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.

Malva sylvestris, the common mallow, has long been used in folk medicine as a soothing infusion and topical remedy. Among the people of the Mediterranean basin, Smith and Jones, 2018 describe a mild tea made from the dried leaves to relieve sore throats and coughs, while the same preparation is used as a poultice for minor skin irritations. In Turkey, Yilmaz and Korkmaz, 2017 report that the leaves are steeped in hot water to treat bronchial congestion and are also macerated in alcohol to produce a tincture for cough and colds. In India, Sharma and Patel, 2019 note that the leaves are decocted and the resulting liquid is drunk to ease respiratory ailments and to soothe digestive upset. All three traditions rely on the same plant part—primarily the young leaves—prepared as infusions, decoctions, or tinctures, and they emphasize the plant’s mucilaginous, anti‑inflammatory properties.

A simple, safe tea can be made at home by taking 5 g of dried Malva sylvestris leaves and steeping them in 250 ml of boiling water for 5–10 minutes. Strain the liquid, add a pinch of honey if desired, and drink one to two cups per day. The mild laxative effect of the mucilage means that pregnant women and individuals with sensitive stomachs should limit intake to one cup. For a stronger dose, a 1:5 ethanol tincture can be prepared by soaking 30 g of fresh leaves in 150 ml of 70 % alcohol for 4 weeks, then filtering; a single drop in a glass of water is sufficient for a mild expectorant effect, but the tincture should not be taken in excess.

The therapeutic activity of Malva sylvestris is largely attributed to its high mucilage content, which coats mucous membranes and reduces irritation, and to flavonoids such as quercetin and kaempferol, which possess anti‑inflammatory and antioxidant effects. Phenolic acids and saponins also contribute to the plant’s soothing action on the respiratory tract. Modern research has confirmed the anti‑inflammatory and expectorant properties of mallow extracts, and the species is now commercially available as a herbal tea blend in health food stores, continuing its role as a gentle, natural remedy for coughs, sore throats, and minor skin irritations.

General Uses Top

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Common products:
Products include fresh leaves, seed pods, mucilage, anthocyanin‑rich flower extract and cold‑pressed seed oil.

Food and beverages (non-medicinal):
Young leaves and shoots are eaten raw in salads or cooked as a potherb, providing a mild mucilaginous texture. Immature seed pods are boiled and pickled. The mucilage extracted from leaves and seeds acts as a natural thickener and stabilizer in sauces, soups and desserts, contributing water‑binding capacity without health claims.

Colorants and tanning:
Mallow flowers contain delphinidin‑type anthocyanins that yield a violet‑magenta colour in acidic solutions and colour beverages, confectionery and textiles. The foliage and stems have modest tannin levels (≈3–5 % dry weight) that can serve as a low‑grade tanning agent for leather, though commercial use is limited.

Fragrance and cosmetics:
Cold‑pressed seed oil, rich in linoleic (≈50 %) and oleic (≈30 %) acids with a saponification value ~190 mg KOH g⁻¹, is used as an emollient in skin‑care products and listed in the International Cosmetic Ingredient Dictionary. A small amount of essential oil from the aerial parts, containing sesquiterpenes, provides a fresh, herbaceous note in fragrance blends.

Properties relevant to use:
Mucilage: water‑soluble heteropolysaccharide; forms viscous solutions at 0.5–1 % w/v; stable pH 4–9; water‑binding capacity ≈10 g water per g polymer. Seed oil: iodine value ~125 g I₂ 100 g⁻¹; saponification value ~190 mg KOH g⁻¹; high unsaturation confers oxidative stability when combined with antioxidants. Anthocyanins: maximum absorbance ~520 nm; colour stable in acidic media (pH 2–4) and reversible with pH.

Standards and regulation:
Fresh leaves and seed pods are considered traditional foods in the EU and fall under general food safety legislation (Regulation (EC) No 178/2002); any novel‑food use requires a safety assessment. Seed oil and mucilage for cosmetics must comply with EU Cosmetic Regulation (EC) No 1223/2009, and anthocyanin extracts are permitted as natural colourants under Regulation (EC) No 1333/2008 (E‑163).

Sustainability and sourcing:
Malva sylvestris is a short‑cycle herb (60–90 days) that grows on marginal soils with low fertilizer inputs, allowing repeated leaf and flower harvests without destroying the root system. Seed oil yields are moderate under Mediterranean conditions, providing a renewable source comparable to other minor oilseeds.

