BIOMAT Database Logo BIOMAT Database Logo

[Derivatives of octahydrodiazocine-1,5 and octahydrodiazocine-1,4 with potential pharmacological action. I. Synthesis of N-alkyl derivatives of octahydrodiazocine-1,5 and octahydrodiazocine-1,4]. 1975

M Majchrzak, and A Kotelko, and R Guryn

UI MeSH Term Description Entries
D007202 Indicators and Reagents Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant & Hackh's Chemical Dictionary, 5th ed, p301, p499) Indicator,Reagent,Reagents,Indicators,Reagents and Indicators
D010084 Oxidation-Reduction A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471). Redox,Oxidation Reduction
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D004232 Diuretics Agents that promote the excretion of urine through their effects on kidney function. Diuretic,Diuretic Effect,Diuretic Effects,Effect, Diuretic,Effects, Diuretic
D006634 Histamine H1 Antagonists Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood. Antihistamines, Classical,Antihistaminics, Classical,Antihistaminics, H1,Histamine H1 Antagonist,Histamine H1 Receptor Antagonist,Histamine H1 Receptor Antagonists,Histamine H1 Receptor Blockaders,Antagonists, Histamine H1,Antagonists, Histamine H1 Receptor,Antihistamines, Sedating,Blockaders, Histamine H1 Receptor,First Generation H1 Antagonists,H1 Receptor Blockaders,Histamine H1 Blockers,Receptor Blockaders, H1,Antagonist, Histamine H1,Classical Antihistamines,Classical Antihistaminics,H1 Antagonist, Histamine,H1 Antagonists, Histamine,H1 Antihistaminics,Sedating Antihistamines
D000959 Antihypertensive Agents Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. Anti-Hypertensive,Anti-Hypertensive Agent,Anti-Hypertensive Drug,Antihypertensive,Antihypertensive Agent,Antihypertensive Drug,Anti-Hypertensive Agents,Anti-Hypertensive Drugs,Anti-Hypertensives,Antihypertensive Drugs,Antihypertensives,Agent, Anti-Hypertensive,Agent, Antihypertensive,Agents, Anti-Hypertensive,Agents, Antihypertensive,Anti Hypertensive,Anti Hypertensive Agent,Anti Hypertensive Agents,Anti Hypertensive Drug,Anti Hypertensive Drugs,Anti Hypertensives,Drug, Anti-Hypertensive,Drug, Antihypertensive,Drugs, Anti-Hypertensive,Drugs, Antihypertensive
D001392 Azocines
D055598 Chemical Phenomena The composition, structure, conformation, and properties of atoms and molecules, and their reaction and interaction processes. Chemical Concepts,Chemical Processes,Physical Chemistry Concepts,Physical Chemistry Processes,Physicochemical Concepts,Physicochemical Phenomena,Physicochemical Processes,Chemical Phenomenon,Chemical Process,Physical Chemistry Phenomena,Physical Chemistry Process,Physicochemical Phenomenon,Physicochemical Process,Chemical Concept,Chemistry Process, Physical,Chemistry Processes, Physical,Concept, Chemical,Concept, Physical Chemistry,Concept, Physicochemical,Concepts, Chemical,Concepts, Physical Chemistry,Concepts, Physicochemical,Phenomena, Chemical,Phenomena, Physical Chemistry,Phenomena, Physicochemical,Phenomenon, Chemical,Phenomenon, Physicochemical,Physical Chemistry Concept,Physicochemical Concept,Process, Chemical,Process, Physical Chemistry,Process, Physicochemical,Processes, Chemical,Processes, Physical Chemistry,Processes, Physicochemical

Related Publications

M Majchrzak, and A Kotelko, and R Guryn
[Synthesis of hexahydroxazepine-1,4 derivatives with expected pharmacological action. I. Synthesis of N-alkyl-derivatives of hexahydrooxazepine-1,4].
January 1967, Acta poloniae pharmaceutica,
M Majchrzak, and A Kotelko, and R Guryn
Synthesis of hexahydro-1,4-thiazepine derivatives with expected pharmacological activity. Part I. N-alkyl(hydroxyalkyl)-hexahydro-1,4-thiazepines and 2-(hexahydro-1,4-thiazepinyl)-ethyl esters of phenoxyacetic acids.
January 1979, Polish journal of pharmacology and pharmacy,
M Majchrzak, and A Kotelko, and R Guryn
[Synthesis of amide derivatives of 3-(1'-alkyl-4'-piperazyl)-propylamines with potential pharmacological action].
January 1974, Acta poloniae pharmaceutica,
M Majchrzak, and A Kotelko, and R Guryn
[Synthesis of Mannich N-bases with potential pharmacological action].
January 1975, Acta poloniae pharmaceutica,
M Majchrzak, and A Kotelko, and R Guryn
[Synthesis of hexahydro-oxazepine -1,4 derivatives with expected pharmacological action. VIII. Hydrazide derivatives of hexahydro-oxazepine-1,4 (homomorpholine) and morpholine].
January 1974, Acta poloniae pharmaceutica,
M Majchrzak, and A Kotelko, and R Guryn
Studies on annelated 1,4-benzothiazines and 1,5-benzothiazepines. I. Synthesis of 4H-s-triazolo[3,4-c]-1,4-benzothiazine and derivatives with potential CNS activity.
April 1985, Il Farmaco; edizione scientifica,
M Majchrzak, and A Kotelko, and R Guryn
[Synthesis of hexahydrooxazepine-1,4 derivatives with expected pharmacological action. 3. Derivatives of hexahydrooxazepine-1,4 containing pharmacologically active ether moieties].
January 1968, Acta poloniae pharmaceutica,
M Majchrzak, and A Kotelko, and R Guryn
1,5-Benzoxathiepin derivatives. I. Synthesis and reaction of 1,5-benzoxathiepin derivatives.
May 1987, Chemical & pharmaceutical bulletin,
M Majchrzak, and A Kotelko, and R Guryn
Synthesis and pharmacological action of some N-alkyl morpholines and their salts.
December 1968, The Journal of pharmacy and pharmacology,
M Majchrzak, and A Kotelko, and R Guryn
[Synthesis of amide deriatives of morpholine and homomorpholine (hexahydrooxazepine-1,4) with potential pharmacological action].
January 1973, Acta poloniae pharmaceutica,
Copied contents to your clipboard!