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Crinodendron hookerianum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401406a266d344488470
Scientific name Crinodendron hookerianum
Authority Gay
First published in Fl. Chil. 1: 341 (1846)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Tricuspidaria lanceolata Miq. Linnaea 25: 650 (1853)
Tricuspidaria hookeriana R.O.Cunn. Notes Str. Magellan : 342 (1871)
Crinodendron eriocladum Gand. Bull. Soc. Bot. France 60: 457 (1913)

Common names Top

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Language Common/alternative name
English chilean lantern tree
Spanish chaquehua
Spanish chaquihue
Spanish chequehue
Spanish coicopio
Spanish coicopío
Spanish copio
Spanish copío
Spanish patagua roja
Hebrew שיח פנס צ'יליאני
Chinese 虎克百合木

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
      • Chile Central
      • Chile South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000626090
Tropicos 11700097
KEW urn:lsid:ipni.org:names:833692-1
The Plant List kew-2742768
Open Tree Of Life 881753
NCBI Taxonomy 112810
IPNI 833692-1
iNaturalist 430899
GBIF 4031017
Freebase /m/0bmdc3g
EPPO KRDHO
EOL 5408641
USDA GRIN 12211
Wikipedia Crinodendron_hookerianum

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Temperate rain forest species partition fine-scale gradients in light availability based on their leaf mass per area (LMA) Fajardo A, Siefert A Ann Bot 06-Sep-2016
PMCID:PMC5155601
doi:10.1093/aob/mcw184
PMID:27604280
The complete nucleotide sequence of the cassava (Manihot esculenta) chloroplast genome and the evolution of atpF in Malpighiales: RNA editing and multiple losses of a group II intron Daniell H, Wurdack KJ, Kanagaraj A, Lee SB, Saski C, Jansen RK Theor Appl Genet 24-Jan-2008
PMCID:PMC2587239
doi:10.1007/s00122-007-0706-y
PMID:18214421
Cucurbitacins and aromatic compounds from Crinodendron hookerianum Magalis Bittner, K.Angela Poyser, J.Philip Poyser, Mario Silva, Eduardo Weldt, Peter G. Sammes Elsevier BV 26-Jul-2002
doi:10.1016/0031-9422(73)80578-3

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 3,4-dihydroxy-5-methoxybenzoate 99622 Click to see COC1=CC(=CC(=C1O)O)C(=O)OC 198.17 unknown https://doi.org/10.1016/0031-9422(73)80578-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1016/0031-9422(73)80578-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(2R,8R,9S,10S,13R,14R,16R,17S)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2S,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 162975165 Click to see 534.70 unknown https://doi.org/10.1016/0031-9422(73)80578-3
(2S,3R,8R,9R,10R,13R,14R,16R,17R)-17-[(E,2S)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163036483 Click to see 518.70 unknown https://doi.org/10.1016/0031-9422(73)80578-3
(2S,3S,8R,9R,10R,13R,14R,16S,17R)-17-[(E,2S)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163189628 Click to see 518.70 unknown https://doi.org/10.1016/0031-9422(73)80578-3
17-(2,6-Dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 429242 Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)C=CC(C)(C)O)O)O)C)C)C)O)O)C 518.70 unknown https://doi.org/10.1016/0031-9422(73)80578-3
2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 4482416 Click to see 534.70 unknown https://doi.org/10.1016/0031-9422(73)80578-3

Gallery Top

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Contributors Top

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Collections Top

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