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Ageratina pichinchensis

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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 UUID643fd245cad56900205757
Scientific name Ageratina pichinchensis
Authority (Kunth) R.M.King & H.Rob.
First published in Phytologia 19: 215 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium pacificum B.L.Rob. 99 1931
Eupatorium huehuetecum Standl. & Steyerm. Publ. Field Mus. Nat. Hist., Bot. Ser. 22: 304. 1940
Eupatorium bustamenta DC. Prodr. 5: 168 (1836)
Eupatorium ciliatum Less. Linnaea 6: 404 (1831)
Eupatorium piurae B.L.Rob. Contr. Gray Herb. 77: 28 (1926)
Ageratina piurae (B.L.Rob.) R.M.King & H.Rob. Phytologia 19: 225 (1970)
Ageratina pacifica (B.L.Rob. ex I.M.Johnst.) R.M.King & H.Rob. Phytologia 19: 215 (1970)
Eupatorium ptaretepuiense V.M.Badillo Bol. Soc. Venez. Ci. Nat. 10: 291 (1946)
Kyrstenia ciliata Greene Leafl. Bot. Observ. Crit. 1: 9 (1903)
Eupatorium pacificum B.L.Rob. ex I.M.Johnst. Proc. Calif. Acad. Sci. , ser. 4, 20: 99 (1931)
Eupatorium tequendamense var. glanduloso-pubescens Hieron. Bot. Jahrb. Syst. 29(1): 6 (1900)
Ageratina articulata (Sch.Bip. ex Hieron.) R.M.King & H.Rob. Phytologia 19: 212 (1970)
Ageratina pichinchensis var. pichinchensis (Kunth) R.M.King & H.Rob. 1970
Eupatorium pichinchense Kunth Nov. Gen. Sp. 4(15): 95 (ed. fol.) (1818)
Bustamenta ovata Mairet ex DC. Prodr. 5: 168 (1836)
Eupatorium articulatum Sch.Bip. ex Hieron. Bot. Jahrb. Syst. 40(3): 385 (1908)
Ageratina ciliata (Less.) R.M.King & H.Rob. Phytologia 19: 213 (1970)
Eupatorium tequendamense var. glabrata Hieron. Bot. Jahrb. Syst. 29(1): 6 (1900)
Eupatorium bustamentum DC. Prodr. 5: 168 (1836)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Southeast
  • Southern America
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000122234
Tropicos 2712307
KEW urn:lsid:ipni.org:names:6988-2
The Plant List gcc-83411
Open Tree Of Life 5739731
NCBI Taxonomy 3015610
IPNI 6988-2
iNaturalist 273997
GBIF 5400249
EOL 5116600

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
Healing of diabetic foot ulcer with topical and oral administrations of herbal products: A systematic review and meta‐analysis of randomized controlled trials Zamanifard M, Nasiri M, Yarahmadi F, Zonoori S, Razani O, Salajegheh Z, Imanipour M, Mohammadi SM, Jomehzadeh N, Asadi M Int Wound J 14-Feb-2024
PMCID:PMC10867296
doi:10.1111/iwj.14760
PMID:38356150
Potential use of the Asteraceae family as a cure for diabetes: A review of ethnopharmacology to modern day drug and nutraceuticals developments Mohanta YK, Mishra AK, Nongbet A, Chakrabartty I, Mahanta S, Sarma B, Panda J, Panda SK Front Pharmacol 03-Aug-2023
PMCID:PMC10441548
doi:10.3389/fphar.2023.1153600
PMID:37608892
A Study of the Essential Oil Isolated from Ageratina dendroides (Spreng.) R.M. King & H. Rob.: Chemical Composition, Enantiomeric Distribution, and Antimicrobial, Antioxidant, and Anticholinesterase Activities Valarezo E, Jaramillo-Jaramillo E, Carrión-Campoverde A, Morocho V, Jaramillo-Fierro X, Cartuche L, Meneses MA Plants (Basel) 28-Jul-2023
PMCID:PMC10420678
doi:10.3390/plants12152796
PMID:37570950
Traditional complementary and alternative medicine (TCAM) for diabetic foot ulcer management: A systematic review Kumar S, Bharali A, Sarma H, Kushari S, Gam S, Hazarika I, Prasad SK, Laloo D J Ayurveda Integr Med 11-Jul-2023
PMCID:PMC10435959
doi:10.1016/j.jaim.2023.100745
PMID:37441954
Acknowledging the use of botanicals to treat diabetic foot ulcer during the 21st century: A systematic review Narzary I, Swarnakar A, Kalita M, Middha SK, Usha T, Babu D, Mochahary B, Brahma S, Basumatary J, Goyal AK World J Clin Cases 16-Jun-2023
PMCID:PMC10303622
doi:10.12998/wjcc.v11.i17.4035
PMID:37388781
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
Phenolic Compounds from Wild Plant and In Vitro Cultures of Ageratina pichichensis and Evaluation of Their Antioxidant Activity Motolinia-Alcántara EA, Franco-Vásquez AM, Nieto-Camacho A, Arreguín-Espinosa R, Rodríguez-Monroy M, Cruz-Sosa F, Román-Guerrero A Plants (Basel) 01-Mar-2023
PMCID:PMC10005229
doi:10.3390/plants12051107
PMID:36903964
Evidence for Natural Products as Alternative Wound-Healing Therapies Moses RL, Prescott TA, Mas-Claret E, Steadman R, Moseley R, Sloan AJ Biomolecules 27-Feb-2023
PMCID:PMC10046143
doi:10.3390/biom13030444
PMID:36979379
Current scenario of traditional medicines in management of diabetic foot ulcers: A review Rayate AS, Nagoba BS, Mumbre SS, Mavani HB, Gavkare AM, Deshpande AS World J Diabetes 15-Jan-2023
PMCID:PMC9850800
doi:10.4239/wjd.v14.i1.1
PMID:36684382
Obtaining 2,3-Dihydrobenzofuran and 3-Epilupeol from Ageratina pichinchensis (Kunth) R.King & Ho.Rob. Cell Cultures Grown in Shake Flasks under Photoperiod and Darkness, and Its Scale-Up to an Airlift Bioreactor for Enhanced Production Sánchez-Ramos M, Marquina-Bahena S, Alvarez L, Bernabé-Antonio A, Cabañas-García E, Román-Guerrero A, Cruz-Sosa F Molecules 06-Jan-2023
PMCID:PMC9865622
doi:10.3390/molecules28020578
PMID:36677637
Guiding stem cells for cutaneous repair Desai S, Jagtap J, Sainani S, Bhonde R Curr Res Pharmacol Drug Discov 06-Dec-2022
PMCID:PMC9761596
doi:10.1016/j.crphar.2022.100145
PMID:36544814
Ethnobotanical study of endemic and non-endemic medicinal plants used by indigenous people in environs of Gullele botanical garden Addis Ababa, central Ethiopia: A major focus on Asteraceae family Woldeamanuel MM, Geda MK, Mohapatra S, Bastia TK, Rath P, Panda AK Front Pharmacol 23-Nov-2022
PMCID:PMC9727095
doi:10.3389/fphar.2022.1020097
PMID:36506590
Updated Perspectives on the Diagnosis and Management of Onychomycosis Falotico JM, Lipner SR Clin Cosmet Investig Dermatol 15-Sep-2022
PMCID:PMC9484770
doi:10.2147/CCID.S362635
PMID:36133401
Complementary and Alternative Therapies for Onychomycosis: A Systematic Review of the Clinical Evidence Nickles MA, Lio PA, Mervak JE Skin Appendage Disord 09-Feb-2022
PMCID:PMC9274952
doi:10.1159/000521703
PMID:35983465
Plant-Derived Natural Antioxidants in Meat and Meat Products Manessis G, Kalogianni AI, Lazou T, Moschovas M, Bossis I, Gelasakis AI Antioxidants (Basel) 02-Dec-2020
PMCID:PMC7761563
doi:10.3390/antiox9121215
PMID:33276503

