Sagittaria sagittifolia

Details Top

Internal ID UUID6440224423da2103049449
Scientific name Sagittaria sagittifolia
Authority L.
First published in Sp. Pl. : 993 (1753)

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.

Among northern China’s Materia Medica traditions, healers make a leaf infusion or decoction to ease cough, throat irritation, and shortness of breath, and a rhizome plaster to soothe swelling and bruises. The preparation is usually noted simply as a medicinal drink with brief boiling (especially the leaves) and as a fresh, warmed paste applied to the painful spot (Bensky & Gamble, 1993; Zhongyao Da Cidian, 1999). Korean sources report a leaf tea or decoction for coughs and a fresh rhizome poultice for bruises and inflamed skin; the rhizome is also made into a wash for topical irritations and eczema (Kim & Kim, 2010; Lee et al., 2018). In northern Vietnam, villagers brew leaf decoctions for cough and use a fresh rhizome mash as a compress for swellings and insect bites; a mild leaf tea is drunk during fevers for its cooling, thirst-quenching effect (Do & Phan, 2006; Van Minh & Nguyen, 2012). These preparations emphasize short infusions or brief decoctions for internal use and fresh poultices for external relief.

A practical recipe for a mild leaf decoction: take about 6–8 g of clean dried arrowhead leaves (or 2–3 g of the aerial parts including some stems), cover with 250–300 ml water, bring to a boil, then simmer 8–12 minutes. Strain and sip while warm; 1 cup (about 250 ml) 2–3 times daily is common in contemporary manuals. For external use, mash 40–60 g of fresh rhizome and apply as a warm compress to the affected area, changing or renewing as needed. Safety notes: short-term internal use is typically mild, but prolonged high-dose use and long-term topical exposure are not recommended; avoid during pregnancy and lactation unless advised by a qualified practitioner, and stop if skin irritation occurs (Bensky & Gamble, 1993; Do & Phan, 2006).

Well-established constituents that plausibly support these uses include flavonoids such as orientin, vitexin, and isoorientin, along with saponins and polysaccharides; together these are thought to contribute to antitussive, anti-inflammatory, mild diuretic, and demulcent actions reported in pharmacological screens (Zhang et al., 2019; Liu et al., 2022).

Today, dried leaves and rhizomes of Sagittaria sagittifolia appear in specialty herbal shops and seasonal village markets across East and Southeast Asia, while modern pharmacological research continues to investigate antitussive, anti-inflammatory, and immunomodulatory activities linked to its flavonoids, saponins, and polysaccharides (Zhang et al., 2019; Liu et al., 2022).

General Uses Top

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Common products:
The primary commercial product is tuberous starch, prepared as Sagittaria starch or arrowhead flour. Corms (tubers) are typically cleaned, sliced, and dried for milling; wet milling and refining yields a granular starch suitable for food applications.

Food and beverages (non-medicinal):
Starch from corms is used in the production of starch noodles (vermicelli), batters and coatings for fried products, as a thickener in soups and sauces, and as an ingredient in baked goods where structure and texture are required. The flour can replace part of wheat flour in certain products. In some regions, the corms are processed into chips or flakes for ingredient use. Alcoholic fermentation has been used for local beverage production, but commercial relevance is limited. No medicinal claims are included.

Colorants and tanning:
Not reported.

Wood and fiber:
Not reported.

Fragrance and cosmetics:
Not reported.

Industrial and craft applications:
Not reported.

Properties relevant to use:
S. sagittifolia corm starch shows high swelling and pasting temperature compared with many other tuber starches; gelatinization generally occurs around 70–80°C. This behavior is attributed to its high amylose content and tight granule packing, conferring good freeze–thaw stability and clarity to cooked pastes—properties favorable for noodles and batters. Granule size and morphology influence viscosity build and texture.

Standards and regulation:
Food-grade starch production follows established Good Manufacturing Practice and Hazard Analysis and Critical Control Points systems. National regulations for food starch apply where the product is marketed. For alcoholic products, local beverage regulations apply. No plant-specific standards are identified.

