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Sparganium stoloniferum

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400b7cefeae366153685
Scientific name Sparganium stoloniferum
Authority (Graebn.) Buch.-Ham. ex Juz.
First published in Fl. URSS 1: 219 (1934)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sparganium carinatum Falc. Proc. Linn. Soc. London 1: 18 (1839)
Sparganium erectum subsp. stoloniferum (Graebn.) H.Hara J. Jap. Bot. 51: 228 (1976)
Sparganium ramosum subsp. stoloniferum Graebn. Pflanzenr. , IV, 10: 14 (1900)

Common names Top

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Language Common/alternative name
English sparganium stoloniferum ex
Chinese 三棱
Chinese 黑三棱
Chinese 理三棱
Chinese 黑三棱*

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Sparganium stoloniferum subsp. choui (D.Yu) K.Sun Fl. China 23: 159 (2010)
Sparganium stoloniferum subsp. stoloniferum Unknown

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
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye
    • Siberia
      • Buryatiya
      • West Siberia
    • Western Asia
      • Afghanistan
      • Iran
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Victoria

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000554193
UNII 873IV8AW3C
Canadensys 25883
Tropicos 29800054
KEW urn:lsid:ipni.org:names:60461195-2
The Plant List kew-266175
Open Tree Of Life 452423
Observations.org 145993
NCBI Taxonomy 203643
IPNI 60461195-2
iNaturalist 842661
GBIF 2702355
EPPO SPGST
EOL 1238534
Elurikkus 286266
USDA GRIN 413529
CMAUP NPO17458

