzymology | Crystallography, X-Ray - methods | Butyrylcholinesterase - chemistry | Cholinesterase Inhibitors - pharmacology | Cholinesterases - chemistry | Butyrylcholinesterase - metabolism | Aminoquinolines - chemistry | Cholinesterases - metabolism | Cholinesterases - pharmacology | Aminoquinolines - pharmacology | Acetylcholinesterase - metabolism | Tacrine - chemistry | Index Medicus | Organic chemistry | Chemical Sciences
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9. Full Text Cholinesterases, a target of pharmacology and toxicology
by Pohanka, Miroslav
Biomedical Papers, ISSN 1213-8118, 2011, Volume 155, Issue 3, pp. 219 - 230
Background. Cholinesterases are a group of serine hydrolases that split the neurotransmitter acetylcholine (ACh) and terminate its action. Of the two types,... 
Myasthenia gravis | Galantamine | Rivastigmine | Donepezil | Acetylcholinesterase | Butyrylcholinesterase | Alzheimer's disease | Huperzine | BUTYRYLCHOLINESTERASE KNOCKOUT MOUSE | MEDICINE, RESEARCH & EXPERIMENTAL | ALZHEIMERS-DISEASE | LONG-TERM EXPOSURE | MOLECULAR-FORMS | 3-DIMENSIONAL STRUCTURE | IN-VITRO | PERIPHERAL ANIONIC SITE | CAPILLARY-ELECTROPHORESIS | SERUM BUTYRYLCHOLINESTERASE | TORPEDO-CALIFORNICA ACETYLCHOLINESTERASE | Alzheimer Disease - physiopathology | Butyrylcholinesterase - physiology | Synaptic Transmission - physiology | Humans | Cholinesterase Inhibitors - chemistry | Cholinesterases - physiology | Chemical Warfare Agents - poisoning | Animals | Acetylcholinesterase - physiology | Cholinesterase Inhibitors - pharmacology | Cholinesterases - chemistry | Cholinesterase Inhibitors - poisoning | Chemical Warfare Agents - pharmacology | Cholinesterases - pharmacology
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10. The biology of cholinesterases
by Silver, Ann
1974, ISBN 0444106529, Volume 36., xiv, 596
Cholinesterases
Book
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11. Comparative enzymology of cholinesterases
by Moralev, Serge N
2007, ISBN 0972077421, xxviii, 484
Book
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12. Full Text A comprehensive evaluation of the efficacy of leading oxime therapies in guinea pigs exposed to organophosphorus chemical warfare agents or pesticides
by Wilhelm, Christina M and Snider, Thomas H and Babin, Michael C and Jett, David A and Platoff, Gennady E and Yeung, David T
Toxicology and Applied Pharmacology, ISSN 0041-008X, 12/2014, Volume 281, Issue 3, pp. 254 - 265
The currently fielded pre-hospital therapeutic regimen for the treatment of organophosphorus (OP) poisoning in the United States (U.S.) is the administration... 
Oxime | Efficacy | Guinea pig | Intramuscular | Toxicity | HYDROXAMIC ACIDS | PYRIDINIUM OXIMES | SOMAN | HUMAN ACETYLCHOLINESTERASE | NERVE AGENTS | TABUN | IN-VIVO REACTIVATION | CYCLOSARIN | SARIN | PHARMACOLOGY & PHARMACY | TOXICOLOGY | BRAIN | Atropine - therapeutic use | Cholinesterase Reactivators - administration & dosage | Cholinesterase Inhibitors - toxicity | Atropine - adverse effects | Oximes - adverse effects | Muscarinic Antagonists - adverse effects | Cholinesterase Inhibitors - chemistry | Oximes - administration & dosage | Pyridinium Compounds - administration & dosage | Pyridinium Compounds - therapeutic use | Oximes - therapeutic use | Male | Organophosphate Poisoning - drug therapy | Pyridinium Compounds - adverse effects | Antidotes - administration & dosage | Muscarinic Antagonists - therapeutic use | Chemical Warfare Agents - chemistry | Cholinesterases - blood | Organophosphate Poisoning - physiopathology | Drug Therapy, Combination - adverse effects | Injections, Subcutaneous | Cholinesterase Reactivators - adverse effects | Guinea Pigs | Drug Administration Schedule | Cholinesterase Reactivators - therapeutic use | Injections, Intramuscular | Pesticides - antagonists & inhibitors | Random Allocation | Muscarinic Antagonists - administration & dosage | Animals | Cholinesterase Inhibitors - administration & dosage | Pesticides - toxicity | Organophosphate Poisoning - blood | Antidotes - adverse effects | Atropine - administration & dosage | Chemical Warfare Agents - toxicity | Drug Monitoring | Antidotes - therapeutic use | Analysis | Enzyme inhibitors | Pesticides | Index Medicus | CHOLINESTERASE | ATROPINE | GUINEA PIGS | CHLORINE | BLOOD-BRAIN BARRIER | CENTRAL NERVOUS SYSTEM | SYMPTOMS | TOXICITY | STANDARD OF LIVING | US FDA | 60 APPLIED LIFE SCIENCES | MOLECULAR WEIGHT | PESTICIDES | LETHAL DOSES | OXIMES | THERAPY | CHEMICAL WARFARE AGENTS | POISONING | BLOOD | toxicity | intramuscular | guinea pig | oxime | efficacy