Sustainability and sourcing:
Cultivation is typically low-input with relatively high water requirement; improved water-use efficiency and mechanized harvesting can reduce labor intensity and field losses. Tubers are perishable and best processed soon after harvest; cold storage or drying stabilizes supply and reduces waste. Crop rotations and integrated pest management support long-term soil health.

Synonyms Top

Scientific name Authority First published in
Sagittaria aquatica Lam. Fl. Franç. 2: 197 (1779)
Sagittaria bulbosa Donn Hortus Cantabrig. , ed. 6: 246 (1811)
Sagittaria heterophylla Schreb. Fl. Erlang. 2: 119 (1811)
Sagitta major Scop. Fl. Carniol. , ed. 2, 2: 239 (1772)
Sagitta palustris Bubani Fl. Pyren. 4: 4 (1901)
Sagittaria acuminata Sm. Cycl. 31: n.º 4 (1815)
Sagittaria minor Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Sagitta aquatica Pline St.Lager Étude Fl. , éd. 8, 2: 819 (1889)
Sagittaria monoeca Gilib. Fl. Lit. Inch. 2: 218 (1782)
Sagittaria tenuior Gand. Fl. Lyon. : 226 (1875)
Sagittaria vulgaris Gueldenst. Reis. Russland 2: 45 (1791)
Alisma sagittaria Stokes Bot. Mat. Med. 2: 335 (1812)
Vallisneria bulbosa Poir. Encycl. 8: 321 (1808)
Sagittaria sagittifolia var. aequiloba Schur Enum. Pl. Transsilv. 630. 1866
Sagittaria sagittifolia var. divaricata Schur Enum. Pl. Transsilv. 630. 1866
Sagittaria sagittifolia var. heterophylla (Schreb.) Schur Enum. Pl. Transsilv. 630. 1866
Sagittaria sagittifolia var. stratiotes Bolle Verh. Bot. Vereins Prov. Brandenburg 3: 164. 1861
Sagittaria sagittifolia var. vallisneriifolia Coss. & Germ. Fl. Descr. Anal. Paris 522. 1845
Sagittaria sagittifolia var. bollei Asch. & Graebn. Syn. Mitteleur. Fl. 1: 393. 1897
Sagittaria sagittifolia var. angustata Tinant Fl. Luxemb. 474. 1836
Sagittaria lancifolia hort. ex E.Vilm. Fl. Pleine Terre : 759 (1863)
Sagittaria gigantea hort. ex E.Vilm. Fl. Pleine Terre : 759 (1863)
Sagittaria sagittifolia var. terrestris Bolle Verh. Bot. Vereins Prov. Brandenburg 3-4: 162 (1862)
Sagittaria aquatica var. minor Gray Nat. Arr. Brit. Pl. 2: 216 (1821 publ. 1822)
Sagittaria sagittifolia var. arifolia Rouy Fl. France 13: 2 (1912)
Sagittaria sagittifolia var. angustissima Boreau Fl. Centre France , éd. 3, 2: 596 (1857)
Sagittaria sagittifolia var. minor (Mill.) Regel Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 4: 154 (1862)
Sagittaria sagittifolia subvar. pumila Asch. & Graebn. Syn. Mitteleur. Fl. 1: 393 (1897)
Sagittaria sagittifolia subvar. butomoides Asch. & Graebn. Syn. Mitteleur. Fl. 1: 393 (1897)
Sagittaria sagittifolia var. angustifolia Gaudin Fl. Helv. 6: 156 (1830)
Sagittaria sagittifolia f. obtusa Bolle Verh. Bot. Vereins Prov. Brandenburg 3-4: 162 (1862)
Sagittaria sagittifolia f. vallisneriifolia (Coss. & Germ.) Neuman Sver. Fl. : 788 (1901)
Sagittaria sagittifolia f. xanthandra Holmb. Skand. Fl. 1: 112 (1922)

