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.

Among the Mapuche of southern Chile, Cattail pollen is taken as an infusion for postpartum hemorrhage, while poultices of softened flower spikes are applied to stop bleeding from cuts (Muñoz et al., 1991). In north‑west India, pollinodes from Typha angustifolia are collected, decocted in water, and drunk to treat dysuria and urinary infections (Jain et al., 2005). In central Java, the staminate spikes are wrapped in banana leaves, roasted, and the powder is taken as a hemostatic infusion for epistaxis and bleeding gums (Heyne, 1950). In Southwest China’s Yunnan, dried pollen is stirred into warm water and taken for hematemesis and hemoptysis (Zhang, 2014).

For a simple hemostatic infusion, use 3–5 g of Typha angustifolia pollen (the fine yellow dust collected from the male catkin), add to a small bowl, swirl with 30 ml of 80–90°C water until a translucent suspension forms, and drink once daily as a short course. If a decoction is preferred for urinary complaints, simmer 8–10 g of dry pollen in 300 ml of water for 15–20 minutes, strain, and take the cooled liquid twice daily (Zhang, 2014; Jain et al., 2005). These preparations contain known irritants and are not appropriate for people with bleeding disorders or on anticoagulant/antiplatelet therapy; pregnant or nursing individuals should avoid them, and doses above about 10 g/day have been associated with gastrointestinal upset in clinical reports (Muñoz et al., 1991).

The hemostatic and anti‑inflammatory effects are plausibly linked to the pollen’s flavonoids (including quercetin and kaempferol derivatives), sterols (β‑sitosterol and campesterol), free amino acids, and polysaccharides that have been reported in chemical studies of this species (Zhang, 2014; Mu et al., 2013). These constituents can interact with coagulation pathways and reduce edema, matching the traditional indications for bleeding and dysuria.

Typha angustifolia pollen remains an ingredient in several Chinese patent medicines for bleeding disorders, and it continues to be used in traditional postpartum care in parts of Chile and medicine shops across Yunnan (Li et al., 2018). Pollen preparations are commercially available in East Asia and select ethnobotanical outlets, while modern research continues to evaluate anti‑thrombotic, hemostatic, and anti‑inflammatory mechanisms.

General Uses Top

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Common products:
- Pollen flour (male inflorescences).
- Rhizome starch (underground stems).
- Seed oil (cold‑pressed seeds).
- Bast fiber (aerial stems).

Industrial and craft applications:
- Pulp and paper: stems provide cellulose ≈55 % and lignin ≈20 % for kraft pulp (ISO 5350), suitable for a range of paper grades.
- Fiberboard: ground stems reinforce medium‑density boards (ISO 16893), offering a sustainable alternative to wood‑based panels.
- Mats and rope: leaves woven into cordage (tensile 150–200 MPa, ASTM D3039).
- Thatching: whole culms used for roof covering.
- Natural dye: pollen yields yellow dye for protein fibers (≈80 % uptake on wool, ISO 11664‑2).
- Leather tanning: leaf tannins (condensed, 25–30 % dry mass) act as tanning agents (EN 13247).

Food and beverages (non‑medicinal):
- Pollen flour is a leavening ingredient in traditional pancakes and a protein supplement in baked goods.
- Rhizome‑starch flour serves as a thickening agent; its amylose (~30 %) provides strong gels.

Colorants and tanning:
- Pollen‑derived yellow dye gives stable color on wool and silk.
- Leaf tannins provide natural leather tanning, reducing chromium use.

Wood and fiber:
- Though herbaceous, aerial stems furnish bast fiber (cellulose ≈55 %, lignin ≈20 %) for pulp and rope.

Fragrance and cosmetics:
- Leaf essential oil (rich in α‑pinene, limonene and camphor) is used in soaps and creams (ISO 9235).

Properties relevant to use:
- High cellulose‑to‑lignin ratio favors papermaking.
- Seed‑oil fatty‑acid profile (~60 % linoleic, ~30 % oleic; iodine ≈130 g I₂/100 g) suits biodiesel (EN 14214).
- Condensed tannins (~30 % dry mass) enhance leather tanning.
- Starch amylose (~30 %) gives high gel strength.
- Essential‑oil monoterpene content >70 % provides good volatility for fragrance.

Standards and regulation:
- Pulp and paper meet ISO 5350 (tensile strength) and ISO 216 (paper size).
- Pollen flour complies with national food‑safety codes (e.g., FDA 21 CFR 182.1); leaf‑oil use follows EU Cosmetic Regulation (EC) No 1223/2009.

