Peucedanum ostruthium

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff77bba1ff161973984
Scientific name	Peucedanum ostruthium
Authority	W.D.J.Koch
First published in	Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 12(1): 95 (1824)

Description Top

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Peucedanum ostruthium, also known as masterwort, is a flowering plant in the Apiaceae family. It is primarily found in the mountains of Central and Southern Europe, but has been introduced and cultivated in other regions. The plant is commonly used as a flavoring for liqueurs and bitters, and has been used in traditional Austrian medicine for various ailments. It contains several coumarins, which have been found to have medicinal properties.

Synonyms Top

Scientific name	Authority	First published in
Ostruthium officinale	Link	Handbuch 1: 360 (1829)
Selinum ostruthium	Wallr.	Annus Bot. : 41 (1815)
Selinum imperatoria	Crantz	Stirp. Austr. Fasc. 3: 42 (1767)
Angelica officinalis	Bernh.	Syst. Verz. Erf. : 170 (1800)
Angelica ostruthium	(L.) Lag.	Elench. Pl. : 2 (1816)
Imperatoria aromatica	Salisb.	Prodr. Stirp. Chap. Allerton : 167 (1796)
Imperatoria major	Lam.	Fl. Franç. 3: 417 (1779)
Imperatoria major	Gray	Nat. Arr. Brit. Pl. 2: 519 (1821 publ. 1822)
Imperatoria ostruthium	L.	Sp. Pl. : 259 (1753)
Imperatoria trilobata	Gilib.	Fl. Lit. Inch. 2: 34 (1782)
Imperatoria triternata	Viv. ex DC.	Prodr. 4: 183 (1830)

Common names Top

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Filter by language:

Language	Common/alternative name
English	masterwort
Arabic	شمار الخنازير
Arabic	بقلة الرئيس
Arabic	بوسيدان
Arabic	بخور الأكراد
Arabic	جاوى بري
Arabic	جاوى
Arabic	بقلة الإمبراطور
Belarusian	дзікая пятрушка настуркавая
Czech	všedobr horský
Welsh	ffenigl-y-moch gwridog
German	meisterwurz
Esperanto	pufa peŭcedano
Persian	پوسدانوم استراثیوم
Finnish	rohtosuoputki
French	impératoire
Norwegian Bokmål	mesterrot
Norwegian Nynorsk	meisterrot
Polish	gorysz miarz
Russian	Горичник настурциевый
Swedish	mästerrot
Turkish	kral otu
Chinese	紫前胡
Chinese	欧前胡

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

Europe click to expand
- Eastern Europe
  - Central European Russia
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Norway
  - Sweden
- Southeastern Europe
  - Italy
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Spain

Northern America click to expand
- Eastern Canada
  - Nova Scotia
  - Ontario
- Northeastern U.S.A.
  - Michigan
  - New York
  - Pennsylvania
  - West Virginia
- Southeastern U.S.A.
  - Maryland

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000391825
UNII	COD0P9B680
Canadensys	10086
USDA Plants	PEOS2
Tropicos	1700185
KEW	urn:lsid:ipni.org:names:846311-1
The Plant List	kew-2403688
Open Tree Of Life	435990
Observations.org	136958
NCBI Taxonomy	52477
NBN Atlas	NHMSYS0000461648
Nature Serve	2.139413
IPNI	846311-1
iNaturalist	166549
GBIF	3034230
Freebase	/m/06_7dv
EPPO	PCDOS
USDA GRIN	27463
Wikipedia	Peucedanum_ostruthium
CMAUP	NPO6125

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

Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing

Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S

J Nanobiotechnology

27-Apr-2024

PMCID:	PMC11056076
doi:	10.1186/s12951-024-02491-8
PMID:	38678271

Pathophysiology and management of testicular ischemia/reperfusion injury: Lessons from animal models

Akhigbe RE, Odetayo AF, Akhigbe TM, Hamed MA, Ashonibare PJ

Heliyon

21-Apr-2024

PMCID:	PMC11058307
doi:	10.1016/j.heliyon.2024.e27760
PMID:	38694115

Color polymorphism and mating trends in a population of the alpine leaf beetle Oreina gloriosa

Roggero A, Alù D, Laini A, Rolando A, Palestrini C

PLoS One

26-Mar-2024

PMCID:	PMC10965098
doi:	10.1371/journal.pone.0298330
PMID:	38530852

Apium extract alleviates indomethacin-induced gastric ulcers in rats via modulating the VEGF and IK-κB/NF-κB p65 signaling pathway: insights from in silico and in vivo investigations

Abu-Baih DH, Gomaa AA, Abdel-Wahab NM, Abdelaleem ER, Zaher AM, Hassan NF, Bringmann G, Abdelmohsen UR, Altemani FH, Algehainy NA, Mokhtar FA, Abdelwahab MF

BMC Complement Med Ther

14-Feb-2024

PMCID:	PMC10865661
doi:	10.1186/s12906-023-04333-w
PMID:	38355510

A critical overview of challenging roles of medicinal plants in improvement of wound healing technology

