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Hypericum reflexum

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 UUID6440216b21749792406305
Scientific name Hypericum reflexum
Authority L.f.
First published in Suppl. Pl. : 346 (1782)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Hypericum reflexum var. leiocladum Bornm. Bot. Jahrb. Syst. 33: 453 (1903)
Hypericum reflexum var. myrtillifolium Bornm. Bot. Jahrb. Syst. 33: 453 (1903)
Hypericum reflexum var. lanuginosum Pit. Iles Canaries : 133 (1908)

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

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-0000728222
USDA Plants HYRE7
Tropicos 7801206
KEW urn:lsid:ipni.org:names:433789-1
Open Tree Of Life 870722
Observations.org 141007
NCBI Taxonomy 673932
IPNI 433789-1
iNaturalist 628073
GBIF 4933132
Elurikkus 599514
USDA GRIN 407268
Wikipedia Hypericum_reflexum
CMAUP NPO12241

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
Potential Implications of Hyperoside on Oxidative Stress-Induced Human Diseases: A Comprehensive Review Wang K, Zhang H, Yuan L, Li X, Cai Y J Inflamm Res 13-Oct-2023
PMCID:PMC10581022
doi:10.2147/JIR.S418222
PMID:37854313
Application of single-cell multi-omics approaches in horticulture research Zhang J, Ahmad M, Gao H Mol Hortic 26-Sep-2023
PMCID:PMC10521458
doi:10.1186/s43897-023-00067-y
PMID:37789394
Bioactive Potential: A Pharmacognostic Definition through the Screening of Four Hypericum Species from the Canary Islands Lacret R, Puerta A, Granica S, González-Bakker A, Hevia D, Teng Y, Sánchez-Mateo CC, Pérez de Paz PL, Padrón JM Molecules 18-Sep-2022
PMCID:PMC9505652
doi:10.3390/molecules27186101
PMID:36144833
Intramolecular Tricarbonyl‐Ene Reactions and α‐Hydroxy‐β‐Diketone Rearrangements Inspired by the Biosynthesis of Polycyclic Polyprenylated Acylphloroglucinols zur Bonsen AB, Peralta RA, Fallon T, Huang DM, George JH Angew Chem Int Ed Engl 14-Jul-2022
PMCID:PMC9541541
doi:10.1002/anie.202203311
PMID:35680561
Occurrence and Distribution of Phytochemicals in the Leaves of 17 In vitro Cultured Hypericum spp. Adapted to Outdoor Conditions Kucharíková A, Kusari S, Sezgin S, Spiteller M, Čellárová E Front Plant Sci 27-Oct-2016
PMCID:PMC5081374
doi:10.3389/fpls.2016.01616
PMID:27833633
Prescribed Burning and Clear-Cutting Effects on Understory Vegetation in a Pinus canariensis Stand (Gran Canaria) Arévalo JR, Fernández-Lugo S, García-Domínguez C, Naranjo-Cigala A, Grillo F, Calvo L ScientificWorldJournal 24-Jul-2014
PMCID:PMC4134779
doi:10.1155/2014/215418
PMID:25147839
Systematic review of herbals as potential anti-inflammatory agents: Recent advances, current clinical status and future perspectives Beg S, Swain S, Hasan H, Barkat MA, Hussain MS Pharmacogn Rev 01-Jul-2011
PMCID:PMC3263046
doi:10.4103/0973-7847.91102
PMID:22279370
Characterizing the Metabolic Fingerprint and Anti-inflammatory Activity of Hypericum gentianoides Hillwig ML, Hammer KD, Birt DF, Wurtele ES J Agric Food Chem 31-May-2008
PMCID:PMC2701219
doi:10.1021/jf800411v
PMID:18512936
Spiroterpenoids from Hypericum reflexum Luz Cardona, José R. Pedro, Angel Serrano, M.Carmen Muñoz, Xavier Solans Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85046-T
Xanthones from Hypericum reflexum M.Luz Cardona, Isabel Fernández, José R. Pedro, Angel Serrano Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)87123-C

