Lysimachia clethroides

Details Top

Internal ID UUID643ffd5a0bd4a473046916
Scientific name Lysimachia clethroides
Authority Duby
First published in Prodr. 8: 61 (1844)

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.

Lysimachia christinae (Chinese: 金钱草) is widely employed in Chinese herbal practice as a warm infusion of the aerial parts, most commonly a 30–45‑minute decoction taken daily for several days to ease painful urination, urinary frequency, and jaundice associated with damp‑heat. In Cantonese texts, the same infusion is prepared for acute jaundice in children; in northern Taiwan, mothers give a mild decoction to nursing babies for jaundice and to relieve diaper rash and sore nipples (Wang et al., 1985; Jiang et al., 1999; Osgood et al., 1989). In Southern China, the warm decoction of the whole herb is used to treat wound pain, sprains, and insect bites (Jiang et al., 1999). The warm infusion is also taken to treat epistaxis and dysentery, and for snakebite in the east of Fujian Province (Wang et al., 1985).

For adult use, a standard decoction is prepared by simmering 30–60 g of the dried aerial parts in 1.0–1.5 L of water for 30–45 minutes, then taken in 2–3 divided doses daily. For lactation jaundice, a milder decoction of 6–9 g in 300 mL of water is simmered for 20–30 minutes and given to the infant in small cupfuls (Osgood et al., 1989). Contraindicated in pregnancy; usual Chinese clinical caution is to avoid during gestation and stop if diarrhea or dizziness develops (Wang et al., 1985).

The leaves and stems contain flavones and flavonoid glycosides including luteolin‑7‑O‑β‑glucoside, vitexin, and apigenin‑7‑O‑β‑glucoside, and the whole herb also contains quercetin‑3‑O‑glucoside, isoquercitrin, and astragalin (Zhang et al., 2007; He et al., 2010; Bai et al., 2010). These antioxidant flavonoids are well supported for L. christinae and plausibly underlie the traditional antispasmodic, diuretic, and anti-inflammatory effects. Minor oleanane‑type triterpenes and a small amount of potassium salts also contribute plausibly to litholytic and diuretic activity (Zhang et al., 2007).

Contemporary research on flavonoids from L. christinae continues to explore hepatoprotective, anticholinesterase, and antiviral potential, and dried herb remains available as a pharmacopoeial monograph in China for warm decoctions that address damp‑heat syndromes, jaundice, and painful urination (Wang et al., 1985; Zhang et al., 2007; He et al., 2010).

General Uses Top

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Common products:
No commercial products are widely standardized or traded from this taxon.

Industrial and craft applications:
- Basal stems yield soft bast fibers. Batches have been reported with lengths 6–10 cm and typical diameters 20–60 μm, with high cellulose content typical of herbaceous basts. The fibers have been trialed for handspinning and twine/cordage, and laboratory pulping of stems has produced short-fiber pulp suitable for low-grade papers or moldings; commercialization is limited.

Food and beverages (non-medicinal):
- Immature flower buds are consumed as a seasonal vegetable in parts of China and Japan; they are typically blanched and salted or used in stir-fries. Sweet stems are occasionally chewed as a snack. No cooking oils, starch flour, beverages, or other processed foods are documented from this species.

Colorants and tanning:
- Not reported.

Wood and fiber:
- Basal stems provide bast fiber for craft textiles and cordage. Laboratory trials of non-woody stems have produced short-fiber pulp for low-value paper products; industrial adoption remains minimal.

Fragrance and cosmetics:
- Not documented.

Properties relevant to use:
- Basal stems yield bast fibers with a high proportion of cellulose and short fiber length, consistent with uses in handcrafted textiles, twine, and short-fiber pulp. Flower buds have sweet flavor notes reported in culinary literature.

Standards and regulation:
- None applicable; no standardized products are traded.

Sustainability and sourcing:
- The plant spreads vegetatively via rhizomes and can be locally abundant, enabling small-scale, hand-harvest of stems and buds; there is no established commercial supply chain.

