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Santalum spicatum

Santalum spicatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440038eb3f88283091179
Scientific name Santalum spicatum
Authority A.DC.
First published in Prodr. 14: 585 (1857)

Description Top

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Synonyms Top

Scientific name Authority First published in
Santalum cygnorum Miq. Pl. Preiss. 1: 615 (1845)
Eucarya spicata Sprague & Summerh. Bull. Misc. Inform. Kew 1927: 196 (1927)
Fusanus cignorum Kuntze Revis. Gen. Pl. 2: 589 (1891)
Fusanus spicatus R.Br. Prodr. Fl. Nov. Holland. : 355 (1810)
Fusanus spicatus var. frutescens Hochr. Candollea 2: 355 (1925)

Common names Top

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Language Common/alternative name
Chinese 澳大利亚檀香

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000492979
UNII O8PUT104O1
Tropicos 100436238
KEW urn:lsid:ipni.org:names:780643-1
Open Tree Of Life 150898
NCBI Taxonomy 453088
IUCN Red List 172724199
IPNI 780643-1
GBIF 3788877
Freebase /m/0c1wt9
Elurikkus 414661
USDA GRIN 33077
Wikipedia Santalum_spicatum

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Bioactive compounds from the parasitic plant Arceuthobium vaginatum inhibit Haemonchus contortus egg hatching Becerril-Gil MM, Estrada-Flores JG, González-Cortazar M, Zamilpa A, Endara-Agramont ÁR, Mendoza-de Gives P, López-Arellano ME, Olmedo-Juárez A Rev Bras Parasitol Vet 22-Dec-2023
PMCID:PMC10878698
doi:10.1590/S1984-29612024004
PMID:38126572
Moringa oleifera as a Natural Alternative for the Control of Gastrointestinal Parasites in Equines: A Review Elghandour MM, Maggiolino A, Vázquez-Mendoza P, Alvarado-Ramírez ER, Cedillo-Monroy J, De Palo P, Salem AZ Plants (Basel) 08-May-2023
PMCID:PMC10181162
doi:10.3390/plants12091921
PMID:37176979
Management of Enteric Methane Emissions in Ruminants Using Feed Additives: A Review Palangi V, Lackner M Animals (Basel) 07-Dec-2022
PMCID:PMC9774182
doi:10.3390/ani12243452
PMID:36552373
Integrated Transcriptomic, Metabolomic, and Physiological Analyses Reveal New Insights into Fragrance Formation in the Heartwood of Phoebe hui Yang H, An W, Wang F, Gu Y, Guo H, Jiang Y, Peng J, Liu M, Chen L, Zhang F, Zhu P, Huang X, Wan X Int J Mol Sci 14-Nov-2022
PMCID:PMC9698381
doi:10.3390/ijms232214044
PMID:36430522
LC-MS/MS Characterization of Phenolic Metabolites and Their Antioxidant Activities from Australian Native Plants Ali A, Cottrell JJ, Dunshea FR Metabolites 24-Oct-2022
PMCID:PMC9698446
doi:10.3390/metabo12111016
PMID:36355099
Essential Oils as Multicomponent Mixtures and Their Potential for Human Health and Well-Being Bunse M, Daniels R, Gründemann C, Heilmann J, Kammerer DR, Keusgen M, Lindequist U, Melzig MF, Morlock GE, Schulz H, Schweiggert R, Simon M, Stintzing FC, Wink M Front Pharmacol 24-Aug-2022
PMCID:PMC9449585
doi:10.3389/fphar.2022.956541
PMID:36091825
Evaluation of the anti-SARS-CoV-2 properties of essential oils and aromatic extracts Strub DJ, Talma M, Strub M, Rut W, Zmudzinski M, Brud W, Neyts J, Vangeel L, Zhang L, Sun X, Lv Z, Nayak D, Olsen SK, Hilgenfeld R, Jochmans D, Drąg M Sci Rep 20-Aug-2022
PMCID:PMC9392441
doi:10.1038/s41598-022-18676-w
PMID:35987981
Anti-Diabesity Middle Eastern Medicinal Plants and Their Action Mechanisms Saad B, Kmail A, Haq SZ Evid Based Complement Alternat Med 18-Jul-2022
PMCID:PMC9313926
doi:10.1155/2022/2276094
PMID:35899227
Aromas Influencing the GABAergic System Hartley N, McLachlan CS Molecules 08-Apr-2022
PMCID:PMC9026314
doi:10.3390/molecules27082414
PMID:35458615
Natural Compounds With Antimicrobial and Antiviral Effect and Nanocarriers Used for Their Transportation Stan D, Enciu AM, Mateescu AL, Ion AC, Brezeanu AC, Stan D, Tanase C Front Pharmacol 06-Sep-2021
PMCID:PMC8450524
doi:10.3389/fphar.2021.723233
PMID:34552489
Knowledge Gaps in Taxonomy, Ecology, Population Distribution Drivers and Genetic Diversity of African Sandalwood (Osyris lanceolata Hochst. & Steud.): A Scoping Review for Conservation Mugula BB, Kiboi SK, Kanya JI, Egeru A, Okullo P, Curto M, Meimberg H Plants (Basel) 26-Aug-2021
PMCID:PMC8465005
doi:10.3390/plants10091780
PMID:34579313
The Assessment of Quality of Products Called Sandalwood Oil Based on the Information Provided by Manufacturer of the Oil on Polish, German, and English Websites Hartman-Petrycka M, Lebiedowska A Evid Based Complement Alternat Med 12-Jul-2021
PMCID:PMC8292048
doi:10.1155/2021/9934143
PMID:34335846
The Diversity of Volatile Compounds in Australia’s Semi-Desert Genus Eremophila (Scrophulariaceae) Sadgrove NJ, Padilla-González GF, Green A, Langat MK, Mas-Claret E, Lyddiard D, Klepp J, Legendre SV, Greatrex BW, Jones GL, Ramli IM, Leuner O, Fernandez-Cusimamani E Plants (Basel) 16-Apr-2021
PMCID:PMC8073941
doi:10.3390/plants10040785
PMID:33923613
A Comparison of the Composition of Selected Commercial Sandalwood Oils with the International Standard Kucharska M, Frydrych B, Wesolowski W, Szymanska JA, Kilanowicz A Molecules 13-Apr-2021
PMCID:PMC8070282
doi:10.3390/molecules26082249
PMID:33924603
Effect of aromatherapy on autonomic nervous system regulation with treadmill exercise-induced stress among adolescents Lin PH, Lin YP, Chen KL, Yang SY, Shih YH, Wang PY PLoS One 13-Apr-2021
PMCID:PMC8043395
doi:10.1371/journal.pone.0249795
PMID:33848307

