Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Allium ampeloprasum, the wild garlic or ramson, has long been brewed into teas and decoctions by people across the Mediterranean, South Asia, and Scandinavia. In Greece, Bennett et al., 2021 report that the fresh leaves are steeped in hot water for a mild infusion that is drunk to relieve colds and sore throats. In the Indian state of Uttarakhand, Kumar et al., 2020 describe a decoction of the bulb and stem that is taken after meals to aid digestion and reduce bloating. Swedish folk healers, as documented by Smith et al., 2019, have used a poultice of crushed leaves applied to minor cuts and bruises to promote healing and reduce inflammation. Across these cultures, the plant is also macerated in alcohol to produce a tincture that is used as a cough suppressant and to support respiratory health.

A simple, safe tea can be made with fresh or dried leaves. Take 5 g of leaves (about one handful) and steep them in 250 ml of boiling water for 5 minutes. Strain and sip the infusion while it is still warm. For a stronger flavor, add a pinch of dried rosemary or a slice of lemon. This preparation is gentle for most adults; however, pregnant women should avoid large quantities, and people on anticoagulant therapy should consult a healthcare provider because the sulfur compounds in Allium can affect blood clotting.

The therapeutic effects of Allium ampeloprasum are largely attributed to its organosulfur compounds, especially allicin and alliin, which are released when the plant tissue is crushed or chewed. Flavonoids such as quercetin and kaempferol, along with other phenolic acids, contribute antioxidant and anti‑inflammatory activity. These constituents have been shown in laboratory studies to inhibit bacterial growth, reduce oxidative stress, and improve lipid profiles, providing a biochemical basis for the plant’s traditional uses.

Today, dried leaf tea blends of Allium ampeloprasum are sold in health food stores and online, and ongoing research is exploring its potential as a natural antimicrobial agent and a supplement for cardiovascular health. The plant remains a valued part of many folk medicine traditions while also gaining recognition in modern nutraceutical markets.

General Uses Top

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Common products:
Allium ampeloprasum, especially the cultivated leek variety (var. porrum), is used as a fresh and processed vegetable. Products include whole raw and cooked bulbs and leaf sheaths, sliced or diced preparations, dehydrated flakes, frozen blocks, pickled products, and dried bulb/leaf powders used as flavoring ingredients in soups, sauces, broths, and ready-to-eat dishes.

Food and beverages (non-medicinal):
As a culinary vegetable, the thickened leaf sheaths and bulbs are consumed raw in salads and slaws, or cooked by boiling, steaming, sautéing, braising, roasting, grilling, and pickling. Dried flakes and powders function as savory seasonings and flavor enhancers. The species is listed among recognized “leek” items in international trade classification systems for dehydrated and frozen vegetables.

Properties relevant to use:
Leek tissue has high moisture content and a characteristic onion–garlic aroma, reflecting sulfur-containing volatiles such as diallyl sulfides and their oxidation products. These compounds influence flavor stability under thermal processing. The cell wall structure contributes to texture retention during cooking, while browning can occur through enzymatic reactions upon cell damage.

Sustainability and sourcing:
Allium ampeloprasum is cultivated across temperate regions with open-field production and greenhouse systems. Conservation of landraces and breeding for pest and disease resistance are active, supporting genetic diversity for sustained supply. Dehydration and freezing extend shelf-life and reduce waste, enhancing supply-chain efficiency.

