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Arisarum vulgare

Arisarum vulgare - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Arisarum vulgare - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Arisarum vulgare - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fe80f220e6129185964
Scientific name Arisarum vulgare
Authority O.Targ.Tozz.
First published in Ann. Mus. Imp. Fis. Firenze 2(2): 67 (1810)

Description Top

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Synonyms Top

Scientific name Authority First published in
Arisarum arisarum Huth Helios 11: 133 (1893)
Arisarum balansae Schott Oesterr. Bot. Wochenbl. 7: 190. 1857 (1857)
Arisarum latifolium Hill Brit. Herb. : 336 (1756)
Arisarum serpentrium Raf. Fl. Tellur. 3: 63. 1837 (1837)
Arum arisarum L. Sp. Pl. : 966 (1753)
Arum calyptrale Salisb. Prodr. Stirp. Chap. Allerton : 261 (1796)
Arum libani Schott Prodr. Syst. Aroid. 21. 1860 (1860)
Balmisa vulgaris Lag. Gen. Sp. Pl. : 17 (1816)
Arisarum vulgare var. veslingii (Schott) Nyman Consp. Fl. Eur. 756. 1882
Arisarum vulgare subsp. veslingii (Schott) K.Richt. Pl. Eur. 1: 174. 1890 (1890)

Common names Top

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Language Common/alternative name
English friar's cowl
Spanish dragontea menor
Arabic شوف
Arabic لنس
Arabic صراخة
Arabic صرين شائع
Arabic ودن الشايب
Arabic ذريرة الشحم
ary أڭرني
Catalan rapa de frare
co ghjallina
Czech áronovec obecný
German krummstab
Greek Αρίσαρον το κοινό
Finnish kypärämunkinhiippa
French capuchon de moine
Hebrew לופית מצויה
Hebrew מטה אהרון
Hebrew מטה אהרן
Kabyle abeqquq n wuccen
Dutch gekapperde kalfsvoet
Portuguese candeias

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Arisarum vulgare subsp. clusii (Schott) K.Richt. Pl. Eur. 1: 174 (1890)
Arisarum vulgare subsp. hastatum (Pomel) Dobignard J. Bot. Soc. Bot. France 46-47: 108 (2009)
Arisarum vulgare subsp. vulgare Unknown

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
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000275694
Tropicos 2105364
INPN 83755
KEW urn:lsid:ipni.org:names:85902-1
The Plant List kew-15835
Open Tree Of Life 974712
Observations.org 106913
NCBI Taxonomy 267624
IPNI 85902-1
iNaturalist 82619
GBIF 2867495
Freebase /m/0h1f62r
EPPO AAUVU
EOL 1134151
USDA GRIN 4021
Wikipedia Arisarum_vulgare
CMAUP NPO11241
PFAF Arisarum vulgare