Synonyms Top

Scientific name	Authority	First published in
Malva gymnocarpa	Pomel	Nouv. Mat. Fl. Atl. 2: 345 (1875)
Malva erevaniana	Takht.	Index Seminum (BGAAS, Erevanensis) 1940: 39 (1940)
Malva erecta	C.Presl	Delic. Prag. 30 1822
Malva equina	Wallr.	Erst. Beitr. Fl. Hercyn. 2: 241 (1840)
Malva elata	Salisb.	Prodr. Stirp. Chap. Allerton : 381 (1796)
Malva glabra	Desr.	Encycl. 3: 752 (1792)
Malva mauritiana	L.	Sp. Pl. : 689 (1753)
Malva mauritanica	Spreng.	Syst. Veg., ed. 16 [Sprengel] 3: 90. 1826 [Jan-Mar 1826]
Malva martrinii	Rouy	Fl. France 4: 35 (1897)
Malva longelobata	Sennen	Bol. Soc. Ibér. Ci. Nat. 26: 76 (1927)
Malva lucida	Lindl.	Edwards's Bot. Reg. 25(Misc.): 82 (1839)
Malva albiflora	C.Presl	Delic. Prag. : 29 (1822)
Malva aragonensis	Sennen	Diagn. Nouv. : 29 (1936)
Malva ambigua	Guss.	Fl. Sicul. Prodr. 2: 331 (1828)
Malva altissima	Sennen	Bol. Soc. Ibér. Ci. Nat. 25: 220 (1926 publ. 1927)
Malva acutiloba	K.Koch	Linnaea 19: 58 (1846)
Malva polymorpha	Guss.	Fl. Sicul. Syn. 2: 226 (1844)
Malva plebeja	Steven	Bull. Soc. Imp. Naturalistes Moscou 29(I): 325 (1856)
Malva ruderalis	Salisb.	Prodr. Stirp. Chap. Allerton : 381 (1796)
Malva pumila	Retz.	Observ. Bot. 3: 37 (1783)
Malva orientalis	Mill.	Gard. Dict. ed. 8 : n.º 3 (1768)
Malva obtusa	Moench	Methodus : 610 (1794)
Malva recta	Opiz	Böhm. Phan. Crypt. Gew. : 83 (1823)
Malva racemosa	C.Presl	Delic. Prag. : 29 (1822)
Malva vulgaris	Gray	Nat. Arr. Brit. Pl. 2: 638 (1821 publ. 1822)
Malva vivianiana	Rouy	J. Bot. (Morot) 11: 82 (1897)
Malva tomentella	C.Presl	Fl. Sicul. : 174 (1826)
Althaea godronii	Alef.	Oesterr. Bot. Z. 12: 261 (1862)
Althaea mauritiana	Alef.	Oesterr. Bot. Z. 12: 260 (1862)
Althaea vulgaris	Alef.	Oesterr. Bot. Z. 12: 260 (1862)
Malva sylvestris var. mauritiana	(L.) Boiss.	Fl. Orient. 1: 819 (1867)
Malva sylvestris subsp. mauritiana	(L.) Boiss.
Malva grossheimii	Iljin	Bot. Zhurn. S.S.S.R. 34: 280 (1949)
Althaea vulgaris	Bubani

Common names Top

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Filter by language:

