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Warionia saharae

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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 UUID643fc7e80ebd5591496320
Scientific name Warionia saharae
Authority Benth. & Coss.
First published in Bull. Soc. Bot. France 19: 166 (1873)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Italian warioniinae

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000018332
Tropicos 50044200
KEW urn:lsid:ipni.org:names:260137-1
The Plant List gcc-117726
Open Tree Of Life 633840
Observations.org 313422
NCBI Taxonomy 40727
IPNI 260137-1
iNaturalist 467542
GBIF 3130270
USDA GRIN 41958

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
Sacha Inchi (Plukenetia volubilis L.) Oil Improves Hepatic Insulin Sensitivity and Glucose Metabolism through Insulin Signaling Pathway in a Rat Model of Type 2 Diabetes Rojanaverawong W, Wongmanee N, Hanchang W Prev Nutr Food Sci 31-Mar-2023
PMCID:PMC10103599
doi:10.3746/pnf.2023.28.1.30
PMID:37066030
Volatile Organic Compound Profiles From Wheat Diseases Are Pathogen-Specific and Can Be Exploited for Disease Classification Ficke A, Asalf B, Norli HR Front Microbiol 07-Jan-2022
PMCID:PMC8776713
doi:10.3389/fmicb.2021.803352
PMID:35069508
Chemical Composition and Antioxidant, Anti-Inflammatory, and Enzyme Inhibitory Activities of an Endemic Species from Southern Algeria: Warionia saharae Rechek H, Haouat A, Hamaidia K, Allal H, Boudiar T, Pinto DC, Cardoso SM, Bensouici C, Soltani N, Silva AM Molecules 30-Aug-2021
PMCID:PMC8434534
doi:10.3390/molecules26175257
PMID:34500690
Ethnobotanical and ethnomedicinal analysis of wild medicinal plants traditionally used in Naâma, southwest Algeria Bouafia M, Amamou F, Gherib M, Benaissa M, Azzi R, Nemmiche S Vegetos 11-Jun-2021
PMCID:PMC8192681
doi:10.1007/s42535-021-00229-7
PMID:34131369
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
Drying Effects on Chemical Composition and Antioxidant Activity of Lippia thymoides Essential Oil, a Natural Source of Thymol do Nascimento LD, Silva SG, Cascaes MM, da Costa KS, Figueiredo PL, Costa CM, Andrade EH, de Faria LJ Molecules 30-Apr-2021
PMCID:PMC8124978
doi:10.3390/molecules26092621
PMID:33946153
Important Flavonoids and Their Role as a Therapeutic Agent Ullah A, Munir S, Badshah SL, Khan N, Ghani L, Poulson BG, Emwas AH, Jaremko M Molecules 11-Nov-2020
PMCID:PMC7697716
doi:10.3390/molecules25225243
PMID:33187049
Essential Oils as Potential Alternative Biocontrol Products against Plant Pathogens and Weeds: A Review Raveau R, Fontaine J, Lounès-Hadj Sahraoui A Foods 21-Mar-2020
PMCID:PMC7143296
doi:10.3390/foods9030365
PMID:32245234
Flavonoid-Enriched Extract from Desert Plant Warionia saharae Improves Glucose and Cholesterol Levels in Diabetic Rats Ajebli M, Eddouks M Cardiovasc Hematol Agents Med Chem 01-May-2019
PMCID:PMC6875866
doi:10.2174/1871525717666190121143934
PMID:30666919
Antimicrobial Properties of Plant Essential Oils against Human Pathogens and Their Mode of Action: An Updated Review Swamy MK, Akhtar MS, Sinniah UR Evid Based Complement Alternat Med 20-Dec-2016
PMCID:PMC5206475
doi:10.1155/2016/3012462
PMID:28090211
Medicinal importance, pharmacological activities, and analytical aspects of hispidulin: A concise report Patel K, Patel DK J Tradit Complement Med 10-Dec-2016
PMCID:PMC5506639
doi:10.1016/j.jtcme.2016.11.003
PMID:28725632
Nerolidol: A Sesquiterpene Alcohol with Multi-Faceted Pharmacological and Biological Activities Chan WK, Tan LT, Chan KG, Lee LH, Goh BH Molecules 28-Apr-2016
PMCID:PMC6272852
doi:10.3390/molecules21050529
PMID:27136520
Sesquiterpene Lactones from Gynoxys verrucosa and their Anti-MRSA Activity Ordóñez PE, Quave CL, Reynolds WF, Varughese KI, Berry B, Breen PJ, Malagón O, Smeltzer MS, Compadre CM J Ethnopharmacol 12-Jul-2011
PMCID:PMC3159821
doi:10.1016/j.jep.2011.07.012
PMID:21782013
Cytotoxic versus anti-inflammatory effects in HeLa, Jurkat T and human peripheral blood cells caused by guaianolide-type sesquiterpene lactones. Hilmi F, Gertsch J, Bremner P, Valovic S, Heinrich M, Sticher O, Heilmann J Bioorg Med Chem 15-Aug-2003
doi:10.1016/S0968-0896(03)00346-8
PMID:12901911
New cytotoxic sesquiterpene lactones from Warionia saharae. Hilmi F, Sticher O, Heilmann J Planta Med 01-May-2003
doi:10.1055/S-2003-39703
PMID:12802731

