A self defense weapon formed as a memo pad and which is easily held by a person's fingers, therefore making it possible to provide protection from a mugger and also to quickly and easily write a record or a message without failure of missing or forgetting significant information under a stressful situation.
Make the Most of Our Site
See this month's Top Inventors and Most Cited Patents.
Stay on top of the latest innovations by subscribing to an RSS feed.
Registered users: Manage your profile.
| Number | Title | Issue Date |
| 8173694 | Therapeutic agent Provided are agents and methods for use in depleting serum amyloid P component (SAP) from a patient in need thereof. ... | 05/08/2012 |
| 8163792 | IAP BIR domain binding compounds Disclosed herein is an isomer, enantiomer, diastereoisomer or tautomer of a compound represented by Formula I: or a prodrug, or a pharmaceutically acceptable salt, or labeled with a detectable label or an affinity tag there... | 04/24/2012 |
| 8124648 | Therapeutic lactams Compounds comprising or a pharmaceutically acceptable salt or a prodrug thereof, are disclosed, wherein J1, J2, B, Y, and A are as described. Methods, compositions, and medicaments related thereto are ... | 02/28/2012 |
| 8088817 | Pyrrole derivative having, as substituents, ureido group, aminocarbonly group and bicyclic group which may have substituent A compound represented by the following formula (1) or a salt thereof: The compound has an inhibitory activity on the production of interleukin-6, and is therefore useful as a therapeutic agent for a disease associated with... | 01/03/2012 |
| 8067457 | Compounds useful as antagonists of CCR2 The present invention provides compounds of general formula I: or a pharmaceutically acceptable salt thereof, wherein X, n, Y, and R1 are defined generally and in subsets herein. Compounds of the invention are inhibitors of CCR2 and accordingly are useful for the tr... | 11/29/2011 |
| 8063096 | Spirocyclic 3-phenyl-3substituted-4-ketolactams and-lactones The present invention relates to novel phenyl-substituted 4-ketolactams and -lactones of the formula (I) in which A, B, Q, G, W, X, Y, Z and R3 are as defined above, to processes and intermedi... | 11/22/2011 |
| 8063095 | IAP BIR domain binding compounds Disclosed is an isomer, enantiomer, diastereoisomer or tautomer of a compound represented by Formula I: or a salt thereof, in which R1, R2, R100, R200, A, A1, B, B... | 11/22/2011 |
| 8044092 | Therapeutic compounds A compound having a substituted five or six-membered carbocycle or heterocycle directly bonded to a substituted aryl or heteroaryl ring, wherein said compound has an EC50 value of 20 nM or less at the prostaglandin EP2 receptor according to the... | 10/25/2011 |
| 8022096 | Pyrrolidine derivatives Pyrrolidine compounds described herein and methods for using them to inhibit dipeptidyl peptidase IV and treat Type II diabetes. ... | 09/20/2011 |
| 8022097 | Adamantane-dipyrromethane derivatives, method of preparation and applications in anion sensing Aamantane dipyrromethane derivatives are obtained by reacting adamantane carbonyl derivatives with pyrrole or pyrrole derivative, in the presence of acid. Adamantane-dipyrromethanes are used to bind anions of the group consisting of: F—, Cl—, Br—, acetate, HSO... | 09/20/2011 |
| 8017647 | Crystalline sodium atorvastatin Crystalline sodium atorvastatin, compositions containing the same and methods for the production thereof. ... | 09/13/2011 |
| 7998998 | Therapeutic substituted lactams Disclosed herein are compounds having a formula: (I) Compositions, methods, and medicaments related thereto are also disclosed. ... | 08/16/2011 |
| 7985765 | Therapeutic substituted pyrroles Disclosed herein is a compound represented by a formula: Therapeutic methods, compositions, and medicaments related thereto are also disclosed. ... | 07/26/2011 |
| 7973071 | Substituted gamma lactams as therapeutic agents A compound comprising or a pharmaceutically acceptable salt, prodrug, or a metabolite thereof is disclosed herein. Y, A, and B are as described herein. Methods, compositions, and medicaments related to these compoun... | 07/05/2011 |
| 7968590 | IAP binding compounds IAP binding molecules and compositions including these are disclosed. The IAP binding molecules interact with IAPs (inhibitor of apoptosis proteins) in cells and may be used to modify apoptosis in cells treated with such molecules. Embodiments of these compounds hav... | 06/28/2011 |
| 7956084 | Phenyl thiophene carboxamide compounds as inhibitors of the enzyme IKK-2 The invention relates to thiophene carboxamides of formula (I), wherein A, R1, R2, R3, n and X are as defined in the specification, processes and intermediates used in their preparation, pharmaceutical compositions containing them an... | 06/07/2011 |
| 7947730 | Piperidinium and pyrrolidinium derivatives as ligands for the muscarinic M3 receptor Compounds of formula I in salt or zwitterionic form wherein, wherein R1, R2, R3, R4, R5, J, L and M have the meanings as indicated in the specification, are useful for ... | 05/24/2011 |
| 7915301 | Inhibitors of cyclin dependent kinases and their use The present invention relates to novel compounds for the inhibition of cyclin-dependent kinases, and more particularly, to chromenone derivatives of formula (Ia), wherein R1, R2, R3, R4... | 03/29/2011 |
| 7897635 | HIV protease inhibitors Compounds useful for inhibiting HIV protease are disclosed. Methods of making the compounds, and their use as therapeutic agents, for example, in treating wild-type HIV and of multidrug-resistant strains of HIV, also are disclosed. ... | 03/01/2011 |
| 7884127 | Inhibitors of cyclin dependent kinases and their use The present invention relates to novel compounds for the inhibition of cyclin-dependent kinases, and more particularly, to chromenone derivatives of formula (Ic) wherein R1, R2, R3, R4 | 02/08/2011 |