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13. Full Text Structure-Based Design and Optimization of Multitarget-Directed 2H-Chromen-2-one Derivatives as Potent Inhibitors of Monoamine Oxidase B and Cholinesterases
by Farina, R and Pisani, L and Catto, M and Nicolotti, O and Gadaleta, D and Denora, N and Soto-Otero, R and Mendez-Alvarez, E and Passos, CS and Muncipinto, G and Altomare, CD and Nurisso, A and Carrupt, PA and Carotti, A
JOURNAL OF MEDICINAL CHEMISTRY, ISSN 0022-2623, 07/2015, Volume 58, Issue 14, pp. 5561 - 5578
The multifactorial nature of Alzheimer's disease calls for the development of multitarget agents addressing key pathogenic processes. To this end, by following... 
CHEMISTRY, MEDICINAL | ALZHEIMERS-DISEASE | BIOLOGICAL EVALUATION | SELECTIVE INHIBITORS | DUAL INHIBITORS | ACETYLCHOLINESTERASE INHIBITORS | HIGHLY POTENT | AMMONIUM-SALTS | A-BETA AGGREGATION | ANTIOXIDANT PROPERTIES | COUMARIN DERIVATIVES | Coumarins - metabolism | Cholinesterase Inhibitors - toxicity | Humans | Cholinesterase Inhibitors - chemistry | Coumarins - chemistry | Structure-Activity Relationship | Monoamine Oxidase - chemistry | Cholinesterase Inhibitors - metabolism | Cholinesterases - chemistry | Drug Design | Madin Darby Canine Kidney Cells | Inhibitory Concentration 50 | Coumarins - toxicity | Monoamine Oxidase Inhibitors - pharmacology | Rats | Permeability | Blood-Brain Barrier - metabolism | Coumarins - pharmacology | Monoamine Oxidase Inhibitors - toxicity | Animals | Cholinesterase Inhibitors - pharmacology | Dogs | Monoamine Oxidase Inhibitors - metabolism | Protein Conformation | Molecular Docking Simulation | Monoamine Oxidase Inhibitors - chemistry | Cholinesterases - metabolism | Monoamine Oxidase - metabolism | Index Medicus
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14. Full Text History and new developments of assays for cholinesterase activity and inhibition
by Miao, Yuqing and He, Nongyue and Zhu, Jun-Jie
Chemical Reviews, ISSN 0009-2665, 09/2010, Volume 110, Issue 9, pp. 5216 - 5234
BRAIN ACETYLCHOLINESTERASE | SERUM-CHOLINESTERASE | ORGANIC-SOLVENTS | OXIDASE BIOSENSOR | CARBON NANOTUBE | ORGANOPHOSPHORUS PESTICIDES | AMPEROMETRIC BIOSENSOR | CARBAMATE PESTICIDES | ACETYLCHOLINESTERASE INHIBITORS | CHEMISTRY, MULTIDISCIPLINARY | MASS-SPECTROMETRY | Cholinesterases - chemistry | History, 21st Century | Enzyme Assays - history | History, 20th Century | Cholinesterase Inhibitors - chemistry | Enzyme Assays - methods | Biosensing Techniques - methods | Electrochemical Techniques - methods | Spectrophotometry - methods | Cholinesterases - metabolism | Usage | Optical properties | Analysis | Ultraviolet spectroscopy | Cholinesterases | Enzyme binding | Research | Chemical properties | Biosensors | Structure | Mass spectrometry
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15. Full Text Cardanol-derived AChE inhibitors: Towards the development of dual binding derivatives for Alzheimer's disease
by Lemes, Laís Flávia Nunes and de Andrade Ramos, Giselle and de Oliveira, Andressa Souza and da Silva, Fernanda Motta R and de Castro Couto, Gina and da Silva Boni, Marina and Guimarães, Marcos Jorge R and Souza, Isis Nem O and Bartolini, Manuela and Andrisano, Vincenza and do Nascimento Nogueira, Patrícia Coelho and Silveira, Edilberto Rocha and Brand, Guilherme D and Soukup, Ondřej and Korábečný, Jan and Romeiro, Luiz Antonio Soares and Romeiro, Nelilma C and Castro, Newton G and Bolognesi, Maria Laura
European Journal of Medicinal Chemistry, ISSN 0223-5234, 01/2016, Volume 108, pp. 687 - 700
Cardanol is a phenolic lipid component of cashew nut shell liquid (CNSL), obtained as the byproduct of cashew nut food processing. Being a waste product, it... 
