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Bisabosquals, Novel Squalene Synthase Inhibitors. II. Physico-chemical Properties and Structure Elucidation
- Source :
- The Journal of Antibiotics. 54:896-903
- Publication Year :
- 2001
- Publisher :
- Japan Antibiotics Research Association, 2001.
-
Abstract
- The squalene synthase inhibitor bisabosqual A was isolated from the culture broth of Stachybotrys sp. RF-7260, and its structure was determined on the basis of spectroscopic methods including detailed 2D NMR analyses. The structures of bisabosquals B, C and D isolated from Stachybotrys ruwenzoriensis RF-6853 were determined by spectroscopic methods and chemical reactions. The absolute stereochemistry of bisabosquals A, B and D was determined by X-ray crystallographic analysis. They have novel cis-fused tetracyclic structures with a bisabolane-type sesquiterpene and phenol moieties.
- Subjects :
- Magnetic Resonance Spectroscopy
Optical Rotation
Spectrophotometry, Infrared
Stereochemistry
Stachybotrys
Stereoisomerism
Crystallography, X-Ray
Sesquiterpene
Gas Chromatography-Mass Spectrometry
chemistry.chemical_compound
Squalene
Drug Discovery
Organic chemistry
Enzyme Inhibitors
Pyrans
Pharmacology
chemistry.chemical_classification
Farnesyl-diphosphate farnesyltransferase
biology
Nuclear magnetic resonance spectroscopy
biology.organism_classification
Molecular Weight
Farnesyl-Diphosphate Farnesyltransferase
Enzyme
chemistry
Spectrophotometry, Ultraviolet
Two-dimensional nuclear magnetic resonance spectroscopy
Subjects
Details
- ISSN :
- 18811469 and 00218820
- Volume :
- 54
- Database :
- OpenAIRE
- Journal :
- The Journal of Antibiotics
- Accession number :
- edsair.doi.dedup.....ab5f2bd531c5ffb2a7167402c88a0bb3
- Full Text :
- https://doi.org/10.7164/antibiotics.54.896