Scientific name	Authority	First published in
Sagittaria chinensis	Sims	Bot. Mag. 39: t. 1631 (1814)
Sagittaria doniana	Sweet	Hort. Brit. : 375 (1826)
Sagittaria edulis	Schltdl.	Linnaea 18: 432 (1844)
Sagittaria leucopetala	(Miq.) Bergmans	Vaste Pl. Rotsheesters : 479 (1924)
Sagittaria japonica	hort. ex E.Vilm.	Fl. Pleine Terre , ed. 3: 1002 (1870)
Sagittaria hirundinacea	Blume	Enum. Pl. Javae : 34 (1827)
Sagittaria sagittata	Thunb.	Fl. Jap. : 242 (1784)
Sagittaria sinensis	Sims	Bot. Mag. 39: t. 1631 (1814)
Sagittaria trifolia var. retusa	J.K.Chen, S.C.Sun & H.Q.Wang	et in Bull. Bot. Res. North-East. Forest. Inst. 4(2): 130 (1984), with latin descr. 1983
Sagittaria sagittifolia var. edulis	Siebold ex Miq.	Ann. Mus. Bot. Lugduno-Batavi 2: 138 (1865)
Sagittaria trifolia var. longiloba	(Turcz.) Kitag.	Neolin. Fl. Manshur. : 62 (1979)
Sagittaria sagittifolia var. diversifolia	M.Michel	Monogr. Phan. 3: 67. 1881
Sagittaria sagittifolia var. leucopetala	Miq.	Ill. Fl. Archip. Ind. 2: 49 (1870)
Sagittaria sagittifolia subsp. leucopetala	(Miq.) Hartog	Fl. Males. 5: 332 (1957)
Sagittaria trifolia var. leucopetala	Miq.	Ill. Fl. Archip. Ind. 2: 49 1870
Sagittaria sagittifolia var. longiloba	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 27(II): 57. 1854
Sagittaria trifolia var. edulis	(Schltdl.) Ohwi ex W.T.Lee	Lin. Fl. Koreae 1221 1996
Sagittaria sagittifolia f. sinensis	(Sims) Makino	J. Jap. Bot. 1: 37. 1918
Sagittaria trifolia var. sinensis	(Sims) Makino	J. Jap. Bot. 1: 37. 1918
Sagittaria trifolia var. angustifolia	Kitag.	Lin. Fl. Manshur. 56. 1939
Sagittaria sagittifolia var. subaequilonga	Regel	Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 VII, 4: 140 1861
Sagittaria sagittifolia var. alismifolia	Makino	Bot. Mag. (Tokyo) 23: 23. 1909
Sagittaria trifolia f. heterophylla	Makino	J. Jap. Bot. 1: 37 1917
Sagittaria trifolia f. subhastata	Makino	J. Jap. Bot. 1: 37 1917
Sagittaria trifolia f. suitensis	Makino	J. Jap. Bot. 1: 36 1917
Sagittaria trifolia f. albida	Makino	J. Jap. Bot. 1: 36 1917
Sagittaria trifolia f. caerulea	Makino	J. Jap. Bot. 1: 36 1917
Sagittaria trifolia f. longiloba	(Turcz.) Makino	J. Jap. Bot. 1: 36 1918
Sagittaria trifolia f. tenuissima	Hand.-Mazz.	Symb. Sin. 7: 1188 1936
Sagittaria trifolia subsp. leucopetala	(Miq.) Q.F.Wang	Fl. China 23: 85 (2010)

Common names Top

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Filter by language:

Language	Common/alternative name
English	threeleaf arrowhead
Arabic	سهم الماء ثلاثي الأوراق
Azerbaijani	Üçyarpaq oxyarpaq
Persian	پیکان آبی
Armenian	Նետաբույս եռատերև
Japanese	オモダカ
Japanese	澤瀉
Korean	벗풀
Korean	소귀나물
Malay	keladi cabang
Russian	Стрелолист трёхлистный
Thai	ขาเขียด
Chinese	野慈菇
Chinese	水芋
Chinese	剪刀草
Chinese	三脚剪
Chinese	剪刀草慈姑
Chinese	野慈姑
Chinese	野慈*(慈菇）
Chinese	慈菇
Chinese	慈姑花
Chinese	慈姑叶
Chinese	慈姑
Chinese	弯喙慈姑
Chinese	三腳剪

