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6177454 Amide derivatives and medicinal compositions thereof  
An amide derivative represented by the following general formula (I) or a salt thereof and a pharmaceutical composition containing the amide derivative and a pharmaceutically acceptable vehicle....
6172076 Inhibitors of prenyl-protein transferase  
The present invention is directed to conformationally constrained compounds which inhibit prenyl-protein transferase and the prenylation of the oncogene protein Ras. The invention is further...
6162798 Inhibitor of atherosclerotic intimal thickening  
An inhibitor of atherosclerotic intimal thickening, which contains an effective amount of a compound of the formula (I): ##STR1## wherein ring X is phenyl, substituted phenyl or 5- or 6-membered...
6159975 Antagonists of gonadotropin releasing hormone  
There are disclosed compounds of formula (I) ##STR1## and pharmaceutically acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety...
6156766 Benzamide compounds and pharmaceutical use thereof  
Benzamide compounds of the formula ##STR1## wherein each symbol is defined in the specification, isomers thereof and pharmaceutically acceptable acid addition salts thereof. Pharmaceutical...
6150371 Method for preventing and for treating autoimmune disease  
A method for preventing or treating autoimmune diseases (excluding type I diabetes) by administering an insulin resistance improving substance as an active ingredient.
6127363 Local administration of Type IV phosphodiesterase inhibitors for the treatment of erectile dysfunction  
A method is provided for treating erectile dysfunction, e.g., vasculogenic erectile dysfunction such as vasculogenic impotence. The method involves the administration of a Type IV phosphodiesterase...
6107312 Thiopyridines for use in the control of helicobacter bacteria  
Thiopyridines of formula (I) ##STR1## in which the substituents and symbols are as defined in the specification are suitable for use in controlling Helicobacter bacteria. They are compounded into...
6107305 Use of pyrazolo [3,4-b] pyridine as cyclin dependent kinase inhibitors  
Compounds of the formula ##STR1## and pharmaceutically acceptable salts thereof for use as inhibitors of cyclin dependent kinases, wherein: X is O, S(O) m ; Y is alkyl, aryl, arylalkyl,...
6100252 Heterocyclic compounds and their use as angiotensin antagonists  
6087374 Anti-viral compounds  
6075016 6,5-fused aromatic ring systems having enhanced phosphodiesterase IV inhibitory activity  
Novel compounds which are effective PDE IV inhibitors are disclosed. The compounds possess improved PDE IV inhibition as compared to theophylline or rolipram, with improved selectivity with regard...
6071931 AT.sub.1 -receptor antagonists for preventing and treating postischemic renal failure and for protecting ischemic kidneys  
The compound (S)-N-(1-carboxy-2-methylprop-1-yl)-N-pentanoyl-N-[2'(1H-tet razol-5-yl)bip henyl-4-yl-methyl]amine (valsartan) of formula ##STR1## or a salt thereof, in particular a pharmaceutically...
6069151 Quinolines and their therapeutic use  
Compounds of the formula ##STR1## have therapeutic utility, as inhibitors of phosphodiesterase IV and TNF release.
6066649 Drug for cardiovascular diseases  
The invention relates to a drug, which contains one or more inhibitors for the cGMP-stimulated phosphodiesterase (PDE II) together with conventional substrates and/or diluents. Preferably the drug...
6060480 Preventives/remedies for muscle tissue degenerations  
An agent for the prophylaxis or treatment of muscle tissue degeneration, containing, as an active ingredient, a quinoline compound of the formula (I): ##STR1## or a pharmaceutically acceptable...
6054466 Inhibitors of farnesyl-protein transferase  
The present invention is directed to compounds which inhibit farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to...
6051572 Azetidine, pyrrolidine and piperidine derivatives  
A class of azetidine, pyrrolidine and piperidine derivatives, substituted by inter alia a phenylmorpholinyl, phenylpiperidinyl or benzimidazolone moiety, are selective agonists of 5-HT 1 -like...
