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

Contributors

Collections

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	جاوى بري
Arabic	جاوى
Arabic	بقلة الرئيس
Arabic	بقلة الإمبراطور
Belarusian	дзікая пятрушка настуркавая
Czech	všedobr horský
Welsh	ffenigl-y-moch gwridog
German	meisterwurz
Esperanto	pufa peŭcedano
Persian	پوسدانوم استراثیوم
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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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

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

Suggest others/fix!

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

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

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

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

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

In vivo anti-inflammatory activities of Plantago major extract and fractions and analysis of their phytochemical components using a high-resolution mass spectrometry

Triastuti A, Pradana DA, Setiawan ID, Fakhrudin N, Himmi SK, Widyarini S, Rohman A

Res Pharm Sci

29-Oct-2022

PMCID:	PMC9872180
doi:	10.4103/1735-5362.359433
PMID:	36704431

Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells

Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T

Molecules

09-Sep-2022

PMCID:	PMC9501561
doi:	10.3390/molecules27185858
PMID:	36144591

Anti-Inflammatory and Wound Healing Properties of Leaf and Rhizome Extracts from the Medicinal Plant Peucedanum ostruthium (L.) W. D. J. Koch

Danna C, Bazzicalupo M, Ingegneri M, Smeriglio A, Trombetta D, Burlando B, Cornara L

Molecules

02-Jul-2022

PMCID:	PMC9268734
doi:	10.3390/molecules27134271
PMID:	35807516

Plants with Therapeutic Potential for Ischemic Acute Kidney Injury: A Systematic Review

Ali A, Lima Sampaio T, Khan H, Jeandet P, Küpeli Akkol E, Bahadar H, Costa Martins AM

Evid Based Complement Alternat Med

23-May-2022

PMCID:	PMC9152371
doi:	10.1155/2022/6807700
PMID:	35656467

Interspecific and intraspecific analysis of Selinum spp. collected from Indian Himalayas using DNA barcoding

Srivastava RP, Saxena G, Singh L, Singh A, Verma PC, Kaur G

J Genet Eng Biotechnol

22-Apr-2022

PMCID:	PMC9033919
doi:	10.1186/s43141-022-00345-0
PMID:	35451659

Diverse in Local, Overlapping in Official Medical Botany: Critical Analysis of Medicinal Plant Records from the Historic Regions of Livonia and Courland in Northeast Europe, 1829–1895

Prakofjewa J, Anegg M, Kalle R, Simanova A, Prūse B, Pieroni A, Sõukand R

Plants (Basel)

13-Apr-2022

PMCID:	PMC9032843
doi:	10.3390/plants11081065
PMID:	35448792

Environmental variation drives the decoupling of leaf and root traits within species along an elevation gradient

Weemstra M, Roumet C, Cruz-Maldonado N, Anthelme F, Stokes A, Freschet GT

Ann Bot

11-Apr-2022

PMCID:	PMC9486920
doi:	10.1093/aob/mcac052
PMID:	35405006

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 / 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/10.1016/0378-8741(86)90156-X https://doi.org/10.1002/ARDP.19092470335 https://doi.org/10.1002/JLAC.19324950112 https://doi.org/10.1055/S-2003-38876 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1007/BF02066241
> 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/ARDP.19092470335 https://doi.org/10.1007/BF02066241 https://doi.org/10.1016/0378-8741(86)90156-X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1002/JLAC.19324950112
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
[(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://doi.org/10.1007/BF02066241 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1002/ARDP.19082460604 https://doi.org/10.1002/ARDP.19092470335
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	928465	Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C	286.28	unknown	https://doi.org/10.1002/ARDP.19082460604 https://doi.org/10.1002/ARDP.19092470335 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1016/0031-9422(75)85329-5 https://doi.org/10.1007/BF02066241
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122331/ https://doi.org/10.1055/S-2003-38876 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