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Ayapana triplinervis

Ayapana triplinervis - Unknown
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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 UUID643fcedb58469044696548
Scientific name Ayapana triplinervis
Authority (Vahl) R.M.King & H.Rob.
First published in Phytologia 20: 212 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium ayapana Vent. Jard. Malmaison 3. t. 3
Eupatorium triplinerve Vahl Symb. Bot. 3: 97 (1794)
Ayapana officinalis Spach Hist. Nat. Vég. (Spach) 10: 290 (1841)
Eupatorium triplinerve Blume 903 1826
Eupatorium luzoniense Llanos Fragm. Pl. Filip. : 88 (1851)

Common names Top

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Language Common/alternative name
Spanish eupatorium ayapana
Spanish ayapana officinalis
Spanish eupatorium luzoniense
Arabic أيابانه
Bengali আয়াপনা ট্রিপলিনেরভিস
French eupatorium ayapana
Indonesian prasman
Malayalam vishalyakarani
Malayalam അയ്യപ്പന
Malayalam അയ്യപ്പാന
Malayalam വിഷല്യകരണി
Malayalam വിശല്യകരണി
Vietnamese ba dót
Chinese 三脉尖佩兰
Chinese 三脈尖佩蘭

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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No forms added yet.

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
  • Africa
    • West Tropical Africa
      • Benin
    • Western Indian Ocean
      • Mauritius
      • Rodrigues
      • Réunion
      • Seychelles
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
    • Indo-China
      • Cambodia
      • Vietnam
    • Malesia
      • Jawa
      • Philippines
  • Southern America
    • Brazil
      • Brazil North
    • Caribbean
      • Dominican Republic
      • Puerto Rico
      • Trinidad-Tobago
    • Northern South America
      • French Guiana
    • Western South America
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000085174
Tropicos 2709519
INPN 448501
KEW urn:lsid:ipni.org:names:27457-2
The Plant List gcc-41590
Open Tree Of Life 786810
NCBI Taxonomy 1090619
IPNI 27457-2
iNaturalist 919365
GBIF 3142644
Freebase /m/026p71j
EOL 487713
USDA GRIN 404707
Wikipedia Ayapana_triplinervis