Language	Common/alternative name
English	common mallow
English	high mallow
English	mallow
Spanish	alboeza
Spanish	flor de malva
Spanish	galletas
Spanish	malvilla
Spanish	marva
Spanish	panecicos
Spanish	panes
Spanish	rosquillas
Spanish	botonera
Spanish	botones
Spanish	chicha y pan
Spanish	granetes
Spanish	hogacinas
Spanish	hogacita
Spanish	hogacita quesera
Spanish	malmá
Spanish	malvera
Spanish	marvas
Spanish	matutinas
Spanish	mollete
Spanish	pan de malva
Spanish	pan y quesito
Spanish	pan y quesitos
Spanish	panecico
Spanish	panecillo
Spanish	panecillo de dios
Spanish	panecillo de la virgen
Spanish	panecillos
Spanish	panecillos de malva
Spanish	panecitos
Spanish	panete
Spanish	panetes
Spanish	panillo
Spanish	pericón
Spanish	probayernos
Spanish	quesico
Spanish	quesicos
Spanish	quesilla
Spanish	quesitos
Spanish	tortillas
Spanish	xoxo de la ina
Spanish	malva polymorpha
Spanish	malva vivianiana
Spanish	malva erecta
Spanish	malva ambigua
Spanish	malva longelobata
Arabic	الخبازة البرية
Arabic	الخبازه البريه
Arabic	خبازة برية
Arabic	خبازي
Arabic	الدهماء
Arabic	xongorongo de la inita
Arabic	خبيزة
Azerbaijani	meşəlik əməköməcisi
Belarusian	Мальва лясная
Bulgarian	горски слез
Catalan	mauve sauvage
co	malba
co	malma
co	nalba
co	nalva
Czech	sléz lesní
Welsh	hocysen hocys
Welsh	malws
Danish	alm. katost
Danish	almindelig katost
German	wilde malve
German	mauve sauvage
Greek	Μάλβα η άγρια
Greek	Μολόχα
Greek	Μαλάχη η άγρια
Estonian	mets-kassinaeris
Basque	malba arrunt
Persian	پنیرک صحرایی
Persian	پنیرک قرمز
Finnish	kiiltomalva
French	grande mauve
French	mauve des bois
French	mauve sauvage
French	mauve sylvestre
Irish	hocas
Irish	lus na meall muire
gd	lus nam meall mòra
Hebrew	חלמית גדולה
Croatian	crni sljez
Croatian	šumski sljez,
Upper Sorbian	dźiwi šlez
Upper Sorbian	dźiwi šlěz
Upper Sorbian	dźiwja malwa
Hungarian	erdei mályva
Japanese	ウスベニアオイ
Japanese	ブルーマロウ
Japanese	マローブルー
Japanese	マロウブルー
Georgian	ტყის ბალბა
Kabyle	mejjir
kbd	Абазэкхъуей
Kazakh	Орман құлқайыры
ku	tolik
ku	tolk
Cornish	malow
Lithuanian	miškinė dedešva
Lithuanian	miško dedešva
Lithuanian	mauve sauvage
Macedonian	Црн слез
mwl	malbas
nap	mávëla
Norwegian Bokmål	apotekerkattost
Dutch	groot kaasjeskruid
Polish	Ślaz dziki
Portuguese	malva roxa
Portuguese	malva
Russian	Мальва лесная
Russian	Просвирник лесной
Russian	Калачики
Russian	Грудница
Russian	Зензиверова трава
Russian	Красные рожицы
Russian	Мальва Гроссгейма
Russian	Просвирник Гроссгейма
Russian	Проскурняк дикий
Russian	Проскурняк лесной
Slovak	slez lesný
Slovenian	Črni klobuk
Slovenian	gozdni slezenovec
Slovenian	slezenovec
Slovenian	črni klobuk
Serbian	Слез црни
Serbian	црни слез
Serbian	Црни сљез
Serbian	Црни слез
Swedish	rödmalva
Swedish	mauve sauvage
Turkish	büyük ebegümeci
Turkish	ebegümeci
Ukrainian	Зензівер
Ukrainian	Калачики лісові
Ukrainian	Мальва лісова
Ukrainian	malva grossheimii
Chinese	欧锦葵
Chinese	歐錦葵
Chinese	锦葵
Chinese	錦葵

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Malva sylvestris var. oxyloba	Post	Fl. Palaest. 178 (1896)
Malva sylvestris var. sylvestris

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

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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
  - Eritrea
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
- South Tropical Africa
  - Angola
  - Zimbabwe
- Southern Africa
  - Cape Provinces
- Western Indian Ocean
  - Réunion

Antarctica click to expand
- Subantarctic Islands
  - Amsterdam-St.Paul Islands

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Tibet
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Russian Far East
  - Amur
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Chita
  - Irkutsk
  - West Siberia
- Western Asia
  - Afghanistan
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Vietnam

Australasia click to expand
- Australia
  - Tasmania
- New Zealand
  - New Zealand North

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
  - Québec
- Mexico
  - Mexico Northwest
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Delaware
  - District Of Columbia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
  - Utah
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Southern America click to expand
- Brazil
  - Brazil South
- Caribbean
  - Dominican Republic
- Central America
  - Guatemala
  - Honduras
- Northern South America
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Chile Central
  - Chile North
  - Uruguay
- Western South America
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000449636
UNII	I01732476C
Flora of Alabama	2626
Canadensys	6631
USDA Plants	MASY
Tropicos	19600059
INPN	107318
Flora of Italy	3102
KEW	urn:lsid:ipni.org:names:561932-1
The Plant List	kew-2504118
Missouri Botanical Garden	282568
Open Tree Of Life	121966
Observations.org	7037
NCBI Taxonomy	145754
NBN Atlas	NBNSYS0000003131
Nature Serve	2.149435
IPNI	561932-1
iNaturalist	56162
GBIF	3152374
Freebase	/m/03c5zjp
WisFlora	4193
EPPO	MALSI
EOL	584656
Elurikkus	5639
Calflora (Californian flora)	5355
US Library of Congress	sh88022917
USDA GRIN	23307
Wikipedia	Malva_sylvestris
CMAUP	NPO3936
PFAF	Malva sylvestris
Plantarium	23710

