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Rolandra fruticosa

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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 UUID643fc760e7df0655690905
Scientific name Rolandra fruticosa
Authority Kuntze
First published in Revis. Gen. Pl. 1: 360 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Echinops nodiflorus Lam. Encycl. 2: 337 (1786)
Rolandra argentea Rottb. Soc. Med. Havn. Collect. ii. (1775) 258.
Echinops fruticosus L. Sp. Pl. : 815 (1753)
Rolandra monacantha Cass. Dict. Sci. Nat., ed. 2. 46: 171 (1827)
Rolandra diacantha Cass. Dict. Sci. Nat., ed. 2. 46: 170 (1827)

Common names Top

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Language Common/alternative name
English yerba de plata

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
    • Caribbean
      • Dominican Republic
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Central American Pacific
      • Costa Rica
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000013942
USDA Plants ROFR
Tropicos 2710919
INPN 630563
KEW urn:lsid:ipni.org:names:221674-2
The Plant List gcc-113485
Open Tree Of Life 4727928
NCBI Taxonomy 1548370
IPNI 221674-2
iNaturalist 985998
GBIF 3114266
EPPO RONFR
EOL 595511
USDA GRIN 412873

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
Germacrene A–A Central Intermediate in Sesquiterpene Biosynthesis Xu H, Dickschat JS Chemistry 30-Sep-2020
PMCID:PMC7821278
doi:10.1002/chem.202002163
PMID:32442350
Phytotherapies in motion: French Guiana as a case study for cross-cultural ethnobotanical hybridization Tareau MA, Bonnefond A, Palisse M, Odonne G J Ethnobiol Ethnomed 16-Sep-2020
PMCID:PMC7493365
doi:10.1186/s13002-020-00404-1
PMID:32938478
Medicinal Plants in the Prevention and Treatment of Colon Cancer Aiello P, Sharghi M, Mansourkhani SM, Ardekan AP, Jouybari L, Daraei N, Peiro K, Mohamadian S, Rezaei M, Heidari M, Peluso I, Ghorat F, Bishayee A, Kooti W Oxid Med Cell Longev 04-Dec-2019
PMCID:PMC7187726
doi:10.1155/2019/2075614
PMID:32377288
Herbal bathing: an analysis of variation in plant use among Saramaccan and Aucan Maroons in Suriname van ‘t Klooster CI, Haabo V, Ruysschaert S, Vossen T, van Andel TR J Ethnobiol Ethnomed 15-Mar-2018
PMCID:PMC5856216
doi:10.1186/s13002-018-0216-9
PMID:29544521
Apoptosis Induction by 13-Acetoxyrolandrolide through the Mitochondrial Intrinsic Pathway Acuña UM, Matthew S, Pan L, Kinghorn AD, Swanson SM, Carcache de Blanco EJ Phytother Res 12-Dec-2013
PMCID:PMC4055509
doi:10.1002/ptr.5091
PMID:24338805
Sesquiterpenoids Lactones: Benefits to Plants and People Chadwick M, Trewin H, Gawthrop F, Wagstaff C Int J Mol Sci 19-Jun-2013
PMCID:PMC3709812
doi:10.3390/ijms140612780
PMID:23783276
Bioactivity-guided isolation of cytotoxic sesquiterpenes of Rolandra fruticosa. Pan L, Lantvit DD, Riswan S, Kardono LB, Chai HB, de Blanco EJ, Farnsworth NR, Soejarto DD, Swanson SM, Kinghorn AD Phytochemistry 01-Apr-2010
PMCID:PMC2847506
doi:10.1016/J.PHYTOCHEM.2010.01.012
PMID:20189206
Bioactivity-guided isolation of cytotoxic sesquiterpenes of Rolandra fruticosa Pan L, Lantvit DD, Riswan S, Kardono LB, Chai HB, Carcache de Blanco EJ, Farnsworth NR, Soejarto DD, Swanson SM, Kinghorn AD Phytochemistry 25-Feb-2010
PMCID:PMC2847506
doi:10.1016/j.phytochem.2010.01.012
PMID:20189206
Structures of the rolandrolides and isorolandrolides, unusual germacradienolides from Rolandra fruticosa Werner Herz, Serengolam V. Govindan, John F. Blount American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00317A022
Sesquiterpene lactones from Rolandra fruticosa J. Jakupovic, M. Grenz, F. Bohlmann, D.C. Wasshausen, R.M. King Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97890-7

