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Wilbrandia ebracteata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffb99283cf537343136
Scientific name Wilbrandia ebracteata
Authority Cogn.
First published in Fl. Bras. 6(4): 33 (1878)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Wilbrandia longisepala var. angustiloba Cogn. Pflanzenr. , IV, 275 I: 74 (1916)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Wilbrandia ebracteata var. bracteata Mart.Crov. Darwiniana 12: 39 (1960)
Wilbrandia ebracteata var. pedunculata Mart.Crov. Darwiniana 12: 39 (1960)

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
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Argentina Northeast
      • Paraguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000427941
Tropicos 9200356
KEW urn:lsid:ipni.org:names:294380-1
The Plant List kew-2466585
Open Tree Of Life 273922
NCBI Taxonomy 703182
IPNI 294380-1
GBIF 7317975
USDA GRIN 464536

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
Recent Advances in the Application of Cucurbitacins as Anticancer Agents Zieniuk B, Pawełkowicz M Metabolites 14-Oct-2023
PMCID:PMC10608718
doi:10.3390/metabo13101081
PMID:37887406
Cucurbitacin-B instigates intrinsic apoptosis and modulates Notch signaling in androgen-dependent prostate cancer LNCaP cells Alafnan A, Khalifa NE, Hussain T, Osman ME Front Pharmacol 28-Jun-2023
PMCID:PMC10338038
doi:10.3389/fphar.2023.1206981
PMID:37448964
Acute Effects of Kawakawa (Piper excelsum) Intake on Postprandial Glycemic and Insulinaemic Response in a Healthy Population Ramzan F, Jayaprakash R, Pook C, Foster M, Miles-Chan JL, Mithen R Nutrients 14-Apr-2022
PMCID:PMC9032225
doi:10.3390/nu14081638
PMID:35458200
Climate change threatens native potential agroforestry plant species in Brazil Lima VP, de Lima RA, Joner F, Siddique I, Raes N, ter Steege H Sci Rep 10-Feb-2022
PMCID:PMC8831634
doi:10.1038/s41598-022-06234-3
PMID:35145191
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Cucurbitacin B Activates Bitter-Sensing Gustatory Receptor Neurons via Gustatory Receptor 33a in Drosophila melanogaster Rimal S, Sang J, Dhakal S, Lee Y Mol Cells 13-May-2020
PMCID:PMC7332364
doi:10.14348/molcells.2020.0019
PMID:32451368
Cucurbitacin B Induces Hypoglycemic Effect in Diabetic Mice by Regulation of AMP-Activated Protein Kinase Alpha and Glucagon-Like Peptide-1 via Bitter Taste Receptor Signaling Kim KH, Lee IS, Park JY, Kim Y, An EJ, Jang HJ Front Pharmacol 21-Sep-2018
PMCID:PMC6161541
doi:10.3389/fphar.2018.01071
PMID:30298009
Brazilian medicinal plants with corroborated anti-inflammatory activities: a review Ribeiro VP, Arruda C, Abd El-Salam M, Bastos JK Pharm Biol 12-Apr-2018
PMCID:PMC6130656
doi:10.1080/13880209.2018.1454480
PMID:29648503
Targeting Cellular Stress Mechanisms and Metabolic Homeostasis by Chinese Herbal Drugs for Neuroprotection Ting HC, Chang CY, Lu KY, Chuang HM, Tsai SF, Huang MH, Liu CA, Lin SZ, Harn HJ Molecules 28-Jan-2018
PMCID:PMC6017457
doi:10.3390/molecules23020259
PMID:29382106
In Vitro and In Vivo Antitumor Activity of a Novel Semisynthetic Derivative of Cucurbitacin B Silva IT, Carvalho A, Lang KL, Dudek SE, Masemann D, Durán FJ, Caro MS, Rapp UR, Wixler V, Schenkel EP, Simões CM, Ludwig S PLoS One 12-Feb-2015
PMCID:PMC4326133
doi:10.1371/journal.pone.0117794
PMID:25674792
Cucurbitacins – A Promising Target for Cancer Therapy Alghasham AA Int J Health Sci (Qassim) 01-Jan-2013
PMCID:PMC3612419
doi:10.12816/0006025
PMID:23559908
Short and Long-Term Effects of Baccharis articulata on Glucose Homeostasis Kappel VD, Pereira DF, Cazarolli LH, Guesser SM, da Silva CH, Schenkel EP, Reginatto FH, Silva FR Molecules 04-Jun-2012
PMCID:PMC6269064
doi:10.3390/molecules17066754
PMID:22664465
Cucurbitacin L 2-O-β-Glucoside Demonstrates Apoptogenesis in Colon Adenocarcinoma Cells (HT-29): Involvement of Reactive Oxygen and Nitrogen Species Regulation Abdelwahab SI, Hassan LE, Abdul Majid AM, Yagi SM, Mohan S, Elhassan Taha MM, Ahmad S, Chuen CS, Narrima P, Rais MM, Syam S, Moharam BA, Hadi AH Evid Based Complement Alternat Med 26-Feb-2012
PMCID:PMC3350939
doi:10.1155/2012/490136
PMID:22685485
Role of phenolic compounds in peptic ulcer: An overview Sumbul S, Ahmad MA, Mohd. A, Mohd. A J Pharm Bioallied Sci 01-Jul-2011
PMCID:PMC3178942
doi:10.4103/0975-7406.84437
PMID:21966156
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467