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Octadec-11-en-9-ynoic acid 92809 Click to see CCCCCCC=CC#CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1007/BF02517979
Ximenynic acid 5312688 Click to see CCCCCCC=CC#CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1007/BF02517979
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geranylacetone 1549778 Click to see CC(=CCCC(=CCCC(=O)C)C)C 194.31 unknown https://doi.org/10.1080/10412905.1991.9697970
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Dendrolasin 5316534 Click to see CC(=CCCC(=CCCC1=COC=C1)C)C 218.33 unknown https://doi.org/10.1080/10412905.1991.9697970
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Bergamotene 86608 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Curcumene 14014430 Click to see CC1=CCC(=CC1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
(+)-Epi-alpha-bisabolol 1201551 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1080/10412905.1991.9697970
(2E)-2-Methyl-6-(4-methylphenyl)-2-hepten-1-ol 6430906 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)CO 218.33 unknown https://doi.org/10.1080/10412905.1991.9697970
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1080/10412905.1991.9697970
(6E,10E)-2,6,10-trimethyldodeca-2,6,10-triene 444108 Click to see CC=C(C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1071/CH9702337
(6E,10Z)-2,6,10-trimethyldodeca-2,6,10-triene 21734683 Click to see CC=C(C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1071/CH9702337
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
(S,Z)-2-Methyl-6-(p-tolyl)hept-2-en-1-ol 67178146 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)CO 218.33 unknown https://doi.org/10.1080/10412905.1991.9697970
(Z)-5-[(1S,3S,6R)-2,3-dimethyl-3-tricyclo[2.2.1.02,6]heptanyl]-2-methylpent-2-en-1-ol 25022145 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO 220.35 unknown https://doi.org/10.1080/10412905.1991.9697970
1-Methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene 5316213 Click to see CC1=CCC(=CC1)C(C)CCCC(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
2,6,10-Trimethyldodeca-2,6,10-triene 4475483 Click to see CC=C(C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1071/CH9702337
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1080/10412905.1991.9697970
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1991.9697970
alpha-Santalene 94164 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
alpha-Santalol 5281531 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO 220.35 unknown https://doi.org/10.1080/10412905.1991.9697970
beta Farnesene 15228937 Click to see CCC(=C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1080/10412905.1991.9697970
beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
beta-Santalene 10889018 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
beta-SANTALOL 6857681 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO 220.35 unknown https://doi.org/10.1080/10412905.1991.9697970
cis-Lanceol 6536796 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)CO 220.35 unknown https://doi.org/10.1080/10412905.1991.9697970
Epi-beta-Santalene 11106484 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
gamma-Bisabolene, (Z)- 3033866 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
Norbornane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)- 10534 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697970
trans-beta-Santalol 6450269 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO 220.35 unknown https://doi.org/10.1080/10412905.1991.9697970
trans-Nerolidol 5284507 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1991.9697970

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