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Hololepis pedunculata

Hololepis pedunculata - Unknown
Part: Unknown
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 UUID643fc87662c66159988139
Scientific name Hololepis pedunculata
Authority DC.
First published in Ann. Mus. Natl. Hist. Nat. xvi. 190 (1810)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vernonia involucrata Less. Linnaea 4: 246 (1829)
Serratula pedunculata Pers. Syn. Pl. 2(2): 391 (1807)
Hololepis involucrata Sch.Bip. Jahresber. Pollichia 20-21: 380 (1863)
Vernonia pedunculata DC. Prodr. 5: 16 (1836)
Haynea pedunculata Spreng. Syst. Veg. 3: 391 (1826)
Proteopsis glauca Mart. ex Baker Fl. Bras. 6(2): 20 (1873)
Heterocoma pedunculata Steud. Nomencl. Bot. : 403 (1821)
Cacalia pedunculata (DC. ex Pers.) Kuntze Revis. Gen. Pl. 2: 970 (1891)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000022678
Tropicos 50158024
KEW urn:lsid:ipni.org:names:224991-1
The Plant List gcc-121917
Open Tree Of Life 5784899
NCBI Taxonomy 1548383
IPNI 224991-1
GBIF 5399485

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
Anti-Leishmania compounds can be screened using Leishmania spp. expressing red fluorescence (tdTomato) Cruz MG, Santi AM, de Morais-Teixeira E, Caldeira AS, de Siqueira EP, Oliveira E, Alves TM, Murta SM Antimicrob Agents Chemother 08-Dec-2023
PMCID:PMC10777850
doi:10.1128/aac.00509-23
PMID:38063403
An empirical assessment of a single family‐wide hybrid capture locus set at multiple evolutionary timescales in Asteraceae Jones KE, Fér T, Schmickl RE, Dikow RB, Funk VA, Herrando‐Moraira S, Johnston PR, Kilian N, Siniscalchi CM, Susanna A, Slovák M, Thapa R, Watson LE, Mandel JR Appl Plant Sci 25-Oct-2019
PMCID:PMC6814182
doi:10.1002/aps3.11295
PMID:31667023
Phylogenomics Yields New Insight Into Relationships Within Vernonieae (Asteraceae) Siniscalchi CM, Loeuille B, Funk VA, Mandel JR, Pirani JR Front Plant Sci 17-Oct-2019
PMCID:PMC6843069
doi:10.3389/fpls.2019.01224
PMID:31749813
Comprehensive untargeted metabolomics of Lychnnophorinae subtribe (Asteraceae: Vernonieae) in a phylogenetic context Martucci ME, Loeuille B, Pirani JR, Gobbo-Neto L PLoS One 11-Jan-2018
PMCID:PMC5764248
doi:10.1371/journal.pone.0190104
PMID:29324799
Constituents of Hololepis pedunculata leaves and their trypanocidal activity V. L. Almeida, A. B. Oliveira, E. Chiari, M. A. D. Boaventura Springer Science and Business Media LLC 21-Feb-2007
doi:10.1007/S10600-006-0266-4

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 / Fatty Acyls / Fatty acid esters
(3-Hydroxy-11-methyl-2,7-dimethylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-1(13)-en-9-yl) 2-methylbut-2-enoate 73312947 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=C)C(C3C1C(=C)C(=O)O3)O)C 374.40 unknown https://doi.org/10.1007/S10600-006-0266-4
Isocentratherin 21634989 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=C)C(C3C1C(=C)C(=O)O3)O)C 374.40 unknown https://doi.org/10.1007/S10600-006-0266-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[2-(Hydroxymethyl)-11-methyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] 2-methylbut-2-enoate 4258953 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 374.40 unknown https://doi.org/10.1007/S10600-006-0266-4
Centratherin 44409502 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 374.40 unknown https://doi.org/10.1007/S10600-006-0266-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1007/S10600-006-0266-4
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1007/S10600-006-0266-4
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1007/S10600-006-0266-4
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1007/S10600-006-0266-4
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/S10600-006-0266-4
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/S10600-006-0266-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12315422 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/S10600-006-0266-4
Luteolin 7-o-rutinoside 10461109 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/S10600-006-0266-4

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