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Piperidine-based drug discovery

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Piperidine-based drug discovery/ Ruben Vardanyan.
作者:	Vardanyan, R. S.
出版者:	Amsterdam, Netherlands :Elsevier, : 2017.,
面頁冊數:	1 online resource :ill.
內容註:	Front Cover; Piperidine-Based Drug Discovery; Copyright Page; Contents; 1. Introduction; 1.1 The Scope of the Material Under Consideration; 1.2 General Methods of the Synthesis of Piperidine Compounds; Nucleophilic Substitution Reactions; Intermolecular Michael Reactions; Catalyzed Hydroamination Reactions; Aza-Diels-Alder Reactions; Intramolecular Ene Reactions; Ring-Closing Metathesis Reactions; Synthesis of Piperidin-4-Ones; The Synthesis of 2,2,6,6-Tetramethyl-4-Oxopiperidine; Petrenko-Kritschenko Reaction for the Synthesis of 2,6-Disubstituted Piperidin-4-Ones.
內容註:	Synthesis of Piperidin-4-Ones by Dieckmann CondensationSynthesis of Piperidin-4-Ones by Miscellaneous Methods; Nucleophilic Addition Reactions to the Carbonyl Group of Piperidin-4-Ones; Nucleophilic Substitution Reactions Involving [alpha]-Carbon of Piperidin-4-Ones; Piperidin-3-Ones; Piperidin-2-Ones; 4-Cyano-4-Phenylpiperidines; References; 2. 1-Substituted Piperidines; 2.1 Derivatives of 1-Phenyl-3-(Piperidin-1-yl)Propan-1-ol; Trihexyphenidyl (2226); Biperiden (1329); Pridinol (157); Cycrimine (82); 2.2 Derivatives of 1-Phenyl-4-(Piperidin-1-yl)Butan-1-ol; Diphenidol (323); Pirmenol (234).
內容註:	2.3 Derivatives of 2-(Piperidin-1-yl)Ethan-1-ol and 3-(Piperidin-1-yl)Propan-1-olCloperastine (199); Benproperine (140); Pipazethate (98); Raloxifene (7685); Flavoxate (452); Piperocaine (266); 2.4 Derivatives of 3-(Piperidin-1-yl)Propane-1,2-Diol and 3-(Piperidin-1-yl)Propane-1,1-Diol; Diperodon (147); Pipoxolan (25); 2.5 Derivatives of 1-Phenyl-3-(Piperidin-1-yl)Propan-1-One; Dyclonine (584); 2.6 Derivatives of 2,2-Diphenyl-4-(Piperidin-1-yl)Butanamide; Fenpiverinium Bromide (83); References; 3. 2-Substituted and 1,2-Disubstituted Piperidines; 3.1 Methylphenidate (11968).
內容註:	3.2 Perhexiline (1216)3.3 Pipradrol (259); 3.4 Mefloquine (5370); 3.5 Mepivacaine (4176); 3.6 Ropivacaine (6847); 3.7 Bupivacaine (21293) and Levobupivacaine (1976); 3.8 Flecainide (3638); 3.9 Encainide (682); 3.10 Thioridazine (6558); 3.11 Rimiterol (219); 3.12 Lobeline (1914); 3.13 Argatroban (2627); 3.14 Ascomycin (752), Pimecrolimus (1645), Tacrolimus (32436), Sirolimus (22468), Everolimus (8972), and Temsirolimus (2859); References; 4. 3-Substituted and 1,3-Disubstituted Piperidines; 4.1 Methixene (92); 4.2 Tipepidine (132); 4.3 Timepidium (83); 4.4 Tiagabine (2008).
內容註:	4.5 Piperidolate (72)4.6 Mepenzolate (137); 4.7 Pipenzolate (109); 4.8 Benidipine (927); 4.9 Paroxetine (12203) and Femoxetine (270); 4.10 Troxipide (110); 4.11 Linagliptin (1133); 4.12 Tofacitinib (1130); References; 5. 4-Substituted and 1,4-Disubstituted Piperidines; 5.1 4-Piperidinols and Their Derivatives; Periciazine (112); Diphenylpyraline (453); Ebastine (990); Bepotastine (236); Lamifiban (257); Eucatropine (90); Propiverine (664); Pentapiperide (22); 5.2 4-Phenylpiperidin-4-ols and Their Derivatives; Haloperidol (41140); Bromperidol (515); Moperone (218); Trifluperidol (613).
標題:	Drugs - Design. -
電子資源:	https://www.sciencedirect.com/science/book/9780128051573
ISBN:	9780128134283 (electronic bk.)

