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Zygogynum pancheri

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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 UUID6440576d36cac188468893
Scientific name Zygogynum pancheri
Authority (Baill.) Vink
First published in Blumea 31: 54 (1985)

Description Top

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Synonyms Top

Scientific name Authority First published in
Belliolum pancheri Tiegh. J. Bot. (Morot) 14: 330 (1900)
Bubbia pancheri (Baill.) B.L.Burtt Hooker's Icon. Pl. 34: t. 3315, 1 (1936)
Drimys pancheri Baill. Adansonia 10: 336 (1872)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Zygogynum pancheri subsp. arrhantum Vink Blumea 34: 518 (1990)
Zygogynum pancheri subsp. deplanchei (v.Tieghem) Vink Blumea 34: 518 (1990)
Zygogynum pancheri subsp. elegans Vink Blumea 34: 518 (1990)
Zygogynum pancheri subsp. rivulare (Vieillard & P.Parm.) Vink Blumea 34: 518 (1990)

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

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-0001260983
Tropicos 50197622
INPN 674406
KEW urn:lsid:ipni.org:names:915621-1
The Plant List tro-50197622
Open Tree Of Life 59238
NCBI Taxonomy 132898
IPNI 915621-1
GBIF 7288437
EOL 5035410

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
Anticancer Activity of Natural and Semi-Synthetic Drimane and Coloratane Sesquiterpenoids Beckmann L, Tretbar US, Kitte R, Tretbar M Molecules 13-Apr-2022
PMCID:PMC9031474
doi:10.3390/molecules27082501
PMID:35458699
Testing the benefits of early vessel evolution Roddy AB J Exp Bot 28-Jun-2019
PMCID:PMC6598055
doi:10.1093/jxb/erz187
PMID:31250904
Selected abstracts from the 26th Conference of the European Cell Death Organization (ECDO): Cell death in disease — from small molecules to translational medicine N/A Cell Death Discov 03-Jan-2019
PMCID:PMC6323120
doi:10.1038/s41420-018-0128-4
Cytotoxic sesquiterpenoids from Winteraceae of Caledonian rainforest. Allouche N, Apel C, Martin MT, Dumontet V, Guéritte F, Litaudon M Phytochemistry 01-Mar-2009
doi:10.1016/J.PHYTOCHEM.2009.01.012
PMID:19251287
Biologically active tetralones from New Caledonian Zygogynum spp. Allouche N, Morleo B, Thoison O, Dumontet V, Nosjean O, Guéritte F, Sévenet T, Litaudon M Phytochemistry 01-May-2008
doi:10.1016/J.PHYTOCHEM.2008.01.025
PMID:18334258

