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Aeollanthus rydingianus

Aeollanthus rydingianus - 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 UUID644029d63af59309690822
Scientific name Aeollanthus rydingianus
Authority van Jaarsv. & A.E.van Wyk
First published in Bothalia 35: 157 (2005)

Description Top

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Synonyms Top

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Common names Top

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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

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Database ID/link to page
World Flora Online wfo-0000807442
KEW urn:lsid:ipni.org:names:77077383-1
The Plant List kew-345683
Open Tree Of Life 6084136
Observations.org 449950
IPNI 77077383-1
iNaturalist 579138
GBIF 3889269
Elurikkus 434307

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)!
Title Authors Publication Released IDs
Isopimarane diterpenoids from Aeollanthus rydingianus and their antimicrobial activity. Rijo P, Simões MF, Duarte A, Rodríguez B Phytochemistry 01-Jun-2009
doi:10.1016/J.PHYTOCHEM.2009.06.008
PMID:19631355

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 / Diterpenoids
(7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-2-yl) acetate 163012835 Click to see CC(=O)OC1CCC2(C3CCC(CC3=CCC2C1(C)C)(C)C=C)C 330.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
(7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl)methanol 15586710 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C 288.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
(7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl)methyl acetate 74974677 Click to see CC(=O)OCC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C=C)C)O)C 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
[(1S,2S,4aR,4bS,7S,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-2-yl] acetate 44250223 Click to see CC(=O)OC1CCC2(C3CCC(CC3=CCC2C1(C)CO)(C)C=C)C 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
[(1S,2S,4aR,4bS,7S,10aR)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl]methyl acetate 44250224 Click to see CC(=O)OCC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C=C)C)O)C 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
[(2S,4aR,4bR,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-2-yl] acetate 163012836 Click to see CC(=O)OC1CCC2(C3CCC(CC3=CCC2C1(C)C)(C)C=C)C 330.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
[(2S,4aR,4bS,7S,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-2-yl] acetate 101488350 Click to see CC(=O)OC1CCC2(C3CCC(CC3=CCC2C1(C)C)(C)C=C)C 330.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
[7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-2-yl] acetate 74974676 Click to see CC(=O)OC1CCC2(C3CCC(CC3=CCC2C1(C)CO)(C)C=C)C 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1S,4aR,4bS,7S,10aR)- 158539 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C 288.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-2-ol 14138913 Click to see CC1(CCC2C(=CCC3C2(CCC(C3(C)CO)O)C)C1)C=C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
Virescenol B 21627909 Click to see CC1(CCC2C(=CCC3C2(CCC(C3(C)CO)O)C)C1)C=C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.008

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