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
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids Xu FF, Chen JQ, Shao DY, Huang PQ Nat Commun 06-Oct-2023
PMCID:PMC10558451
doi:10.1038/s41467-023-41846-x
PMID:37803030
Recent insights about pyrrolidine core skeletons in pharmacology Poyraz S, Döndaş HA, Döndaş NY, Sansano JM Front Pharmacol 06-Sep-2023
PMCID:PMC10512268
doi:10.3389/fphar.2023.1239658
PMID:37745071
Natural Medicine a Promising Candidate in Combating Microbial Biofilm Shamim A, Ali A, Iqbal Z, Mirza MA, Aqil M, Kawish SM, Siddiqui A, Kumar V, Naseef PP, Alshadidi AA, Saheer Kuruniyan M Antibiotics (Basel) 02-Feb-2023
PMCID:PMC9952808
doi:10.3390/antibiotics12020299
PMID:36830210
A Quantitative Study on the Ethnobotanical Knowledge about Wild Edible Plants among the Population of Messiwa Ghanimi R, Ouhammou A, Babahmad RA, Cherkaoui M Ethiop J Health Sci 01-Nov-2022
PMCID:PMC9692160
doi:10.4314/ejhs.v32i6.22
PMID:36475263
Ethnobotanical study on wild edible plants traditionally used by Messiwa people, Morocco Ghanimi R, Ouhammou A, Ahouach A, Cherkaoui M J Ethnobiol Ethnomed 15-Mar-2022
PMCID:PMC8922891
doi:10.1186/s13002-022-00500-4
PMID:35292058
Phytocompound Mediated Blockage of Quorum Sensing Cascade in ESKAPE Pathogens Ghosh S, Lahiri D, Nag M, Dey A, Pandit S, Sarkar T, Pati S, Abdul Kari Z, Ishak AR, Edinur HA, Ray RR Antibiotics (Basel) 05-Jan-2022
PMCID:PMC8773049
doi:10.3390/antibiotics11010061
PMID:35052938
Ethnobotany of the Aegadian Islands: safeguarding biocultural refugia in the Mediterranean La Rosa A, Cornara L, Saitta A, Salam AM, Grammatico S, Caputo M, La Mantia T, Quave CL J Ethnobiol Ethnomed 28-Jul-2021
PMCID:PMC8320050
doi:10.1186/s13002-021-00470-z
PMID:34321030
Potential Toxicity of Medicinal Plants Inventoried in Northeastern Morocco: An Ethnobotanical Approach Kharchoufa L, Bouhrim M, Bencheikh N, Addi M, Hano C, Mechchate H, Elachouri M Plants (Basel) 31-May-2021
PMCID:PMC8226742
doi:10.3390/plants10061108
PMID:34072709
Reductive Functionalization of Amides in Synthesis and for Modification of Bioactive Compounds Czerwiński PJ, Furman B Front Chem 26-Apr-2021
PMCID:PMC8107389
doi:10.3389/fchem.2021.655849
PMID:33981672
Herbal Medicine Used in the Treatment of Human Diseases in the Rif, Northern Morocco Chaachouay N, Douira A, Zidane L Arab J Sci Eng 07-Apr-2021
PMCID:PMC8024440
doi:10.1007/s13369-021-05501-1
PMID:33842189
Floristic and Vegetation Changes on a Small Mediterranean Island over the Last Century Sciandrello S, Cambria S, Giusso del Galdo G, Guarino R, Minissale P, Pasta S, Tavilla G, Cristaudo A Plants (Basel) 01-Apr-2021
PMCID:PMC8065674
doi:10.3390/plants10040680
PMID:33916121
Ecological and Plant Community Implication on Essential Oils Composition in Useful Wild Officinal Species: A Pilot Case Study in Apulia (Italy) Perrino EV, Valerio F, Gannouchi A, Trani A, Mezzapesa G Plants (Basel) 18-Mar-2021
PMCID:PMC8002985
doi:10.3390/plants10030574
PMID:33803659
Amino acid–derived defense metabolites from plants: A potential source to facilitate novel antimicrobial development Parthasarathy A, Borrego EJ, Savka MA, Dobson RC, Hudson AO J Biol Chem 19-Feb-2021
PMCID:PMC8024917
doi:10.1016/j.jbc.2021.100438
PMID:33610552
Natural Anti-biofilm Agents: Strategies to Control Biofilm-Forming Pathogens Mishra R, Panda AK, De Mandal S, Shakeel M, Bisht SS, Khan J Front Microbiol 29-Oct-2020
PMCID:PMC7658412
doi:10.3389/fmicb.2020.566325
PMID:33193155

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
> Alkaloids and derivatives
(2R,3R,6S)-2-methyl-6-(9-phenylnonyl)piperidin-3-ol 10925178 Click to see CC1C(CCC(N1)CCCCCCCCCC2=CC=CC=C2)O 317.50 unknown https://doi.org/10.1055/S-2006-957490
https://doi.org/10.1080/10575639508043196
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Dehydrodigallic acid 14057208 Click to see C1=C(C=C(C(=C1O)O)OC2=C(C(=C(C=C2C(=O)O)O)O)O)C(=O)O 338.22 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
(2R)-2-[9-(2-methoxyphenyl)nonyl]-1-methylpyrrolidine 53921662 Click to see CN1CCCC1CCCCCCCCCC2=CC=CC=C2OC 317.50 unknown https://doi.org/10.1055/S-2006-957490
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
methyl 2-[(2R,4aR,8aS)-8a-hydroperoxy-4a-methyl-8-methylidene-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoate 162856359 Click to see CC12CCCC(=C)C1(CC(CC2)C(=C)C(=O)OC)OO 280.36 unknown https://doi.org/10.1055/S-2006-957490
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
(2R)-1-Methyl-2-(9-phenylnonyl)pyrrolidine 461558 Click to see CN1CCCC1CCCCCCCCCC2=CC=CC=C2 287.50 unknown https://doi.org/10.1055/S-2006-957490
https://doi.org/10.1016/S0041-0101(99)00232-9
https://doi.org/10.1021/NP50085A016
https://doi.org/10.1080/10575639308043815
https://doi.org/10.1080/10575639508043196
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
(2R)-1-methyl-2-tetradecylpyrrolidine 461557 Click to see CCCCCCCCCCCCCCC1CCCN1C 281.50 unknown https://doi.org/10.1080/10575639508043196
https://doi.org/10.1021/NP50085A016
https://doi.org/10.1080/10575639308043815
https://doi.org/10.1016/S0378-4274(98)00375-0
https://doi.org/10.1055/S-2006-957490
(2S)-1-methyl-2-tetradecylpyrrolidine 11196781 Click to see CCCCCCCCCCCCCCC1CCCN1C 281.50 unknown https://doi.org/10.1016/S0944-7113(00)80087-2
2-tetradecyl 1-N-methylpyrrolidine 24796983 Click to see CCCCCCCCCCCCCCC1CCCN1C 281.50 unknown https://doi.org/10.1016/S0378-4274(98)00375-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol 3,7-di-O-sulfate 12988285 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)O)O)OS(=O)(=O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
Tamarixetin 5281699 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
[5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-3-sulfonatooxychromen-7-yl] sulfate 21676171 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)[O-])O)OS(=O)(=O)[O-])O 474.40 unknown via CMAUP database

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