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Duroia hirsuta

Duroia hirsuta - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644038ecebacd947738025
Scientific name Duroia hirsuta
Authority K.Schum.
First published in Fl. Bras. (Martius) 6(6): 367. 1889 [15 Jun 1889]

Description Top

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Synonyms Top

Scientific name Authority First published in
Schachtia dioica H.Karst. Linnaea 30: 157 (1859)
Duroia spraguei Wernham Bull. Misc. Inform. Kew 1914: 66 (1914)
Amaioua hirsuta Poepp. Nov. Gen. Sp. Pl. 3: 25 (1841)

Common names Top

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Language Common/alternative name
Spanish borojocillo
Spanish casa del diablo
Spanish huitillo
Spanish turma de mono
Arabic نبات نمل الليمون
Arabic دورويا المشعرة
Quechua añanku kaspi
Quechua tubi abiyu
Quechua añanku k'aspi

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000946928
Tropicos 27904163
KEW urn:lsid:ipni.org:names:86135-2
The Plant List kew-65315
Open Tree Of Life 919378
NCBI Taxonomy 114473
IUCN Red List 210263630
IPNI 748664-1
iNaturalist 706977
GBIF 2892105
Freebase /m/0gmfp39
EOL 1111097
Wikipedia Duroia_hirsuta

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
Patterns of Plumericin Concentration in Leaves of Himatanthus tarapotensis (Apocynaceae) and Its Interactions with Herbivory in the Peruvian Amazon Amasifuen Guerra CA, Patel K, Delprete PG, Spina AP, Grados J, Vásquez-Ocmín P, Gadea A, Rojas R, Guzmán J, Sauvain M Plants (Basel) 08-Apr-2022
PMCID:PMC9027084
doi:10.3390/plants11081011
PMID:35448739
Fungal Endophytes: A Potential Source of Antibacterial Compounds Deshmukh SK, Dufossé L, Chhipa H, Saxena S, Mahajan GB, Gupta MK J Fungi (Basel) 08-Feb-2022
PMCID:PMC8877021
doi:10.3390/jof8020164
PMID:35205918
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
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
Natural Products from Endophytic Fungi Associated with Rubiaceae Species Cruz JS, da Silva CA, Hamerski L J Fungi (Basel) 07-Aug-2020
PMCID:PMC7558492
doi:10.3390/jof6030128
PMID:32784526
Cuticular Lipids as a Cross-Talk among Ants, Plants and Butterflies Barbero F Int J Mol Sci 24-Nov-2016
PMCID:PMC5187766
doi:10.3390/ijms17121966
PMID:27886144
The Biochemical Toxin Arsenal from Ant Venoms Touchard A, Aili SR, Fox EG, Escoubas P, Orivel J, Nicholson GM, Dejean A Toxins (Basel) 20-Jan-2016
PMCID:PMC4728552
doi:10.3390/toxins8010030
PMID:26805882
Stelliosphaerols A and B, Sesquiterpene–Polyol Conjugates from an Ecuadorian Fungal Endophyte Forcina GC, Castro A, Bokesch HR, Spakowicz DJ, Legaspi ME, Kucera K, Villota S, Narvaez-Trujillo A, McMahon JB, Gustafson KR, Strobel SA J Nat Prod 14-Dec-2015
PMCID:PMC6318786
doi:10.1021/acs.jnatprod.5b00749
PMID:26651879
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Triterpenes and the Antimycobacterial Activity of Duroia macrophylla Huber (Rubiaceae) Martins D, Carrion LL, Ramos DF, Salomé KS, da Silva PE, Barison A, Nunez CV Biomed Res Int 12-Feb-2013
PMCID:PMC3583080
doi:10.1155/2013/605831
PMID:23509750
Spatio-temporal changes of photosynthesis in carnivorous plants in response to prey capture, retention and digestion Pavlovič A Plant Signal Behav 01-Nov-2010
PMCID:PMC3115228
doi:10.4161/psb.5.11.11906
PMID:20523127
The devil to pay: a cost of mutualism with Myrmelachista schumanni ants in ‘devil's gardens’ is increased herbivory on Duroia hirsuta trees Frederickson ME, Gordon DM Proc Biol Sci 13-Feb-2007
PMCID:PMC2124481
doi:10.1098/rspb.2006.0415
PMID:17301016
Substances, relationships and the omnipresence of the body: an overview of Ashéninka ethnomedicine (Western Amazonia) Lenaerts M J Ethnobiol Ethnomed 10-Nov-2006
PMCID:PMC1654146
doi:10.1186/1746-4269-2-49
PMID:17096839
Identification of a plant growth inhibiting iridoid lactone fromDuroia hirsuta, the allelopathic tree of the ‘Devil's Garden’ J. E. Page, S. Madriñán, G. H. N. Towers Springer Science and Business Media LLC 02-Aug-2005
doi:10.1007/BF01956467
New 3-methyoxyflavones, an iridoid lactone and a flavonol from duroia hirsuta. Aquino R, Tommasi ND, Tapia M, Lauro MR, Rastrelli L J Nat Prod 01-Apr-1999
doi:10.1021/NP9803631
PMID:10217708

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 / Terpene lactones
(1S,4S,8R,10R,11R,14S)-11-acetyl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-dien-12-one 100936158 Click to see CC(=O)C1C2C3(C=CC4C3C(O2)OC=C4COC5C(C(C(C(O5)CO)O)O)O)OC1=O 440.40 unknown https://doi.org/10.1021/NP9803631
(1S,4S,8R,10S,11R,14S)-11-acetyl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-dien-12-one 163194506 Click to see CC(=O)C1C2C3(C=CC4C3C(O2)OC=C4COC5C(C(C(C(O5)CO)O)O)O)OC1=O 440.40 unknown https://doi.org/10.1021/NP9803631
11-Acetyl-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-dien-12-one 85243626 Click to see CC(=O)C1C2C3(C=CC4C3C(O2)OC=C4COC5C(C(C(C(O5)CO)O)O)O)OC1=O 440.40 unknown https://doi.org/10.1021/NP9803631
methyl (1R,4R,8S,10S,11E,14S)-11-ethylidene-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate 161287690 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1007/BF01956467
Plumericin 5281545 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1007/BF01956467
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(25S)-11alpha,20,26-trihydroxyecdysone 16755647 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O)O 512.60 unknown https://doi.org/10.1007/BF01956467
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,4'-Dihydroxy-7,3',5'-trimethoxyflavone 10807373 Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C(=C3)OC)O)OC)O 344.30 unknown https://doi.org/10.1021/NP9803631
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-3,7,3',5'-tetramethoxyflavone 10642125 Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C(=C3)OC)O)OC)OC 358.30 unknown https://doi.org/10.1021/NP9803631
4',5'-Dihydroxy-3,7,3'-trimethoxyflavone 10593524 Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C(=C3)OC)O)O)OC 344.30 unknown https://doi.org/10.1021/NP9803631

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