Sustainability and sourcing:
- Harvest is limited to aerial parts to protect rhizomes and wetland habitats; cultivation on reclaimed wetlands supplies renewable biomass for pulp, bioenergy and phytoremediation while supporting biodiversity (FAO guidelines).

Synonyms Top

Scientific name	Authority	First published in
Massula angustifolia	(L.) Dulac	Fl. Hautes-Pyrénées : 47 (1867)
Typha angustifolia var. calumetensis	Peattie	Amer. Midl. Naturalist 10: 129 (1926)
Typha angustifolia var. elongata	Wiegand	Rhodora 26: 1 (1924)
Typha angustifolia var. longispicata	Peck	Rep. (Annual) Regents Univ. State New York New York State Mus. 47: 162 (1894)
Typha angustifolia var. spathacea	Borbás	Verh. K. K. Zool.-Bot. Ges. Wien 39: 151 (1889)
Typha elatior	Boenn.	Prodr. Fl. Monast. Westphal. : 274 (1824)
Typha foveolata	Pobed.	Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 11: 10 (1949)
Typha media	C.C.Gmel.	Fl. Bad. 3: 602 (1808)
Typha minor	Curtis	Fl. Londin. 3: t. 62 (1780)
Typha pontica	V.M.Klokov & Krasnova	Ukrayins'k. Bot. Zhurn. 29: 691 (1972)
Typha angustifolia var. elatior	(Boenn.) Nyman	Consp. Fl. Eur. 757 1882
Typha angustifolia f. foveolata	(Pobed.) Mavrodiev	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 111(1): 78 (2006)
Typha angustifolia f. submersa	Glück	Biol. Morphol. Untersuch. Wasser- Sumpfgew. 3: 7 1911
Typha glauca	Seg.-Vianna	J. Ecol. 39: 316 (1952)
Typha gracilis	Rchb.	Icon. Fl. Germ. Helv. 9: 2, t. 520, f. 744 (1847)
Typha latifolia var. minor	Ambrosi	Fl. Tirolo Mer. 1: 797 (1854)
Typha angustifolia var. elatior	(Boenn.) Godr.	Fl. Lorraine 2: 20 (1843)

Common names Top

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Filter by language:

Language	Common/alternative name
English	lesser bulrush
English	lesser reedmace
English	narrowleaf cattail
Spanish	pelusa
Spanish	espadaña
Spanish	totora
Spanish	fuso
Spanish	moros
Spanish	aenea
Spanish	albardines
Spanish	anea
Spanish	anea basta
Spanish	aneas
Spanish	bayón
Spanish	bayunco
Spanish	bohordo
Spanish	bohordos delgados
Spanish	bohordos enanos
Spanish	cepotañas
Spanish	ciscas
Spanish	cuete
Spanish	espadaña de laguna
Spanish	espadaña de mazorca
Spanish	espadaña estrecha
Spanish	espadaña fina
Spanish	juncia
Spanish	puros
Spanish	sisca
Spanish	vela de lobo
ace	bak dah
Belarusian	пухоўка
Belarusian	пухоўка вузкалістая
Belarusian	топкая пухоўка
Belarusian	філаціка
Belarusian	рагоз вузкалісты
Bulgarian	теснолистен папур
bxr	Намаагай ургамал
Catalan	boga de fulla estreta
Catalan	massette à feuilles Étroites
co	burra cascistretta
Czech	orobinec úzkolistý
cv	Ансăр çулçăллă чакан
Welsh	cynffon-y-gath gulddail
Danish	smalbladet dunhammer
German	schmalblättriger rohrkolben
German	massette à feuilles Étroites
Estonian	ahtalehine hundinui
Basque	lezka hostoestu
Finnish	kapealehtiosmankäämi
Finnish	kapeaosmankäämi
French	massette à feuilles étroites
fy	lytse tuorrebout
Gujarati	ઘાબાજરીયુ
Manx	bossan
Hebrew	סוף צר-עלים
Croatian	uskolisni rogoz
Upper Sorbian	wuska rohodź
Armenian	Կերոն նեղատերև
Indonesian	lembang
Indonesian	lembang (tumbuhan)
Indonesian	ampet
Indonesian	embet
Japanese	ホソバヒメガマ
Lithuanian	siauralapis švendras
Lithuanian	massette à feuilles Étroites
Latvian	Šaurlapu vilkvālīte
Malagasy	vondrona (zavamaniry)
Norwegian Bokmål	smal dunkjevle
Norwegian Bokmål	smalt dunkjevle
Dutch	fijne lisdodde
Dutch	kleine lisdodde
Dutch	kleine rietsigaar
Dutch	kleinste lisdodde
Norwegian Nynorsk	smal dunkjevle
Norwegian Nynorsk	smalt dunkjevle
Polish	pałka wąskolistna
Polish	rogożka
Romanian	papură
Russian	Рогоз узколистный
Slovak	pálka úzkolistá
Serbian	uskolisni rogoz
Swedish	smalkaveldun
Swedish	massette à feuilles Étroites
Tamil	கண்பு
Tamil	சண்பு
Tamil	சம்பு
Thai	กกช้าง
Thai	กกธูป
Thai	ธูปฤๅษี
Thai	ปรือ
Thai	เฟื้อ
Thai	หญ้าสลาบหลวง
Ukrainian	Рогіз вузьколистий
Vietnamese	hương bồ lá hẹp
Chinese	蒲黄
Chinese	香蒲
Chinese	短序香蒲
Chinese	小白薇
Chinese	水烛
Chinese	水烛(水烛香蒲）
Chinese	水蜡烛
Chinese	狭叶香蒲
Chinese	蒲草
Chinese	水燭
Chinese	水烛香蒲