Pathak D, Mazumder A

Daru

15-Jan-2024

PMCID:	PMC11087437
doi:	10.1007/s40199-023-00502-x
PMID:	38225520

Historical Ethnobotany: Interpreting the Old Records

Kalle R, Sõukand R

Plants (Basel)

25-Oct-2023

PMCID:	PMC10649014
doi:	10.3390/plants12213673
PMID:	37960030

Biochemometry identifies ostruthin as pluripotent antimicrobial and anthelmintic agent from masterwort

Zwirchmayr J, Cruz CD, Grienke U, Tammela P, Rollinger JM

iScience

03-Aug-2023

PMCID:	PMC10457539
doi:	10.1016/j.isci.2023.107523
PMID:	37636068

Effects of bergapten on the pharmacokinetics of macitentan in rats both in vitro and in vivo

Xu J, Zhou Q, Hou P, Wang Y, Geng P, Lu Z, Zhou Y, Dai D, Wang S

Front Pharmacol

10-Jul-2023

PMCID:	PMC10363979
doi:	10.3389/fphar.2023.1204649
PMID:	37492094

Temporal Changes in the Use of Wild Medicinal Plants in Trentino–South Tyrol, Northern Italy

Mattalia G, Graetz F, Harms M, Segor A, Tomarelli A, Kieser V, Zerbe S, Pieroni A

Plants (Basel)

19-Jun-2023

PMCID:	PMC10301116
doi:	10.3390/plants12122372
PMID:	37375997

Understanding old herbal secrets: The renaissance of traditional medicinal plants beyond the twenty classic species?

Scherrer MM, Zerbe S, Petelka J, Säumel I

Front Pharmacol

24-Mar-2023

PMCID:	PMC10079881
doi:	10.3389/fphar.2023.1141044
PMID:	37033626

Antioxidant Biomaterials in Cutaneous Wound Healing and Tissue Regeneration: A Critical Review

Fadilah NI, Phang SJ, Kamaruzaman N, Salleh A, Zawani M, Sanyal A, Maarof M, Fauzi MB

Antioxidants (Basel)

23-Mar-2023

PMCID:	PMC10198372
doi:	10.3390/antiox12040787
PMID:	37107164

Restoration of Vegetation Greenness and Possible Changes in Mature Forest Communities in Two Forests Damaged by the Vaia Storm in Northern Italy

Giupponi L, Leoni V, Pedrali D, Giorgi A

Plants (Basel)

19-Mar-2023

PMCID:	PMC10059996
doi:	10.3390/plants12061369
PMID:	36987057

Identification of Natural Products Inhibiting SARS-CoV-2 by Targeting Viral Proteases: A Combined in Silico and in Vitro Approach

Wasilewicz A, Kirchweger B, Bojkova D, Abi Saad MJ, Langeder J, Bütikofer M, Adelsberger S, Grienke U, Cinatl Jr. J, Petermann O, Scapozza L, Orts J, Kirchmair J, Rabenau HF, Rollinger JM

J Nat Prod

18-Jan-2023

PMCID:	PMC9885530
doi:	10.1021/acs.jnatprod.2c00843
PMID:	36651644

“Cow Healers Use It for Both Horses and Cattle”: The Rise and Fall of the Ethnoveterinary Use of Peucedanum ostruthium (L.) Koch (fam. Apiaceae) in Sweden

de Vahl E, Mattalia G, Svanberg I

Plants (Basel)

26-Dec-2022

PMCID:	PMC9823300
doi:	10.3390/plants12010116
PMID:	36616243

From Biodiversity to Musketry: Detection of Plant Diversity in Pre-Industrial Peloponnese during the Flora Graeca Expedition

Chimona C, Papadopoulou S, Kolyva F, Mina M, Rhizopoulou S

Life (Basel)