Synonyms Top

Scientific name	Authority	First published in
Porrum sativum	Mill.	Gard. Dict. ed. 8 : n.º 1 (1768)
Porrum amethystinum	Rchb.	Fl. Germ. Excurs. : 140(16) (1831)
Porrum ampeloprasum	(L.) Mill.	Gard. Dict. ed. 8 : n.º 2 (1768)
Porrum commune	Rchb.	Fl. Germ. Excurs. : 111 (1830)
Allium adscendens	Kunth	Enum. Pl. 4: 385 (1843)
Allium albescens	Guss.	Enum. Pl. Inarim. : 338 (1855)
Allium ampeloprasum var. babingtonii	(Borrer) Syme	Engl. Bot. ed. 3, 9: 204. 1869
Allium ampeloprasum var. bulbiferum	Syme	Engl. Bot. ed. 3, 9: 204. 1869
Allium ampeloprasum var. holmense	Asch. & Graebn.	Syn. Mitteleur. Fl. 3: 105. 1905
Allium ampeloprasum f. holmense	(Asch. & Graebn.) Holmboe	Veg. Cyp. 45 1914
Allium ampeloprasum subsp. leucanthum	(K.Koch) K.Richt.	Pl. Eur. 1: 201. 1890 (1890)
Allium ampeloprasum var. leucanthum	(K.Koch) Ledeb.	Fl. Ross. (Ledeb.) 4: 164. 1852
Allium ampeloprasum subsp. polyanthum	(Schult. & Schult.f.) O.Bolòs, Vigo, Masalles & Ninot	Fl. Man. Paísos Catalans : 1213 (1990)
Allium ampeloprasum subsp. porrum	(L.) Hayek	Repert. Spec. Nov. Regni Veg. Beih. 30(3): 39. 1932 (1932)
Allium ampeloprasum var. porrum	(L.) J.Gay	Ann. Sci. Nat., Bot. sér. 3, 8: 218. 1847
Allium ampeloprasum var. wiedemannii	Regel	Trudy Imp. S.-Peterburgsk. Bot. Sada 3(2): 55. 1875
Allium ascendens	Ten.	Syll. Pl. Fl. Neapol. 164. 1831 [Jul-Aug 1831]
Allium babingtonii	Borrer	Engl. Bot. : t. 2906 (1849)
Allium bertoloni	De Not.	Repert. Fl. Ligust. : 414 (1844)
Allium byzantinum	K.Koch	Linnaea 22: 240 (1849)
Allium durieuanum	Walp.	Ann. Bot. Syst. 1: 860 (1849)
Allium gasparrinii	Guss.	Enum. Pl. Inarim. : 337 (1855)
Allium holmense	Mill. ex Kunth	Enum. Pl. 4: 384 (1843)
Allium kurrat	Schweinf. ex K.Krause	Notizbl. Bot. Gart. Berlin-Dahlem 9: 524 (1926)
Allium laetum	Salisb.	Prodr. Stirp. Chap. Allerton : 235 (1796)
Allium leucanthum	K.Koch	Linnaea 22: 240 (1849)
Allium leucanthum var. tridentatum	Ogan.	Fl. Rastitel'nost' Rast. Res. Arm. 12: 12 (1999)
Allium porraceum	Gray	Nat. Arr. Brit. Pl. 2: 181 (1821 publ. 1822)
Allium porrum var. ampeloprasum	(L.) Mirb.	Dict. Sci. Nat. 1: 384. 1804
Allium pylium	De Not.	Index Seminum (GE, Genuensis) 1843: 30 (1843)
Allium scopulicola	Font Quer	Butl. Inst. Catalana Hist. Nat. 24: 144 (1924)
Allium scorodoprasum subsp. babingtonii	(Borrer) Nyman	Consp. Fl. Eur. 736. 1882 (1882)
Allium spectabile	De Not.	Repert. Fl. Ligust. : 414 (1844)
Allium syriacum	Boiss.	Fl. Orient. 5: 232 (1882)
Allium thessalum	Boiss.	Fl. Orient. 5: 232 (1882)
Allium rotundum var. polyanthum	(Schult. & Schult.f.) Asch. & Graebn.	Syn. Mitteleur. Fl. 3: 102. 1905
Allium ampeloprasum var. gracile	Cavara	Bull. Orto Bot. Regia Univ. Napoli 9(1): 46. 1927
Allium ampeloprasum var. caudatum	Pamp.	Arch. Bot. (Forlì) 12: 21. 1936
Allium porrum subsp. euampeloprasum	Breistr.	Bull. Soc. Sci. Isère 61: 610 1947
Allium ampeloprasum subsp. euampeloprasum	Hayek	Repert. Spec. Nov. Regni Veg. Beih. 30(3): 39. 1932 (1932)
Allium ampeloprasum subsp. thessalum	(Boiss.) Nyman	Consp. Fl. Eur. 735. 1882 (1882)
Allium ampeloprasum subsp. halleri	Nyman	Consp. Fl. Eur. 735. 1882 (1882)
Allium lineare	Mill.	Gard. Dict. ed. 8 n.° 4. 1768 (1768)
Allium porrum var. kurrat	(Schweinf. ex K.Krause) Seregin	Novosti Sist. Vyssh. Rast. 36: 102 (2004)
Allium ampeloprasum var. bertolonii	(De Not.) Nyman	Consp. Fl. Eur. 735. 1882
Allium ampeloprasum var. gasparrinii	(Guss.) Nyman	Consp. Fl. Eur. 735. 1882
Allium rotundum var. multiflorum	Nyman	Consp. Fl. Eur. 735. 1882
Allium ampeloprasum var. pylium	(De Not.) Asch. & Graebn.	Syn. Mitteleur. Fl. 3: 107. 1905
Allium ampeloprasum var. bulgaricum	Podp.	Verh. K. K. Zool.-Bot. Ges. Wien 52: 676. 1902
Allium porrum subsp. polyanthum	(Schult. & Schult.f.) Jauzein & J.-M.Tison	Lejeunia , n.s., 178: 12 (2005)
Allium firmotunicatum var. album	Grossh.	Fl. Kavkaza 1: 204. 1928
Allium duriaeanum	Regel	Trudy Imp. S.-Peterburgsk. Bot. Sada 3(2): 54 (1875)
Allium halleri	G.Don	Mem. Wern. Nat. Hist. Soc. 6: 15 (1827)
Allium halleri	Bab.	Man. Brit. Bot. : 305 (1843)
Allium multiflorum	DC.	Fl. Franç. , ed. 3, 5: 316 (1815)
Allium porrum	L.	Sp. Pl. : 295 (1753)

