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Lychnophora salicifolia

Lychnophora salicifolia - Unknown
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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 UUID643fd01f85263751574488
Scientific name Lychnophora salicifolia
Authority Mart.
First published in Denkschr. Königl. Bot. Ges. Regensburg ii. 157 (1822)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vernonia salicifolia Less. Linnaea 4: 249 (1829)
Cacalia salicifolia (Mart.) Kuntze Revis. Gen. Pl. 2: 971 (1891)
Lychnophora columnaris Mattf. Notizbl. Bot. Gart. Berlin-Dahlem 8: 433 (1923)
Lychnophora hakeaefolia Spreng. 1827
Lychnophora arrojadoana Mattf. Notizbl. Bot. Gart. Berlin-Dahlem 8: 432 (1923)
Lychnophora hakeifolia Mart. Denkschr. Bot. Ges. Regensb. ii. 156. 1822
Lychnophora urbaniana Glaz. Bull. Soc. Bot. France 56(Mém. 3d): 378 (1909)
Lychnophora luetzelburgii Mattf. Notizbl. Bot. Gart. Berlin-Dahlem 8: 431 (1923)
Vernonia hakeaefolia (Mart.) Less. Linnaea 4: 249 (1829)
Vernonia hakeifolia Less. Linnaea 4: 249 (1829)

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000096396
Tropicos 2706826
KEW urn:lsid:ipni.org:names:231315-1
The Plant List gcc-52540
Open Tree Of Life 1013816
NCBI Taxonomy 375932
IUCN Red List 149210645
IPNI 231315-1
iNaturalist 939734
GBIF 5399368
CMAUP NPO8020

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
Machine-Learning- and Structure-Based Virtual Screening for Selecting Cinnamic Acid Derivatives as Leishmania major DHFR-TS Inhibitors Muñoz-Vega MC, López-Hernández S, Sierra-Chavarro A, Scotti MT, Scotti L, Coy-Barrera E, Herrera-Acevedo C Molecules 28-Dec-2023
PMCID:PMC10779987
doi:10.3390/molecules29010179
PMID:38202763
Metabolomics-Guided Elucidation of Plant Abiotic Stress Responses in the 4IR Era: An Overview Tinte MM, Chele KH, van der Hooft JJ, Tugizimana F Metabolites 08-Jul-2021
PMCID:PMC8305945
doi:10.3390/metabo11070445
PMID:34357339
ChemInform Abstract: A NEW TYPE OF SESQUITERPENE LACTONES FROM LYCHNOPHORA SALICIFOLIA F. BOHLMANN, C. ZDERO, R. M. KING, H. ROBINSON Wiley 05-May-2016
doi:10.1002/CHIN.198349348
Mass spectrometry imaging for plant biology: a review Boughton BA, Thinagaran D, Sarabia D, Bacic A, Roessner U Phytochem Rev 13-Oct-2015
PMCID:PMC4870303
doi:10.1007/s11101-015-9440-2
PMID:27340381
Mass Spectrometry of Flavonoid Vicenin-2, Based Sunlight Barriers in Lychnophora species Silva DB, Turatti IC, Gouveia DR, Ernst M, Teixeira SP, Lopes NP Sci Rep 07-Mar-2014
PMCID:PMC3945490
doi:10.1038/srep04309
PMID:24603617
Biogenic trypanocidal sesquiterpenes: lead compounds to design future trypanocidal drugs - a mini review Saeidnia S, Gohari AR, Haddadi A Daru 15-May-2013
PMCID:PMC3663703
doi:10.1186/2008-2231-21-35
PMID:23676125
Ein neuer Typ von Sesquiterpenlactonen aus <i>Lychnophora salicifolia</i> Ferdinand Bohlmann, Christa Zdero, Robert M. King, Harold Robinson Wiley 19-Jul-2007
doi:10.1002/JLAC.198319830820
Antimicrobial Activity of Constituents Isolated fromLychnophora salicifolia (Asteraceae) Obdulio G. Miguel, Edeltrudes O. Lima, Verônica M. F. Morais, Sosigenas T. A. Gomes, Franco Delle Monache, Alexandre Bella Cruz, Rosana C. Bella Cruz, Valdir Cechinel Filho Wiley 10-Sep-2002
doi:10.1002/(SICI)1099-1573(199612)10:8<694::AID-PTR923>3.0.CO;2-X
Caryophyllene derivatives and a heliangolide from Lychnophora species Ferdinand Bohlmann, Christa Zdero, Harold Robinson, Robert M. King Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)91032-X