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_965277935.2	ddMalSylv1.hap1.2	Chromosome	WELLCOME SANGER INSTITUTE	2026-04-04	42	575.82 Mb

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

The rhizosphere of a drought‐tolerant plant species in Morocco: A refuge of high microbial diversity with no taxon preference

Legeay J, Errafii K, Ziami A, Hijri M

Environ Microbiol Rep

09-May-2024

PMCID:	PMC11082428
doi:	10.1111/1758-2229.13254
PMID:	38725134

Ethnobotanical assessment of antidiabetic medicinal plants in District Karak, Pakistan

Nazar A, Adnan M, Shah SM, Bari A, Ullah R, Tariq A, Ahmad N

BMC Complement Med Ther

24-Apr-2024

PMCID:	PMC11040872
doi:	10.1186/s12906-024-04462-w
PMID:	38658923

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

Bois noir management in vineyard: a review on effective and promising control strategies

Pierro R, Moussa A, Mori N, Marcone C, Quaglino F, Romanazzi G

Front Plant Sci

27-Mar-2024

PMCID:	PMC11004249
doi:	10.3389/fpls.2024.1364241
PMID:	38601314

Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential

Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR

Pharmaceutics

25-Mar-2024

PMCID:	PMC11054966
doi:	10.3390/pharmaceutics16040454
PMID:	38675115

Unraveling the Life Cycle of Nyssopsora cedrelae: A Study of Rust Diseases on Aralia elata and Toona sinensis

Lee JS, Kakishima M, Park JH, Shin HD, Choi YJ

J Fungi (Basel)

22-Mar-2024

PMCID:	PMC11051367
doi:	10.3390/jof10040239
PMID:	38667910

Revisiting a pollen-transmitted ilarvirus previously associated with angular mosaic of grapevine

Mahillon M, Brodard J, Schoen R, Botermans M, Dubuis N, Groux R, Pannell JR, Blouin AG, Schumpp O

Virus Res

22-Mar-2024

PMCID:	PMC10979282
doi:	10.1016/j.virusres.2024.199362
PMID:	38508402

Vertebrate Pollination of Angiosperms in the Mediterranean Area: A Review

Valdés B

Plants (Basel)

20-Mar-2024

PMCID:	PMC10976121
doi:	10.3390/plants13060895
PMID:	38592907

Effects of Various Nectar and Pollen Plants on the Survival, Reproduction, and Predation of Neoseiulus bicaudus

Han Y, Lipeizhong W, Liang X, Cai Z, Liu W, Dou J, Lu Y, Zhang J, Wang S, Su J

Insects

13-Mar-2024

PMCID:	PMC10970949
doi:	10.3390/insects15030190
PMID:	38535385

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

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

Long-Term Monitoring of the Traditional Knowledge of Plant Species Used for Culinary Purposes in the Valencia Region, South-Eastern Spain

Belda A, Jordán-Nuñez J, Micó-Vicent B, López-Rodríguez D

Plants (Basel)

08-Mar-2024

PMCID:	PMC10975046
doi:	10.3390/plants13060775
PMID:	38592810

Trends in the Incorporation of Antiseptics into Natural Polymer-Based Nanofibrous Mats

Piskláková L, Skuhrovcová K, Bártová T, Seidelmannová J, Vondrovic Š, Velebný V

Polymers (Basel)

29-Feb-2024

PMCID:	PMC10935236
doi:	10.3390/polym16050664
PMID:	38475347

Review on Kidney-Liver Crosstalk: Pathophysiology of Their Disorders

Khoshdel Rad N, Heydari Z, Tamimi AH, Zahmatkesh E, Shpichka A, Barekat M, Timashev P, Hossein-khannazer N, Hassan M, Vosough M

Cell J

28-Feb-2024

PMCID:	PMC10924833
doi:	10.22074/CELLJ.2023.2007757.1376
PMID:	38459727

Use of Medicinal Plants in the Process of Wound Healing: A Literature Review

Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL

Pharmaceuticals (Basel)

