Industrial and craft applications:
- Hypericum aucheri is employed as a reference taxon in molecular phylogenetic studies of the genus Hypericum, providing nuclear ribosomal internal transcribed spacer (ITS) and chloroplast trnL‑F sequence data that support systematic research and comparative genomics within Hypericaceae.

Synonyms Top

Scientific name	Authority	First published in
Hypericum apterum	Velen.	Sitzungsber. Königl. Böhm. Ges. Wiss., Math.-Naturwiss. Cl. 1887: 443 (1888)
Hypericum jankae	Nyman	Consp. Fl. Eur. , Suppl. 2(1): 75 (1889)
Hypericum kazdaghense	Y.Gemici & E.Leblebici	Candollea 50: 46 (1995)
Hypericum aucheri var. aegeum	Rech.f.	Bot. Jahrb. Syst. 69: 463. 1939
Hypericum aucheri var. macranthum	D.Jord. & Kožuharov	in Fl. Rast. Res. Kaz. 4: 709 1970
Hypericum aucheri var. simplex	D.Jord. & Kožuharov	in Fl. Rast. Res. Kaz. 4: 709 1970
Hypericum aucheri f. minutum	D.Jord. & Kožuharov	in Fl. Rast. Res. Kaz. 4: 709 1970
Hypericum tenellum	Janka	Oesterr. Bot. Z. 22: 175 (1872)

Common names Top

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Filter by language:

Language	Common/alternative name
Bulgarian	аухерова звъника
Czech	třezalka aucherova

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Asia-temperate click to expand
- Western Asia
  - Turkey

Europe click to expand
- Southeastern Europe
  - Bulgaria
  - Greece
  - Turkey-in-Europe

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000727382
KEW	urn:lsid:ipni.org:names:433222-1
The Plant List	kew-2857768
Open Tree Of Life	4730066
Observations.org	118874
NCBI Taxonomy	1321321
IPNI	433222-1
GBIF	3715193
EPPO	HYPAW
EOL	5707308
Elurikkus	401224
Wikipedia	Hypericum_aucheri

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

Therapeutic potential of mangiferin in cancer: Unveiling regulatory pathways, mechanisms of action, and bioavailability enhancements – An updated review

Iqbal H, Inam‐Ur‐Raheem M, Munir S, Rabail R, Kafeel S, Shahid A, Mousavi Khaneghah A, Aadil RM

Food Sci Nutr

20-Dec-2023

PMCID:	PMC10916574
doi:	10.1002/fsn3.3869
PMID:	38455223

Co-Treatment of Caco-2 Cells with Doxorubicin and Gold Nanoparticles Produced from Cyclopia intermedia Extracts or Mangiferin Enhances Drug Effects

Aboyewa JA, Sibuyi NR, Goboza M, Murtz LA, Oguntibeju OO, Meyer M

Nanomaterials (Basel)

07-Nov-2022

PMCID:	PMC9654788
doi:	10.3390/nano12213918
PMID:	36364694

Natural Products Inhibitors of Monoamine Oxidases—Potential New Drug Leads for Neuroprotection, Neurological Disorders, and Neuroblastoma

Chaurasiya ND, Leon F, Muhammad I, Tekwani BL

Molecules

04-Jul-2022

PMCID:	PMC9268457
doi:	10.3390/molecules27134297
PMID:	35807542

Gold Nanoparticles Synthesized Using Extracts of Cyclopia intermedia, Commonly Known as Honeybush, Amplify the Cytotoxic Effects of Doxorubicin

Aboyewa JA, Sibuyi NR, Meyer M, Oguntibeju OO

Nanomaterials (Basel)

08-Jan-2021

PMCID:	PMC7826697
doi:	10.3390/nano11010132
PMID:	33429945

A Toxicological Evaluation of Mango Leaf Extract (Mangifera indica) Containing 60% Mangiferin

Reddeman RA, Glávits R, Endres JR, Clewell AE, Hirka G, Vértesi A, Béres E, Szakonyiné IP

J Toxicol

01-Aug-2019

PMCID:	PMC6699309
doi:	10.1155/2019/4763015
PMID:	31467524

Radical scavenging and antioxidant activities of methanolic extracts from Hypericum species growing in Bulgaria

Zheleva-Dimitrova D, Nedialkov P, Kitanov G

Pharmacogn Mag

05-May-2010

PMCID:	PMC2900065
doi:	10.4103/0973-1296.62889
PMID:	20668569

Biflavone, flavonol, and xanthone glycosides from Hypericum aucheri

G. M. Kitanov

Springer Science and Business Media LLC

24-Nov-2004

doi:	10.1007/BF00598599

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1007/BF00598599
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1007/BF00598599
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Isomangiferin	5318597	Click to see	422.30	unknown	https://doi.org/10.1007/BF00598599
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1007/BF00598599
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,4S,5R,6R)-6-[[(2S,3R)-5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	163002454	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O	496.40	unknown	https://doi.org/10.1007/BF00598599
6-(2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-4-Oxochromen-3-Yl)Oxy-3,4,5-Trihydroxyoxane-2-Carboxylic Acid	12004528	Click to see	478.40	unknown	https://doi.org/10.1007/BF00598599
6-[[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	163002453	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O	496.40	unknown	https://doi.org/10.1007/BF00598599
Querciturone	5274585	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1007/BF00598599
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2S,3R)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	162901081	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	482.40	unknown	https://doi.org/10.1007/BF00598599
(2S,3R)-5,7-dihydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	162884414	Click to see	466.40	unknown	https://doi.org/10.1007/BF00598599
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one	51402807	Click to see	464.40	unknown	https://doi.org/10.1007/BF00598599
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl)Oxy-Chromen-4-one	12304323	Click to see	464.40	unknown	https://doi.org/10.1007/BF00598599
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	https://doi.org/10.1007/BF00598599
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	40486293	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/10.1007/BF00598599
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside	5353915	Click to see	448.40	unknown	https://doi.org/10.1007/BF00598599
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00598599
5,7-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	73322072	Click to see	482.40	unknown	https://doi.org/10.1007/BF00598599
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00598599
Dihydromyricetin 3-rhamnoside	3754658	Click to see	466.40	unknown	https://doi.org/10.1007/BF00598599
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/10.1007/BF00598599
Myricetin 3-glucoside	44259426	Click to see	480.40	unknown	https://doi.org/10.1007/BF00598599
Myricitrin	5281673	Click to see	464.40	unknown	https://doi.org/10.1007/BF00598599

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Hypericum aucheri

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top