Author pages are created from data sourced from our academic publisher partnerships and public sources.
- Publications
- Influence
Potential neuroleptic agents. 3. Chemistry and antidopaminergic properties of substituted 6-methoxysalicylamides.
- T. de Paulis, Y. Kumar, +5 authors S. O. Ógren
- Chemistry, Medicine
- Journal of medicinal chemistry
- 1 September 1985
A series of substituted 6-methoxysalicylamides were synthesized from their corresponding 2,6-dimethoxybenzamides by demethylation of one methoxy group with boron tribromide. Substituted… Expand
Potential neuroleptic agents. 4. Chemistry, behavioral pharmacology, and inhibition of [3H]spiperone binding of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides.
- T. de Paulis, Y. Kumar, +5 authors S. O. Ógren
- Chemistry, Medicine
- Journal of medicinal chemistry
- 1986
A series of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl) methyl]-6-methoxysalicylamides was synthesized, starting from the 2,6-dimethoxybenzoic acids, by boron tribromide demethylation of the… Expand
New selective dopamine D-2 antagonists as antipsychotic agents. Pharmacological, chemical, structural and theoretical considerations.
- T. Hoegberg, S. Raemsby, S. Ogren, U. Norinder
- Chemistry, Medicine
- Acta pharmaceutica Suecica
- 1987
Antidepressant agents. 1. Chemistry and pharmacology of amino-substituted spiro(5H-dibenzo(a,d)cycloheptene-5,1'-cycloalkanes).
- B. Carnmalm, E. Jacupovic, +6 authors S. O. Ógren
- Chemistry, Medicine
- Journal of medicinal chemistry
- 1974
Potential Neuroleptic Agents. Part 4. Chemistry, Behavioral Pharmacology and Inhibition of [3H]Spiperone Binding of 3,5‐Disubstituted N‐[(1‐Ethyl‐2‐pyrrolidinyl)methyl]‐6‐methoxysalicylamides.
- T. D. Paulis, Y. Kumar, +5 authors S. O. Ögren
- Chemistry
- 20 May 1986
Die Carbonsauren (II) werden in die Amide (III) und (IV) umgewandelt, von denen (III) (R′, R2 = C1) auf Grund der Voruntersu-g chungsergebnisse klinisch gegen Schizophrenie untersucht werden soll.
Synthesis of Npi- and Ntau-(2-Hydroxyethyl)-L-histidines.
- C. Calleman, C. A. Wachtmeister, +5 authors C. Yanaihara
- Chemistry
- 25 September 1979
POTENTIAL NEUROLEPTIC AGENTS. 3. CHEMISTRY AND ANTIDOPAMINERGIC PROPERTIES OF F SUBSTITUTED 6-METHOXYSALICYLAMIDES
- T. D. Paulis, Y. Kumar, +5 authors S. O. Ögren
- Chemistry
- 31 December 1985
Cyanide as an efficient and mild catalyst in the aminolysis of esters
- T. Hoegberg, P. Stroem, M. Ebner, S. Raemsby
- Chemistry
- 1 May 1987
Crystallographic, theoretical and molecular modelling studies on the conformations of the salicylamide, raclopride, a selective dopamine‐D2 antagonist *
- T. Hoegberg, U. Norinder, S. Raemsby, B. Stensland
- Medicine, Chemistry
- The Journal of pharmacy and pharmacology
- 1 October 1987
The structure of the potent dopamine‐D2 antagonist, raclopride, (S)‐3,5‐dichloro‐N‐[(1‐ethyl‐2‐pyrrolidinyl)methyl]‐6‐methoxysalicylamide (+)‐tartrate, has been determined by X‐ray crystallography.… Expand
Solid state conformations and antidopaminergic effects of remoxipride hydrochloride and a closely related salicylamide, FLA 797, in relation to dopamine receptor models.
- T. Hoegberg, S. Raemsby, T. de Paulis, B. Stensland, I. Csöregh, A. Wägner
- Chemistry, Medicine
- Molecular pharmacology
- 1 October 1986
The X-ray structures of two new 2,6-disubstituted benzamides, i.e., remoxipride hydrochloride monohydrate [-)-(S)-3-bromo-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2,6-dimethoxybenza mide hydrochloride… Expand