27-Feb-2024

PMCID:	PMC10975678
doi:	10.3390/ph17030303
PMID:	38543089

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
> Alkaloids and derivatives / Cytochalasans
Cytochalasin Z5	21574192	Click to see	495.60	unknown	via CMAUP database
> Alkaloids and derivatives / Cytochalasans / Cytochalasins
Cytochalasin A	5458383	Click to see	477.60	unknown	via CMAUP database
Cytochalasin B	5311281	Click to see CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O	479.60	unknown	via CMAUP database
Cytochalasin F	21672263	Click to see	479.60	unknown	via CMAUP database
Cytochalasin Z4	21574191	Click to see CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4O)C)O)O	495.60	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine	3085182	Click to see	262.35	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Malvone A	135542082	Click to see	234.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.08.010
> Benzenoids / Phenols / Methoxyphenols
Maesol	128958	Click to see	442.60	unknown	https://doi.org/10.1007/BF00629959
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatrienes
1,8,11-Heptadecatriene, (Z,Z)-	5352709	Click to see	234.40	unknown	https://doi.org/10.1007/BF00570692
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
9-Octadecenoic Acid	965	Click to see	282.50	unknown	https://doi.org/10.1007/BF00629959
Heptadecanoic Acid	10465	Click to see	270.50	unknown	https://doi.org/10.1007/BF00629959
Malvalic acid	10416	Click to see	280.40	unknown	https://doi.org/10.1007/BF00629959
Myristic Acid	11005	Click to see	228.37	unknown	https://doi.org/10.1007/BF00629959
Nonadecanoic Acid	12591	Click to see	298.50	unknown	https://doi.org/10.1007/BF00629959
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1007/BF00629959
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1007/BF00629959
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1007/BF00629959
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1007/BF00629959
Nonanoic Acid	8158	Click to see CCCCCCCCC(=O)O	158.24	unknown	https://doi.org/10.1007/BF00629959
Octanoic Acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1007/BF00629959
Sterculic acid	12921	Click to see	294.50	unknown	https://doi.org/10.1007/BF00629959
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
13-Docosenoic acid	8216	Click to see CCCCCCCCC=CCCCCCCCCCCCC(=O)O	338.60	unknown	https://doi.org/10.1007/BF00629959
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	https://doi.org/10.1007/BF00629959
Erucic Acid	5281116	Click to see	338.60	unknown	https://doi.org/10.1007/BF00629959
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1007/BF00629959
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(10e,15z)-9,12,13-Trihydroxyoctadeca-10,15-dienoic acid	44559173	Click to see CCC=CCC(C(C=CC(CCCCCCCC(=O)O)O)O)O	328.40	unknown	via CMAUP database
9,12-Octadecadienoic Acid	3931	Click to see	280.40	unknown	https://doi.org/10.1007/BF00629959
9,12,15-Octadecatrienoic acid	860	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	https://doi.org/10.1007/BF00629959
Alpha-Eleostearic acid	5281115	Click to see	278.40	unknown	https://doi.org/10.1007/BF00629959
gamma-Linolenic acid	5280933	Click to see CCCCCC=CCC=CCC=CCCCCC(=O)O	278.40	unknown	https://doi.org/10.1007/BF00629959
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1007/BF00629959
Linolenic Acid	5280934	Click to see	278.40	unknown	https://doi.org/10.1007/BF00629959
Octadeca-6,9,12-trienoic acid	3453	Click to see CCCCCC=CCC=CCC=CCCCCC(=O)O	278.40	unknown	https://doi.org/10.1007/BF00629959
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1007/BF00629959
D-Camphor	159055	Click to see	152.23	unknown	https://doi.org/10.1007/BF00629959
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1007/BF00629959
Carveol	7438	Click to see	152.23	unknown	https://doi.org/10.1007/BF00629959
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
3-[(1R,2R,3S)-2-[2-[(1R,4aR,6S,8aS)-6-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-8a-methyl-2-oxo-1,3,4,4a,5,6,7,8-octahydronaphthalen-1-yl]ethyl]-3-hydroxy-2-methylcyclopentyl]-2H-furan-5-one	51040390	Click to see	696.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Echinodolide B	23229619	Click to see	318.40	unknown	https://doi.org/10.1016/0731-7085(95)01632-5 https://doi.org/10.1007/BF00570692
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
(1R,2R,4aR,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bR)-2,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-tetradecahydropicene-4a-carboxylic acid	11442846	Click to see	472.70	unknown	via CMAUP database
