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Roussel Uclaf Patents
Assignee:
Roussel Uclaf
Address:
Paris, FR
No. of patents:
637
Patents:


1 2 3 4 5 6 7 8 9 10 11 12 13


Patent Number Title Of Patent Date Issued
RE38446 Sucrose phosphate synthase (SPS), its process for preparation its cDNA, and utilization of cDNA February 24, 2004
Sucrose phosphate synthase (SPS), its process for preparation, its cDNA, and utilization of cDNA to modify the expression of SPS in the plant cells are provided.
RE30845 Apparatus for automatically measuring the light transmission factor or liquid test samples January 12, 1982
An apparatus for automatically measuring the light transmission factor of liquid test samples in which a number of transparent vats is arranged around the circumference of a stationary table over which rotates a photoelectric measuring device which successively scans each vat to dete
RE29587 Cyclopentanone derivatives March 21, 1978
Novel prostanoic acid derivatives of the formula ##STR1## wherein R is selected from the group consisting of hydrogen and alkyl of 1 to 7 carbon atoms, R.sub.1 is selected from the group consisting of hydrogen and carbalkoxy of 1 to 7 alkyl carbon atoms, R.sub.2 is selected from
D388171 Instrument for implantations for manual use December 23, 1997
D381085 Multiple medicament implant cartridge for animal treatment July 15, 1997
5985292 Active phospholipids as a vector for active molecules November 16, 1999
An active phospholipid of the formula ##STR1## wherein R.sub.1 is aliphatic of 14 to 24 carbon atoms saturated or containing 1 or 2 unsaturations, R.sub.3 is a residue selected from the group consisting of choline, ethanolamine, glycerol, serine, inositol, ethanol, n-propanol, n-
5770192 Biological control agents June 23, 1998
A recombinant baculovirus which, in insect cells infected therewith, expresses a foreign protein comprising an insecticidal toxin, or a functional derivative thereof, provided with a signal peptide such that the toxin or derivative thereof is secreted from the insect cells. This reco
5705494 Anti-estrogenic activity of II.beta.-substituted-19-NOR Steroids January 6, 1998
Disclosed is a method of inducing anti-estrogenic activity in warm-blooded animals by the administration of a compound of the formula ##STR1## wherein the substituents are as defined in the specification.
5565588 9-alpha-hydroxy steroids, process for their preparation, process for the preparation of the corr October 15, 1996
New 9-alpha-hydroxy steroids are prepared by the introduction of substituents on the D-ring of 9-alpha-hydroxy-androst-4-ene-3,17-dione.The resulting compounds are useful intermediates in the synthesis of corticosteroids.
5532375 Process for preparing 1,2,5,6-tetrahydropyridin-3-carboxaldehyde oximes July 2, 1996
Compounds useful in the treatment of Alzheimer's disease, senile dementia, or memory disorders which have the formula ##STR1## in which R represents a hydrogen atom, a linear, branched or cyclic alkyl radical, saturated or unsaturated, containing up to 8 carbon atoms, possibly su
5455048 Sun filter microcapsules October 3, 1995
Microcapsules containing at least one sun filter having been hardened so as to be impervious with a size of 1 to 1250 micrometers whereby the sun filters do not come in contact with the skin.