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene 12308843 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
3H-3a,7-Methanoazulene, 2,4,5,6,7,8-hexahydro-1,4,9,9-tetramethyl-, [3aR-(3aalpha,4beta,7alpha)]- 99856 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
Hinesene 11310242 Click to see CC1CCC=C(C12CCC(C2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(4R,6S,8S,9E,11E)-8-acetyloxy-3-(ethoxymethyl)-6-hydroxy-6,10-dimethyl-2-oxo-4,5,7,8-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 21634138 Click to see CCOCC1=C2C(CC(CC(C=C(C=C2OC1=O)C)OC(=O)C)(C)O)OC(=O)C(=C)C 434.50 unknown https://doi.org/10.1021/JO00317A022
[(4R,6S,8S,9E,11E)-8-acetyloxy-6-hydroxy-3-(hydroxymethyl)-6,10-dimethyl-2-oxo-4,5,7,8-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 21634139 Click to see CC1=CC(CC(CC(C2=C(C(=O)OC2=C1)CO)OC(=O)C(=C)C)(C)O)OC(=O)C 406.40 unknown https://doi.org/10.1021/JO00317A022
[(4R,6Z,8R,10S,11E)-8-acetyloxy-10-hydroxy-3-(hydroxymethyl)-6,10-dimethyl-2-oxo-4,5,8,9-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 162859490 Click to see CC1=CC(CC(C=C2C(=C(C(=O)O2)CO)C(C1)OC(=O)C(=C)C)(C)O)OC(=O)C 406.40 unknown https://doi.org/10.1021/JO00317A022
[(4R,6Z,8R,10S,11E)-8-acetyloxy-3-(acetyloxymethyl)-10-hydroxy-6,10-dimethyl-2-oxo-4,5,8,9-tetrahydrocyclodeca[b]furan-4-yl] (E)-2-methylbut-2-enoate 162898605 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(C=C2C1=C(C(=O)O2)COC(=O)C)(C)O)OC(=O)C)C 462.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
[(4S,6E,8S,10S,11Z)-8-acetyloxy-10-hydroxy-3-(methoxymethyl)-6,10-dimethyl-2-oxo-4,5,8,9-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 162974552 Click to see CC1=CC(CC(C=C2C(=C(C(=O)O2)COC)C(C1)OC(=O)C(=C)C)(C)O)OC(=O)C 420.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
[8-Acetyloxy-10-hydroxy-3-(hydroxymethyl)-6,10-dimethyl-2-oxo-4,5,8,9-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 162859489 Click to see CC1=CC(CC(C=C2C(=C(C(=O)O2)CO)C(C1)OC(=O)C(=C)C)(C)O)OC(=O)C 406.40 unknown https://doi.org/10.1021/JO00317A022
[8-Acetyloxy-10-hydroxy-3-(methoxymethyl)-6,10-dimethyl-2-oxo-4,5,8,9-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 75151786 Click to see CC1=CC(CC(C=C2C(=C(C(=O)O2)COC)C(C1)OC(=O)C(=C)C)(C)O)OC(=O)C 420.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
[8-Acetyloxy-3-(acetyloxymethyl)-10-hydroxy-6,10-dimethyl-2-oxo-4,5,8,9-tetrahydrocyclodeca[b]furan-4-yl] 2-methylbut-2-enoate 162898604 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(C=C2C1=C(C(=O)O2)COC(=O)C)(C)O)OC(=O)C)C 462.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
[8-Acetyloxy-3-(acetyloxymethyl)-10-hydroxy-6,10-dimethyl-2-oxo-4,5,8,9-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 5231779 Click to see CC1=CC(CC(C=C2C(=C(C(=O)O2)COC(=O)C)C(C1)OC(=O)C(=C)C)(C)O)OC(=O)C 448.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
https://doi.org/10.1021/JO00317A022
[8-Acetyloxy-3-(ethoxymethyl)-6-hydroxy-6,10-dimethyl-2-oxo-4,5,7,8-tetrahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 73816636 Click to see CCOCC1=C2C(CC(CC(C=C(C=C2OC1=O)C)OC(=O)C)(C)O)OC(=O)C(=C)C 434.50 unknown https://doi.org/10.1021/JO00317A022
Acetylrolandrolide 5384465 Click to see CC1=CC(CC(C=C2C(=C(C(=O)O2)COC(=O)C)C(C1)OC(=O)C(=C)C)(C)O)OC(=O)C 448.50 unknown https://doi.org/10.1021/JO00317A022
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
Ethoxyisorolandrolide 163184520 Click to see CCOCC1=C2C(CC(CC(C=C(C=C2OC1=O)C)OC(=O)C)(C)O)OC(=O)C(=C)C 434.50 unknown https://doi.org/10.1021/JO00317A022
Isorolandrolide 163184521 Click to see CC1=CC(CC(C=C2C(=C(C(=O)O2)CO)C(C1)OC(=O)C(=C)C)(C)O)OC(=O)C 406.40 unknown https://doi.org/10.1021/JO00317A022
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(1S,2R,4R,6R,7E,10S)-6-acetyloxy-12-(acetyloxymethyl)-4,8-dimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradeca-7,11-dien-10-yl] 2-methylprop-2-enoate 14355841 Click to see CC1=CC(CC2(C(O2)C3C(=C(C(=O)O3)COC(=O)C)C(C1)OC(=O)C(=C)C)C)OC(=O)C 448.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
[6-Acetyloxy-12-(acetyloxymethyl)-4,8-dimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradeca-7,11-dien-10-yl] 2-methylprop-2-enoate 74151575 Click to see CC1=CC(CC2(C(O2)C3C(=C(C(=O)O3)COC(=O)C)C(C1)OC(=O)C(=C)C)C)OC(=O)C 448.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847506/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)97890-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides
[(2R)-2-methyl-1-(2-oxooxolan-3-yl)pentyl] (2R)-2-[[(2S)-2-[[(E)-4-amino-4-oxobut-2-enoyl]amino]propanoyl]amino]-3-methylbutanoate 162893828 Click to see CCCC(C)C(C1CCOC1=O)OC(=O)C(C(C)C)NC(=O)C(C)NC(=O)C=CC(=O)N 453.50 unknown https://doi.org/10.1021/JO00317A022

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