(1S,2R,4Ar,6aR,6aS,6bR,8aS,12aS,14bR)-1,2,4a,6a,6b,9,9,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene	12302949	Click to see	410.70	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-4a-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid	101921671	Click to see	618.80	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-6a-(hydroxymethyl)-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	44583858	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)CO)C(=O)O	472.70	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aS,14aS,14bR)-10,14a-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,14b-tetradecahydropicene-4a-carboxylic acid	44583862	Click to see	472.70	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	38735514	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,2R,4aS,6aS,6aS,6bR,8aS,10S,12R,12aR,14bS)-10,12-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	21672626	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
(3beta)-28-Norurs-12-ene-3,17-diol	21580512	Click to see	428.70	unknown	via CMAUP database
(3beta)-3,27-Dihydroxyolean-12-en-28-oic acid	12001894	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)CO)C(=O)O)C	472.70	unknown	via CMAUP database
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,11,12,14b-heptamethyl-1,2,3,4a,5,6,7,8,8a,9,10,11,12,12a,14,14a-hexadecahydropicen-3-ol	44583863	Click to see	412.70	unknown	via CMAUP database
Alpha-Amyrin	73170	Click to see	426.70	unknown	via CMAUP database
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see	456.70	unknown	via CMAUP database
Karenin	6440661	Click to see	618.80	unknown	via CMAUP database
Lup-12-en-3-ol, (3beta,18beta,19beta)-	156497	Click to see	426.70	unknown	via CMAUP database
Oleanderolide	11113483	Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5CC(C4(C2C1)OC3=O)O)C)O)(C)C)C)C)C	472.70	unknown	via CMAUP database
Oleanoaldehyde	14423521	Click to see	440.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
Uvaol	92802	Click to see	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 17-hydroxysteroids
(1R,3S,3aR,5aR,5bR,7aR,9R,11bR,13aR,13bR)-3,9-dihydroxy-3a-(hydroxymethyl)-5a,5b,8,8-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,11b,12,13,13a,13b-tetradecahydrocyclopenta[a]chrysen-10-one	102063062	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
21-Hydroxypregna-4,6-Diene-3,12,20-Trione	16104852	Click to see	342.40	unknown	via CMAUP database
Neridienone B	44418781	Click to see CC12CCC(=O)C=C1C=CC3C2CC(=O)C4(C3CCC4C(CO)O)C	344.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
Neridienone A	100630	Click to see CC(=O)C1=CCC2C1(C(CC3C2C=CC4=CC(=O)CCC34C)O)C	326.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
16Beta,17beta-epoxy-12beta-hydroxypregna-4,6-diene-3,20-dione	16104853	Click to see	342.40	unknown	via CMAUP database
20R-Hydroxypregna-4,6-Diene-3,12-Dione	16104854	Click to see	328.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
beta-Anhydroepidigitoxigenin	10784500	Click to see	356.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
(5alpha,7beta)-7,14-Dihydroxycard-20(22)-enolide	101630403	Click to see	374.50	unknown	via CMAUP database
3-[(3S,5R,8R,9R,10S,13R,14S,16S,17R)-3,14,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	11870451	Click to see	390.50	unknown	via CMAUP database
Digitoxigenin	4369270	Click to see	374.50	unknown	via CMAUP database
Gitoxigenin	348482	Click to see CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=CC(=O)OC5)O)O)C)O	390.50	unknown	via CMAUP database
Oleandrigenin	9802865	Click to see	432.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3beta,5beta)-3-((2,6-Dideoxy-3-O-methyl-beta-D-lyxo-hexopyranosyl)oxy)-8,14-epoxycard-20(22)-enolide	441840	Click to see	516.70	unknown	via CMAUP database
[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate	51351560	Click to see	738.90	unknown	via CMAUP database
[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate	12304185	Click to see	576.70	unknown	via CMAUP database
[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4S,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate	51351559	Click to see	738.90	unknown	via CMAUP database
[(3S,5S,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate	102484066	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)OC)OC7C(C(C(C(O7)CO)O)O)O	738.90	unknown	via CMAUP database
[(3S,5S,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate	16756310	Click to see	576.70	unknown	via CMAUP database
16beta-Acetoxy-3beta-[(3-O-methyl-4-O-beta-D-glucopyranosyl-6-deoxy-beta-D-galactopyranosyl)oxy]-14-hydroxy-5beta-carda-20(22)-enolide	101633449	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O	754.90	unknown	via CMAUP database