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 / Benzene and substituted derivatives / Acetophenones
[(2S,3R)-5-acetyl-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-3-yl] (E)-2-methylbut-2-enoate 163187938 Click to see CC=C(C)C(=O)OC1C(OC2=C1C=C(C=C2)C(=O)C)C(C)(C)O 318.40 unknown https://doi.org/10.1080/14786410902843301
[(2S,3R)-5-acetyl-2-(2-hydroxypropan-2-yl)-6-methoxy-2,3-dihydro-1-benzofuran-3-yl] (E)-2-methylbut-2-enoate 163190534 Click to see CC=C(C)C(=O)OC1C(OC2=CC(=C(C=C12)C(=O)C)OC)C(C)(C)O 348.40 unknown https://doi.org/10.1080/14786410902843301
[5-Acetyl-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-3-yl] 2-methylbut-2-enoate 78412635 Click to see CC=C(C)C(=O)OC1C(OC2=C1C=C(C=C2)C(=O)C)C(C)(C)O 318.40 unknown https://doi.org/10.1080/14786410902843301
[5-Acetyl-2-(2-hydroxypropan-2-yl)-6-methoxy-2,3-dihydro-1-benzofuran-3-yl] 2-methylbut-2-enoate 78412636 Click to see CC=C(C)C(=O)OC1C(OC2=CC(=C(C=C12)C(=O)C)OC)C(C)(C)O 348.40 unknown https://doi.org/10.1080/14786410902843301
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 521215 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1080/14786410902843301
beta-Eudesmol cis epimer 12309818 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1080/14786410902843301
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1080/14786410902843301
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1080/14786410902843301
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(5-Acetyl-2-methoxy-phenyl)-3-methyl-butan-1-one 3009228 Click to see CC(C)CC(=O)C1=C(C=CC(=C1)C(=O)C)OC 234.29 unknown https://doi.org/10.1080/14786410902843301
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2H-1-Benzopyran-6-methanol, 7-methoxy-alpha,2,2-trimethyl-, (alphaR)- 3009229 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC)O 234.29 unknown https://doi.org/10.1080/14786410902843301
6-(1-Methoxyethyl)-2,2-dimethylchromen-7-ol 188665 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)O)OC 234.29 unknown https://doi.org/10.1080/14786410902843301
6-[(1R)-1-methoxyethyl]-2,2-dimethylchromen-7-ol 162913404 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)O)OC 234.29 unknown https://doi.org/10.1080/14786410902843301
7-Methoxy-6-(1-methoxyethyl)-2,2-dimethyl-2H-1-benzopyran 14427467 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC)OC 248.32 unknown https://doi.org/10.1080/14786410902843301
7-methoxy-6-[(1R)-1-methoxyethyl]-2,2-dimethylchromene 162953649 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC)OC 248.32 unknown https://doi.org/10.1080/14786410902843301
Encecalin 114703 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 232.27 unknown https://doi.org/10.1080/14786410902843301
Encecalol 184893 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC)O 234.29 unknown https://doi.org/10.1055/S-2003-45113
https://doi.org/10.1080/14786410902843301

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