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Class 514/408 - The five-membered hetero ring consists of one nitrogen and four carbons


Subclass of Class 514 - Drug, bio-affecting and body treating compositions
Definition: Subject matter wherein the five-membered hetero ring consists
No. of applications: 521
Last issue date: 05/24/2012


1                      
Application No.Application TitleIssue Date
20120129860STYRENYL DERIVATIVE COMPOUNDS FOR TREATING OPHTHALMIC DISEASES AND DISORDERS
The present invention relates generally to compositions and methods for treating neurodegenerative diseases and disorders, particularly ophthalmic diseases and disorders. Provided herein are styrenyl derivative compounds, including but not limited to stilbene derivative...
05/24/2012
20120129906MODULATORS OF S1P RECEPTORS
The present invention relates to novel diphenylethyne derivatives, processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals as modulators of sphingosine-1-phosphate receptors....
05/24/2012
20120046291Extended Triterpene Derivatives
The present invention concerns novel pharmaceutically active triterpene derivatives, pharmaceutical compositions containing the same, their use as medicaments, and the use of the compounds for the manufacture of specific medicaments. The present invention also concerns ...
02/23/2012
20120035154Modulators of Cellular Adhesion
The present invention provides compounds having formula (I):

and pharmaceutically acceptable derivatives thereof, wherein R1-R4, n, p, A, B, D, E, L and AR1 are as described g...

02/09/2012
20120027700SKIN CARE COMPOSITIONS COMPRISING SUBSTITUTED DIAMINES
Skin care compositions comprising certain substituted diamines, which are particularly beneficial for skin lightening and achieving evenness of color, especially for face and underarm skin....
02/02/2012
20120022039NOVEL SUBSTITUTED INDANES, METHOD FOR THE PRODUCTION THEREOF, AND USE THEREOF AS DRUGS
The invention relates to substituted indanes and derivatives thereof, to physiologically acceptable salts and physiologically functional derivatives thereof, to the production thereof, to drugs containing at least one substituted indane according to the invention or der...
01/26/2012
20110294767BILE ACID RECYCLING INHIBITORS AND SATIOGENS FOR TREATMENT OF DIABETES, OBESITY, AND INFLAMMATORY GASTROINTESTINAL CONDITIONS
Provided herein are methods of utilizing bile acid transport inhibitors and/or enteroendocrine peptide enhancing agents for the treatment of obesity, diabetes, and inflammatory gastrointestinal conditions....
12/01/2011
20110245244PHENOXY ACETIC ACIDS AS PPAR DELTA ACTIVATORS
Novel compounds of the general formula (I), the use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds and methods of treatment employing these compounds and compositions. The present compounds are activators of PPARÎ...
10/06/2011
20110237538TREATMENT OF LYSOSOMAL STORAGE DISORDERS AND OTHER PROTEOSTATIC DISEASES
Described are various compounds, in particular iminosugars, and methods for the treatment of proteostatic diseases, in particular lysosomal storage disorders. The compound may be a pharmacoperone of an enzyme selected from: (a) Acid alpha-glucosidase; (b) Acid beta-gluc...
09/29/2011
20110172258INDENE DERIVATIVES AS PHARMACEUTICAL AGENTS
Compounds of formula (Ia):

    • wherein R1, R2, R3, R4a...
07/14/2011
20110117219HAIR TREATMENT PRODUCT AND HAIR AFTER-TREATMENT PRODUCT CONTAINING ETHER GUANIDINES AS ACTIVE SUBSTANCES, FOR PROTECTING FROM DAMAGE CAUSED BY CHEMICAL TREATMENT AND FOR REPAIRING ALREADY DAMAGED HAIR
The invention relates to ether guanidines of the general formulae (I)

and/or salts or hydrates thereof, in which R1=—CH2—CH2—CH2—O—R3 where R

05/19/2011
20110111068Inhibitors of cognitive decline
Compounds that are central nervous system drug candidates for the treatment of cognitive decline and, more particularly, Alzheimer's disease are provided. Methods of treating, inhibiting, and/or abatement of cognitive decline and Alzheimer's disease with a derivative of...
05/12/2011
20110098309METHODS OF INHIBITING THE FORMATION OF AMYLOID-BETA DIFFUSABLE LIGANDS USING ACYLHYDRAZIDE COMPOUNDS
Disclosed are methods of inhibiting, regulating, and/or modulating the formation of soluble, globular, non-fibrillar, neurotoxic amyloid β1-42 oligomers from amyloid β1-42 monomers using acylhydrazide compounds. Also disclosed are methods of treating a patient sufferi...
04/28/2011
20110071202ANTI-HEPATITIS C VIRUS AGENTS AND ANTI-HIV AGENTS
An anti-hepatitis C virus agent or anti-HIV agent comprising, as an active ingredient, a fullerene derivative which has a nitrogen atom forming a ring together with adjacent bonded carbon atom pairs constituting the carbon cluster skeleton of the fullerene or a quaterna...
03/24/2011
20100292279Bis-(Sulfonylamino) Derivatives in Therapy
The invention provides compounds of formula

