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Baccharis quitensis

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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 UUID643fd205bc061523948196
Scientific name Baccharis quitensis
Authority Kunth
First published in Nov. Gen. Sp. 4(14): 44 (ed. fol.) (1818)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis pendula Heering Jahrb. Hamburg. Wiss. Anst. 31, Beiheft 3: 86 (1915)
Pingraea flexuosa Baker Candollea 48: 217. 1993
Pingraea flexuosa (Baker) F.H.Hellw. Candollea 48(1): 217 (1993): (1993)
Baccharis mapiriiensis Rusby
Baccharis mattogrossensis Heering ex Malme Ark. Bot. 24A, n.° 8: 36 (1932)
Baccharis mapirensis Rusby Mem. Torrey Bot. Club 6: 61 (1896)
Baccharis flexuosa Baker Fl. Bras. 6(3): 83 (1882)

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
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Argentina Northwest
    • Western South America
      • Bolivia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000120131
Tropicos 2704846
KEW urn:lsid:ipni.org:names:183661-1
The Plant List gcc-81406
Open Tree Of Life 7600145
NCBI Taxonomy 2707514
IPNI 183661-1
iNaturalist 704885
GBIF 3129668

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)!
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Title Authors Publication Released IDs
Flavonoids and Terpenoids from the Exudates of Some Baccharis Species Eckhard Wollenweber, Ingrid Schober, Pia Dostal, Dagmar Hradetzky, Francisco J. Arriaga-Giner, George Yatskievych Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1986-1-214
Diterpenes from Baccharis species Ferdinand Bohlmann, Wolfgang Kramp, Michael Grenz, Harold Robinson, Robert M. King Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)84033-2

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
1-[(2S)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]ethanone 12414274 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 202.25 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Benzenoids / Phenols / Benzenediols / Resorcinols
5-Pentadecylresorcinol 76617 Click to see CCCCCCCCCCCCCCCC1=CC(=CC(=C1)O)O 320.50 unknown https://doi.org/10.1016/0031-9422(81)84033-2
5-Tetradecylbenzene-1,3-diol 21532618 Click to see CCCCCCCCCCCCCCC1=CC(=CC(=C1)O)O 306.50 unknown https://doi.org/10.1016/0031-9422(81)84033-2
Grevillol 174862 Click to see CCCCCCCCCCCCCC1=CC(=CC(=C1)O)O 292.50 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
methyl (2E,8Z)-deca-2,8-dien-4,6-diynoate 6443002 Click to see CC=CC#CC#CC=CC(=O)OC 174.20 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
methyl (2E,8E)-10-[(Z)-2-methylbut-2-enoyl]oxydeca-2,8-dien-4,6-diynoate 10061778 Click to see CC=C(C)C(=O)OCC=CC#CC#CC=CC(=O)OC 272.29 unknown https://doi.org/10.1016/0031-9422(81)84033-2
methyl (2E,8Z)-10-[(Z)-2-methylbut-2-enoyl]oxydeca-2,8-dien-4,6-diynoate 6475134 Click to see CC=C(C)C(=O)OCC=CC#CC#CC=CC(=O)OC 272.29 unknown https://doi.org/10.1016/0031-9422(81)84033-2
Methyl 10-(2-methylbut-2-enoyloxy)deca-2,8-dien-4,6-diynoate 470964 Click to see CC=C(C)C(=O)OCC=CC#CC#CC=CC(=O)OC 272.29 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(14-Formyl-5,9-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl 3-(4-hydroxyphenyl)propanoate 162975689 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)C=O)C)COC(=O)CCC5=CC=C(C=C5)O 452.60 unknown https://doi.org/10.1016/0031-9422(81)84033-2
(5,9-Dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl 3-(4-hydroxyphenyl)propanoate 163014389 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)COC(=O)CCC5=CC=C(C=C5)O 436.60 unknown https://doi.org/10.1016/0031-9422(81)84033-2
[(1S,4S,5R,9S,10R,13R,14R)-14-formyl-5,9-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl 3-(4-hydroxyphenyl)propanoate 162975690 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)C=O)C)COC(=O)CCC5=CC=C(C=C5)O 452.60 unknown https://doi.org/10.1016/0031-9422(81)84033-2
[(1S,4S,5R,9S,10R,13R)-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl 3-(4-hydroxyphenyl)propanoate 163014390 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)COC(=O)CCC5=CC=C(C=C5)O 436.60 unknown https://doi.org/10.1016/0031-9422(81)84033-2
[(1S,4S,5R,9S,10S,13R)-14-(hydroxymethyl)-5,9-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methyl 3-(4-hydroxyphenyl)propanoate 163040693 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C4)CO)C)COC(=O)CCC5=CC=C(C=C5)O 452.60 unknown https://doi.org/10.1016/0031-9422(81)84033-2
[14-(Hydroxymethyl)-5,9-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methyl 3-(4-hydroxyphenyl)propanoate 163040692 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C4)CO)C)COC(=O)CCC5=CC=C(C=C5)O 452.60 unknown https://doi.org/10.1016/0031-9422(81)84033-2
CID 433869 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(81)84033-2
ent-16-Kauren-19-ol 529650 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1016/0031-9422(81)84033-2
ent-Kaur-16-en-19-ol 443465 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Methyl 2-(furan-3-yl)-5-hydroxy-6a,10b-dimethyl-4-oxo-2,4,6,6a,10a,10b-hexahydro-1h-benzo[f]isochromene-7-carboxylate 132279003 Click to see CC12CC(OC(=O)C1=C(CC3(C2C=CC=C3C(=O)OC)C)O)C4=COC=C4 370.40 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(2,2-Dimethylchromen-6-yl)ethanone 177040 Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)C 202.25 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Oxalicumone D 139583111 Click to see CC1=CC(=C2C(=C1)OC3=C(C2=O)CC(S3)C(CC(C(=O)O)O)(C(=O)OC)O)O 410.40 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-(3,8-Dimethylnona-3,7-dienoxy)chromen-2-one 163049508 Click to see CC(=CCCC=C(C)CCOC1=CC2=C(C=C1)C=CC(=O)O2)C 312.40 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
8-Methoxycirsilineol 181092 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown https://doi.org/10.1016/0031-9422(81)84033-2
Gardenin D 3080750 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown https://doi.org/10.1515/ZNC-1986-1-214
Sideritoflavone 155493 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC 360.30 unknown https://doi.org/10.1515/ZNC-1986-1-214
Xanthomicrol 73207 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC 344.30 unknown https://doi.org/10.1016/0031-9422(81)84033-2
https://doi.org/10.1515/ZNC-1986-1-214

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