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Internal ID UUID643fc681e6f17744419629
Scientific name Haplopappus remyanus
Authority Wedd.
First published in Chlor. Andina 1: 210 (1857)

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Synonyms Top

Scientific name Authority First published in
Haplopappus prinophyllus Phil.
Aster remyanus Kuntze Revis. Gen. Pl. 1: 318. 1891 [5 Nov 1891]
Pyrrocoma ilicifolia J.Rémy Fl. Chil. 4(1): 67 (1849)

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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-0000005727
Tropicos 2702585
KEW urn:lsid:ipni.org:names:178077-1
The Plant List gcc-105511
Open Tree Of Life 7599243
IPNI 178077-1
GBIF 3100629

Genomes (via NCBI) Top

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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
Friedolabdanes and other constituents from chileanHaplopappus species C. Zdero, F. Bohlmann, H.M. Niemeyer Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80089-J

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,8-Trihydroxy-2-methyl-1,2-dihydroanthracene-9,10-dione 149814611 Click to see CC1C(C2=C(C=C1O)C(=O)C3=C(C2=O)C(=CC=C3)O)O 272.25 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Benzenoids / Benzene and substituted derivatives / Toluenes
[(2R)-2-hydroxy-2-(4-methylphenyl)propyl] 3-phenylpropanoate 162931343 Click to see CC1=CC=C(C=C1)C(C)(COC(=O)CCC2=CC=CC=C2)O 298.40 unknown https://doi.org/10.1016/0031-9422(91)80089-J
[(2R)-2-hydroxy-2-(4-methylphenyl)propyl] acetate 10330683 Click to see CC1=CC=C(C=C1)C(C)(COC(=O)C)O 208.25 unknown https://doi.org/10.1016/0031-9422(91)80089-J
[2-Hydroxy-2-(4-methylphenyl)propyl] 3-phenylpropanoate 15109629 Click to see CC1=CC=C(C=C1)C(C)(COC(=O)CCC2=CC=CC=C2)O 298.40 unknown https://doi.org/10.1016/0031-9422(91)80089-J
[2-Hydroxy-2-(4-methylphenyl)propyl] acetate 10330684 Click to see CC1=CC=C(C=C1)C(C)(COC(=O)C)O 208.25 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13E)-18-(3-Phenylpropanoyloxy)labda-7,13-dien-15-oic acid 15109625 Click to see CC1=CCC2C(CCCC2(C1CCC(=CC(=O)O)C)C)(C)COC(=O)CCC3=CC=CC=C3 452.60 unknown https://doi.org/10.1016/0031-9422(91)80089-J
(E)-5-[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 101616658 Click to see CC1=CCC2C(CCCC2(C1CCC(=CC(=O)O)C)C)(C)CO 320.50 unknown https://doi.org/10.1016/0031-9422(91)80089-J
5-[2,5,8a-Trimethyl-5-(3-phenylpropanoyloxymethyl)-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 163069550 Click to see CC1=CCC2C(CCCC2(C1CCC(=CC(=O)O)C)C)(C)COC(=O)CCC3=CC=CC=C3 452.60 unknown https://doi.org/10.1016/0031-9422(91)80089-J
5-[5-(Hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 85317777 Click to see CC1=CCC2C(CCCC2(C1CCC(=CC(=O)O)C)C)(C)CO 320.50 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
[(2R)-2-hydroxy-2-[(1R)-4-methylcyclohex-3-en-1-yl]propyl] 3-phenylpropanoate 163186020 Click to see CC1=CCC(CC1)C(C)(COC(=O)CCC2=CC=CC=C2)O 302.40 unknown https://doi.org/10.1016/0031-9422(91)80089-J
[2-Hydroxy-2-(4-methylcyclohex-3-en-1-yl)propyl] 3-phenylpropanoate 163039220 Click to see CC1=CCC(CC1)C(C)(COC(=O)CCC2=CC=CC=C2)O 302.40 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
[(2S)-2-hydroxy-2-[(1R)-4-methylidenecyclohex-2-en-1-yl]propyl] acetate 162908036 Click to see CC(=O)OCC(C)(C1CCC(=C)C=C1)O 210.27 unknown https://doi.org/10.1016/0031-9422(91)80089-J
[2-Hydroxy-2-(4-methylidenecyclohex-2-en-1-yl)propyl] acetate 101415777 Click to see CC(=O)OCC(C)(C1CCC(=C)C=C1)O 210.27 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[(2R)-2-hydroxy-2-[(1R)-4-methylcyclohex-3-en-1-yl]propyl] (E)-3-phenylprop-2-enoate 26176653 Click to see CC1=CCC(CC1)C(C)(COC(=O)C=CC2=CC=CC=C2)O 300.40 unknown https://doi.org/10.1016/0031-9422(91)80089-J
[2-Hydroxy-2-(4-methylcyclohex-3-en-1-yl)propyl] 3-phenylprop-2-enoate 74488963 Click to see CC1=CCC(CC1)C(C)(COC(=O)C=CC2=CC=CC=C2)O 300.40 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2-Methyl-6-methylideneocta-2,7-dienyl) 3-(4-hydroxyphenyl)prop-2-enoate 162927632 Click to see CC(=CCCC(=C)C=C)COC(=O)C=CC1=CC=C(C=C1)O 298.40 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(91)80089-J
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(91)80089-J
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(5-Hydroxy-7-methoxy-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl) acetate 72745200 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC=CC=C3 328.30 unknown https://doi.org/10.1016/0031-9422(91)80089-J
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(91)80089-J
5-Hydroxy-7-methoxyflavanone 4101463 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(91)80089-J
Alpinone 3-acetate 15109631 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC=CC=C3 328.30 unknown https://doi.org/10.1016/0031-9422(91)80089-J
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(91)80089-J

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