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Journal ArticleDOI

Structure of FK506, a novel immunosuppressant isolated from Streptomyces

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This article is published in Journal of the American Chemical Society.The article was published on 1987-08-01. It has received 523 citations till now. The article focuses on the topics: Streptomyces tsukubaensis & Streptomyces.

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Journal ArticleDOI

Application of coil centrifugal counter-current chromatography to the separation of macrolide antibiotic analogues III. Effects of flow-rate, mass load and rotation speed on the peak resolution.

TL;DR: The results show that the retention percentage of the stationary phase has linear relationships with both flow-rate at 1 to 3 ml/min and rotation speed at 100 to 700 rpm, but their correlation coefficients are negative (-1.000) and positive (0.9821).
Journal ArticleDOI

Novel derivatives at the C21 position of the FK-506 macrocycle

TL;DR: In this paper, a number of derivatives of FK-506 were prepared and their immunosuppressant properties evaluated in a T-cell proliferation assay, and some of these compounds are surprisingly potent antagonists of Fk-506-mediated immuno-suppression.
Journal ArticleDOI

Aerobic oxidative amidation of alkynes using titanium oxide encapsulated cuprous iodide nanoparticles (CuI@TiO2)

TL;DR: In this article, a catalyst consisting of titanium oxide encapsulated cuprous iodide nanoparticles was prepared via a sol-gel method using inexpensive raw materials and was harnessed successfully in the oxidative amidation of alkynes via an environmentally benign and sustainable protocol.
Book ChapterDOI

Chapter 22. Mechanism-Based Immunosuppressants

TL;DR: While macrocyclic immunosuppressants exert their effects through a variety of paths, the total elucidation and refinement of their mechanism(s) of action are ongoing, and the utility of traditional, clinically used immuno-pharmaceuticals is largely limited to transplantation.
Journal ArticleDOI

Thermal rearrangement of the immunosuppressant fk-506

TL;DR: In this article, FK-506 in xylene at reflux results in a [3,3] sigmropic rearrangement of the allylic ester portion of the molecule to give a new ring expanded macrolide.
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