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Lychnophora pinaster

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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 UUID643fc808f11b4972942142
Scientific name Lychnophora pinaster
Authority Mart.
First published in Denkschr. Königl.-Baier. Bot. Ges. Regensburg 2: 152 (1822)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vernonia pinaster Less. Linnaea 4: 249 (1829)
Lychnophora affinis Gardner London J. Bot. 5: 233 (1846)
Lychnophora rosmarinus Pohl ex Sch.Bip. Jahresber. Pollichia 20-21: 361 (1863)
Lychnophora piptocoma Sch.Bip. ex Baker Fl. Bras. 6(2): 155 (1873)
Piptocoma lychnophorioides Less. Linnaea 4: 315 (1829)
Lychnophora trichocarpha (Spreng.) Spreng. ex Sch.Bip. Jahresber. Pollichia 20/21: 363. 1863
Lychnophora brunioides var. pinifolia Mart. Fl. Bras. 6(2): 155 (1873)
Vernonia trichocarpha Spreng. Syst. Veg. 3: 437 (1826)
Lychnophora brunioides var. affinis (Gardner) Baker Fl. Bras. 6(2): 155 (1873)
Lychnophora rosmarinus var. normalis Sch.Bip. Jahresber. Pollichia 20-21: 362 (1863)
Lychnophora trichocarpha (Spreng.) Spreng. Syst. Veg. (ed. 16) [Sprengel] 4(2, Cur. Post.): 298 1827
Lychnophora rosmarinus var. affinis Sch.Bip. Jahresber. Pollichia 20-21: 363 (1863)

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-0000019293
Tropicos 2738593
KEW urn:lsid:ipni.org:names:146424-2
Open Tree Of Life 980366
Observations.org 304097
NCBI Taxonomy 437899
IPNI 146424-2
iNaturalist 939742
GBIF 5399362
CMAUP NPO12064

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
Ethanolic Extract from Limonia acidissima L. Fruit Attenuates Serum Uric Acid Level via URAT1 in Potassium Oxonate-Induced Hyperuricemic Rats Yusnaini R, Nasution R, Saidi N, Arabia T, Idroes R, Ikhsan I, Bahtiar R, Iqhrammullah M Pharmaceuticals (Basel) 09-Mar-2023
PMCID:PMC10054421
doi:10.3390/ph16030419
PMID:36986518
Assessing the Biocontrol Potential of Clonostachys Species Isolated as Endophytes from Coffea Species and as Mycoparasites of Hemileia Rusts of Coffee in Africa Kapeua-Ndacnou M, de Abreu LM, de Macedo DM, da Nóbrega TF, Pereira CM, Evans HC, Barreto RW J Fungi (Basel) 13-Feb-2023
PMCID:PMC9962503
doi:10.3390/jof9020248
PMID:36836362
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Indirect in vitro Regeneration of the Medicinal Plant, Aspilia africana, and Histological Assessment at Different Developmental Stages Okello D, Yang S, Komakech R, Chung Y, Rahmat E, Gang R, Omujal F, Lamwaka AV, Kang Y Front Plant Sci 17-Dec-2021
PMCID:PMC8719492
doi:10.3389/fpls.2021.797721
PMID:34975987
Toxicological Profile of the Aqueous Extract of Tectona grandis L.F. (Verbenaceae) Leaves: A Medicinal Plant Used in the Treatment of Typhoid Fever in Traditional Cameroonian Medicine Kamsu GT, Djamen Chuisseu DP, Fodouop Chegaing SP, Laure Feudjio HB, Ndel Famen LC, Kodjio N, Sokoudjou JB, Gatsing D J Toxicol 05-Apr-2021
PMCID:PMC8046569
doi:10.1155/2021/6646771
PMID:33880119
Brazilian Ironstone Plant Communities as Reservoirs of Culturable Bacteria With Diverse Biotechnological Potential Caneschi WL, Felestrino ÉB, Fonseca NP, Villa MM, Lemes CG, Cordeiro IF, Assis RD, Sanchez AB, Vieira IT, Kamino LH, do Carmo FF, Garcia CC, Moreira LM Front Microbiol 23-Jul-2018
PMCID:PMC6064971
doi:10.3389/fmicb.2018.01638
PMID:30083146
Phylogeny strongly drives seed dormancy and quality in a climatically buffered hotspot for plant endemism Dayrell RL, Garcia QS, Negreiros D, Baskin CC, Baskin JM, Silveira FA Ann Bot 27-Aug-2016
PMCID:PMC5321058
doi:10.1093/aob/mcw163
PMID:27568299
Canga biodiversity, a matter of mining Skirycz A, Castilho A, Chaparro C, Carvalho N, Tzotzos G, Siqueira JO Front Plant Sci 24-Nov-2014
PMCID:PMC4241825
doi:10.3389/fpls.2014.00653
PMID:25505476
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
Anti-inflammatory effects in muscle injury by transdermal application of gel with Lychnophora pinaster aerial parts using phonophoresis in rats Abreu VG, Correa GM, Silva TM, Fontoura HS, Cara DC, Piló-Veloso D, Alcântara AF BMC Complement Altern Med 20-Oct-2013
PMCID:PMC3874755
doi:10.1186/1472-6882-13-270
PMID:24138803
Constituents of Lychnophora pinaster Hydroalcoholic Extract A. A. Ferreira, A. O. Azevedo, D. Silveira, P. M. Oliveira, M. S. A. Castro, D. S. Raslan Springer Science and Business Media LLC 08-Nov-2005
doi:10.1007/S10600-005-0179-7
Seed germination, phenology, and antiedematogenic activity of Peperomia pellucida (L.) H. B. K. Arrigoni-Blank MD, Oliveira RL, Mendes SS, Silva PD, Antoniolli ÂR, Vilar JC, Cavalcanti SC, Blank AF BMC Pharmacol 09-May-2002
PMCID:PMC113267
doi:10.1186/1471-2210-2-12
PMID:12019026

