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Ophryosporus macrodon

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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 UUID643fd1d03bb2c952638668
Scientific name Ophryosporus macrodon
Authority Griseb.
First published in Abh. Königl. Ges. Wiss. Göttingen 24: 173 (1879)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium kuntzei Hieron. Bot. Jahrb. Syst. 22(4-5): 766 (1897)

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
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000118441
Tropicos 2707263
KEW urn:lsid:ipni.org:names:235508-1
The Plant List gcc-7977
Open Tree Of Life 7604283
IPNI 235508-1
iNaturalist 1146877
GBIF 3140116

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
Diprenylated derivatives of p-hydroxyacetophenone from Ophryosporus macrodon Elizabeth Sigstad, César A.N. Catalán, Jesús G. Diaz, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85415-N

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
12-Hydroxy-2,3-dihydroeuparin 10036992 Click to see CC(=O)C1=C(C=C2C(=C1)CC(O2)C(=C)CO)O 234.25 unknown https://doi.org/10.1016/0031-9422(93)85415-N
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
1-[5-Acetyl-2-(2-hydroxypropan-2-yl)-1-benzofuran-7-yl]-3-methylbutan-1-one 162847354 Click to see CC(C)CC(=O)C1=C2C(=CC(=C1)C(=O)C)C=C(O2)C(C)(C)O 302.40 unknown https://doi.org/10.1016/0031-9422(93)85415-N
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(2R,4aR,7R,8S,8aR)-8-[(3R)-3-hydroxy-3-methylpent-4-enyl]-4,4a,7,8-tetramethyl-1,2,5,6,7,8a-hexahydronaphthalen-2-ol 5318244 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CC(C=C2C)O)C 306.50 unknown https://doi.org/10.1016/0031-9422(93)85415-N
3-[[(4aR,5S,6R,8aR)-5-[2-[(3R,5S)-5-[(2S,4R)-4-[2-[(1S,2R,4aR,8aR)-5-[(2-carboxyacetyl)oxymethyl]-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]oxolan-2-yl]oxyoxolan-3-yl]ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 162903609 Click to see CC1CCC2(C(C1(C)CCC3CC(OC3)OC4CC(CO4)CCC5(C(CCC6(C5CCC=C6COC(=O)CC(=O)O)C)C)C)CCC=C2COC(=O)CC(=O)O)C 799.00 unknown https://doi.org/10.1016/0031-9422(93)85415-N
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-[5-Acetyl-2-hydroxy-3-(3-hydroxy-3-methyl-1-butenyl)phenyl]-3-methyl-1-butanone 78385075 Click to see CC(C)CC(=O)C1=CC(=CC(=C1O)C=CC(C)(C)O)C(=O)C 304.40 unknown https://doi.org/10.1016/0031-9422(93)85415-N
beta-Methyl-2'-hydroxy-3'-(3-hydroxy-3-methyl-1-butenyl)-5'-acetylbutyrophenone 5318238 Click to see CC(C)CC(=O)C1=CC(=CC(=C1O)C=CC(C)(C)O)C(=O)C 304.40 unknown https://doi.org/10.1016/0031-9422(93)85415-N
> Organoheterocyclic compounds / Benzofurans
1-[2-(2-Hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-1-benzofuran-5-yl]ethanone 162899083 Click to see CC(=CCC1=C2C(=CC(=C1)C(=O)C)C=C(O2)C(C)(C)O)C 286.40 unknown https://doi.org/10.1016/0031-9422(93)85415-N
1-[5-Acetyl-2-(2-hydroxypropan-2-yl)-1-benzofuran-7-yl]-3-methylbut-2-en-1-one 162877460 Click to see CC(=CC(=O)C1=C2C(=CC(=C1)C(=O)C)C=C(O2)C(C)(C)O)C 300.30 unknown https://doi.org/10.1016/0031-9422(93)85415-N
1-[7-(2,3-Dihydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-1-benzofuran-5-yl]ethanone 163071148 Click to see CC(=O)C1=CC(=C2C(=C1)C=C(O2)C(C)(C)O)CC(C(C)(C)O)O 320.40 unknown https://doi.org/10.1016/0031-9422(93)85415-N
1-[7-(3-Hydroxy-3-methylbut-1-enyl)-2-(2-hydroxypropan-2-yl)-1-benzofuran-5-yl]ethanone 163004479 Click to see CC(=O)C1=CC(=C2C(=C1)C=C(O2)C(C)(C)O)C=CC(C)(C)O 302.40 unknown https://doi.org/10.1016/0031-9422(93)85415-N
1-[7-[(2S)-2,3-dihydroxy-3-methylbutyl]-2-(2-hydroxypropan-2-yl)-1-benzofuran-5-yl]ethanone 163071149 Click to see CC(=O)C1=CC(=C2C(=C1)C=C(O2)C(C)(C)O)CC(C(C)(C)O)O 320.40 unknown https://doi.org/10.1016/0031-9422(93)85415-N
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(93)85415-N
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(93)85415-N

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