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Didymocheton pettigrewianus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID68f908625d900473386996
Scientific name Didymocheton pettigrewianus
Authority (F.M.Bailey) Hauenschild & Holzmeyer
First published in Taxon 70(6): 1260 (2021)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Dysoxylum whiteanum Merr. & L.M.Perry J. Arnold Arbor. 22: 256 (1941)
Dysoxylum pettigrewianum F.M.Bailey Bot. Bull. Dept. Agric. Queensland 5: 9 (1892)

Common names Top

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Language Common/alternative name
English cairns satinwood
English spur mahogany
English spurwood

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
Tropicos 100327756
KEW urn:lsid:ipni.org:names:578274-1
The Plant List kew-2780119
Open Tree Of Life 477028
NCBI Taxonomy 715773
IPNI 578274-1
iNaturalist 858957
GBIF 3852280
Freebase /m/0h3wj4p
EOL 6954658
Wikipedia Dysoxylum_pettigrewianum
World Flora Online wfo-1000026722
KEW urn:lsid:ipni.org:names:77222449-1
IPNI 77222449-1
GBIF 11609468
EOL 65037935

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
Nitrogen concentration and physical properties are key drivers of woody tissue respiration Westerband AC, Wright IJ, Eller AS, Cernusak LA, Reich PB, Perez-Priego O, Chhajed SS, Hutley LB, Lehmann CE Ann Bot 04-Mar-2022
PMCID:PMC9113292
doi:10.1093/aob/mcac028
PMID:35245930
Antitumor Profile of Carbon-Bridged Steroids (CBS) and Triterpenoids Dembitsky VM, Gloriozova TA, Poroikov VV Mar Drugs 03-Jun-2021
PMCID:PMC8228860
doi:10.3390/md19060324
PMID:34205074
The Translation Inhibitor Rocaglamide Targets a Biomolecular Cavity between eIF4A and Polypurine RNA Iwasaki S, Iwasaki W, Takahashi M, Sakamoto A, Watanabe C, Shichino Y, Floor SN, Fujiwara K, Mito M, Dodo K, Sodeoka M, Imataka H, Honma T, Fukuzawa K, Ito T, Ingolia NT Mol Cell 27-Dec-2018
PMCID:PMC6386617
doi:10.1016/j.molcel.2018.11.026
PMID:30595437
Broad Anatomical Variation within a Narrow Wood Density Range—A Study of Twig Wood across 69 Australian Angiosperms Ziemińska K, Westoby M, Wright IJ PLoS One 23-Apr-2015
PMCID:PMC4408027
doi:10.1371/journal.pone.0124892
PMID:25906320
The Overlooked Biodiversity of Flower-Visiting Invertebrates Wardhaugh CW, Stork NE, Edwards W, Grimbacher PS PLoS One 19-Sep-2012
PMCID:PMC3446946
doi:10.1371/journal.pone.0045796
PMID:23029246
Triterpenoids from Dysoxylum pettigrewianum Dulcie A. Mulholland, Jerald J. Nair Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90421-7

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 / Prenol lipids / Triterpenoids
(E,6S)-6-[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-7-acetyloxy-3-hydroxy-2,6,6,10-tetramethyl-15-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl]-2-methylhept-2-enoic acid 101677476 Click to see 514.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
(Z,6S)-6-[(1S,2R,3R,5R,10R,11R,14R,15S)-3-acetyloxy-2,6,6,10-tetramethyl-7-oxo-15-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl]-2-methylhept-2-enoic acid 163008023 Click to see 512.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
(Z,6S)-6-[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-7-acetyloxy-3-hydroxy-2,6,6,10-tetramethyl-15-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl]-2-methylhept-2-enoic acid 163185952 Click to see CC(CCC=C(C)C(=O)O)C1CCC23C1(C2)CCC4C3(C(CC5C4(CCC(C5(C)C)OC(=O)C)C)O)C 514.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-2-enoic acid 346346 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
3Alpha-Hydroxymasticadienonic Acid 70692334 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
6-(3-Acetyloxy-2,6,6,10-tetramethyl-7-oxo-15-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl)-2-methylhept-2-enoic acid 163008022 Click to see 512.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 73719044 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
6-(7-Acetyloxy-3-hydroxy-2,6,6,10-tetramethyl-15-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl)-2-methylhept-2-enoic acid 163065297 Click to see CC(CCC=C(C)C(=O)O)C1CCC23C1(C2)CCC4C3(C(CC5C4(CCC(C5(C)C)OC(=O)C)C)O)C 514.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
Masticadienonic acid 11340012 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7
Terebinthone 15560138 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(00)90421-7

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