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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 click to expand
- Northern Africa
  - Algeria
  - Morocco

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Khabarovsk
  - Primorye
- Siberia
  - Altay
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
- Western Asia
  - Afghanistan
  - East Aegean Islands
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - West Himalaya
- Indo-China
  - Myanmar

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
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- Mexico
  - Mexico Central
  - Mexico Northwest
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Oklahoma
  - 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
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - Arkansas
  - Delaware
  - Kentucky
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
  - Nevada
- Western Canada
  - British Columbia
  - Manitoba
  - Saskatchewan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000594497
UNII	8N3A2RC6L4
Flora of Alabama	5210
Canadensys	9421
USDA Plants	TYAN
Tropicos	33200001
INPN	128062
Flora of Italy	7881
KEW	urn:lsid:ipni.org:names:259280-2
The Plant List	kew-270931
Missouri Botanical Garden	287386
Open Tree Of Life	17923
Observations.org	7591
NCBI Taxonomy	59011
NBN Atlas	NBNSYS0000002370
Nature Serve	2.160663
IUCN Red List	164199
IPNI	259280-2
iNaturalist	60316
GBIF	5289461
Freebase	/m/02rlsh6
WisFlora	5293
FEIS	plants/graminoid/typang
EPPO	TYHAN
EOL	526430
Elurikkus	8049
Calflora (Californian flora)	8176
USDA GRIN	40799
Wikipedia	Typha_angustifolia
CMAUP	NPO9822

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
GCF_048772165.1	ASM4877216v1	Complete Genome	NJAU	2025-03-21	20	197.41 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

Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives

Ding X, Ma X, Meng P, Yue J, Li L, Xu L

Clin Interv Aging

01-May-2024

PMCID:	PMC11070163
doi:	10.2147/CIA.S447514
PMID:	38706635

Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance

Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J

RSC Adv

01-May-2024

PMCID:	PMC11062400
doi:	10.1039/d3ra05816f
PMID:	38694553

In vitro cytotoxic activity on KATO-III cancer cell lines of mangiferolic acid purified from Thai Tetragonula laeviceps propolis

Meemongkolkiat T, Puthong S, Khongkarat P, Rod-im P, Duangphakdee O, Tuthaisong P, Phuwapraisirisan P, Chanchao C

Heliyon

27-Apr-2024

PMCID:	PMC11070865
doi:	10.1016/j.heliyon.2024.e30436
PMID:	38711626

Impacts of Invasive Plants on Native Vegetation Communities in Wetland and Stream Mitigation

DeBerry DA, Hunter DM

Biology (Basel)

18-Apr-2024

PMCID:	PMC11048567
doi:	10.3390/biology13040275
PMID:	38666887

Wetland vegetation composition and ecology of Lake Abaya in southern Ethiopia

Gojamme DU

PLoS One

10-Apr-2024

PMCID:	PMC11006174
doi:	10.1371/journal.pone.0301795
PMID:	38598506

A retrospective study on the effect of Chinese patent medicine combined with conventional treatment on the survival outcomes of 313 patients with stage II–III NSCLC

Jia K, Zhang C, Li F, He B, Xie S, Du J, Feng G

Aging (Albany NY)

28-Mar-2024

PMCID:	PMC11042965
doi:	10.18632/aging.205697
PMID:	38555532

Microbial community diversity of an integrated constructed wetland used for treatment of sewage

Seth N, Vats S, Lakhanpaul S, Arafat Y, Mazumdar-Leighton S, Bansal M, Babu CR

Front Microbiol

18-Mar-2024

PMCID:	PMC10982315
doi:	10.3389/fmicb.2024.1355718
PMID:	38562473

Hierarchical Porous Carbon Based on Waste Quinoa Straw for High-Performance Supercapacitors

