Transformation of the marine natural product cyclotheonamide A by aqueous base. X-ray analysis of a novel ligand complexed with human α-thrombin
- 20 May 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (21) , 3667-3670
- https://doi.org/10.1016/0040-4039(96)00658-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Total Synthesis of Cyclotheonamide B, a Facile Route towards AnaloguesTetrahedron Letters, 1995
- Macrocyclic Peptide Inhibitors of Serine Proteases. Convergent Total Synthesis of Cyclotheonamides A and B via a Late-Stage Primary Amine Intermediate. Study of Thrombin Inhibition under Diverse ConditionsJournal of the American Chemical Society, 1995
- Synthesis of Cyclotheonamide B and Its DerivativesAngewandte Chemie International Edition in English, 1994
- Atomic structure of the trypsin-cyclotheonamide A complex: lessons for the design of serine protease inhibitorsJournal of the American Chemical Society, 1993
- Total synthesis of cyclotheonamide AThe Journal of Organic Chemistry, 1993
- Inhibition of thrombin and other trypsin-like serine proteinases by cyclotheonamide AThrombosis Research, 1993
- Reassignment of stereochemistry and total synthesis of the thrombin inhibitor cyclotheonamide BJournal of the American Chemical Society, 1992
- Structure of the hirugen and hirulog 1 complexes of α-thrombinJournal of Molecular Biology, 1991
- Bioactive marine metabolites. 33. Cyclotheonamides, potent thrombin inhibitors, from a marine sponge Theonella spJournal of the American Chemical Society, 1990