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Uvaria welwitschii

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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 UUID643ffa228951c648392566
Scientific name Uvaria welwitschii
Authority Engl. & Diels
First published in Monogr. Afrik. Pflanzen-Fam. 6: 18 (1901)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oxymitra welwitschii Hiern Cat. Afr. Pl. (Hiern) 1(1): 10. 1896
Uvaria valvata De Wild. Pl. Bequaert. 1: 460 (1922)

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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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • South Tropical Africa
      • Angola
      • Zambia
    • West-central Tropical Africa
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000416184
Tropicos 1601915
KEW urn:lsid:ipni.org:names:75994-1
The Plant List kew-2447940
Open Tree Of Life 830708
NCBI Taxonomy 1144419
IPNI 75994-1
GBIF 3154356
EOL 304960

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)!
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Title Authors Publication Released IDs
Chemical studies on the roots of Uvaria welwitschii. Moriyasu M, Nakatani N, Ichimaru M, Nishiyama Y, Kato A, Mathenge SG, Juma FD, Chalo Mutiso PB J Nat Med 01-Apr-2011
doi:10.1007/S11418-010-0498-2
PMID:21234693

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 / Phenols / Methoxyphenols
2-[(2S,3S)-3-[(S)-hydroxy(phenyl)methyl]oxiran-2-yl]-3,5,6-trimethoxyphenol 162917882 Click to see COC1=CC(=C(C(=C1C2C(O2)C(C3=CC=CC=C3)O)O)OC)OC 332.30 unknown https://doi.org/10.1007/S11418-010-0498-2
2-Hydroxy-3,4,6-trimethoxybenzaldehyde 12494693 Click to see COC1=CC(=C(C(=C1C=O)O)OC)OC 212.20 unknown https://doi.org/10.1007/S11418-010-0498-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(5aR,12S)-1,3,4,7,8,10-hexamethoxy-5a-phenyl-12-(2-phenylethenyl)-12H-chromeno[2,3-b]chromene 162867174 Click to see COC1=CC(=C(C2=C1C=C3C(C4=C(C(=C(C=C4OC)OC)OC)OC3(O2)C5=CC=CC=C5)C=CC6=CC=CC=C6)OC)OC 594.60 unknown https://doi.org/10.1007/S11418-010-0498-2
(5aR,12S)-1,3,4,7,8,10-hexamethoxy-5a-phenyl-12-[(E)-2-phenylethenyl]-12H-chromeno[2,3-b]chromene 163191310 Click to see COC1=CC(=C(C2=C1C=C3C(C4=C(C(=C(C=C4OC)OC)OC)OC3(O2)C5=CC=CC=C5)C=CC6=CC=CC=C6)OC)OC 594.60 unknown https://doi.org/10.1007/S11418-010-0498-2
[(2R)-5,5',6',7,7',8,8'-heptamethoxy-2'-phenyl-2,4'-spirobi[chromene]-3-yl]-phenylmethanone 162851869 Click to see COC1=CC(=C(C2=C1C=C(C3(O2)C=C(OC4=C3C(=C(C(=C4OC)OC)OC)OC)C5=CC=CC=C5)C(=O)C6=CC=CC=C6)OC)OC 638.70 unknown https://doi.org/10.1007/S11418-010-0498-2
[(2R)-5,5',7,7',8,8'-hexamethoxy-2'-phenyl-2,4'-spirobi[chromene]-3-yl]-phenylmethanone 162867170 Click to see COC1=CC(=C(C2=C1C=C(C3(O2)C=C(OC4=C3C(=CC(=C4OC)OC)OC)C5=CC=CC=C5)C(=O)C6=CC=CC=C6)OC)OC 608.60 unknown https://doi.org/10.1007/S11418-010-0498-2
Norwogonin 5,7,8-trimethyl ether 14756218 Click to see COC1=CC(=C(C2=C1C(=O)C=C(O2)C3=CC=CC=C3)OC)OC 312.30 unknown https://doi.org/10.1007/S11418-010-0498-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
(3R)-5,7-dihydroxy-3-(4-hydroxy-2,3-dimethoxyphenyl)-2,3-dihydrochromen-4-one 163018342 Click to see COC1=C(C=CC(=C1OC)O)C2COC3=CC(=CC(=C3C2=O)O)O 332.30 unknown https://doi.org/10.1007/S11418-010-0498-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
2-Hydroxy-3,4,6-trimethoxydihydrochalcone 42607736 Click to see COC1=CC(=C(C(=C1CCC(=O)C2=CC=CC=C2)O)OC)OC 316.30 unknown https://doi.org/10.1007/S11418-010-0498-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
2-Hydroxy-3,4,6-trimethoxychalcone 54080897 Click to see COC1=CC(=C(C(=C1C=CC(=O)C2=CC=CC=C2)O)OC)OC 314.30 unknown https://doi.org/10.1007/S11418-010-0498-2
Tepanone 42607663 Click to see COC1=CC(=C(C(=C1C=CC(=O)C2=CC=CC=C2)O)OC)OC 314.30 unknown https://doi.org/10.1007/S11418-010-0498-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
(r)-(+)-2-(3-Hydroxy-3-phenylpropyl)-3,5,6-trimethoxyphenol 129844565 Click to see COC1=CC(=C(C(=C1CCC(C2=CC=CC=C2)O)O)OC)OC 318.40 unknown https://doi.org/10.1007/S11418-010-0498-2
[(1S)-3-(2-hydroxy-3,4,6-trimethoxyphenyl)-1-phenylpropyl] acetate 163048194 Click to see CC(=O)OC(CCC1=C(C(=C(C=C1OC)OC)OC)O)C2=CC=CC=C2 360.40 unknown https://doi.org/10.1007/S11418-010-0498-2
2-(3-Phenyl-2-propenyl)-3,5,6-trimethoxyphenol 129844573 Click to see COC1=CC(=C(C(=C1CC=CC2=CC=CC=C2)O)OC)OC 300.30 unknown https://doi.org/10.1007/S11418-010-0498-2

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