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Institution

Roussel Uclaf

About: Roussel Uclaf is a based out in . It is known for research contribution in the topics: Alkyl & Alkoxy group. The organization has 1888 authors who have published 2338 publications receiving 36508 citations.
Topics: Alkyl, Alkoxy group, Aryl, Carbon, Carboxylic acid


Papers
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Journal ArticleDOI
TL;DR: The autoradiographic distribution of glucocorticosteroid binding sites in the brain of adrenalectomized rats was studied and a specific and dense labeling was revealed in the pyramidal cell layer of the Ammon's horn and in the granular cell layers of the dentate gyrus of the hippocampus.

33 citations

Journal ArticleDOI
TL;DR: In vivo corticosterone modulates its own number of binding sites demonstrated by in vitro binding on brain sections, in a manner which is reminiscent of changes in cytosol receptors demonstrated by conventional biochemical methods, Thus, this in vitro method provides an alternative way to study the plasticity of hippocampal glucocorticoid receptors.

33 citations

Patent
13 Feb 1981
TL;DR: In this article, it was shown that a linear or branched alkyl, alkenyl, alkynyl or cycloalkyl radical having at most 6 carbon atoms can be substituted by one or more radicals.
Abstract: 1. Claims for Contracting States : BE CH DE GB IT LI LU NL SE Products of general formula (I') : see diagramm : EP0104671,P40,F2 syn isomers in which R, A, X', R'a, n have the following significances either A] R represents, either a linear or branched alkyl, alkenyl, alkynyl or cycloalkyl radical having at most 6 carbon atoms, or an acetyl, propionyl, butyryl, valeryl, hexanoyl, acryloyl, crotonyl, benzoyl or carbamoyl radical, each of these radicals being optionally substituted by one or more radicals chosen from the following radicals ; carboxy optionally salified or esterified, methoxy, carboxyl, ethoxy carbonyl, carbamoyl, amino dimethylcarbamoyl, methylamino, dimethylamino, halogen, methoxy, ethoxy, propyloxy, methylthio, phenyl ethylthio, tetrazolyl, phenylthio, tetrazolylthio or thiadiazolylthio optionally substituted by methyl, or R represents a methoxycarbonyl or ethoxycarbonyl radical, A represents a hydrogen atom, an equivalent of an alkali metal, of an alkaline earth metal, of magnesium, of ammonium or of an aminated organic base, or A represents the remainder of an easily cleavable ester group, R'a represents an alkyl radical optionally interrupted by a heteroatom, linear or branched alkenyl or alkynyl radical having at most 6 carbon atoms, or a benzyl or phenylethyl radical optionally substituted by a carboxy, amino or dimethylaminoethyl radical, n is equal to 0, 1 or 2, X' represents a sulphur atom optionally oxidised in the form of the sulphoxide or sulphone, or an oxygen atom, it being understood that R does not represent an alkenyl or alkynyl radical having at most 6 carbon atoms or a linear or branched alkyl radical having at most 6 carbon atoms optionally substituted by one or more radicals chosen from the following, carboxy optionally salified or esterified, alkoxycarbonyl, amino, alkylamino, dialkylamino or heterocyclic aryl, when the radical -X'-R'a represents an alkoxy, alkylthio or alkenylthio radical ; or B] n is equal to 0, A represents a hydrogen atom and either R represents a -CH2 -CH2 -NH2 , -CH2 CO2 H or -C(CH3 )2 CO2 H radical, X' represents a sulphur or oxygen atom and R'a represents a methyl or ethyl radical or R represents a see diagramm : EP0104671,P41,F1 radical, X' represents an oxygen or sulphur atom and R'a represents a methyl radical as well as the salts of products of formula (I') with mineral or organic acids. 1. Claims for Contracting State : AT Preparation process for products of general formula (I') see diagramm : EP0104671,P45,F1 syn isomers in which R, A, X', R'a, n have the following significances either A] R represents, either a linear or branched alkyl radical, an alkenyl, alkynyl or cycloalkyl radical having at most 6 carbon atoms, carbamoyl each of these radicals being optionally substituted by one or more of the following radicals, carboxy optionally salified or esterified, methoxy carboxyl, ethoxy carbonyl, carbamoyl, amino-dimethylcarbamoyl, methylamino, dimethylamino, halogen, methoxy, ethoxy, propyloxy, methylthio, phenyl ethylthio, tetrazolyl, phenylthio, tetrazolylthio