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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 click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Uzbekistan
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Buryatiya
  - Chita
  - Krasnoyarsk
- Western Asia
  - Afghanistan
  - Iran
  - Iraq

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Philippines
  - Sulawesi
  - Sumatera

Europe click to expand
- Eastern Europe
  - South European Russia
  - Ukraine

Pacific click to expand
- South-central Pacific
  - Marquesas
  - Society Islands
  - Tubuai Islands
- Southwestern Pacific
  - Fiji

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000738042
USDA Plants	SATR11
Tropicos	900125
INPN	446101
KEW	urn:lsid:ipni.org:names:58596-1
The Plant List	kew-287453
PFAF	Sagittaria trifolia
Open Tree Of Life	962775
NCBI Taxonomy	63789
IUCN Red List	168772
IPNI	58596-1
iNaturalist	206167
GBIF	5328972
Freebase	/m/010ffn0s
EPPO	SAGTR
EOL	1082270
USDA GRIN	400322
Wikipedia	Sagittaria_trifolia

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

Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China

Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C

J Ethnobiol Ethnomed

15-Jan-2024

PMCID:	PMC10790445
doi:	10.1186/s13002-023-00638-9
PMID:	38225656

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Yao-Shan of traditional Chinese medicine: an old story for metabolic health

Yang S, Yang H, Zhang Y

Front Pharmacol

16-Aug-2023

PMCID:	PMC10468577
doi:	10.3389/fphar.2023.1194026
PMID:	37663255

Chemical Modification of Polysaccharides: A Review of Synthetic Approaches, Biological Activity and the Structure–Activity Relationship

Liu T, Ren Q, Wang S, Gao J, Shen C, Zhang S, Wang Y, Guan F

Molecules

15-Aug-2023

PMCID:	PMC10457902
doi:	10.3390/molecules28166073
PMID:	37630326

Physicochemical characterization and antioxidant activity of polysaccharides from Chlorella sp. by microwave-assisted enzymatic extraction

Peng H, Xv X, Cui X, Fu Y, Zhang S, Wang G, Chen X, Song W

Front Bioeng Biotechnol

10-Aug-2023

PMCID:	PMC10448769
doi:	10.3389/fbioe.2023.1264641
PMID:	37635998

IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors

Zhang J, Zhang R, Li W, Ma XC, Qiu F, Sun CP

Int J Biol Sci

06-Aug-2023

PMCID:	PMC10496512
doi:	10.7150/ijbs.85158
PMID:	37705738

The Roles of Hormone Signals Involved in Rhizosphere Pressure Response Induce Corm Expansion in Sagittaria trifolia

Li E, Tang J, Liu J, Zhang Z, Hua B, Jiang J, Miao M

Int J Mol Sci

02-Aug-2023

PMCID:	PMC10419225
doi:	10.3390/ijms241512345
PMID:	37569720

Selection of Reliable Reference Genes for Gene Expression Normalization in Sagittaria trifolia

Tang J, Li E, Liu J, Zhang Z, Hua B, Jiang J, Miao M

Genes (Basel)

23-Jun-2023

PMCID:	PMC10379039
doi:	10.3390/genes14071321
PMID:	37510226

Chinese medicinal herbs for reducing endocrine therapy-induced side effects in patients with hormone receptor‐positive breast cancer: a systematic review and meta-analysis

Chen S, Gao Y, Liu H, Jing J, Yang Z, Zhu H, Chen B, Wang Y, Zhang T, Wang S, Lin J

Pharm Biol

25-Apr-2023

PMCID:	PMC10132232
doi:	10.1080/13880209.2023.2203193
PMID:	37096936

Physiological and Biochemical Responses of Sagittaria trifolia L. to Phytotoxic Ethyl Acetate Fungal Extract from Curvularia lunata Strain CLST-01

Wang K, Xu C, Li D, Gu Z

Plants (Basel)

25-Apr-2023

PMCID:	PMC10180700
doi:	10.3390/plants12091758
PMID:	37176815

WRA-Net: Wide Receptive Field Attention Network for Motion Deblurring in Crop and Weed Image

