Abstract: The present invention relates to furanopyrimidine compounds having the general Formula I: and stereoisomers, tautomers, solvates, pharmaceutically acceptable salts and derivatives, and prodrugs thereof. The invention also includes pharmaceutical compositions comprising a compound of Formula I, methods of treating various diseases and conditions in a mammal, including inflammation, inhibition of T cell activation, proliferation, arthritis, organ transplant, ischemic or reperfusion injury, myocardial infarction, stroke, multiple sclerosis, inflammatory bowel disease, Crohn's disease, lupus, hypersensitivity, type 1 diabetes, psoriasis, dermatitis, Hashimoto's thyroiditis, Sjogren's syndrome, autoimmune hyperthyroidism, Addison's disease, autoimmune diseases, glomerulonephritis, allergic diseases, asthma, hayfever, eczema, cancer, colon carcinoma and thymoma, comprising administering to the mammal a therapeutically effective amount of a compound of Formula I.

Abstract: Compounds that modulate the action of ACK1 and LCK, and related compositions methods for treating ACK1- and LCK-mediated diseases are described. In one aspect, the compounds have the general structure: where the values of the substituents are provided herein.

Abstract: Compounds of formula (I) are pesticides having activity against arthropods: ##STR1## wherein R.sup.1, R.sup.2 and R.sup.3 are H, alkyl, alkoxy, halo, cyano or trifluoromethyl, or two of R.sup.1, R.sup.2 and R.sup.3 are linked to form a 3 or 4 carbon atom group;X is O or NA where A is H or alkyl;R is H or alkyl; andR.sup.4 and R.sup.5 are H, alkenyl or haloalkenyl or optionally substituted alkyl, aryl or aralkyl, or NR.sup.4 R.sup.5 represents a heterocyclic ring; or an acid addition salt thereof.The invention further provides methods for the preparation of the compounds, pesticidal formulations containing them, and their use in controlling arthropod pests.

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: Compounds of formula (I) are pesticides active against arthropods. ##STR1## wherein R.sup.1, R.sup.2, and R.sup.3 are H, alkyl, alkoxy, halo, CN or CF.sub.3 or two are linked to form a 3 or 4 carbon atom group;X is O or NA where A is H or alkyl;R is H or alkyl;R.sup.4 is H or optionally substituted alkyl, aryl, aralkyl, alkenyl or alkynyl; andR.sup.5 is --CB. R.sup.6 where B is O, S or NR.sup.7 where R.sup.7 is H, alkyl, alkoxy, or optionally substituted aryl or aralkyl;R.sup.6 is H, R.sup.8, OR.sup.8, SR.sup.8 or NR.sup.9 R.sup.10 where R.sup.8 is alkyl, alkenyl or optionally substituted aryl, aralkyl or aryloxyalkyl; and R.sup.9 and R.sup.10 are H, alkyl or optionally substituted aryl or aralkyl;The invention also comprises processes for the preparation of compounds (I), formulations containing them, and their use as pesticides.

Abstract: Imidazoline compounds of formula (I): ##STR1## wherein Ar is selected from a phenyl or a mono-, di- or tri-substituted phenyl radical in which the substituents are selected from alkyl, alkoxy, halogen, hydroxy, cyano, amino, trihalomethyl and nitro and in which any two adjacent carbon atoms of the phenyl ring may be joined by a carbon chain containing 3 or 4 carbon atoms;X.sup.1 is S, NR.sup.3 or NZ.sup.1 ;R.sup.1 and R.sup.2 are selected from hydrogen or alkyl;R.sup.3 is alkyl or aryl;m is 0 or 1; andZ.sup.1 and Z.sup.2 are a group SO.sub.n R.sup.9 or a group ##STR2## in which X.sup.2 is O, S or NR.sup.5 ; R.sup.4 is alkyl, aryl, alkoxy, aryloxy, amino or amido;R.sup.5 is alkyl, aryl, alkoxy, aryloxy, alkylthio, arylthio, amino or amido;the alkyl or alkoxy radicals containing from 1 to 4 carbon atoms each; or an acid addition salt of the imidazoline compound.Methods of preparing the compounds are provided, as are pesticidal formulations containing them.

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.