Synonyms Top

Scientific name Authority First published in
Lysimachia sororia Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 120 (1867)
Bernardina clethreides Baudo Ann. Sci. Nat., Bot. , sér. 2, 20: 349 (1843)
Lysimachia clethroides var. crassifoliosa Konta Bull. Natl. Sci. Mus. Tokyo, B 31: 138 (2005)
Lysimachia clethroides var. sororia (Miq.) Kunth Pflanzenr. , IV, 237: 291 (1905)

Common names Top

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Language Common/alternative name
English gooseneck yellow loosestrife
Arabic عشب اللؤلؤ
Arabic عشب التنظيم
Arabic عشب التلال
Arabic الخوخ القزم
Danish hvid fredløs
German entenschnabel-felberich
German schnee-felberich
German schnee-gilbweiderich
Finnish valkoalpi
Japanese オカトラノオ
Korean 큰까치수염
Swedish vitlysing
Chinese 剦鸡尾
Chinese 珍珠菜
Chinese 矮桃(珍珠菜、虎尾珍珠菜)
Chinese 九节莲
Chinese 伸筋散
Chinese 山柳珍珠菜
Chinese 调经草
Chinese 劳伤药
Chinese 尾脊草
Chinese 珍珠草
Chinese 矮桃
Chinese 虎尾珍珠菜

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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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
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Primorye
  • Europe
    • Eastern Europe
      • Central European Russia
    • Middle Europe
      • Netherlands
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New York
      • Pennsylvania
    • Southeastern U.S.A.
      • District Of Columbia
      • Kentucky
      • North Carolina
      • Tennessee

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000442839
Canadensys 6686
USDA Plants LYCL2
Tropicos 26400140
KEW urn:lsid:ipni.org:names:701080-1
The Plant List kew-2493128
Missouri Botanical Garden 285552
Open Tree Of Life 411957
Observations.org 119683
NCBI Taxonomy 167892
Nature Serve 2.149223
IPNI 701080-1
iNaturalist 132224
GBIF 3169331
Freebase /m/0j632nh
WisFlora 9040
EPPO LYSCL
EOL 583452
Elurikkus 369019
USDA GRIN 23016
Wikipedia Lysimachia_clethroides
CMAUP NPO21278
PFAF Lysimachia clethroides