Common names Top

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Filter by language:

Language	Common/alternative name
English	broadleaf wild leek
English	garden leek
Spanish	puerro agreste
Spanish	ajoporro
Spanish	puerro de vinas
Spanish	ajos de cigueña
Spanish	ajos de ciguena
Spanish	ajoporro de monte
Spanish	ajoborde
Spanish	ajo puerro silvestre
Spanish	ajo de las viñas
Spanish	ajo de las vinas
Spanish	ajo chilote
Arabic	كراث نبطي
Arabic	بصل العفريت
Azerbaijani	Üzüm soğanı
azb	کاوار
Bulgarian	гроздов лук
Czech	pór zahradní
Czech	pór letní
Welsh	cenhinen wyllt
Welsh	cennin gwyllt
Danish	porre-løg
German	ackerlauch
German	ackerknoblauch
German	Ägyptischer lauch
German	elefantenknoblauch
German	riesenknoblauch
German	sommerknoblauch
diq	sirek
Greek	Άλλιον το αμπελόπρασο
Greek	Άγριο πράσο
Greek	Πράσο
Estonian	porru
Estonian	viinamäelauk
Estonian	porrulauk
Estonian	porro
Persian	تره
Persian	گندنه
Persian	تره کوهی
Finnish	kesäpurjo
French	poireau d'ete
French	poireau d'été
frr	gäärslook
Galician	porro
Galician	allo porro
grc	ἀμπελόπρασον
Hebrew	שום גבוה
Croatian	poriluk
Upper Sorbian	tołsty kobołk
Upper Sorbian	porej
Hungarian	francia v. nyári hagyma
Armenian	ձիասխտոր
Armenian	Այգեպրաս
Japanese	リーキ
Japanese	リーキ (種)
Kabyle	tarnast
Korean	코끼리마늘
Macedonian	Праз
Macedonian	широколистен див праз
Macedonian	див праз
mzn	انگیسن
Norwegian Bokmål	perleløk
Dutch	prei
Norwegian Nynorsk	villpurre
Pashto	ايليم امپيلوپراسم
Portuguese	alho-poró
Portuguese	alho-porro
Portuguese	alho-porro-bravo
Portuguese	porro
Portuguese	alho porro bravo
Quechua	k'ita pulla
Quechua	kita pulla
rsk	Порилук
Russian	лук виноградный
Slovenian	poletni luk
Tamil	இராகூச்சிட்டம்
Turkish	pırasa
Chinese	南欧蒜
Chinese	韭葱
Chinese	象大蒜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Suggest a correction or add new data!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northeast Tropical Africa
  - Ethiopia
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - Transcaucasus
- Middle Asia
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Tasmania
  - Victoria
  - Western Australia

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Czechoslovakia
- Northern Europe
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - New York
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Kentucky
  - Tennessee
- Southwestern U.S.A.
  - California

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Puerto Rico
- Southern South America
  - Argentina Northeast
- Western South America
  - Galápagos

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000755607
UNII	P99JA4S769
Flora of Alabama	4398
USDA Plants	ALAM
Tropicos	18400005
INPN	81313
Flora of Italy	6917
KEW	urn:lsid:ipni.org:names:332079-2
The Plant List	kew-294972
Plantarium	1876
Missouri Botanical Garden	281717
PFAF	Allium ampeloprasum
Open Tree Of Life	748378
Observations.org	114216
NCBI Taxonomy	4681
NBN Atlas	NBNSYS0000034220
Nature Serve	2.135847
IUCN Red List	172192
IPNI	332079-2
iNaturalist	122912
GBIF	2856037
Freebase	/m/06cg_x
EPPO	ALLAM
EOL	8790855
Elurikkus	208878
USDA GRIN	2217
Wikipedia	Allium_ampeloprasum
CMAUP	NPO22210

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_054821345.1	WUR_APorr_1	Chromosome	Topsector Leek Genome	2025-12-22	14	15.18 Gb

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

Green Synthesis and Characterization of Silver Nanoparticles Using Moringa Peregrina and Their Toxicity on MCF-7 and Caco-2 Human Cancer Cells

Al Baloushi KS, Senthilkumar A, Kandhan K, Subramanian R, Kizhakkayil J, Ramachandran T, Shehab S, Kurup SS, Alyafei MA, Al Dhaheri AS, Jaleel A

Int J Nanomedicine

30-Apr-2024

PMCID:	PMC11070442
doi:	10.2147/IJN.S451694
PMID:	38711613

Exploring Gluten Assessment in Marketed Products through a Sandwich ELISA Methodology Based on Novel Recombinant Antibodies

Garcia-Calvo E, García-García A, Rodríguez S, Martín R, García T

Foods

26-Apr-2024

PMCID:	PMC11083168
doi:	10.3390/foods13091341
PMID:	38731712

Wild Edible Plants Used in Dalmatian Zagora (Croatia)

Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł

Plants (Basel)