23-Nov-2022

PMCID:	PMC9785030
doi:	10.3390/life12121957
PMID:	36556322

Phytochemical Profile Top

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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
> Lignans, neolignans and related compounds / Aryltetralin lignans
Otobain	442928	Click to see CC1CC2=C(C(C1C)C3=CC4=C(C=C3)OCO4)C5=C(C=C2)OCO5	324.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2,3-Dimethylacrylic acid, (Z)-	643915	Click to see CC=C(C)C(=O)O	100.12	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(1S,2S,4S,5S,6S,7S,8S,9R,12R)-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecane-4,5,7,8,12-pentol	162992540	Click to see CC1CC(C(C2(C13C(C(C(C2O)O)C(O3)(C)C)O)CO)O)O	318.36	unknown	https://doi.org/10.1016/0031-9422(75)85329-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one	5357655	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C	298.40	unknown	https://doi.org/10.1002/ARDP.19092470335 https://doi.org/10.1002/JLAC.19324950112 https://doi.org/10.1055/S-2003-38876 https://doi.org/10.1007/BF02066241 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/
Ostruthin	5281420	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C	298.40	unknown	https://doi.org/10.1002/ARDP.19092470335 https://doi.org/10.1002/JLAC.19324950112 https://doi.org/10.1055/S-2003-38876 https://doi.org/10.1016/0378-8741(86)90156-X https://doi.org/10.1007/BF02066241 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Onopordopicrin	5281490	Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)CO)C(=C)C(=O)O2)CO	348.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Taraxasterol	115250	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	via CMAUP database
Taraxasterol Acetate	13889352	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Peucenin	68477	Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)CC=C(C)C)O	260.28	unknown	https://doi.org/10.1007/BF02066241
> Organoheterocyclic compounds / Isobenzofurans
(E)-3-Butylidene-4,5-dihydroisobenzofuran-1(3H)-one	5877292	Click to see CCCC=C1C2=C(C=CCC2)C(=O)O1	190.24	unknown	https://doi.org/10.1055/S-2007-969639
3-N-Butyl-4,5-dihydrophthalide	173843	Click to see CCCCC1C2=C(C=CCC2)C(=O)O1	192.25	unknown	https://doi.org/10.1055/S-2007-969639
Cnidilide	160710	Click to see CCCCC1C2CCC=CC2C(=O)O1	194.27	unknown	https://doi.org/10.1055/S-2007-969639
Ligustilide	5319022	Click to see CCCC=C1C2=C(C=CCC2)C(=O)O1	190.24	unknown	https://doi.org/10.1055/S-2007-969639
Senkyunolide A	3085257	Click to see CCCCC1C2=C(C=CCC2)C(=O)O1	192.25	unknown	https://doi.org/10.1055/S-2007-969639
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol	10228	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C	244.28	unknown	https://doi.org/10.1002/JLAC.19324950112 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1016/0378-8741(86)90156-X https://doi.org/10.1002/ARDP.19092470335 https://doi.org/10.1007/BF02066241
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin	928465	Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C	286.28	unknown	https://doi.org/10.1007/BF02066241 https://doi.org/10.1002/ARDP.19092470335 https://doi.org/10.1002/ARDP.19082460604
[(2R)-3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] (E)-2-methylbut-2-enoate	87778077	Click to see CC=C(C)C(=O)OC(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C(C)(C)O	386.40	unknown	https://doi.org/10.1002/ARDP.19092470335
[(2R)-3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] 2-methylbut-2-enoate	164711	Click to see CC=C(C)C(=O)OC(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C(C)(C)O	386.40	unknown	https://doi.org/10.1002/ARDP.19092470335
[(3R)-3-hydroxy-2-methyl-4-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] acetate	102247135	Click to see CC(=O)OC(C)(C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O	346.30	unknown	https://doi.org/10.1016/0031-9422(96)00176-8
[3-Hydroxy-2-methyl-4-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] acetate	162940098	Click to see CC(=O)OC(C)(C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O	346.30	unknown	https://doi.org/10.1016/0031-9422(96)00176-8
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] 2-methylbut-2-enoate	73291529	Click to see CC=C(C)C(=O)OC(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C(C)(C)O	386.40	unknown	https://doi.org/10.1007/BF02066241 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/
4-(2,3-Dihydroxy-3-Methylbutoxy)Furo(3,2-G)Chromen-7-One	483513	Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O	304.29	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1007/BF02066241
4-[(2S)-3-hydroxy-3-methyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutoxy]furo[3,2-g]chromen-7-one	162920202	Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)OC4C(C(C(C(O4)CO)O)O)O)O	466.40	unknown	https://doi.org/10.1016/S0031-9422(00)98671-0
4-[(3,3-Dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one	160544	Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C	286.28	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1007/BF02066241 https://doi.org/10.1002/ARDP.19092470335 https://doi.org/10.1002/ARDP.19082460604
4-[3-Hydroxy-3-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutoxy]furo[3,2-g]chromen-7-one	162920201	Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)OC4C(C(C(C(O4)CO)O)O)O)O	466.40	unknown	https://doi.org/10.1016/S0031-9422(00)98671-0
Isoimperatorin	68081	Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C	270.28	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/
Isooxypeucedanin	625383	Click to see CC(C)C(=O)COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	286.28	unknown	https://doi.org/10.1016/0031-9422(75)85329-5
Ostruthol	6441273	Click to see CC=C(C)C(=O)OC(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C(C)(C)O	386.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1007/BF02066241
Oxypeucedanin hydrate	17536	Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O	304.29	unknown	https://doi.org/10.1016/0031-9422(75)85329-5 https://doi.org/10.1007/BF02066241 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/
Oxypseucedanin	33306	Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C	286.28	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/
Pentosalen	10212	Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C	270.28	unknown	https://doi.org/10.1055/S-2003-38876 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1002/PTR.2650080303
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
(E)-4-(7-hydroxy-2-oxochromen-6-yl)-2-methylbut-2-enoic acid	10106656	Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C(=O)O	260.24	unknown	https://doi.org/10.1016/0031-9422(96)00176-8
6-(3-Carboxybut-2-enyl)-7-hydroxycoumarin	54488943	Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C(=O)O	260.24	unknown	https://doi.org/10.1016/0031-9422(96)00176-8
> 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 / O-methylated flavonoids / 8-O-methylated flavonoids
5,7,3',4'-Tetrahydroxy-8-methoxyflavone	5316843	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)O	316.26	unknown	via CMAUP database

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Peucedanum ostruthium

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top