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Class 546/265 - Having -C(=X)-, wherein X is chalcogen, bonded directly to the acyclic nitrogen


Subclass of Class 546 - Organic compounds -- part of the class 532-570 series
Definition: Compounds in which the acyclic nitrogen is bonded directly
No. of applications: 41
Last issue date: 01/05/2012


1    
Application No.Application TitleIssue Date
20120004381RAFT POLYMERISATION
A method of preparing polymer, the method comprising polymerising one or more ethylenically unsaturated monomers of formula (I)

    • ...
01/05/2012
20110312974HETEROARYL ANTAGONISTS OF PROSTAGLANDIN D2 RECEPTORS
Described herein are compounds that are antagonists of PGD2 receptors. Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well as methods of using such antagonists of PGD2 receptors, alone...
12/22/2011
20110312875PEPTIDIC COMPOUNDS
The present invention provides a compound of formula I, II, III and IV as defined herein and pharmaceutically acceptable derivatives thereof. The present invention further provides use of the compounds of the present invention in the treatment of bacterial infection and...
12/22/2011
20110305729Scriptaid Isosteres and Their Use in Therapy
Compounds of the invention are of the formula (I); wherein: custom-character is a double bond and X is C; or 12/15/2011
20110275674Small Molecules Modulator of Epigenetic Regulation and Their Therapeutic Applications
Disclosed are methods and compositions for modulating the function of transcription factors, especially transcription factors that recruit epigenetic regulators (histone modifying enzymes) to specific DNA promoters. The targeted transcription factors include but are not...
11/10/2011
20110269966SEMICONDUCTING ARTICLES
An amic acid or amic ester precursor can be applied to a substrate and thermally converted into a thin organic semiconducting layer of the corresponding arylene diimide. This semiconducting layer can be used in various semiconductive articles such as organic light emitt...
11/03/2011
20110269967AROMATIC AMIC ACIDS OR AMIC ESTERS AND COMPOSITIONS
Novel amic acids and amic esters can be thermally converted into corresponding arylene diimides. These amic acids and amic ester can be used as precursors to prepare semiconducting thin films that can be used in various articles including thin-film transistor devices th...
11/03/2011
20110237578AMIDE COMPOUNDS, COMPOSITIONS AND USES THEREOF
Compounds are provided according to formula (I), where A, B, W, X′, L, R1, R3, R4b, and m′ are as defined herein. Provided compounds and pharmaceutical compositions thereof are useful for the prevention and treatment of a variety of ...
09/29/2011
20110237573N- (HETERO)ARYL, 2- (HETERO)ARYL-SUBSTITUTED ACETAMIDES FOR USE AS WNT SIGNALING MODULATORS
The present invention relates to compounds of formulae 1 and 2 and methods for modulating the Wnt signaling pathway using these compounds, wherein A1, A2, B, Y and Z all represent rings.

...

09/29/2011
20110224225Inhibitors of protein kinases
Compounds of general Formula (I):

wherein R1, R2, R3, Ra, A, B and x are as defined herein are inhibitors of protein kinases in particular members of the cyclin-dep...

09/15/2011
20110166132Gamma Secretase Modulators
The present invention provides compounds that are gamma secretase modulators and are therefore useful for the treatment of diseases treatable by modulation of gamma secretase such as Alzheimer's disease. Also provided are pharmaceutical compositions containing such comp...
07/07/2011
20110152323Histone deacetylase inhibitors and uses thereof
The present invention discloses a group of histone deacetylase inhibitors and use thereof. The histone deacetylase inhibitors are useful in the treatment of malignant tumors and the diseases associated with differentiation and proliferation. The histone deacetylase inhi...
06/23/2011
20110118234Urea Compounds as Gamma Secretase Modulators
The present invention provides compounds Formula (I) that are gamma secretase modulators and are therefore useful for the treatment of diseases treatable by modulation of gamma secretase such as Alzheimer's disease. Also provided are pharmaceutical compositions containi...
05/19/2011
20110077160PESTICIDES
Compounds having the following generic formula are disclosed.

...

