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Hypericum beanii

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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 UUID6440214919fb4745643342
Scientific name Hypericum beanii
Authority N.Robson
First published in J. Roy. Hort. Soc. 95: 490 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hypericum lagarocladum N.Robson Bull. Brit. Mus. (Nat. Hist.), Bot. 12: 247 (1985)
Hypericum patulum var. henryi Veitch ex Bean Gard. Chron. ser. 3, 38: 179. 1905

Common names Top

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Language Common/alternative name
Chinese 栽秧花
Chinese 赶山鞭
Chinese 黄花香

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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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

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Database ID/link to page
World Flora Online wfo-0000727403
USDA Plants HYBE3
Tropicos 7801284
KEW urn:lsid:ipni.org:names:433246-1
The Plant List kew-2857796
Missouri Botanical Garden 279230
Open Tree Of Life 811246
NCBI Taxonomy 268979
IPNI 433246-1
GBIF 3714996
EPPO HYPBE
EOL 2889762
USDA GRIN 104668
Wikipedia Hypericum_beanii

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
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
New secondary metabolites with cytotoxicity from fungus Penicillium roqueforti Mo S, Zhao Z, Ye Z, Huang Z, Zhang Y, Yang W, Wang J, Hu Z, Zhang Y Nat Prod Bioprospect 01-Jun-2023
PMCID:PMC10235286
doi:10.1007/s13659-023-00381-4
PMID:37261606
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
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL Chem Rev 09-Nov-2020
PMCID:PMC8183567
doi:10.1021/acs.chemrev.0c00922
PMID:33164487
Methicillin-resistant Staphylococcus aureus, Vancomycin-resistant Enterococcus faecalis and Enterococcus faecium active Dimeric Isobutyrylphloroglucinol from Ivesia gordonii Ahmed MH, Ibrahim MA, Zhang J, Melek FR, El-Hawary SS, Jacob MR, Muhammad I Nat Prod Commun 01-Feb-2014
PMCID:PMC4130393
PMID:24689296
Inhibition of Bacterial Growth and Biofilm Production by Constituents from Hypericum spp Sarkisian SA, Janssen MJ, Matta H, Henry GE, LaPlante KL, Rowley DC Phytother Res 15-Dec-2011
PMCID:PMC3339047
doi:10.1002/ptr.3675
PMID:22170780
Spirocyclic acylphloroglucinol derivatives from Hypericum beanii. Chen XQ, Li Y, Li KZ, Peng LY, He J, Wang K, Pan ZH, Cheng X, Li MM, Zhao QS, Xu G Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.1250
PMID:21963634
Dermatological remedies in the traditional pharmacopoeia of Vulture-Alto Bradano, inland southern Italy Quave CL, Pieroni A, Bennett BC J Ethnobiol Ethnomed 06-Feb-2008
PMCID:PMC2275234
doi:10.1186/1746-4269-4-5
PMID:18254949
Anti-staphylococcal acylphloroglucinols from Hypericum beanii. Shiu WK, Gibbons S Phytochemistry 01-Dec-2006
doi:10.1016/J.PHYTOCHEM.2006.09.037
PMID:17092525