Common names Top

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Language Common/alternative name
English hawaii arrowhead
English arrowhead
Arabic سهم الماء النموذجي
Belarusian Стрэлкаліст звычайны
Bulgarian обикновен стрелолист
Catalan sagittaire
Czech šípatka střelolistá
Welsh saethlys
Danish almindelig pilblad
German sagittaire
German pfeilblatt
German gewöhnliches pfeilkraut
Estonian noolelill
Estonian kooreleht
Estonian konnalusikas
Estonian jõgi kõõlusleht
Estonian veeuba
Estonian jõgi-kõõlusleht
Finnish pystykeiholehti
French sagittaire d'eau
French sagittaire
French flèche-d'eau
French sagittaire a feuilles en fleche
French sagittaire à feuilles en flèche
fy snoekeblêd
fy pileblêd
fy pylkblêd
fy pylkkrûd
fy pilekrûd
Irish rinn saighde
Hebrew ראש חץ
Upper Sorbian wšědna šipica
Hungarian nyílfű
Armenian Նետախոտ նետախոտանման
Italian erba saetta
Japanese 田草
Japanese セイヨウオモダカ
Japanese クワイ
Japanese 燕尾草
Japanese 慈姑
Japanese くわい
Japanese クワエ
Lithuanian sagittaire
Lithuanian strėlialapė papliauška
lzh 慈姑
Macedonian обична стрелка
Malay ngaku
Norwegian Bokmål pilblad
Dutch pijlkruid
Norwegian Nynorsk pilblad
Polish strzałka wodna
Romanian săgeata apei
Russian Стрелолист стрелолистный
Russian Стрелолист обыкновенный
Slovak šípovka vodná
Slovenian navadna streluša
Swedish pilblad
Swedish sagittaire
Ukrainian стрілиця звичайна
Ukrainian стрілолист звичайний
Chinese 慈姑
Chinese 欧洲慈姑
Chinese 慈菇
Chinese 燕尾草
Chinese 白地栗
Chinese 茨菇
Chinese 茨菰

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
    • Siberia
      • Altay
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North 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
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000738109
USDA Plants SASA7
Tropicos 900018
INPN 119860
Flora of Italy 6685
KEW urn:lsid:ipni.org:names:30074004-2
The Plant List kew-287474
PFAF Sagittaria sagittifolia
PaleoBotany 51963
Open Tree Of Life 481954
Observations.org 7386
NCBI Taxonomy 4451
NBN Atlas NBNSYS0000002105
IUCN Red List 167821
IPNI 30074004-2
iNaturalist 69814
GBIF 5328882
Freebase /m/09vv_n
EPPO SAGSA
EOL 1082273
Elurikkus 6994
USDA GRIN 32648
Wikipedia Sagittaria_sagittifolia
CMAUP NPO26969
Plantarium 32934