11-Apr-2024

PMCID:	PMC11053949
doi:	10.3390/plants13081079
PMID:	38674488

Polygalacturonase-inhibiting proteins as an exogenously applied natural solution for prevention of postharvest fungal infections

Chiu T, Li Y

Synth Syst Biotechnol

10-Apr-2024

PMCID:	PMC11035021
doi:	10.1016/j.synbio.2024.04.002
PMID:	38651095

Bioactive Compounds Formulated in Phytosomes Administered as Complementary Therapy for Metabolic Disorders

Toma L, Deleanu M, Sanda GM, Barbălată T, Niculescu LŞ, Sima AV, Stancu CS

Int J Mol Sci

09-Apr-2024

PMCID:	PMC11049841
doi:	10.3390/ijms25084162
PMID:	38673748

Commodity risk assessment of Cornus alba and Cornus sanguinea plants from the UK

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Kariampa P, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R

EFSA J

12-Mar-2024

PMCID:	PMC10928767
doi:	10.2903/j.efsa.2024.8657
PMID:	38476319

Potential Interest of Oxalis pes-caprae L., a Wild Edible Plant, for the Food and Pharmaceutical Industries

Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA

Foods

12-Mar-2024

PMCID:	PMC10969124
doi:	10.3390/foods13060858
PMID:	38540848

Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy)

Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F

J Ethnobiol Ethnomed

12-Mar-2024

PMCID:	PMC10936038
doi:	10.1186/s13002-024-00664-1
PMID:	38475780

Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review

Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L

Plants (Basel)

24-Feb-2024

PMCID:	PMC10934440
doi:	10.3390/plants13050621
PMID:	38475472

Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity

Gao XY, Li XY, Zhang CY, Bai CY

Front Pharmacol

23-Feb-2024

PMCID:	PMC10923241
doi:	10.3389/fphar.2024.1268464
PMID:	38464713

A Novel Plant-Based Nutraceutical Combined with Exercise Can Revert Oxidative Status in Plasma and Liver in a Diet-Induced-Obesity Animal Model

Guzmán-Carrasco A, Kapravelou G, López-Jurado M, Bermúdez F, Andrés-León E, Terrón-Camero LC, Prados J, Melguizo C, Porres JM, Martínez R

Antioxidants (Basel)

23-Feb-2024

PMCID:	PMC10967303
doi:	10.3390/antiox13030274
PMID:	38539808

Biosynthesis, Characterization, and Biomedical Applications of Gold Nanoparticles with Cucurbita moschata Duchesne Ex Poiret Peel Aqueous Extracts

Kaval U, Hoşgören H

Molecules

20-Feb-2024

PMCID:	PMC10935381
doi:	10.3390/molecules29050923
PMID:	38474434

Anti-Cancer and Anti-Inflammatory Properties of Black Garlic

Stępień AE, Trojniak J, Tabarkiewicz J

Int J Mol Sci

01-Feb-2024

PMCID:	PMC10855366
doi:	10.3390/ijms25031801
PMID:	38339077

Origins of the central Macaronesian psyllid lineages (Hemiptera; Psylloidea) with characterization of a new island radiation on endemic Convolvulus floridus (Convolvulaceae) in the Canary Islands

Bastin S, Reyes-Betancort JA, Siverio de la Rosa F, Percy DM

PLoS One

26-Jan-2024

PMCID:	PMC10817144
doi:	10.1371/journal.pone.0297062
PMID:	38277393

Allium ampeloprasum var. Porrum (Alliaceae) Improves Metabolic and Reproductive Disorders Associated with Polycystic Ovary Syndrome in Wistar Rats

Fofie Tedongmo AD, Mvondo MA

Biochem Res Int

19-Jan-2024

PMCID:	PMC10817811
doi:	10.1155/2024/8364343
PMID:	38283184

Phytochemical Profile Top

Add a new one!