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 521215 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1021/NP0104222
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(3aS,6S,8S,9R,9aS,9bR)-6,9-dihydroxy-6,9-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9a,9b-hexahydroazuleno[4,5-b]furan-8-yl] 2-[(2R,4aS,8aR)-4a-methyl-8-methylidene-7-oxo-2,3,4,8a-tetrahydro-1H-naphthalen-2-yl]prop-2-enoate 162911068 Click to see CC12CCC(CC1C(=C)C(=O)C=C2)C(=C)C(=O)OC3C=C4C(C3(C)O)C5C(CCC4(C)O)C(=C)C(=O)O5 508.60 unknown https://doi.org/10.1016/S0968-0896(03)00346-8
[(3aS,6S,8S,9R,9aS,9bS)-6,9-dihydroxy-6,9-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9a,9b-hexahydroazuleno[4,5-b]furan-8-yl] 2-[(2R,4aS,8aR)-4a-methyl-8-methylidene-7-oxo-2,3,4,8a-tetrahydro-1H-naphthalen-2-yl]prop-2-enoate 162911069 Click to see CC12CCC(CC1C(=C)C(=O)C=C2)C(=C)C(=O)OC3C=C4C(C3(C)O)C5C(CCC4(C)O)C(=C)C(=O)O5 508.60 unknown https://doi.org/10.1016/S0968-0896(03)00346-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Reynosin 482788 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1055/S-2003-39703
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1,10-Dimethyl-6-methylidene-5-oxo-4,13-dioxatetracyclo[10.1.1.02,11.03,7]tetradec-10-en-14-yl) 2-methylbutanoate 73880621 Click to see CCC(C)C(=O)OC1C2C3=C(CCC4C(C3C1(O2)C)OC(=O)C4=C)C 346.40 unknown https://doi.org/10.1021/NP0104222
(1R,2S,3R,7S,12S,14S)-14-hydroxy-1,10-dimethyl-6-methylidene-4,13-dioxatetracyclo[10.1.1.02,11.03,7]tetradec-10-en-5-one 11139915 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C4(C(C2O4)O)C 262.30 unknown https://doi.org/10.1021/NP0104222
[(1R,2S,3R,7S,12S,14S)-1,10-dimethyl-6-methylidene-5-oxo-4,13-dioxatetracyclo[10.1.1.02,11.03,7]tetradec-10-en-14-yl] (2R)-2-methylbutanoate 163021362 Click to see CCC(C)C(=O)OC1C2C3=C(CCC4C(C3C1(O2)C)OC(=O)C4=C)C 346.40 unknown https://doi.org/10.1021/NP0104222
14-Hydroxy-1,10-dimethyl-6-methylidene-4,13-dioxatetracyclo[10.1.1.02,11.03,7]tetradec-10-en-5-one 75072238 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C4(C(C2O4)O)C 262.30 unknown https://doi.org/10.1021/NP0104222
3beta-O-(2-Methylbutyryl)moroccolide A 9997743 Click to see CCC(C)C(=O)OC1C2C3=C(CCC4C(C3C1(O2)C)OC(=O)C4=C)C 346.40 unknown https://doi.org/10.1021/NP0104222
Fpluwngzvamknr-uwbbwcmesa- 11046234 Click to see CCC(C)C(=O)OC1C2C3=C(CCC4C(C3C1(O2)C)OC(=O)C4=C)C 346.40 unknown https://doi.org/10.1021/NP0104222
