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Haplopappus rigidus

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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 UUID643fc9de3cfdd496911946
Scientific name Haplopappus rigidus
Authority Phil.
First published in Fl. Atacam. 204. 1860

Description Top

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Synonyms Top

Scientific name Authority First published in
Aster atacamensis Kuntze Revis. Gen. Pl. 1: 315 (1891)
Haplopappus villanuevae Phil. Anales Univ. Chile 87: 592 (1894)
Haplopappus doellianus Phil. Anales Univ. Chile (1873) 489.

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000033867
Tropicos 2706445
KEW urn:lsid:ipni.org:names:178082-1
The Plant List gcc-13274
Open Tree Of Life 7051164
NCBI Taxonomy 2528747
IPNI 117756-2
iNaturalist 825572
GBIF 3100648
EOL 6162312

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
Targeting metabolic disorders by natural products Tabatabaei-Malazy O, Larijani B, Abdollahi M J Diabetes Metab Disord 08-Jul-2015
PMCID:PMC4495701
doi:10.1186/s40200-015-0184-8
PMID:26157708
RIGIDUSIDO, UN NUEVO GLICODITERPENOIDE DE Haplopappus rigidus GLAUCO MORALES, PATRICIA SIERRA, JORGE BORQUEZ, LUIS A. LOYOLA SciELO Agencia Nacional de Investigacion y Desarrollo (ANID) 04-Aug-2009
doi:10.4067/S0366-16442000000400014
Diterpenoids from Haplopappus rigidus. Morales G, Sierra P, Loyola LA, Borquez J Phytochemistry 01-Dec-2000
doi:10.1016/S0031-9422(00)00321-6
PMID:11140515

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1S,2R,4aS,8aR)-alpha-Ethenyl-1,2,3,4,4a,7,8,8a-octahydro-5-(hydroxymethyl)-alpha,1,2,4a-tetramethyl-1-naphthalenepropanol 101717365 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2CO)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)00321-6
(3R)-5-[(1S,2R,4aS,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol 163018751 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2CO)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)00321-6
(3S)-5-[(1S,2R,4aS,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol 163190539 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2CO)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)00321-6
[(4aR,5S,6R,8aS)-5-(3-hydroxy-3-methylpent-4-enyl)-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl acetate 22297648 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2COC(=O)C)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)00321-6
[(4aR,5S,6R,8aS)-5-[(3S)-3-hydroxy-3-methylpent-4-enyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl acetate 637218 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2COC(=O)C)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)00321-6
[5-(3-Hydroxy-3-methylpent-4-enyl)-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl acetate 22297649 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2COC(=O)C)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)00321-6
Sagittariol 101603339 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2CO)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)00321-6
> 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/10.4067/S0366-16442000000400014

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