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Biomedical subjects

R Dahlbom

Publications and source records attributed to R Dahlbom.

At least 37 records · Page 2Linked to original sources

PubMed1978

Stereoselectivity of oxotremorine antagonists containing a chiral pyrrolidine group.

Oxotremorine (Ia) and its succinimide analogue (IIa) have been substituted in the pyrrolidine ring with a methyl group in the 2- or 3-positions. The compounds are oxotremorine antagonists. The 2-methyl-substituted enantiomers show stereoselectivity, the S-isomers being the most active.

Animals↗

PubMed1978

Acetylene compounds of potential pharmacological value. XXV. N-(4-pyrrolidino-2-butynyl)-N-alkylcarboxamides.

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Alkynes↗

PubMed1978

Acetylene compounds of potential pharmacological value. XXXVI. N-(4-tert-Amino-2-butynyl)-substituted 2(3H)-thiazolones and 2(3H)-oxazolones.

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Animals↗

PubMed1978

Acetylene compounds of potential pharmacological value. XXVII. Stereoselectivity of oxotremorine antagonists containing a chiral pyrrolidine group.

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Animals↗

PubMed1975

The crystal and molecular structure of oxotremorine sesquioxalate.

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Chemical Phenomena↗

PubMed1975

Acetylene compounds of potential pharmacological value. XIX. N-(dialkylaminoalkynyl)-substituted succinimides and 2-pyrrolidones as partial cholinergic agonists.

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Alkynes↗

PubMed1975

Acetylene compounds of potential pharmacological value. XX. N-(t-aminoalkynyl)substituted phthalimides.

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Alkynes↗

PubMed1975

Acetylene compounds of potential pharmacological value. XXI. Further studies on the effect of branching the intermediate chain of N-(t-aminoalkynyl)-substituted succinimides and 2-pyrrolidones.

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Alkynes↗

PubMed1975

Acetylene compounds of potential pharmacological value. XXII. Base strength and biological activity in oxotremorine antagonists.

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Alkynes↗

PubMed1975

Acetylene compounds of potential pharmacological value. XXIII. N-(1-Methyl-5-pyrrolidino-3-pentynyl)-substituted succinimide and 2-pyrrolidone.

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Alkynes↗

PubMed1974

Stereospecificity of oxotremorine antagonists.

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Acetylcholine↗

PubMed1974

On the inhibitory power of some further pyrazole derivatives of horse liver alcohol dehydrogenase.

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Alcohol Oxidoreductases↗

PubMed1974

Cyclizing compounds. IV. Tertiary N-(2-(3,4,5-trimethoxybenzoyloxy)ethyl)-N-haloalkylamines with hemicholinium-like activity.

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Acetylcholine↗

PubMed1973

Cyclizing compounds. I. Tertiary N-(2-bromobenzyl)-N-haloalkylamines with adrenergic blocking action.

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Adrenergic alpha-Antagonists↗

PubMed1973

Cyclizing compounds. II. Tertiary N-(2-(2,6-dimethylphenoxy)ethyl)-N-haloalkylamines with local anaesthetic action.

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Amines↗

PubMed1973

Acetylene compounds of potential pharmacological value. 18. N-(t-aminoalkynyl)-substituted 2-pyrrolidones, a new series of potent oxotremorine antagonists.

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Acetylcholine↗

PubMed1972

Studies on carbanilic acid esters of cyclic amino alcohols. 5. Local anesthetic potency of the enantiomers of two N-butyl-3-piperidyl carbanilates.

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Action Potentials↗

PubMed1972

Synthesis and pharmacology of 1-(2-thioxopyrrolidino)-4-pyrrolidino-2-butyne, the thiolactam analogue of oxotremorine.

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Acetylcholine↗