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Baccharis conferta

Baccharis conferta - 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 UUID643fc64beff14247831816
Scientific name Baccharis conferta
Authority Kunth
First published in Nov. Gen. Sp. 4(14): 43 (ed. fol.) (1818)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis orizabaensis Sch.Bip. ex Hemsl. Biol. Cent.-Amer., Bot. 2: 130 (1881)
Baccharis xalapensis Kunth Nov. Gen. Sp. 4(14): 44 (ed. fol.) (1818)
Baccharis resinosa Kunth Nov. Gen. Sp. 4(14): 41 (ed. fol.) (1818)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000004046
Tropicos 2704662
KEW urn:lsid:ipni.org:names:183207-1
The Plant List gcc-10390
Open Tree Of Life 6056140
NCBI Taxonomy 3015672
IPNI 183207-1
iNaturalist 244807
GBIF 3129932

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
Humboldt’s legacy: explaining the influence of environmental factors on the taxonomic and phylogenetic diversity of angiosperms along a Neotropical elevational gradient Gómez-Díaz JA, Carvajal-Hernández CI, Bautista-Bello AP, Monge-González ML, Guzmán-Jacob V, Kreft H, Krömer T, Villalobos F AoB Plants 07-Nov-2022
PMCID:PMC9840209
doi:10.1093/aobpla/plac056
PMID:36654988
Environment‐driven changes in diversity of riparian plant communities along a mountain river Flores‐Galicia N, Trejo I, Ramírez‐Marcial N Ecol Evol 25-Mar-2021
PMCID:PMC8131774
doi:10.1002/ece3.7472
PMID:34026040
Plant-Based Natural Products for the Discovery and Development of Novel Anthelmintics against Nematodes Liu M, Panda SK, Luyten W Biomolecules 09-Mar-2020
PMCID:PMC7175113
doi:10.3390/biom10030426
PMID:32182910
Ixcatec ethnoecology: plant management and biocultural heritage in Oaxaca, Mexico Rangel-Landa S, Casas A, Rivera-Lozoya E, Torres-García I, Vallejo-Ramos M J Ethnobiol Ethnomed 20-Jul-2016
PMCID:PMC4955254
doi:10.1186/s13002-016-0101-3
PMID:27439512
Plant management and biodiversity conservation in Náhuatl homegardens of the Tehuacán Valley, Mexico Larios C, Casas A, Vallejo M, Moreno-Calles AI, Blancas J J Ethnobiol Ethnomed 06-Nov-2013
PMCID:PMC3827996
doi:10.1186/1746-4269-9-74
PMID:24195962
Weitere Inhaltsstoffe aus <i>Baccharis conferta</i> H. B. K. Ferdinand Bohlmann, Christa Zdero Wiley 29-Jun-2007
doi:10.1002/CBER.19761090430
Spasmolytic effects of baccharis conferta and some of its constituents. Weimann C, Goransson U, Pongprayoon-Claeson U, Claeson P, Bohlin L, Rimpler H, Heinrich M J Pharm Pharmacol 01-Jan-2002
doi:10.1211/0022357021771797
PMID:11829135

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 / Benzene and substituted derivatives / Acetophenones
2-(6-Acetyl-5-hydroxy-2,3-dihydrobenzo[d]furan-2-yl)prop-2-enyl acetate 481690 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)COC(=O)C)O 276.28 unknown https://doi.org/10.1002/CBER.19761090430
2-[(2S)-6-acetyl-5-hydroxy-2,3-dihydro-1-benzofuran-2-yl]prop-2-enal 163034065 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)C=O)O 232.23 unknown https://doi.org/10.1002/CBER.19761090430
2-[(2S)-6-acetyl-5-hydroxy-2,3-dihydro-1-benzofuran-2-yl]prop-2-enyl acetate 163030891 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)COC(=O)C)O 276.28 unknown https://doi.org/10.1002/CBER.19761090430
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Methyl 9-hydroxyoctadec-11-enoate 163074698 Click to see CCCCCCC=CCC(CCCCCCCC(=O)OC)O 312.50 unknown https://doi.org/10.1002/CBER.19761090430
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1211/0022357021771797
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1211/0022357021771797
methyl (4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate 122541 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1211/0022357021771797
Methyl oleanolate 92900 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1211/0022357021771797
Olean-12-ene-3,28-diol 608886 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1211/0022357021771797
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1211/0022357021771797
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1211/0022357021771797
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(S)-5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)chroman-4-one 14057196 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 300.30 unknown https://doi.org/10.1211/0022357021771797
5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 321346 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 300.30 unknown https://doi.org/10.1211/0022357021771797
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.1211/0022357021771797
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1211/0022357021771797

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