| 7858657 | Wortmannin analogs and methods of using same in combination with chemotherapeutic agents Novel wortmannin analogs and their use in inhibiting PI-3-kinase activity in mammals and the treatment or prevention of cancer and tumor formation in a subject are described herein. Preferably, the wortmannin analogs may be administered with other chemotherapeutic a... | 12/28/2010 |
| 7842715 | N-benzoyl- and N-benzylpyrrolidin-3-ylamines as histamine-3 antagonists The present invention provides a compound of formula I and the use thereof for the treatment of a central nervous system disorder related to or affected by the histamine-3 receptor. ... | 11/30/2010 |
| 7803836 | Aminophenylsulfonamide derivatives as HIV protease inhibitor The present invention concerns substituted aminophenylsulfonamide compounds and derivatives, their use as protease inhibitors, in particular as broadspectrum HIV protease inhibitors, processes for their preparation as well as pharmaceutical compositions and diagnost... | 09/28/2010 |
| 7799822 | Phenyl sulfonamides as modulators of ion channels The present invention relates to phenyl sulfonamides useful as inhibitors of ion channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of variou... | 09/21/2010 |
| 7799821 | Therapeutic compounds A compound having a substituted five or six-membered carbocycle or heterocycle directly bonded to a substituted aryl or heteroaryl ring, wherein said compound has an EC50 value of 20 nM or less at the prostaglandin EP2 receptor according to the... | 09/21/2010 |
| 7795298 | IAP BIR domain binding compounds Disclosed is an isomer, enantiomer, diastereoisomer or tautomer of a compound represented by Formula I: or a salt thereof, in which R1, R2, R100, R200, A, A1, B, B... | 09/14/2010 |
| 7781482 | Substituted gamma lactams as therapeutic agents A compound comprising or a pharmaceutically acceptable salt thereof, or a prodrug thereof is disclosed herein. Y, A, and B are as described herein. Methods, compositions, and medicaments related to these compounds a... | 08/24/2010 |
| 7776908 | Wortmannin analogs and methods of using same Novel Wortmannin analogs and their use in inhibiting inhibiting PI-3-kinase activity in mammals as well, as tumor formation in a subject are described herein. ... | 08/17/2010 |
| 7759389 | Chroman derivatives and uses thereof Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein m, p, q, Ar, R1, R2, R3 and R4 are as defined herein. Also provided are methods for pre... | 07/20/2010 |
| 7737175 | Methods and compositions for regulating HDAC4 activity The present invention provides methods and compositions for modulating HDAC4 activity and modulating the activity of proteins downstream of HDAC4 in the muscle transcriptional pathway in a cell by modulating HDAC4 activity. Further provided are methods and compositi... | 06/15/2010 |
| RE41356 | Hepatitis C inhibitor tri-peptides Racemates, diastereolsomers and optical isomers of a compound of formula (I): wherein B is H, a C6 or C10 aryl, C7-16 aralkyl; Het or (lower alkyl)-Het, all of which optionally substituted with C | 05/25/2010 |
| 7723375 | Metabolites of wortmannin analogs and methods of using the same Novel metabolites of wortmannin and wortmannin analogs and their use in inhibiting PI-3 kinase activity in mammals and the treatment and prevention of cancer or tumor formation in a subject are described herein. ... | 05/25/2010 |
| 7718691 | Compounds as inhibitors of hepatitis C virus NS3 serine protease The present invention discloses novel compounds which have HCV protease inhibitory activity as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising such compounds as well as methods of us... | 05/18/2010 |
| 7691897 | Therapeutic agent Agent for the depletion of an unwanted protein population from the plasma of a subject, which agent comprises a plurality of ligands covalently co-linked so as to form a complex with a plurality of the proteins in the presence thereof, wherein at least two of the li... | 04/06/2010 |
| 7652059 | Pyrrolcarboxamides and pyrrolcarbothioamides The invention relates to novel pesticidal pyrrolcarboxamides of formula I wherein X is oxygen or sulfur; R1 is CF3, CF2H or CFH2; R2 | 01/26/2010 |
| 7652060 | Small molecule rotamase enzyme inhibitors This invention relates to neurotrophic compounds having an affinity for FKBP-type immunophilins, their preparation and use as inhibitors of the enzyme activity associated with immunophilin proteins, and particularly inhibitors of peptidyl-prolyl isomerase or rotamas... | 01/26/2010 |
| 7638550 | Pyrrolic derivatives with histone deacetylase inhibitory activity The invention describes new compounds derived from formula I pyrroles, methods for obtaining them and their application as drugs in pharmaceutical compositions for the treatment of cancer due to their inhibitory activity on certain histone deacetylases. ... | 12/29/2009 |
| 7638549 | Mitotic kinesin inhibitors The present invention relates to dihydropyrrole compounds that are useful for treating cellular proliferative diseases, for treating disorders associated with KSP kinesin activity, and for inhibiting KSP kinesin. The invention is also related to compositions which c... | 12/29/2009 |
| 7632857 | Histamine H3 receptor agents, preparation and therapeutic uses The present invention discloses novel compounds of Formula (I) or pharmaceutically acceptable salts thereof, which have histamine-H3 receptor antagonist or inverse agonist activity, as well as methods for preparing such compounds. In another embodiment, the inventio... | 12/15/2009 |
| 7615573 | Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors Disclosed is a novel enantiomeric synthesis ceramide-like inhibitors of UDP-glucose: N-acylsphingosine glucosyltransferase. Also disclosed are novel intermediates formed during the synthesis. ... | 11/10/2009 |