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Caiophora coronata

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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 UUID64400e88ef251488966859
Scientific name Caiophora coronata
Authority Hook. & Arn.
First published in Bot. Misc. 3: 327. 1833

Description Top

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Synonyms Top

Scientific name Authority First published in
Loasa pilosa Meyen Observ. Bot. 1: 470 (1834)
Blumenbachia coronata Haage & Schmidt Rev. Hort. [Paris]. (1874) 58.
Caiophora absinthiifolia C.Presl Reliq. Haenk. 2: 41 (1831)
Caiophora pycnophylla Urb. & Gilg Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 76: 274 (1900)
Loasa coronata Gillies ex Arn. Edinburgh J. Nat. Geogr. Sci. 3: 274 (1831)

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-0000578565
Tropicos 50134084
KEW urn:lsid:ipni.org:names:1056723-2
The Plant List kew-2690211
Open Tree Of Life 148464
NCBI Taxonomy 310862
IPNI 545041-1
iNaturalist 704934
GBIF 4021135
EOL 5740282
CMAUP NPO13392

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
Warming impacts potential germination of non-native plants on the Antarctic Peninsula Bokhorst S, Convey P, Casanova-Katny A, Aerts R Commun Biol 25-Mar-2021
PMCID:PMC7994377
doi:10.1038/s42003-021-01951-3
PMID:33767327
Extreme Drought Affects Visitation and Seed Set in a Plant Species in the Central Chilean Andes Heavily Dependent on Hummingbird Pollination Arroyo MT, Robles V, Tamburrino Í, Martínez-Harms J, Garreaud RD, Jara-Arancio P, Pliscoff P, Copier A, Arenas J, Keymer J, Castro K Plants (Basel) 12-Nov-2020
PMCID:PMC7697181
doi:10.3390/plants9111553
PMID:33198222
A case of behavioural diversification in male floral function – the evolution of thigmonastic pollen presentation Henning T, Mittelbach M, Ismail SA, Acuña-Castillo RH, Weigend M Sci Rep 19-Sep-2018
PMCID:PMC6145904
doi:10.1038/s41598-018-32384-4
PMID:30232353
A first report of hydroxylated apatite as structural biomineral in Loasaceae – plants’ teeth against herbivores Ensikat HJ, Geisler T, Weigend M Sci Rep 19-May-2016
PMCID:PMC4872142
doi:10.1038/srep26073
PMID:27194462
Exploring the ontogenetic scaling hypothesis during the diversification of pollination syndromes in Caiophora (Loasaceae, subfam. Loasoideae) Strelin MM, Benitez-Vieyra S, Fornoni J, Klingenberg CP, Cocucci AA Ann Bot 06-Apr-2016
PMCID:PMC4845809
doi:10.1093/aob/mcw035
PMID:27056974
An Overview of Antimicrobial Properties of Different Classes of Phytochemicals Patra AK Dietary Phytochemicals and Microbes 18-Feb-2012
PMCID:PMC7121617
doi:10.1007/978-94-007-3926-0_1
Nectar, Floral Morphology and Pollination Syndrome in Loasaceae subfam. Loasoideae (Cornales) ACKERMANN M, WEIGEND M Ann Bot 01-Sep-2006
PMCID:PMC2803572
doi:10.1093/aob/mcl136
PMID:16820408
A novel antibacterial iridoid and triterpene from Caiophora coronata. Khera S, Woldemichael GM, Singh MP, Suarez E, Timmermann BN J Nat Prod 01-Dec-2003
doi:10.1021/NP030314A
PMID:14695811

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Larreatricin 26389403 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown via CMAUP database
Meso-3,3'-Didemethoxynectandrin B 14213224 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,4R,4aS,5S,7S,7aS)-5-hydroxy-7-(hydroxymethyl)-1-methoxy-4-methyl-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-3-one 3009696 Click to see CC1C2C(CC(C2C(OC1=O)OC)CO)O 230.26 unknown https://doi.org/10.1021/NP030314A
(1S,4R,5S,7S,7aS)-5-hydroxy-7-(hydroxymethyl)-1-methoxy-4-methyl-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-3-one 163195140 Click to see CC1C2C(CC(C2C(OC1=O)OC)CO)O 230.26 unknown https://doi.org/10.1021/NP030314A
(4aR,6S,7R,7aR)-6-hydroxy-7-methyl-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-3-one 44566204 Click to see CC1C(CC2C1COC(=O)C2)O 170.21 unknown https://doi.org/10.1021/NP030314A
(4aS,6S,7R,7aS)-6-hydroxy-7-methyl-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-3-one 10725829 Click to see CC1C(CC2C1COC(=O)C2)O 170.21 unknown https://doi.org/10.1021/NP030314A
5-hydroxy-7-(hydroxymethyl)-1-methoxy-4-methyl-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-3-one 78297594 Click to see CC1C2C(CC(C2C(OC1=O)OC)CO)O 230.26 unknown https://doi.org/10.1021/NP030314A
Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-hydroxy-7-methyl-, [4aR-(4aalpha,6alpha,7alpha,7aalpha)]-; (4aR,6S,7R,7aS)-Hexahydro-6-hydroxy-7-methylcyclopenta[c]pyran-3(1H)-one 13715189 Click to see CC1C(CC2C1COC(=O)C2)O 170.21 unknown https://doi.org/10.1021/NP030314A
Isoboonein 10899112 Click to see CC1C(CC2C1COC(=O)C2)O 170.21 unknown https://doi.org/10.1021/NP030314A
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10,12-dihydroxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 73797058 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C2C1C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP030314A
1beta,3beta-Dihydroxyurs-12-ene-27-oic acid 21574214 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C2C1C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP030314A
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2-Hydroxy-4-methoxyphenyl)-5-(3-hydroxypropyl)benzofuran 14213211 Click to see COC1=CC(=C(C=C1)C2=CC3=C(O2)C=CC(=C3)CCCO)O 298.30 unknown via CMAUP database
2-(4-hydroxyphenyl)-5-(E)-propenylbenzofuran 53483951 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)O 250.29 unknown via CMAUP database
2-(4-Methoxyphenyl)-5-(1-propenyl)benzofuran 91991396 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)OC 264.30 unknown via CMAUP database
4-[(2S,3R)-3-(hydroxymethyl)-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol 71460125 Click to see CC=CC1=CC2=C(C=C1)OC(C2CO)C3=CC=C(C=C3)O 282.30 unknown via CMAUP database
4-{5-[(1E)-prop-1-en-1-yl]-1-benzofuran-2-yl}benzene-1,3-diol 10355545 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)O 266.29 unknown via CMAUP database
5-(3-Hydroxypropyl)-2-(2-methoxy-4-hydroxyphenyl)benzofuran 14213209 Click to see COC1=C(C=CC(=C1)O)C2=CC3=C(O2)C=CC(=C3)CCCO 298.30 unknown via CMAUP database
Conocarpan 10999992 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown via CMAUP database
Eupomatenoid 6 6261723 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown via CMAUP database
Rataniaphenol I 6440631 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)OC)O 280.30 unknown via CMAUP database

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