Highly Substituted Terphenyls as Inhibitors of Parasite cGMP-Dependent Protein Kinase Activity

Highly Substituted Terphenyls as Inhibitors of Parasite cGMP-Dependent Protein Kinase Activity Tenellones A and B from a <i>Diaporthe</i> sp.:  Two Highly Substituted Benzophenone Inhibitors of Parasite cGMP-Dependent Protein Kinase Activity Tenellones A and B from a <i>Diaporthe</i> sp.:  Two Highly Substituted Benzophenone Inhibitors of Parasite cGMP-Dependent Protein Kinase Activity Terferol, an inhibitor of cyclic adenosine 3',5'-monophosphate phosphodiesterase. I Isolation and characterization. Terferol, an inhibitor of cyclic adenosine 3',5'-monophosphate phosphodiesterase. II Structural elucidation. Trisubstituted thiazoles as potent and selective inhibitors of Plasmodium falciparum protein kinase G (PfPKG) Synthesis and SAR of 2,3-diarylpyrrole inhibitors of parasite cGMP-dependent protein kinase as novel anticoccidial agents Bioactive <i>p</i>-Terphenyl Derivatives from a <i>Cordyceps</i>-Colonizing Isolate of <i>Gliocladium</i> sp. Benzoylbenzimidazole-based selective inhibitors targeting Cryptosporidium parvum and Toxoplasma gondii calcium-dependent protein kinase-1 Three New Pigment Protein Tyrosine Phosphatases Inhibitors from the Insect Parasite Fungus Cordyceps gracilioides: Terreusinone A, Pinophilin C and Cryptosporioptide A