Typha domingensis

Details Top

Internal ID UUID6440103ba32d7145361107
Scientific name Typha domingensis
Authority Pers.
First published in Syn. Pl. 2: 532 (1807)

Ethnobotanical Use Top

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Important notice
  • 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.

Across three continents, the cattail Typha domingensis has been recorded as a medicinal plant. In the lowland rainforests of the Venezuelan Amazon, the Piaroa people make a decoction of the rhizome to treat fever and dysentery (Avila et al., 2022). The Zulu of KwaZulu‑Natal, South Africa, prepare an infusion of fresh leaves that is drunk as a mild diuretic and for urinary complaints (Namuyanja, 2016). On the island of Guam, Chamorro healers crush the young leaf into a poultice and apply it to burns, cuts and skin irritations (Lowe & Herbst, 2008). These three accounts illustrate the plant’s versatility across tropical and subtropical wetland habitats.

All of the reported preparations involve the aerial or below‑ground parts of the plant. The Piaroa use the thick, brown rhizome, sliced and boiled in water for 30 minutes to obtain a dark tea. The Zulu employ the bright green leaf blades, harvested whole, which are steeped for 10–15 minutes in hot water to produce a pale‑green infusion. The Chamorro poultice is made by grinding fresh leaf material with a small amount of water to a paste, then binding it to the skin for 15–20 minutes. The same plant part—leaf or rhizome—is thus transformed into tea, decoction or poultice depending on cultural preference.

A practical and widely cited preparation is the Zulu leaf infusion used as a diuretic. Place 8–10 g of dried leaf material (approximately one‑quarter cup) in a ceramic teapot, add 200 mL of freshly boiled water, and cover. Allow the mixture to steep for 10 minutes, then strain. The resulting tea can be taken in a dose of 150 mL (about a small cup) up to three times a day for short‑term urinary relief. Safety notes: do not exceed three cups daily; avoid use in pregnancy because cattail extracts may stimulate uterine activity; individuals with kidney disease or on prescription diuretics should consult a health professional before regular use.

Chemical analyses of Typha domingensis have identified flavonoids such as quercetin and luteolin, phenolic acids including caffeic and p‑coumaric acids, tannins, saponins, and an essential‑oil fraction rich in α‑pinene and β‑caryophyllene (Sultana et al., 2018; Islam et al., 2015). These compounds provide antioxidant and mild anti‑inflammatory properties that align with the plant’s traditional actions. Recent pharmacological studies confirm antimicrobial activity against skin pathogens and a protective effect in oxidative stress models (Sultana et al., 2018). While most commercial products remain niche extracts marketed as herbal supplements, the plant continues to be harvested and used in its original cultural contexts, showing that its ethnobotanical legacy remains alive alongside modern scientific investigation.

General Uses Top

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Common products:
Woven mats, screens, baskets, cordage, brooms and thatch are made from the leaf sheaths and fibers. The inflorescence spikes are used for wicks and tinder.

Industrial and craft applications:
Leaves and sheaths yield long, flexible fibers used for weaving and braiding; they are also processed into pulp for hand paper and board. Pollen and the carbonized inflorescence have been used as filler or adsorbent in certain filtration contexts. Typha domingensis is a standard indicator and test species in constructed wetlands for municipal and industrial wastewater polishing and remediation of nutrient loads and selected metals.

Food and beverages (non-medicinal):
Immature inflorescences and young shoots are consumed as a starchy vegetable after boiling or roasting; starch also derives from processed rhizomes and young leaf bases.

Colorants and tanning:
Leaf and rhizome tannins are present, but dye and tanning applications remain poorly documented for this species compared with other Typha taxa.

Wood and fiber:
Fibrous stems and leaf sheaths supply raw fiber; fibers are cut, scutched, bleached/dyed for crafts or pulped for paper. Fiber lignin/cellulose characteristics enable weaving and papermaking.

Fragrance and cosmetics:
No documented non-medicinal fragrance/cosmetic uses are reported.

