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Allium minutiflorum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644024ad722e4189109603
Scientific name Allium minutiflorum
Authority Regel
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 3(2): 242 (1875)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

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Common names Top

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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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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-0000756739
Tropicos 100144298
KEW urn:lsid:ipni.org:names:528415-1
The Plant List kew-296021
Open Tree Of Life 357130
NCBI Taxonomy 543691
IPNI 528415-1
iNaturalist 1101345
GBIF 2857918
EOL 1084725

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 Review of Effect of Saponins on Ruminal Fermentation, Health and Performance of Ruminants Kholif AE Vet Sci 10-Jul-2023
PMCID:PMC10385484
doi:10.3390/vetsci10070450
PMID:37505855
Chemical Constituents, Biological Activities, and Proposed Biosynthetic Pathways of Steroidal Saponins from Healthy Nutritious Vegetable—Allium Wang H, Zheng Q, Dong A, Wang J, Si J Nutrients 08-May-2023
PMCID:PMC10180908
doi:10.3390/nu15092233
PMID:37432450
Phytochemical Classification of Medicinal Plants Used in the Treatment of Kidney Disease Based on Traditional Persian Medicine Rabizadeh F, Mirian MS, Doosti R, Kiani-Anbouhi R, Eftekhari E Evid Based Complement Alternat Med 31-Jul-2022
PMCID:PMC9357710
doi:10.1155/2022/8022599
PMID:35958915
Checklist of African Soapy Saponin—Rich Plants for Possible Use in Communities’ Response to Global Pandemics Kunatsa Y, Katerere DR Plants (Basel) 22-Apr-2021
PMCID:PMC8143558
doi:10.3390/plants10050842
PMID:33922037
Dual Mode of the Saponin Aescin in Plant Protection: Antifungal Agent and Plant Defense Elicitor Trdá L, Janda M, Macková D, Pospíchalová R, Dobrev PI, Burketová L, Matušinsky P Front Plant Sci 28-Nov-2019
PMCID:PMC6893899
doi:10.3389/fpls.2019.01448
PMID:31850004
Computational approaches to the in vitro antibacterial activity of Allium hirtifolium Boiss against gentamicin-resistant Escherichia coli: focus on ribosome recycling factor Ali SE, Chehri K, Karimi N, Karimi I In Silico Pharmacol 30-Aug-2017
PMCID:PMC5577348
doi:10.1007/s40203-017-0027-z
PMID:28924532
Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli Wojnicz D, Kucharska AZ, Sokół-Łętowska A, Kicia M, Tichaczek-Goska D Urol Res 23-Aug-2012
PMCID:PMC3495101
doi:10.1007/s00240-012-0499-6
PMID:22915095
Saponins from Allium minutiflorum with antifungal activity. Barile E, Bonanomi G, Antignani V, Zolfaghari B, Sajjadi SE, Scala F, Lanzotti V Phytochemistry 01-Mar-2007
doi:10.1016/J.PHYTOCHEM.2006.10.009
PMID:17118413

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 / Triterpenoids
(2beta,3beta,5alpha,6beta,25R)-Spirostan-2,3,6-triol 12312669 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.009
5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16,18,19-tetrol 3761894 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6(C5(CC(C(C6)O)O)C)O)O)C)C)OC1 464.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.009
Alliogenin 14656689 Click to see 464.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.009
Neoagigenin 52931439 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.009
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
2-[[(E,2S,3R,6S)-2,3-dimethyl-6-[(3S,5S,6S,8S,9R,10S,13R,14S,15R,17R)-6,8,15-trihydroxy-10,13-dimethyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]hept-4-enoyl]amino]ethanesulfonic acid 162800513 Click to see CC(C=CC(C)C(C)C(=O)NCCS(=O)(=O)O)C1CC(C2C1(CCC3C2(CC(C4C3(CCC(C4)OC5C(C(C(CO5)O)O)O)C)O)O)C)O 717.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.009
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(3S,5S,6S,8S,9R,10S,13R,14S,15R,17R)-6,8,15-trihydroxy-10,13-dimethyl-17-[(E,2S,5R)-6-methyl-5-[(2R,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyhept-3-en-2-yl]-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] hydrogen sulfate 162814270 Click to see 662.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.009

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