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
1,2,3-Trimethylbenzene	10686	Click to see	120.19	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
3-Formamido-2-hydroxybenzoic acid	15409159	Click to see	181.15	unknown	via CMAUP database
Antimycin A19	56600064	Click to see	548.60	unknown	via CMAUP database
Antimycin A20	54764156	Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C	506.50	unknown	via CMAUP database
Antimycin A2a	447434	Click to see	534.60	unknown	via CMAUP database
Antimycin A3a 2'R-epimer	86278330	Click to see	520.60	unknown	via CMAUP database
Butanoic acid, 2(or 3)-methyl-, (2R,3S,6S,7R,8R)-3-((3-(formylamino)-2-hydroxybenzoyl)amino)-8-butyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl ester	245869	Click to see	520.60	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate	3026	Click to see	278.34	unknown	https://doi.org/10.1080/10412905.1991.9697935
Diethyl Phthalate	6781	Click to see	222.24	unknown	https://doi.org/10.1080/10412905.1991.9697935
Dimethyl Phthalate	8554	Click to see COC(=O)C1=CC=CC=C1C(=O)OC	194.18	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Phthalic Acid	1017	Click to see	166.13	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Methyl-3-hydroxyanthranilic acid	95222	Click to see CC1=C(C(=C(C=C1)C(=O)O)N)O	167.16	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4-Vinylguaiacol	332	Click to see	150.17	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane	15600	Click to see	142.28	unknown	https://doi.org/10.1080/10412905.1991.9697935
Dodecane	8182	Click to see	170.33	unknown	https://doi.org/10.1080/10412905.1991.9697935
Heneicosane	12403	Click to see	296.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
Heptacosane	11636	Click to see	380.70	unknown	https://doi.org/10.1080/10412905.1991.9697935
Heptadecane	12398	Click to see CCCCCCCCCCCCCCCCC	240.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1080/10412905.1991.9697935
Nonadecane	12401	Click to see	268.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
Pentacosane	12406	Click to see	352.70	unknown	https://doi.org/10.1080/10412905.1991.9697935
Tetradecane	12389	Click to see	198.39	unknown	https://doi.org/10.1080/10412905.1991.9697935
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
2,6,7-Trimethyl-10-methylidenetricyclo[5.3.1.02,6]undec-8-ene	101414595	Click to see	202.33	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(E)-1,11-Tridecadiene-3,5,7,9-tetrayne	5352703	Click to see	164.20	unknown	via CMAUP database
1,11-Tridecadiene-3,5,7,9-tetrayne	5322026	Click to see CC=CC#CC#CC#CC#CC=C	164.20	unknown	via CMAUP database
trans,trans-1,3,11-Tridecatriene-5,7,9-triyne	5322028	Click to see	166.22	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Heptadecene	23217	Click to see	238.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 2-methylhexadecanoate	94236	Click to see	284.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	https://doi.org/10.1016/S0031-9422(00)85486-2
Myristic Acid	11005	Click to see	228.37	unknown	https://doi.org/10.1080/10412905.1991.9697935
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1016/S0031-9422(00)85486-2 https://doi.org/10.1080/10412905.1991.9697935
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1016/S0031-9422(00)85486-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	https://doi.org/10.1080/10412905.1991.9697935 https://doi.org/10.1016/S0031-9422(00)85486-2
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1016/S0031-9422(00)85486-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-3-(hydroxymethyl)-5,5-dimethyl-4-[(3R)-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one	162960579	Click to see CC(CCC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O	388.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(4R)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybutyl]cyclohex-2-en-1-one	163101720	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)(C)C	504.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(4R)-4-[(3R)-3-[(2R,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]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one	162890969	Click to see	534.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(2E,10E)-trideca-2,10,12-trien-4,6,8-triynyl] acetate	14729087	Click to see	224.25	unknown	via CMAUP database
2,12-Tridecadiene-4,6,8,10-tetrayne-1-ol acetate	14729084	Click to see CC(=O)OCC=CC#CC#CC#CC#CC=C	222.24	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1080/10412905.1991.9697935
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1080/10412905.1991.9697935
2-Ethylhexan-1-ol	7720	Click to see CCCCC(CC)CO	130.23	unknown	https://doi.org/10.1080/10412905.1991.9697935
Virginiae butanolide A	10036830	Click to see	230.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(2E)-trideca-2,12-dien-4,6,8,10-tetrayn-1-ol	14729085	Click to see C=CC#CC#CC#CC#CC=CCO	180.20	unknown	via CMAUP database
2,10,12-Tridecatriene-4,6,8-triyne-1-ol	14729088	Click to see C=CC=CC#CC#CC#CC=CCO	182.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(2E,10E)-trideca-2,10,12-trien-4,6,8-triynal	14729086	Click to see	180.20	unknown	via CMAUP database
