Allium stipitatum

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID644024cb6a8c6239950877
Scientific name	Allium stipitatum
Authority	Regel
First published in	Trudy Imp. S.-Peterburgsk. Bot. Sada 7: 546 (1881)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Allium atropurpureum var. hirtulum	Regel	Trudy Imp. S.-Peterburgsk. Bot. Sada 3(2): 248. 1875
Allium hirtifolium	Boiss.	Fl. Orient. 5: 281 (1882)

Common names Top

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Filter by language:

Language	Common/alternative name
English	persian shallot
azb	سووآلاق
Czech	česnek stopečkatý
Persian	موسیر ایرانی
Japanese	アリウム・スティピタトゥム
Korean	무시르
Russian	Лук стебельчатый
tg	модари сиёҳалаф
Chinese	长柄葱
Chinese	波斯红葱
Chinese	波斯紅蔥

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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Sow seeds directly at 4°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Iran
  - Iraq
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Europe click to expand
- Middle Europe
  - Czechoslovakia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000757441
UNII	P03I5D3H6I
Tropicos	18400464
KEW	urn:lsid:ipni.org:names:528920-1
The Plant List	kew-296677
Open Tree Of Life	942173
NCBI Taxonomy	70767
IPNI	528920-1
iNaturalist	871320
GBIF	2856593
Freebase	/m/0gvvx7q
EOL	1084999
USDA GRIN	2391
Wikipedia	Allium_stipitatum
CMAUP	NPO13010
PFAF	Allium stipitatum

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

Wild mushrooms as potential reservoirs of plant pathogenic bacteria: a case study on Burkholderia gladioli

Hamidizade M, Taghavi SM, Soleimani A, Bouazar M, Abachi H, Portier P, Osdaghi E

Microbiol Spectr

21-Feb-2024

PMCID:	PMC10986547
doi:	10.1128/spectrum.03395-23
PMID:	38380912

New Antimicrobial Strategies to Treat Multi-Drug Resistant Infections Caused by Gram-Negatives in Cystic Fibrosis

Scoffone VC, Barbieri G, Irudal S, Trespidi G, Buroni S

Antibiotics (Basel)

11-Jan-2024

PMCID:	PMC10812592
doi:	10.3390/antibiotics13010071
PMID:	38247630

Structure-dependent activity of plant natural products against methicillin-resistant Staphylococcus aureus

Moreno Cardenas C, Çiçek SS

Front Microbiol

15-Aug-2023

PMCID:	PMC10463185
doi:	10.3389/fmicb.2023.1234115
PMID:	37649631

The Antibacterial and Wound Healing Properties of Natural Products: A Review on Plant Species with Therapeutic Potential against Staphylococcus aureus Wound Infections

Morguette AE, Bartolomeu-Gonçalves G, Andriani GM, Bertoncini GE, de Castro IM, Spoladori LF, Bertão AM, Tavares ER, Yamauchi LM, Yamada-Ogatta SF

Plants (Basel)

29-May-2023

PMCID:	PMC10255540
doi:	10.3390/plants12112147
PMID:	37299127

Applications and Opportunities in Using Disulfides, Thiosulfinates, and Thiosulfonates as Antibacterials

Blume L, Long TE, Turos E

Int J Mol Sci

12-May-2023

PMCID:	PMC10218091
doi:	10.3390/ijms24108659
PMID:	37240003

Effect of dietary garlic (Allium sativum) on the zootechnical performance and health indicators of aquatic animals: A mini-review

Delgado DL, Caceres LL, Gómez SA, Odio AD

Vet World

11-May-2023

PMCID:	PMC10420702
doi:	10.14202/vetworld.2023.965-976
PMID:	37576751

Pyridine-N-Oxide Alkaloids from Allium stipitatum and Their Synthetic Disulfide Analogs as Potential Drug Candidates against Mycobacterium tuberculosis: A Molecular Docking, QSBAR, and ADMET Prediction Approach

Amengor CD, Orman E, Danquah CA, Ben IO, Biniyam PD, Harley BK

Biomed Res Int

07-Oct-2022

PMCID:	PMC9568345
doi:	10.1155/2022/6261528
PMID:	36246961

An overview of remote monitoring methods in biodiversity conservation

Kerry RG, Montalbo FJ, Das R, Patra S, Mahapatra GP, Maurya GK, Nayak V, Jena AB, Ukhurebor KE, Jena RC, Gouda S, Majhi S, Rout JR

Environ Sci Pollut Res Int

05-Oct-2022

PMCID:	PMC9534007
doi:	10.1007/s11356-022-23242-y
PMID:	36197618

Comparative Analysis of the Complete Chloroplast Genomes in Allium Section Bromatorrhiza Species (Amaryllidaceae): Phylogenetic Relationship and Adaptive Evolution

