✦ LIBER ✦

Biosynthetic origins of the large macrolide, oligomycin A

✍ Scribed by John D. Bu'Lock; Gareth A. Morris; Michelle K. Richards

Publisher: Elsevier Science
Year: 1986
Tongue: French
Weight: 229 KB
Volume: 27
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)84680-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Biosynthetic Origins of the Carbon Skele

Biosynthetic Origins of the Carbon Skeleton of Heme d1

✍ J.C. Matthews; R. Timkovich 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 483 KB

\({ }^{13}\)-labeling experiments were performed to determine the simple precursor metabolites that contribute to the tetrapyrrole skeleton of heme \(\mathrm{d}_{1}\). By use of \(5-\left[4^{-13} \mathrm{C}\right]\) aminolevulinic acid it was determined that the skeleton is derived from \(8 \mathrm{

Biosynthetic origin of the gem-methyls o

Biosynthetic origin of the gem-methyls of geraniol

✍ Anand Akhila; Derek V. Banthorpe 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 274 KB

The biosynthetic origin of the pyridone

The biosynthetic origin of the pyridone ring of efrotomycin

✍ Gary Darland; Byron Arison; Louis Kaplan 📂 Article 📅 1991 🏛 Springer-Verlag 🌐 English ⚖ 543 KB

Biosynthetic Origin of the Oxygen Atoms

Biosynthetic Origin of the Oxygen Atoms of Tetracenomycin C

✍ Dipl.-Ing. Györgyi Udvarnoki; Dr. Christina Wagner; Dipl.-Chem. Reinhard Machine 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 391 KB

Biosynthetic origin of the tetrahydropyr

Biosynthetic origin of the tetrahydropyranyl side chain of verucopeptin

✍ Youla S. Tsantrizos; Jianhua Shen; Laird A. Trimble 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 238 KB

The biosynthesis of the tetrahydropyranyl side chain of verucopeptin (1) in cultures of Actinomadura verrucosospora was investigated. Incorporation experiments using 13C-labeled acetate and propionate, followed by analysis of the labeled metabolite by NMR, revealed that the tetrahydropyranyl side ch

The chemistry of unusual macrolides, 2.

The chemistry of unusual macrolides, 2. Spectroscopic and biosynthetic investigations of the V-type ATPase inhibitor concanamycin A

✍ Bindseil, Kai U. ;Zeeck, Axel 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 769 KB

## Abstract The ^1^H‐ and ^13^C‐NMR spectra of the conformationally flexible macrolide concanamycin A (1) have been assigned by the use of 2D NMR techniques at low temperatures and have enabled biosynthetic studies on this most potent inhibitor of vacuolar ATPases. By feeding of different [^13^C]‐l