Cashew nut shell liquid | Acetylcholinesterase | Dual binding site AChE inhibitors | Alzheimer's disease | Multitarget compounds | TARGET-DIRECTED LIGANDS | DESIGN | CHEMISTRY, MEDICINAL | DRUG-DEVELOPMENT | PREDICTION | MULTITARGET LIGANDS | BIVALENT LIGANDS | BIOLOGICAL EVALUATION | PHARMACOLOGICAL EVALUATION | AGGREGATION | Phenols - chemical synthesis | Humans | Cholinesterase Inhibitors - chemistry | Alzheimer Disease - drug therapy | Cholinesterase Inhibitors - chemical synthesis | Structure-Activity Relationship | Alzheimer Disease - enzymology | Dose-Response Relationship, Drug | HT29 Cells | Cholinesterase Inhibitors - pharmacology | Phenols - chemistry | Molecular Structure | Cholinesterases - metabolism | Binding Sites - drug effects | Phenols - pharmacology | Enzyme inhibitors | Chemical properties | Surface active agents | Drug therapy | Index Medicus
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16. Cholinesterase-inhibiting insecticides
: their impact on wildlife and the environment
by Mineau, P. 1955- (Pierre)
1991, Chemicals in agriculture, ISBN 0444887075, Volume 2, 348
Measurement | Cholinesterase-inhibiting insecticides | Toxicology | Pesticides and wildlife | Cholinesterases | Carbamates | Environmental aspects | Organophosphorus compounds
Book
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17. Full Text Donepezil and Memantine for Moderate-to-Severe Alzheimer's Disease
by Howard, Robert and McShane, Rupert and Lindesay, James and Ritchie, Craig and Baldwin, Ashley and Barber, Robert and Burns, Alistair and Dening, Tom and Findlay, David and Holmes, Clive and Hughes, Alan and Jacoby, Robin and Jones, Roy and Jones, Rob and McKeith, Ian and Macharouthu, Ajay and O'Brien, John and Passmore, Peter and Sheehan, Bart and Juszczak, Edmund and Katona, Cornelius and Hills, Robert and Knapp, Martin and Ballard, Clive and Brown, Richard and Banerjee, Sube and Onions, Caroline and Griffin, Mary and Adams, Jessica and Gray, Richard and Johnson, Tony and Bentham, Peter and Phillips, Patrick
The New England Journal of Medicine, ISSN 0028-4793, 03/2012, Volume 366, Issue 10, pp. 893 - 903
In patients with moderate or severe Alzheimer's disease receiving donepezil, those assigned to continue donepezil had less cognitive decline than did those... 