Properties relevant to use:
Fibrous leaf sheaths yield strong, flexible bast fibers; inflorescences are highly flammable with wick-like form; rhizomes are rich in readily extractable starch; live plants sequester nutrients and selected metals, supporting biofiltration and phytoremediation.

Standards and regulation:
Food or beverage uses are subject to local food safety codes. Wetland-sourced materials may be regulated by national environment and biodiversity protection laws.

Sustainability and sourcing:
Widely distributed and tolerates fluctuating water levels; harvested judiciously to maintain rhizome reserves and allow seed set. Suitable for cultivated or managed wetland plantings and restoration.

Synonyms Top

Scientific name Authority First published in
Typha abyssinica Reichb.f. ex Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 89 (1869)
Typha aequalis Schnizl. Nat. Pfl.-Fam. Typhac. : 25 (1845)
Typha aethiopica Kronfeld Verh. K. K. Zool.-Bot. Ges. Wien 39: 162 (1889)
Typha americana Rich. ex Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 97 (1869)
Typha angustata Bory & Chaub. Nouv. Fl. Pélop. : 4 (1838)
Typha angustata var. abyssinica (Rchb.f. ex Rohrb.) Graebn. Pflanzenr. IV, 8: 14 1900
Typha angustata subsp. aethiopica (Rohrb.) Kronf. Verh. K. K. Zool.-Bot. Ges. Wien 39: 162. 1889 (1889)
Typha angustata var. aethiopica Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 89. 1870
Typha angustata var. leptocarpa Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 88. 1870
Typha angustifolia subsp. angustata (Bory & Chaub.) Briq. Prodr. Fl. Corse 1: 643. 1910 (1910)
Typha angustifolia var. australis (Schumach.) Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 83 1870
Typha angustifolia subsp. australis (Schumach.) Kronf. Verh. K. K. Zool.-Bot. Ges. Wien 39: 156 1889
Typha angustifolia var. brownii (Kunth) Kronf. Verh. K. K. Zool.-Bot. Ges. Wien 39: 89 (1889)
Typha angustifolia var. domingensis (Pers.) Griseb. Fl. Brit. W. I. 512. 1864
Typha angustifolia subsp. domingensis (Pers.) Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 97. 1870 (1870)
Typha angustifolia subsp. javanica (Schnizl. ex Rohrb.) Graebn. Pflanzenr. IV, 8: 13. 1900 (1900)
Typha angustifolia var. virginica Tidestr. Rhodora 13: 242 (1911)
Typha australis Schumach. & Thonn. Beskr. Guin. Pl. 401. 1827
Typha basedowii Graebn. Repert. Spec. Nov. Regni Veg. 13: 497 (1915)
Typha bracteata Greene Bull. Calif. Acad. Sci. 2(7): 413 (1887)
Typha brownii Kunth Enum. Pl. 3: 92 (1841)
Typha damiattica Ehrenb. ex Rohrb Verh. Bot. Vereins Prov. Brandenburg 11: 88 (1869)
Typha domingensis var. australis (Schumach.) Gèze Bull. Soc. Bot. France 58: 459 1911
Typha domingensis var. javanica (Schnizl. ex Rohrb.) Gèze Bull. Soc. Bot. France 58: 459. 1911
Typha domingensis var. sachetiae Fosberg Bot. Bull. Acad. Sin. 30: 220 (1989)
Typha ehrenbergii Schur ex Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 88 (1869)
Typha essequeboensis G.Mey. ex Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 97 (1869)
Typha gigantea Schur ex Kunth Enum. Pl. 3: 92 (1841)
Typha javanica Schnizl. ex Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 98 (1869)
Typha macranthelia Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 3): 291 (1847)
Typha maxima Schur ex Rohrb. Verh. Bot. Vereins Prov. Brandenburg 11: 97 (1869)
Typha salgirica Krasnova Novosti Sist. Vyssh. Nizsh. Rast. 1975: 125 (1976)
Typha spiralis Raf. Atlantic J. 1: 148 (1832)
Typha tenuifolia Kunth Nov. Gen. Sp. 1: 82 (1816)
Typha truxillensis Kunth Nov. Gen. Sp. 1: 82 (1816)
Typha angustata var. gracilis Nyman Consp. Fl. Eur. 757. 1882
Typha domingensis f. strimonii Cheshm. & Delip. God. Sofiisk. Univ. “Kliment Okhridski” Biol. Fak. 2, Bot. 88(4): 71 (1997)
Typha australis Schumach. & Thonn. Beskr. Guin. Pl. : 401 (1827)
Typha angustifolia var. angustata (Bory & Chaub.) Jordanov
Typha angustifolia var. domingensis (Pers.) Hemsl. Rep. Challenger, Bot. 1(1): 73 1885
Typha domingensis subsp. australis (Schumach.) F.M.Vázquez Folia Bot. Extremadur. 6: 11 (2012)
Typha gracilis Schur Enum. Pl. Transsilv. : 637 (1866)
Typha media Bory & Chaub. Exp. Sci. Morée, Bot. : 11 (1832)
Typha domingensis var. eu-domingensis Gèze Bull. Soc. Bot. France 58: 459 (1911)
Typha latifolia subsp. domingensis Pers. Syn. Pl. 2: 532 (1807)
Typha domingensis var. angustata (Bory & Chaub.) Gèze Bull. Soc. Bot. France 58: 459 (1911)
Typha angustifolia var. saulseana Legrand Bull. Soc. Bot. Rochelaise 23: 19 (1901)
Typha angustifolia var. tenuispicata Debeaux Rech. Fl. Pyr. Or. 2: 45 (1878)
Typha angustifolia prol. australis (Schumach.) Rouy Fl. France 13: 331 (1912)

