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Baccharis alaternoides

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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 UUID643fcc712d15f155822833
Scientific name Baccharis alaternoides
Authority Kunth
First published in Nov. Gen. Sp. 4(14): 40 (ed. fol.) (1818)

Description Top

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It is a medium-sized shrub, growing up to 1.5 m tall, with a woody stem and branches. The leaves are alternate, oblong-lanceolate, and up to 8 cm long. The flowers are small, white, and clustered in heads. The fruit is a small, dry, one-seeded achene.

Baccharis alaternoides is a shrub of the Asteraceae family found in the Andes region of Ecuador and Peru. It is a medium-sized shrub, growing up to 1.5 m tall, with woody stems and branches. The leaves are alternate, oblong-lanceolate, and up to 8 cm long. The flowers are small, white, and clustered in heads, while the fruit is a small, dry, one-seeded achene.

Synonyms Top

Scientific name Authority First published in
Baccharis tridentata Poepp. ex DC. Prodr. 5: 411 (1836)
Baccharis resinosa Hook. & Arn. Bot. Beechey Voy. : 31 (1830)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000062775
Tropicos 2704617
KEW urn:lsid:ipni.org:names:183084-1
The Plant List gcc-19771
Open Tree Of Life 7599820
IPNI 183084-1
iNaturalist 925182
GBIF 3129393
Wikipedia Baccharis_alaternoides

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
Diterpenes from Baccharis species Ferdinand Bohlmann, Wolfgang Kramp, Jasmin Jakupovic, Harold Robinson, Robert M. King Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95275-0

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
> 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/10.1016/S0031-9422(00)95275-0
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/10.1016/S0031-9422(00)95275-0
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/10.1016/S0031-9422(00)95275-0
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2,8-Decadiene-4,6-diynoic acid, methyl ester 5319573 Click to see CC=CC#CC#CC=CC(=O)OC 174.20 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
Lachnophyllum ester 642290 Click to see CCCC#CC#CC=CC(=O)OC 176.21 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
Methyl deca-2,8-dien-4,6-diynoate 185530 Click to see CC=CC#CC#CC=CC(=O)OC 174.20 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
Methyl-dec-2-en-4,6-diynoate 96905 Click to see CCCC#CC#CC=CC(=O)OC 176.21 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
> 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/10.1016/S0031-9422(00)95275-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
3-[[(4aR,5S,6R,8aR)-5-[(3S)-5-hydroxy-3-methylpentyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 162906649 Click to see CC1CCC2(C(C1(C)CCC(C)CCO)CCC=C2COC(=O)CC(=O)O)C 394.50 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
3-[[(4aR,5S,6R,8aR)-5-[2-[(3R,5S)-5-hydroxyoxolan-3-yl]ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 163189782 Click to see CC1CCC2(C(C1(C)CCC3CC(OC3)O)CCC=C2COC(=O)CC(=O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
3-[[5-(5-Hydroxy-3-methylpentyl)-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 162906648 Click to see CC1CCC2(C(C1(C)CCC(C)CCO)CCC=C2COC(=O)CC(=O)O)C 394.50 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(1R,2R,5S,7R,10R,11R,14R,16S)-2,5,7,10,15,15-hexamethyl-7-(4-methylpent-3-enyl)-19-oxapentacyclo[14.2.1.01,14.02,11.05,10]nonadecane 162960565 Click to see CC(=CCCC1(CCC2(C3CCC4C(C5CCC4(C3(CCC2(C1)C)C)O5)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
D:B-Friedo-18,19-secolup-19-ene, 3,10-epoxy-, (3beta,10beta)- 550409 Click to see CC(=CCCC1(CCC2(C3CCC4C(C5CCC4(C3(CCC2(C1)C)C)O5)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)95275-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
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)95275-0

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