| Identification | Back Directory | [Name]
1H-Naphtho[2,1-b]pyran,3-e | [CAS]
596-84-9 | [Synonyms]
Manoyl
Manoyl oxide
1H-Naphtho[2,1-b]pyran,3-e
(3R,6aα,10bα)-3α-Vinyl-3,4aβ,7,7,10aβ-pentamethyldodecahydro-1H-naphtho[2,1-b]pyran
(3R,6aα,10bα)-Dodecahydro-3,4aβ,7,7,10aβ-pentamethyl-3-vinyl-1H-naphtho[2,1-b]pyran
1H-Naphtho[2,1-b]pyran, 3-ethenyldodecahydro-3,4a,7,7,10a-pentamethyl-, (3R,4aR,6aS,10aS,10bR)- (9CI) | [Molecular Formula]
C20H34O | [MOL File]
596-84-9.mol | [Molecular Weight]
290.48 |
| Hazard Information | Back Directory | [Uses]
Manoyl oxide is a labdane-type diterpenoid. Manoyl oxide is the precursor of Forskolin (HY-15371)[1]. | [Definition]
ChEBI: (13R)-epi-8,13-epoxylabd-14-ene is a tricyclic diterpenoid that is isolated from plants and fungi and exhibits anti-bacterial protperties. It has a role as a plant metabolite, an antibacterial agent and a fungal metabolite. It is a labdane diterpenoid, a cyclic ether, an organic heterotricyclic compound and a tricyclic diterpenoid. | [References]
[1] García-Granados A, et al., Manoyl-oxide biotransformations with filamentous fungi[J]. Current Organic Chemistry, 2007, 11(8): 679-692. |
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