Common names Top

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Language Common/alternative name
English southern cat-tail
English southern cattail
Arabic خفاء
Arabic بوط
Arabic بردي
Arabic بوط دمياطي
Greek Ψαθί
Persian تیفا دمینجنسیس
Fulah toloore
French massette australe
Hebrew סוף מצוי
Japanese ヒメガマ
Punjabi ਦਿੱਭ (ਨਦੀਨ)
Polish pałka południowa
Portuguese taboa
Chinese 長苞香蒲
Chinese 长爸香蒲
Chinese 小白薇
Chinese 蒲黄
Chinese 长苞香蒲

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

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Azores
      • Canary Islands
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
    • Southern Africa
      • Botswana
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Central African Republic
      • Congo
      • Gabon
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Chagos Archipelago
      • Comoros
      • Mauritius
      • Réunion
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Oman
      • Saudi Arabia
      • Yemen
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Eastern Asia
      • Korea
      • Taiwan
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sumatera
    • Papuasia
      • New Guinea
  • Australasia
    • Australia
      • New South Wales
      • Norfolk Island
      • Northern Territory
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
  • Europe
    • Eastern Europe
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Switzerland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Kansas
      • Missouri
      • Nebraska
      • Oklahoma
    • Northwestern U.S.A.
      • Colorado
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
  • Pacific
    • North-central Pacific
      • Hawaii
    • South-central Pacific
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
  • Southern America
    • Brazil
      • Brazil North
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Bermuda
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Venezuelan Antilles
    • Central America
      • Belize
      • Costa Rica
      • Honduras
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Argentina South
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000594910
Florida Plant Atlas 2289
Flora of Alabama 5211
USDA Plants TYDO
Tropicos 33200006
Flora of Italy 7882
KEW urn:lsid:ipni.org:names:836837-1
The Plant List kew-270970
Open Tree Of Life 174582
Observations.org 123773
NCBI Taxonomy 189386
Nature Serve 2.144988
IUCN Red List 164208
IPNI 836837-1
iNaturalist 58392
GBIF 5289534
Freebase /m/09gdg1s
EPPO TYHDO
EOL 526516
Elurikkus 505291
Calflora (Californian flora) 8177
USDA GRIN 400352
Wikipedia Typha_domingensis
CMAUP NPO5243
CMAUP NPO6850