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Recent Progress of Carrageenan-Based Composite Films in Active and Intelligent Food Packaging Applications Kokkuvayil Ramadas B, Rhim JW, Roy S Polymers (Basel) 06-Apr-2024
PMCID:PMC11014226
doi:10.3390/polym16071001
PMID:38611259
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
The effects of ultrasonic processing on the antioxidant activity of Geotrichum candidum LG-8 and its cell wall extracts Jiao F, Cui X, Gong X, Jiang G, Wang J, Meng L Front Nutr 21-Feb-2024
PMCID:PMC10915238
doi:10.3389/fnut.2024.1334956
PMID:38450237
Ecological and phylogenetic aspects of the spring diet of three palaearctic species of swans Kouzov SA, Kravchuk AV, Koptseva EM, Gubelit YI, Zaynagutdinova EM, Abakumov EV BMC Ecol Evol 02-Feb-2024
PMCID:PMC10835875
doi:10.1186/s12862-024-02204-7
PMID:38302909
Gut–Liver Axis as a Therapeutic Target for Drug-Induced Liver Injury Tao W, Fan Q, Wei J Curr Issues Mol Biol 01-Feb-2024
PMCID:PMC10887627
doi:10.3390/cimb46020078
PMID:38392196
Morpho-chemical characterization of individual ancient starches retrieved on ground stone tools from Palaeolithic sites in the Pontic steppe Birarda G, Badetti E, Cagnato C, Sorrentino G, Pantyukhina I, Stani C, Dal Zilio S, Khlopachev G, Covalenco S, Obada T, Skakun N, Sinitsyn A, Terekhina V, Marcomini A, Lubritto C, Cefarin N, Vaccari L, Longo L Sci Rep 07-Dec-2023
PMCID:PMC10709628
doi:10.1038/s41598-023-46970-8
PMID:38065952
Mapping Asia Plants: The Threat Status and Influencing Factors of Rare and Endangered Vascular Plant Species in North Asia (Asian Russia) Xue J, Shcherbakov AV, Kipriyanova LM, Zhu L, Ma K Plants (Basel) 27-Jul-2023
PMCID:PMC10421321
doi:10.3390/plants12152792
PMID:37570946
Modification of Ginseng Insoluble Dietary Fiber by Enzymatic Method: Structural, Rheological, Thermal and Functional Properties Jiang G, Ramachandraiah K, Tan C, Cai N, Ameer K, Feng X Foods 24-Jul-2023
PMCID:PMC10379364
doi:10.3390/foods12142809
PMID:37509900
Methods of crop improvement and applications towards fortifying food security Patel A, Miles A, Strackhouse T, Cook L, Leng S, Patel S, Klinger K, Rudrabhatla S, Potlakayala SD Front Genome Ed 07-Jul-2023
PMCID:PMC10361821
doi:10.3389/fgeed.2023.1171969
PMID:37484652
Macrophyte communities as bioindicator of stormwater pollution in rivers: a quantitative analysis Babko R, Diachenko T, Zaburko J, Danko Y, Kuzmina T, Szulżyk-Cieplak J, Czarnota J, Łagód G PeerJ 01-Jun-2023
PMCID:PMC10239615
doi:10.7717/peerj.15248
PMID:37283889
The Alien Plant Species Impact in Rice Crops in Northwestern Italy Vagge I, Chiaffarelli G Plants (Basel) 17-May-2023
PMCID:PMC10223007
doi:10.3390/plants12102012
PMID:37653929
Extraction optimization, structure features, and bioactivities of two polysaccharides from Corydalis decumbens Wang Z, Luo D PLoS One 13-Apr-2023
PMCID:PMC10101462
doi:10.1371/journal.pone.0284413
PMID:37053219
Evolutionary honing in and mutational replacement: how long-term directed mutational responses to specific environmental pressures are possible Livnat A, Melamed D Theory Biosci 11-Mar-2023
PMCID:PMC10209271
doi:10.1007/s12064-023-00387-z
PMID:36899155
Research progress on the therapeutic effects of polysaccharides on non-alcoholic fatty liver diseases Hu YL, Ma Q, Dong X, Kong Y, Cai J, Li J, Dong C Front Nutr 10-Mar-2023
PMCID:PMC10036344
doi:10.3389/fnut.2023.1107551
PMID:36969821
Advances in health-promoting effects of natural polysaccharides: Regulation on Nrf2 antioxidant pathway Luo JH, Li J, Shen ZC, Lin XF, Chen AQ, Wang YF, Gong ES, Liu D, Zou Q, Wang XY Front Nutr 16-Feb-2023
PMCID:PMC9978827
doi:10.3389/fnut.2023.1102146
PMID:36875839

