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Hymenodictyon floribundum

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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 UUID643fdf55ad2bb558451366
Scientific name Hymenodictyon floribundum
Authority B.L.Rob.
First published in Proc. Amer. Acad. Arts 45: 404 (1910)

Description Top

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Synonyms Top

Scientific name Authority First published in
Kurria floribunda Hochst. & Steud. Flora 24(1): 28 (1841)
Hymenodictyon kurria var. elongatum Hochst. Fl. Trop. Afr. 3: 42. 1877
Hymenodictyon kurria var. bequaertii De Wild. Pl. Bequaert. 2: 201. 1923
Hymenodictyon kurria var. claessensii De Wild. Pl. Bequaert. 2: 202. 1923

Common names Top

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Language Common/alternative name
Chinese 多花土连翘

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
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Namibia
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Rwanda
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000216092
Tropicos 27904439
KEW urn:lsid:ipni.org:names:753550-1
The Plant List kew-101229
Open Tree Of Life 243675
NCBI Taxonomy 60056
IUCN Red List 146208815
IPNI 753550-1
iNaturalist 507326
GBIF 2904461
EOL 1105258

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
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
Phytochemicals as alternative fungicides for controlling plant diseases: A comprehensive review of their efficacy, commercial representatives, advantages, challenges for adoption, and possible solutions Deresa EM, Diriba TF Heliyon 17-Feb-2023
PMCID:PMC9984788
doi:10.1016/j.heliyon.2023.e13810
PMID:36879959
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
An ethnobotanical study of medicinal plants in Wayu Tuka District, East Welega Zone of Oromia Regional State, West Ethiopia Megersa M, Asfaw Z, Kelbessa E, Beyene A, Woldeab B J Ethnobiol Ethnomed 25-Sep-2013
PMCID:PMC3851437
doi:10.1186/1746-4269-9-68
PMID:24295044
Iridoids from Hymenodictyon floribundum Cristina M. P. Borges, Carlos Diakanawma, Dina I. M. D. de Mendonça FapUNIFESP (SciELO) 21-Jul-2010
doi:10.1590/S0103-50532010000600023
Glycoside derivatives of scopoletin and β-sitosterol from Hymenodictyon floribundum A.-C Mitaine-Offer, L.A Tapondjou, J.D Djoukeng, H Bouda, M.-A Lacaille-Dubois Elsevier BV 17-Jan-2003
doi:10.1016/S0305-1978(02)00086-8

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 / Sesquiterpenoids
4-Hydroxy-4-(3-hydroxybut-1-en-1-yl)-3,3,5-trimethylcyclohexan-1-one 71344200 Click to see CC1CC(=O)CC(C1(C=CC(C)O)O)(C)C 226.31 unknown https://doi.org/10.1590/S0103-50532010000600023
4,5-Dihydroblumenol A 21630916 Click to see CC1CC(=O)CC(C1(C=CC(C)O)O)(C)C 226.31 unknown https://doi.org/10.1590/S0103-50532010000600023
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 162943803 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1590/S0103-50532010000600023
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1590/S0103-50532010000600023
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0305-1978(02)00086-8
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0305-1978(02)00086-8
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(3E,4S)-3-ethylidene-4-(2-hydroxyethyl)oxan-2-one 162934563 Click to see CC=C1C(CCOC1=O)CCO 170.21 unknown https://doi.org/10.1590/S0103-50532010000600023
3-Ethylidene-4-(2-hydroxyethyl)oxan-2-one 162934562 Click to see CC=C1C(CCOC1=O)CCO 170.21 unknown https://doi.org/10.1590/S0103-50532010000600023
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Hymexelsin 14136086 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O 486.40 unknown https://doi.org/10.1016/S0305-1978(02)00086-8
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1016/S0305-1978(02)00086-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1590/S0103-50532010000600023
https://doi.org/10.1016/S0305-1978(02)00086-8

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