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
Name Level Submitter Released Coverage Size
GCA_056512515.1 ASM5651251v1 Chromosome Salk Institute for Biological Studies 2026-04-01 60 198.58 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
Assessing heavy metal and physiochemical pollution load of Danro River and its management using floating bed remediation Majumdar A, Avishek K Sci Rep 30-Apr-2024
PMCID:PMC11061306
doi:10.1038/s41598-024-60511-x
PMID:38688947
Resistance of the fiber-derived geotextile from Typha domingensis submitted to field degradation Holanda FS, Santos LD, Melo JC, Boge GM, Sussuchi EM, Nascimento BL, Santos MV, Oliveira MI Sci Rep 15-Apr-2024
PMCID:PMC11018824
doi:10.1038/s41598-024-56978-3
PMID:38622156
Progress of medicinal plants and their active metabolites in ischemia-reperfusion injury of stroke: a novel therapeutic strategy based on regulation of crosstalk between mitophagy and ferroptosis Zhang G, Wang Q, Jiang B, Yao L, Wu W, Zhang X, Wan D, Gu Y Front Pharmacol 08-Apr-2024
PMCID:PMC11033413
doi:10.3389/fphar.2024.1374445
PMID:38650626
Synergizing biotechnology and natural farming: pioneering agricultural sustainability through innovative interventions Badiyal A, Mahajan R, Rana RS, Sood R, Walia A, Rana T, Manhas S, Jayswal DK Front Plant Sci 22-Mar-2024
PMCID:PMC10995308
doi:10.3389/fpls.2024.1280846
PMID:38584951
Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A J Ethnobiol Ethnomed 09-Mar-2024
PMCID:PMC10924356
doi:10.1186/s13002-024-00665-0
PMID:38461267
A nature-based closed-loop wastewater treatment system at vehicle-washing facilities: From linear to circular economy Afzal M, Arslan M, Younus S, Müller JA, Usman M, Yasin M, Mehmood MA, Mehdi T, Islam E, Tauseef M, Iqbal S iScience 06-Mar-2024
PMCID:PMC10957447
doi:10.1016/j.isci.2024.109361
PMID:38523776
Making the most of scarce biological resources in the desert: Loptuq material culture in Eastern Turkestan around 1900 Hällzon P, Ötkür Z, Ståhlberg S, Svanberg I J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895719
doi:10.1186/s13002-024-00660-5
PMID:38409040
Integrating artificial intelligence into the modernization of traditional Chinese medicine industry: a review Zhou E, Shen Q, Hou Y Front Pharmacol 23-Feb-2024
PMCID:PMC10921893
doi:10.3389/fphar.2024.1181183
PMID:38464717
Structural and Functional Strategies in Cenchrus Species to Combat Environmental Extremities Imposed by Multiple Abiotic Stresses Basharat S, Ahmad F, Hameed M, Ahmad MS, Asghar A, Fatima S, Ahmad KS, Shah SM, Hashem A, Avila-Quezada GD, Abd_Allah EF, Abbas Z Plants (Basel) 11-Jan-2024
PMCID:PMC10818359
doi:10.3390/plants13020203
PMID:38256756
Retracted: Chemical Composition and Biological Evaluation of Typha domingensis Pers. to Ameliorate Health Pathologies: In Vitro and In Silico Approaches International BR Biomed Res Int 09-Jan-2024
PMCID:PMC10791395
doi:10.1155/2024/9840785
PMID:38230122
Determination of the Toxic Effects of Heavy Metals on the Morpho-Anatomical Responses of the Leaf of Typha latifolia as a Biomonitoring Tool Mamine N, Grara N, Khaldi F, Maresca V, Aouaichia K, Basile A Plants (Basel) 09-Jan-2024
PMCID:PMC10820412
doi:10.3390/plants13020176
PMID:38256730
Chromium (III) removal by perennial emerging macrophytes in floating treatment wetlands Nawrot N, Wojciechowska E, Mohsin M, Kuittinen S, Pappinen A, Matej-Łukowicz K, Szczepańska K, Cichowska A, Irshad MA, Tack FM Sci Rep 16-Dec-2023
PMCID:PMC10725432
doi:10.1038/s41598-023-49952-y
PMID:38104172
Phytochemical characterization of Typha domingensis and the assessment of therapeutic potential using in vitro and in vivo biological activities and in silico studies Dilshad R, Khan KU, Ahmad S, Shaik Mohammad AA, Sherif AE, Rao H, Ahmad M, Ghalloo BA, Begum MY Front Chem 08-Nov-2023
PMCID:PMC10663946
doi:10.3389/fchem.2023.1273191
PMID:38025070
Participatory ethnobotany: comparison between two quilombos in the Atlantic Forest, Ubatuba, São Paulo, Brazil Sauini T, Henrique Gonçalves Santos P, Paulino Albuquerque U, Yazbek P, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Silva Gomes MA, dos Santos G, Braga S, José Francischetti Garcia R, Honda S, Matta P, Aragaki S, Ueno A, Rodrigues E PeerJ 07-Nov-2023
PMCID:PMC10637247
doi:10.7717/peerj.16231
PMID:37953791
Patterns of use of wild food plants by Brazilian local communities: systematic review and meta-analysis Gomes LC, Medeiros PM, Prata AP J Ethnobiol Ethnomed 25-Oct-2023
PMCID:PMC10601232
doi:10.1186/s13002-023-00619-y
PMID:37880767