or thiadiazolylthio optionally substituted by methyl, or R represents a methoxycarbonyl or ethoxycarbonyl radical, A represents a hydrogen atom, an equivalent of an alkali metal, of an alkaline earth metal, of magnesium, of ammonium or of an aminated organic base, or A represents the remainder of an easily cleavable ester group, R'a represents an alkyl radical optionally interrupted by a heteroatom, linear or branched alkenyl or alkynyl radical having at most 6 carbon atoms, or a benzyl or phenylethyl radical optionally substituted by a carboxy, amino or dimethylaminoethyl radical, n is equal to 0, 1 or 2, X' represents a sulphur atom optionally oxidised in the form of the sulphoxide or sulphone, or an oxygen atom, it being understood that R does not represent an alkenyl or alkynyl radical having at most 6 carbon atoms or a linear or branched alkyl radical having at most 6 carbon atoms optionally substituted by one or more of the following carboxy optionally salified or esterified, alkoxycarbonyl, amino, alkylamino, dialkylamino or heterocyclic aryl, when the -X'-R'a radical represents an alkoxy, alkylthio or alkenylthio radical ; or B] n is equal to 0, A represents a hydrogen atom and either R represents a CH2 -CH2 -NH2 , -CH2 CO2 H or -C(CH3 )2 CO2 H radical, X' represents a sulphur or oxygen atom and R'a represents a methyl or ethyl radical or R represents a see diagramm : EP0104671,P45,F2 radical, X' represents an oxygen or sulphur atom and R'a represents a methyl radical as well as the salts of products of formula (I') with mineral or organic acids characterised in that a product of formula (II) see diagramm : EP0104671,P46,F1 in which n, X' and R'a have the significance indicated previously and A' represents a hydrogen atom or the remainder of an easily cleavable ester group, is treated by a product of formula (III) : see diagramm : EP0104671,P46,F2 or a functional derivative of this acid, formula (III) in which R1 represents a hydrogen atom or a protector group of the amino radical and either R' represents a linear or branched alkyl radical, an alkenyl, alkynyl or cycloalkyl radical having at most 6 carbon atoms, or R' represents one of the following radicals, acetyl, propionyl, butyryl, valeryl, hexanoyl, acryloyl, crotonoyl, benzoyl, carbamoyl or alkoxycarbonyl, each of these radicals being optionally substituted, to obtain a product of formula (IV) : see diagramm : EP0104671,P46,F3 in which R1 , R', A', R'a, X' and n have the previous significance, which product, if desired, in the case where n is equal to 0 and X' represents a sulphur or oxygen atom, is treated with an oxidation agent, to obtain a product of formula (IV) in which n is equal to 1 or 2 and X' represents a sulphur atom oxidised in the form of the sulphoxide or sulphone or an oxygen atom and, which product of formula IV, if necessary or if desired, is subjected to one or more of the following reactions, in any order : a) detachment by hydrolysis, hydrogenolysis or by the action of thiourea of all or part of the ester groups or the protector groups of the amino radical or radicals, b) esterification or salification of the carboxylic radical or radicals by a base, c) salification of the amino radical or radicals by an acid.

33 citations

Journal ArticleDOI
TL;DR: Trandolapril produced dose-related reductions in BP, total peripheral resistance and heart work in dogs pretreated with hydrochlorothiazide to increase plasma renin activity, and was 2.3-10-fold more potent than enalapril in all experiments, depending on species or route of administration.

33 citations

Journal ArticleDOI
TL;DR: Combined treatment of adult male rats with the LHRH agonist, [D-Ser(TBU)6, des-Gly-NH2(10)]LHRH ethylamide, and a non-steroid antiandrogen led to a rapid and marked atrophy of the ventral prostate and seminal vesicles.

33 citations


Authors

Showing all 1888 results

NameH-indexPapersCitations
Fernand Labrie11088548308
Lionel H. Opie8451925964
Alain Bélanger7024416469
Michel J. Tremblay5327310485
Pierre Monsan512168049
Samir Z. Zard5057510739
Alejandro Aruffo4712314084
Samuel S.C. Yen47966865
Dominique Maraninchi471888108
Serge Erlinger461528200
Romain Lefebvre402215269
William B. Motherwell393056357
Jean-Pierre Raynaud381045075
André Lemay381144264
Patrick J. Creaven321023435
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20181
20114
20104
20091
20084
20072