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Uvaria pandensis

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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 UUID644046ba0266c647366361
Scientific name Uvaria pandensis
Authority Verdc.
First published in Kew Bull. 43: 99 (1988)

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-0001066200
Tropicos 1601775
KEW urn:lsid:ipni.org:names:934501-1
The Plant List tro-1601775
Open Tree Of Life 363735
NCBI Taxonomy 673193
IUCN Red List 158332
IPNI 934501-1
iNaturalist 444569
GBIF 3154243
EOL 304978

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
Oxygenated Cyclohexene Derivatives from the Stem and Root Barks of Uvaria pandensis Maeda G, Gilissen PJ, Rudenko A, van der Wal J, Bourgard C, Gupta AK, Sunnerhagen P, Munissi JJ, Nyandoro SS, Erdélyi M J Nat Prod 22-Nov-2021
PMCID:PMC8713284
doi:10.1021/acs.jnatprod.1c00811
PMID:34802242
3-Farnesylindole from Uvaria pandensis verdc. Mayunga H.H. Nkunya, Hugo Weenen, Nazarius J. Koyi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84730-5
Cyclohexene epoxides, (+)-pandoxide, (+)β-senepoxide and (−)-pipoxide, from Uvaria pandensis Mayunga H.H. Nkunya, Hugo Weenen, Nazarius J. Koyi, Lambertus Thijs, Binne Zwanenburg Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83878-9
Two indolosesquiterpenes from Uvaria pandensis Mayunga H.H. Nkunya, Hugo Weenen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97952-4

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
(-)-Pipoxide 11969921 Click to see C1=CC=C(C=C1)C(=O)OCC23C(O2)C=CC(C3O)OC(=O)C4=CC=CC=C4 366.40 unknown https://doi.org/10.1016/S0031-9422(00)83878-9
https://doi.org/10.1016/S0031-9422(00)97952-4
(2-Acetyloxy-3-methoxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl)methyl benzoate 162866580 Click to see CC(=O)OC1C(C=CC2C1(O2)COC(=O)C3=CC=CC=C3)OC 318.32 unknown https://doi.org/10.1016/S0031-9422(00)97952-4
https://doi.org/10.1016/S0031-9422(00)84730-5
(3-Acetyloxy-2-hydroxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl)methyl benzoate 162882629 Click to see CC(=O)OC1C=CC2C(C1O)(O2)COC(=O)C3=CC=CC=C3 304.29 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
(4-Benzoyloxy-5-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-6-yl)methyl benzoate 494920 Click to see C1=CC=C(C=C1)C(=O)OCC23C(O2)C=CC(C3O)OC(=O)C4=CC=CC=C4 366.40 unknown https://doi.org/10.1016/S0031-9422(00)83878-9
https://doi.org/10.1016/S0031-9422(00)97952-4
[(1R,2R,3R,6R)-2-acetyloxy-3-methoxy-1-bicyclo[4.1.0]hept-4-enyl]methyl benzoate 101624710 Click to see CC(=O)OC1C(C=CC2C1(C2)COC(=O)C3=CC=CC=C3)OC 316.30 unknown https://doi.org/10.1016/S0031-9422(00)83878-9
https://doi.org/10.1016/S0031-9422(00)97952-4
[(1R,2R,3S,6S)-3-acetyloxy-2-hydroxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl]methyl benzoate 162882630 Click to see CC(=O)OC1C=CC2C(C1O)(O2)COC(=O)C3=CC=CC=C3 304.29 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
[(1R,2R,3S,6S)-3-benzoyloxy-2-hydroxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl]methyl benzoate 14283282 Click to see C1=CC=C(C=C1)C(=O)OCC23C(O2)C=CC(C3O)OC(=O)C4=CC=CC=C4 366.40 unknown https://doi.org/10.1016/S0031-9422(00)97952-4
[(1R,2S,3R,6R)-2-acetyloxy-3-methoxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl]methyl benzoate 162866581 Click to see CC(=O)OC1C(C=CC2C1(O2)COC(=O)C3=CC=CC=C3)OC 318.32 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
https://doi.org/10.1016/S0031-9422(00)97952-4
[(1R,2S,3R,6R)-2,3-diacetyloxy-7-oxabicyclo[4.1.0]hept-4-en-1-yl]methyl benzoate 10871693 Click to see CC(=O)OC1C=CC2C(C1OC(=O)C)(O2)COC(=O)C3=CC=CC=C3 346.30 unknown https://doi.org/10.1016/S0031-9422(00)83878-9
https://doi.org/10.1016/S0031-9422(00)84730-5
https://doi.org/10.1016/S0031-9422(00)97952-4
d,l-Senepoxyde 329239 Click to see CC(=O)OC1C=CC2C(C1OC(=O)C)(O2)COC(=O)C3=CC=CC=C3 346.30 unknown https://doi.org/10.1016/S0031-9422(00)97952-4
https://doi.org/10.1016/S0031-9422(00)84730-5
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
Covi-ox 6560141 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4S,5S,6E,10E)-12-(1H-indol-3-yl)-2,6,10-trimethyldodeca-2,6,10-triene-4,5-diol 163189244 Click to see CC(=CC(C(C(=CCCC(=CCC1=CNC2=CC=CC=C21)C)C)O)O)C 353.50 unknown https://doi.org/10.1016/S0031-9422(00)97952-4
(4S,5S,6R,10E)-12-(1H-indol-3-yl)-2,6,10-trimethyldodeca-2,10-diene-4,5-diol 163194290 Click to see CC(CCCC(=CCC1=CNC2=CC=CC=C21)C)C(C(C=C(C)C)O)O 355.50 unknown https://doi.org/10.1016/S0031-9422(00)97952-4
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
12-(1H-indol-3-yl)-2,6,10-trimethyldodeca-2,10-diene-4,5-diol 163006573 Click to see CC(CCCC(=CCC1=CNC2=CC=CC=C21)C)C(C(C=C(C)C)O)O 355.50 unknown https://doi.org/10.1016/S0031-9422(00)97952-4
12-(1H-indol-3-yl)-2,6,10-trimethyldodeca-2,6,10-triene-4,5-diol 162879611 Click to see CC(=CC(C(C(=CCCC(=CCC1=CNC2=CC=CC=C21)C)C)O)O)C 353.50 unknown https://doi.org/10.1016/S0031-9422(00)97952-4
3-(3,7,11-Trimethyl-2,6,10-dodecatrienyl)-1H-indole 5388343 Click to see CC(=CCCC(=CCCC(=CCC1=CNC2=CC=CC=C21)C)C)C 321.50 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
3-(3,7,11-trimethyldodeca-2,6,10-trienyl)-1H-indole 366505 Click to see CC(=CCCC(=CCCC(=CCC1=CNC2=CC=CC=C21)C)C)C 321.50 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
3-Farnesylindole 49768248 Click to see CC(=CCCC(=CCCC(=CCC1CNC2=CC=CC=C12)C)C)C 323.50 unknown https://doi.org/10.1016/S0031-9422(00)84730-5
Farnesol 3327 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)84730-5

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