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American Home Products, Corp. Patents
Assignee:
American Home Products, Corp.
Address:
New York, NY
No. of patents:
84
Patents:


1 2


Patent Number Title Of Patent Date Issued
D275788 Diagnostic test device October 2, 1984
D269949 Container for a liquid or a gel August 2, 1983
D260607 Container for liquid September 8, 1981
D259662 Tourniquet and vein delineator June 23, 1981
D257171 Combined electric shocking device for personal protection and guard therefor or the like September 30, 1980
D257126 Pharmaceutical dispensing container or the like September 30, 1980
D254477 Combined bottle and squeegee March 18, 1980
D253127 Necropsy board for small animals October 9, 1979
D253126 Necropsy board for small animals October 9, 1979
D252106 Necropsy board for large animals June 12, 1979
D252105 Necropsy board for large animals June 12, 1979
D249641 Dispensing container or the like September 26, 1978
D249157 Deodorant container or the like August 29, 1978
6787319 .beta.-amyloid peptide-binding proteins and polynucleotides encoding the same September 7, 2004
Novel proteins which bind human .beta.-amyloid peptide, polynucleotides which encode these proteins, and methods for producing these proteins are provided. Diagnostic, therapeutic, and screening methods employing the polynucleotides and polypeptides of the present invention are also
6559127 Compounds which inhibit leukocyte adhesion mediated by VLA-4 May 6, 2003
Disclosed are compounds which bind VLA-4. Certain of these compounds also inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such compounds are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, such as asthma, Alzheime
6492421 Substituted phenylalanine type compounds which inhibit leukocyte adhesion mediated by VLA-4 December 10, 2002
Disclosed are compounds which bind VLA-4. Certain of these compounds aslo inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such compounds are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, such as asthma, Alzheime
6423688 Dipeptide and related compounds which inhibit leukocyte adhesion mediated by VLA-4 July 23, 2002
Disclosed are compounds which bind VLA-4. Certain of these compounds aslo inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such compounds are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, such as asthma, Alzheime
6403617 Diaminopyridine-containing thiourea inhibitors of herpes viruses June 11, 2002
Compounds of the formula ##STR1##Useful in the treatment of diseases associated with herpes viruses including human cytomegalovirus, herpes simplex viruses, Epstein-Barr virus, varicella-zoster virus, humanherpesviruses-6 and -7, and Kaposi herpesvirus.
6369197 Potassium channel interactors and uses therefor April 9, 2002
The invention provides isolated nucleic acids molecules, designated PCIP nucleic acid molecules, which encode proteins that bind potassium channels and modulate potassium channel mediated activities. The invention also provides antisense nucleic acid molecules, recombinant expression vec
6333167 Methods and reagents for identifying inhibitors of proteolysis of membrane-associated proteins December 25, 2001
The present disclosure provides DNA constructs, genetically modified host cells and methods for identifying inhibitors of proteolysis of membrane-associated protease substrates including, but not limited to, amyloid precursor protein, a Notch protein and sterol response element bindi
6313126 Arylpiperazinyl-cyclohexyl indole derivatives for the treatment of depression November 6, 2001
Compounds are provided which are useful for the treatment of serotonin-affected neurological disorders which comprise ##STR1##Wherein:R.sub.1, R.sub.2 and R.sub.3 are each, independently, hydrogen, halogen, CF.sub.3, alkyl, alkoxy, MeSO.sub.2, or together can form a 5-7 membered carb
6313114 3,4-Dihydro-2H-benzo[1,4]oxazinyl-methyl)-[3-(1H-indol-3yl)-alkyl]- amines November 6, 2001
Compounds are provided which have the following formula: ##STR1##wherein:R is hydrogen, alkyl of 1 to 6 carbon atoms, phenyl, or substituted phenyl;X and Y are each, independently, hydrogen, halogen, cyano, or alkoxy of 1 to 6 carbon atoms; andm is 1 to 5; ora pharmaceutically acceptable sal
6310066 Antipsychotic indolyl derivatives October 30, 2001
The present invention provides novel compounds of the general formula: ##STR1##wherein R.sub.1 and R.sub.2 are H, OH, F, Cl, Br, I, 1 to 6 carbon alkyl or alkenyl, 1 to 6 carbon alkoxy, aryl, OR.sub.5, nitro, amino, CF.sub.3 or R.sub.1 and R.sub.2 are taken together to form a fused ring
6291683 N-arloxyethyl-alkylamines for the treatment of depression September 18, 2001
