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Pluchea lanceolata

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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 UUID643fce1ba17f3668500452
Scientific name Pluchea lanceolata
Authority (DC.) C.B.Clarke
First published in Compos. Ind. : 94 (1876)

Description Top

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Synonyms Top

Scientific name Authority First published in
Conyza proteiformis Perr. ex DC. Prodr. 5: 376 (1836)
Conyza rubra Buch.-Ham. ex DC. Prodr. 5: 376 (1836)
Saussurea mucronata Spreng. ex DC. Prodr. 5: 376 (1836)
Berthelotia lanceolata DC. Prodr. 5: 376 (1836)
Pluchea lanceolata (DC.) Oliv. & Hiern Fl. Trop. Afr. 3: 329 (1877)

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
  • Africa
    • East Tropical Africa
      • Tanzania
    • Northeast Tropical Africa
      • Chad
    • West Tropical Africa
      • Senegal
    • Western Indian Ocean
      • Comoros
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000078455
UNII 379LVI0J88
Tropicos 2736151
KEW urn:lsid:ipni.org:names:77124381-1
The Plant List gcc-35054
Open Tree Of Life 7051748
NCBI Taxonomy 1950228
IPNI 77124381-1
iNaturalist 961566
GBIF 3132718
EPPO PLULA
USDA GRIN 401818
Wikipedia Pluchea_lanceolata
CMAUP NPO19742

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
Phytocompounds and Regulation of Flavonoids in In Vitro-Grown Safflower Plant Tissue by Abiotic Elicitor CdCl2 Ejaz B, Mujib A, Syeed R, Mamgain J, Malik MQ, Birat K, Dewir YH, Magyar-Tábori K Metabolites 16-Feb-2024
PMCID:PMC10891796
doi:10.3390/metabo14020127
PMID:38393019
Screening herbal extracts as biostimulant to increase germination, plant growth and secondary metabolite production in wheatgrass Yadav A, Singh S, Yadav V Sci Rep 05-Jan-2024
PMCID:PMC10770375
doi:10.1038/s41598-023-50513-6
PMID:38182633
Enhanced wedelolactone content in in vitro-raised genetically uniform Wedelia chinensis under the influence of CuSO4 Swami RK, Nimker S, Narula A, Farooqi H Front Plant Sci 19-Dec-2023
PMCID:PMC10758438
doi:10.3389/fpls.2023.1281445
PMID:38169740
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
Uttarabasti in bladder neck contracture following transurethral resection of prostate: A case report Pokhrel SM, Sharma A, Singh M J Ayurveda Integr Med 25-Jul-2023
PMCID:PMC10388190
doi:10.1016/j.jaim.2023.100772
PMID:37499589
Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives Dubey S, Dixit AK J Ayurveda Integr Med 24-Feb-2023
PMCID:PMC9988554
doi:10.1016/j.jaim.2023.100688
PMID:36841194
Pharmacodynamic appraisal of wound-healing herbs of Sushruta Samhita Kumar V, Nesari TM, Ghildiyal S, Sherkhane R Ayu 07-Dec-2022
PMCID:PMC9893898
doi:10.4103/ayu.AYU_34_20
PMID:36743272
Hyperhydricity in Plant Tissue Culture Polivanova OB, Bedarev VA Plants (Basel) 30-Nov-2022
PMCID:PMC9738826
doi:10.3390/plants11233313
PMID:36501352
Genome size and gas chromatography-mass spectrometry (GC–MS) analysis of field-grown and in vitro regenerated Pluchea lanceolata plants Mamgain J, Mujib A, Syeed R, Ejaz B, Malik MQ, Bansal Y J Appl Genet 30-Sep-2022
PMCID:PMC9522435
doi:10.1007/s13353-022-00727-7
PMID:36175751
Effect of heavy metals on in vitro growth and development of the Momordica cymbalaria Fenzl Chaitanya G, Pavani C, Shasthree T Int J Environ Sci Technol (Tehran) 27-Jul-2022
PMCID:PMC9326134
doi:10.1007/s13762-022-04437-9
PMID:35909798
“An integrative approach with Ayurveda and Traditional Chinese Acupuncture in post covid parosmia – A case study” Bhat AK, Krishna Kumar V, Johnson JD J Ayurveda Integr Med 16-Jul-2022
PMCID:PMC9287594
doi:10.1016/j.jaim.2022.100560
PMID:35851219
Phytochemicals for the Prevention and Treatment of Renal Cell Carcinoma: Preclinical and Clinical Evidence and Molecular Mechanisms Bajalia EM, Azzouz FB, Chism DA, Giansiracusa DM, Wong CG, Plaskett KN, Bishayee A Cancers (Basel) 04-Jul-2022
PMCID:PMC9265746
doi:10.3390/cancers14133278
PMID:35805049
An In-vitro evaluation of a polyherbal formulation, against SARS-Cov-2 Kanchibhotla D, Subramanian S, Ravi Kumar RM, Venkatesh Hari KR, Pathania M J Ayurveda Integr Med 23-Jun-2022
PMCID:PMC9222090
doi:10.1016/j.jaim.2022.100581
PMID:35753154
Ayurvedic formulations: Potential COVID-19 therapeutics? Mahaboob Ali AA, Bugarcic A, Naumovski N, Ghildyal R Phytomed Plus 20-Apr-2022
PMCID:PMC9020642
doi:10.1016/j.phyplu.2022.100286
PMID:35474908
Traditional Knowledge to Contemporary Medication in the Treatment of Infectious Disease Dengue: A Review Dhiman M, Sharma L, Dadhich A, Dhawan P, Sharma MM Front Pharmacol 14-Mar-2022
PMCID:PMC8963989
doi:10.3389/fphar.2022.750494
PMID:35359838

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Phloroglucinols and derivatives
Phloroglucinol 359 Click to see C1=C(C=C(C=C1O)O)O 126.11 unknown https://doi.org/10.1111/J.1399-3054.1994.TB03025.X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3beta-Acetoxytaraxasterane-20-ene-22-one 100936445 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C=C1C)C)C)C)(C)C)OC(=O)C)C 482.70 unknown via CMAUP database
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown via CMAUP database
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.3109/13880209009082796
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Lup-12-en-3-ol, (3beta,18beta,19beta)- 156497 Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1076/PHBI.34.1.73.13183
methyl (1R,3aS,5aR,5bR,7aR,9S,10R,11aR,11bR,13aR,13bR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 21672694 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)OC 486.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / C24-propyl sterols and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 90694767 Click to see CCC(CCC(C)C1CCC2C1(C=CC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(94)85091-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3109/13880209009082796
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3109/13880209009082796
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.3109/13880209009082796
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.3109/13880209009082796
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1111/J.1399-3054.1994.TB03025.X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44257215 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1007/BF00994609
https://doi.org/10.1111/J.1399-3054.1994.TB03025.X
Ononin 442813 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1007/BF00994609
https://doi.org/10.1111/J.1399-3054.1994.TB03025.X

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