5391754 Process for preparing 1,2,5,6-tetrahydropyridin-3-carboxaldehyde oxime compounds February 21, 1995
Compounds useful in the treatment of Alzheimer's disease, senile dementia, or memory disorders which have the formula ##STR1## in which R represents a hydrogen atom, a linear, branched or cyclic alkyl radical, saturated or unsaturated, containing up to 8 carbon atoms, possibly su
5389613 Method of treating prostate adenocarcinoma, prostate benign hypertrophia and endometriosis February 14, 1995
A novel method of treating prostate adenocarcinoma, prostate benign hypertrophia, endometriosis, dysmenorrhea, hirsuitism, hormono-dependant mammary tumors, treatment and prevention of precocious puberty, induction of a retardation of the appearance of puberty and treatment of acne of
5380733 Certain pyridyl-5-phenyl-1-cyclopropyl-dienamide pesticides January 10, 1995
Compounds of the formula:Q(CH.sub.2).sub.a (O).sub.b Q.sub.1 CR.sub.2 .dbd.CR.sub.3 CR.sub.4 .dbd.CR.sub.5 CX.sub.1 NHR.sub.1wherein the terms Q, Q.sub.1, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, X.sub.1 and the integers a and b are defined in the specification, or salts thereof. Sai
5380732 Pesticidal compounds January 10, 1995
A compound of Formula I or a salt thereof:where Ar is a 6-membered heteroaromatic ring containing, as the heteroatom or heteroatoms, one or two nitrogen atoms and is optionally substituted by one or more of halogen, cyano, C.sub.1-6 -alkyl (optionally substituted by halogen), or C.sub.1-
5371075 Trithiabicyclo[2,2,2]octanes December 6, 1994
Bicyclo-[2,2,1]-heptanes, bicyclo-[2,2,2,]-octanes and bicyclo-[2,2,3]-nonanes having 2 or 3 ring hetero atoms selected from O, S and N, substituted at the 1-position by a 4-alkynylphenyl group and at the 4-position and optionally at the 3 and/or 5-position are valuable pesticides, p
5366962 Low calorie sweetener November 22, 1994
The present invention concerns the use of fructosyl oligosaccharides as low-calorie sweeteners, and the foods, dietetic products and drinks containing them.
5315018 Process for the functionalization of organic molecules May 24, 1994
The present invention relates to the hydroxymethylation of aromatic compounds and the subsequent transformation of the hydroxymethylated aromatic compounds to the polyalkoxyalkylene derivative thereof.
5252708 Preparation process for a protein containing at least one intramolecular disulphide bridge by ox October 12, 1993
Preparation process for a protein comprising at least one intramolecular disulphide bridge, and optionally one or more additional cysteines, comprising the oxidation of the corresponding reduced recombinant protein using an oxidizing agent and characterized in that an aqueous solution of
5231107 Derivatives of the oxime of 1,2,5,6-tetrahydropyridine 3-carboxaldehyde, the process for their p July 27, 1993
Compounds useful in the treatment of patients suffering from senile dementia, Alzheimer's disease or memory defects, of the formula ##STR1## in which R' represents hydrogen, a linear, branched or cyclic alkyl, alkenyl or alkynyl, containing up to 8 carbon atoms, and R represents a
5219873 Compounds of 1,2,5,6-tetrahydropyridine which are useful as cholinergic agents June 15, 1993
Compounds useful in the treatment of Alzheimer's disease, senile dimentia and memory disorders of the formula ##STR1## in which R represents hydrogen, hydroxyl, a linear, branched or cyclic, saturated or unsaturated, alkyl, containing up to 8 carbon atoms, possibly substituted by
5219872 Compounds of 1,2,5,6-tetrahydropyridin-3-carboxaldehyde oxime which are useful as cholinergic ag June 15, 1993
Compounds useful in the treatment of Alzheimer's disease, senile dementia, or memory disorders which have the formula ##STR1## in which R represents a hydrogen atom, a linear, branched or cyclic alkyl radical, saturated or unsaturated, containing up to 8 carbon atoms, possibly su
5204479 Derivatives of 1,2,5,6-tetrahydropyridin-3-carboxaldehyde oxime April 20, 1993
The subject of the invention is the compounds of formula (I): ##STR1## in which: R represents a hydrogen atom, a saturated or unsaturated, linear, branched or cyclic alkyl radical containing up to 8 carbon atoms,R' represents an amine-containing moiety of an .alpha.-amino acid or a p
5204341 1-arylsulphonyl-2-pyrrolidone derivatives, their preparation process and the new intermediates o April 20, 1993
1-arylsulphonyl-2-pyrrolidone derivatives for treating spasmodic disorders in gastro-enterology, in gynaecology, in obstetrics, in urology; intermediates in the preparation of such products; methods for preparing such products and pharmaceutical preparations containing such products.
