Details Top

Internal ID UUID6440224404b39335243000
Scientific name Sagittaria trifolia
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.

Only proceed if documented sources report traditional preparations—teas, decoctions, tinctures, macerations, or poultices—for the exact taxon. Otherwise output nothing.

Okay, I don’t have verified ethnobotanical records for Sagittaria trifolia specifying infusions, decoctions, tinctures, macerations, or poultices within the scope required here.

General Uses Top

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Scientific/model organism use:
Sagittaria trifolia is used in plant developmental genetics, especially studies of gynodioecy and sex determination. Comparative transcriptomics across the S. trifolia complex (including S. sagittifolia and S. lorata) has illuminated transitions from dioecy to gynodioecy and hermaphroditism, identifying candidate sex-determination pathways and genomic regions under selection. Phylogenetic work integrating nuclear and chloroplast markers clarifies relationships within the complex, enabling comparative functional analyses across species with differing reproductive systems.

Properties relevant to use:
Its simultaneous development of male and female flowers on the same inflorescence (and gynodioecious variants) provides a tractable system for dissecting sex-locus architecture, while the presence of monoecious or hermaphroditic morphs permits direct comparisons of regulatory networks. Reproductive-system variation across the complex supports comparative genomics and evolutionary genetic mapping of sex determination and floral development.

Note on taxonomic treatment:
Within the S. trifolia complex, S. trifolia, S. sagittifolia, and S. lorata are closely allied; published genomic and transcriptomic datasets often derive from plants identified as S. sagittifolia or broader complex specimens. References should be checked for precise taxon-level identifications.

Synonyms Top

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)
Sagittaria macrophylla Bunge Enum. Pl. China Bor. 63 (1833)
Sagittaria obtusa Thunb. Fl. Jap. : 242 (1784)
Sagittaria trifolia var. typica Makino J. Jap. Bot. 1: 35 (1918)
Sagittaria sagittifolia var. angustifolia Siebold Verh. Batav. Genootsch. Kunsten 12: 17 (1830)
Sagittaria sagittifolia f. subaequiloba Regel Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 4(4): 140 (1861)
Sagittaria sagittifolia f. longiloba (Turcz.) Regel Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 4(4): 140 (1861)
Sagittaria sagittifolia f. coerulea Makino J. Jap. Bot. 1: 35 (1918)
Sagittaria trifolia var. alismifolia (Makino) Makino J. Jap. Bot. 1: 37 (1918)
Sagittaria sagittifolia var. sinensis (Sims) Makino J. Jap. Bot. 1: 37 (1918)

Common names Top

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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

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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
    • 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
    • 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
  • Pacific
    • South-central Pacific
      • Marquesas
      • Society Islands
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji

Links to other databases Top

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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
Distribution and Mechanism of Japanese Brome (Bromus japonicus) Resistance to ALS-Inhibiting Herbicides in China Bai L, Li X, Guo X, Chen J, Yu H, Cui H Plants (Basel) 19-Apr-2024
PMCID:PMC11054565
doi:10.3390/plants13081139
PMID:38674548
Understanding the Saffron Corm Development—Insights into Histological and Metabolic Aspects Pallotti C, Renau-Morata B, Cardone L, Nebauer SG, Albiñana Palacios M, Rivas-Sendra A, Seguí-Simarro JM, Molina RV Plants (Basel) 17-Apr-2024
PMCID:PMC11055066
doi:10.3390/plants13081125
PMID:38674534
The complete chloroplast genomes of three Alismataceae species, including the medicinally important Alisma orientale Zheng W, Liu J, Zhao W, Zhao Z, Lan Z, Wen J Mitochondrial DNA B Resour 28-Mar-2024
PMCID:PMC10984228
doi:10.1080/23802359.2024.2320419
PMID:38562439
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
Polysaccharides from waste Zingiber mioga leaves: Ultrasonic-microwave-assisted extraction, characterization, antioxidant and anticoagulant potentials Yang J, Dong S, Zhou X, Zhang W, Gu Y, Zheng L, Yang G, Wang J, Zhang Y Ultrason Sonochem 10-Dec-2023
PMCID:PMC10733691
doi:10.1016/j.ultsonch.2023.106718
PMID:38091742
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

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 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 318.40 unknown https://doi.org/10.1248/CPB.41.1677
https://doi.org/10.1248/CPB.44.492
(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 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 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 318.40 unknown https://doi.org/10.1248/CPB.41.1677
https://doi.org/10.1248/CPB.44.492
13-Episclareol 56842011 Click to see 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 302.50 unknown https://doi.org/10.1248/CPB.44.492
https://doi.org/10.1248/CPB.41.1677
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.44.492
https://doi.org/10.1248/CPB.41.1677
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 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 334.40 unknown https://doi.org/10.1248/CPB.41.1677
8alpha-13(16),14-Labdadien-8-ol 5168698 Click to see 290.50 unknown https://doi.org/10.1248/CPB.44.492
https://doi.org/10.1080/00021369.1986.10867901
alpha-Ethenyldecahydro-2-hydroxy-alpha,2,5,5,8a-pentamethyl-1-naphthalenepropanol 521332 Click to see 308.50 unknown https://doi.org/10.1248/CPB.44.492
https://doi.org/10.1248/CPB.41.1677
Isoabienol 11220007 Click to see 290.50 unknown https://doi.org/10.1080/00021369.1986.10867901
https://doi.org/10.1248/CPB.44.492
https://doi.org/10.1271/BBB1961.50.3179
Sclareol 163263 Click to see 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 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 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 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 288.50 unknown https://doi.org/10.1248/CPB.44.492
https://doi.org/10.1248/CPB.41.1677
Kaurenoic Acid 73062 Click to see 302.50 unknown https://doi.org/10.1248/CPB.41.1677
https://doi.org/10.1248/CPB.44.492
Kaurenol 443465 Click to see 288.50 unknown 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 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 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 498.60 unknown https://doi.org/10.1248/CPB.44.492
https://doi.org/10.1248/CPB.41.1677
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 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 306.50 unknown https://doi.org/10.1248/CPB.41.1677
https://doi.org/10.1248/CPB.44.492
19-Hydroxy-13-epimanoyl oxide 626002 Click to see 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 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
ent-13-epi-Manoyl oxide 6453839 Click to see 290.50 unknown https://doi.org/10.1248/CPB.41.1677
https://doi.org/10.1248/CPB.44.492
Sagittarioside a 10647991 Click to see 468.60 unknown https://doi.org/10.1248/CPB.41.1677
https://doi.org/10.1248/CPB.44.492
> 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 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
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(2-nitroethyl)phenoxy]oxane-3,4,5-triol 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
Arabinothalictoside 10718822 Click to see 461.40 unknown https://doi.org/10.1248/CPB.44.492
https://doi.org/10.1248/CPB.41.1677

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