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Pseudowintera axillaris

Pseudowintera axillaris - 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 UUID6440555976b33882151726
Scientific name Pseudowintera axillaris
Authority (J.R.Forst. & G.Forst.) Dandy
First published in J. Bot. 71: 121 (1933)

Description Top

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Synonyms Top

Scientific name Authority First published in
Wintera terminalis Tiegh. J. Bot. (Morot) 14: 291 (1900)
Wintera axillaris J.F.Gmel. Syst. Nat. ed. 13[bis] : 852 (1791)

Common names Top

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Language Common/alternative name
Persian لولند هرپیتو

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-0001240756
Tropicos 50108850
KEW urn:lsid:ipni.org:names:871219-1
The Plant List tro-50108850
Open Tree Of Life 59243
NCBI Taxonomy 132897
IPNI 871219-1
iNaturalist 366714
GBIF 4020824
Freebase /m/0jk_v22
EOL 5037120
USDA GRIN 100979
Wikipedia Pseudowintera_axillaris

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
Comparative De Novo Transcriptome Analysis of Fertilized Ovules in Xanthoceras sorbifolium Uncovered a Pool of Genes Expressed Specifically or Preferentially in the Selfed Ovule That Are Potentially Involved in Late-Acting Self-Incompatibility Zhou Q, Zheng Y PLoS One 20-Oct-2015
PMCID:PMC4616620
doi:10.1371/journal.pone.0140507
PMID:26485030
Self-Sterility in Camellia oleifera May Be Due to the Prezygotic Late-Acting Self-Incompatibility Liao T, Yuan DY, Zou F, Gao C, Yang Y, Zhang L, Tan XF PLoS One 13-Jun-2014
PMCID:PMC4057179
doi:10.1371/journal.pone.0099639
PMID:24926879
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Chemotaxonomy of Pseudowintera: sesquiterpene dialdehyde variants are species markers. Wayman KA, de Lange PJ, Larsen L, Sansom CE, Perry NB Phytochemistry 01-May-2010
doi:10.1016/J.PHYTOCHEM.2010.01.017
PMID:20176388
Fungicidal sesquiterpene dialdehyde cinnamates from Pseudowintera axillaris. Brennan NJ, Larsen L, Lorimer SD, Perry NB, Chapin EL, Werk TL, Henry MJ, Hahn DR J Agric Food Chem 25-Jan-2006
doi:10.1021/JF052585S
PMID:16417306
The Causes of Self‐sterility in Natural Populations of the Relictual Angiosperm, Illicium floridanum (Illiciaceae) KOEHL V, THIEN LB, HEIJ EG, SAGE TL Ann Bot 01-Jul-2004
PMCID:PMC4242369
doi:10.1093/aob/mch113
PMID:15155377
Evidence for Ovarian Self‐incompatibility as a Cause of Self‐sterility in the Relictual Woody Angiosperm, Pseudowintera axillaris (Winteraceae) SAGE TL, SAMPSON FB Ann Bot 01-Jun-2003
PMCID:PMC4242389
doi:10.1093/aob/mcg085
PMID:12730068