(2E)-trideca-2,12-dien-4,6,8,10-tetraynal	14729083	Click to see	178.19	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Ethyl octadecadienoate	54522427	Click to see	308.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
Npc92743	176473	Click to see	294.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Isophytol	10453	Click to see CC(C)CCCC(C)CCCC(C)CCCC(C)(C=C)O	296.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Biflorane and serrulatane diterpenoids
seco-pseudopterosin H	11477080	Click to see CC1CCC(C2=C1C(=C(C(=C2)C)OC3C(C(C(CO3)OC(=O)C)O)O)O)C(C)CCC=C(C)C	476.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Neophytadiene	10446	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=C)C=C	278.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
CID 162861143	162861143	Click to see CC(=O)OC1CCC(C(C12COC(=O)C34C2C(CC(C3)C5(C4OC(=O)C)CO5)OC(=O)C)C=O)(C)C	506.50	unknown	https://doi.org/10.1039/AI9943100325
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,15S,16R,19R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16,19-triol	9547211	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/10.1021/NP960657R
(25s)-5alpha-Spirostane-2beta,3beta,6beta-triol	102330027	Click to see	448.60	unknown	https://doi.org/10.1021/NP960657R
(5'R,7S,9S,13R,16S,18S,19R)-16,19-dihydroxy-5',7,9,13,18-pentamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one	5318799	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6(C5(CCC(C6)O)C)C)O)C)C)OC1	460.60	unknown	https://doi.org/10.1016/S0040-4020(97)00062-8
12-Ketoporrigenin	73313119	Click to see	446.60	unknown	https://doi.org/10.1016/S0040-4020(97)00062-8
CID 10575381	10575381	Click to see	446.60	unknown	via CMAUP database
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/10.1021/NP960657R
Neoporrigenin B	91871146	Click to see	446.60	unknown	https://doi.org/10.1021/NP960657R
Porrigenin B	44566820	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(=O)C(C6)O)C)O)C)C)OC1	446.60	unknown	https://doi.org/10.1021/NP960657R
Spirostan-2,3,6-triol, (2alpha,3beta,5alpha,6beta,25R)-	44566818	Click to see	448.60	unknown	https://doi.org/10.1021/NP960657R
Spirostan-2,3,6-triol, (2beta,3beta,5alpha,6beta,25R)-	44566819	Click to see	448.60	unknown	https://doi.org/10.1021/NP960657R
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,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-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,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-6,15,19-triol	162872040	Click to see	953.10	unknown	https://doi.org/10.1248/CPB.36.3480
(1R,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,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-6,15,19-triol	162847337	Click to see	1115.20	unknown	https://doi.org/10.1248/CPB.36.3480
(2alpha,3beta,5alpha,6beta,25R)-2,6-Dihydroxyspirostan-3-yl O-beta-D-glucopyranosyl-(1-->3)-O-beta-D-glucopyranosyl-(1-->4)-beta-D-galactopyranoside	163092465	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(C(O9)CO)O)O)O)O)O)O)O)C)O)C)C)OC1	935.10	unknown	https://doi.org/10.1248/CPB.36.3480
(2R,3R,4S,5R,6R)-2-[(2R,3S,4R,5R,6R)-6-[(5'R,7S,9S,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-6-(hydroxymethyl)oxane-3,4,5-triol	6325838	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)O)O)O)O)O)C)O)C)C)OC1	772.90	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-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-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	101609012	Click to see	1067.20	unknown	https://doi.org/10.1016/0305-1978(87)90089-5 https://doi.org/10.1271/BBB.62.1904 https://doi.org/10.1248/CPB.47.738 https://doi.org/10.1021/JF000331V
16-[5-[3-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15-one	131751416	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(=O)C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1	1227.30	unknown	https://doi.org/10.1271/BBB.62.1904
Ampeloside Bf1	14187144	Click to see	1115.20	unknown	https://doi.org/10.1248/CPB.36.3480
Ampeloside Bf2	14187146	Click to see	953.10	unknown	https://doi.org/10.1248/CPB.36.3480
Ampeloside Bs1	14187142	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(C(O9)CO)O)O)O)O)O)O)O)C)O)C)C)OC1	935.10	unknown	https://doi.org/10.1248/CPB.36.3480
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	https://doi.org/10.1248/CPB.47.738 https://doi.org/10.1271/BBB.62.1904
Yayoisaponin A	5101819	Click to see	1229.30	unknown	https://doi.org/10.1271/BBB.62.1904
Yayoisaponin C	85125467	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(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1	1097.20	unknown	https://doi.org/10.1248/CPB.47.738 https://doi.org/10.1271/BBB.62.1904
> Mixed metal/non-metal compounds / Other mixed metal/non-metal oxoanionic compounds / Non-metal selenates
Hydroxysulfanyl hydrogen selenate	163192398	Click to see OSO[Se](=O)(=O)O	193.05	unknown	https://doi.org/10.1039/AI9943100325
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Methiin	9578071	Click to see CS(=O)CC(C(=O)O)N	151.19	unknown	https://doi.org/10.1021/JF990938F
S-Methylcysteine sulfoxide	82142	Click to see CS(=O)CC(C(=O)O)N	151.19	unknown	https://doi.org/10.1021/JF990938F
S-propyl-L-cysteine sulfoxide	87309	Click to see	179.24	unknown	https://doi.org/10.1021/JF990938F https://doi.org/10.1016/0305-1978(95)00072-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
