"The production of too many useful things results in too many useless people."
Karl Marx
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 |
| 5955507 | Therapeutic substituted guanidines The present invention provides therapeutically useful substituted guanidines and methods of treatment and pharmaceutical compositions that utilize or comprise one or more of such guanidines.... | 09/21/1999 |
| 5922772 | Therapeutic substituted guanidines The present invention provides therapeutically useful substituted guanidines and methods of treatment and pharmaceutical compositions that utilize or comprise one or more of such guanidines.... | 07/13/1999 |
| 5883133 | Substituted cinnamic acid guanidides, a process for their preparation, their use as medicaments or diagnostic agents and medicaments comprising them Compounds of the formula I ##STR1## are described in which at least one of the substituents R(1), R(2), R(3), R(4) and R(5) is a nitrogen-containing heterocyclic radical. They are outstanding cardiovascular therapeutic agents. They are obtained by ... | 03/16/1999 |
| 5856344 | Sulfonylamino-substituted benzoylguanidines, a process for their preparation, their use as a medicament or diagnostic aid, and medicament containing them Benzoylguanidines of the formula I ##STR1## in which R(1) to R(6) have the meanings stated in the claims, are antiarrhythmic pharmaceuticals which have excellent activity and a cardioprotective component and are highly suitable for the prophylaxis of... | 01/05/1999 |
| 5847006 | Therapeutic guanidines The present invention provides N,N'-diaryl substituted guanidines having therapeutic utility. The compounds of the present invention are represented by the formula: ##STR1## wherein R and R1 represent hydrogen or other group and Ar and ... | 12/08/1998 |
| 5830917 | L-N6 -(1-iminoethyl) lysine derivatives useful as nitric oxide synthase inhibitors There is disclosed a novel amino alcohol amine derivatives of L-N6 -(1-iminoethyl)lysine, pharmaceutical compositions containing these novel compounds, and to their use in therapy, in particular their use as nitric oxide synthase inhibitors.... | 11/03/1998 |
| 5807896 | Arylbenzoylguanidines Arylbenzoylguanidines of the formula I ##STR1## in which R1 R2, R3 and Ph have the given meanings herein, and also the physiologically harmless salts thereof, exhibit antiarrhythmic properties and act as inhibitors of... | 09/15/1998 |
| 5798390 | Tri- and tetra-substituted guanidines and their use as excitatory amino acid antagonists Tri- and tetra-substituted guanidines which exhibit a high binding affinity to phencyclidine (PCP) receptors and, more preferably, low affinity to the brain sigma receptors. These guanidine derivatives act as non-competitive inhibitors of glutamate induce... | 08/25/1998 |
| 5792769 | Guanidino protease inhibitors Compounds of the formula: ##STR1## wherein R1 --R4, R7 --R8, Ra, Rb, Rc, Y, Z, n and m are set forth in the specification, as well as hydrates, solvates or pharmaceutically ... | 08/11/1998 |
| 5773469 | Diaryl antimicrobial agents The invention relates to diaryl antimicrobial compounds of the general formula: ##STR1## where G, E L, J, q, m, X, Ar, W, p, n and A are as described herein, pharmaceutical compositions containing the compounds, methods for their production and ... | 06/30/1998 |
| 5767162 | Tri-and tetra-substituted guanidines and their use as excitatory amino acid antagonists Tri- and tetra-substituted guanidines which exhibit a high binding affinity to phencyclidine (PCP) receptors and, more preferably, low affinity to the brain sigma receptors. These guanidine derivatives act as non-competitive inhibitors of glutamate induce... | 06/16/1998 |
| 5753715 | 2-disubstituted cyclohexenyl and cyclohexyl antimicrobial agents The invention relates to cyclohexenyl antibacterial compounds of the formula I: ##STR1## and pharmaceutical compositions containing the compounds, methods for their production and use.... | 05/19/1998 |
| 5753710 | Substituted benzyloxycarbonylguanidines, a process for their preparation, their use as a medicament or diagnostic, and a medicament containing them Substituted benzyloxycarbonylguanidines, a process for their preparation, their use as a medicament or diagnostic, and a medicament containing them. There are described compounds of the formula I ##STR1## in which the substituents R(1) to R(7) and X ... | 05/19/1998 |
