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ACD/Labs Blog

Sikorska et al isolated and investigated the unusual polyketide macrolides Mandelalides A-D which were isolated from a new species of Lissoclinum ascidian. Their planar structures were elucidated from sub-milligram samples by comprehensive analysis of 1D and 2D NMR data, and supported by mass spectrometry. Here we will describe the elucidation of Mandelalide A (molecular formula C33H52O11) using ACD/Structure Elucidator Suite.

This example clearly shows how an improper axiom assumption by a researcher can lead to an incorrect structure. Employing an unbiased analysis of spectral data using Structure Elucidator Suite would allow the authors to infer the correct structure (Viridol, molecular formula C20H18O6) unambiguously in several seconds.

Lorente and co-workers isolated two known compounds, pretomaymycin and oxotomaymycin, plus the previously unknown compound barmumycin from the culture broth of the marine actinomycete Streptomyces sp. BOSC-022A. Barmumycin (molecular formula C15H19NO4)and its diacetate show antitumor activity at micromolar concentrations.

A reinvestigation of the NMR and IR results for natural schizocommunin led the researchers to propose a revised structure, quinazolinone. We suggested that if a CASE approach were used elucidate the structure when this compound was firstly isolated, the structure revision would be not necessary: for final structure confirmation X-ray crystallographic analysis would be sufficient.

This month we re-visit the example of structure revision of Epohelmin A with structure revision utilizing ACD/Structure Elucidator Suite, which demonstrates how the software allows a researcher to avoid complex multi-stage synthesis to refute a wrong proposed structure and prove the revised one.

To understand the molecular mechanism underlying the genus-specificity of ascidians' sperm chemotaxis, Matsumori et al investigated the structure of a novel compound Ascidia-SAAF 2 (molecular formula C27H44O10S2Na2), which was isolated from the eggs of the ascidian Ascidia sydneiensis. Utilizing Structure Elucidator Suite allowed the correct structure of unknown, and its configuration upon a double bond to be determined.

Kim et al isolated and identified two unprecedented phosphorus-containing iodinated polyacetylenes, Phosphoiodyn A and B, from a Korean marine sponge Placospongia sp. Here we will describe the structural elucidation of Phosphoiodyn A (molecular formula C16H24O4PI).

Aquatolide is a humulane-derived sesquiterpenoid lactone isolated from Asteriscus aquaticus. The structure originally proposed on the basis of 1D and 2D NMR analysis contains an exceedingly rare ladderane substructure. As a result of the quantum-chemical (QM) calculations of the 13C and 1H chemical shifts and associated coupling constants for a series of possible structures, it was shown that the proposed structure was incorrect. We applied a well-established Computer Assisted Structure Elucidation (CASE) method to the problem, in order to compare results with the QM method.

Wang and co-workers isolated Jatrophalactam (molecular formula C20H29NO3), a novel diterpenoid lactam possessing an unprecedented skeleton from the roots of Jatropha curcas.

To understand the molecular mechanism underlying the genus-specificity of sperm chemotaxis of ascidians (a type of marine invertebrate filter feeders), Matsumori et al have investigated the structure of a novel compound Ascidia-SAAF 2 (molecular formula C27H44O10S2Na2) isolated from the eggs of the ascidian Ascidia sydneiensis.