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Baccharis macraei

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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 UUID643fcd725f15d836907947
Scientific name Baccharis macraei
Authority Hook. & Arn.
First published in J. Bot. (Hooker) 3: 32 (1840)

Description Top

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Baccharis macraei is a shrub species that is native to Chile and Peru. It typically grows to be 50-150 cm tall and has a wide branching angle. The stems are initially covered in dense trichomes, giving the appearance of a round stem, but as the plant ages, the stems become greyish brown, shiny, and wrinkled. The leaves are firm, waxy, and have a toothed margin, and only last for one year. They are clustered at the top of branches and surround the singular, terminal, sessile inflorescences. This species is also involved in natural hybridization with Baccharis linearis, forming the hybrid Baccharis intermedia.

Synonyms Top

Scientific name Authority First published in
Baccharis macraei var. lucida Heering Jahrb. Hamburg. Wiss. Anst. 31, Beiheft 3: 125 (1915)

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
  • Southern America
    • Southern South America
      • Chile Central
    • Western South America
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000072372
Tropicos 2704755
KEW urn:lsid:ipni.org:names:273029-2
The Plant List gcc-29124
Open Tree Of Life 7600018
IPNI 273029-2
iNaturalist 861001
GBIF 3129149
Wikipedia Baccharis_macraei
CMAUP NPO12376

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
Hybridization in the Genus Baccharis : Baccharis linearis χ B. macraei Francesca Faini, Frank Hellwlg, Cecilia Labbé, Mariano Castillo Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(91)90113-E
Neo-clerodane diterpenoids from Baccharis macraei Vicente Gambaro, María C. Chamy, Juan A. Garbarino, Aurelio San-Martin, Mariano Castillo Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)80085-1
Neo-clerodane diterpenoids from Baccharis macraei Vicente Gambaro, María C. Chamy, Juan A. Garbarino Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81436-3

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
5-(2'-Oxoheneicosyl)Resorcinol 56683379 Click to see CCCCCCCCCCCCCCCCCCCC(=O)CC1=CC(=CC(=C1)O)O 418.70 unknown https://doi.org/10.1016/0305-1978(91)90113-E
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Octadecene 8217 Click to see CCCCCCCCCCCCCCCCC=C 252.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(+)-Hardwickiic Acid 15559627 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C 316.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
(4aR,5S,6R,8aS)-8a-(acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-5,6-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 162891447 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)COC(=O)C 374.50 unknown https://doi.org/10.1016/S0031-9422(00)81436-3
5-(2-(Furan-3-YL)ethyl)-8A-(hydroxymethyl)-5,6-dimethyl-3,4,4A,6,7,8-hexahydronaphthalene-1-carboxylic acid 12310371 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)CO 332.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
8a-(Acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-5,6-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 53396110 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)COC(=O)C 374.50 unknown https://doi.org/10.1016/S0031-9422(00)81436-3
Hardwickiic acid 15559629 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C 316.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
https://doi.org/10.1016/0305-1978(91)90113-E
https://doi.org/10.1016/S0031-9422(00)81436-3
Hautriwaic acid 12310372 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)CO 332.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
https://doi.org/10.1016/S0031-9422(00)81436-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
Yuanhuacine 5358691 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown via CMAUP database
Yuanhuaoate E 73348817 Click to see CCCCCC=CC=CC(=O)OC1C2C3C(O3)(C(C4(C(C2(C(C(C1(C(=C)C)O)OC(=O)C5=CC=CC=C5)C)O)C=C(C4=O)C)O)O)CO 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(3aS,6aR,7R,8S,10aR)-7-[2-(furan-3-yl)ethyl]-3a-hydroxy-7,8-dimethyl-6,6a,8,10-tetrahydro-1H-benzo[d][2]benzofuran-3,9-dione 162955576 Click to see CC1C(=O)CC23COC(=O)C2(C=CCC3C1(C)CCC4=COC=C4)O 344.40 unknown https://doi.org/10.1016/S0031-9422(00)81436-3
(5S,6aR,7R,8S,10aS)-7-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethyl-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-3,9-dione 162974871 Click to see CC1C(=O)CC23COC(=O)C2=CC(CC3C1(C)CCC4=COC=C4)O 344.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
(6aR,7R,8S,10aS)-7-[2-(furan-3-yl)ethyl]-7,8-dimethyl-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-3,9-dione 14262615 Click to see CC1C(=O)CC23COC(=O)C2=CCCC3C1(C)CCC4=COC=C4 328.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
7-[2-(furan-3-yl)ethyl]-3a-hydroxy-7,8-dimethyl-6,6a,8,10-tetrahydro-1H-benzo[d][2]benzofuran-3,9-dione 162955575 Click to see CC1C(=O)CC23COC(=O)C2(C=CCC3C1(C)CCC4=COC=C4)O 344.40 unknown https://doi.org/10.1016/S0031-9422(00)81436-3
7-[2-(Furan-3-yl)ethyl]-5-hydroxy-7,8-dimethyl-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-3,9-dione 162974870 Click to see CC1C(=O)CC23COC(=O)C2=CC(CC3C1(C)CCC4=COC=C4)O 344.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
7-[2-(Furan-3-yl)ethyl]-7,8-dimethyl-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-3,9-dione 14262614 Click to see CC1C(=O)CC23COC(=O)C2=CCCC3C1(C)CCC4=COC=C4 328.40 unknown https://doi.org/10.1016/0031-9422(86)80085-1
> 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/10.1016/0031-9422(86)80085-1
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/S0031-9422(00)81436-3
https://doi.org/10.1016/0031-9422(86)80085-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives
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/10.1016/0305-1978(91)90113-E
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,2'R,3'S,8'S)-3',4,5',6-tetrahydroxy-2',8'-bis(4-hydroxyphenyl)spiro[1-benzofuran-2,9'-2,3,4,8-tetrahydrofuro[2,3-h]chromene]-3-one 100885566 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(O3)C5=CC=C(C=C5)O)C(=O)C6=C(C=C(C=C6O4)O)O)O)C7=CC=C(C=C7)O)O 542.50 unknown via CMAUP database
Daphnodorin A 72426 Click to see C1CC2=C(C3=C(C=C2O)OC(=C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown via CMAUP database
Daphnodorin B 72427 Click to see C1C(C(OC2=C1C(=CC3=C2C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5O)O)O)O)C6=CC=C(C=C6)O)O 542.50 unknown via CMAUP database
Daphnodorin C 72428 Click to see C1CC2=C(C3=C(C=C2O)OC(C34C(=O)C5=C(C=C(C=C5O4)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 526.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnetin-8-glucoside 5316301 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O 352.30 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5S,6R,13S)-1,6,9,17,19-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 15984107 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(=O)C5=C(C=C(C=C5OC4(O3)C6=CC=C(C=C6)O)O)O)O)O)C7=CC=C(C=C7)O)O 558.50 unknown via CMAUP database
(1S,5S,13R)-1,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 76317993 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown via CMAUP database
(1S,5S,6R,13R)-1,6,9,17,19-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 15984106 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(=O)C5=C(C=C(C=C5OC4(O3)C6=CC=C(C=C6)O)O)O)O)O)C7=CC=C(C=C7)O)O 558.50 unknown via CMAUP database
daphnodorin D2 13941113 Click to see C1CC2=C(C(=C(C=C2O)O)C3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown via CMAUP database
Daphnodorin F 70688394 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown via CMAUP database
> 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/10.1016/0305-1978(91)90113-E
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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/10.1016/0305-1978(91)90113-E
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1016/0305-1978(91)90113-E

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