| 5739142 | 4-aminobenzoylguanidine derivatives 4-Aminobenzoylguanidines of the formula I ##STR1## in which A, R1, R2 and R3 have the meanings given, and the physiologically unobjectionable salts thereof exhibit antiarrhythmic properties and are active as inhibitor... | 04/14/1998 |
| 5733934 | Antiarrythmic and cardioprotective substituted indenoylguanidines Indenoylguanidines of formula I and formula II, the process for their preparation, their use as medicaments, medicaments containing them, their use as diagnostic agents and medicaments containing them are described. Compounds I are useful for treating car... | 03/31/1998 |
| 5723133 | Cosmetics containing guanidine derivatives A guanidine derivative represented by formula (1), (2), (3) or its acid addition salt and a production process thereof ##STR1## wherein each of A and B is a C2 -C8 alkylene, D is a single bond, --CO-- or a C1 -C5... | 03/03/1998 |
| 5719187 | Compounds having a guanidine structure and pharmaceutical composition containing same Guanidine derivatives are provided useful for promoting growth, repair and regeneration of a neuronal axon and for treating neuropathies and myopathies. The compounds have the formula: ##STR1## wherein R1 is an isopropyl radical, a benzyl ... | 02/17/1998 |
| 5696290 | Synthesis of penta-substituted guanidines The present invention is the novel synthesis of sterically hindered penta-substituted guanidines by a process in which (1a) an isocyanate is reacted first with a di-substituted amine or (1b) a urea is reacted with two moles of a mono-substituted amine to ... | 12/09/1997 |
| 5696138 | Urea derivatives and their use A compound having the formula ##STR1## or a pharmaceutically acceptable salt thereof, wherein X, Z, Y, A, D, E, F, R1, R2, R3, R4, R11, R12 have the meanings set forth in the specification,... | 12/09/1997 |
| 5693672 | 3,4,5-substituted benzoylguanidines, process for their preparation, their use as a medicament or diagnostic and medicament containing them 3,4,5-Substituted benzoylguanidines, process for their preparation, their use as a medicament or diagnostic and medicament containing them Benzoylguanidines of the formula I ##STR1## where R(1) is R(4)--SOm or R(5)R(6)N--SO2 --, wher... | 12/02/1997 |
| 5670544 | Substituted benzoylguanidines process for their preparation their use as a medicament or diagnostic and medicament containing them There are described benzoylguanidines of the formula I ##STR1## where R(1) is hydrogen, Hal, --NO2, --CN, --CF3, R(4)--SOm or R(5)R(6)N--SO2 --, where m is zero to 2, R(4) and R(5) are alk(en)yl or --C... | 09/23/1997 |
| 5646188 | Polyamine derivatives of 1-aminoindan A compound of general formula I ##STR1## wherein n is 1 or 2; R1 and R2 are each independently hydrogen, hydroxy, substituted or unsubstituted C1-4 alkyl, substituted or unsubstituted C1-4 alkoxy or halogen... | 07/08/1997 |
| 5643950 | Triphenylalkyl antimicrobial agents The invention relates to triphenylalkyl antibacterial compounds of the general formula: ##STR1## pharmaceutical compositions containing the compounds, and methods for their production and use. These compounds are effective in inhibiting the acti... | 07/01/1997 |
| 5637621 | Methods and compositions for treating Botrytis infections The invention provides fungicidal compounds having the general formula: X1 -A1 -B1 -C-B2 -A2 -X2 (I) wherein X1 is an amidine, a guanidine, or an imidazole group. A1 is either a ... | 06/10/1997 |
| 5629348 | Methods and compositions for treating septoria infections The invention provides fungicidal compounds having the general formula: X1 -A1 -B1 -C-B2 -A2 -X2 (I) wherein X1 is an amidine, a guanidine, or an imidazole group. A1 is either a... | 05/13/1997 |
| 5614630 | Acenaphthyl substituted guanidines and methods of use thereof Modulators of neurotransmitter release including substituted guanidines, N"-aminoguanidines, and N,N'N",N'"-tetrasubstituted hydrazinedicarboximidamides, and pharmaceutical compositions thereof are disclosed. Also disclosed are methods involving the use o... | 03/25/1997 |