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
> Alkaloids and derivatives / Strychnos alkaloids
[(1S,9S,10R,11R,17S)-12-[(E)-2-[(4S,12S,13R,16S,17S,18S,20S,21S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-21-yl]ethenyl]-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,12-tetraen-10-yl]methanol 162913727 Click to see CC1C2C3CC4C5(CCN4C2C=CC6=CN7CCC89C7CC6C(C8NC2=CC=CC=C92)CO)C(C3CO1)NC1=CC=CC=C51 588.80 unknown https://doi.org/10.1248/CPB.59.1250
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
(2,4-Dihydroxyphenyl)-[5-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]methanone 14162794 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=C(C=C(C=C3)O)O)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 514.50 unknown https://doi.org/10.1248/CPB.59.1250
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
5,9-Dimethyl-14-methylidene-2-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 162945795 Click to see CC12CCCC(C1CC(=O)C34C2CCC(C3)C(=C)C4)(C)C(=O)O 316.40 unknown https://doi.org/10.1248/CPB.59.1250
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1S,3S,3aS,4R,5S,8S,8aS)-3,8-dimethyl-5-propan-2-yl-1,2,3,3a,4,5,6,7,8,8a-decahydroazulene-1,4-diol 162962785 Click to see CC1CCC(C(C2C1C(CC2C)O)O)C(C)C 240.38 unknown https://doi.org/10.1248/CPB.59.1250
(1S,3S,3aS,5S,8aR)-3,8-dimethyl-4-methylidene-5-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulen-1-ol 163000214 Click to see CC1CC(C2C1C(=C)C(CC=C2C)C(C)C)O 234.38 unknown https://doi.org/10.1248/CPB.59.1250
1alphaH,5alphaH-Guaia-6-ene-4beta,10beta-diol 71773128 Click to see CC(C)C1=CC2C(CCC2(C)O)C(CC1)(C)O 238.37 unknown https://doi.org/10.1248/CPB.59.1250
Guaianediol 10243299 Click to see CC(C)C1=CC2C(CCC2(C)O)C(CC1)(C)O 238.37 unknown https://doi.org/10.1248/CPB.59.1250
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(E)-5-[(1S,2S,4aS,5S,8aR)-5-(acetyloxymethyl)-2,5,8a-trimethyl-2-[(2R,3S,4R,5S,6S)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enyl] acetate 163045401 Click to see CC(=CCOC(=O)C)CCC1C2(CCCC(C2CCC1(C)OC3C(C(C(C(O3)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)(C)COC(=O)C)C 738.90 unknown https://doi.org/10.1248/CPB.59.1250
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-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 12314479 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/J.PHYTOCHEM.2006.09.037
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.09.037
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.09.037
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxyxanthone 5376036 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O 212.20 unknown https://doi.org/10.1248/CPB.59.1250
1,2,5-Trihydroxyxanthone 10060362 Click to see C1=CC2=C(C(=C1)O)OC3=C(C2=O)C(=C(C=C3)O)O 244.20 unknown https://doi.org/10.1248/CPB.59.1250
1,3-Dihydroxy-6-methoxy-9H-xanthen-9-one 46866697 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)O)O 258.23 unknown https://doi.org/10.1248/CPB.59.1250
1,5-Dihydroxy-2-methoxyxanthone 5377509 Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C=CC=C3O)O 258.23 unknown https://doi.org/10.1248/CPB.59.1250
2,5-Dihydroxyxanthone 182216 Click to see C1=CC2=C(C(=C1)O)OC3=C(C2=O)C=C(C=C3)O 228.20 unknown https://doi.org/10.1248/CPB.59.1250
Alloathyriol 44575387 Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(C=C(C=C3O2)O)O)O 274.22 unknown https://doi.org/10.1248/CPB.59.1250
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.09.037
Montixanthone 86096014 Click to see COC1=CC(=CC2=C1C(=O)C3=CC(=C(C=C3O2)O)O)O 274.22 unknown https://doi.org/10.1248/CPB.59.1250
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Ugaxanthone 5321880 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=C(C=C3)O)O)C 328.30 unknown https://doi.org/10.1248/CPB.59.1250
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R,4R)-2-(4-hydroxyphenyl)-6-[(2S,3R,4S)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7,8-tetrol 101193697 Click to see C1=CC(=CC=C1C2C(C(C3=C(O2)C(=C(C=C3)O)O)C4=CC5=C(C(=C4O)O)OC(C(C5O)O)C6=CC=C(C=C6)O)O)O 562.50 unknown https://doi.org/10.1248/CPB.59.1250
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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/10.1248/CPB.59.1250
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/10.1248/CPB.59.1250
Quercetin 3-O-rhamnoside 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/10.1248/CPB.59.1250
Quercitrin 5280459 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/10.1248/CPB.59.1250

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