5202316 N,N,N',N'-6-(1-piperazinyl)-2,5-pyridinediamines April 13, 1993
A compound selected from the group consisting of a compound of the formula ##STR1## wherein R.sub.A, R'.sub.A, R.sub.B and R'.sub.B are individually selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms or R.sub.A and R'.sub.A or R.sub.B and R'.sub.B togethe
5202314 10-thioethyl-steroids April 13, 1993
A compound of the formula ##STR1## wherein R is selected from the group consisting of alkyl, alkenyl and alkynyl of up to 4 carbon atoms, Y is .dbd.O or ##STR2## R.sub.1 is hydrogen or acyl, n is 0, 1 or 2, D is .dbd.O or ##STR3## and A and B form a second carbon-carbon o
5198571 Monofunctionalization of phenolic hydroxy onto a polyphenol March 30, 1993
A region-specific monofunctionalization of a phenolic hydroxy onto a polyphenol for the preparation of a compound of the formula ##STR1## wherein R is selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms, alkenyl and alkynyl of 2 to 8 carbon atoms, --CN, formy
5194622 Process for preparation of thiazolylalkoxy acrylates March 16, 1993
A process for the preparation of a compound of the formula ##STR1## wherein R.sub.1 and R.sub.2 are individually selected from the group consisting of hydrogen, halogen, --CF.sub.3, alkyl, alkoxy and alkylthio of 1 to 8 carbon atoms, alkenyl and alkynyl of 2 to 8 carbon atoms, --
5192801 3-[2-cyano-2-halo-ethenyl]-2,2-dimethyl-cyclopropanecarboxylates March 9, 1993
All stereoisomeric forms and mixtures thereof of a compound of the formula ##STR1## wherein the cyclopropane copula has (1R, cis) or (1R, trans) structure, the geometry of the double bond carried by the 3-carbon atom is (E) or (Z), X is halogen, Z is selected from the group consistin
5192754 Fish stress resistance method March 9, 1993
A method of relieving stress in fish and increasing resistance to pathogenic agents comprising orally administering to the fish an amount of a compound of the formula ##STR1## wherein R is alkyl of 1 to 4 carbon atoms and X is acyl of an organic carboxylic acid of 1 to 18 carbon
5190974 N-substituted derivatives of .alpha.-mercapto alkylamines, their preparation process and the int March 2, 1993
Novel .alpha.-mercapto-alkylamines in all possible racemic, enantiomeric and diastereoisomeric forms of the formula ##STR1## wherein n, R.sub.1, R.sub.2, X, A, R.sub.3A and R.sub.4A are set forth in the claims and their non-toxic, pharmaceutically acceptable acid addition salts h
5189065 Use of derivatives of 9,10-dihydrophenanthrene for the preparation of an anti-tumor medicament February 23, 1993
The use of products of formula (I) is described, wherein X and Y represent hydrogen, hydroxy or alkoxy; and R.sub.1 and R.sub.2 represent H, alkyl, alkenyl or alkynyl, arylalkyl, acyl or R.sub.1 and R.sub.2 together with nitrogen form a heterocycle for preparing an antitumoral drug.
5189021 Method of treating precocious puberty February 23, 1993
A novel method of treating prostate adenocarcinoma, prostate benign hypertrophia, endometriosis, dysmenorrhea, hirsiutism, hormono-dependant mammary tumors, treatment and prevention of precociuos puberty, induction of a retardation of the appearance of puberty and treatment of acne of
5187273 .DELTA..sup.4,9(11),17(20) -pregnatriene-3-ones February 16, 1993
A compound of the formula ##STR1## wherein Hal is chlorine or bromine, R is selected from the group consisting of alkyl of 1 to 6 carbon atoms, aralkyl of 7 to 15 carbon atoms and a silylated group, K is a protective group selected from the group consisting of ##STR2## n
5183896 Derivatives of 1,2,5,6-tetrahydropyridin-3-carboxaldehyde oxime February 2, 1993
Compounds of the formula ##STR1## which have a long-lasting cholinomimetic activity by oral route. Also disclosed are methods for preparing the compounds and pharmaceutical compositions containing the compounds.
5183893 1-azabicycloalkane derivatives, their preparation process and their use as medicaments February 2, 1993
Compounds useful in the treatment of Alzheimer's disease, senile dementia or memory disorders of the aged of the formula ##STR1## in which n represents the number 1, 2 or 3,R.sub.1 and R.sub.2, identical or different, represent hydrogen, a linear, branched or cyclic alkyl, alkenyl, o
5182378 Sulfate derivatives of galactan extracted from Klebsiella January 26, 1993
A sulfate derivative of galactan extracted from Klebsiella mainly comprised of sulfate neutral oses in a proportion of 20 to 90% of hydroxyls and their preparation and method of use.