wherein R1, R2, R3, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceu...

11/18/2010
20100291069METHODS OF TREATING A DIABETIC EMBRYOPATHY
Maternal diabetes can lead to a developmental malformation of an embryo. A developmental malformation caused by maternal diabetes is commonly referred to as a diabetic embryopathy. There is currently no effective treatment for reducing or inhibiting a diabetic embryopat...
11/18/2010
20100292288CRYSTALLINE FORMS OF (R)-1-{2-[4`- (3-METHOXY-PROPANE-1- SULFONYL)-BIPHENYL-4-YL]-ETHYL}-2-METHYL-PYRROLIDINE, AND COMPOSITIONS, AND METHODS RELATED THERETO
The present invention is directed to novel salts of (R)-1-{2-[4′-(3-methoxy-propane-1-sulfonyl)-biphenyl-4-yl]-ethyl}-2-methyl-pyrrolidine, and crystalline forms, and compositions thereof that modulate the activity of the histamine H3-receptor and are useful in the tr...
11/18/2010
20100273778TREATMENT OF OSTEOARTHRITIS PAIN
This invention discloses a method of treatment of osteoarthritis pain by administration of a histamine H3 receptor antagonist, described herein, a salt thereof, or a composition comprising such compound or salt....
10/28/2010
20100267690TRICYCLIC GUANIDINE DERIVATIVES AS SODIUM-PROTON EXCHANGE INHIBITORS
Guanidine derivatives having a condensed tricyclic ring of formula 1:

are disclosed, wherein U is C(O), CRaRb, O, NRa or S(O)m; V is CRaRb or ...

10/21/2010
20100260671COMPOUNDS AND METHODS FOR THE DIAGNOSIS AND TREATMENT OF AMYLOID ASSOCIATED DISEASES
The invention is in general directed to compounds, such as tannic acid, nicotine, nicotine derivatives and pyrrolid derivatives of nicotine, and methods for diagnosing, preventing or alleviating the symptoms of amyloid-associated diseases, for example, neuronal diseases...
10/14/2010
20100256213Tosylate Salt Of Trans-N-Isobutyl-3-Fluoro-3- [3-Fluoro-4-(Pyrrolidin-1-YL-Methyl)-Phenyl] Cyclobut Anecarboxamide
The present invention is directed to the tosylate salt of trans-N-isobutyl-3-fluoro-3-[3-fluoro-4-(pyrrolidin-1-ylmethyl)-phenyl]-cyclobutanecarboxamide Formula (I):

to solvates (e.g., hydrates) thereof, to p...

10/07/2010
20100256214EPH RECEPTOR LIGANDS AND METHODS OF USE
Disclosed are methods and compositions relating to binder, modulators and inhibitors of EphA4 and EphA2....
10/07/2010
20100240653BIPHENYL SULFONYL AND PHENYL-HETEROARYL SULFONYL MODULATORS OF THE HISTAMINE H3-RECEPTOR USEFUL FOR THE TREATMENT OF DISORDERS RELATED THERETO
The present invention relates to certain biphenyl sulfonamide derivatives of Formula (Ia) and pharmaceutical compositions thereof that modulate the activity of the histamine H3-receptor. Compounds of the present invention and pharmaceutical compositions thereof are dire...
09/23/2010
20100222406T Type Calcium Channel Blockers and the Treatment of Diseases
The present invention provides a method for treating a disease or condition in a mammal associated with influx of extracellular calcium via T type calcium channels, which comprises administering to the mammal a therapeutically effective amount of a T type calcium channe...
09/02/2010
20100210630Diamine Derivatives as Inhibitors of Leukotriene A4 Hydrolase
This invention is directed to compounds of formula (I):