03/31/2011
20110064657LABELED INHIBITORS OF PROSTATE SPECIFIC MEMBRANE ANTIGEN (PSMA), BIOLOGICAL EVALUATION, AND USE AS IMAGING AGENTS
The prostate-specific membrane antigen (PSMA) is increasingly recognized as a viable target for imaging and therapy of cancer. Various 99mTc/Re-labeled compounds were prepared by attaching known Tc/Re chelating agents to an amino-functionalized PSMA inhibitor with or wi...
03/17/2011
20110003859N- (6-AMINOPYRIDIN-3-YL) -3- (SULFONAMIDO) BENZAMIDE DERIVATIVES AS B-RAF INHIBITORS FOR THE TREATMENT OF CANCER
Compounds of Formula (I) are useful for inhibition of Raf kinases. Methods of using compounds of Formula I and stereoisomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammali...
01/06/2011
20100331549Novel compounds useful for modulating abnormal cell proliferation
There is described compounds of Formulæ I, II, III, IV and V. The compounds of Formulæ I, II, III, IV and/or V are useful: in therapeutic methods and compositions for modulating cell proliferation, in diagnostic assays and as research tools....
12/30/2010
20100324092PYRIDYL AND PYRIMIDINYL DERIVATIVES AS HISTONE DEACETYLASE INHIBITORS
The present invention relates to a novel class of pyridyl and pyrimidinyl derivatives. The pyridyl and pyrimidinyl compounds can be used to treat cancer. The pyridyl and pyrimidinyl compounds can also inhibit histone deacetylase and are suitable for use in selectively i...
12/23/2010
201003240464-CARBOXYBENZYLAMINO DERIVATIVES AS HISTONE DEACETYLASE INHIBITORS
The present invention relates to a novel class of 4-carboxybenzylamino derivatives. The 4-carboxybenzylamino compounds can be used to treat cancer. The 4-carboxybenzylamino compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing t...
12/23/2010
20100266714P2X3 RECEPTOR ANTAGONISTS FOR TREATMENT OF PAIN
The subject invention relates to novel P2X3 receptor antagonists that play a critical role in treating disease states associated with pain, in particular peripheral pain, inflammatory pain, or tissue injury pain that can be treated using a P2X3 rec...
10/21/2010
20100267697ION CHANNEL MODULATORS
The present teachings provide compounds of Formula (I)

and pharmaceutically acceptable salts, hydrates, and esters thereof, wherein Ar, R1, R2, R3, p, and X are defined herein...

10/21/2010
20100190788Amide derivatives as kinase inhitors
The present invention relates to new AGC kinase inhibitors, in particular to compounds of Formula (I) or (II) or a stereoisomer, tautomer, racemic, metabolite, pro- or predrug, salt, hydrate, or solvate thereof, wherein Ar1, Ar2, R1, R
07/29/2010
20100178247CA-IX SPECIFIC RADIOPHARMACEUTICALS FOR THE TREATMENT AND IMAGING OF CANCER
A compound that recognizes and binds to the CA-IX protein has Formula I, II, III, or IV. The compounds may include a radioactive element for radioimaging or therapeutic applications. Thus, pharmaceutical compositions may be prepared with one or more of the compounds of ...
07/15/2010
20100178246TECHNETIUM- AND RHENIUM-BIS(HETEROARYL) COMPLEXES AND METHODS OF USE THEREOF FOR INHIBITING PSMA
A compound of Formula I, a pharmaceutically acceptable salt, or solvate thereof:

complexes with metals such as rhenium, technetium, and others to provide a complex for imaging tissues or treating disease, par...

07/15/2010
20100168070COMPOUNDS FOR THE TREATMENT OF ALZHEIMER'S DISEASE
The invention relates to substituted 1,2-ethylenediamines of general formula (I),

wherein the radicals R1-R13, A, B, L and i are as defined in the description and in the claims. The inve...

07/01/2010
20100099881SPHINGOSINE COMPOUND, METHOD FOR PRODUCING THE SAME, AND SPHINGOMYELINASE INHIBITOR
An object of the invention is to provide a novel sphingosine compound with an inhibitory activity against sphingomyelinase, and a method for producing the sphingosine compound.

