C10 N-Acyl modified FK-506: A possible hybrid analogue of the transition state of peptidyl-prolyl cis-trans isomerization.
- 1 March 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (10) , 1375-1378
- https://doi.org/10.1016/s0040-4039(00)79671-7
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Molecular cloning and overexpression of the human FK506-binding protein FKBPNature, 1990
- Inhibition of FKBP Rotamase Activity by Immunosuppressant FK506: Twisted Amide SurrogateScience, 1990
- A receptor for the immuno-suppressant FK506 is a cis–trans peptidyl-prolyl isomeraseNature, 1989
- A cytosolic binding protein for the immunosuppressant FK506 has peptidyl-prolyl isomerase activity but is distinct from cyclophilinNature, 1989
- Kinetic β‐deuterium isotope effects suggest a covalent mechanism for the protein folding enzyme peptidylprolyl cis/trans‐isomeraseFEBS Letters, 1989
- Total synthesis of immunosuppressant (-)-FK-506Journal of the American Chemical Society, 1989
- Cyclophilin and peptidyl-prolyl cis-trans isomerase are probably identical proteinsNature, 1989
- Peptidyl-prolyl cis-trans isomerase is the cyclosporin A-binding protein cyclophilinNature, 1989
- A synthetic route to the tricarbonyl region of FK-506The Journal of Organic Chemistry, 1989
- Rapamycin (AY-22,989), a new antifungal antibiotic. I. Taxonomy of the producing streptomycete and isolation of the active principle.The Journal of Antibiotics, 1975