Compounds useful for alleviating symptoms of depression are provided which have the following formula: ##STR1##wherein:R.sub.1 is hydrogen, lower alkyl or aryl;R.sub.2 is hydrogen, lower alkyl, phenyl or substituted phenyl;X and Y are each, independently, hydrogen, lower alkyl, lower alkoxy,
6291453 4-amino-phenylalanine type compounds which inhibit leukocyte adhesion mediated by VLA-4 September 18, 2001
Disclosed are compounds which bind VLA-4. Certain of these compounds also inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such compounds are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, such as asthma, Alzheime
6291434 Benzylmaltotriosides as inhibitors of smooth muscle cell proliferation September 18, 2001
This invention provides smooth muscle cell proliferation inhibitors of formula I having the structure ##STR1##whereinX is ##STR2##R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.9 and R.sup.10, are each, independently, hydrogen, acyl of 2-7 carbon at
6258784 Acetal benzylmaltosides as inhibitors of smooth muscle cell proliferation July 10, 2001
This invention provides smooth muscle cell proliferation inhibitors of formula I having the structure ##STR1##whereinW is S, SO, SO.sub.2, NR;Y is O, S, NR, or CH.sub.2 ;R is hydrogen or alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, acyl of 2-7 carbon atoms, perfluoroacy
6245799 [(Indol-3-yl)-cycloalkyl]-3-substituted azetidines for the treatment of central nervous system d June 12, 2001
This invention provides novel compounds and pharmaceutical compositions and methods of using the compounds in the treatment of central nervous system disorders, such as anxiety and depression, the compounds having the formula I: ##STR1##wherein:X is N--R, O, S(O).sub.m ; m is 0 to 2;
6245780 Tetrahydroisoquinolinyl-indole derivatives for the treatment of depression June 12, 2001
Compounds are provided which have the formula: ##STR1##wherein:R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are, independently, hydrogen, halogen, alkoxy, or carboxamide;R.sub.5 is hydrogen, halogen, CF.sub.3, CN, carbamide or alkoxy; andX is (CH.sub.2).sub.n or a 4-6 membered carbocyclic ring, wh
6239134 Diazole derivatives as serotonergic agents May 29, 2001
The present invention provides compounds of the general formula (1): ##STR1##wherein:two atoms of X, Y, or Z are nitrogen and the third atom is sulfur or oxygen;R is H, halogen, OH, SH, C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, C.sub.1 -C.sub.6 thioalkyl, phenoxy, thiophenoxy, phe
6228880 4-amino-(ethylamino)-oxindole dopamine autoreceptor agonists May 8, 2001
Compounds having dopaminegic activity are provided, having the formula: ##STR1##wherein R.sup.1 and R.sup.2 are each, independently, hydrogen, C.sub.1-10 alkyl, or (CH.sub.2).sub.m R.sup.4, wherein R.sup.4 is phenyl or naphthyl which may be substituted by one or two substituents selected
6221863 3,4-dihydro-2H-benzo[1,4]oxazine derivatives April 24, 2001
Compounds are provided having the following formula: ##STR1##wherein:R.sub.1 is hydrogen or halogen;R.sub.2 is hydrogen, alkoxy or carboximide;R.sub.3 is hydrogen, alkyl, alkylaryl, aryl or substituted aryl;R.sub.4 is hydrogen, CN, halogen, or carboximide; andX is CH or N; or pharmaceutically ac
6200994 1,4-Disubstituted cyclohexane derivatives for the treatment of depression March 13, 2001
Compounds useful for the treatment of disorders of the serotonin-affected neurological systems are provided which have the following formula: ##STR1##wherein:X is carbon or nitrogen;R.sub.1 and R.sub.2 are each, independently, hydrogen, halogen, CF.sub.3, alkyl, alkoxy, or MeSO2.sub.4 ;R
6168918 Method of detecting foreign DNA integrated in eukaryotic chromosomes January 2, 2001
Methods of detecting the presence of a plasmid DNA sequence integrated in a chromosomal DNA molecule of a eukaryotic cell in a sample that contains chromosomal DNA molecules of eukaryotic cells and free plasmid DNA molecules are disclosed. According to the invention, chromosomal DNA of
6162803 Indol-3-yl-cyclohexyl amine derivatives for the treatment of depression December 19, 2000
Compounds effective in treating disorders of the serotonin-affected neurological symptoms are provided, such compounds having the following formula: ##STR1## wherein: R.sub.1 and R.sub.5 are each, independently, hydrogen, halogen, lower alkoxy, lower alkyl, cyano, or trifluoromet
6150533 N-aryloxyethyl-indoly-alkylamines for the treatment of depression November 21, 2000
Compounds effective in treating disorders of the serotonin-affected neurological systems are provided, such compounds having the following formula: ##STR1## wherein: R.sub.1 is hydrogen, lower alkyl, phenyl, or substituted phenyl;X and Y together complete a lactam, imidazole, imidazo
6140485 Nucleic acid encoding human neuronal calcium channel subunits October 31, 2000
