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Iphiona mucronata

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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 UUID643fcde3d66a3992942820
Scientific name Iphiona mucronata
Authority (Forssk.) Asch. & Schweinf.
First published in Mém. Inst. Égypte 2: 86. 1887 [10 Feb 1887] ; preprint

Description Top

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Synonyms Top

Scientific name Authority First published in
Alkibias mucronata Raf. Fl. Tellur. 4: 119 (1838)
Conyza pungens Lam. Encycl. 2: 86 (1786)
Iphiona spinosa DC. ex Steud. Nomencl. Bot. 1: 815 (1840)
Iphiona juniperifolia Cass. Dict. Sci. Nat., ed. 2. 23: 610 (1822)
Serratula spinosa Poir. ex DC. Prodr. 5: 475 (1836)
Chrysocoma mucronata Forssk. Fl. Aegypt.-Arab. : 147 (1775)
Serratula subulata Poir. Encycl. 6: 558 (1805)
Staehelina spinosa Vahl Symb. Bot. i. 69 (1790)
Iphiona dubia Cass. Bull. Sci. Soc. Philom. Paris (1817) 153

Common names Top

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Language Common/alternative name
Arabic ظفرة

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
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Western Asia
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000076430
Tropicos 2728560
KEW urn:lsid:ipni.org:names:226226-1
The Plant List gcc-33088
Open Tree Of Life 7051743
NCBI Taxonomy 2072397
IPNI 226226-1
iNaturalist 634032
GBIF 3125389

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
Polyphenols of the Inuleae-Inulinae and Their Biological Activities: A Review Malarz J, Michalska K, Stojakowska A Molecules 27-Apr-2024
PMCID:PMC11085778
doi:10.3390/molecules29092014
PMID:38731504
Pulicaria incisa (Lam.) DC. as a Potential Source of Antioxidant, Antibacterial, and Anti-Enzymatic Bioactive Molecules: Phytochemical Constituents, In Vitro and In Silico Pharmacological Analysis Alreshidi M, Abdulhakeem MA, Badraoui R, Amato G, Caputo L, De Martino L, Nazzaro F, Fratianni F, Formisano C, De Feo V, Snoussi M Molecules 05-Nov-2023
PMCID:PMC10648406
doi:10.3390/molecules28217439
PMID:37959858
Distinguishing features of Lycium L. species (family Solanaceae) distributed in Egypt based on their anatomical, metabolic, molecular, and ecological characteristics Ragab OG, Mamdouh D, Bedair R, Smetanska I, Gruda NS, Yousif SK, Omer RM, Althobaiti AT, Abd El-Raouf HS, El-Taher AM, El-Sayed AS, Eldemerdash MM Front Plant Sci 12-May-2023
PMCID:PMC10213676
doi:10.3389/fpls.2023.1162695
PMID:37251766
Iphiona mucronata (Forssk.) Asch. & Schweinf. A Comprehensive Phytochemical Study via UPLC-Q-TOF-MS in the Context of the Embryo- and Cytotoxicity Profiles Pecio Ł, Otify AM, Saber FR, El-Amier YA, Shalaby ME, Kozachok S, Elmotayam AK, Świątek Ł, Skiba A, Skalicka-Woźniak K Molecules 03-Nov-2022
PMCID:PMC9656354
doi:10.3390/molecules27217529
PMID:36364367
Effect of explant type (leaf, stem) and 2,4-D concentration on callus induction: influence of elicitor type (biotic, abiotic), elicitor concentration and elicitation time on biomass growth rate and costunolide biosynthesis in gazania (Gazania rigens) cell suspension cultures Mahood HE, Sarropoulou V, Tzatzani TT Bioresour Bioprocess 16-Sep-2022
PMCID:PMC10991164
doi:10.1186/s40643-022-00588-2
Impacts of Anthropogenic Disturbance on Vegetation Dynamics: A Case Study of Wadi Hagul, Eastern Desert, Egypt Bedair R, Ibrahim AA, Alyamani AA, Aloufi S, Ramadan S Plants (Basel) 14-Sep-2021
PMCID:PMC8466335
doi:10.3390/plants10091906
PMID:34579436
Interspecific variations in the habitats of Reichardia tingitana (L.) Roth leading to changes in its bioactive constituents and allelopathic activity Abd-ElGawad AM, El-Amier YA, Assaeed AM, Al-Rowaily SL Saudi J Biol Sci 25-Nov-2019
PMCID:PMC6933205
doi:10.1016/j.sjbs.2019.11.015
PMID:31889875
Endophytic Actinobacteria and the Interaction of Micromonospora and Nitrogen Fixing Plants Trujillo ME, Riesco R, Benito P, Carro L Front Microbiol 01-Dec-2015
PMCID:PMC4664631
doi:10.3389/fmicb.2015.01341
PMID:26648923
New Dehydrothymol Derivative from Iphiona mucronata Mohamed Metwally Walter de Gruyter GmbH 03-Mar-2015
doi:10.1515/ZNB-1985-1134
Sesquiterpene Xylosides from Iphiona mucronata Ahmed A. Ahmed, Ahmed A. Seif El-Din American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50070A047

