Abstract: Since sulfonamide derivatives of the present invention show strong inhibitory activity against cysteine protease such as calpain papain, cathepsin B, cathepsin H, cathepsin L, they can be used as remedies for muscular dystrophy, cataract, myocardial infarction, stroke, Alzheimer's disease, amyotrophia, osteoporosis, hypercalcemia or the like.

Abstract: Disclosed are benztropine and CFT analogs useful for imaging of cocaine receptors and treatment of cocaine abuse. Also disclosed are analogs useful for imaging and treatment of Parkinson's disease.

Abstract: Disclosed is a gel or stick composition for reduction of body malodor, containing active deodorant and/or antiperspirant ingredients, a polyamide gelling agent and a solvent system for the polyamide gelling agent. The polyamide gelling agent has good stability, even in the presence of acidic antiperspirant metal salts, and can provide a clear deodorant or antiperspirant gel or stick. The composition has good pay-off characteristics and application properties, and good structural integrity. Moreover, the composition can be formulated so as not to leave any undesirable residue, such as a white residue left after applying conventional antiperspirant sticks.

Abstract: The present invention relates to a new isoindolinone derivative of formula: ##STR1## in racemic form or in the form of its enantiomers, as well as its salts, its preparation and the pharmaceutical compositions which contain it.

Abstract: This invention relates to polycyclic compounds containing two mono- and/or bicyclic rings and a basic tertiary amino group capable of forming an ammonium ion at biological pH and which reduces levels of serum cholesterol in the body without significantly reducing mevalonic metabolite synthesis. This invention relates also to pharmacological compositions and method of treatment for lowering serum cholesterol levels using the compounds of this invention.

Abstract: Fibrinogen receptor antagonists having the formula ##STR1## for example ##STR2##

Abstract: Compounds of the formulas: ##STR1## or pharmaceutically acceptable salts thereof. These compounds are obtainable by cultivation of a pure culture of Actinoplanes sp. SCC2314, ATCC 55600. These compounds are useful as antifungal agents.

Abstract: A clear antiperspirant gel is made by combining and mixing together (A) an astringent compound having a refractive index of 1.48 to 1.53 which is an antiperspirant salt in the form of (i) a tray dried compound, (ii) an encapsulated salt, or (iii) a solvent solution of a salt compound; and (B) a clear anhydrous organic oil free gel formed with a gelator which is 12-hydroxystearic acid or its metal salts, and an aromatic containing silicone fluid or blend of silicone fluids.

Abstract: This invention relates to 2-(1'-azabicyclo[2.2.2]oct-3'S-yl)-6-hydroxy-2,4,5,6-tetrahydro-1H-benz[de ]isoquinolin-1-one and 2-(1'-azabicyclo[2.2.2]oct-3'S-yl)-6-hydroxy-2,3,3a,4,5,6-hexahydro-1H-ben z[de]isoquinolin-1-one and their individual stereoisomers and uses and the processes for their making.

Abstract: The invention relates to an emulsion containing an aqueous phase dispersed in an oily phase using a mixed ester of isostearic acid and succinic acid with glycerol, and at least 10% by weight of polyol relative to the total weight of the emulsion.This emulsion is intended in particular for the cosmetic and/or dermatological treatment of hands.

Abstract: A cosmetic sunscreen composition is described that includes an emulsion formed from water, an emollient oil and an organic sunscreen agent capable of absorbing ultraviolet radiation within the range of 290 to 400 nm. Further included in the sunscreen composition is a microfluidized medium formulated and microfluidized separately and prior to blending with the other aforementioned components. This medium includes water, a phospholipid, and an organic sunscreen agent identical to that in the emulsion. The combination of identical sunscreen agents in different environments provides an overall increase in SPF for the overall sunscreen composition.

Abstract: An antisun product which contains, besides cosmetic auxiliaries and sunscreen agents and/or sun blocks, an effective amount of deproteinated haemodialysate of mammalian blood or an active fraction thereof results in improving the condition of the skin and in reducing or avoiding the adverse effects of exposure to the sun. The composition is suitable for both prophylaxis and aftercare.

Abstract: The present invention relates to novel imidazonaphthyridine derivatives represented by the following formulae: ##STR1## wherein R represents hydrogen, lower alkyl or --CH.sup.2 R.sup.1 (where R.sup.1 represents phenyl or pyridyl) and pharmaceutically acceptable salts thereof.The compounds exhibit excellent anti-allergic, anti-inflammatory and anti-asthmatic activities.

