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Details Top

Internal ID UUID643fcb335e282475087975
Scientific name Blumea densiflora
Authority DC.
First published in Prodr. 5: 446 (1836)

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Synonyms Top

Scientific name Authority First published in
Placus grandis Baill. Hist. Pl. 8: 303 (1882)
Conyza amygdalina Spreng. ex DC. Prodr. 5: 446 (1836)
Blumea excisa DC. Prodr. 5: 446 (1836)
Blumea hookeri C.B.Clarke ex Hook.f. Fl. Brit. India 3(8): 269 (1881)
Blumea klossii S.Moore J. Nat. Hist. Soc. Siam 4: 145 (1921)
Blumea densiflora var. hookeri (C.B.Clarke ex Hook.f.) C.C.Chang & Y.Q.Tseng Fl. Reipubl. Popularis Sin. 75: 23 (1979)
Blumea densiflora var. excisa (DC.) C.B.Clarke 89 1876
Blumea dasycoma var. pinnatifida (Miq.) Boerl. 239 1891
Conyza excisa Wall. Numer. List : n.° 3011 (1831)
Conyza falcigera Wall. Numer. List : n.° 2048 (1829)
Conyza densiflora B.Heyne Numer. List [Wallich] n. 2997. 1831
Conyza densiflora Wall. 1831
Placus milnei Kuntze Revis. Gen. Pl. 1: 357 (1891)

Common names Top

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Language Common/alternative name
Chinese 密花艾纳香

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000044404
UNII VRG77CBE8P
Tropicos 50055277
INPN 671053
KEW urn:lsid:ipni.org:names:185543-1
The Plant List gcc-142951
Open Tree Of Life 628039
NCBI Taxonomy 441178
IPNI 185543-1
iNaturalist 1146384
GBIF 5395751
USDA GRIN 429482

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
Comparative Pollen Morphology of Selected Species of Blumea DC. and Cyathocline Cass. and Its Taxonomic Significance Peng Y, Pu X, Yu Q, Zhou H, Huang T, Xu B, Gao X Plants (Basel) 09-Aug-2023
PMCID:PMC10459363
doi:10.3390/plants12162909
PMID:37631121
Mosquitoes Larvicidal Activity of Ocimum kilimandscharicum Oil Formulation under Laboratory and Field-Simulated Conditions Ochola JB, Mutero CM, Marubu RM, Haller BF, Hassanali A, Lwande W Insects 16-Feb-2022
PMCID:PMC8877965
doi:10.3390/insects13020203
PMID:35206778
A Review of Resistance Mechanisms of Synthetic Insecticides and Botanicals, Phytochemicals, and Essential Oils as Alternative Larvicidal Agents Against Mosquitoes Senthil-Nathan S Front Physiol 25-Feb-2020
PMCID:PMC7052130
doi:10.3389/fphys.2019.01591
PMID:32158396
Phylogenetic Reconstruction and Divergence Time Estimation of Blumea DC. (Asteraceae: Inuleae) in China Based on nrDNA ITS and cpDNA trnL-F Sequences Zhang YB, Yuan Y, Pang YX, Yu FL, Yuan C, Wang D, Hu X Plants (Basel) 08-Jul-2019
PMCID:PMC6681236
doi:10.3390/plants8070210
PMID:31288447
Essential Oils as an Alternative to Pyrethroids’ Resistance against Anopheles Species Complex Giles (Diptera: Culicidae) Gnankiné O, Bassolé IH Molecules 22-Sep-2017
PMCID:PMC6151604
doi:10.3390/molecules22101321
PMID:28937642
Prioritizing fodder species based on traditional knowledge: a case study of mithun (Bos frontalis) in Dulongjiang area, Yunnan Province, Southwest China Geng Y, Hu G, Ranjitkar S, Wang Y, Bu D, Pei S, Ou X, Lu Y, Ma X, Xu J J Ethnobiol Ethnomed 04-May-2017
PMCID:PMC5418811
doi:10.1186/s13002-017-0153-z
PMID:28472968
Isoalantolactone derivatives and germacranolides from Blumea densiflora Umesh C. Pandey, Ram P. Sharma, Palaniappan Kulanthaivel, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81056-0