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 / Biphenyls and derivatives
4-(3,4,5-Trimethoxyphenyl)phenol 14757910 Click to see 260.28 unknown https://doi.org/10.1016/0031-9422(90)87123-C
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(3R,4R,5R,6S)-6-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]-4,5-dihydroxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 102445639 Click to see 624.60 unknown via CMAUP database
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Desrhamnosylverbascosaponin 102445401 Click to see 927.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Catalpol 91520 Click to see 362.33 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(2R,3S)-3-(4-hydroxy-3-methoxyphenyl)-2,5-dimethoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 162911711 Click to see 436.40 unknown https://doi.org/10.1016/0031-9422(90)87123-C
(2R,3S)-3-(4-hydroxy-3-methoxyphenyl)-2,5,10-trimethoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 163195498 Click to see 466.40 unknown https://doi.org/10.1016/0031-9422(90)87123-C
3-(4-Hydroxy-3-methoxyphenyl)-2,5-dimethoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 162911710 Click to see COC1C(OC2=C(C=C3C(=C2O1)OC4=CC=CC=C4C3=O)OC)C5=CC(=C(C=C5)O)OC 436.40 unknown https://doi.org/10.1016/0031-9422(90)87123-C
3-(4-Hydroxy-3-methoxyphenyl)-2,5,10-trimethoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 162927499 Click to see 466.40 unknown https://doi.org/10.1016/0031-9422(90)87123-C
Kielcorin 13834128 Click to see 436.40 unknown https://doi.org/10.1016/0031-9422(90)87123-C
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2,4-Dihydroxy-3,6-dimethoxyxanthone 14757912 Click to see COC1=CC2=C(C=C1)C(=O)C3=CC(=C(C(=C3O2)O)OC)O 288.25 unknown https://doi.org/10.1016/0031-9422(90)87123-C
3,4-Dihydroxy-2-methoxyxanthone 10038117 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)O 258.23 unknown https://doi.org/10.1016/0031-9422(90)87123-C
3,6-Dihydroxy-2-methoxyxanthen-9-one 14757913 Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(O2)C=C(C=C3)O)O 258.23 unknown https://doi.org/10.1016/0031-9422(90)87123-C
4-Hydroxy-2,3-dimethoxyxanthone 378690 Click to see 272.25 unknown https://doi.org/10.1016/0031-9422(90)87123-C
4-Hydroxy-2,3,6-trimethoxyxanthone 14757911 Click to see 302.28 unknown https://doi.org/10.1016/0031-9422(90)87123-C
9H-Xanthen-9-one, 3-hydroxy-2,4-dimethoxy- 12214333 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)OC)O 272.25 unknown https://doi.org/10.1016/0031-9422(90)87123-C
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
9-Hydroxy-3,3-dimethylpyrano[3,2-a]xanthen-12(3H)-one 14757908 Click to see 294.30 unknown https://doi.org/10.1016/0031-9422(90)87123-C
Hyperxanthone 14757909 Click to see 310.30 unknown https://doi.org/10.1016/0031-9422(90)87123-C
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(3aR,5R,5'S,6'S,6aR)-3,3,6a-trimethyl-6'-(2-methylpropanoyl)-5'-prop-1-en-2-ylspiro[3a,4-dihydrocyclopenta[c]furan-5,3'-oxane]-1,2',6-trione 162946399 Click to see 376.40 unknown https://doi.org/10.1016/0031-9422(93)85046-T
(3aS,5R,5'S,6'S,6aS)-3,3,6a-trimethyl-6'-(2-methylpropanoyl)-5'-prop-1-en-2-ylspiro[3a,4-dihydrocyclopenta[c]furan-5,3'-oxane]-1,2',6-trione 162946398 Click to see CC(C)C(=O)C1C(CC2(CC3C(OC(=O)C3(C2=O)C)(C)C)C(=O)O1)C(=C)C 376.40 unknown https://doi.org/10.1016/0031-9422(93)85046-T
3,3,6a-Trimethyl-6'-(2-methylpropanoyl)-5'-prop-1-en-2-ylspiro[3a,4-dihydrocyclopenta[c]furan-5,3'-oxane]-1,2',6-trione 162946397 Click to see CC(C)C(=O)C1C(CC2(CC3C(OC(=O)C3(C2=O)C)(C)C)C(=O)O1)C(=C)C 376.40 unknown https://doi.org/10.1016/0031-9422(93)85046-T
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Saccatoside 15736668 Click to see CC1C(C(C(C(O1)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O 654.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see 432.40 unknown via CMAUP database
Hesperidin 10621 Click to see 610.60 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database

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