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
2-[(Carboxymethyl)amino]-4-chlorobenzoic acid 11107141 Click to see 229.62 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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
3,5-Dihydroxybenzoic Acid 7424 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Secoisolariciresinol, (+)- 6336781 Click to see 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Acyl carnitines
2-(Acetyloxy)-3-carboxy-N,N,N-trimethylpropan-1-aminium 2 Click to see 204.24 unknown via CMAUP database
Hexanoylcarnitine 6426853 Click to see 259.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Heptanol 8129 Click to see 116.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,7R)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 5316148 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
(3S)-5-[(1R,4aS,8aS)-2-(hydroxymethyl)-5,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol 162994951 Click to see 306.50 unknown https://doi.org/10.1016/0031-9422(75)85185-5
5-[2-(Hydroxymethyl)-5,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol 162994950 Click to see CC1(CCCC2(C1CC=C(C2CCC(C)(C=C)O)CO)C)C 306.50 unknown https://doi.org/10.1016/0031-9422(75)85185-5
Sagittine G 11616743 Click to see 320.50 unknown via CMAUP database
Sclareol 163263 Click to see 308.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Sagittariol 101603339 Click to see CC1CCC2(C(C1(C)CCC(C)(C=C)O)CCC=C2CO)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)82644-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(1R)-1,6,6-trimethyl-1,2,6,7,8,9-hexahydrophenanthro[1,2-b]furan-10,11(3aH,11aH)-dione 25181389 Click to see CC1COC2C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Cyclohexene, 1-methyl-3-(1-methylethenyl)- 10354 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown via CMAUP database
1,3-Dimethyl-8-(1-methylethyl)-tricyclo(4.4.0.02,7)dec-3-ene 25245021 Click to see 204.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown via CMAUP database
Sagittine A 11493191 Click to see CC1(CCC2(C3CCCC(C3=CCC2C1)(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1021/NP050479E
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(7S,8R)-6,6,8-trimethyl-2-methylidenetricyclo[5.3.1.01,5]undecane 24883561 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Sagittine B 11647447 Click to see 420.60 unknown https://doi.org/10.1021/NP050479E
Sagittine C 11496338 Click to see 462.60 unknown https://doi.org/10.1021/NP050479E
Sagittine D 11641229 Click to see 462.60 unknown https://doi.org/10.1021/NP050479E
Sagittine E 11598594 Click to see CC(=O)OCC1C(C(C(O1)OCC2(CCCC3C2=CCC4C3(CCC(C4)(C)C=C)C)C)OC(=O)C)O 504.70 unknown https://doi.org/10.1021/NP050479E
Sagittine F 11497064 Click to see CC(=O)OCC1C(C(C(O1)OCC2(CCCC3C2=CCC4C3(CCC(C4)(C)C=C)C)C)O)OC(=O)C 504.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Labd-14-ene, 8,13-epoxy-, (13S)- 6432025 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6R)-2-[[(3S,8R,9S,10R,13R,14R,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163042762 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/10.1016/0031-9422(75)85133-8
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/10.1016/0031-9422(75)85133-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1016/0305-1978(86)90092-X
> Organic oxygen compounds / Organooxygen compounds
Heptylidyneoxidanium 53630757 Click to see [CH2-]CCCCCC#[O+] 112.17 unknown via CMAUP database
Hexylidyneoxidanium 53628050 Click to see 98.14 unknown via CMAUP database
Methylhydroxycarbene 11262180 Click to see 44.05 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Cyclooctanemethanol 77196 Click to see 142.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R)-1-[2-(hydroxymethyl)-5,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-2-methylbut-3-en-2-ol 5321053 Click to see 292.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Pentanal 8063 Click to see 86.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(111C)octanal 451254 Click to see 127.21 unknown via CMAUP database
Decanal 8175 Click to see 156.26 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Acetone 180 Click to see CC(=O)C 58.08 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Triazoles / Phenyltriazoles / Phenyl-1,2,4-triazoles
Fenchlorazole-ethyl 3033865 Click to see CCOC(=O)C1=NN(C(=N1)C(Cl)(Cl)Cl)C2=C(C=C(C=C2)Cl)Cl 403.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
1-(Benzo[d][1,3]dioxol-5-yl)butan-1-ol 10375365 Click to see 194.23 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines
2-Ethylpyrazine 26331 Click to see CCC1=NC=CN=C1 108.14 unknown via CMAUP database
Trimethylpyrazine 26808 Click to see 122.17 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines / Pyrazine carboxylic acids and derivatives / Pyrazine carboxylic acids
Methyl pyrazinoate 72662 Click to see 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol 8369 Click to see 126.11 unknown via CMAUP database
> Organosulfur compounds / Sulfoxides
Dimethyl Sulfoxide 679 Click to see CS(=O)C 78.14 unknown via CMAUP database
> Organosulfur compounds / Thioethers / Dialkylthioethers
Di((2H3)methyl) sulphide 2724139 Click to see CSC 68.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Hemiphloin 160711 Click to see 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 102467789 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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
Quercetin 3-robinobioside 10371536 Click to see 610.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Sagittatin A 44258946 Click to see 710.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Aspalathin 11282394 Click to see 452.40 unknown via CMAUP database
Nothofagin 21722188 Click to see 436.40 unknown via CMAUP database

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