Chen J, Xie D, He X, Yang Y, Li X

Genes (Basel)

19-Jul-2022

PMCID:	PMC9324613
doi:	10.3390/genes13071279
PMID:	35886061

In Vitro Growth-Inhibitory Synergistic Effect of Zinc Pyrithione in Combination with Gentamicin against Bacterial Skin Pathogens of Livestock

Mala L, Lalouckova K, Skrivanova E, Houdkova M, Strakova M, Kokoska L

Antibiotics (Basel)

17-Jul-2022

PMCID:	PMC9311854
doi:	10.3390/antibiotics11070960
PMID:	35884214

Pyridine Compounds with Antimicrobial and Antiviral Activities

Marinescu M, Popa CV

Int J Mol Sci

18-May-2022

PMCID:	PMC9147400
doi:	10.3390/ijms23105659
PMID:	35628466

Efficacy of Dimethyl Trisulfide on the Suppression of Ring Rot Disease Caused by Botryosphaeria dothidea and Induction of Defense-Related Genes on Apple Fruits

Sun M, Duan Y, Liu JP, Fu J, Huang Y

Front Microbiol

07-Feb-2022

PMCID:	PMC8859264
doi:	10.3389/fmicb.2022.796167
PMID:	35197948

Bioactive small-molecule constituents of Lao plants

Ren Y, Elkington BG, Henkin JM, Sydara K, Kinghorn AD, Soejarto DD

J Med Plant Res

31-Dec-2021

PMCID:	PMC8849567
doi:	10.5897/jmpr2021.7137
PMID:	35178192

A review of the phytochemical mediated synthesis of AgNP (silver nanoparticle): the wonder particle of the past decade

Shaikh WA, Chakraborty S, Owens G, Islam RU

Appl Nanosci

30-Oct-2021

PMCID:	PMC8556825
doi:	10.1007/s13204-021-02135-5
PMID:	34745812

Environmentally Safe Biosynthesis of Gold Nanoparticles Using Plant Water Extracts

Hassanisaadi M, Bonjar GH, Rahdar A, Pandey S, Hosseinipour A, Abdolshahi R

Nanomaterials (Basel)

