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Didymocheton gaudichaudianum

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 UUID68f91e5343019902649786
Scientific name Didymocheton gaudichaudianum
Authority A.Juss.
First published in Mém. Mus. Hist. Nat. 19: 231 (1830 publ. 1831)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Turraea decandra Blanco Fl. Filip. : 347 (1837)
Alliaria ammoorodes Kuntze Revis. Gen. Pl. 1: 108. 1891 [5 Nov 1891]
Alliaria gaudichaudiana Kuntze Revis. Gen. Pl. 1: 109. 1891 [5 Nov 1891]
Alliaria otophora Kuntze Revis. Gen. Pl. 1: 109. 1891 [5 Nov 1891]
Alliaria spanoghei Kuntze Revis. Gen. Pl. 1: 109. 1891 [5 Nov 1891]
Didymocheton albiflorum (C.DC.) Harms Nat. Pflanzenfam. ed. 2 , 19b: 157 (1940)
Didymocheton amooroides (Miq.) Harms Nat. Pflanzenfam. ed. 2 , 19b: 157 (1940)
Didymocheton betchei (C.DC.) Harms Nat. Pflanzenfam. ed. 2 , 19b: 157 (1940)
Didymocheton decandrum (Blanco) Harms Nat. Pflanzenfam. ed. 2 , 19b: 157 (1940)
Didymocheton spanoghei (Miq.) Harms Nat. Pflanzenfam. ed. 2 , 19b: 157 (1940)
Dysoxylum albiflorum C.DC. Annuaire Conserv. Jard. Bot. Genève 15-16: 245 (1912)
Dysoxylum amooroides Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 16 (1868)
Dysoxylum bakerarum Guillaumin J. Linn. Soc., Bot. 51: 550 (1938)
Dysoxylum betchei C.DC. Bull. Herb. Boissier , sér. 2, 3: 178 (1903)
Dysoxylum blancoi S.Vidal Cat. Met. Pl. Leños : 22 (1880)
Dysoxylum decandrum Merr. Sp. Blancoan. : 209 (1918)
Dysoxylum intermedium Merr. & L.M.Perry J. Arnold Arbor. 29: 157 (1948)
Dysoxylum macrophyllum Teijsm. & Binn. Cat. Hort. Bot. Bogor. (Teijsmann & Binnendijk) 211, nomen. 1866
Dysoxylum maota Reinecke Bot. Jahrb. Syst. 25: 643 (1898)
Dysoxylum otophorum Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 15 (1868)
Dysoxylum pubescens Teijsm. & Binn. Cat. Hort. Bot. Bogor. (Teijsmann & Binnendijk) 211, nomen. 1866
Dysoxylum quaifei C.DC. Bull. Herb. Boissier , sér. 2, 6: 982 (1906)
Dysoxylum rufum var. glabrescens Benth. Fl. Austral. 1: 382 (1863)
Dysoxylum salutare Fern.-Vill. Nov. App. 42. 1880
Dysoxylum spanoghei Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 14 (1868)
Dysoxylum vestitum Warb. Bot. Jahrb. Syst. 13: 343 (1891)
Dysoxylum gaudichaudianum (A.Juss.) Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 15 (1868)

Common names Top

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Language Common/alternative name
English ivory mahogany

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 50310944
INPN 706219
KEW urn:lsid:ipni.org:names:578141-1
The Plant List kew-2779969
Open Tree Of Life 430660
NCBI Taxonomy 201015
IUCN Red List 156217920
IPNI 578141-1
iNaturalist 348331
GBIF 3850172
Freebase /m/013cd3tk
Wikipedia Dysoxylum_gaudichaudianum
World Flora Online wfo-0000647066

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
Fascinating Furanosteroids and Their Pharmacological Profile Dembitsky VM Molecules 26-Jul-2023
PMCID:PMC10419491
doi:10.3390/molecules28155669
PMID:37570639
Seedling diversity in actively and passively restored tropical forest understories Wills J, Herbohn J, Wells J, Maranguit Moreno MO, Ferraren A, Firn J Ecol Appl 01-Mar-2021
PMCID:PMC8047924
doi:10.1002/eap.2286
PMID:33421244
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
Cytotoxic Compounds from Wrightia pubescens (R.Br.) De Los Reyes MM, Oyong GG, S. Ng VA, Shen CC, Ragasa CY Pharmacognosy Res 01-Jan-2018
PMCID:PMC5855380
doi:10.4103/pr.pr_45_17
PMID:29568181
Gaudichaudysolin A, a New Limonoid from the Bark of Dysoxylum gaudichaudianum Hiroshi Morita, Yuta Nagakura, Reiko Yamanaka, Yusuke Hirasawa, Takahiro Hosoya, Abdul Rahman, Idha Kusumawati, Noor Cholies Zaini The Japan Institute of Heterocyclic Chemistry 03-Feb-2010
doi:10.3987/COM-09-S(S)106
The evolution of bat pollination: a phylogenetic perspective Fleming TH, Geiselman C, Kress WJ Ann Bot 29-Sep-2009
PMCID:PMC2766192
doi:10.1093/aob/mcp197
PMID:19789175
Making the most of Papua New Guinea’s biodiversity: Establishment of an integrated set of programs that link botanical survey with pharmacological assessment in “The Land of the Unexpected” Barrows LR, Matainaho TK, Ireland CM, Miller S, Carter GT, Bugni T, Rai P, Gideon O, Manoka B, Piskaut P, Banka R, Kiapranis R, Noro JN, Pond CD, Andjelic CD, Koch M, Harper MK, Powan E, Pole AR, Jensen JB Pharm Biol 01-Aug-2009
PMCID:PMC2794140
doi:10.1080/13880200902991599
PMID:20016761
Dysoxylins A-D, tetranortriterpenoids with potent anti-RSV activity from Dysoxylum gaudichaudianum. Chen JL, Kernan MR, Jolad SD, Stoddart CA, Bogan M, Cooper R J Nat Prod 01-Feb-2007
doi:10.1021/NP060398Y
PMID:17315968