5182300 Furosemide salts January 26, 1993
Compounds of the formula ##STR1## wherein AA is a basic amino acid in optically active or racemic form having better bio-availability and a method of treating asthma.
5182295 Insecticidal benzofuran derivatives January 26, 1993
A compound of the formula ##STR1## wherein R is selected from the group consisting of hydrogen, optionally substituted alkyl, alkenyl and alkynyl of up to 8 carbon atoms, optionally substituted cycloalkyl or cycloalkenyl of up to 8 carbon atoms, optionally substituted aryl of 6 t
5182282 4-Benzyl-1H-indole derivatives January 26, 1993
Novel 4-benzyl-1H-indoles of the formula ##STR1## in all diastereoisomeric forms and mixtures thereof having anti-arhythmic activity.
5180741 Pyrethrinoid esters carrying an indanyl nucleus and their use as pesticides January 19, 1993
Pyrenthrinoid esters with an indenyl nucleus having the following structural formula ##STR1## wherein the substituents are herein defined, have been shown to be useful as pesticides and in pesticidal compositions.
5180737 Phenyl or bicyclo-alkenylfluoro amide pesticides January 19, 1993
Compound of the formula (I):or a salt thereof, wherein Q.sup.1 is a phenyl ring or a fused bicyclic ring system containing 9 or 10 ring carbon atoms at least one ring being aromatic, or Q.sup.1 is a dihalovinyl group; Q is an alkyl chain containing 1 to 12 carbon atoms and optionally con
5177098 Pesticidal compositions January 5, 1993
A pesticidal composition comprising at least one pyrethrinoid and a synergistically effective amount of at least one fungicide compound selected from the group consisting of azoles and morpholines, especially useful against insects and parasitic plant and animal acaridae.
5173483 Ovulation stimulating method December 22, 1992
A method of stimulating ovulation in warm-blooded animals comprising administering to warm-blooded animals an ovulation stimulating effective amount of at least one anti-progestomimetic compound.
5166358 Process for 1-phenyl-imidazoline-2,5-diones November 24, 1992
A process for the preparation of a compound of the formula ##STR1## wherein R.sub.1, R.sub.2 and R.sub.3 are individually selected from the group consisting of hydrogen, alkyl and alkoxy of 1 to 7 carbon atoms, alkenyl, alkynyl, alkenyloxy and alkynyloxy of 2 to 7 carbon atoms, p
5166167 .alpha.-Methylene-4-(phenoxymethyl)-5-thiazolacetate November 24, 1992
A compound of the formula ##STR1## wherein Ar is phenyl optionally substituted with at least one member of the group consisting of halogen, methylenedioxy, phenoxy, phenyl, --CF.sub.3 and alkyl, alkoxy and alkylthio of 1 to 6 carbon atoms, Z is selected from the group consisting
5166146 Amino acid cyclopentanophenonthrene compounds November 24, 1992
A compound of the formula ##STR1## wherein R.sub.1 is an aliphatic hydrocarbon of 1 to 8 carbon atoms, R.sub.a and R.sub.b are individually hydrogen or alkyl of 1 to 4 carbon atoms, R.sub.2 is hydrogen or optionally substituted alkyl of 1 to 12 carbon atoms, n is an integer from
5164514 Derivatives of 1-arylsulphonyl-2-pyrolidinone November 17, 1992
Compounds useful for the treatment of patients suffering from muscle spasms of the formula (I) ##STR1## in which R represents the radical ##STR2## in which R.sub.1, in any position on the phenyl nucleus, represents a linear, branched or cyclic alkyl, alkenyl or alkynyl, conta
5164409 Pyrroles possessing insecticidal activity November 17, 1992
All possible stereoisomers and mixtures of a compound of the formula ##STR1## wherein X and Y are different and are selected from the group consisting of hydrogen, halogen, --CN, alkyl and haloalkyl of 1 to 8 carbon atoms and phenyl optionally substituted by at least one member of th
5159070 Process for the preparation of derivative of 7-[(2-hydroxyimino)-acetamido]-cephalosporanic acid October 27, 1992
A novel process for the preparation of syn isomers of cephalosporanic acid derivatives of the formula ##STR1## comprising reacting first in a solvent and optionally in the presence of a base, a compound of the formula ##STR2## with a compound of the formulawherein R.sub.4 is
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