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Heterophyllaea pustulata

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 UUID64403e2f2c99b136370768
Scientific name Heterophyllaea pustulata
Authority Hook.f.
First published in Hooker's Icon. Pl. 12: 31 (1873)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Heterophyllaea fiebrigii (K.Krause) Standl. Publ. Field Columb. Mus., Bot. Ser. 11: 214 (1936)
Heterophyllaea lanceolata Griseb. Abh. Königl. Ges. Wiss. Göttingen 24: 154 (1879)
Hindsia fiebrigii K.Krause Bot. Jahrb. Syst. 40: 320 (1908)

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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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
    • Southern South America
      • Argentina Northwest
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000981966
Tropicos 27907048
KEW urn:lsid:ipni.org:names:753052-1
The Plant List kew-98811
Open Tree Of Life 1041897
NCBI Taxonomy 60145
IPNI 753052-1
GBIF 2903405
EPPO HTRPU
EOL 1105460

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
Fungal Anthraquinone Photoantimicrobials Challenge the Dogma of Cationic Photosensitizers Hammerle F, Fiala J, Höck A, Huymann L, Vrabl P, Husiev Y, Bonnet S, Peintner U, Siewert B J Nat Prod 14-Sep-2023
PMCID:PMC10616806
doi:10.1021/acs.jnatprod.2c01157
PMID:37708055
Optimization of the Extraction Conditions of Bioactive Compounds from Ocimum basilicum Leaves Using Ultrasound-Assisted Extraction via a Sonotrode Aloisio C, Razola-Díaz MD, Aznar-Ramos MJ, Longhi MR, Andreatta AE, Verardo V Molecules 07-Jul-2023
PMCID:PMC10343415
doi:10.3390/molecules28135286
PMID:37446947
Efficacy of Acacia nilotica, Eucalyptus camaldulensis, and Salix safsafs on the mortality and development of two vector-borne mosquito species, Culex pipiens and Aedes aegypti, in the laboratory and field Baeshen RS, Baz MM Heliyon 19-May-2023
PMCID:PMC10220238
doi:10.1016/j.heliyon.2023.e16378
PMID:37251815
Plants causing poisoning outbreaks of livestock in South America: A review Riet-Correa F, Machado M, Micheloud JF Toxicon X 21-Jan-2023
PMCID:PMC9898795
doi:10.1016/j.toxcx.2023.100150
PMID:36747993
Primary Photosensitization by Chamaecrista serpens in Santa Inês Sheep Mendonça MF, Caymmi LG, Silva AW, Biscarde CE, Silva RD, Leal PV, Pimentel LA, Riet-Correa F, Peixoto TC Animals (Basel) 13-Nov-2022
PMCID:PMC9686935
doi:10.3390/ani12223132
PMID:36428360
Insights into Antiviral Properties and Molecular Mechanisms of Non-Flavonoid Polyphenols against Human Herpesviruses Hassan ST, Šudomová M, Mazurakova A, Kubatka P Int J Mol Sci 11-Nov-2022
PMCID:PMC9693824
doi:10.3390/ijms232213891
PMID:36430369
Antiviral potential of anthraquinones from Polygonaceae, Rubiaceae and Asphodelaceae: Potent candidates in the treatment of SARS-COVID-19, A comprehensive review Ntemafack A, Singh RV, Ali S, Kuiate JR, Hassan QP S Afr J Bot 29-Sep-2022
PMCID:PMC9519529
doi:10.1016/j.sajb.2022.09.043
PMID:36193345
Extraction of High-Value Chemicals from Plants for Technical and Medical Applications Kapadia P, Newell AS, Cunningham J, Roberts MR, Hardy JG Int J Mol Sci 07-Sep-2022
PMCID:PMC9499410
doi:10.3390/ijms231810334
PMID:36142238
Photoactive Herbal Compounds: A Green Approach to Photodynamic Therapy Sulaiman C, George BP, Balachandran I, Abrahamse H Molecules 10-Aug-2022
PMCID:PMC9413332
doi:10.3390/molecules27165084
PMID:36014325
Some Natural Photosensitizers and Their Medicinal Properties for Use in Photodynamic Therapy Kubrak TP, Kołodziej P, Sawicki J, Mazur A, Koziorowska K, Aebisher D Molecules 10-Feb-2022
PMCID:PMC8879555
doi:10.3390/molecules27041192
PMID:35208984
Photosensitization of a subcutaneous tumour by the natural anthraquinone parietin and blue light Mugas ML, Calvo G, Marioni J, Céspedes M, Martinez F, Vanzulli S, Sáenz D, Di Venosa G, Nuñez Montoya S, Casas A Sci Rep 10-Dec-2021
PMCID:PMC8664885
doi:10.1038/s41598-021-03339-z
PMID:34893702
The use of ultrasound in the South Cone region. Advances in organic and inorganic synthesis and in analytical methods Lo Fiego MJ, Lorenzetti AS, Silbestri GF, Domini CE Ultrason Sonochem 16-Nov-2021
PMCID:PMC8608658
doi:10.1016/j.ultsonch.2021.105834
PMID:34814046
Hybrid high-intensity ultrasound and microwave treatment: A review on its effect on quality and bioactivity of foods Muñoz-Almagro N, Morales-Soriano E, Villamiel M, Condezo-Hoyos L Ultrason Sonochem 16-Nov-2021
PMCID:PMC8626613
doi:10.1016/j.ultsonch.2021.105835
PMID:34826725
Chemistry, Biosynthesis, Physicochemical and Biological Properties of Rubiadin: A Promising Natural Anthraquinone for New Drug Discovery and Development Watroly MN, Sekar M, Fuloria S, Gan SH, Jeyabalan S, Wu YS, Subramaniyan V, Sathasivam KV, Ravi S, Mat Rani NN, Lum PT, Vaijanathappa J, Meenakshi DU, Mani S, Fuloria NK Drug Des Devel Ther 03-Nov-2021
PMCID:PMC8576757
doi:10.2147/DDDT.S338548
PMID:34764636
Kinetic Study of Subcritical Water Extraction of Scopoletin, Alizarin, and Rutin from Morinda citrifolia Jamaludin R, Kim DS, Salleh LM, Lim SB Foods 24-Sep-2021
PMCID:PMC8534878
doi:10.3390/foods10102260
PMID:34681309