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 / Limonoids
[(1R,2R,4S,5S,6S,10R,11S,12R,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-[(3R)-5-oxooxolan-3-yl]-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] (E)-2-methylbut-2-enoate 162871652 Click to see 628.70 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,12R,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-[(3R)-5-oxooxolan-3-yl]-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] (E)-3,4-dimethylpent-2-enoate 162958966 Click to see 656.80 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,12R,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-[(3R)-5-oxooxolan-3-yl]-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] benzoate 162967199 Click to see 650.80 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,12R,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-[(3S)-5-oxooxolan-3-yl]-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] (2R)-2-methylbutanoate 162940085 Click to see 630.80 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,12R,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-[(3S)-5-oxooxolan-3-yl]-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] (E)-2-methylbut-2-enoate 162871651 Click to see 628.70 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,12R,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-[(3S)-5-oxooxolan-3-yl]-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] (E)-3,4-dimethylpent-2-enoate 162958967 Click to see 656.80 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,12R,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-[(3S)-5-oxooxolan-3-yl]-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] benzoate 162967200 Click to see 650.80 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] (E)-2-methylbut-2-enoate 102401803 Click to see 628.70 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] (E)-3,4-dimethylpent-2-enoate 102401806 Click to see 656.80 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] 2-methylbutanoate 102401805 Click to see 630.80 unknown https://doi.org/10.1021/NP060398Y
[(1R,2R,4S,5S,6S,10R,11S,15R,16R,18S,19R)-4,18-diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] benzoate 102401804 Click to see 650.80 unknown https://doi.org/10.1021/NP060398Y
[4,18-Diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] 2-methylbut-2-enoate 162871650 Click to see 628.70 unknown https://doi.org/10.1021/NP060398Y
[4,18-Diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] 2-methylbutanoate 162940084 Click to see CCC(C)C(=O)OC1C2C3C(CO2)(C(CC(C3(C4C1(C5=CCC(C5(C(C4)OC(=O)C)C)C6CC(=O)OC6)C)C)OC(=O)C)O)C 630.80 unknown https://doi.org/10.1021/NP060398Y
[4,18-Diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] 3,4-dimethylpent-2-enoate 162958965 Click to see 656.80 unknown https://doi.org/10.1021/NP060398Y
[4,18-Diacetyloxy-16-hydroxy-1,5,10,15-tetramethyl-6-(5-oxooxolan-3-yl)-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadec-8-en-11-yl] benzoate 162967198 Click to see 650.80 unknown https://doi.org/10.1021/NP060398Y
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(3R,3aR,4R,5R,6R,7aS)-6-[(2R,3S)-3-acetyloxy-2-[(2S,3R)-2-(hydroxymethyl)-2-methyl-5-oxooxolan-3-yl]-5-methoxy-5-oxopentan-2-yl]-5-formyloxy-7a-hydroxy-3-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-3a-methyl-7-methylidene-1-oxo-3,4,5,6-tetrahydro-2H-inden-4-yl] (3R,4S)-3-hydroxy-4-methylhexanoate 163024977 Click to see 766.80 unknown https://doi.org/10.3987/COM-09-S(S)106
[6-[3-acetyloxy-2-[2-(hydroxymethyl)-2-methyl-5-oxooxolan-3-yl]-5-methoxy-5-oxopentan-2-yl]-5-formyloxy-7a-hydroxy-3-(2-hydroxy-5-oxo-2H-furan-3-yl)-3a-methyl-7-methylidene-1-oxo-3,4,5,6-tetrahydro-2H-inden-4-yl] 3-hydroxy-4-methylhexanoate 163024976 Click to see 766.80 unknown https://doi.org/10.3987/COM-09-S(S)106

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