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
> Alkaloids and derivatives / Aporphines
(-)-Isoboldine 6971182 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine 442168 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC 355.40 unknown via CMAUP database
(+)-Caryachine 12305286 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 3082467 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol 10948236 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC(=C(C=C25)OC)OC)O)OCO4 355.40 unknown via CMAUP database
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol 11110561 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4 339.30 unknown via CMAUP database
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 11869664 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 102304441 Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-] 341.40 unknown via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 102304443 Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4)[O-] 341.40 unknown via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 11823545 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene 11012304 Click to see C1C2C3=CC4=C(C=C3CC(N2)C5=CC6=C(C=C51)OCO6)OCO4 309.30 unknown via CMAUP database
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol 92856799 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O 327.40 unknown via CMAUP database
(1S,9S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 12300156 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
Caryachine 44575219 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
Crychine 193382 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
Escholtzine 12304178 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-8,9-Dihydrostepharine 13819281 Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC 299.40 unknown via CMAUP database
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol 10870351 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC 301.40 unknown via CMAUP database
Isoamuronine 12306127 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)OC)OC 313.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cryptocaryone 10379026 Click to see C1C2C(C=CC(=O)C2=C(C=CC3=CC=CC=C3)O)OC1=O 282.29 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium 2753983 Click to see C[N+]1=CC2=CC3=C(C=C2C=C1)OCO3 188.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-(6,7-Dimethoxyisoquinoline-1-ylmethyl)phenol 21814573 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC=C(C=C3)O)OC 295.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin 12998814 Click to see CN1C=CC2=CC3=C(C=C2C1=O)OCO3 203.19 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
7-O-Methylcryptochinone A 46939685 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
Cryptocaryanone A 10356404 Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O 282.29 unknown via CMAUP database
Cryptochinone A 46939683 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone B 46939684 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone D 46939686 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol 10914050 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC 315.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
3,5,7-Trihydroxyflavanone; Dihydrogalangin 3519897 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown https://doi.org/10.1007/S10600-005-0179-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone 21632881 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Larrein 9993268 Click to see COC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O 270.28 unknown via CMAUP database

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