6040327 Benzimidazole, benzoxazole and benzothiazole compounds  
A compound of formula (I): ##STR1## wherein: R 1 represents halogen or a different group as defined in the description, Ra and Rb, which mnay be identical or different, represent hydrogen,...
6037349 Imidazopyridines  
Imidazopyridine derivatives ad pharmacologically acceptable salts having antagonistic properties towards angiotensin II can be used for the treatment of hypertension, aldosteronism and cardiac...
6020340 Imidazopyridines  
Compounds of formula I wherein one of A and B is a nitrogen atom and the other is CH, and Ar has one of the meanings stated in the specification, are effective bronchial therapeutics and are also...
6017923 Carbo-acyclic nucleoside derivatives as antiviral and antineoplastic agents  
5972975 Substituted 2-aminopyridines as inhibitors of nitric oxide synthase  
Substituted 2-aminopyridine compounds of Formula (I) and pharmaceutically acceptable salts which have been found useful in the treatment of nitric oxide synthase mediated diseases and disorders....
5965582 N-benzylindole and benzopyrazole derivatives with anti-asthmatic, anti-allergic, anti-inflammatory and immunemodulating effect  
The N-benzylindole- and benzopyrazole derivatives of the general formula 1 ##STR1## possess anti-asthmatic, anti-allergic, anti-inflammatory and immunomodulating effect and are suitable for the...
5929114 Arylthio compounds  
Arylthiol and dithiobisarylamide antibacterial and antiviral agents have the general formula ##STR1## where A is monocyclic or bicyclic aryl which can contain up to 3 heteroatoms selected from O,...
5922720 Piperazinothiopyridines for the control of Helicobacter bacteria  
Compounds of formula I are piperazinothiopyridines which are useful for controlling Helicobacter bacteria. They are useful as active compounds for treating diseases based on such bacteria, and are...
5900428 Pharmacological use of AII-receptor antagonists  
A method for the prophylaxis and treatment of MOF using certain angiotensin II type 1 receptor antagonists and a pharmaceutical preparation comprising these compounds.
5900414 Methods for administering integrin receptor antagonists  
The compositions and methods of the invention provide a convenient means for systemically administering an integrin receptor antagonist or a pharmaceutically effective amount thereof to a patient...
5891904 Use of inhibitors of phosphodiesterase IV  
The invention relates to the use of inhibitors of phosphodiesterase IV for the modulation of the motility and peristalsis of the hollow organs of the urogenital and gastrointestinal tract.
5889020 Treatment of normotensive glaucoma with angiotensin II antagonists  
The present invention relates to the use of angiotensin antagonist or a pharmaceutically acceptable salt thereof for the treatment of normal tension glaucoma, wherein said angiotensin antagonist...
5866588 Imidazopyridine derivatives  
This invention relates to imidazopyridine derivatives with the general formula II: ##STR1## These compounds are useful as dual histamine (H 1 ) and platelet activating factor (PAF) receptor...
5866603 Derivatives of estra 1,3,5(10)triene-17-one, 3-amino compounds and their use  
This invention discloses compounds useful as steroid sulfatase inhibitors. The compounds comprise the formula (1) ##STR1## wherein (a) R is selected from the group consisting of hydrogen, a lower...
5861389 Methods of treating androgen deficiency in men using selective aromatase inhibitors  
Male menopause is characterized by significant decreases in serum levels of bioavailable androgens. The administration of aromatase inhibitors to men experiencing male menopause can remedy the...
5859030 Substituted arylalkylthioalkylthiopyridines for use in the control of helicobacter bacteria  
A compound of the formula I ##STR1## Wherein all the variables are defined in the specification. The compounds are used for controlling Helicobacter bacteria.
