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Patent No. 6650315

Mouse device with a built-in printer

A mouse device for use as an input device of a computer is provided that includes a housing in which recording paper is loadable, and a printer unit provided within the housing for printing on the recording paper print information received from the computer.

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Class 546/86 - Chalcogen bonded directly to ring carbon of the tricyclo ring system


Subclass of Class 546 - Organic compounds -- part of the class 532-570 series
Definition: Compounds in which chalcogen (i.e., oxygen, sulfur, selenium,
No. of patents: 194
Last issue date: 05/24/2011


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NumberTitleIssue Date
7947838Radiolabelled benzamide analogues, their synthesis and use in diagnostic imaging
Fluoroalkoxybenzamide compounds which selectively bind Sigma-2 receptors are disclosed. These compounds, when labelled with 18F, can be used as radiotracers for imaging of tumors by positron emission tomography (PET). In addition, these compounds, when la...
05/24/2011
7893266Detection of cancer cells in vitro using sigma-2 receptor ligands as radiotracers
Methods for detection of cancer cells and for determining the proliferative status of cells in a tissue sample in vitro are disclosed. These methods comprise contacting a tissue sample with a radiolabeled compound or salt thereof of Formula
02/22/2011
7659400Radiolabelled benzamide analogues, their synthesis and use in diagnostic imaging
Fluoroalkoxybenzamide compounds which selectively bind Sigma-2 receptors are disclosed. These compounds, when labelled with 18F, can be used as radiotracers for imaging of tumors by positron emission tomography (PET). In addition, these compounds, when la...
02/09/2010
7649093Naphthalene compounds as selective estrogen receptor modulators
The present invention relates to cycloalkylidene compounds with a variety of therapeutic uses, more particularly novel naphthalene compounds that are particularly useful for selective estrogen receptor modulation. ...
01/19/2010
7612206Sigma-2 receptor radiotracers for imaging the proliferative status of solid tumors
Novel benzamide compounds of Formula (I), Formula (II), and Formula (III), salts, water soluble salts, analogs and radiolabeled counterparts thereof as sigma-2 receptor radiotracers for imaging the proliferative status of solid tumors. A method for diagnosing a mamm...
11/03/2009
7390902Sigma-2 receptor radiotracers for imaging the proliferative status of solid tumors
Novel benzamide compounds of Formula (I), Formula (II) and Formula (III, salts, water soluble salts, analogs and radiolabeled counterparts thereof as sigma-2 receptor radiotracers for imaging the proliferative status of solid tumors. A method for diagnosing a mammal...
06/24/2008
7358364Substituted carboxylic acids
The present invention relates to compounds and pharmaceutically acceptable salts of formula (I): which are useful in the treatment of metabolic disorders related to insulin resistance or hyperglycemia. These compounds inclu...
04/15/2008
7297796Sulfamoyl benzamide derivatives and methods of their use
Novel sulfamoyl benzamide compounds, pharmaceutical compositions containing the sulfamoyl benzamide compounds, and methods of their pharmaceutical use are disclosed. In certain embodiments, the sulfamoyl benzamide compounds are agonists and/or modulating ligands of ...
11/20/2007
7211572Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor
The present invention relates to a nitrogen-containing fused ring compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt th...
05/01/2007
7189851Condensed heterocyclic compounds as calcitonin agonists
The present invention relates to novel fused heterocyclic ring system compounds and methods for their use in the treatment and prevention of diseases or conditions. ...
03/13/2007
71258865-HT3 receptor antagonists and methods of use
The subject invention provides useful and novel 5-HT3 antagonists. The subject invention also provides methods for synthesizing the compounds of invention. The invention also provides methods for the treatment of irritable bowel syndrome and other such conditions.
10/24/2006
7122554Carboline derivatives
Compounds of the general structural formula and use of the compounds and salts and solvates thereof, as therapeutic agents. ...
10/17/2006
7109339Substituted tricyclic gamma-carbolines as serotonin receptor agonists and antagonists
The present invention is directed to novel compounds represented by structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein R1, R4a, R5, R6, R
09/19/2006
70841542-(aminomethyl) arylamide analgesics
A chemical genus of 2-(aminomethyl)arylamides, which are useful as analgesics, is disclosed. The genus is represented by the formula I: A representative example is:
08/01/2006
7022856Carboline derivatives
Compounds of the general structural formula and use of the compounds and salts and solvates thereof, as therapeutic agents. ...
04/04/2006
7001911Fused cyclic modulators of nuclear hormone receptor function
The invention pertains to fused cyclic compounds having the formula, wherein G is an optionally substituted aryl or heterocyclo, L is an optional linker, M is a bond, O, CR7R7′ or NR10
02/21/2006
6987115Antibacterial compounds
Compounds of the formula (I) are disclosed and are useful in the treatment bacterial infections: wherein: R1 is Ar or Het; R2 is C1-6a...
01/17/2006
6984646Imidazopyridinones as p38 map kinase inhibitors
The invention relates to imidazopyridinones of the formula wherein the groups R1, R2, R3, and R4 are as defined in claim 1, to the process for their preparation, to pharmaceu...
01/10/2006
6964970Antibacterial compounds
Compounds of the formula (I) are disclosed which are Fab I inhibitors and are useful in the treatment bacterial infections: wherein: R1 is Ar or Het; R
11/15/2005
6933303Heteroaryl-fused nitrogen heterocycles as therapeutic agents
This invention provides compounds which are useful as inhibitors of protein tyrosine phosphatases (PTPases). As inhibitors of PTPases, the compounds of the invention are useful for the management, treatment, control and adjunct treatment of diseases mediated by PTPa...