The novel sphingosine compound or a salt thereof according to t...

04/22/2010
20100081673HETEROARYL ANTAGONISTS OF PROSTAGLANDIN D2 RECEPTORS
Described herein are compounds that are antagonists of PGD2 receptors. Also described are pharmaceutical compositions that include the compounds described herein, and methods of using such antagonists of PGD2 receptors, alone or in combination with...
04/01/2010
20100062937BENZANILIDES WITH INSECTICIDAL ACTIVITY
Benzanilides of the formula:

in which X represents hydrogen, halogen, nitro, C1-6 alkylthio, C1-6 alkylsulfinyl, C1-6 alkylsulfonyl or C1-6 alkylsulfonyloxy; Y repr...

03/11/2010
20100000028Styryl sulfide dyes
Disclosed are styryl sulfide dyes of formula (1), wherein R1, R′1, R2, R′2, R3 and R′3, independently from each other are hydrogen; C1-C20alkyl or C1-C20a...
01/07/2010
20090312314HETEROAROMATIC MONOAMIDES AS OREXININ RECEPTOR ANTAGONISTS
The present invention is concerned with novel sulfonamides of formula

wherein R1, R2, R3, R4, R5, Ar, Ar1, Ar2, n, o and p are as d...

12/17/2009
20090275550Pyridyl Amide T-Type Calcium Channel Antagonists
The present invention is directed to pyridyl amide compounds which are antagonists of T-type calcium channels, and which are useful in the treatment or prevention of disorders and diseases in which T-type calcium channels are involved. The invention is also directed to ...
11/05/2009
20090172897STYRYL THIOL/DISULFIDE COMPOUND WITH A HYDROXY(CYCLO)ALKYLAMINO UNIT, PROCESS FOR LIGHTENING KERATIN MATERIALS USING SAME
The disclosure relates to the dyeing of keratin materials using styryl hydroxy(cyclo)alkylamino thiol/disulfide fluorescent dyes. Disclosed herein is a dye composition comprising a styryl hydroxy(cyclo)alkylamino thiol/disulfide fluorescent dye and a dyeing process with...
07/09/2009
20090042867COMPOUNDS FOR THE TREATMENT OF ALZHEIMER'S DISEASE
The invention relates to substituted 1,2-ethylenediamines of general formula (I),

wherein the radicals R1 to R13, A, B, L, and i are defined as indicated in the description and the claim...

02/12/2009
20090030042Amide Addition Reaction
A method of making a compound of formula II

comprising the reaction of a compound of formula RCONH2 with a compound of formula III

R be...

01/29/2009
20090018141KINASE INHIBITORS, COMPOSITIONS THEREOF, AND METHODS OF USE THEREWITH
Provided herein are Compounds having the following structure:

    • wherein A, L, X and ring B...
01/15/2009
20080242702Paclitaxel enhancer compound
One embodiment of the present invention is a compound represented by the Structural Formula (I):

10/02/2008
20080090794Potassium Channel Inhibitors
The present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like. ...
04/17/2008
20080039490PYRIDINES FOR TREATING INJURED MAMMALIAN NERVE TISSUE
The invention provides novel pyridines, pharmaceutical compositions comprising such pyridines, and the use of such compositions in treating injured mammalian nerve tissue, including but not limited to an injured spinal cord, in one embodiment, the compounds, composition...
02/14/2008
20070293501Thioalkeneamides as Transketolase Inhibitors
The present invention provides thioalkeneamides of formula (I) which are useful as transketolase inhibitors: wherein R1, R2, R3, R4, R5, R6, Ra-Rd, n and ring A are as defined herein...
12/20/2007
20070219244Histone deacetylase inhibitors as therapeutics for neurological diseases
The invention provides HDAC inhibitors that may be used as therapeutics for the treatment of a neurodegenerative or neuromuscular condition. The invention provides compounds of formula I: The invention also provides pharmaceutical compositions and articles of manufa...
09/20/2007
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