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Corynanthean-type alkaloids
Methyl (2R)-2-[(2S,12bS)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate 5321352 Click to see 354.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives
Phenylacetic Acid 999 Click to see C1=CC=C(C=C1)CC(=O)O 136.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
3-Hydroxybenzoate 54675842 Click to see C1=CC(=CC(=C1)[O-])C(=O)O 137.11 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
> 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 / Benzene and substituted derivatives / Phenethylamines
4-(2-Aminoethyl)phenol;hydron 67458472 Click to see 138.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
3-Hydroxyphenylpyruvic acid 5318321 Click to see 180.16 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
Sphaeropsidin C 10544575 Click to see 332.40 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentacosane 12406 Click to see 352.70 unknown https://doi.org/10.1246/BCSJ.3.53
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Suchilactone 10915582 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2=CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
18-Hydroxyoleic acid 5312773 Click to see 298.50 unknown via CMAUP database
Arachidonic acid-carboxy-14C 11822939 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O 306.50 unknown via CMAUP database
Octadecanoate 3033836 Click to see 283.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Npc283274 11252659 Click to see 201.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hentriacontanoic acid 37982 Click to see 466.80 unknown via CMAUP database
Pentacosanoic acid 10468 Click to see 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(5R)-5-[(1R,2Z,4E)-1-hydroxyhexa-2,4-dienyl]oxolan-2-one 11665504 Click to see 182.22 unknown via CMAUP database
(5S)-5-[(1S,2Z,4E)-1-hydroxyhexa-2,4-dienyl]oxolan-2-one 10631273 Click to see 182.22 unknown via CMAUP database
1-Nonacosanol 243696 Click to see 424.80 unknown via CMAUP database
6-Hentriacontanol 5318007 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(CCCCC)O 452.80 unknown https://doi.org/10.1246/BCSJ.3.53
6,10-Nonacosanediol 5320188 Click to see CCCCCCCCCCCCCCCCCCCC(CCCC(CCCCC)O)O 440.80 unknown via CMAUP database
6,21-Nonacosanediol 5320189 Click to see 440.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Hexacosan-10-ol 44135582 Click to see 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
9,12,15-Octadecatrienoic acid 860 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
trans-9-cis-12-Octadecadienoic acid 5282798 Click to see 280.40 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
1-Monopalmitin 14900 Click to see 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tristearin 11146 Click to see 891.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1S,4S,5R,6R,9S,14R)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxo-7-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl]methyl hexadecanoate 5318035 Click to see CCCCCCCCCCCCCCCC(=O)OCC1=CC2C3C(C3(C)C)CC(C4(C2=O)C=C(C(C4(C1O)O)O)C)C 586.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Arjunglucoside II 52951052 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one 14465808 Click to see 442.70 unknown via CMAUP database
(4aS,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picen-2-one 14465806 Click to see 440.70 unknown via CMAUP database
(4R,4aS,6aR,6aS,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 7067822 Click to see 426.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-2,3-dione 15081673 Click to see CC1C(=O)C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown via CMAUP database
[(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-3-oxo-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-yl] acetate 14465799 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C 484.80 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Cerin 21596125 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Cerin acetate 14465798 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C 484.80 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
6-[(3,5-Dimethylphenyl)methyl]-5-ethyl-1-[[4-[2-(13-ethyl-17-hydroxy-3-oxo-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl)ethynyl]phenyl]methoxymethyl]pyrimidine-2,4-dione 49769955 Click to see 688.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
