Pseudotheonamides, Serine Protease Inhibitors from the Marine Sponge Theonella swinhoei¹

This publication has 10 references indexed in Scilit:

• Cyclotheonamides E2 and E3, New Potent Serine Protease Inhibitors from the Marine Sponge of the Genus Theonella
  Journal of Natural Products, 1998
• Transformation of the marine natural product cyclotheonamide A by aqueous base. X-ray analysis of a novel ligand complexed with human α-thrombin
  Tetrahedron Letters, 1996
• Comparison of the structures of the cyclotheonamide a complexes of human α‐thrombin and bovine β‐trypsin
  Protein Science, 1996
• Three more cyclotheonamides, C, D, and E, potent thrombin inhibitors from the marine sponge Theonella swinhoei
  Bioorganic & Medicinal Chemistry, 1995
• Theonellamides A-E, cytotoxic bicyclic peptides, from a marine sponge Theonella sp.
  The Journal of Organic Chemistry, 1995
• Molecular basis for the inhibition of human alpha-thrombin by the macrocyclic peptide cyclotheonamide A.
  Proceedings of the National Academy of Sciences, 1993
• Bioactive marine metabolites. 33. Cyclotheonamides, potent thrombin inhibitors, from a marine sponge Theonella sp
  Journal of the American Chemical Society, 1990
• Stereochemistry associated with the addition of 2-(trimethylsilyl)thiazole to differentially protected .alpha.-amino aldehydes. Applications toward the synthesis of amino sugars and sphingosines
  The Journal of Organic Chemistry, 1990
• First observation of electroluminescence at the p-type semiconductor/electrolyte interface caused by electron injection. Energetics of adsorbed hydrogen at the p-gallium arsenide electrode
  Journal of the American Chemical Society, 1986
• Synthesis of alternating hydroxy- and methyl-substituted hydrocarbons by oxymercuration of cyclopropylcarbinols
  Journal of the American Chemical Society, 1986