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Aldama robusta

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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 UUID64405ce9caf69751722756
Scientific name Aldama robusta
Authority (Gardner) E.E.Schill. & Panero
First published in Bot. J. Linn. Soc. 167(3): 324 (2011)

Description Top

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Synonyms Top

Scientific name Authority First published in
Viguiera ovatifolia DC.
Rhysolepis robusta (Gardner) H.Rob. & A.J.Moore Proc. Biol. Soc. Washington 117(3): 431 (2004)
Viguiera radula Baker Fl. Bras. 6(3): 223 (1884)
Rhysolepis radula (Baker) H.Rob. & A.J.Moore Proc. Biol. Soc. Washington 117(3): 431 (2004)
Rhysolepis ovatifolia (DC.) H.Rob. & A.J.Moore Proc. Biol. Soc. Washington 117(3): 430 (2004)
Viguiera ovatifolia (DC.) Baker Fl. Bras. (Martius) 6(3): 226. 1884 [1 May 1884]
Leighia ovatifolia DC. Prodr. 5: 583 (1836)
Viguiera scabra Pohl ex Baker Fl. Bras. 6(3): 227 (1884)
Viguiera robusta Gardner London J. Bot. 7: 403 (1848)
Rhysolepis macrocalyx (S.F.Blake) H.Rob. & A.J.Moore Proc. Biol. Soc. Washington 117(3): 429 (2004)
Viguiera macrocalyx S.F.Blake Contr. Gray Herb. 54: 171 (1918)
Aldama macrocalyx (S.F.Blake) E.E.Schill. & Panero Bot. J. Linn. Soc. 167(3): 324 (2011)
Aldama ovatifolia (DC.) E.E.Schill. & Panero Bot. J. Linn. Soc. 167(3): 324 (2011)
Aldama radula (Baker) E.E.Schill. & Panero Bot. J. Linn. Soc. 167(3): 324 (2011)

Common names Top

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil South
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001318127
Tropicos 100439042
KEW urn:lsid:ipni.org:names:77115702-1
NCBI Taxonomy 2805000
IPNI 77115702-1
iNaturalist 1098301
GBIF 7666394
Elurikkus 612911