Abstract: Compositions, for conditioning human hair, comprising from about 0.1% to about 10% of a silicone conditioning agent, from about 0.01% to about 10% of a dimethicone copolyol, from about 0.1% to about 10% of a lipid vehicle material, from about 0.05% to about 5% of a cationic surfactant vehicle material, and the balance of water. Preferably the lipid vehicle materials are fatty alcohols or fatty esters. Also preferably, the silicone conditioning agent is an unsubstituted, amine substituted, or alkoxy substituted polydimethyl siloxane.

Abstract: A tricyclic compound represented by the following formula (I): ##STR1## wherein R.sup.1 represents hydrogen, halogen or lower alkyl; A represents cyano, carboxyl, tetrazolyl, cyano-substituted phenyl, carboxyl-substituted phenyl or tetrazolyl-substituted phenyl; V represents --(CH.sub.2).sub.m --(wherein m is an integer of 0 to 2); W represents ##STR2## (wherein R.sup.2, R.sup.3 and R.sup.4 independently represent hydrogen, halogen, lower alkyl, cycloalkyl, halogenated lower alkyl, hydroxy, lower alkoxy, amino, lower alkylamino, carboxyl or lower alkoxycarbonyl; and Q.sup.1 --Q.sup.2 --Q.sup.3 --Q.sup.4 represents N.dbd.CH--CH.dbd.CH; X.sup.1 --X.sup.2 --X.sup.3 represents CH.dbd.CH--CH.dbd.CH, S--CH.dbd.CH or CH.dbd.CH--S; Y represents a single bond, CH.sub.2, O, S, CH.sub.2 O, OCH.sub.2, CH.sub.2 S, SCH.sub.2, CH.sub.2 CH.sub.2 or CH.dbd.CH; and Z.sup.1 --Z.sup.2 represents C.dbd.CH, CH--CH.sub.2 or CH--CH(COOH)-- or a pharmaceutically acceptable salt thereof.

Abstract: The invention relates to the use of an extract of Cyperus, in particular Cyperus rotundus L. for the preparation of a cosmetic or pharmaceutical composition, especially dermatological composition, intended for promoting the pigmentation of the skin or hair and/or for treating pigmentation disorders.

Abstract: This invention relates to compounds of formula I and pharmaceutically acceptable salts thereof ##STR1## in which R.sub.1 represents hydrogen, alkyl, hydroxy, carboxyalkenyl, alkoxycarbonyalkenyl, hydroxyalkyl, carboxyalkyl, alkoxycarbonylalkyl, alkoxy, halogenated alkyl, carboxy alkoxycarbonyl or alkanoylamino; R.sub.2 represents hydrogen, halo, alkoxy, hydroxy, alkanoyloxy, or phenoxy; R.sub.3 represents hydrogen or alkyl; R.sub.4 represents hydrogen, halo, alkoxycarbonyl, a benzyloxycarbonyl, alkanoyl, benzoyl, carbamoyl, alkyl, carboxy, hydroxyalkyl or alkylthio; R.sub.5 represents hydrogen or alkyl; R.sub.6 represents hydrogen, alkyl [optionally substituted by one or more of the following: hydroxy, halo or an amino group of formula --NR.sub.12 R.sub.13 ], a C.sub.3-12 alicyclic hydrocarbon group, phenyl, (cycloalkyl)alkyl or benzyl; R.sub.7 represents hydrogen, halo, trifluoromethyl, trifluoromethoxy, alkyl, carboxy, or alkoxy; R.sub.

Abstract: A clear antiperspirant gel is made by combining and mixing together (A) an astringent compound having a refractive index of 1.48 to 1.53 which is an antiperspirant salt in the form of (i) a tray dried compound, (ii) an encapsulated salt, or (iii) a solvent solution of a salt compound; and (B) a clear anhydrous organic oil free gel formed with the gelator 12-hydroxystearic acid and a blend of aromatic containing silicone fluid and volatile silicone fluids.

Abstract: A process for preparing imidazopyridines of the general formula: ##STR1## wherein R.sub.1 is an alkyl, cycloalkyl, aryl or aralkyl group or is a heterocyclic radical, R.sub.2 and R.sub.4 are identical or different and are hydrogen, a hydroxy, a cyano, alkyl, cycloalkyl, aryl or aralkyl group or are an alkanoyl or an alkoxy-carbonyl group, and R.sub.3 is hydrogen, an alkyl, aryl or aralkyl group or a halogen atom. In the key step of the process, an amidine of the formula: ##STR2## is cyclized with a 1,3-dicarbonyl compound of the general formula: ##STR3## The imidazopyridines are valuable intermediates for the preparation of angiotensin II antagonists.