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Baccharis ochracea

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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 UUID643fcf25a9989684834784
Scientific name Baccharis ochracea
Authority Spreng.
First published in Syst. Veg. 3: 460 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis velutina DC. Prodr. 5: 415 (1836)
Lanugothamnus ochraceus (Spreng.) Deble Balduinia 37: 15 (2012)

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 South
    • Southern South America
      • Argentina Northeast
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000087775
Tropicos 2741680
KEW urn:lsid:ipni.org:names:183525-1
The Plant List gcc-4412
Open Tree Of Life 7600063
NCBI Taxonomy 2707479
IPNI 183525-1
iNaturalist 1017885
GBIF 3129610

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
Bio-Guided Isolation of New Compounds from Baccharis spp. as Antifungal against Botrytis cinerea Pinto AA, Ruano-González A, Ezzanad A, Pinedo-Rivilla C, Sánchez-Maestre R, Amaro-Luis JM Metabolites 19-Dec-2022
PMCID:PMC9781812
doi:10.3390/metabo12121292
PMID:36557330
An unusual diterpene and other constituents from Baccharis ochracea Eloir P. Schenkel, AndreáM. Sobottka, Peter P. Lankhorst, Jan Schripsema Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(96)00565-1

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
(E,2R)-6-methyl-2-(4-methylpent-3-enyl)-9-(5-oxo-2H-furan-3-yl)non-6-enoic acid 162894903 Click to see CC(=CCCC(CCCC(=CCCC1=CC(=O)OC1)C)C(=O)O)C 334.40 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
6-methyl-2-(4-methylpent-3-enyl)-9-(5-oxo-2H-furan-3-yl)non-6-enoic acid 162894902 Click to see CC(=CCCC(CCCC(=CCCC1=CC(=O)OC1)C)C(=O)O)C 334.40 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(5S,9S,10S,13R,14R)-17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 137706369 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 521229 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
Isochlorogensaure 12310829 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(96)00565-1
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(96)00565-1

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