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Haplopappus foliosus

Haplopappus foliosus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd390b3569616860136
Scientific name Haplopappus foliosus
Authority DC.
First published in Prodr. 5: 346 (1836)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Haplopappus foliosus subsp. foliosus
Haplopappus foliosus subsp. meyenii (Walp.) Klingenb. Biblioth. Bot. 157: 142 (2007)

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000133131
Tropicos 2702566
KEW urn:lsid:ipni.org:names:177949-1
The Plant List gcc-93951
Open Tree Of Life 929838
NCBI Taxonomy 147773
IPNI 177949-1
iNaturalist 705287
GBIF 3100485
Freebase /m/0w338w4
EOL 466923
USDA GRIN 413822
Wikipedia Haplopappus_foliosus

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Effects of Piper nigrum L. Fruit Essential Oil Toxicity against Stable Fly (Diptera: Muscidae) Weluwanarak T, Changbunjong T, Leesombun A, Boonmasawai S, Sungpradit S Plants (Basel) 24-Feb-2023
PMCID:PMC10005248
doi:10.3390/plants12051043
PMID:36903904
Removal of Heavy Metals from Mine Tailings in Central Chile Using Solidago chilensis Meyen, Haplopappus foliosus DC, and Lycium chilense Miers ex Bertero Lazo P, Lazo A, Hansen HK, Ortiz-Soto R, Hansen ME, Arévalo F, Gutiérrez C Int J Environ Res Public Health 03-Feb-2023
PMCID:PMC9916048
doi:10.3390/ijerph20032749
PMID:36768113
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
Leaf traits in Chilean matorral: sclerophylly within, among, and beyond matorral, and its environmental determinants Read J, Sanson G, Pérez Trautmann MF Ecol Evol 03-Feb-2016
PMCID:PMC4739351
doi:10.1002/ece3.1970
PMID:26865953
A Structure-Activity Study of Antibacterial Diterpenoids Urzúa A, Rezende MC, Mascayano C, Vásquez L Molecules 17-Apr-2008
PMCID:PMC6245368
doi:10.3390/molecules13040822
PMID:18463590
Haplopappin, ein 8‐(α‐Methylbenzyl)flavonoid aus <i>Haplopapus foliosus</i> Rudolf Tschesche, M. Sualaheen Delhvi, Silvia Sepúlveda‐Boza, Fritz Zilliken, Armin Kirfel, Georg Will Wiley 19-Jul-2007
doi:10.1002/JLAC.198519851215
Flavonoids From Haplopappus foliosus Ayhan Ulubelen, Eser Ayanoglu, W. Dennis Clark, Gregory K. Brown, Tom J. Mabry American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50021A021
Antibacterial new clerodane diterpenes from the surface of Haplopappus foliosus. Urzúa A, Torres R, Mendoza L, Delle Monache F Planta Med 01-Jul-2003
doi:10.1055/S-2003-41118
PMID:12898428
A new diterpenic acid and other constituents of Haplopappus foliosus and H. Angustifolius Mario Silva, Peter G. Sammes Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)80397-8
Guaiane sesquiterpenoids from Haplopappus foliosus Cecilia Labbé, Francesca Faini, Josep Coll, Pere Carbonell Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00871-6
Comparative chemical composition of the resinous exudates from Haplopappus foliosus and H. uncinatus. Urzúa AA, Andrade L, Jara F Biochem Syst Ecol 01-Jun-2000
doi:10.1016/S0305-1978(99)00080-0
PMID:10725607

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 / Cumenes
2-Isopropylphenol 6943 Click to see CC(C)C1=CC=CC=C1O 136.19 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1016/0031-9422(73)80397-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown https://doi.org/10.1016/0031-9422(73)80397-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4aR,5S,6R,8aS)-5-[(E)-4-carboxy-3-methylbut-3-enyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 102117108 Click to see CC1CCC2(C(C1(C)CCC(=CC(=O)O)C)CCC=C2C(=O)O)C 334.40 unknown https://doi.org/10.1016/0031-9422(73)80397-8
(4aS,5S,6R,8aR)-5-[(E)-4-carboxy-3-methylbut-3-enyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 162983069 Click to see CC1CCC2(C(C1(C)CCC(=CC(=O)O)C)CCC=C2C(=O)O)C 334.40 unknown https://doi.org/10.1016/0031-9422(73)80397-8
Agn-PC-0JT8DC 580305 Click to see CC1CCC2(C(C1(C)CCC(=CC(=O)O)C)CCC=C2C(=O)O)C 334.40 unknown https://doi.org/10.1016/0031-9422(73)80397-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(Z)-alpha-ocimene 5463455 Click to see CC(=C)CCC=C(C)C=C 136.23 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
Thujane 79017 Click to see CC1CCC2(C1C2)C(C)C 138.25 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1R)-4-methyl-1-propan-2-ylcyclohex-2-en-1-ol 163187984 Click to see CC1CCC(C=C1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
5-(2-hydroxypropan-2-yl)-3,8-dimethyl-4,5,6,7,8,8a-hexahydro-1H-azulen-2-one 14610252 Click to see CC1CCC(CC2=C(C(=O)CC12)C)C(C)(C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(97)00871-6
Hydroxycolorenone 11447720 Click to see CC1CCC(CC2=C(C(=O)CC12)C)C(C)(C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(97)00871-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4R,4aS,6aR,6aS,6bS,8aR,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol 162967127 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/0031-9422(73)80397-8
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80397-8
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80397-8
Friedelinol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/0031-9422(73)80397-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9R,10R,13S,14S,17S)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163081991 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(73)80397-8
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(73)80397-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/S0305-1978(99)00080-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1021/NP50021A021
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Haplopappin 21721935 Click to see CC(C1=CC=C(C=C1)O)C2=C(C=C(C3=C2OC(=C(C3=O)OC)C4=CC=C(C=C4)OC)O)O 434.40 unknown https://doi.org/10.1002/JLAC.198519851215
Haplopappin A 44259574 Click to see CC(C1=CC=C(C=C1)O)C2=C(C=C(C3=C2OC(=C(C3=O)O)C4=CC=C(C=C4)OC)O)OC 434.40 unknown https://doi.org/10.1002/JLAC.198519851215
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Betuletol 5459196 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1002/JLAC.198519851215
Eupatolitin 5317291 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O)OC 346.30 unknown https://doi.org/10.1021/NP50021A021
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1021/NP50021A021
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP50021A021
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50021A021
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP50021A021
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51521831 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP50021A021
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50021A021
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402809 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1021/NP50021A021
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50021A021
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP50021A021
Quercetin 3-alloside 12304327 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP50021A021
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1021/NP50021A021
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/10.1002/JLAC.198519851215
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown https://doi.org/10.1002/JLAC.198519851215
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown https://doi.org/10.1055/S-2003-41118

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