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
> Benzenoids / Phenol esters
(4-Methoxy-5-methyl-2-prop-1-en-2-ylphenyl) 3-methylbutanoate 163071454 Click to see CC1=CC(=C(C=C1OC)C(=C)C)OC(=O)CC(C)C 262.34 unknown https://doi.org/10.1515/ZNB-1985-1134
[2-[(2R)-2-(acetyloxymethyl)oxiran-2-yl]-4-methoxy-5-methylphenyl] 3-methylbutanoate 162912182 Click to see CC1=CC(=C(C=C1OC)C2(CO2)COC(=O)C)OC(=O)CC(C)C 336.40 unknown https://doi.org/10.1515/ZNB-1985-1134
[2-[2-(Acetyloxymethyl)oxiran-2-yl]-4-methoxy-5-methylphenyl] 3-methylbutanoate 162912181 Click to see CC1=CC(=C(C=C1OC)C2(CO2)COC(=O)C)OC(=O)CC(C)C 336.40 unknown https://doi.org/10.1515/ZNB-1985-1134
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(2S,3R,4S,5R)-2-[2-[(3S,3aS,5R,7aS)-3-acetyl-3a-hydroxy-7a-methyl-2,3,4,5,6,7-hexahydro-1H-inden-5-yl]propan-2-yloxy]-4,5-dihydroxyoxan-3-yl] acetate 14756449 Click to see CC(=O)C1CCC2(C1(CC(CC2)C(C)(C)OC3C(C(C(CO3)O)O)OC(=O)C)O)C 428.50 unknown https://doi.org/10.1021/NP50070A047
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2S,3R,4S,5R)-2-[2-[(2R,4aR,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-yloxy]oxane-3,4,5-triol 163009944 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)OC3C(C(C(CO3)O)O)O)C 354.50 unknown https://doi.org/10.1021/NP50070A047
[(2S,3R,4S,5R)-2-[2-[(2R,4aR,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-yloxy]-4,5-dihydroxyoxan-3-yl] acetate 162857709 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)OC3C(C(C(CO3)O)O)OC(=O)C)C 396.50 unknown https://doi.org/10.1021/NP50070A047
[(2S,3R,4S,5R)-2-[2-[(2R,4aR,8aS)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]propan-2-yloxy]-4,5-dihydroxyoxan-3-yl] acetate 163003010 Click to see CC(=O)OC1C(C(COC1OC(C)(C)C2CCC3(CCCC(=C)C3C2)C)O)O 396.50 unknown https://doi.org/10.1021/NP50070A047
[(2S,3R,4S,5R)-2-[2-[(2R,4aR)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-yloxy]-4,5-dihydroxyoxan-3-yl] acetate 14756445 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)OC3C(C(C(CO3)O)O)OC(=O)C 396.50 unknown https://doi.org/10.1021/NP50070A047
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(2S,3R,4S,5R)-4,5-dihydroxy-2-[2-[(1R,4R)-4-methyl-3-oxo-4-(4-oxopentyl)cyclohexyl]propan-2-yloxy]oxan-3-yl] acetate 163048924 Click to see CC(=O)CCCC1(CCC(CC1=O)C(C)(C)OC2C(C(C(CO2)O)O)OC(=O)C)C 428.50 unknown https://doi.org/10.1021/NP50070A047

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