POPULATION | MEDICINE, GENERAL & INTERNAL | DEMENTIA | EFFICACY | SAFETY | DOUBLE-BLIND | 24-WEEK | QUALITY-OF-LIFE | CHOLINESTERASE-INHIBITORS | RECEIVING DONEPEZIL | Indans - adverse effects | Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors | Excitatory Amino Acid Antagonists - therapeutic use | Double-Blind Method | Humans | Kaplan-Meier Estimate | Alzheimer Disease - drug therapy | Male | Treatment Outcome | Patient Dropouts | Indans - therapeutic use | Drug Synergism | Piperidines - therapeutic use | Piperidines - adverse effects | Aged, 80 and over | Cholinesterase Inhibitors - adverse effects | Female | Aged | Psychological Tests | Cholinesterase Inhibitors - therapeutic use | Drug Therapy, Combination | Memantine - therapeutic use | Excitatory Amino Acid Antagonists - adverse effects | Memantine - adverse effects | Caregivers | Activities of daily living | Neurodegenerative diseases | Cognitive ability | Clinical trials | Patients | Cholinesterase | Memantine | Cognition & reasoning | Older people | Donepezil | Alzheimers disease | Alzheimer's disease
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18. Full Text Oximes in organophosphate poisoning: 60 years of hope and despair
by Worek, Franz and Thiermann, Horst and Wille, Timo
Chemico-Biological Interactions, ISSN 0009-2797, 11/2016, Volume 259, Issue Pt B, pp. 93 - 98
The high number of annual fatalities following suicidal poisoning by organophosphorus (OP) pesticides and the recent homicidal use of the chemical warfare... 
Oxime | Organophosphorus compounds | Acetylcholinesterase | Nerve agents | Pesticides | CHOLINESTERASE | SUBSTITUTED BETA-CYCLODEXTRIN | DETOXIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | NERVE AGENT | REAL-TIME DETERMINATION | HUMAN ACETYLCHOLINESTERASE | REACTIVATORS | IN-VITRO | CYCLOSARIN | PYRIDINIUM ALDOXIMES | PHARMACOLOGY & PHARMACY | TOXICOLOGY | Atropine - therapeutic use | Atropine - metabolism | Atropine - chemistry | Cholinesterase Reactivators - metabolism | Humans | Cholinesterase Inhibitors - chemistry | Cholinesterase Reactivators - therapeutic use | Oximes - therapeutic use | Chemical Warfare Agents - poisoning | Organophosphate Poisoning - drug therapy | Acetylcholinesterase - chemistry | Cholinesterase Reactivators - chemistry | Chemical Warfare Agents - chemistry | Oximes - chemistry | Cholinesterase Inhibitors - metabolism | Paraoxon - metabolism | Oximes - metabolism | Paraoxon - chemistry | Erythrocytes - enzymology | Kinetics | Acetylcholinesterase - metabolism | Nerve gas | Analysis | Poisoning
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19. Full Text Conjugates of salicylaldoximes and peripheral site ligands: Novel efficient nonquaternary reactivators for nerve agent-inhibited acetylcholinesterase
by Wei, Zhao and Liu, Yan-qin and Liu, Xue-Ying and Wang, Yong-an and Wang, Sheng-zheng and Yao, Lin and Nie, Hui-fang and Zheng, Zhi-bing and Li, Song
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 08/2017, Volume 25, Issue 16, pp. 4497 - 4505
Based on a dual site binding strategy, the salicylaldoximes were conjugated to different peripheral site ligands through alkyl chains for construction of novel... 
Human acetylcholinesterase | Nonquaternary reactivator | Salicylaldoxime conjugates | Peripheral site ligand | Nerve agent | CHEMISTRY, MEDICINAL | UNCHARGED REACTIVATORS | CLICK CHEMISTRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | PYRIDINIUM OXIMES | CHEMISTRY, ORGANIC | BLOOD-BRAIN-BARRIER | ALDOXIME | ADMET PREDICTION | SARIN | ORGANOPHOSPHORUS COMPOUNDS | CHOLINESTERASES | IN-SITU | Cholinesterase Reactivators - chemical synthesis | Cholinesterase Reactivators - pharmacology | Humans | Cholinesterase Inhibitors - chemistry | Cholinesterase Inhibitors - chemical synthesis | Structure-Activity Relationship | Oximes - chemical synthesis | Cholinesterase Reactivators - chemistry | Dose-Response Relationship, Drug | Oximes - chemistry | Cholinesterase Inhibitors - pharmacology | Oximes - pharmacology | Ligands | Molecular Structure | Acetylcholinesterase - metabolism | Nerve gas | Phosphates | Surface active agents | Chemical tests and reagents | Index Medicus
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