10-Aug-2021

PMCID:	PMC8400837
doi:	10.3390/nano11082033
PMID:	34443864

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
> Benzenoids / Benzene and substituted derivatives
Methyl phenyl disulfide	84234	Click to see CSSC1=CC=CC=C1	156.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Menadione	4055	Click to see CC1=CC(=O)C2=CC=CC=C2C1=O	172.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane	12410	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	436.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin	91458	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid	7163172	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,15R,16R,18R)-15,16,18-trihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one	90412196	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6(C5(CC(C(C6)O)O)C)O)C)C)OC1	462.60	unknown	https://doi.org/10.1007/BF00629988
(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18R,19R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16,18,19-triol	9803727	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6(C5(CCC(C6)O)C)O)O)C)C)OC1	448.60	unknown	https://doi.org/10.1007/BF00629988
15,16,18-Trihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one	3726126	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6(C5(CC(C(C6)O)O)C)O)C)C)OC1	462.60	unknown	https://doi.org/10.1007/BF00629988 https://doi.org/10.1007/BF00597575
2alpha,3beta,5beta-Trihydroxy-(25r)-spirostan-6-one	11518301	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6(C5(CC(C(C6)O)O)C)O)C)C)OC1	462.60	unknown	https://doi.org/10.1007/BF00597575
2alpha,5alpha-Epoxy-(25r)-spirostan-3beta,6beta-diol	21607745	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C67C5(CC(O6)C(C7)O)C)O)C)C)OC1	446.60	unknown	https://doi.org/10.1007/BF00596746 https://doi.org/10.1007/BF00598985
5',10,12,16-Tetramethylspiro[8,21-dioxahexacyclo[16.2.1.01,16.04,15.05,12.07,11]henicosane-9,2'-oxane]-2,19-diol	4979371	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C67C5(CC(O6)C(C7)O)C)O)C)C)OC1	446.60	unknown	https://doi.org/10.1007/BF00596746
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/10.1007/BF00597575
5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16,18,19-triol	76374852	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6(C5(CCC(C6)O)C)O)O)C)C)OC1	448.60	unknown	https://doi.org/10.1007/BF00629988
Alliogenin	14656689	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/10.1007/BF00597575
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	https://doi.org/10.1007/BF00597575
Spirost-5-en-2,3-diol	3777347	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CC(C(C6)O)O)C)C)C)OC1	430.60	unknown	https://doi.org/10.1007/BF00597575
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
Yuccagenin	3083608	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CC(C(C6)O)O)C)C)C)OC1	430.60	unknown	https://doi.org/10.1007/BF00597575
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5R,6R)-2-[[(8S,9S,10R,13S,14S,17R)-1,3-dihydroxy-17-[(2S)-3-hydroxy-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-16-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101608677	Click to see CC(C)CCC(C(C)C1C(CC2C1(CCC3C2CC=C4C3(C(CC(C4)O)O)C)C)OC5C(C(C(C(O5)CO)O)O)O)O	596.80	unknown	https://doi.org/10.1007/BF00629759
Alloside B	3072500	Click to see CC(C)CCC(C(C)C1C(CC2C1(CCC3C2CC=C4C3(C(CC(C4)O)OC5C(C(C(C(O5)CO)O)O)O)C)C)OC6C(C(C(C(O6)CO)O)O)O)O	758.90	unknown	https://doi.org/10.1007/BF00629759
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,6R,7S,8R,9S,12S,13S,15R,16R,18S)-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,16-triol	162967653	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O	612.80	unknown	https://doi.org/10.1055/S-2005-873134
(1R,2S,4S,6S,7S,8R,9S,12S,13S,15R,16R,18S)-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,16-triol	162967652	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O	612.80	unknown	https://doi.org/10.1055/S-2005-873134
(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,15R,16R,18R,19R)-5',7,9,13-tetramethyl-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,18,19-triol	162881436	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6(C5(CC(C(C6)OC7C(C(C(C(O7)CO)O)O)O)O)C)O)O)C)C)OC1	626.80	unknown	https://doi.org/10.1055/S-2005-873134
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1R,2S,4S,6R,7S,8R,9S,12S,13S,15R,16R,18S)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,15-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162944980	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1069.20	unknown	https://doi.org/10.1055/S-2005-873134
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1R,2S,4S,6S,7S,8R,9S,12S,13S,15R,16R,18S)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,15-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162944979	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1069.20	unknown	https://doi.org/10.1055/S-2005-873134
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1R,2S,4S,8S,9S,12S,13S,15R,16R,18S)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162888206	Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)O)O)O)O)C)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O	1051.20	unknown	https://doi.org/10.1055/S-2005-873134
(2S,3R,4S,5R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,15R,16R,18S,19R)-15,19-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol	163001252	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)O)O)O)O)C)O)C)C)OC1	905.00	unknown	https://doi.org/10.1055/S-2005-873134
(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162907422	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)C)C)OC1	756.90	unknown	https://doi.org/10.1055/S-2005-873134
2-[2-[6-(15,19-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol	163001251	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)O)O)O)O)C)O)C)C)OC1	905.00	unknown	https://doi.org/10.1055/S-2005-873134
2-[4-[16-[5-[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162888205	Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)O)O)O)O)C)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O	1051.20	unknown	https://doi.org/10.1055/S-2005-873134
2-[4-[16-[5-[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,15-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162944978	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1069.20	unknown	https://doi.org/10.1055/S-2005-873134
5',7,9,13-Tetramethyl-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,18,19-triol	162881435	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6(C5(CC(C(C6)OC7C(C(C(C(O7)CO)O)O)O)O)C)O)O)C)C)OC1	626.80	unknown	https://doi.org/10.1055/S-2005-873134
7,9,13-Trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,16-triol	162967651	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O	612.80	unknown	https://doi.org/10.1055/S-2005-873134
Capsicoside B1	73800784	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)C)C)OC1	756.90	unknown	https://doi.org/10.1055/S-2005-873134
