Widdringtonia whytei - Unknown
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Internal ID UUID643ffb99e5c9d418228385
Scientific name Widdringtonia whytei
Authority Rendle
First published in Trans. Linn. Soc. London, Bot. 4: 60 (1894)

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Synonyms Top

Scientific name Authority First published in
Widdringtonia nodiflora var. whytei (Rendle) Silba Phytologia 68: 74 (1990)
Widdringtonia nodiflora subsp. whytei (Rendle) Silba J. Int. Conifer Preserv. Soc. 13(1): 20 (2006)
Callitris whytei (Rendle) Engl. Pflanzenw. Ost-Afrikas , C: 93 (1895)

Common names Top

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Language Common/alternative name
English mulanje cedar
English mulanje cedarwood
English mulanje cypress
Persian سرو مولانجی
French widdringtonia whitei
Russian Виддрингтония Уайта
Chinese 姆兰杰南非柏

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000427973
Tropicos 9400129
KEW urn:lsid:ipni.org:names:264042-1
The Plant List kew-2466624
Open Tree Of Life 305714
NCBI Taxonomy 1075059
IUCN Red List 33216
IPNI 264042-1
iNaturalist 135523
GBIF 2684261
Freebase /m/02vv13q
EPPO WIDWH
EOL 1034888
USDA GRIN 42028
Wikipedia Widdringtonia_whytei

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
A biogeographical appraisal of the threatened South East Africa Montane Archipelago ecoregion Bayliss J, Bittencourt-Silva GB, Branch WR, Bruessow C, Collins S, Congdon TC, Conradie W, Curran M, Daniels SR, Darbyshire I, Farooq H, Fishpool L, Grantham G, Magombo Z, Matimele H, Monadjem A, Monteiro J, Osborne J, Saunders J, Smith P, Spottiswoode CN, Taylor PJ, Timberlake J, Tolley KA, Tovela É, Platts PJ Sci Rep 12-Mar-2024
PMCID:PMC10933300
doi:10.1038/s41598-024-54671-z
PMID:38472297
Seed viability of five wild Saudi Arabian species by germination and X-ray tests Al-Hammad BA, Al-Ammari BS Saudi J Biol Sci 12-Apr-2017
PMCID:PMC5562476
doi:10.1016/j.sjbs.2017.04.004
PMID:28855841
Determination of seed viability of eight wild Saudi Arabian species by germination and X-ray tests Al-Turki TA, Baskin CC Saudi J Biol Sci 05-Jul-2016
PMCID:PMC5415129
doi:10.1016/j.sjbs.2016.06.009
PMID:28490953
Environmental Gap Analysis to Prioritize Conservation Efforts in Eastern Africa van Breugel P, Kindt R, Lillesø JP, van Breugel M PLoS One 09-Apr-2015
PMCID:PMC4391866
doi:10.1371/journal.pone.0121444
PMID:25855968
A polyphasic taxonomy of Daldinia (Xylariaceae) Stadler M, Læssøe T, Fournier J, Decock C, Schmieschek B, Tichy HV, Peršoh D Stud Mycol 15-Mar-2014
PMCID:PMC3953824
doi:10.3114/sim0016
PMID:24790283
A re‐examination of mulanje cedarwood oil (<i>Widdringtonia whytei</i> Rendle) C. L. Green, A. B. Wood, J. M. Robinson Wiley 04-Nov-2006
doi:10.1002/FFJ.2730030303
Prediction of Desiccation Sensitivity in Seeds of Woody Species: A Probabilistic Model Based on Two Seed Traits and 104 Species DAWS MI, GARWOOD NC, PRITCHARD HW Ann Bot 01-Apr-2006
PMCID:PMC3291879
doi:10.1093/aob/mcl022
PMID:16464874

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids
Arhimachalene 11458355 Click to see CC1CCCC(C2=C1C=CC(=C2)C)(C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1R,4S,5R)-1,8-Dimethyl-4-(prop-1-en-2-yl)spiro[4.5]dec-7-ene 20055537 Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
(1R)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene 5316209 Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
Acoradiene 90351 Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
alpha-Alaskene 6428487 Click to see CC1CCC(=C(C)C)C12CCC(=CC2)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Bergamotene, (E)-(-)- 6429302 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
alpha-CIS-BERGAMOTENE 6429303 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
1-methyl-4-[(1S)-1,2,2-trimethylcyclopentyl]cyclohexa-1,3-diene 5316205 Click to see CC1=CC=C(CC1)C2(CCCC2(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
Thujopsadiene 6428961 Click to see CC1=CCC2(CC=CC(C23C1C3)(C)C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730030303
Thujopsen 97829 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
Thujopsene 442402 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(+)-beta-Cedrene 102432 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
beta-Cedrene 11106485 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown https://doi.org/10.1002/FFJ.2730030303
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1002/FFJ.2730030303
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[7]annulene 15095 Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
beta-Himachalene 11586487 Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1 204.35 unknown https://doi.org/10.1002/FFJ.2730030303
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
1H-Benzocyclohepten-7-ol, 2,3,4,4a,5,6,7,8-octahydro-1,1,4a,7-tetramethyl-, cis- 5315300 Click to see CC1(CCCC2(C1=CCC(CC2)(C)O)C)C 222.37 unknown https://doi.org/10.1002/FFJ.2730030303
Widdrol 94334 Click to see CC1(CCCC2(C1=CCC(CC2)(C)O)C)C 222.37 unknown https://doi.org/10.1002/FFJ.2730030303

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