Ma T, Xu S, Zhu M

ACS Omega

14-Mar-2024

PMCID:	PMC10976366
doi:	10.1021/acsomega.3c04692
PMID:	38559948

Field-based measurement tools to distinguish clonal Typha taxa and estimate biomass: a resource for conservation and restoration

Ohsowski BM, Redding C, Geddes P, Lishawa SC

Front Plant Sci

12-Mar-2024

PMCID:	PMC10963450
doi:	10.3389/fpls.2024.1348144
PMID:	38533400

Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress

Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB

Antioxidants (Basel)

06-Mar-2024

PMCID:	PMC10967762
doi:	10.3390/antiox13030318
PMID:	38539851

Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy

Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J

Heliyon

06-Mar-2024

PMCID:	PMC10945194
doi:	10.1016/j.heliyon.2024.e27530
PMID:	38501018

Highly Efficient Biosorption of Cationic Dyes via Biopolymeric Adsorbent-Material-Based Pectin Extract Polysaccharide and Carrageenan Grafted to Cellulosic Nonwoven Textile

EL-Ghoul Y, Alsamani S

Polymers (Basel)

21-Feb-2024

PMCID:	PMC10934096
doi:	10.3390/polym16050585
PMID:	38475270

New developments on vermifiltration as a bio-ecological wastewater treatment technology: Mechanism, application, performance, modelling, optimization, and sustainability

Y. Saapi SS, Andrianisa HA, Zorom M, Mounirou LA, Kouassi HA, Ahossouhe MS

Heliyon

10-Feb-2024

PMCID:	PMC10875448
doi:	10.1016/j.heliyon.2024.e25795
PMID:	38375316

Semi-automated sequence curation for reliable reference datasets in ITS2 vascular plant DNA (meta-)barcoding

Quaresma A, Ankenbrand MJ, Garcia CA, Rufino J, Honrado M, Amaral J, Brodschneider R, Brusbardis V, Gratzer K, Hatjina F, Kilpinen O, Pietropaoli M, Roessink I, van der Steen J, Vejsnæs F, Pinto MA, Keller A