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-3-pyridin-2-ylsulfinylpropanoic acid	163036726	Click to see C1=CC=NC(=C1)S(=O)CC(C(=O)O)N	214.24	unknown	https://doi.org/10.1021/JF902294C
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2R)-2-amino-3-[(S)-pyridin-2-ylsulfinyl]propanoic acid	163036727	Click to see C1=CC=NC(=C1)S(=O)CC(C(=O)O)N	214.24	unknown	https://doi.org/10.1021/JF902294C
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)Glc(b1-2b)Fruf	44420456	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O	504.40	unknown	via CMAUP database
Stachyose	439531	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O	666.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives
2-(Methyldithio)pyrimidine	12278995	Click to see CSSC1=NC=CC=N1	158.20	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
> Organoheterocyclic compounds / Heteroaromatic compounds
2-(Methyldithio)thiophene	45272211	Click to see CSSC1=CC=CS1	162.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine	190	Click to see C1=NC2=NC=NC(=C2N1)N	135.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
5-(1-hydroxybutyl)-4-methoxy-6-methyl-2H-pyran-2-one	38357481	Click to see CCCC(C1=C(OC(=O)C=C1OC)C)O	212.24	unknown	https://doi.org/10.1021/JF902294C
> Organoheterocyclic compounds / Pyridines and derivatives
2-(Methylsulfanylmethylsulfanylsulfinyl)pyridine	162842947	Click to see CSCSS(=O)C1=CC=CC=N1	219.40	unknown	https://doi.org/10.1021/JF902294C
2-[(S)-[(S)-pyridin-2-ylsulfinyl]sulfinyl]pyridine	162970890	Click to see C1=CC=NC(=C1)S(=O)S(=O)C2=CC=CC=N2	252.30	unknown	https://doi.org/10.1021/JF902294C
2-[(S)-methylsulfanylmethylsulfanylsulfinyl]pyridine	162842948	Click to see CSCSS(=O)C1=CC=CC=N1	219.40	unknown	https://doi.org/10.1021/JF902294C
2-[(S)-methylsulfanylsulfinyl]pyridine	163014456	Click to see CSS(=O)C1=CC=CC=N1	173.30	unknown	https://doi.org/10.1021/JF902294C
2-Methylsulfanylsulfinylpyridine	101466389	Click to see CSS(=O)C1=CC=CC=N1	173.30	unknown	https://doi.org/10.1021/JF902294C
2-Pyridin-2-ylsulfinylsulfinylpyridine	162970889	Click to see C1=CC=NC(=C1)S(=O)S(=O)C2=CC=CC=N2	252.30	unknown	https://doi.org/10.1021/JF902294C
2,2'-Dithiodipyridine	65093	Click to see C1=CC=NC(=C1)SSC2=CC=CC=N2	220.30	unknown	https://doi.org/10.1021/JF902294C
Methyl 2-pyridyl disulfide	173923	Click to see CSSC1=CC=CC=N1	157.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
S-pyridin-2-yl Pyridine-2-sulfinothioate	85765250	Click to see C1=CC=NC(=C1)SS(=O)C2=CC=CC=N2	236.30	unknown	https://doi.org/10.1021/JF902294C
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinium derivatives
2-((Methylthiomethyl)Dithio)Pyridine-N-Oxide	45267926	Click to see CSCSSC1=CC=CC=[N+]1[O-]	219.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
2-(Methyldithio)Pyridine-N-Oxide	13386157	Click to see CSSC1=CC=CC=[N+]1[O-]	173.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
Dipyrithione	3109	Click to see C1=CC=[N+](C(=C1)SSC2=CC=CC=[N+]2[O-])[O-]	252.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
> Organoheterocyclic compounds / Quinolines and derivatives
2-(Methyldithio)quinoline	45270487	Click to see CSSC1=NC2=CC=CC=C2C=C1	207.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
> Organoheterocyclic compounds / Quinolines and derivatives / 8-hydroxyquinolines
8-Hydroxyquinoline	1923	Click to see C1=CC2=C(C(=C1)O)N=CC=C2	145.16	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765505/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-[(E)-3-(beta-D-glucopyranosyloxy)-1-propenyl]-7-methoxy-2,3-dihydrobenzofuran-3beta-methanol	11027727	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCOC4C(C(C(C(O4)CO)O)O)O	520.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4S,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	5320625	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O	478.40	unknown	via CMAUP database
[(2R,3R,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	110062419	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
Calceolarioside A	5273566	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O	478.40	unknown	via CMAUP database
Calceolarioside B	5273567	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
Hellicoside	5281778	Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(OC(C(C2OC3C(C(C(C(O3)CO)O)O)O)O)OCC(C4=CC(=C(C=C4)O)O)O)CO)O)O	656.60	unknown	via CMAUP database
Isoacteoside	6476333	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
Isomartynoside	91895373	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O	652.60	unknown	via CMAUP database
Leucosceptoside A	10394343	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	638.60	unknown	via CMAUP database
Martynoside	5319292	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	652.60	unknown	via CMAUP database
Plantainoside B	9847922	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O	478.40	unknown	via CMAUP database
Plantamajoside	5281788	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	640.60	unknown	via CMAUP database
Plantasioside	44423103	Click to see C1C(OC2C(C(C(OC2O1)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)C4=CC(=C(C=C4)O)O	476.40	unknown	via CMAUP database
Sanangoside	6915840	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O	478.40	unknown	via CMAUP database
Scroside B	9831187	Click to see COC1=C(C=C(C=C1)CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	668.60	unknown	via CMAUP database
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Plantagoside	174157	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O	466.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-(((2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-(((2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one	10008639	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1055/S-2005-873134
3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	21722032	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1055/S-2005-873134
3-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	13940971	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1055/S-2005-873134
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1055/S-2005-873134
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1055/S-2005-873134
Kaempferol-3-O-glucorhamnoside	13915496	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1055/S-2005-873134
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Homoplantaginin	5318083	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	via CMAUP database
kaempferol 7-O-glucoside	10095180	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1055/S-2005-873134
Kaempferol-7-o-glucoside	5480982	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1055/S-2005-873134
Plantaginin	5320623	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database

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Allium stipitatum

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