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Baccharis neaei

Baccharis neaei - 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 UUID643fca8751292988195035
Scientific name Baccharis neaei
Authority DC.
First published in Prodr. 5: 411 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis bezanilleana J.Rémy in Gay Fl. Chil. 4: 98 (-99) (1849)
Baccharis talcareguensis Heering Anales de la Universidad de Chile 111: 174 1902
Baccharis solierii J.Rémy in Gay Fl. Chil. 4: 98 (1849)
Baccharis solierii var. williamsii Heering
Baccharis rhetinodes Meyen & Walp. Nov. Actorum Acad. Caes. Leop.-Carol. Nat. Cur. 19(Suppl. 1): 265 (1843)
Baccharis bezanilleana var. solisi (Phil.) Heering Fl. Chile 4: 22 (1902)
Baccharis solisi Phil. Anales Univ. Chile 36: 330 (1865)
Baccharis williamsii F.Phil. Anales Univ. Chile 87: 701 (1894)
Baccharis talcareguensis Heering ex Reiche Anales Univ. Chile 111: 174 (1903)
Baccharis benzanilleana var. solisi (Phil.) Reiche Anales Univ. Chile 111: 172 1902

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
    • Southern South America
      • Argentina Northwest
      • Argentina South
      • Chile Central
      • Chile South

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000039104
Tropicos 2704784
KEW urn:lsid:ipni.org:names:183503-1
The Plant List gcc-137811
Open Tree Of Life 5738967
NCBI Taxonomy 1654445
IPNI 183503-1
iNaturalist 864762
GBIF 3129461

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
Alien plant species on roadsides of the northwestern Patagonian steppe (Argentina) Chichizola GA, Gonzalez SL, Rovere AE PLoS One 11-Feb-2021
PMCID:PMC7877596
doi:10.1371/journal.pone.0246657
PMID:33571278
Secondary Metabolites from Chilean Baccharis species C. Labbe, J. Rovirosa, F. Faini, M. Mahu, A. San-Martin, M. Castillo American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50045A025
Diterpene glycosides and other constituents from argentinian baccharis species C. Zdero, F. Bohlmann, R.M. King, H. Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83754-1
Diterpenoids from Baccharis neaei Francesca Faini, Cecilia Labbe, M.Inés Polanco Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83494-J
Insect antifeedant activity of clerodane diterpenoids. Sosa ME, Tonn CE, Giordano OS J Nat Prod 01-Sep-1994
doi:10.1021/NP50111A012
PMID:7798961

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 / Diterpenoids
(3S)-5-[(1S,2S,4aS,5S,8aR)-2-hydroxy-5-(hydroxymethyl)-2,5,8a-trimethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanal 163097188 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)CO)C)CC=O 324.50 unknown https://doi.org/10.1016/0031-9422(92)83494-J
(3S)-5-[(1S,2S,4aS,5S,8aR)-5-(3-carboxypropanoyloxymethyl)-2-hydroxy-2,5,8a-trimethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 163052073 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)COC(=O)CCC(=O)O)C)CC(=O)O 440.60 unknown https://doi.org/10.1016/0031-9422(92)83494-J
4-[[(1S,4aR,5S,6S,8aS)-6-hydroxy-1,4a,6-trimethyl-5-[(3S)-3-methyl-5-oxopentyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-4-oxobutanoic acid 162995225 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)COC(=O)CCC(=O)O)C)CC=O 424.60 unknown https://doi.org/10.1016/0031-9422(92)83494-J
4-[[(1S,4aR,5S,6S,8aS)-6-hydroxy-5-[(3S)-5-hydroxy-3-methylpentyl]-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-4-oxobutanoic acid 163056591 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)COC(=O)CCC(=O)O)C)CCO 426.60 unknown https://doi.org/10.1016/0031-9422(92)83494-J
4-[[6-hydroxy-1,4a,6-trimethyl-5-(3-methyl-5-oxopentyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-4-oxobutanoic acid 162995224 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)COC(=O)CCC(=O)O)C)CC=O 424.60 unknown https://doi.org/10.1016/0031-9422(92)83494-J
4-[[6-hydroxy-5-(5-hydroxy-3-methylpentyl)-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-4-oxobutanoic acid 163056590 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)COC(=O)CCC(=O)O)C)CCO 426.60 unknown https://doi.org/10.1016/0031-9422(92)83494-J
5-[2-hydroxy-5-(hydroxymethyl)-2,5,8a-trimethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanal 163097187 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)CO)C)CC=O 324.50 unknown https://doi.org/10.1016/0031-9422(92)83494-J
5-[5-(3-carboxypropanoyloxymethyl)-2-hydroxy-2,5,8a-trimethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 163052072 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)COC(=O)CCC(=O)O)C)CC(=O)O 440.60 unknown https://doi.org/10.1016/0031-9422(92)83494-J
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
3-[[(4aR,5S,6R,8aS)-8a-(acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-5,6-dimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 162959213 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2COC(=O)CC(=O)O)COC(=O)C 446.50 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
3-[[(4aS,7R,8S,8aR)-8-[2-(furan-3-yl)ethyl]-4-(hydroxymethyl)-7,8-dimethyl-1,2,5,6,7,8a-hexahydronaphthalen-4a-yl]methoxy]-3-oxopropanoic acid 163009995 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2CO)COC(=O)CC(=O)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
3-[[8-[2-(Furan-3-yl)ethyl]-4-(hydroxymethyl)-7,8-dimethyl-1,2,5,6,7,8a-hexahydronaphthalen-4a-yl]methoxy]-3-oxopropanoic acid 163009994 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2CO)COC(=O)CC(=O)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
3-[[8a-(Acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-5,6-dimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 162959212 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2COC(=O)CC(=O)O)COC(=O)C 446.50 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1016/0031-9422(92)83494-J
https://doi.org/10.1021/NP50045A025
> Organoheterocyclic compounds / Naphthopyrans
7-(Furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-13-ene-5,15-dione 326832 Click to see CC12CC(OC(=O)C1CCC34C2CCC=C3C(=O)OC4)C5=COC=C5 342.40 unknown https://doi.org/10.1021/NP50111A012
Bacchotricuneatin A 14021509 Click to see CC12CC(OC(=O)C1CCC34C2CCC=C3C(=O)OC4)C5=COC=C5 342.40 unknown https://doi.org/10.1021/NP50111A012
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0031-9422(92)83494-J
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown https://doi.org/10.1021/NP50045A025
Desmethoxycentaureidin 5469524 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1021/NP50045A025
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Demethoxysudachitin 3083845 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)O 330.29 unknown https://doi.org/10.1021/NP50045A025

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