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
Plant-Derived Epi-Nutraceuticals as Potential Broad-Spectrum Anti-Viral Agents Gabbianelli R, Shahar E, de Simone G, Rucci C, Bordoni L, Feliziani G, Zhao F, Ferrati M, Maggi F, Spinozzi E, Mahajna J Nutrients 08-Nov-2023
PMCID:PMC10675658
doi:10.3390/nu15224719
PMID:38004113
Do índio Passos ao doutor Chernoviz: experiências de cura da lepra no Pará do século XIX Henrique MC Hist Cienc Saude Manguinhos 04-Aug-2023
PMCID:PMC10402912
doi:10.1590/S0104-59702023000100027
PMID:37556716
Natural Products and Derivatives as Potential Zika virus Inhibitors: A Comprehensive Review Pereira RS, Santos FC, Campana PR, Costa VV, de Pádua RM, Souza DG, Teixeira MM, Braga FC Viruses 20-May-2023
PMCID:PMC10222392
doi:10.3390/v15051211
PMID:37243296
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Antiviral Effect of Stenocline ericoides DC. and Stenocline inuloides DC., Two Flavonoid-Rich Endemic Plants from Madagascar, against Dengue and Zika Viruses Ramiharimanana FD, Haddad JG, Andrianavalonirina MA, Apel C, Olivon F, Diotel N, Desprès P, Ramanandraibe VV, El Kalamouni C Pharmaceuticals (Basel) 30-Nov-2022
PMCID:PMC9787939
doi:10.3390/ph15121500
PMID:36558951
Essential Oils from Vietnamese Asteraceae for Environmentally Friendly Control of Aedes Mosquitoes Hoi TM, Satyal P, Huong LT, Hau DV, Binh TD, Duyen DT, Dai DN, Huy NG, Chinh HV, Hoa VV, Hung NH, Setzer WN Molecules 17-Nov-2022
PMCID:PMC9699393
doi:10.3390/molecules27227961
PMID:36432060
A First Look at the Inhibitory Potential of Urospatha sagittifolia (Araceae) Ethanolic Extract for Bothrops atrox Snakebite Envenomation Vera-Palacios AL, Sacoto-Torres JD, Hernández-Altamirano JA, Moreno A, Peñuela-Mora MC, Salazar-Valenzuela D, Mogollón NG, Almeida JR Toxins (Basel) 17-Jul-2022
PMCID:PMC9315696
doi:10.3390/toxins14070496
PMID:35878234
The co-adsorption of thymohydroquinone dimethyl ether (THQ) and coumarin present in the aqueous extract of Ayapana triplinervis on mild steel and its protection in hydrochloric acid up to 323 K: computational and physicochemical studies Rani AT J, Thomas A, Kuruvilla M, Arshad M, Joseph A RSC Adv 12-May-2022
PMCID:PMC9096429
doi:10.1039/d2ra02109a
PMID:35702201
Bacterial Skin Infections in Livestock and Plant-Based Alternatives to Their Antibiotic Treatment Mala L, Lalouckova K, Skrivanova E Animals (Basel) 23-Aug-2021
PMCID:PMC8388705
doi:10.3390/ani11082473
PMID:34438930
An in vitro Propagation of Aspilia africana (Pers.) C. D. Adams, and Evaluation of Its Anatomy and Physiology of Acclimatized Plants Okello D, Yang S, Komakech R, Rahmat E, Chung Y, Gang R, Kim YG, Omujal F, Kang Y Front Plant Sci 29-Jul-2021
PMCID:PMC8358661
doi:10.3389/fpls.2021.704896
PMID:34394159
Determination of Phenolics and Flavonoids of Some Useful Medicinal Plants and Bioassay-Guided Fractionation Substances of Sclerocarya birrea (A. Rich) Hochst Stem (Bark) Extract and Their Efficacy Against Salmonella typhi Abdallah MS, Mustafa M, Nallappan MA, Choi S, Paik JH, Rusea G Front Chem 27-Jul-2021
PMCID:PMC8353516
doi:10.3389/fchem.2021.670530
PMID:34386478
Development of nano-emulsions based on Ayapana triplinervis essential oil for the control of Aedes aegypti larvae Lobato Rodrigues AB, Martins RL, Rabelo ÉD, Tomazi R, Santos LL, Brandão LB, Faustino CG, Ferreira Farias AL, dos Santos CB, de Castro Cantuária P, Galardo AK, de Almeida SS PLoS One 09-Jul-2021
PMCID:PMC8270136
doi:10.1371/journal.pone.0254225
PMID:34242328
Brazilian essential oils as source for the discovery of new anti-COVID-19 drug: a review guided by in silico study Amparo TR, Seibert JB, Silveira BM, Costa FS, Almeida TC, Braga SF, da Silva GN, dos Santos OD, de Souza GH Phytochem Rev 13-Apr-2021
PMCID:PMC8042356
doi:10.1007/s11101-021-09754-4
PMID:33867898
Nanoemulsions: The rising star of antiviral therapeutics and nanodelivery system—current status and prospects Franklyne JS, Gopinath PM, Mukherjee A, Chandrasekaran N Curr Opin Colloid Interface Sci 30-Mar-2021
PMCID:PMC8007535
doi:10.1016/j.cocis.2021.101458
PMID:33814954
Composition of Essential Oils from Roots and Aerial Parts of Carpesium cernuum and Their Antibacterial and Cytotoxic Activities Wajs-Bonikowska A, Malarz J, Szoka Ł, Kwiatkowski P, Stojakowska A Molecules 26-Mar-2021
PMCID:PMC8038092
doi:10.3390/molecules26071883
PMID:33810440

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2,5-Dimethoxy-p-cymene 6427071 Click to see CC1=CC(=C(C=C1OC)C(C)C)OC 194.27 unknown https://doi.org/10.1002/CBER.19080410195
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3R,4aR,8aR)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 12309812 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)94483-2
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)94483-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
Thymoquinone 10281 Click to see CC1=CC(=O)C(=CC1=O)C(C)C 164.20 unknown https://doi.org/10.1055/S-2006-959619
> Phenylpropanoids and polyketides / Coumarins and derivatives
7,8-Dimethoxycoumarin 142768 Click to see COC1=C(C2=C(C=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/0031-9422(71)85045-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
8-Hydroxy-7-methoxycoumarin 146487 Click to see COC1=C(C2=C(C=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0031-9422(71)85045-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown https://doi.org/10.1016/0031-9422(71)85045-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-8-methoxycoumarin 5316302 Click to see COC1=C(C=CC2=C1OC(=O)C=C2)O 192.17 unknown https://doi.org/10.1016/0031-9422(71)85045-8
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/0031-9422(71)85045-8

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