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
Anti-Leishmania compounds can be screened using Leishmania spp. expressing red fluorescence (tdTomato) Cruz MG, Santi AM, de Morais-Teixeira E, Caldeira AS, de Siqueira EP, Oliveira E, Alves TM, Murta SM Antimicrob Agents Chemother 08-Dec-2023
PMCID:PMC10777850
doi:10.1128/aac.00509-23
PMID:38063403
Role of NLRP3 in the pathogenesis and treatment of gout arthritis Liu YR, Wang JQ, Li J Front Immunol 27-Mar-2023
PMCID:PMC10083392
doi:10.3389/fimmu.2023.1137822
PMID:37051231
Overview of Bioactive Fungal Secondary Metabolites: Cytotoxic and Antimicrobial Compounds Conrado R, Gomes TC, Roque GS, De Souza AO Antibiotics (Basel) 11-Nov-2022
PMCID:PMC9687038
doi:10.3390/antibiotics11111604
PMID:36421247
Sulfur-Containing Compounds from Endophytic Fungi: Sources, Structures and Bioactivities Fan Y, Ma Z, Zhang Y, Wang Y, Ding Y, Wang C, Cao S J Fungi (Basel) 13-Jun-2022
PMCID:PMC9224594
doi:10.3390/jof8060628
PMID:35736111
Evaluation of Antiarthritic and Antinociceptive Effects of Cedrol in a Rat Model of Arthritis Forouzanfar F, Pourbagher-Shahri AM, Ghazavi H Oxid Med Cell Longev 25-Apr-2022
PMCID:PMC9060983
doi:10.1155/2022/4943965
PMID:35509836
Anti-Inflammatory and Immunoregulatory Action of Sesquiterpene Lactones Paço A, Brás T, Santos JO, Sampaio P, Gomes AC, Duarte MF Molecules 08-Feb-2022
PMCID:PMC8839508
doi:10.3390/molecules27031142
PMID:35164406
Chaetomugilins and Chaetoviridins—Promising Natural Metabolites: Structures, Separation, Characterization, Biosynthesis, Bioactivities, Molecular Docking, and Molecular Dynamics Omar AM, Mohamed GA, Ibrahim SR J Fungi (Basel) 27-Jan-2022
PMCID:PMC8875349
doi:10.3390/jof8020127
PMID:35205880
Biotransformation ability of endophytic fungi: from species evolution to industrial applications Liu X, Zhou ZY, Cui JL, Wang ML, Wang JH Appl Microbiol Biotechnol 09-Sep-2021
PMCID:PMC8426592
doi:10.1007/s00253-021-11554-x
PMID:34499202
Plant Metabolites Involved in the Differential Development of a Heliantheae-Specialist Insect Gallon ME, Gobbo-Neto L Metabolites 25-Feb-2021
PMCID:PMC7996590
doi:10.3390/metabo11030134
PMID:33669112
Endophytic Penicillium species and their agricultural, biotechnological, and pharmaceutical applications Toghueo RM, Boyom FF 3 Biotech 08-Feb-2020
PMCID:PMC7007919
doi:10.1007/s13205-020-2081-1
PMID:32095421
Occurrence and Properties of Thiosilvatins Salvatore MM, Nicoletti R, DellaGreca M, Andolfi A Mar Drugs 26-Nov-2019
PMCID:PMC6950259
doi:10.3390/md17120664
PMID:31779089
Editorial: Ethnopharmacological Studies for the Development of Drugs With Special Reference to Asteraceae Panda SK, da Silva LC, Sahal D, Leonti M Front Pharmacol 03-Sep-2019
PMCID:PMC6737279
doi:10.3389/fphar.2019.00955
PMID:31551771
Therapeutic Interventions for Countering Leishmaniasis and Chagas’s Disease: From Traditional Sources to Nanotechnological Systems Souto EB, Dias-Ferreira J, Craveiro SA, Severino P, Sanchez-Lopez E, Garcia ML, Silva AM, Souto SB, Mahant S Pathogens 01-Aug-2019
PMCID:PMC6789685
doi:10.3390/pathogens8030119
PMID:31374930
Budlein A, a Sesquiterpene Lactone From Viguiera robusta, Alleviates Pain and Inflammation in a Model of Acute Gout Arthritis in Mice Fattori V, Zarpelon AC, Staurengo-Ferrari L, Borghi SM, Zaninelli TH, Da Costa FB, Alves-Filho JC, Cunha TM, Cunha FQ, Casagrande R, Arakawa NS, Verri WA Jr Front Pharmacol 25-Sep-2018
PMCID:PMC6167909
doi:10.3389/fphar.2018.01076
PMID:30319413
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

