Chemistry:Viridiflorol
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IUPAC name
6β,11-Cyclo-1β,4α,5β,10α-guaian-10-ol
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Systematic IUPAC name
(1aR,4S,4aS,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol | |
Other names
(+)-Viridiflorol
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Identifiers | |
3D model (JSmol)
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ChEBI | |
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PubChem CID
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Properties | |
C15H26O | |
Molar mass | 222.372 g·mol−1 |
Hazards | |
GHS pictograms | |
GHS Signal word | Warning |
H315, H319 | |
P264, P280, P302+352, P305+351+338, P321, P332+313, P337+313, P362 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Tracking categories (test):
Viridiflorol is a chemical compound, classified as a sesquiterpenoid, that has been isolated from the essential oils of a variety of plants including Melaleuca quinquenervia[1] (broad-leaved paperbark), Melaleuca alternifolia[2] (tea tree), and Allophylus edulis.[3]
Viridiflorol has shown moderate antibacterial activity against Mycobacterium tuberculosis, the causative agent of tuberculosis, in an in vitro assay. [1] It is also produced by the endophytic root fungus Serendipita indica and exhibits antifungal activity against Colletotrichum truncatum [4]
References
- ↑ 1.0 1.1 Ireland, B.F.; Hibbert, D.B.; Goldsack, R.J.; Doran, J.C.; Brophy, J.J. (2002). "Chemical variation in the leaf essential oil of Melaleuca quinquenervia (Cav.). It is also produced by the endopytic fungus Serendipita indica S.T. Blake". Biochemical Systematics and Ecology 30 (5): 457–470. doi:10.1016/s0305-1978(01)00112-0.
- ↑ "Essential oil of Melaleuca, terpene-4-ol (tea tree oil): ISO 4730: 2017 (E)". International Organization for Standardization (ISO), Geneva, Switzerland. 2017. https://www.sis.se/api/document/preview/921469. Retrieved 6 March 2019.
- ↑ Trevizan, Lucas Noboru Fatori; Nascimento, Kamilla Felipe do; Santos, Joyce Alencar; Kassuya, Candida Aparecida Leite; Cardoso, Claudia Andrea Lima; Vieira, Maria do Carmo; Moreira, Flora Martinez Figueira; Croda, Julio et al. (2016). "Anti-inflammatory, antioxidant and anti- Mycobacterium tuberculosis activity of viridiflorol: The major constituent of Allophylus edulis (A. St.-Hil., A. Juss. & Cambess.) Radlk". Journal of Ethnopharmacology 192: 510–515. doi:10.1016/j.jep.2016.08.053. PMID 27612433.
- ↑ Ntana, F.; Bhat, W.W.; Johnson, S.R.; Jørgensen, H.J.L.; Collinge, D.B.; Jensen, B.; Hamberger, B. (2021). "A Sesquiterpene Synthase from the Endophytic Fungus Serendipita indica Catalyzes Formation of Viridiflorol.". Biomolecules 11: 898. doi:10.3390/biom11060898.
Original source: https://en.wikipedia.org/wiki/Viridiflorol.
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