08/23/2005
6916825Alkylated imidazopyridine derivatives
Compounds of the formula 1 in which the substituents have the meanings mentioned in the description are suitable for the prevention and treatment of gastrointestinal diseases. ...
07/12/2005
6911543Azabicyclic-substituted fused-heteroaryl compounds for the treatment of disease
The invention provides compounds of Formula I: wherein Azabicyclo is These compounds may be in the form of pharmaceutical salts or co...
06/28/2005
6908928Crystalline tiotropium bromide monohydrate, processes for the preparation thereof, and pharmaceutical compositions
Crystalline monohydrate of (1α,2β,4β,5α,7β)-7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonane bromide (tiotropium bromide monohydrate), processes for the preparation thereof, pharmaceutical compositions thereof,...
06/21/2005
6890933Kinesin inhibitors
The present invention provides for compounds, compositions, methods and systems for inhibiting cell growth. More specifically, the present invention provides for methods, compounds and compositions which are capable of inhibiting mitosis in metabolically active cell...
05/10/2005
6849640Therapeutic 1H-pyrido [4,3-b] indoles
The present invention provides 2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indoles and 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles. These compounds are 5-HT ligands that are useful for treating diseases wherein modulation of 5-HT activity is desired. ...
02/01/2005
6841555Lavendamycin analogs, quinoline-5,8-diones and methods of using them
The invention provides novel lavendamycin analogs having the following general formula: and quinoline-5,8-diones having the following formula: Methods of making and using...
01/11/2005
67706555-HT3 receptor antagonists and methods of use
The subject invention provides useful and novel 5-HT3 antagonists. The subject invention also provides methods for synthesizing the compounds of invention. The invention also provides methods for the treatment of irritable bowel syndrome and other such conditions.
08/03/2004
6720330Somatostatin antagonists and agonists that act at the SST subtype 2 receptor
Compounds according to the formula A—Z—W as herein described, wherein A is selected from the groups consisting of: A′—(CH2)n—, A′—(CH2)nSO2—, and A′—(CH2)nCO—, where n...
04/13/2004
67203311-substituted 1,2,3,4-tetrahydro-β-carboline and 3,4-dihydro-β-carboline and analogs as antitumor agents
A composition includes a substituted dihydro- or tetrahydro-β-carboline of formula (II) or (III), wherein the aromatic ring of the carboline may include one or more substituents selected from the group consisting of hydroxy, C1-6 alkoxy, benzyloxy, C
04/13/2004
6699865Pyrazole compositions useful as inhibitors of ERK
Described herein are compounds that are useful as protein kinase inhibitors having the formula: ##STR1## where R1-4, Q, and T are described in the specification. The compounds are useful for treating disease states in mammals that are alleviate...
03/02/2004
6686372Selective 댣 adrenergic agonists
The present invention is in the field of medicine, particularly in the treatment of Type II diabetes and obesity. More specifically, the present invention relates to selective 댣 receptor agonists useful in the treatment of Type II diabet...
02/03/2004
6673781Tricyclic compounds having sPLA2-inhibitory activities
The present invention provides a compound having sPLA2 inhibiting activity. The compound represented by the formula (I): ##STR1## wherein R1 is (a) C1 to C20 alkyl, C2 to C20 alkenyl, C2 to C20 alkynyl, carbocyclic groups, heterocycl...
01/06/2004
6608098Isoindole derivatives
This invention relates to compounds represented by the general formula [I] ##STR1## wherein, R represents an azido group, etc., R1 and R2 are the same or different and represent hydrogen atoms, etc., R3 and R4 are th...
08/19/2003
6573272Antibacterial compounds
Compounds of the formula (I) are disclosed which are FabI inhibitors and are useful in the treatment bacterial infections: ##STR1## wherein: R1 is Ar or Het; R2 is H, C1-6 alkyl or Ar--C0-6 alkyl; X is H, C1-4
06/03/2003
6528509Pyrazole compositions useful as inhibitors of ERK
Described herein are compounds that are useful as protein kinase inhibitors having the formula: ##STR1## where R1-4, Q, and T are described in the specification. The compounds are useful for treating disease states in mammals that are alleviate...
03/04/2003
6528649Imidazoloisoquinolines
Disclosed are compounds of the formula: ##STR1## and the pharmaceutically acceptable salts, prodrugs and solvates thereof, wherein n, R1, R2, R3, W, Q, and X are defined herein, which compounds bind with high selectivity a...
03/04/2003
6511987Bicyclic and tricyclic heteroaromatic compounds
Disclosed are compounds of the formula: ##STR1## and the pharmaceutically acceptable salts thereof, wherein W, Q, X, X1, Y and Z are as defined herein. These compounds bind with high selectivity and/or high affinity to the benzodiazepine site o...
01/28/2003
6492364Triazolo and derivatives as chemokine inhibitors
Novel triazolo derivatives represented by the following formula and pharmaceutically acceptable salts thereof, as well as chemokine inhibitors containing the same as an effective component. These are useful as therapeutic agents for allergic diseases such...
12/10/2002
6492358ଲ-carboline derivatives useful as inhibitors of phosphodiesterase
The present invention relates to novel ଲ-carboline derivatives of the general formula ##STR1## wherein all the variables are as described within the specification, useful as phosphodiesterase inhibitors. The present invention further relates to ...
12/10/2002
6451809Oxo-pyridoimidazole-carboxamides: GABA brain receptor ligands
Disclosed are compounds of the formula: ##STR1## or the pharmaceutically acceptable non-toxic salts thereof where R1 -R4 and A are defined herein, which compounds are highly selective agonists, antagonists or inverse agonists for GAB...
09/17/2002
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