5849753 Pyridyl imidazole derivatives and processes for the preparation thereof  
Substituted pyridyl imidazole derivatives of formula (I) inhibit effectively the action of angiotensin II and have a superior anti-hypertensive activity. ##STR1##
5824677 Substituted amino alcohol compounds  
Disclosed are compounds having a straight or branched aliphatic hydrocarbon structure of formula I: ##STR1## In formula I, n is an integer from one to four and m is an integer from four to twenty....
5824696 Medicaments  
The present invention relates to the use of an angiotensin II receptor antagonist in the manufacture of a medicament for the treatment of chronic inflammatory disease states.
5821241 Fibrinogen receptor antagonists  
Compounds of the invention have the formula ##STR1## The compounds have fibrinogen receptor antagonist activity.
5789415 Azacyclic-heterocyclic compounds as angiotension II receptor antagonists  
Compounds of the formula ##STR1## wherein: Q is naphthyl, heterocyclic or heterobicyclic; R 1 and R 2 , when taken separately, are hydrogen, hydroxy, alkyl, alkylthio, alkylsulfinyl,...
5780482 Condensed 4-aminopyridines with antirheumatic activity  
Compounds of formula I ##STR1## and pharmaceutically acceptable salts thereof in which one of A or B represents N and the other represents N or C--R 3 ; R 1 represents hydrogen, halo, alkyl,...
5753671 Imidazopyridine derivatives as dual histamine (H.sub.1) and platelet activating factor (PAF) antagonists  
Described herein are compounds of formula (II) ##STR1## pharmaceutical or veterinary compositions thereof, and methods of treating diseases or conditions mediated by histamine and/or PAF in mammals.
5753651 Method of modifying angiotensin receptor activity for mediation of pain  
The present invention relates to a method of modifying Angiotensin II subtype 1 (AT 1 ) receptor activity for the treatment of premenstrual syndrome (PMS) and the symptoms associated therewith, and...
5753672 Imidazopyridine derivatives and process for preparing the same  
An imidazopyridine derivative of the formula I!: ##STR1## wherein R 1 is a lower alkyl group, R 2 is a lower alkanoyl group, and R 3 and R 4 are each lower alkyl groups, or both combine at the...
5741794 Heterocyclic sulfonamide derivatives as antagonists of PAF and angiotensin II  
Compounds of formula (I), wherein: A represents: a) a --VR 6 group wherein v is --C(O), --C(O)O--, --CH 2 O--, --CH 2 OC(O)--, --C(S)--, --CH 2 OC(O)NH--, --C(S)O--, --CH 2 ...
5739147 Cyclohexane derivatives, process for their preparation, and the use of the compounds for the treatment of diseases  
Cyclohexane derivatives, process for their preparation, and the use of the compounds for the treatment of diseases Cyclohexane derivatives of the formula I ##STR1## wherein R 2 , R 4 and R 5 have...
5736554 Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties  
Compounds of the Formula ##STR1## wherein: K is N or N➝O; Q is CH 2 or O; T is ##STR2## or R 3 O--CH 2 ; X is a straight or branched chain alkylene, cycloalkylene or cycloalkenylene group,...
5710159 Integrin receptor antagonists  
This invention relates to novel heterocycle compounds including but not limited to 3- 3- 3-(imidazolin-2-yl amino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(benzyloxycarb onylamino)-pro pionic acid,...
5705504 Piperidine derivatives with PAF antagonist activity  
Compounds of general formula I and their salts and solvates are PAF antagonists and as such are useful in the treatment of various diseases or disorders mediated by PAF. Pharmaceutical compositions...
5703092 Hydroxamic acid compounds as metalloprotease and TNF inhibitors  
The present invention provides novel hydroxamic acids and carbocyclic acids and derivatives thereof and to pharmaceutical compositions and methods of use of these novel compounds for the inhibition...
5693633 Angiotensin II antagonists  
This invention provides novel heterocyclic derivatives, their pharmaceutical formulations, and their use for antagonizing angiotensin II receptors in mammals.