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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,6-Dihydroxy-7-methoxy-2-methylanthracene-9,10-dione 11652118 Click to see 284.26 unknown https://doi.org/10.1021/NP050181O
https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
2-Hydroxy-3-methoxy-7-methyl anthraquinone 11587079 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC(=C(C=C3C2=O)O)OC 268.26 unknown https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
https://doi.org/10.1021/NP050181O
2-Hydroxy-3-methylanthraquinone 10889963 Click to see 238.24 unknown https://doi.org/10.1078/094471103322331854
5,5'-Bisoranjidiol 11677810 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3C4=C(C=CC5=C4C(=O)C6=C(C5=O)C(=C(C=C6)C)O)O)O)O 506.50 unknown https://doi.org/10.1021/NP050181O
https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
6-Hydroxy-1-methoxy-2-methylanthracene-9,10-dione 44715573 Click to see 268.26 unknown https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
Damnacanthal 2948 Click to see COC1=C2C(=CC(=C1C=O)O)C(=O)C3=CC=CC=C3C2=O 282.25 unknown https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
https://doi.org/10.1078/094471103322331854
Damnacanthol 160474 Click to see 284.26 unknown https://doi.org/10.1078/094471103322331854
https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1078/094471103322331854
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
https://doi.org/10.1078/094471103322331854
Soranjidiol 124063 Click to see 254.24 unknown https://doi.org/10.1078/094471103322331854
https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[5-(hexopyranosyloxy)-1-oxo-2a,4a,5,7b-tetrahydro-1H-2,6-dioxacyclopenta[cd]inden-4-yl]methyl acetate 233330 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1021/NP050181O
Asperuloside 84298 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1021/NP050181O
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1021/NP050181O
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1021/NP050181O
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1021/NP050181O
Quercetin 3-O-(6-O-acetyl-beta-D-glucopyranoside) 10006384 Click to see 506.40 unknown https://doi.org/10.1021/NP050181O
Quercetin-3-O-glucosyl-6''-acetate 15596585 Click to see 506.40 unknown https://doi.org/10.1021/NP050181O

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