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 / Fatty Acyls / Fatty acid esters
(2,11-Dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-1(13)-en-9-yl) 2-methylbut-2-enoate 162971531 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(CC3C1C(=C)C(=O)O3)C)C 360.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(2R,4R,8S,9R,11R)-2,11-dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-1(13)-en-9-yl] (Z)-2-methylbut-2-enoate 101939161 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(CC3C1C(=C)C(=O)O3)C)C 360.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4aR,7S,8R,8aS)-8-[5-(6-amino-9-methylpurin-9-ium-7-yl)-3-methylpent-3-enyl]-4,4a,7,8-tetramethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one 163186917 Click to see CC1CCC2(C(C1(C)CCC(=CCN3C=[N+](C4=NC=NC(=C43)N)C)C)CC(=O)C=C2C)C 436.60 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10S,15S)-15-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 139031795 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0305-1978(96)00057-9
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0367-326X(01)00365-3
Grandifloric acid 433554 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0305-1978(96)00057-9
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0367-326X(01)00365-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(2,11-Dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl) 2-methylbut-2-enoate 500211 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(2Z,4S,8R,9R,11R)-2-(hydroxymethyl)-11-methyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] (E)-2-methylbut-2-enoate 14807488 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 374.40 unknown https://doi.org/10.1016/J.PHYMED.2009.04.002
[(2Z,8R,9R,11R)-2-(hydroxymethyl)-11-methyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] 2-methylbut-2-enoate 163185002 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 374.40 unknown https://doi.org/10.1016/J.PHYMED.2009.04.002
Atripliciolidtiglate 14314512 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
https://doi.org/10.1016/0305-1978(96)00057-9
Budlein A 5281430 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 374.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2013.09.022
https://doi.org/10.1016/J.PHYMED.2009.04.002
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1,12-Dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl) 2-methylbut-2-enoate 162960437 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(CC3C1C(=C)C(=O)O3)C)O)O)C 380.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
(3aR,4R,6Z,10Z,11aR)-4-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 99720499 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
(8-Acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl) 2-methylbut-2-enoate 78410063 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)C 404.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(1R,2R,4S,6R,8S,9Z,11R)-8-hydroxy-4-(hydroxymethyl)-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (Z)-2-methylbut-2-enoate 162910695 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)CO 378.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(1R,2R,4S,6R,9Z,11R)-4-(hydroxymethyl)-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (Z)-2-methylbut-2-enoate 162923550 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CCC(=CC3C1C(=C)C(=O)O3)C)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(1R,2S,4R,8S,9R,11R,12S)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] (Z)-2-methylbut-2-enoate 162960438 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(CC3C1C(=C)C(=O)O3)C)O)O)C 380.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(3aR,4R,6Z,10Z,11aR)-6-(acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162989534 Click to see CC1C(O1)(C)C(=O)OC2CC(=CCCC(=CC3C2C(=C)C(=O)O3)C)COC(=O)C 404.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(3aR,4R,6Z,10Z,11aR)-6-(acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2S,3S)-2,3-dimethyloxirane-2-carboxylate 162989535 Click to see CC1C(O1)(C)C(=O)OC2CC(=CCCC(=CC3C2C(=C)C(=O)O3)C)COC(=O)C 404.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(3aR,4R,6Z,10Z,11aR)-6-(acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162877090 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 404.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[(3aR,4R,6Z,8R,10Z,11aR)-8-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 92254803 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[4-(Acetyloxymethyl)-8-hydroxy-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-methylbut-2-enoate 163022175 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)COC(=O)C 420.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[4-(Hydroxymethyl)-9-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-methylbut-2-enoate 162923548 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CCC(=CC3C1C(=C)C(=O)O3)C)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[6-(Acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2,3-dimethyloxirane-2-carboxylate 162989531 Click to see CC1C(O1)(C)C(=O)OC2CC(=CCCC(=CC3C2C(=C)C(=O)O3)C)COC(=O)C 404.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[6-(Acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 4-hydroxy-2-methylbut-2-enoate 137796477 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 404.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
[8-Hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylbut-2-enoate 122744 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
4-Hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 72656715 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
CID 3478765 3478765 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
Epoxynobilin 9998730 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
Leptocarpin 6438714 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
Leptocarpin acetate 10408931 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)C 404.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
Rotundin 73354911 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)COC(=O)C 420.50 unknown https://doi.org/10.1016/S0031-9422(02)00747-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,12-diol 162949840 Click to see CC(CCC=C(C)C)C1CCC2(C1(C(CC3=C2CCC4C3(CCC(C4(C)C)O)C)O)C)C 442.70 unknown https://doi.org/10.1016/0305-1978(96)00057-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
2-(5-Ethyl-5-methyl-10-methylidene-4-tricyclo[7.2.1.01,6]dodecanyl)-2-methylpropanoic acid 162884783 Click to see CCC1(C2CCC3CC2(CCC1C(C)(C)C(=O)O)CC3=C)C 304.50 unknown https://doi.org/10.1016/S0367-326X(01)00365-3
2-[(1S,4S,5S,6R,9R)-5-ethyl-5-methyl-10-methylidene-4-tricyclo[7.2.1.01,6]dodecanyl]-2-methylpropanoic acid 162884784 Click to see CCC1(C2CCC3CC2(CCC1C(C)(C)C(=O)O)CC3=C)C 304.50 unknown https://doi.org/10.1016/S0367-326X(01)00365-3
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/0305-1978(96)00057-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1016/0305-1978(96)00057-9
Prenyletin 3873459 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)O)C 246.26 unknown https://doi.org/10.1016/0305-1978(96)00057-9

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