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Baccharis salicifolia subsp. salicifolia

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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 UUID64406db840425277947092
Scientific name Baccharis salicifolia subsp. salicifolia

Description Top

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Common names Top

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Language Common/alternative name
English nominate mule fat

Varieties (abbr. var.) 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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000055436
Tropicos 50283808
KEW urn:lsid:ipni.org:names:77179887-1
iNaturalist 79641
GBIF 7338554
Calflora (Californian flora) 11371
USDA GRIN 461196

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)!
Title Authors Publication Released IDs
13- EPI-NEOCLERODANES FROM BACCHARIS MARGINALIS AURELIO SAN-MARTÍN, LUIS ASTUDILLO, MARGARITA GUTIÉRREZ, MARÍA CRISTINA CHAMY, SILVIA OREJARENA, PATRICIO RIVERA, KAREN VERGARA SciELO Agencia Nacional de Investigacion y Desarrollo (ANID) 03-May-2010
doi:10.4067/S0717-97072010000100028
Cyclohexanecarboxylic‐Acid Derivatives from <i>Psiadia trinervia</i> Ying Wang, Matthias Hamburger, Joseph Gueho, Kurt Hostettmann Wiley 28-Dec-2004
doi:10.1002/HLCA.19920750122
Neo-clerodane diterpenoids and other constituents from Baccharis species Francesca Faini, Patricio Rivera, Manuel Mahú, Mariano Castillo Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82487-5
Antimicrobial flavonoids from Psiadia trinervia and their methylated and acetylated derivatives Ying Wang, Matthias Hamburger, Joseph Gueho, Kurt Hostettmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97976-7

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
[[4-[(7-Methoxy-1,3-benzodioxol-5-yl)methyl]-2-oxooxolan-3-yl]-(3,4,5-trimethoxyphenyl)methyl] acetate 162876896 Click to see CC(=O)OC(C1C(COC1=O)CC2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC 488.50 unknown https://doi.org/10.4067/S0717-97072010000100028
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
3-methyl-5-(5,6,7-trihydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)pentanoic acid 13967135 Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)O)CC(C(C2(C)O)O)O)C 356.50 unknown https://doi.org/10.1016/S0031-9422(00)82487-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(6aR,7S,8R,10aS)-7,8-dimethyl-7-[2-(5-oxo-2H-furan-3-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 162943149 Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CCC4=CC(=O)OC4 330.40 unknown https://doi.org/10.4067/S0717-97072010000100028
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S)-3,4-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 129316855 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1002/HLCA.19920750122
3,4-Di-O-Caffeoylquinic acid 3802778 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1002/HLCA.19920750122
3,5-Dicaffeoyl-epi-quinic acid 60150332 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1002/HLCA.19920750122
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1002/HLCA.19920750122
Isochlorogenic acid A 6474310 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1002/HLCA.19920750122
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1002/HLCA.19920750122
> 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 https://doi.org/10.1002/HLCA.19920750122
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1002/HLCA.19920750122
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
https://doi.org/10.1002/HLCA.19920750122
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
https://doi.org/10.1002/HLCA.19920750122
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,7-Di-O-methylquercetin 5280417 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)82487-5
7-O-Methyleriodictyol 1268276 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(00)82487-5
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
Ayanin 5280682 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
Penduletin 5320462 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC 344.30 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)82487-5
Sternbin 4872981 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(00)82487-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
https://doi.org/10.1002/HLCA.19920750122
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)97976-7
Gossypetin 3,8,3',4'-tetramethyl ether 13872458 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)OC 374.30 unknown https://doi.org/10.1016/S0031-9422(00)97976-7

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