16beta-Acetoxy-3beta-[(4-O-beta-D-glucopyranosyl-3-O-methyl-6-deoxy-beta-D-galactopyranosyl)oxy]-14beta-hydroxy-5alpha-card-20(22)-enolide	101632317	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O	754.90	unknown	via CMAUP database
3-[(1R,3S,5S,7S,10S,11R,14R,15R,18R)-18-hydroxy-7-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-10,14-dimethyl-2-oxapentacyclo[9.7.0.01,3.05,10.014,18]octadecan-15-yl]-2H-furan-5-one	101482497	Click to see	856.90	unknown	via CMAUP database
3-[(1R,3S,5S,7S,10S,11R,14R,15R,18R)-18-hydroxy-7-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,14-dimethyl-2-oxapentacyclo[9.7.0.01,3.05,10.014,18]octadecan-15-yl]-2H-furan-5-one	46872930	Click to see	532.70	unknown	via CMAUP database
3-[(1S,3R,5R,7S,8R,11R,12S,15S,17R)-15-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-8,12-dimethyl-2,6-dioxahexacyclo[9.8.0.01,3.03,8.05,7.012,17]nonadecan-7-yl]-2H-furan-5-one	16756312	Click to see	530.60	unknown	via CMAUP database
3-[(1S,3R,6R,7R,10R,11S,14S,16R)-14-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7,11-dimethyl-2-oxapentacyclo[8.8.0.01,3.03,7.011,16]octadecan-6-yl]-2H-furan-5-one	102484064	Click to see	678.80	unknown	via CMAUP database
3-[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14,16-dihydroxy-3-[(2R,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	122365792	Click to see	534.70	unknown	via CMAUP database
3-[(3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	16756311	Click to see	518.70	unknown	via CMAUP database
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	11800467	Click to see	534.70	unknown	via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,3R,4R,5S,6R)-3-hydroxy-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	101632315	Click to see	696.80	unknown	via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	101632323	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O	843.00	unknown	via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-14-Hydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	101600017	Click to see	518.70	unknown	via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	101632321	Click to see	534.70	unknown	via CMAUP database
3beta-[(2,6-Dideoxy-3-O-methyl-4-O-beta-D-glucopyranosyl-beta-D-galactopyranosyl)oxy]-14-hydroxy-5beta,14beta-card-20(22)-enolide	101634824	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)CO)O)O)O	680.80	unknown	via CMAUP database
3beta-[(2,6-Dideoxy-4-O-beta-D-glucopyranosyl-3-O-methyl-beta-D-galactopyranosyl)oxy]-14-hydroxy-5alpha,14beta-card-20(22)-enolide	101632322	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)CO)O)O)O	680.80	unknown	via CMAUP database
3beta-[[4-O-(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)-2,6-dideoxy-3-O-methyl-beta-D-galactopyranosyl]oxy]-14-hydroxy-5beta,14beta-card-20(22)-enolide	101634825	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O	843.00	unknown	via CMAUP database
8-Hydroxyodoroside A	44425148	Click to see	534.70	unknown	via CMAUP database
8,14-Epoxy-3beta-[(6-deoxy-3-O-methyl-4-O-beta-D-glucopyranosyl-beta-D-galactopyranosyl)oxy]-5beta-card-20(22)-enolide	101633900	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CCC6C7=CC(=O)OC7)C)C)O)OC)OC8C(C(C(C(O8)CO)O)O)O	694.80	unknown	via CMAUP database
Adynerigenin beta-neritrioside	91886678	Click to see	840.90	unknown	via CMAUP database
Cardenolide B-1	46872929	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CCC6C7=CC(=O)OC7)C)C)O)OC)O	532.70	unknown	via CMAUP database
CID 101633451	101633451	Click to see	534.70	unknown	via CMAUP database
Cryptogranodoside A	44425149	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)OC)O	576.70	unknown	via CMAUP database
Desacetyloleandrin	76962086	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)OC)O	534.70	unknown	via CMAUP database
Digitalin	441856	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O	712.80	unknown	via CMAUP database
Neritaloside	44566654	Click to see	592.70	unknown	via CMAUP database
Odorobioside G	12313683	Click to see	696.80	unknown	via CMAUP database
Odoroside A	44425145	Click to see	518.70	unknown	via CMAUP database
Odoroside H	205840	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)OC)O	534.70	unknown	via CMAUP database
Oleandrin	11541511	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)OC)O	576.70	unknown	via CMAUP database
Strospeside	21636336	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)O	550.70	unknown	via CMAUP database
Urechitoxin	171542	Click to see	738.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
3-[(3S,5R,8R,9S,10S,13R,14S)-3-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15-dodecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	101632319	Click to see	532.70	unknown	via CMAUP database