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 / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(6,8-Dihydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-7-yl) 3-methylbutanoate 162965984 Click to see CC(C)CC(=O)OC1C(C(=C)C2CC3C(CC2(C1O)C)OC(=O)C3=C)O 364.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
(8-Acetyloxy-5,8a-dimethyl-3-methylidene-2,7-dioxo-3a,4,4a,8,9,9a-hexahydrobenzo[f][1]benzofuran-6-yl) 3-methylbutanoate 162865674 Click to see CC1=C(C(=O)C(C2(C1CC3C(C2)OC(=O)C3=C)C)OC(=O)C)OC(=O)CC(C)C 404.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
(8-Acetyloxy-6-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-7-yl) 3-methylbutanoate 163023105 Click to see CC(C)CC(=O)OC1C(C(=C)C2CC3C(CC2(C1OC(=O)C)C)OC(=O)C3=C)O 406.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
(8-Acetyloxy-7-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl) 3-methylbutanoate 163015303 Click to see CC(C)CC(=O)OC1C(C(C2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)OC(=O)C)O 406.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
(8-Hydroxy-5,8a-dimethyl-3-methylidene-2,7-dioxo-3a,4,4a,8,9,9a-hexahydrobenzo[f][1]benzofuran-6-yl) 3-methylbutanoate 163014462 Click to see CC1=C(C(=O)C(C2(C1CC3C(C2)OC(=O)C3=C)C)O)OC(=O)CC(C)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
(8-Hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl) 2-methylpropanoate 76538164 Click to see CC(C)C(=O)OC1CC(C2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)O 334.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
(8-Hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl) 3-methylbutanoate 163039227 Click to see CC(C)CC(=O)OC1CC(C2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(3aR,4aR,6R,8S,8aR,9aR)-8-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl] 2-methylpropanoate 163051643 Click to see CC(C)C(=O)OC1CC(C2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)O 334.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(3aR,4aR,6R,8S,8aR,9aR)-8-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl] 3-methylbutanoate 163192976 Click to see CC(C)CC(=O)OC1CC(C2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(3aR,4aR,8R,8aR,9aR)-8-acetyloxy-5,8a-dimethyl-3-methylidene-2,7-dioxo-3a,4,4a,8,9,9a-hexahydrobenzo[f][1]benzofuran-6-yl] 3-methylbutanoate 162865675 Click to see CC1=C(C(=O)C(C2(C1CC3C(C2)OC(=O)C3=C)C)OC(=O)C)OC(=O)CC(C)C 404.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(3aR,4aR,8R,8aR,9aR)-8-hydroxy-5,8a-dimethyl-3-methylidene-2,7-dioxo-3a,4,4a,8,9,9a-hexahydrobenzo[f][1]benzofuran-6-yl] 3-methylbutanoate 163014463 Click to see CC1=C(C(=O)C(C2(C1CC3C(C2)OC(=O)C3=C)C)O)OC(=O)CC(C)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(3aR,4aS,6S,7S,8R,8aR,9aR)-6,8-dihydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-7-yl] 3-methylbutanoate 162965985 Click to see CC(C)CC(=O)OC1C(C(=C)C2CC3C(CC2(C1O)C)OC(=O)C3=C)O 364.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(3aR,4aS,6S,7S,8R,8aR,9aR)-8-acetyloxy-6-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-7-yl] 3-methylbutanoate 163023106 Click to see CC(C)CC(=O)OC1C(C(=C)C2CC3C(CC2(C1OC(=O)C)C)OC(=O)C3=C)O 406.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(3aR,4aS,6S,7S,8R,8aR,9aR)-8-acetyloxy-7-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl] 3-methylbutanoate 163015304 Click to see CC(C)CC(=O)OC1C(C(C2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)OC(=O)C)O 406.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1-Ethoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl) 2-methylpropanoate 74035546 Click to see CCOC12CCC(O1)(CC(C3C(CC2C)OC(=O)C3=C)OC(=O)C(C)C)C 380.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(1S,2S,4R,8S,9R,11R)-1-ethoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] 2-methylpropanoate 163011911 Click to see CCOC12CCC(O1)(CC(C3C(CC2C)OC(=O)C3=C)OC(=O)C(C)C)C 380.50 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(1S,2S,4R,8S,9R,11S,12S)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] 2-methylpropanoate 163007652 Click to see CC1CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 368.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
[(2S,4R,8S,9R,12R)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] 2-methylpropanoate 102004628 Click to see CC1CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 368.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0
CID 13855920 13855920 Click to see CC1CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 368.40 unknown https://doi.org/10.1016/S0031-9422(00)81056-0

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