摘要:
A method of controlling parasites in or on an animal comprising administering to the animal a parasiticidally effecive, substantially non-emetic 1-arylpyrazole.
摘要:
Compounds of Formula (I) are provided, as are methods for their preparation. The variables W, X, Y, Z, R 5 , R 8 and Ar in the above formula are defined herein. Such compounds may be used to modulate ligand binding to GABA A receptorsin vivo or in vitro, and are particularly useful in the treatment of a variety of central nervous system (CNS) disorders in humans, domesticated companion animals and livestock animals. Compounds provided herein may be administered alone or in combination with one or more other CNS agents to potentiate the effects of the other CNS agent(s). Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting GABA A receptors (e.g., receptor localization studies).
摘要:
Benzimidazole derivatives having the general formula (I) are provided. These compounds are useful as tyrosine kinase inhibitors, especially for the treatment of cancer.
摘要:
The present invention is a radiation sensitive composition that includes a polymer resin, a photoacid generator, a solvent, and a heterocyclic additive selected from the group consisting of: compounds of the formulas (I), (II), (III), and (IV): where R is H, -NH2-, -OH, -N(CH3)2, -NH-CO-CH3, or (II) where R is CH3 or benzoyl; (III) where R is H, or C1-C4 alkyl; W, X, Y, and Z are each independently selected from CH2-, -C-, -CH(CH3)-, -C(CH3)2-, -NH-, or N(CH3)-, with the proviso that at least one of W, X, Y, or Z is C-, and at least one of W, X, Y, or Z is NH- or N(CH3)-; (IV) where A is CH= or C-; R is H, -CH3, or CH2-CH(CH3)2; R is H, -CH3, or CH2-CH(OH)-CH2(OH); R is H; B and D are identical and selected from C- or CH-; one p and q is 0 and the other p and q is 1, when A is CH=; and p and q are both 1, when A is C-; and mixtures thereof.
摘要:
A method of controlling parasites in or on an animal comprising administering to the animal a parasiticidally effecive, substantially non-emetic 1-arylpyrazole.
摘要:
The invention concerns fungicidal compounds and compositions containing them, of general formula (I) in which the different symbols represent various organic groups. The invention also concerns methods for treating plants using said compounds and the use of said compounds as synthesis intermediates of compounds with fungicidal action.
摘要:
Provided are inhbitors of Rho GTPase activation, and, in particular, compounds that inhibit RhoA activation by an RhoGEF. Also provided are related pharmaceutical compositions and methods. Also provided are methods of inhibiting Rho GTPase activation. Also provided are methods of screening for compounds that inhibit Rho GTPase activation by a RhoGEF.
摘要:
This invention relates to novel homotopic prodrugs and medicaments and methods for their preparation, testing and use. In one embodiment, the homotopic prodrug has the general formula (I) wherein (II) is a biologically-active moiety comprising a carboxylic acid functional group, and Rb is a homotopically-symmetrical alcohol bonded to the biologically-active moiety through the carboxylic acid functional group to form an ester linkage, as well as optical isomers, enantiomers, pharmaceutically acceptable salts, biohydrolyzable amides, esters, and imides thereof and combinations thereof.
摘要:
Neue substituierte Pyrazoline der Formel (I), in welcher R?1¿, R?2¿, R?3¿ und R?4¿ die in der Beschreibung angegebenen Bedeutungen haben,mehrere Verfahren zur Herstellung dieser Stoffe und deren Verwendung zur Bekämpfung von Schädlingen, sowie neue Zwischenprodukte und Verfahren zu deren Herstellung.
摘要:
This invention provides compounds of formula (I) and their pharmaceutically acceptable salts, pharmaceutical formulations of said compounds, and methods for treating hyperglycemia associated with non-insulin dependent diabetes and for treating hyperlipidemia.