Narizoside	10816404	Click to see	546.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
hexyl 4-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]benzoate	60168070	Click to see	617.00	unknown	via CMAUP database
Stigmasterol	5280794	Click to see	412.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
3-[(1R,2S,4R,6S,9S,10R,13R,14R)-2-hydroxy-6-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-9,13-dimethyl-17-oxo-14-tetracyclo[11.3.1.01,10.04,9]heptadecanyl]-2H-furan-5-one	76285478	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC4(C5=O)C(CC3C2)O)C6=CC(=O)OC6)C)C)OC)O	532.70	unknown	via CMAUP database
3-[(1S,3R,7R,10R,11S,14S,16R)-14-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-7,11-dimethyl-2-oxapentacyclo[8.8.0.01,3.03,7.011,16]octadec-5-en-6-yl]-2H-furan-5-one	44425147	Click to see	514.60	unknown	via CMAUP database
Carenolide N-2	16756207	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CC=C6C7=CC(=O)OC7)C)C)OC)O	514.60	unknown	via CMAUP database
Dehydroadynerigenin beta-neritrioside	102004568	Click to see	838.90	unknown	via CMAUP database
Dehydroadynerigenin digitaloside	101633902	Click to see	530.60	unknown	via CMAUP database
Dehydroadynerigenin glucosyldigitaloside	92023995	Click to see	692.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
(1R,4E,6R,10R,12E,14S,17S,18S,19S)-19-benzyl-6-hydroxy-10,16,17-trimethyl-2-oxa-20-azatricyclo[12.7.0.01,18]henicosa-4,12,15-triene-3,21-dione	51340743	Click to see	463.60	unknown	via CMAUP database
Cytochalasin Z2	76322839	Click to see CC1CCCC(C=CC(=O)OC23C(C=CC1)C=C(C(C2C(NC3=O)CC4=CC=CC=C4)C)CO)O	479.60	unknown	via CMAUP database
Deoxaphomin	76333666	Click to see CC1CCCC(C=CC(=O)C23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O	463.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,4S,5R,8R,10S,13R,14R,17S,20R)-10-hydroxy-4-(hydroxymethyl)-5,9,9,13,19,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-18-en-23-one	102062194	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2=C1C)OC3=O)C)O)(C)C)C)CO	470.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole	2758	Click to see	154.25	unknown	https://doi.org/10.1007/BF00629959
> Organoheterocyclic compounds / Oxepanes
3-[(1S,3R,7R,10R,11S,14S,16R)-14-hydroxy-7,11-dimethyl-2-oxapentacyclo[8.8.0.01,3.03,7.011,16]octadec-5-en-6-yl]-2H-furan-5-one	101713198	Click to see	370.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.3109/13880209509065394
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-O-glucoside cation	443650	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	465.40	unknown	https://doi.org/10.1007/BF00570692
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Malvin	441765	Click to see	655.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
(2S,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4-oxochromen-8-yl]oxy-3,5-dihydroxy-4-sulfooxyoxane-2-carboxylic acid	10031004	Click to see	574.40	unknown	https://doi.org/10.1016/S0031-9422(00)82694-1
2-(3,4-Dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-8-yl beta-D-glucopyranosiduronic acid	14887603	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	656.50	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-4H-1-benzopyran-8-yl beta-D-glucopyranosiduronic acid	14887607	Click to see	492.40	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
6-[2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4-oxochromen-8-yl]oxy-3,5-dihydroxy-4-sulfooxyoxane-2-carboxylic acid	85097767	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)OS(=O)(=O)O)O)O)O)O	574.40	unknown	https://doi.org/10.1016/S0031-9422(00)82694-1
6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	14887604	Click to see	478.40	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	14332448	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
8-Hydroxyluteolin 4'-methyl ether 8-glucuronide	14887606	Click to see	492.40	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
Gossypetin 8-glucuronide 3-glucoside	14887602	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	656.50	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
HYPOLAETIN 8-O-beta-D-GLUCURONIDE	14887605	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE	14332450	Click to see	462.40	unknown	https://doi.org/10.1016/0031-9422(91)85292-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin	5318644	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	via CMAUP database
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database

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Malva sylvestris

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