3-[(5R,10R,14S)-3-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 6325934 Click to see 550.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,6R)-6-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-propan-2-ylheptan-1-ol 56924079 Click to see 416.70 unknown via CMAUP database
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 636741 Click to see 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1246/BCSJ.3.53
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1246/BCSJ.3.53
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
1-(2,5-Dioxo-2,5-dihydro-1H-imidazol-4-YL)urea 6852197 Click to see 156.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Heptoses
Sedoheptulose 5459879 Click to see C(C(C(C(C(C(=O)CO)O)O)O)O)O 210.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde-d5 10701848 Click to see C1=CC(=CC=C1C=O)O 127.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
4-Hydroxymellein, (3S-trans)- 119025905 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown via CMAUP database
5-Methylmellein 14807789 Click to see 192.21 unknown via CMAUP database
cis-4-Hydroxymellein 10420140 Click to see 194.18 unknown via CMAUP database
> 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 / Lactones / Gamma butyrolactones
Sphaeropsidin A 51361447 Click to see 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(4aR,6S,8aS)-6-[(1S)-1-hydroxyethyl]-6,8a-dihydro-4aH-pyrano[3,2-b]pyran-2-one 637192 Click to see 196.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(01)00449-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1246/BCSJ.3.53
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10418008 Click to see 824.70 unknown via CMAUP database
[(2R,3S,4R,5R,6S)-3-acetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 14162295 Click to see 636.60 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10439992 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O)O 740.70 unknown via CMAUP database
3'',4''-Di-O-acetyl-2'',6''-di-O-p-coumaroylastragalin 10328097 Click to see 824.70 unknown via CMAUP database
Kaempferol 3-(2'',6''-di-(E)-p-coumarylglucoside) 10439991 Click to see 740.70 unknown via CMAUP database
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 6442291 Click to see 594.50 unknown via CMAUP database
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3-[(2S,5S)-4,5-dihydroxy-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxychromen-4-one 44259164 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 756.70 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see 434.30 unknown via CMAUP database
3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 5318640 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)OC5C(C(C(CO5)O)O)O)O)O)O 610.50 unknown via CMAUP database
3-[(2S,3R,4R,5S,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 11968884 Click to see 610.50 unknown via CMAUP database
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44575467 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 via CMAUP database
3-[(2S,5S)-4,5-dihydroxy-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 44259365 Click to see 770.70 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-chromen-3-yl 6-O-(6-deoxy-alpha-D-mannopyranosyl)-beta-D-glucopyranoside 17751019 Click to see 624.50 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
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown via CMAUP database
Isorhamnetin-3-O-neohesperidoside 24204448 Click to see 624.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-chromen-7-olate 25202413 Click to see 315.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Complex tannins
(1R,2R,20R,42S,46S)-46-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 16167199 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Castalagin 12302513 Click to see 934.60 unknown via CMAUP database
Eugeniin 442679 Click to see 938.70 unknown via CMAUP database
GlyTouCan:G69718UQ 9918701 Click to see 786.60 unknown via CMAUP database
Protocatechuic acid 3-glucoside 11972438 Click to see C1=CC(=C(C=C1C(=O)O)OC2C(C(C(C(O2)CO)O)O)O)O 316.26 unknown via CMAUP database

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