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 / Naphthalenes / Phenylnaphthalenes
(8R)-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-8,9-dihydro-7H-benzo[g]chromen-6-one 24863960 Click to see CC1(C=CC2=C(O1)C=C3CC(CC(=O)C3=C2O)C4=CC=C(C=C4)O)C 336.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-8,9-dihydro-7H-benzo[g]chromen-6-one 74337436 Click to see CC1(C=CC2=C(O1)C=C3CC(CC(=O)C3=C2O)C4=CC=C(C=C4)O)C 336.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
8-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-8,9-dihydro-7H-benzo[g]chromen-6-one 74343933 Click to see CC1(C=CC2=C(O1)C=C3CC(CC(=O)C3=C2O)C4=CC(=C(C=C4)O)O)C 352.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
Zygolone A 24882527 Click to see CC1(C=CC2=C(O1)C=C3CC(CC(=O)C3=C2O)C4=CC(=C(C=C4)O)O)C 352.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
> Organic oxygen compounds / Organic oxides
5,5,8a-Trimethyl-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 5080908 Click to see CC1(CCCC2(C1CC=C(C2C=O)C=O)C)C 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
Tadeonal 72503 Click to see CC1(CCCC2(C1CC=C(C2C=O)C=O)C)C 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
https://doi.org/10.1016/J.PHYTOCHEM.2009.01.012
> Organoheterocyclic compounds / Naphthofurans
(1,5-Dihydroxy-6,6,9a-trimethyl-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-9-yl) 3-phenylprop-2-enoate 74820602 Click to see CC1(CCC(C2(C1C(C=C3C2C(OC3)O)O)C)OC(=O)C=CC4=CC=CC=C4)C 398.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
[(1R,5S,5aS,9R,9aS,9bS)-1,5-dihydroxy-6,6,9a-trimethyl-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-9-yl] (E)-3-phenylprop-2-enoate 42611884 Click to see CC1(CCC(C2(C1C(C=C3C2C(OC3)O)O)C)OC(=O)C=CC4=CC=CC=C4)C 398.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
6,6,9a-trimethyl-3a,4,5,5a,7,8,9,9b-octahydro-3H-benzo[g][2]benzofuran-1-one 69782495 Click to see CC1(CCCC2(C1CCC3C2C(=O)OC3)C)C 236.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
7-Ketoisodrimenin 13281820 Click to see CC1(CCCC2(C1CC(=O)C3=C2C(=O)OC3)C)C 248.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
Benzo[e]isobenzofuran-1,4-dione,1,3,4,5,5a,6,7,8,9,9a-decahydro-6,6,9a-trimethyl 563311 Click to see CC1(CCCC2(C1CC(=O)C3=C2C(=O)OC3)C)C 248.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
Jeekfyiezdnhgk-ohtbphcpsa- 10331685 Click to see CC1(CCCC2(C1CCC3C2C(=O)OC3)C)C 236.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
(7,8-Diformyl-4,4,8a-trimethyl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl) 3-phenylprop-2-enoate 74820548 Click to see CC1(CCC(C2(C1CC=C(C2C=O)C=O)C)OC(=O)C=CC3=CC=CC=C3)C 380.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
(7,8-diformyl-4a-hydroxy-4,4,8a-trimethyl-2,3,5,8-tetrahydro-1H-naphthalen-1-yl) 3-phenylprop-2-enoate 74820547 Click to see CC1(CCC(C2(C1(CC=C(C2C=O)C=O)O)C)OC(=O)C=CC3=CC=CC=C3)C 396.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
(7,8-Diformyl-5-hydroxy-4,4,8a-trimethyl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl) 3-phenylprop-2-enoate 74820546 Click to see CC1(CCC(C2(C1C(C=C(C2C=O)C=O)O)C)OC(=O)C=CC3=CC=CC=C3)C 396.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
[(1R,4aR,8R,8aS)-7,8-diformyl-4a-hydroxy-4,4,8a-trimethyl-2,3,5,8-tetrahydro-1H-naphthalen-1-yl] (E)-3-phenylprop-2-enoate 42611764 Click to see CC1(CCC(C2(C1(CC=C(C2C=O)C=O)O)C)OC(=O)C=CC3=CC=CC=C3)C 396.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
[(1R,4aS,5S,8R,8aS)-7,8-diformyl-5-hydroxy-4,4,8a-trimethyl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] (E)-3-phenylprop-2-enoate 163186781 Click to see CC1(CCC(C2(C1C(C=C(C2C=O)C=O)O)C)OC(=O)C=CC3=CC=CC=C3)C 396.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
[(1R,4aS,5S,8S,8aS)-7,8-diformyl-5-hydroxy-4,4,8a-trimethyl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] (E)-3-phenylprop-2-enoate 42611763 Click to see CC1(CCC(C2(C1C(C=C(C2C=O)C=O)O)C)OC(=O)C=CC3=CC=CC=C3)C 396.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025
[(1R,4aS,8R,8aS)-7,8-diformyl-4,4,8a-trimethyl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] (E)-3-phenylprop-2-enoate 42611765 Click to see CC1(CCC(C2(C1CC=C(C2C=O)C=O)C)OC(=O)C=CC3=CC=CC=C3)C 380.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.025

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