Piperidine-based drug discovery
Vardanyan, R. S.

Piperidine-based drug discovery[electronic resource] /Ruben Vardanyan. - Amsterdam, Netherlands :Elsevier,2017. - 1 online resource :ill. - Heterocyclic drug discovery series. - Heterocyclic drug discovery series..

Includes bibliographical references and index.

Front Cover; Piperidine-Based Drug Discovery; Copyright Page; Contents; 1. Introduction; 1.1 The Scope of the Material Under Consideration; 1.2 General Methods of the Synthesis of Piperidine Compounds; Nucleophilic Substitution Reactions; Intermolecular Michael Reactions; Catalyzed Hydroamination Reactions; Aza-Diels-Alder Reactions; Intramolecular Ene Reactions; Ring-Closing Metathesis Reactions; Synthesis of Piperidin-4-Ones; The Synthesis of 2,2,6,6-Tetramethyl-4-Oxopiperidine; Petrenko-Kritschenko Reaction for the Synthesis of 2,6-Disubstituted Piperidin-4-Ones.

Piperidine-Based Drug Discovery outlines the complexities of Piperidine scaffold use in drug discovery, including derivative chemistry, structural properties, methods of synthesis and practical implementations. Piperidine scaffolds are the cornerstones of over 70 commercialized drugs (including multiple blockbusters). Designed as a guide for both experts and students working in this and related areas, it is hoped that this volume will encourage and inspire the continued design and development of novel pharmaceuticals based on Piperidine and its derivatives. Heterocyclic compounds are of central importance to medicinal chemistry, as demonstrated by the high percentage of marketable drugs that feature heterocyclic fragments in their structures. As starting points for drug discovery they offer a broad range of attractive properties, and a detailed understanding of the particular characteristics of each is of great benefit to researchers. The most commonly used heterocycle among US FDA approved pharmaceuticals, Piperidine is an extremely important building block in the synthesis of medicinal agents. This heterocycle and its derivatives exhibit a number of important functionalities and have been employed variously as CNS modulators, antiaggregants, anticoagulants, antihistamines, anti-cancer drugs and analgesics.

ISBN: 9780128134283 (electronic bk.)Subjects--Topical Terms:

