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Patent No. 6637447

Beerbrella

A small umbrella which may be removably attached to a beverage container in order to shade the beverage container from the direct rays of the sun.

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Class 544/230 - Spiro


Subclass of Class 544 - Organic compounds -- part of the class 532-570 series
Definition: Compounds which contain a spiro ring system.
No. of applications: 282
Last issue date: 05/03/2012


1                
Application No.Application TitleIssue Date
20120108602Carbamoyl Compounds as DGAT1 Inhibitors 190
DGAT-1 inhibitor compounds of formula (1), pharmaceutically-acceptable salts and pro-drugs thereof are described, together with pharmaceutical compositions, processes for making them and their use in treating, for example, obesity

    05/03/2012
20120083488TETRACYCLIC COMPOUND
A compound represented by the general Formula (I) below, or a salt or solvate thereof, which is useful as an ALK inhibitor, and is useful for prophylaxis or treatment of a disease accompanied by abnormality in ALK, for example, cancer, cancer metastasis, depression or c...
04/05/2012
20120083501COMPOUNDS FOR TREATING NEURODEGENERATIVE DISEASES
The invention provides novel tricyclic compounds of Formula I′ that inhibit β-secretase cleavage of APP and are useful as therapeutic agents for treating neurodegenerative diseases.

...

04/05/2012
20120083476HETEROARYL-SUBSTITUTED SPIROCYCLIC DIAMINE UREA MODULATORS OF FATTY ACID AMIDE HYDROLASE
Certain heteroaryl-substituted spirocyclic diamine urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty a...
04/05/2012
20120071479PYRAZINE DERIVATIVES AS ENAC BLOCKERS
Compounds of Formula I:

and pharmaceutically acceptable salts and solvates thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8

03/22/2012
20120053164CYCLIC PYRIMIDIN-4-CARBOXAMIDES AS CCR2 RECEPTOR ANTAGONISTS FOR TREATMENT OF INFLAMMATION, ASTHMA AND COPD
The present invention relates to novel antagonists for CCR2 (CC chemokine receptor 2) and their use for providing medicaments for treating conditions and diseases, especially pulmonary diseases like asthma and COPD. Formula (I), wherein A is selected from among a single...
03/01/2012
20120052096NOVEL DIOXO-IMIDAZOLIDINE DERIVATIVES, WHICH INHIBIT THE ENZYME SOAT-1, AND PHARMACEUTICAL AND COSMETIC COMPOSITIONS CONTAINING THEM
SOAT-1 inhibitors of general formula (I)

and cosmetic and pharmaceutical compositions containing such a compound are described....

03/01/2012
20120046277BENZOFURAN DERIVATIVES
The present invention provides a compound represented by the following formula (I): wherein: Ring A represents an optionally substituted piperazine ring, an optionally substituted morpholine ring, or an optionally substituted bromopiperazine ring; R1 and R
02/23/2012
20120046304TRICYCLIC PYRIDINE DERIVATIVES, MEDICAMENTS CONTAINING SUCH COMPOUNDS, THEIR USE AND PROCESS FOR THEIR PREPARATION
The present invention relates to compounds defined by formula I

wherein the variables R1-R8 are defined as in the description, possessing valuable pharmacological activity. Particularly,...

02/23/2012
20120046306Substituted Heteroaryl Spiropyrrolidine MDM2 Antagonists
There are provided compounds of the general formula

wherein A, B, V, W, R1, R2, R3, R3, and R4, are as described herein and enantiomers and pharmaceutica...

02/23/2012
20120041012SUBSTITUTED SPIROCYCLIC AMINES USEFUL AS ANTIDIABETIC COMPOUNDS
Substituted spirocyclic amines of structural formula I are selective antagonists of the somatostatin sub-type receptor 5 (SSTR5) and are useful for the treatment, control or prevention of disorders responsive to antagonism of SSTR5, such as Type 2 diabetes, insulin resi...
02/16/2012
20120040020COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE
The present disclosure relates to pyrazine compounds of formula I:

wherein L, n, R1, and R2 are as described in the specification. These compounds are useful as inhibitors of ATR protein...