Yun C, Kim YH, Lee SJ, Im SJ, Park KR

Plant Phenomics

05-Apr-2023

PMCID:	PMC10243196
doi:	10.34133/plantphenomics.0031
PMID:	37287583

Emerging Role of Plant-Based Dietary Components in Post-Translational Modifications Associated with Colorectal Cancer

Rodríguez-García C, Gutiérrez-Santiago F

Life (Basel)

18-Jan-2023

PMCID:	PMC9962725
doi:	10.3390/life13020264
PMID:	36836621

Rotations improve the diversity of rhizosphere soil bacterial communities, enzyme activities and tomato yield

Feng C, Yi Z, Qian W, Liu H, Jiang X

PLoS One

12-Jan-2023

PMCID:	PMC9836298
doi:	10.1371/journal.pone.0270944
PMID:	36634092

Novel RNA Viruses Discovered in Weeds in Rice Fields

Chao S, Wang H, Zhang S, Chen G, Mao C, Hu Y, Yu F, Wang S, Lv L, Chen L, Feng G

Viruses

10-Nov-2022

PMCID:	PMC9717734
doi:	10.3390/v14112489
PMID:	36366587

Sexual selection on male but not female function in monoecious and dioecious populations of broadleaf arrowhead (Sagittaria latifolia)