where r, q, R, R2, R3, R4, R5a, R5b, R5c, R6a, R6b, R6c

08/19/2010
20100204294Methods For Assessing, Improving, Or Maintaining Urogenital Health in Postmenopausal Woman
This invention relates to methods and kits useful for improving or maintaining urogenital health using an estrogen agonist/antagonist. The methods of treatment are effective for improving or maintaining urogenital health while substantially reducing the concomitant liab...
08/12/2010
20100197640NOVEL SULFAMOYL-PHENYL-UREIDO COMPOUNDS AND THEIR USE AS MEDICAMENT
The present invention relates to novel sulfamoyl-phenyl-ureido compounds having the formula (I) or a physiologically acceptable salt or derivative thereof which are suitable for the therapy of infections caused by protozoa and in particular uncomplicated or severe malar...
08/05/2010
20100158818ANTIMICROBIAL N-CHLORINATED COMPOSITIONS
The present application relates to N-chlorinated cationic compounds of Formula I

or a salt thereof, and associated compositions and methods of use as antimicrobial agents....

06/24/2010
20100152220INDENE DERIVATIVES AS PHARMACEUTICAL AGENTS
Compounds of formula (Ia):

    • wherein R1, R2, R3, R4a...
06/17/2010
20100152179TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS
A method for treating a patient suffering from disorders and deficits of the central nervous system associated with diabetes, associated with aging and neurodegeneration, comprising attention deficit disorder in general, attention deficit hyperactivity disorder (ADHD), ...
06/17/2010
20100130472BILE ACID RECYCLING INHIBITORS FOR TREATMENT OF OBESITY AND DIABETES
Provided herein are methods of utilizing bile acid transport inhibitors for the treatment of obesity and diabetes....
05/27/2010
201001206154-CYCLOALKYL OR 4-SUBSTITUTED PHENOXYPHENYLAMIDINES AND USE THEREOF AS FUNGICIDES
The present invention relates to 4-cycloalkyl- or 4-aryl-substituted phenoxyphenylamidines of the general formula (I), to a process for their preparation, to the use of the amidines according to the invention for controlling unwanted microorganisms and also to a composi...
05/13/2010
20100105753Inhibitors of Fibroblast Activation Protein, and Methods of Use Thereof
One aspect of the present invention relates to synthetic peptide derivatives that inhibit fibroblast activation protein α (FAP) activity. Another aspect of the invention relates to methods for treating a mammal suffering from cancer by administering a therapeutically e...
04/29/2010
20100093672USE OF S1P RECEPTOR MODULATOR
Use of an S1P receptor modulator in the treatment or prevention of a disease or condition dependent on brain-derived neurotrophic factor (BDNF) expression....
04/15/2010
20100093673PAIN RELIEVING PATCH
Described here are patches for the treatment of pain. The patches include a carrier material, which itself, in the absence of an active agent, is capable of relieving pain. Methods of treating pain using the patches are also described....
04/15/2010
20100076036HETEROCYCLYL-SUBSTITUTED SULFONAMIDES FOR THE TREATMENT OF COGNITIVE OR FOOD INGESTION RELATED DISORDERS
The present invention relates to heterocyclyl-substituted sulfonamides with 5-HT6 receptor affinity, and compositions thereof, and the use of said compounds for the treatment or prophylaxis of various disorders....
03/25/2010
201000760342-ARYL-2-FLUOROPROPANOIC ACIDS AND DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
The present invention relates to (R,S) 2-aryl-2-fluoropropanoic acids, their single enantiomers (R) and (S), their derivatives amides and acylsulfonamides and to pharmaceutical compositions containing them, which are used in the prevention and treatment of tissue damage...
03/25/2010
20100076024Novel Compounds as Serine Protease Inhibitors
The invention relates to compounds of formula (I) wherein the substituents are as defined in claim 1; to compositions comprising said compounds and to their use as pharmaceutical agents, in particular as inhibitors of serine proteases.

03/25/2010

20100063090Composition for Repelling and Deterring Vermin
The invention describes essentially a non-therapeutical process for deterring vermin, which is based on the usage of the largely known beta amino-alcohol derivatives of formula (I), as defined herein before. Furthermore, it describes the corresponding vermin-deterring c...
03/11/2010
20100063135POLYETHYLENE GLYCOL LIPID CONJUGATES AND USES THEREOF
Polyethylene glycol (PEG)-lipid conjugates, polyethylene glycol (PEG)-lipid conjugate based drug delivery systems, ways to make them and methods of treating diseases using them are disclosed....
03/11/2010
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