02/16/2012
20120040968DIAMINO HETEROCYCLIC CARBOXAMIDE COMPOUND
Provided is a compound useful as an inhibitor against the kinase activity of EML4-ALK fusion protein.

As a result of intensive and extensive studies on compounds having inhibitory activity against the kinase activity of EML4-ALK fusion prot...

02/16/2012
20120040975BRIDGED BICYCLIC HETEROCYCLE DERIVATIVES AND METHODS OF USE THEREOF
The present invention relates to Bridged Bicyclic Heterocycle Derivatives, compositions comprising a Bridged Bicyclic Heterocycle Derivative, and methods of using the Bridged Bicyclic Heterocycle Derivatives for treating or preventing obesity, diabetes, a metabolic diso...
02/16/2012
20120041011SUBSTITUTED BENZOFUSED DERIVATIVES AND THEIR USE AS VANILLOID RECEPTOR LIGANDS
The present invention relates to substituted benzofused derivatives, which can he used as vanilloid receptor ligands, method of treating diseases, conditions and/or disorders modulated by vanilloid receptors with them, and processes for preparing them....
02/16/2012
20120035189Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands
The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous sy...
02/09/2012
20120028954Substituted Pyridine, Pyridazine, Pyrazine And Pyrimidine Compounds And Methods For Using The Same
Disclosed are substituted pyridine compounds as well as pharmaceutical compositions and methods of use. One embodiment is a compound having the structure

wherein E, J, T, the ring system denoted by “B”, T...

02/02/2012
201200289585-ALKYNYL-PYRIMIDINES
The present invention encompasses compounds of general formula (1)

wherein

R1 to R4 R3 are defined as in claim 1, which are suitable for the trea...

02/02/2012
201200289525-ALKYNYL-PYRIMIDINES
The present invention encompasses compounds of general formula (1)

    • wherein
    • ...
02/02/2012
20120021976BICYCLIC PIPERIDINE AND PIPERAZINE DERIVATIVES AS GPCR MODULATORS FOR THE TREATMENT OF OBESITY, DIABETES AND OTHER METABOLIC DISORDERS
The present invention relates to Bicyclic Piperidine and piperazine Derivatives, compositions comprising a Bicyclic Piperidine and piperazine Derivative, and methods of using the Bicyclic Piperidine and piperazine Derivatives for treating or preventing obesity, diabetes...
01/26/2012
20120022030Tetracyclic Lactame Derivatives
The present invention describes tetracyclic compounds of formula (IA) or (IB),

wherein the symbols R, X, A, Y, R2, R3 and D are as defined in the specification, their use in the treatment of certain diseases,...

01/26/2012
20120010193CGRP RECEPTOR ANTAGONISTS
Compounds of Formula (I) (wherein variables A1, A2, A3, ring-B, m, n, J, E1, E2, E3, R5, RPG and Y are as described herein), which are useful as antagonists of CGRP receptors, and useful in the...
01/12/2012
201200102086-CYCLOAMINO-3-(1H-PYRROLO[2,3-b]PYRIDIN-4-YL)IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
The invention relates to 6-cycloamino-3-(1H-pyrrolo[2,3-b]pyridin-4-yl)imidazo[1,2-b]pyridazine derivatives corresponding to the general formula (I) in which R2 represents an aryl group optionally substituted with one or more halogen atoms or C1-6-...
01/12/2012
20120004218NOVEL TETRAHYDRO-QUINOLINE DERIVATIVES
A compound of formula (I)

or a pharmaceutically acceptable salt or ester thereof, wherein A1 to A3 and R1 to R10 have the significance given in claim 1, can ...

