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Monotes engleri

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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 UUID644053dd8d5ab610510999
Scientific name Monotes engleri
Authority Gilg
First published in Bot. Jahrb. Syst. 41: 291 (1908)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Afrikaans pienkpapierkelk

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
  • Africa
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001221376
Tropicos 50008584
KEW urn:lsid:ipni.org:names:321075-1
The Plant List tro-50008584
Open Tree Of Life 6115011
NCBI Taxonomy 1902362
IUCN Red List 50762899
IPNI 321075-1
GBIF 4097039
EOL 5713222

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
Synthesis and structure-activity relationship study of monotesone-A, an antifungal component of Monotes engleri. Kenéz A, Lestár Z, Lenkey B, Antus S Nat Prod Res 20-Mar-2008
doi:10.1080/14786410701339055
PMID:18404558
Prenylated Flavanones from <i>Monotes engleri</i>: On‐line Structure Elucidation by LC/UV/NMR Eliane Garo, Jean‐Luc Wolfender, Kurt Hostettmann, Wolf Hiller, SÁNdor Antus, Steven Mavi Wiley 28-Dec-2004
doi:10.1002/HLCA.19980810325
5-(4-Hydroxyphenethenyl)-4,7-dimethoxycoumarin, a new constituent of Monotes engleri. Seo EK, Chai HB, Chagwedera TE, Farnsworth NR, Cordell GA, Pezzuto JM, Kinghorn AD Planta Med 01-Mar-2000
doi:10.1055/S-0029-1243128
PMID:10763599
Cytotoxic prenylated flavanones from Monotes engleri. Seo EK, Silva GL, Chai HB, Chagwedera TE, Farnsworth NR, Cordell GA, Pezzuto JM, Kinghorn AD Phytochemistry 01-Jun-1997
doi:10.1016/S0031-9422(96)00871-0
PMID:9190085

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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-8-[(E)-3-methylbut-1-enyl]-2,3-dihydrochromen-4-one 163186280 Click to see CC(C)C=CC1=C2C(=C(C(=C1O)CC(C(=C)C)O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O 440.50 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-8-(3-methylbut-1-enyl)-2,3-dihydrochromen-4-one 85191061 Click to see CC(C)C=CC1=C2C(=C(C(=C1O)CC(C(=C)C)O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O 440.50 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-bis(3-methyl-2-butenyl)-4H-1-benzopyran-4-one 14542255 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)CC=C(C)C)O)C 438.50 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
2-(3,5-Dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 10622240 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=CC(=C3)O)O)CC=C(C)C)O)C 424.50 unknown https://doi.org/10.1002/HLCA.19980810325
Monotesone B 26213315 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=CC(=C3)O)O)CC=C(C)C)O)C 424.50 unknown https://doi.org/10.1002/HLCA.19980810325
Senegalensin 124035 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 408.50 unknown https://doi.org/10.1002/HLCA.19980810325
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6,8-bis[(E)-3-methylbut-1-enyl]-2,3-dihydrochromen-4-one 10455035 Click to see CC(C)C=CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)C=CC(C)C)O 424.50 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
(2S)-5,7,3',4'-Tetrahydroxy-6-(1,1-dimethylallyl)flavanone 10498462 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)O)O 356.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
(2S)-5,7,4'-Trihydroxy-6-(1,1-dimethylallyl)flavanone 10759582 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O 340.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(2-methylbut-3-en-2-yl)-2,3-dihydrochromen-4-one 85160884 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)O)O 356.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-1-enyl)-2,3-dihydrochromen-4-one 85147621 Click to see CC(C)C=CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)C=CC(C)C)O 424.50 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
5,7-Dihydroxy-2-[3-hydroxy-4-(3-methylbut-2-enoxy)phenyl]chroman-4-one 85160885 Click to see CC(=CCOC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)C 356.40 unknown https://doi.org/10.1002/HLCA.19980810325
https://doi.org/10.1080/14786410701339055
5,7-Dihydroxy-2-[4-(3-methylbut-2-enoxy)phenyl]chroman-4-one 12305191 Click to see CC(=CCOC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 340.40 unknown https://doi.org/10.1002/HLCA.19980810325
6-(1,1-Dimethylallyl)naringenin 10315196 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O 340.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
Archangelenone 71586977 Click to see CC(=CCOC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 340.40 unknown https://doi.org/10.1002/HLCA.19980810325
Monotesone A 10498463 Click to see CC(=CCOC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)C 356.40 unknown https://doi.org/10.1002/HLCA.19980810325
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)chromen-4-one 10669924 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)CC=C(C)C)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
> Phenylpropanoids and polyketides / Flavonoids / Furanoflavonoids and dihydrofuranoflavonoids
(2R,7S)-4-hydroxy-7-(4-hydroxyphenyl)-2,3,3-trimethyl-6,7-dihydro-2H-furo[3,2-g]chromen-5-one 163042218 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)CC(O3)C4=CC=C(C=C4)O)(C)C 340.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
4-hydroxy-7-(4-hydroxyphenyl)-2,3,3-trimethyl-6,7-dihydro-2H-furo[3,2-g]chromen-5-one 85224524 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)CC(O3)C4=CC=C(C=C4)O)(C)C 340.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2S)-5,7,4'-Trihydroxy-3'-methoxy-6-(1,1-dimethylallyl)flavanone 10761665 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(2-methylbut-3-en-2-yl)-2,3-dihydrochromen-4-one 85258903 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00871-0
> Phenylpropanoids and polyketides / Stilbenes
5-[(E)-2-(4-hydroxyphenyl)ethenyl]-4,7-dimethoxychromen-2-one 10358875 Click to see COC1=CC(=C2C(=C1)OC(=O)C=C2OC)C=CC3=CC=C(C=C3)O 324.30 unknown https://doi.org/10.1055/S-0029-1243128
5-[2-(4-Hydroxyphenyl)ethenyl]-4,7-dimethoxychromen-2-one 54261202 Click to see COC1=CC(=C2C(=C1)OC(=O)C=C2OC)C=CC3=CC=C(C=C3)O 324.30 unknown https://doi.org/10.1055/S-0029-1243128

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