Kwok A, Dorken ME

Proc Biol Sci

09-Nov-2022

PMCID:	PMC9653219
doi:	10.1098/rspb.2022.0919
PMID:	36350202

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,2R,4aR,8aR)-1-[(3S)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	7067321	Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C	308.50	unknown	https://doi.org/10.1248/CPB.44.492
(1S,2R,4aR,8aR)-2,5,5,8a-tetramethyl-1-(3-methylidenepent-4-enyl)-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	21579290	Click to see CC1(CCCC2(C1CCC(C2CCC(=C)C=C)(C)O)C)C	290.50	unknown	https://doi.org/10.1248/CPB.44.492
(1S,4aR,4bS,7S,9S,10aS)-7-ethenyl-9-hydroxy-1-(hydroxymethyl)-1,4a,7-trimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	10805526	Click to see CC1(CCC2C(=C1)C(CC3C2(CC(=O)CC3(C)CO)C)O)C=C	318.40	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
(1S,4aS,4bR,7S,10aS)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	10494596	Click to see CC1(CCC2C(=C1)CCC3C2(CC(=O)CC3(C)CO)C)C=C	302.50	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
(4aR,4bS,7S,9S,10aS)-7-ethenyl-9-hydroxy-1,1-bis(hydroxymethyl)-4a,7-dimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	10568746	Click to see CC1(CCC2C(=C1)C(CC3C2(CC(=O)CC3(CO)CO)C)O)C=C	334.40	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
(4aS,4bR,7S,10aS)-7-ethenyl-1,1-bis(hydroxymethyl)-4a,7-dimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	10829382	Click to see CC1(CCC2C(=C1)CCC3C2(CC(=O)CC3(CO)CO)C)C=C	318.40	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-alpha,2,5,5,8a-pentamethyl-, [1R-[1alpha(R*),2beta,4abeta,8aalpha]]-	521332	Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C	308.50	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
13-Episclareol	56842011	Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C	308.50	unknown	https://doi.org/10.1248/CPB.44.492
7-Ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	85145840	Click to see CC1(CCC2C(=C1)CCC3C2(CC(=O)CC3(C)CO)C)C=C	302.50	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
7-Ethenyl-1,1-bis(hydroxymethyl)-4a,7-dimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	85079689	Click to see CC1(CCC2C(=C1)CCC3C2(CC(=O)CC3(CO)CO)C)C=C	318.40	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
7-Ethenyl-9-hydroxy-1-(hydroxymethyl)-1,4a,7-trimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	71346514	Click to see CC1(CCC2C(=C1)C(CC3C2(CC(=O)CC3(C)CO)C)O)C=C	318.40	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
7-Ethenyl-9-hydroxy-1,1-bis(hydroxymethyl)-4a,7-dimethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one	85133848	Click to see CC1(CCC2C(=C1)C(CC3C2(CC(=O)CC3(CO)CO)C)O)C=C	334.40	unknown	https://doi.org/10.1248/CPB.41.1677
8alpha-13(16),14-Labdadien-8-ol	5168698	Click to see CC1(CCCC2(C1CCC(C2CCC(=C)C=C)(C)O)C)C	290.50	unknown	https://doi.org/10.1080/00021369.1986.10867901 https://doi.org/10.1248/CPB.44.492
Isoabienol	11220007	Click to see CC1(CCCC2(C1CCC(C2CCC(=C)C=C)(C)O)C)C	290.50	unknown	https://doi.org/10.1080/00021369.1986.10867901 https://doi.org/10.1271/BBB1961.50.3179 https://doi.org/10.1248/CPB.44.492
Sclareol	163263	Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C	308.50	unknown	https://doi.org/10.1248/CPB.41.1677
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,5S,9S,10R,13R,14S)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	162934980	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O	336.50	unknown	https://doi.org/10.1248/CPB.44.492
(1S,4S,5S,9S,10R,13R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	11722476	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O	302.50	unknown	https://doi.org/10.1248/CPB.44.492
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	49775756	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O	302.50	unknown	https://doi.org/10.1248/CPB.44.492
16,17-Dihydroxykauran-18-oic acid	5088391	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O	336.50	unknown	https://doi.org/10.1248/CPB.44.492
5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	433869	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O	302.50	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
Candol B	101289732	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO	288.50	unknown	https://doi.org/10.1248/CPB.44.492
ent-16-Kauren-19-ol	529650	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO	288.50	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
ent-Kaur-16-en-19-ol	443465	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO	288.50	unknown	https://doi.org/10.1248/CPB.41.1677
Kaurenoic acid	73062	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O	302.50	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-5,9-dimethyl-14-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	162892236	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(COC5C(C(C(C(O5)CO)O)O)O)O)(C)C(=O)O	498.60	unknown	https://doi.org/10.1248/CPB.41.1677
(1S,4S,5R,9S,10R,13R,14S)-14-hydroxy-5,9-dimethyl-14-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	101692676	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(COC5C(C(C(C(O5)CO)O)O)O)O)(C)C(=O)O	498.60	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
(2R,3R,4S,5S,6R)-2-[[(2S,4aS,5R,6R,8aR)-6-hydroxy-5-[(3R)-3-hydroxy-3-methylpent-4-enyl]-1,1,4a,6-tetramethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101612224	Click to see CC1(C2CCC(C(C2(CCC1OC3C(C(C(C(O3)CO)O)O)O)C)CCC(C)(C=C)O)(C)O)C	486.60	unknown	https://doi.org/10.1248/CPB.41.1677
14-Hydroxy-5,9-dimethyl-14-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	72245822	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(COC5C(C(C(C(O5)CO)O)O)O)O)(C)C(=O)O	498.60	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
2-[[6-hydroxy-5-(3-hydroxy-3-methylpent-4-enyl)-1,1,4a,6-tetramethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	44715758	Click to see CC1(C2CCC(C(C2(CCC1OC3C(C(C(C(O3)CO)O)O)O)C)CCC(C)(C=C)O)(C)O)C	486.60	unknown	https://doi.org/10.1248/CPB.41.1677
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13R)-ent-8,13-epoxylabd-14-ene	44346478	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1248/CPB.44.492
[(3R,4aS,6aS,7R,10aR,10bS)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-7-yl]methanol	13996012	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)CO	306.50	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
19-Hydroxy-13-epimanoyl oxide	626002	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)CO	306.50	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
2-[(3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-7-yl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85218496	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)COC4C(C(C(C(O4)CO)O)O)O	468.60	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	518574	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
Labd-14-ene, 8,13-epoxy-, (13R)-	6453839	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
Sagittarioside a	10647991	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)COC4C(C(C(C(O4)CO)O)O)O	468.60	unknown	https://doi.org/10.1248/CPB.44.492 https://doi.org/10.1248/CPB.41.1677
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(1S,2S,5S,6R,9S,10R,15S)-5-(5,6-dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol	129316892	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	https://doi.org/10.1021/NP060222W
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1248/CPB.44.492
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/10.1248/CPB.44.492
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Arabinothalictoside	10718822	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)CC[N+](=O)[O-])O)O)O)O)O)O	461.40	unknown	https://doi.org/10.1248/CPB.41.1677 https://doi.org/10.1248/CPB.44.492
Thalictoside	21629843	Click to see C1=CC(=CC=C1CC[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O	329.30	unknown	https://doi.org/10.1021/NP060222W

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Sagittaria trifolia

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