S-Allyl-L-cysteine sulfoxide	15558642	Click to see C=CCS(=O)CC(C(=O)O)N	177.22	unknown	https://doi.org/10.1021/JF990938F
> 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
3-(allylsulphinyl)-L-alanine	87310	Click to see C=CCS(=O)CC(C(=O)O)N	177.22	unknown	https://doi.org/10.1016/0305-1978(95)00072-0 https://doi.org/10.1021/JF990938F
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids and derivatives
Antimycin A	14957	Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C	548.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Mercaptomethyl acetate	15354425	Click to see CC(=O)OCS	106.15	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Ketomycin	19489	Click to see	154.16	unknown	via CMAUP database
> Organic acids and derivatives / Organic thiosulfuric acids and derivatives / S-alkyl thiosulfates
S-Propyl thiosulfate	3083960	Click to see	156.20	unknown	https://doi.org/10.1021/NP0503350
> Organic acids and derivatives / Thiosulfinic acid esters
1-Propanesulfinothioic acid, S-methyl ester	20209223	Click to see	138.30	unknown	https://doi.org/10.1021/NP0503350
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Penten-3-Ol	12020	Click to see	86.13	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
Oleandomycin	72493	Click to see	687.90	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
9-[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]-3H-purin-6-one	21785357	Click to see C1C(C(C(C(O1)N2C=NC3=C2NC=NC3=O)O)O)O	268.23	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Acetoin	179	Click to see	88.11	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
3-Methylbutanal	11552	Click to see	86.13	unknown	https://doi.org/10.1080/10412905.1991.9697935
Pentanal	8063	Click to see	86.13	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Thiophene-2,3-dicarbaldehyde	573752	Click to see	140.16	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexanal	6184	Click to see	100.16	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
2-Methyl-2-pentenal	12177	Click to see	98.14	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
1-Octen-3-one	61346	Click to see	126.20	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
(2R)-2-[(2R,5S,6R)-6-[(3E,5E,7E,9E,11S)-11-ethyl-16-oxo-16-(1H-pyrrol-2-yl)hexadeca-3,5,7,9-tetraen-3-yl]-5-methyloxan-2-yl]propanoic acid	101789368	Click to see	495.70	unknown	via CMAUP database
Indanomycin	10345604	Click to see	493.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals
Acetal	7765	Click to see	118.17	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Ethers / Hemiacetals
1-(Ethylthio)ethanethiol	12499749	Click to see	122.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
Ethylthiopropanethiol	21516151	Click to see	136.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organoheterocyclic compounds / Azacyclic compounds
Trimethyldihydrodithiazine	129676057	Click to see CC1(C=CSSN1C)C	161.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Porric acid A	478958	Click to see	302.28	unknown	https://doi.org/10.1002/(SICI)1099-0690(199804)1998:4<661::AID-EJOC661>3.0.CO;2-V
Porric acid B	478957	Click to see	288.25	unknown	https://doi.org/10.1002/(SICI)1099-0690(199804)1998:4<661::AID-EJOC661>3.0.CO;2-V
Porric acid C	478956	Click to see CC1=CC(=CC2=C1C3=C(O2)C(=CC(=C3)O)C(=O)O)O	258.23	unknown	https://doi.org/10.1002/(SICI)1099-0690(199804)1998:4<661::AID-EJOC661>3.0.CO;2-V
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
methyl (2R)-6',10-dihydroxy-7',9'-dimethoxy-4',5',9-trioxospiro[3,4-dihydropyrano[4,3-g]chromene-2,2'-3H-benzo[g][1]benzofuran]-7-carboxylate	97042233	Click to see COC1=CC(=C(C2=C1C3=C(CC4(O3)CCC5=C(O4)C(=C6C(=C5)C=C(OC6=O)C(=O)OC)O)C(=O)C2=O)O)OC	536.40	unknown	via CMAUP database
Methyl (2S)-4,5',8',9-tetrahydro-4',9',10-trihydroxy-7'-methoxy-5',8',9-trioxospiro(benzo(1,2-b:5,4-c')dipyran-2(3H),2'(3'H)-naphtho(2,3-b)furan)-7-carboxylate	5464075	Click to see	522.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Bi- and oligothiophenes
2-ethenyl-5-[5-[(E)-prop-1-enyl]thiophen-2-yl]thiophene	14704544	Click to see	232.40	unknown	via CMAUP database
2,2':5',2''-Terthiophene	65067	Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3	248.40	unknown	via CMAUP database
5-(3-Buten-1-ynyl)-2,2'-bithienyl	70813	Click to see	216.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinoxalines / Phenazines and derivatives
6-Acetylphenazine-1-carboxylic acid	443635	Click to see	266.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Ethylfuran	18554	Click to see CCC1=CC=CO1	96.13	unknown	https://doi.org/10.1080/10412905.1991.9697935
2-Pentylfuran	19602	Click to see	138.21	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organoheterocyclic compounds / Imidazodiazepines
(8R)-3-[(2R,4R,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7,8-dihydro-4H-imidazo[4,5-d][1,3]diazepin-8-ol	44283251	Click to see	268.27	unknown	via CMAUP database
Pentostatin	439693	Click to see C1C(C(OC1N2C=NC3=C2NC=NCC3O)CO)O	268.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4R,5S)-3-hexyl-4-hydroxy-5-methyloxolan-2-one	11030843	Click to see	200.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
2,3-Secoporrigenin	10837674	Click to see	460.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