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 / Steroids and steroid derivatives / Cucurbitacins
(2S,3R,8S,9R,10R,13R,14S,16R,17R)-17-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163037198 Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(CC=CC(C)(C)O)O)O)C)C)C)O)O)C 504.70 unknown https://doi.org/10.1016/0031-9422(92)80284-L
(8S,9R,10S,13R,14S)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 138113434 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1055/S-2006-959668
17-(2,6-Dihydroxy-6-methylhept-4-en-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163037197 Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(CC=CC(C)(C)O)O)O)C)C)C)O)O)C 504.70 unknown https://doi.org/10.1016/0031-9422(92)80284-L
23,24-dihydrocucurbitacin E 21577087 Click to see 558.70 unknown https://doi.org/10.1016/S0024-3205(03)00602-7
https://doi.org/10.1055/S-2006-959668
Cucurbitacin B 5281316 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1055/S-2006-959668
https://doi.org/10.1016/S0024-3205(03)00602-7
https://doi.org/10.1016/S0024-3205(99)00200-3
https://doi.org/10.1055/S-2006-957755
Cucurbitacin B, dihydro- 588303 Click to see CC(=O)OC(C)(C)CCC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O)O 560.70 unknown https://doi.org/10.1016/J.LFS.2006.12.021
Cucurbitacin D 5281318 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1055/S-2006-959668
Cucurbitacin E 5281319 Click to see 556.70 unknown https://doi.org/10.1055/S-2006-959668
https://doi.org/10.1055/S-2006-957755
https://doi.org/10.1016/S0024-3205(03)00602-7
Cucurbitacin H 441818 Click to see 534.70 unknown https://doi.org/10.1055/S-2006-959668
Cucurbitacin P 441822 Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)O)C 520.70 unknown https://doi.org/10.1055/S-2006-959668
Cucurbitacin R 180535 Click to see 518.70 unknown https://doi.org/10.1016/S0024-3205(03)00602-7
Dihydrocucurbitacin B 267250 Click to see 560.70 unknown https://doi.org/10.1016/J.LFS.2006.12.021
https://doi.org/10.1055/S-2006-959668
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 11-oxosteroids
8,16,17-Trihydroxy-2,8,10,13,18,18-hexamethyl-6-(2-methylprop-1-enyl)-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicos-19-en-12-one 155978633 Click to see 486.70 unknown https://doi.org/10.1016/0031-9422(92)80284-L
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1080/14786410701782544
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
8-Hydroxyquercetagetin 44260065 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C(=C(C(=C3O2)O)O)O)O)O)O)O 334.23 unknown https://doi.org/10.1080/14786410701782544
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5-Hydroxy-2-(4-Hydroxyphenyl)-7-Methoxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 369636 Click to see 446.40 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
https://doi.org/10.1016/J.FITOTE.2010.07.022
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 4475102 Click to see 432.40 unknown https://doi.org/10.1080/14786410701782544
Isoorientin 114776 Click to see 448.40 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
https://doi.org/10.1080/14786410701782544
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
https://doi.org/10.1080/14786410701782544
Spinosin 155692 Click to see 608.50 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
Swertisin 124034 Click to see 446.40 unknown https://doi.org/10.1016/J.FITOTE.2010.07.022
https://doi.org/10.1076/PHBI.34.4.300.13233
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1080/14786410701782544
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1080/14786410701782544
Isoswertisin 44258317 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1076/PHBI.34.4.300.13233
https://doi.org/10.1080/14786410701782544

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