664528
Drugs
--Design.Index Terms--Genre/Form:

542853
Electronic books.

LC Class. No.: RS420

Dewey Class. No.: 615.19

National Library of Medicine Call No.: QV 745

Piperidine-based drug discovery
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505 0 $a Front Cover; Piperidine-Based Drug Discovery; Copyright Page; Contents; 1. Introduction; 1.1 The Scope of the Material Under Consideration; 1.2 General Methods of the Synthesis of Piperidine Compounds; Nucleophilic Substitution Reactions; Intermolecular Michael Reactions; Catalyzed Hydroamination Reactions; Aza-Diels-Alder Reactions; Intramolecular Ene Reactions; Ring-Closing Metathesis Reactions; Synthesis of Piperidin-4-Ones; The Synthesis of 2,2,6,6-Tetramethyl-4-Oxopiperidine; Petrenko-Kritschenko Reaction for the Synthesis of 2,6-Disubstituted Piperidin-4-Ones.
505 8 $6 880-01 $a Synthesis of Piperidin-4-Ones by Dieckmann CondensationSynthesis of Piperidin-4-Ones by Miscellaneous Methods; Nucleophilic Addition Reactions to the Carbonyl Group of Piperidin-4-Ones; Nucleophilic Substitution Reactions Involving [alpha]-Carbon of Piperidin-4-Ones; Piperidin-3-Ones; Piperidin-2-Ones; 4-Cyano-4-Phenylpiperidines; References; 2. 1-Substituted Piperidines; 2.1 Derivatives of 1-Phenyl-3-(Piperidin-1-yl)Propan-1-ol; Trihexyphenidyl (2226); Biperiden (1329); Pridinol (157); Cycrimine (82); 2.2 Derivatives of 1-Phenyl-4-(Piperidin-1-yl)Butan-1-ol; Diphenidol (323); Pirmenol (234).
505 8 $a 2.3 Derivatives of 2-(Piperidin-1-yl)Ethan-1-ol and 3-(Piperidin-1-yl)Propan-1-olCloperastine (199); Benproperine (140); Pipazethate (98); Raloxifene (7685); Flavoxate (452); Piperocaine (266); 2.4 Derivatives of 3-(Piperidin-1-yl)Propane-1,2-Diol and 3-(Piperidin-1-yl)Propane-1,1-Diol; Diperodon (147); Pipoxolan (25); 2.5 Derivatives of 1-Phenyl-3-(Piperidin-1-yl)Propan-1-One; Dyclonine (584); 2.6 Derivatives of 2,2-Diphenyl-4-(Piperidin-1-yl)Butanamide; Fenpiverinium Bromide (83); References; 3. 2-Substituted and 1,2-Disubstituted Piperidines; 3.1 Methylphenidate (11968).
505 8 $a 3.2 Perhexiline (1216)3.3 Pipradrol (259); 3.4 Mefloquine (5370); 3.5 Mepivacaine (4176); 3.6 Ropivacaine (6847); 3.7 Bupivacaine (21293) and Levobupivacaine (1976); 3.8 Flecainide (3638); 3.9 Encainide (682); 3.10 Thioridazine (6558); 3.11 Rimiterol (219); 3.12 Lobeline (1914); 3.13 Argatroban (2627); 3.14 Ascomycin (752), Pimecrolimus (1645), Tacrolimus (32436), Sirolimus (22468), Everolimus (8972), and Temsirolimus (2859); References; 4. 3-Substituted and 1,3-Disubstituted Piperidines; 4.1 Methixene (92); 4.2 Tipepidine (132); 4.3 Timepidium (83); 4.4 Tiagabine (2008).
505 8 $a 4.5 Piperidolate (72)4.6 Mepenzolate (137); 4.7 Pipenzolate (109); 4.8 Benidipine (927); 4.9 Paroxetine (12203) and Femoxetine (270); 4.10 Troxipide (110); 4.11 Linagliptin (1133); 4.12 Tofacitinib (1130); References; 5. 4-Substituted and 1,4-Disubstituted Piperidines; 5.1 4-Piperidinols and Their Derivatives; Periciazine (112); Diphenylpyraline (453); Ebastine (990); Bepotastine (236); Lamifiban (257); Eucatropine (90); Propiverine (664); Pentapiperide (22); 5.2 4-Phenylpiperidin-4-ols and Their Derivatives; Haloperidol (41140); Bromperidol (515); Moperone (218); Trifluperidol (613).
520 $a Piperidine-Based Drug Discovery outlines the complexities of Piperidine scaffold use in drug discovery, including derivative chemistry, structural properties, methods of synthesis and practical implementations. Piperidine scaffolds are the cornerstones of over 70 commercialized drugs (including multiple blockbusters). Designed as a guide for both experts and students working in this and related areas, it is hoped that this volume will encourage and inspire the continued design and development of novel pharmaceuticals based on Piperidine and its derivatives. Heterocyclic compounds are of central importance to medicinal chemistry, as demonstrated by the high percentage of marketable drugs that feature heterocyclic fragments in their structures. As starting points for drug discovery they offer a broad range of attractive properties, and a detailed understanding of the particular characteristics of each is of great benefit to researchers. The most commonly used heterocycle among US FDA approved pharmaceuticals, Piperidine is an extremely important building block in the synthesis of medicinal agents. This heterocycle and its derivatives exhibit a number of important functionalities and have been employed variously as CNS modulators, antiaggregants, anticoagulants, antihistamines, anti-cancer drugs and analgesics.
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