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 / Sesquiterpenoids
(1R,3S,5S,5aS,7S,9R,9aS,9bR)-1,3-dimethoxy-7,9a-dimethyl-6-methylidene-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-5,9-diol 11522458 Click to see CC1CC(C2(C(C1=C)C(C=C3C2C(OC3OC)OC)O)C)O 310.40 unknown https://doi.org/10.1021/JF052585S
(1R,3S,5S,5aS,7S,9R,9aS,9bR)-1,3,5-trimethoxy-7,9a-dimethyl-6-methylidene-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-9-ol 11551567 Click to see CC1CC(C2(C(C1=C)C(C=C3C2C(OC3OC)OC)OC)C)O 324.40 unknown https://doi.org/10.1021/JF052585S
(1R,4aS,6S,8R,8aS)-8-hydroxy-6,8a-dimethyl-5-methylidene-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 11536109 Click to see CC1CC(C2(C(C1=C)CC=C(C2C=O)C=O)C)O 248.32 unknown https://doi.org/10.1021/JF052585S
(1R,4aS,6S,8R,8aS)-8-methoxy-6,8a-dimethyl-5-methylidene-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 11557991 Click to see CC1CC(C2(C(C1=C)CC=C(C2C=O)C=O)C)OC 262.34 unknown https://doi.org/10.1021/JF052585S
(1R)-4alpha-Hydroxy-5-methylene-6beta,8abeta-dimethyl-8beta-(cinnamoyloxy)-1,4,4aalpha,5,6,7,8,8a-octahydronaphthalene-1beta,2-dicarbaldehyde 11682657 Click to see CC1CC(C2(C(C(=CC(C2C1=C)O)C=O)C=O)C)OC(=O)C=CC3=CC=CC=C3 394.50 unknown https://doi.org/10.1021/JF052585S
(7,8-Diformyl-3,8a-dimethyl-4-methylidene-1,2,3,4a,5,8-hexahydronaphthalen-1-yl) 3-phenylprop-2-enoate 73060542 Click to see CC1CC(C2(C(C1=C)CC=C(C2C=O)C=O)C)OC(=O)C=CC3=CC=CC=C3 378.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.01.017
https://doi.org/10.1021/JF052585S
(7,8-Diformyl-5-hydroxy-3,8a-dimethyl-4-methylidene-1,2,3,4a,5,8-hexahydronaphthalen-1-yl) 3-phenylprop-2-enoate 73002072 Click to see CC1CC(C2(C(C(=CC(C2C1=C)O)C=O)C=O)C)OC(=O)C=CC3=CC=CC=C3 394.50 unknown https://doi.org/10.1021/JF052585S
[(1R,3S,4aS,5R,8R,8aS)-7,8-diformyl-5-hydroxy-3,8a-dimethyl-4-methylidene-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] (E)-3-phenylprop-2-enoate 11545661 Click to see CC1CC(C2(C(C(=CC(C2C1=C)O)C=O)C=O)C)OC(=O)C=CC3=CC=CC=C3 394.50 unknown https://doi.org/10.1021/JF052585S
[(1R,3S,4aS,8S,8aS)-7,8-bis(hydroxymethyl)-3,8a-dimethyl-4-methylidene-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] (E)-3-phenylprop-2-enoate 11625136 Click to see CC1CC(C2(C(C1=C)CC=C(C2CO)CO)C)OC(=O)C=CC3=CC=CC=C3 382.50 unknown https://doi.org/10.1021/JF052585S
[(1R,3S,5aS,7S,9R,9aR,9bR)-1,3-dimethoxy-7,9a-dimethyl-6-methylidene-5-oxo-3,5a,7,8,9,9b-hexahydro-1H-benzo[e][2]benzofuran-9-yl] (E)-3-phenylprop-2-enoate 11611881 Click to see CC1CC(C2(C3C(OC(C3=CC(=O)C2C1=C)OC)OC)C)OC(=O)C=CC4=CC=CC=C4 438.50 unknown https://doi.org/10.1021/JF052585S
[(1R,3S,5aS,7S,9R,9aS,9bR)-1,3-dimethoxy-7,9a-dimethyl-6-methylidene-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-9-yl] (E)-3-phenylprop-2-enoate 11626008 Click to see CC1CC(C2(C(C1=C)CC=C3C2C(OC3OC)OC)C)OC(=O)C=CC4=CC=CC=C4 424.50 unknown https://doi.org/10.1021/JF052585S
[(1R,3S,5S,5aS,7S,9R,9aS,9bR)-5-hydroxy-1,3-dimethoxy-7,9a-dimethyl-6-methylidene-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-9-yl] (E)-3-phenylprop-2-enoate 11553981 Click to see CC1CC(C2(C(C1=C)C(C=C3C2C(OC3OC)OC)O)C)OC(=O)C=CC4=CC=CC=C4 440.50 unknown https://doi.org/10.1021/JF052585S
[(1R,3S,5S,5aS,7S,9R,9aS,9bR)-5-hydroxy-1,3-dimethoxy-7,9a-dimethyl-6-methylidene-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-9-yl] 3-phenylpropanoate 11704895 Click to see CC1CC(C2(C(C1=C)C(C=C3C2C(OC3OC)OC)O)C)OC(=O)CCC4=CC=CC=C4 442.50 unknown https://doi.org/10.1021/JF052585S
Paxidal 11682335 Click to see CC1CC(C2(C(C1=C)CC=C(C2C=O)C=O)C)OC(=O)C=CC3=CC=CC=C3 378.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.01.017
https://doi.org/10.1021/JF052585S
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[(1R,4aS,8R,8aS)-7,8-diformyl-3,4,8a-trimethyl-2,4a,5,8-tetrahydro-1H-naphthalen-1-yl] (E)-3-phenylprop-2-enoate 101509247 Click to see CC1=C(C2CC=C(C(C2(C(C1)OC(=O)C=CC3=CC=CC=C3)C)C=O)C=O)C 378.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.01.017
[(1R,4aS,8R,8aS)-7,8-diformyl-3,4,8a-trimethyl-2,4a,5,8-tetrahydro-1H-naphthalen-1-yl] 3-phenylprop-2-enoate 162970231 Click to see CC1=C(C2CC=C(C(C2(C(C1)OC(=O)C=CC3=CC=CC=C3)C)C=O)C=O)C 378.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.01.017

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