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
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methoxyanthraquinone 80103 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
1-Methoxy-2-methyl-anthraquinone 3534338 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)OC 252.26 unknown via CMAUP database
1,3-Dimethoxyanthraquinone 361511 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=CC=CC=C3C2=O 268.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxyanthraquinone 196978 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)O)O 240.21 unknown via CMAUP database
2-Hydroxyanthraquinone 11796 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)O 224.21 unknown via CMAUP database
Alizarin 6293 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)O)O 240.21 unknown via CMAUP database
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Lucidin 10163 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)CO)O 270.24 unknown via CMAUP database
Purpurin 6683 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O 256.21 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
4-Methoxy-1-naphthol 66542 Click to see COC1=CC=C(C2=CC=CC=C21)O 174.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see CC#CC#CC#CC#CC#CC=C 162.19 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
1,11-Tridecadien-3,5,7,9-tetrayne 528754 Click to see CC=CC#CC#CC#CC#CC=C 164.20 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
1,11-Tridecadiene-3,5,7,9-tetrayne 5322026 Click to see CC=CC#CC#CC#CC#CC=C 164.20 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(1,10-Dimethyl-5-methylidene-4,13-dioxo-3,14-dioxatricyclo[9.2.1.02,6]tetradeca-9,11-dien-8-yl) 2-methylbut-2-enoate 163059184 Click to see CC=C(C)C(=O)OC1CC2C(C3(C(=O)C=C(O3)C(=C1)C)C)OC(=O)C2=C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
[(1S,2R,6R,8R,9Z)-1,10-dimethyl-5-methylidene-4,13-dioxo-3,14-dioxatricyclo[9.2.1.02,6]tetradeca-9,11-dien-8-yl] (Z)-2-methylbut-2-enoate 163059185 Click to see CC=C(C)C(=O)OC1CC2C(C3(C(=O)C=C(O3)C(=C1)C)C)OC(=O)C2=C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-beta-Caryophyllene 20831623 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
(1R,4R,9R)-11,11-dimethyl-8-methylidenebicyclo[7.2.0]undecane-4-carboxylic acid 162848991 Click to see CC1(CC2C1CCC(CCCC2=C)C(=O)O)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
(1S,2S,4Z,9R)-2-acetyloxy-11,11-dimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene-4-carboxylic acid 163018102 Click to see CC(=O)OC1CC(=CCCC(=C)C2C1C(C2)(C)C)C(=O)O 292.40 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
(1S,2S,4Z,9R)-2-hydroxy-11,11-dimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene-4-carboxylic acid 38359278 Click to see CC1(CC2C1C(CC(=CCCC2=C)C(=O)O)O)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
(1S,4Z,9R)-11,11-dimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene-4-carboxylic acid 162843443 Click to see CC1(CC2C1CCC(=CCCC2=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
11,11-Dimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene-4-carboxylic acid 496471 Click to see CC1(CC2C1CCC(=CCCC2=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
11,11-Dimethyl-8-methylidenebicyclo[7.2.0]undecane-4-carboxylic acid 162848990 Click to see CC1(CC2C1CCC(CCCC2=C)C(=O)O)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
2-Acetyloxy-11,11-dimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene-4-carboxylic acid 163018101 Click to see CC(=O)OC1CC(=CCCC(=C)C2C1C(C2)(C)C)C(=O)O 292.40 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
2-Hydroxy-11,11-dimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene-4-carboxylic acid 74208368 Click to see CC1(CC2C1C(CC(=CCCC2=C)C(=O)O)O)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)- 26318 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
Lychnopholic acid 134747151 Click to see CC1(CC2C1C(CC(=CCCC2=C)C(=O)O)O)C 250.33 unknown https://doi.org/10.1002/(SICI)1099-1573(199612)10:8<694::AID-PTR923>3.0.CO;2-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,6aR,9aR,9bS)-6-methyl-3,9-dimethylidene-4,6a,7,8,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2-one 98659233 Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
Vanillosmin 591383 Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11876093 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/10.1016/S0031-9422(00)91032-X
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 162942499 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
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/10.1016/S0031-9422(00)91032-X
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)91032-X
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/10.1002/(SICI)1099-1573(199612)10:8<694::AID-PTR923>3.0.CO;2-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Alpha,beta-unsaturated carboxylic esters / Enoate esters
(1R,2R,5S)-1-(hydroxymethyl)-4,4-dimethyl-12-oxatricyclo[6.3.2.02,5]tridec-8-en-13-one 162929851 Click to see CC1(CC2C1CCC3=CCCC2(OC3=O)CO)C 250.33 unknown https://doi.org/10.1002/JLAC.198319830820
(1S,2R,5S)-1-(hydroxymethyl)-4,4-dimethyl-12-oxatricyclo[6.3.2.02,5]tridec-8-en-13-one 162929852 Click to see CC1(CC2C1CCC3=CCCC2(OC3=O)CO)C 250.33 unknown https://doi.org/10.1002/JLAC.198319830820
1-(Hydroxymethyl)-4,4-dimethyl-12-oxatricyclo[6.3.2.02,5]tridec-8-en-13-one 162929849 Click to see CC1(CC2C1CCC3=CCCC2(OC3=O)CO)C 250.33 unknown https://doi.org/10.1002/JLAC.198319830820
https://doi.org/10.1002/CHIN.198349348
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(4,4-Dimethyl-13-oxo-12-oxatricyclo[6.3.2.02,5]tridec-8-en-1-yl)methyl acetate 162884571 Click to see CC(=O)OCC12CCC=C(CCC3C1CC3(C)C)C(=O)O2 292.40 unknown https://doi.org/10.1002/JLAC.198319830820
[(1S,2R,5S)-4,4-dimethyl-13-oxo-12-oxatricyclo[6.3.2.02,5]tridec-8-en-1-yl]methyl acetate 162884572 Click to see CC(=O)OCC12CCC=C(CCC3C1CC3(C)C)C(=O)O2 292.40 unknown https://doi.org/10.1002/JLAC.198319830820
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Asperuloside 84298 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3,4-Dihydroxy cinnamic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database

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