01/05/2012
20120004252NEW CCR2 RECEPTOR ANTAGONISTS AND USES THEREOF
The present invention relates to novel antagonists for CCR2 (CC chemokine receptor 2) and their use for providing medicaments for treating conditions and diseases, especially pulmonary diseases like asthma and COPD....
01/05/2012
20110319381DERIVATIVES OF AZASPIRANYL-ALKYLCARBAMATES OF 5-MEMBER HETEROCYCLIC COMPOUNDS, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
The invention relates to a compound of the general formula (I) in which R2 is a hydrogen or fluorine atom or a hydroxyl, cyano, trifluoromethyl, C1-6-alkyl, C1-6-alkoxy, NR8R9 group; m, n, o and p are independently ...
12/29/2011
20110319392Thiazole Sulfonamide And Oxazole Sulfonamide Kinase Inhibitors
The present invention provides thiazole sulfonamide and oxazole sulfonamide compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents....
12/29/2011
20110306589NITROGEN CONTAINING HETEROARYL COMPOUNDS
The invention is concerned with novel nitrogen-containing heteroaryl compounds of formula (I)

wherein A1, A2,

R1,...

12/15/2011
201103066043- AND 6-QUINOLINES WITH N-ATTACHED HETEROCYCLIC CGRP RECEPTOR ANTAGONISTS
Compounds of Formula (I): (where variables R1A, R1B, R2, R3, R4, A, and Z are as defined herein) which are useful as antagonists of CGRP receptors, and useful in the treatment or prevention of diseases in which CGRP...
12/15/2011
20110306587UNSATURATED NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS
Unsaturated nitrogen heterocyclic compounds of formula (I):

as defined in the specification, compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treat...

12/15/2011
20110306588HETEROARYLOXYHETEROCYCLYL COMPOUNDS AS PDE10 INHIBITORS
Heteroaryloxyheterocyclyl compounds, and compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, non-insulin dependent diabetes, schiz...
12/15/2011
20110300104HEPATITIS C VIRUS INHIBITORS
The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof:

which inhibit RNA-containing virus, particularly the Hepatitis C Virus (HCV). Conse...

12/08/2011
20110284835Quinoxaline Derivative, and Light-Emitting Element, Light-Emitting Device, and Electronic Device Using the Same
The present invention provides a quinoxaline derivative represented by a general formula (G1). In the formula, α1 and α2 each independently represent an arylene group which has 13 or less carbon atoms forming a ring; Ar represents an aryl group w...
11/24/2011
20110288068AZA SPIRO ALKANE DERIVATIVES AS INHIBITORS OF METALLOPROTEASES
The present invention provides a compound of Formula I or Formula II:

enantiomer, diastereomer, prodrug, solvate, metabolite, or pharmaceutically acceptable salt thereof, wherein constituent variables are pro...

11/24/2011
20110288067Pyrrolopyrazine Kinase Inhibitors
The present invention relates to the use of novel pyrrolopyrazine derivatives of Formula I,

wherein the variables Q and R, R2, and R3 are defined as described herein, which inhibit JAK a...

11/24/2011
20110288087FUSED RING COMPOUND AND USE THEREOF
Provided is a novel compound represented by the following formula

Wherein each symbol is as defined in the specification, or a salt thereof, which has an angiotensin II receptor antagonistic activity and a pe...

11/24/2011
20110263605Azabicyclo[2.2.1]Heptane Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands
The disclosure provides compounds of formula I, including Ia, Ib, Ic, or Id, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disord...
10/27/2011
20110257162HIV INTEGRASE INHIBITORS
Compounds of Formula I are inhibitors of HIV integrase and inhibitors of HIV replication:

wherein m, n, X, R1, R2, R3, R4, R5, R6, R7

10/20/2011
20110251207BIARYL-SPIROAMINOOXAZOLINE ANALOGUES AS ALPHA 2C ADRENERGIC RECEPTOR MODULATORS
In its many embodiments, the present invention provides a novel class of biaryi spiroaminooxazoline analogues as modulators of α2C adrenergic receptor agonists, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, meth...
10/13/2011
20110251169Arylethynyl derivatives
The present invention relates to ethynyl compounds of formula I

wherein

  • R1, R2, R2′, R3, R3′, R4, R4′, U, V, W, Y, m, and n are as ...
10/13/2011
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