2-(3-Buten-1-ynyl)-5-[(E)-3-penten-1-ynyl]thiophene	14550074	Click to see	198.29	unknown	via CMAUP database
2-(But-3-en-1-ynyl)-5-(penta-1,3-diynyl)-thiophene	14262770	Click to see	196.27	unknown	via CMAUP database
> Organosulfur compounds
Oxo-prop-1-enyl-propoxy-sulfanylidene-lambda6-sulfane	54203861	Click to see	180.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
Propyl sulfinothioic acid	19020798	Click to see	124.23	unknown	https://doi.org/10.1021/JF00024A018 https://doi.org/10.1021/JF00024A017
> Organosulfur compounds / Allyl sulfur compounds
3-(Prop-2-enyldisulfanyl)pentane	163195820	Click to see	176.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
3-(Propylthio)propene	98781	Click to see	116.23	unknown	https://doi.org/10.1080/10412905.1991.9697935
Allyl methyl disulfide	62434	Click to see	120.20	unknown	https://doi.org/10.1080/10412905.1991.9697935
Allyl propyl disulfide	16591	Click to see CCCSSCC=C	148.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
Allylthiosulfinsaure	53743786	Click to see	122.21	unknown	https://doi.org/10.1021/JF00024A017
Diallyl disulfide	16590	Click to see C=CCSSCC=C	146.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Organic disulfides
1-(Methyldithio)-1-propene	521863	Click to see	120.20	unknown	https://doi.org/10.1080/10412905.1991.9697935
Dipropenyldisulfid	171311	Click to see	146.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
1-Ethylsulfanyl-1-(1-ethylsulfanylethyldisulfanyl)ethane	163192318	Click to see CCSC(C)SSC(C)SCC	242.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
1-Ethylsulfanyl-1-(1-ethylsulfanylhexyldisulfanyl)hexane	163195823	Click to see CCCCCC(SCC)SSC(CCCCC)SCC	354.70	unknown	https://doi.org/10.1080/10412905.1991.9697935
2-Ethylsulfanyl-1-(2-ethylsulfanylbutyldisulfanyl)butane	163192583	Click to see	298.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
2-Methylsulfanyl-1-(2-methylsulfanylbutyldisulfanyl)butane	163195731	Click to see	270.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
2-Methylsulfanyl-1-(2-methylsulfanylpentyldisulfanyl)pentane	163192316	Click to see	298.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
3-Methylsulfanyl-1-(3-methylsulfanylbutyldisulfanyl)butane	163192417	Click to see	270.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
3-Propylsulfanyl-1-(3-propylsulfanylbutyldisulfanyl)butane	163195821	Click to see CCCSC(C)CCSSCCC(C)SCCC	326.70	unknown	https://doi.org/10.1080/10412905.1991.9697935
3-Propylsulfanyl-1-(3-propylsulfanylpentyldisulfanyl)pentane	163192250	Click to see CCCSC(CC)CCSSCCC(CC)SCCC	354.70	unknown	https://doi.org/10.1080/10412905.1991.9697935
Dipropyl disulfide	12377	Click to see	150.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
Ethyl-1-(ethylthio)ethyldisulfid	129890562	Click to see	298.60	unknown	https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl disulfide	16592	Click to see	122.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Organic trisulfides
Allyl propyl trisulfide	525330	Click to see	180.40	unknown	https://doi.org/10.1080/10412905.1991.9697935
Dipropyl trisulfide	22383	Click to see CCCSSSCCC	182.40	unknown	https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl trisulfide	5319765	Click to see	154.30	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Sulfenyl compounds
1-(Methylpentasulfanyl)prop-1-ene	85619639	Click to see	216.40	unknown	https://doi.org/10.1080/10412905.1991.9697935
1-(Prop-1-enyltetrasulfanyl)propane	528717	Click to see CCCSSSSC=CC	212.40	unknown	https://doi.org/10.1080/10412905.1991.9697935
Dipropyl tetrasulfide	104285	Click to see	214.40	unknown	https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl pentasulfide	528716	Click to see	218.50	unknown	https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl tetrasulphide	528709	Click to see CCCSSSSC	186.40	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Thioacetals / Dithioacetals
1-Methylsulfanyl-1-(1-methylsulfanylethylsulfanyl)ethane	12687136	Click to see CC(SC)SC(C)SC	182.40	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Thioethers / Dialkylthioethers
3-(Ethylsulfanyl)pentane	15709057	Click to see	132.27	unknown	https://doi.org/10.1080/10412905.1991.9697935
Propyl sulfide	8118	Click to see	118.24	unknown	https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Thiols / Alkylthiols
1-Propanethiol, 3-amino-	97436	Click to see	91.18	unknown	via CMAUP database
2-Propanethiol	6364	Click to see	76.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Anthracyclines
Cinerubin B	73593	Click to see	825.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-Phenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	22446905	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=CC=CC=C3O2)OC4C(C(C(C(O4)CO)O)O)O	400.40	unknown	https://doi.org/10.1021/NP0503350
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/10.1016/S0031-9422(01)00039-5
Kaempferol 3-neohesperidoside	5318761	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/10.1016/S0031-9422(01)00039-5
> Phenylpropanoids and polyketides / Macrolactams
Desferrioxamine X5	85625752	Click to see	598.70	unknown	https://doi.org/10.1016/S0031-9422(00)85486-2

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Allium ampeloprasum

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