| 5574054 | Quaternary ammonium salts and use thereof as medicine Novel quaternary ammonium salts having utility in the medical field for treating gastrointestinal disorders.... | 11/12/1996 |
| 5565185 | Process for the preparation of radiolabeled meta-halobenzylguanidine The present invention provides a no-carrier-added synthesis of radiolabeled meta-halobenzylguanidine by halodestannylation which comprises reacting a meta-trialkylstannylbenzylguanidine with a source of radionuclide of a halogen. The present invention als... | 10/15/1996 |
| 5559154 | Tri- and tetra-substituted guanidines and their use as excitatory amino acid antagonists Tri- and tetra-substituted guanidines which exhibit a high binding affinity to phencyclidine (PCP) receptors and, more preferably, low affinity to the brain sigma receptors. These guanidine derivatives act as non-competitive inhibitors of glutamate induce... | 09/24/1996 |
| 5494934 | Guanidine compounds A compound of formula (I): ##STR1## in which: R1 represents substituted or unsubstituted phenyl or (C3 -C7) cycloalkyl, R2 represents trifluoromethyl or (C3 -C4) cycloalkyl, A represents --... | 02/27/1996 |
| 5489709 | Preparation of substituted guanidines A process for the preparation of a substituted guanidine by reacting a substituted cyanamide with ammonia or a substituted amine in the presence of a Lewis acid catalyst. Also disclosed is a process for the preparation of a tri-substituted guanidine by re... | 02/06/1996 |
| 5428065 | 1,3-benzenedimethanamines useful as central nervous system active agents Pharmaceutical compounds of the formula: ##STR1## R1 to R8 are each hydrogen or C1-4 alkyl, m, n and p are each 0, 1, or 2, q is 0, 1, 2 or 3, X and Z are each C1-4 alkyl, C1-4 alkoxy, hydroxy, n... | 06/27/1995 |
| 5399570 | Aspartic acid derivatives, and their use for inhibiting platelete aggregation Aspartic acid derivatives of the formula ##STR1## in which X denotes, for example, ##STR2## and R denotes, for example, cyclohexylamino, have useful pharmacological properties.... | 03/21/1995 |
| 5395853 | Anti-atherosclerotic diaryl compounds The present invention is concerned with compounds of formula (I) ##STR1## wherein m is 0 or 1; W is hydrogen, a C1-16 straight, branched, or cyclic alkyl group, or a C2-16 straight, branched, or cyclic alkenyl or alkynyl group, or Ph... | 03/07/1995 |
| 5373024 | 3,5-Substituted benzoylguanidines, process for their preparation, their use as a medicament of diagnostic and medicament containing them Benzoylguanidines of the formula I ##STR1## are described where R(1) is R(4)--SOm or R(5)R(6)N--SOz --, where R(4) and R(5) are alk(en)yl or --Cn H2n --R(7), and where R(7) is a cycloalkyl or phenyl, where ... | 12/13/1994 |
| 5364868 | Amino-substituted benzoylguanidines, process for their preparation, their use as a medicament and medicament containing them Amino-substituted benzoylguanidines, process for their preparation, their use as a medicament and medicament containing them Benzoylguanidines of the formula I ##STR1## are described in which R(1) or R(2) is an amino group --NR(3)R(4), where R(3) and... | 11/15/1994 |
| 5360938 | Asymmetric syntheses This invention relates to asymmetric syntheses in which a prochiral or chiral compound is contacted in the presence of an optically active metal-ligand complex catalyst to produce an optically active product.... | 11/01/1994 |
| 5336689 | Tri- and tetra-substituted guanidines and their use as excitatory amino acid antagonists Tri- and tetra-substituted guanidines which exhibit a high binding affinity to phencyclidine (PCP) receptors and, more preferably, low affinity to the brain sigma receptors. These guanidine derivatives act as non-competitive inhibitors of glutamate induce... | 08/09/1994 |
| 5296498 | Guanidine compounds A compound of formula (I): ##STR1## in which: R1 represents substituted or unsubstituted phenyl or (C3 -C7) cycloalkyl, R2 represents trifluoromethyl or (C3 -C4) cycloalkyl, A represents --... | 03/22/1994 |
| 5292755 | USPA benzolyguanidines Benzoylguanidines of the formula I ##STR1## where R(1) or R(2) is equal to R(6)--S(O)n -- or R(7)R(8)N--O2 S-- and the other substituent R(1) or R(2) is in each case equal to H, F, Cl, Br, I, alkyl, alkoxy or phenoxy, R(6)--S(O)... | 03/08/1994 |