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Pteronia paniculata

Pteronia paniculata - 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 UUID643fc6e91c9e0267318654
Scientific name Pteronia paniculata
Authority Thunb.
First published in Prodr. Pl. Cap. 2: 143 (1800)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aster pteronia Kuntze Revis. Gen. Pl. 3[3]: 131 (1898)
Pteronia flexicaulis DC. Prodr. 5: 360 (1836)

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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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-0000010227
Tropicos 2718235
KEW urn:lsid:ipni.org:names:240293-1
The Plant List gcc-109900
Open Tree Of Life 7599757
NCBI Taxonomy 2930444
IPNI 240293-1
iNaturalist 592711
GBIF 5394753
Wikipedia Pteronia_paniculata

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
Umbelactonyl cinnamate derivatives from Crypteronia paniculata that mediate DNA strand scission. Deng JZ, Newman DJ, Hecht SM J Nat Prod 01-Mar-2005
doi:10.1021/NP0401112
PMID:15787463
Diterpenes and other constituents from Pteronia species C. Zdero, J. Jakupovic, F. Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85434-H

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 / Fatty Acyls / Fatty acid esters
[(2Z,5R,8S)-2-penta-2,4-diynylidene-1,10-dioxaspiro[4.5]dec-3-en-8-yl] 3-methylbutanoate 163185434 Click to see CC(C)CC(=O)OC1CCC2(C=CC(=CC#CC#C)O2)OC1 300.30 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3R)-5-[(1S,2S,4R,4aR,8aR)-1,2,4a,5-tetramethyl-4-[(Z)-2-methylbut-2-enoyl]oxy-3-oxo-4,7,8,8a-tetrahydro-2H-naphthalen-1-yl]-3-methylpentanoic acid 163040413 Click to see CC=C(C)C(=O)OC1C(=O)C(C(C2C1(C(=CCC2)C)C)(C)CCC(C)CC(=O)O)C 418.60 unknown https://doi.org/10.1016/0031-9422(90)85434-H
(3S)-5-[(1R,2S,4aR,8aR)-1,2,4a,5-tetramethyl-3-oxo-4,7,8,8a-tetrahydro-2H-naphthalen-1-yl]-3-methylpentanoic acid 163045769 Click to see CC1C(=O)CC2(C(C1(C)CCC(C)CC(=O)O)CCC=C2C)C 320.50 unknown https://doi.org/10.1016/0031-9422(90)85434-H
(3S)-5-[(1S,2R,4S,4aS,5R,8aR)-5-hydroxy-1,2,4a,5-tetramethyl-4-[(Z)-2-methylbut-2-enoyl]oxy-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-3-methylpentanoic acid 162993961 Click to see CC=C(C)C(=O)OC1CC(C(C2C1(C(CCC2)(C)O)C)(C)CCC(C)CC(=O)O)C 422.60 unknown https://doi.org/10.1016/0031-9422(90)85434-H
(3S)-5-[(1S,2S,4R,4aR,8aR)-1,2,4a,5-tetramethyl-4-(2-methylpropoxy)-3-oxo-4,7,8,8a-tetrahydro-2H-naphthalen-1-yl]-3-methylpentanoic acid 162956106 Click to see CC1C(=O)C(C2(C(C1(C)CCC(C)CC(=O)O)CCC=C2C)C)OCC(C)C 392.60 unknown https://doi.org/10.1016/0031-9422(90)85434-H
(3S)-5-[(1S,2S,4R,4aR,8aR)-4-hydroxy-1,2,4a,5-tetramethyl-3-oxo-4,7,8,8a-tetrahydro-2H-naphthalen-1-yl]-3-methylpentanoic acid 162965032 Click to see CC1C(=O)C(C2(C(C1(C)CCC(C)CC(=O)O)CCC=C2C)C)O 336.50 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
O-Geranylconiferyl alcohol 6439279 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)C 316.40 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
Bionectin F 145720713 Click to see CC(=CCCC(C)(CCCC(C)(CCCC(C)(CCCC(C)(CCCC(C)(CCCC(C)(CCCC(C)(CCCC(=CCCC(=CCO)C)C)O)O)O)O)O)O)O)C 825.30 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(90)85434-H
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85434-H
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3Z-Hexenylferulate 14589009 Click to see CCC=CCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 276.33 unknown https://doi.org/10.1016/0031-9422(90)85434-H
Isopentyl ferulate 14589006 Click to see CC(C)CCOC(=O)C=CC1=CC(=C(C=C1)O)OC 264.32 unknown https://doi.org/10.1016/0031-9422(90)85434-H
Isovaleryl-cis-ferulate 14589007 Click to see CC(C)CCOC(=O)C=CC1=CC(=C(C=C1)O)OC 264.32 unknown https://doi.org/10.1016/0031-9422(90)85434-H
Phenylethyl 3-methylcaffeate 5284444 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=CC=C2)O 298.30 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(3-methyl-5-oxo-2H-furan-2-yl)methyl 3-(4-hydroxyphenyl)prop-2-enoate 72790268 Click to see CC1=CC(=O)OC1COC(=O)C=CC2=CC=C(C=C2)O 274.27 unknown https://doi.org/10.1021/NP0401112
[(2R)-3-methyl-5-oxo-2H-furan-2-yl]methyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate 11460006 Click to see CC1=CC(=O)OC1COC(=O)C=CC2=CC=C(C=C2)O 274.27 unknown https://doi.org/10.1021/NP0401112

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