Moroccolide A 44566947 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C4(C(C2O4)O)C 262.30 unknown https://doi.org/10.1021/NP0104222
https://doi.org/10.1055/S-2003-39703
https://doi.org/10.1016/S0968-0896(03)00346-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1R,2S,6S,10S,12R,14S)-10-hydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradec-8-en-4-one 11777480 Click to see CC1=CCC2C(C3C1(CC4C3(O4)C)O)OC(=O)C2=C 262.30 unknown https://doi.org/10.1021/NP0104222
(1S,2R,3R,7S,11R,12R)-11-hydroxy-1,10-dimethyl-6-methylidene-4,13-dioxatetracyclo[10.1.1.02,11.03,7]tetradec-9-en-5-one 11139916 Click to see CC1=CCC2C(C3C1(C4CC3(O4)C)O)OC(=O)C2=C 262.30 unknown https://doi.org/10.1021/NP0104222
(3aS,6aR,7R,9S,9aR,9bR)-6a-hydroxy-9-methyl-3,6-bis(methylene)decahydro-7,9-epoxyazuleno[4,5-b]furan-2(3H)-one 642934 Click to see CC12CC(O1)C3(C2C4C(CCC3=C)C(=C)C(=O)O4)O 262.30 unknown https://doi.org/10.1021/NP0104222
(3aS,6aS,7aR,8aS,8bR,8cS)-6a-hydroxy-8a-methyl-3,6-bis(methylene)decahydrooxireno[2,3]azuleno[4,5-b]furan-2(3H)-one 642935 Click to see CC12C(O1)CC3(C2C4C(CCC3=C)C(=C)C(=O)O4)O 262.30 unknown https://doi.org/10.1021/NP0104222
10-Hydroxy-14-methyl-5,9-dimethylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 78201181 Click to see CC12C(O1)CC3(C2C4C(CCC3=C)C(=C)C(=O)O4)O 262.30 unknown https://doi.org/10.1021/NP0104222
10-Hydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradec-8-en-4-one 73097213 Click to see CC1=CCC2C(C3C1(CC4C3(O4)C)O)OC(=O)C2=C 262.30 unknown https://doi.org/10.1021/NP0104222
11-Hydroxy-1-methyl-6,10-dimethylidene-4,13-dioxatetracyclo[10.1.1.02,11.03,7]tetradecan-5-one 75072243 Click to see CC12CC(O1)C3(C2C4C(CCC3=C)C(=C)C(=O)O4)O 262.30 unknown https://doi.org/10.1021/NP0104222
11-Hydroxy-1,10-dimethyl-6-methylidene-4,13-dioxatetracyclo[10.1.1.02,11.03,7]tetradec-9-en-5-one 75072242 Click to see CC1=CCC2C(C3C1(C4CC3(O4)C)O)OC(=O)C2=C 262.30 unknown https://doi.org/10.1021/NP0104222
Saharanolide A 44566953 Click to see CC1=CCC2C(C3C1(C4CC3(O4)C)O)OC(=O)C2=C 262.30 unknown https://doi.org/10.1021/NP0104222
Saharanolide B 44566954 Click to see CC12CC(O1)C3(C2C4C(CCC3=C)C(=C)C(=O)O4)O 262.30 unknown https://doi.org/10.1021/NP0104222
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown https://doi.org/10.1055/S-2003-39703
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1055/S-2003-39703

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