Nucleic acids encoding each of three subunits, .alpha.1B, .alpha.2.delta., and .beta.3, of a calcium channel, are disclosed. Also disclosed are vectors containing the nucleic acids encoding the subunits; host cells containing the nucleic acids encoding the subunits; methods of isolating
6121307 N-aryloxyethyl-indoly-alkylamines for the treatment of depression September 19, 2000
Compounds useful for alleviating symptoms of depression are provided which have the following formula: wherein:R.sub.1 is hydrogen, lower alkyl or aryl;R.sub.2 is hydrogen, lower alkyl, phenyl or substituted phenyl;X and Y are each, independently, hydrogen, lower alkyl, lower alkoxy, or halo
6110956 N-aryloxyethylamine derivatives for the treatment of depression August 29, 2000
Compounds effective in treating disorders of the serotonin-affected neurological systems are provided, such compounds having the following formula: ##STR1## wherein: R.sub.1 and R.sub.2 are each, independently, hydrogen, halogen, CF.sub.3, lower alkyl, lower alkoxy, MeSO.sub.2, o
6049006 Elevation of HDL cholesterol by N-[2-[(aminothioxomethyl) hydrazono]-2-arylethyl]amides April 11, 2000
This invention relates to the treatment of atherosclerosis via raising the level of HDL cholesterol by administration of a compound of the formula ##STR1## wherein: R.sup.1, R.sup.2, and R.sup.3 are independently hydrogen, C.sub.1 -C.sub.6 alkyl or --(CH.sub.2).sub.0-6 Ph where Ph is
5610154 Bicyclic carboxamides March 11, 1997
Bicyclic carboxamides of formula I ##STR1## and the pharmaceutically acceptable acid addition salts are 5-HT.sub.1A binding agents, particularly 5-HT.sub.1A antagonists and may be used, for example, as anxiolytics. In the formulaX represents --CR.sup.2 .dbd.CR.sup.2 -- or --(CR.sup.2
5221745 Psychotropic piperidinylmethyl benzodioxans June 22, 1993
The compounds ##STR1## in which Z is ##STR2## where R.sup.4 is -H or alkyl; q is one of the integers 0, 1 or 2; Y is H.sub.2 or O; or Z, taken with R.sup.1 forms ##STR3## R.sup.1 is hydrogen or alkyl or combined with Z as described above; R.sup.2 and R.sup.3 are, ind
5010102 Anti-ulcer 5-(2-substituted ethenyl)-3(2H)-furanones April 23, 1991
A compound of the formula: ##STR1## in which R is alkyl, phenyl or halophenyl; R.sup.2 is substituted phenyl having from 1 to 3 substiuents selected from halo, alkyl, alkylthio, alkylsulfonyl, cyano, trifluoromethyl, or R.sup.2 is pyridinyl, pyrazinyl, quinolinyl, N-alkylpyrrolyl
4988814 Tertiary alkyl functionalized piperazine derivatives January 29, 1991
Compounds of the formula: ##STR1## in which R.sup.1 is alkyl; R.sup.2 and R.sup.3 are alkyl or taken together they are polymethylene, R.sup.2 and R.sup.3 complete a 5-norbornen-2-yl moiety; X is --CO.sub.2 --, --OCO--, --OCO.sub.2 --, --N(R.sup.7)CO--, --NHNHCO--, --ON(R.sup.7)CO
4957913 Antihypertensive polycyclic imides September 18, 1990
Hypertension in the mammal is controlable by administration of a compound of the formula: ##STR1## wherein R is ##STR2## in which X is methylene, ethylene or ethylidene and Q is alkylene, alkylidene, or Q is a ##STR3## in which the dotted line represents optional uns
4955481 Tablet package having alternative indicators and method of use September 11, 1990
Packaging for a course of tablets comprises a base for a blister pack and a cover flap. Rub-off indicators are provided on the inner surface of the flap to permit indication of one of a range of alternatives related to the course. The indicators may be color keyed to particular doses of
4933184 Menthol enhancement of transdermal drug delivery June 12, 1990
Disclosed herein are compositions and methods for enhancing the transdermal delivery of physiologically active agents across mammalian skin or membranes and which comprise a percutaneous transfer enhancing amount of menthol and a drug.
4931283 Menthol enhancement of transdermal drug delivery June 5, 1990
Disclosed herein are compositions and methods for enhancing the transdermal delivery of physiologically active agents across mammalian skin or membranes and which comprise a percutaneous transfer enhancing amount of menthol and a drug.
4904799 Preparation of tryptophols February 27, 1990
Indole derivatives characterized by having a 1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid nucleus bearing a substituent in position 1-, 4-, 5-, 6-, 7- and 8- are disclosed. The derivatives are useful anti-inflammatory and analgesic agents and methods for their preparation and
4900739 Novel spirosuccinimides as aldose reductase inhibitors and antihyperglycemic agents February 13, 1990
This invention relates to novel spirosuccinimide derivatives, to the processes for their preparation, to methods for using the compounds, and to pharmaceutical preparations thereof. The compounds have pharmaceutical properties which render them beneficial for the treatment of diabetes
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