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
Gut microbes combined with metabolomics reveal the protective effects of Qijia Rougan decoction against CCl4-induced hepatic fibrosis Li X, Xu X, Tao S, Su Y, Wen L, Wang D, Liu J, Feng Q Front Pharmacol 28-Mar-2024
PMCID:PMC11007057
doi:10.3389/fphar.2024.1347120
PMID:38606180
Effectiveness of adjuvant traditional Chinese medicine on macrovascular invasion in patients with hepatocellular carcinoma: a real-world propensity score-matched study Yan H, Wang X, Yu L, Liu X, Yan F, Xie Y, Pu Q, Yang Z Front Pharmacol 23-Feb-2024
PMCID:PMC10923102
doi:10.3389/fphar.2024.1353720
PMID:38464727
Integrative traditional Chinese medicine treatment for children with obstructive sleep apnea Lai WY, Wei CC, Lin CH, Hang LW, Shih YH, Huang FW, Yen HR J Tradit Complement Med 07-Aug-2023
PMCID:PMC10785241
doi:10.1016/j.jtcme.2023.08.002
PMID:38223810
Jianpi Yangzheng Xiaozheng decoction alleviates gastric cancer progression via suppressing exosomal PD-L1 Chen Y, Liu J, Chen Y, Zhang R, Tao J, Chen X, Wang H, Sun Q, Wu J, Liu S Front Pharmacol 03-Aug-2023
PMCID:PMC10434994
doi:10.3389/fphar.2023.1159829
PMID:37601051
Discovering the anti-cancer phytochemical rutin against breast cancer through the methodical platform based on traditional medicinal knowledge Lee J, Lee J, Sim W, Kim JH, Choi C, Jeon J BMB Rep 05-Jul-2023
PMCID:PMC10689086
doi:10.5483/BMBRep.2023-0057
PMID:37357538
Molecular mechanism and research progress on pharmacology of ferulic acid in liver diseases Shi Y, Shi L, Liu Q, Wang W, Liu Y Front Pharmacol 31-May-2023
PMCID:PMC10264600
doi:10.3389/fphar.2023.1207999
PMID:37324465
Efficacy and safety of the herbal formula Naesohwajung-tang for functional dyspepsia: a randomized, double-blind, placebo-controlled, multi-center trial Ha NY, Ko SJ, Park JW, Kim J Front Pharmacol 12-May-2023
PMCID:PMC10213234
doi:10.3389/fphar.2023.1157535
PMID:37251334
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
Gastrodia elata BI.:A Comprehensive Review of Its Traditional Use, Botany, Phytochemistry, Pharmacology, and Pharmacokinetics Wu YN, Wen SH, Zhang W, Yu SS, Yang K, Liu D, Zhao CB, Sun J Evid Based Complement Alternat Med 18-Apr-2023
PMCID:PMC10129437
doi:10.1155/2023/5606021
PMID:37114145
Ginseng-containing traditional medicine preparations in combination with fluoropyrimidine-based chemotherapy for advanced gastric cancer: A systematic review and meta-analysis Hu J, Cheng M, Li Y, Shi B, He S, Yao Z, Jiang J, Yu H, He Z, Zhao Y, Zheng H, Hua B, Liu R PLoS One 17-Apr-2023
PMCID:PMC10109524
doi:10.1371/journal.pone.0284398
PMID:37068063
Fufang shenhua tablet, astragali radix and its active component astragaloside IV: Research progress on anti-inflammatory and immunomodulatory mechanisms in the kidney Li R, Shi C, Wei C, Wang C, Du H, Hong Q, Chen X Front Pharmacol 05-Apr-2023
PMCID:PMC10113559
doi:10.3389/fphar.2023.1131635
PMID:37089929
Effect of oral Xiao-xian decoction combined with acupoint application therapy on pediatric adenoid hypertrophy: A randomized trial Zhao X, Xu J, Wang MY, Hou ZW, Shi HS, Zhang XX Medicine (Baltimore) 03-Feb-2023
PMCID:PMC9901993
doi:10.1097/MD.0000000000032804
PMID:36749267
Kidney tonifying traditional Chinese medicine: Potential implications for the prevention and treatment of osteoporosis Duan Y, Su YT, Ren J, Zhou Q, Tang M, Li J, Li SX Front Pharmacol 09-Jan-2023
PMCID:PMC9868177
doi:10.3389/fphar.2022.1063899
PMID:36699069
Integrating HPLC-Q-TOF-MS/MS, network pharmacology and experimental validation to decipher the chemical substances and mechanism of modified Gui-shao-liu-jun-zi decoction against gastric cancer Huang W, Wen F, Ruan S, Gu P, Gu S, Song S, Zhou J, Li Y, Liu J, Shu P J Tradit Complement Med 08-Jan-2023
PMCID:PMC10148141
doi:10.1016/j.jtcme.2023.01.002
PMID:37128200
A reappraisal of the phylogeny and historical biogeography of Sparganium (Typhaceae) using complete chloroplast genomes Zhang Q, Belyakov EA, Lapirov AG, Zhao Y, Freeland J, Xu X BMC Plant Biol 15-Dec-2022
PMCID:PMC9753266
doi:10.1186/s12870-022-03981-3
PMID:36522739

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 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 / Phenols / Tyrosols and derivatives
Hydroxytyrosol Acetate 155240 Click to see CC(=O)OCCC1=CC(=C(C=C1)O)O 196.20 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol 82755 Click to see C1=CC(=C(C=C1CCO)O)O 154.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(E)-6,9,10-trihydroxyoctadec-7-enoic acid 5321100 Click to see CCCCCCCCC(C(C=CC(CCCCC(=O)O)O)O)O 330.50 unknown via CMAUP database
2-Dodecyl-3-methylbutanedioic acid 99891 Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
alpha-Sanshool 6440935 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aS,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 11897956 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol 51340201 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde 317607 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown via CMAUP database
Monogynol B (6CI) 44586882 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3beta,9xi,10xi)-24-Methylene-9,19-cyclolanostan-3-ol 5273649 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown via CMAUP database
(6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 21157981 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown via CMAUP database
24-Methylene-cycloartanol 9547213 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown via CMAUP database
24-Methylenecycloartanol 94204 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown via CMAUP database
3beta-24-Methylenecycloartan-3-ol 544165 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Fungisterol 5283646 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,7,2',3'-Tetrahydroxyflavone 5321864 Click to see C1=CC(=C(C(=C1)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 286.24 unknown via CMAUP database
Kaempferol oxoanion 25202062 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O 285.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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-chromen-3-yl 6-O-(6-deoxy-alpha-D-mannopyranosyl)-beta-D-glucopyranoside 17751019 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
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
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database

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