Nobilonin
Structural formula | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
General | ||||||||||
Surname | Nobilonin | |||||||||
other names |
δ-nobilonin |
|||||||||
Molecular formula | C 17 H 27 NO 3 | |||||||||
External identifiers / databases | ||||||||||
|
||||||||||
properties | ||||||||||
Molar mass | 293.4 | |||||||||
Melting point |
87-88 ° C |
|||||||||
safety instructions | ||||||||||
|
||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Nobilonin is a natural product from the group of dendrobium alkaloids . The isolation from the orchid Dendrobium nobile and the structure elucidation was published in 1964. Next to dendrobin , nobilonin is the second most common alkaloid from the orchid Dendrobium nobile and occurs in three other dendrobium species.
structure
Nobilonin is a tricyclic compound in which a cyclohexanone structural element is fused with a cyclopentane ring and bridged by a lactone unit . The compound is possibly a biosynthetic precursor of dendrobin with an open pyrrolidine ring .
Individual evidence
- ↑ a b Shosuke Yamamura, Yoshimasa Hirata: Structures of nobiline and dendrobine . In: Tetrahedron Letters . tape 5 , no. January 2 , 1964, p. 79 , doi : 10.1016 / s0040-4039 (00) 90333-2 .
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ a b Epidendroideae (Part Three) . In: Alec M. Pridgeon, Phillip H. Cribb, Mark W. Chase, Finn N. Rasmussen (Eds.): Genera Orchidacearum . tape 6 . Oxford University Press, 2014, ISBN 978-0-19-964651-7 , pp. 75 ( limited preview in Google Book search).