Structures and Anatomical Distribution of Oxygenated Diterpenes in the Australian Nudibranch Chromodoris reticulata

Suciati and Lynette K. Lambert and Mary J. Garson (2011) Structures and Anatomical Distribution of Oxygenated Diterpenes in the Australian Nudibranch Chromodoris reticulata. Australian Journal of Chemistry, 64 (6). pp. 757-765. ISSN 0004-9425

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Official URL: http://www.publish.csiro.au/CH/CH11036

Abstract

The structures and stereochemistry of six new diterpenes (1–6), two of which contain cyclic imine functionality, have been deduced by 2D NMR spectroscopy. The anatomical distribution of these, and of 17 other diterpenes (7–23) that were also isolated, has been investigated. The known compound aplyroseol-2 (14) was the major compound in the mantle tissue along with some dialdehydes, while the linear furan ambliofuran (7) was the only diterpene found solely in the internal organs. The presence of lactone-acetal-hemiacetal functionality in many of the isolated compounds is a consequence of the reactive dialdehydes present in the mollusc.

Item Type: Article
Subjects: R Medicine
R Medicine > RS Pharmacy and materia medica
Divisions: 05. Fakultas Farmasi
Creators:
CreatorsNIM
SuciatiNIDN0004117905
Lynette K. LambertUNSPECIFIED
Mary J. GarsonUNSPECIFIED
Depositing User: Mr M. Fuad Sofyan
Date Deposited: 24 Jan 2020 07:17
Last Modified: 05 Feb 2020 04:08
URI: http://repository.unair.ac.id/id/eprint/93602
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