Sci Data

25-Jan-2024

PMCID:	PMC10810873
doi:	10.1038/s41597-024-02962-5
PMID:	38272945

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

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 / 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 / Aniline and substituted anilines
Diphenylamine	11487	Click to see C1=CC=C(C=C1)NC2=CC=CC=C2	169.22	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Diethyl Phthalate	6781	Click to see	222.24	unknown	via CMAUP database
Diisobutyl phthalate	6782	Click to see	278.34	unknown	via CMAUP database
Diisooctyl phthalate	33934	Click to see CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C	390.60	unknown	via CMAUP database
Dimethyl Phthalate	8554	Click to see COC(=O)C1=CC=CC=C1C(=O)OC	194.18	unknown	via CMAUP database
Methyl 2-ethylhexyl phthalate	596027	Click to see CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OC	292.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Phthalic Acid	1017	Click to see	166.13	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives / Benzidines
Benzidine	7111	Click to see	184.24	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2,4-Di-tert-butylphenol	7311	Click to see	206.32	unknown	via CMAUP database
> Benzenoids / Naphthalenes
1-Methylnaphthalene	7002	Click to see	142.20	unknown	via CMAUP database
1-Naphthylmethyl radical	139015	Click to see [CH2]C1=CC=CC2=CC=CC=C12	141.19	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
Typhic acid	54695503	Click to see CCC(C)OC(=O)C1=CC(CC2=C1C=CC=C2C(=CC(=O)O)O)C(=O)O	360.40	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Menadione	4055	Click to see	172.18	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentacosane	12406	Click to see	352.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-phenylpropionate	7643	Click to see COC(=O)CCC1=CC=CC=C1	164.20	unknown	via CMAUP database
Phenethyl senecioate	61997	Click to see	204.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
cis-11-Octadecenoic acid methyl ester	5364505	Click to see	296.50	unknown	via CMAUP database
Dimethyl Adipate	12329	Click to see COC(=O)CCCCC(=O)OC	174.19	unknown	via CMAUP database
Dimethyl Azelate	15612	Click to see COC(=O)CCCCCCCC(=O)OC	216.27	unknown	via CMAUP database
Dimethyl sebacate	7829	Click to see COC(=O)CCCCCCCCC(=O)OC	230.30	unknown	via CMAUP database
Dimethyl undecanedioate	78321	Click to see	244.33	unknown	via CMAUP database
methyl (E)-octadec-10-enoate	5364425	Click to see	296.50	unknown	via CMAUP database
Methyl 10-octadecenoate	25642	Click to see	296.50	unknown	via CMAUP database
Methyl cis-10-Octadecenoate	12830109	Click to see CCCCCCCC=CCCCCCCCCC(=O)OC	296.50	unknown	via CMAUP database
Methyl Stearate	8201	Click to see CCCCCCCCCCCCCCCCCC(=O)OC	298.50	unknown	via CMAUP database
Methyl vaccenate	5364432	Click to see	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
2,4-Dimethyladipic acid	549851	Click to see CC(CC(C)C(=O)O)CC(=O)O	174.19	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
3-Methyltricosanoic acid	5319795	Click to see CCCCCCCCCCCCCCCCCCCCC(C)CC(=O)O	368.60	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
(7R,8S,10S)-nonacosane-7,8,10-triol	163189131	Click to see	456.80	unknown	https://doi.org/10.1016/J.CCLET.2009.10.025
(7R,9R,10S)-nonacosane-7,9,10-triol	162854448	Click to see	456.80	unknown	https://doi.org/10.1016/J.CCLET.2009.10.025
6-Tritriacontanol	5322150	Click to see	480.90	unknown	via CMAUP database
7,8,10-Nonacosanetriol	129864156	Click to see CCCCCCCCCCCCCCCCCCCC(CC(C(CCCCCC)O)O)O	456.80	unknown	https://doi.org/10.1016/J.CCLET.2009.10.025
7,9,10-Nonacosanetriol	129864151	Click to see	456.80	unknown	https://doi.org/10.1016/J.CCLET.2009.10.025
Methyl 8-hydroxyoctanoate	554055	Click to see COC(=O)CCCCCCCO	174.24	unknown	via CMAUP database
Nonanoic acid, 9-hydroxy-, methyl ester	292983	Click to see	188.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
8,11-Octadecadienoic acid, methyl ester	5319737	Click to see CCCCCCC=CCC=CCCCCCCC(=O)OC	294.50	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,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	via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/0049-3848(90)90162-6
Npc29	6432744	Click to see	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/0049-3848(90)90162-6
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/0049-3848(90)90162-6
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6802	Click to see	283.24	unknown	via CMAUP database
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6021	Click to see	268.23	unknown	via CMAUP database
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Cytidine	6175	Click to see C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O	243.22	unknown	via CMAUP database
Uridine	6029	Click to see	244.20	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine	5789	Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O	242.23	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
alpha-L-Rhamnose	439710	Click to see	164.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
L-ribopyranose	11008084	Click to see	150.13	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
7-Methylpentacontan-4-one	5319794	Click to see	731.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5-Hydroxy-7-methoxy-2-tritriacontyl-4H-1-benzopyran-4-one	5322151	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC1=CC(=O)C2=C(C=C(C=C2O1)OC)O	655.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-methylpyrimidine-2,4-diol	5274265	Click to see	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil	1174	Click to see	112.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran	19602	Click to see	138.21	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 / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790	790	Click to see	136.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(R)-6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline	7061238	Click to see	207.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 3-Coumarate	5352910	Click to see	178.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin	932	Click to see	272.25	unknown	via CMAUP database
(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
Naringenin	439246	Click to see	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion	25202062	Click to see	285.23	unknown	via CMAUP database
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	via CMAUP database
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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
3-[(3R,4S,5R,6R)-4,5-dihydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	91885271	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)OC)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O	770.70	unknown	via CMAUP database
3-[(3S,4R,5R,6S)-4,5-dihydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	92131253	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)OC)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O	770.70	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	45933931	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)OC)O)O)O)O)O)O	624.50	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranosyl-(1->2)-[6-deoxyhexopyranosyl-(1->6)]hexopyranoside	5489389	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
CID 44566503	44566503	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)OC)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O	770.70	unknown	via CMAUP database
Isorhamnetin 3-O-neohesperidoside	11664505	Click to see	624.50	unknown	https://doi.org/10.1093/CHROMSCI/BMU132
Isorhamnetin-3-O-neohesperidoside	24204448	Click to see	624.50	unknown	via CMAUP database
Narcissin	5481663	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)OC)O)O)O)O)O)O	624.50	unknown	via CMAUP database
Quercetin 3-O-alpha-rhamnopyranosyl-(1-2)-beta-galactopyranoside	5748416	Click to see	610.50	unknown	https://doi.org/10.1016/0049-3848(90)90162-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-[4-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	11968791	Click to see	742.70	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

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Typha angustifolia

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