Abstract: 3,5-Diamino-6-(2,3-dichlorophenyl)-1,2,4-triazine isethionate is provided. This salt has high water solubility and thus advantageously allows parenteral administration in the form of a sterile aqueous solution suitable for injection.

Abstract: Compounds of formula (I) ##STR1## inhibit both the cyclo-oxygenase and lipoxygenase pathways of arachidonic acid oxygenation and are useful in medicine as, e.g., anti-inflammatory and anti-asthmatic agents.The compounds may be administered as the raw chemical or in association with a carrier as a pharmaceutical formulation.The compounds may be prepared by methods analogous to those known in the art, e.g., by the method of Duffin and Kendall in J. Chem. Soc. (1954), 408-415, or by other methods.

Abstract: Heterocyclic compounds of formula (I) and acid addition salts thereof inhibit arachidonic acid oxygenation and are useful in medicine, for example as anti-inflammatory agents. ##STR1## The compounds of formula (I) may be prepared by any method analogous to those known in the art, for example by the method of G. F. Duffin and J. D. Kendall in J. Chem. Soc. (1954), 408-415. When used in medicine, the compounds of formula (I) may be administered as the compound alone or as a pharmaceutical formulation together with a pharmaceutically acceptable carrier.

Abstract: Heterocyclic compounds of formula (I) ##STR1## and their acid addition salts, when administered topically, exhibit anti-inflammatory activity and do not produce the side-effects associated with the administration of certain other anti-inflammatories. The compounds of formula (I) may be administered topically as the compound alone or in a suitable topical pharmaceutical formulation.

Abstract: Compounds of formula (I) ##STR1## inhibit both the cyclo-oxygenase and lipoxygenase pathways of arachidonic acid oxygenation and are useful in medicine as, e.g., anti-inflammatory and anti-asthmatic agents.The compounds may be administered as the raw chemical or in association with a carrier as a pharmaceutical formulation.The compounds may be prepared by methods analogous to those known in the art, e.g. by the method of Duffin and Kendall in J. Chem. Soc. (1954), 408-415, or by other methods.

Abstract: 1-Phenoxyalkyl- and 1-anilinoalkyl imidazolines, methods for the preparation thereof, the use thereof as intermediates and pesticides and pesticidal formulations containing such compounds.

Abstract: Glycinamides of formula (1):NH.sub.2 CH.sub.2 CONHE (1)wherein E has seven to nine carbon atoms and is branched alkyl, alkylcycloalkyl or cycloalkylalkyl or their acid addition salts, methods of preparing them, pharmaceutical compositions containing them and their use in medicine as anti-depressants.

Abstract: Compounds of formula (I): ##STR1## wherein Ar is an unsubstituted or mono-, di or tri-substituted phenyl radical in which the substituents are the same or different and are selected from alkyl, alkoxy, halogen, hydroxy, cyano, amino, trifluoromethyl or nitro and in which any two adjacent carbon atoms on the phenyl ring may optionally be joined by a carbon chain having 3 or 4 carbon atoms;X.sup.1 is O or NH;R.sup.1 and R.sup.2 are the same or different and are hydrogen or alkyl; andZ is a group SO.sub.n R.sup.8 or a group ##STR2## in which X.sup.2 is O, S or NR.sup.4 ; R.sup.3 is alkyl, aryl, alkyloxy, aryloxy or NR.sup.5 R.sup.6 ;R.sup.4 is alkyl, aryl, alkyloxy, aryloxy, alkylthio, arylthio or NR.sup.5 R.sup.6 ;R.sup.5 and R.sup.6 are the same or different and are hydrogen, alkyl, aryl, COR.sup.7 or SO.sub.2 R.sup.7 ;R.sup.7 is alkyl, aryl, alkoxy or aryloxy;n is 1 or 2;R.sup.8 is alkyl, aryl or NR.sup.9 R.sup.10 ; andR.sup.9 and R.sup.