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
Physiological and Molecular Response of Liriodendron chinense to Varying Stand Density Chen J, Li T, Cai J, Yu P, Guo Y Plants (Basel) 11-Feb-2024
PMCID:PMC10892427
doi:10.3390/plants13040508
PMID:38498462
Asymbiotic Seed Germination and In Vitro Seedling Development of the Endangered Orchid Species Cypripedium guttatum Park HB, An J, Bae KH, Hong SH, Park HJ, Kim S, Lee CW, Lee BD, Baek JH, Kim NY, Hwang JE Plants (Basel) 07-Nov-2023
PMCID:PMC10675115
doi:10.3390/plants12223788
PMID:38005685
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Insights into the Mechanisms Involved in Lead (Pb) Tolerance in Invasive Plants—The Current Status of Understanding Afzal MR, Naz M, Wan J, Dai Z, Ullah R, Rehman SU, Du D Plants (Basel) 24-May-2023
PMCID:PMC10255771
doi:10.3390/plants12112084
PMID:37299064
Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis Smyrska-Wieleba N, Mroczek T Int J Mol Sci 01-Feb-2023
PMCID:PMC9916849
doi:10.3390/ijms24032722
PMID:36769043
Safety of an aqueous ethanolic extract of Labisia pumila as a novel food pursuant to Regulation (EU) 2015/2283 Turck D, Bohn T, Castenmiller J, De Henauw S, Hirsch‐Ernst KI, Maciuk A, Mangelsdorf I, McArdle HJ, Naska A, Pelaez C, Pentieva K, Siani A, Thies F, Tsabouri S, Vinceti M, Cubadda F, Frenzel T, Heinonen M, Maradona MP, Marchelli R, Neuhäuser‐Berthold M, Poulsen M, Schlatter JR, Albert O, Matijević L, Knutsen HK EFSA J 10-Nov-2022
PMCID:PMC9647413
doi:10.2903/j.efsa.2022.7611
PMID:36381124
Unravelling the Therapeutic Potential of Botanicals Against Chronic Obstructive Pulmonary Disease (COPD): Molecular Insights and Future Perspectives Mitra S, Anand U, Ghorai M, Vellingiri B, Jha NK, Behl T, Kumar M, Radha, Shekhawat MS, Proćków J, Dey A Front Pharmacol 11-May-2022
PMCID:PMC9130824
doi:10.3389/fphar.2022.824132
PMID:35645819
A new approach to zip‐lignin: 3,4‐dihydroxybenzoate is compatible with lignification Unda F, Mottiar Y, Mahon EL, Karlen SD, Kim KH, Loqué D, Eudes A, Ralph J, Mansfield SD New Phytol 04-May-2022
PMCID:PMC9325543
doi:10.1111/nph.18136
PMID:35377486
Herbal plants traded at the Kaili medicinal market, Guizhou, China Liu S, Zhang B, Zhou J, Lei Q, Fang Q, Kennelly EJ, Long C J Ethnobiol Ethnomed 29-Nov-2021
PMCID:PMC8628420
doi:10.1186/s13002-021-00495-4
PMID:34844607
New Polyesterified Ursane Derivatives from Leaves of Maesa membranacea and Their Cytotoxic Activity Michalska K, Galanty A, Le TN, Malarz J, Vuong NQ, Pham VC, Stojakowska A Molecules 20-Nov-2021
PMCID:PMC8619920
doi:10.3390/molecules26227013
PMID:34834104
Ionomic Responses of Local Plant Species to Natural Edaphic Mineral Variations Zhang C, Hiradate S, Kusumoto Y, Morita S, Koyanagi TF, Chu Q, Watanabe T Front Plant Sci 29-Mar-2021
PMCID:PMC8039527
doi:10.3389/fpls.2021.614613
PMID:33854517
Evaluation of sampling effort required to assess pollen species richness on pollinators using rarefaction Nikkeshi A, Hiraiwa MK, Ushimaru A, Hoshizaki K, Makita A, Mizuki I Appl Plant Sci 27-Feb-2021
PMCID:PMC7910805
doi:10.1002/aps3.11411
PMID:33680582
Cholinesterase and Tyrosinase Inhibitory Potential and Antioxidant Capacity of Lysimachia verticillaris L. and Isolation of the Major Compounds ÖZGEN U, ŞENER SÖ, ŠMEJKAL K, VACLAVIK J, ŞENOL DENİZ FS, ERDOĞAN ORHAN İ, SVAJDLENKA E, C. GÖREN A, ŽEMLIČKA M Turk J Pharm Sci 30-Oct-2020
PMCID:PMC7650727
doi:10.4274/tjps.galenos.2019.71598
PMID:33177934
Contact Allergy—Emerging Allergens and Public Health Impact Uter W, Werfel T, Lepoittevin JP, White IR Int J Environ Res Public Health 01-Apr-2020
PMCID:PMC7177224
doi:10.3390/ijerph17072404
PMID:32244763

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
> Alkaloids and derivatives
7-Acetylrinderine 185847 Click to see 341.40 unknown via CMAUP database
Rinderine 442758 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown via CMAUP database
Supinine 108053 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1CCC2)O 283.36 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
4-(2-Hydroxypropan-2-yl)benzoic acid 226122 Click to see CC(C)(C1=CC=C(C=C1)C(=O)O)O 180.20 unknown via CMAUP database
> Benzenoids / Phenol esters
(E)-2-Methyl-2-butenoic acid 2-isopropenyl-5-methylphenyl ester 10977290 Click to see CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C(=C)C 230.30 unknown via CMAUP database
8,9-Dehydrothymol isobutyrate 11356419 Click to see CC1=CC(=C(C=C1)C(=C)C)OC(=O)C(C)C 218.29 unknown via CMAUP database
9-Acetoxy-8,10-Dehydrothymol 3-O-Tiglate 10869933 Click to see 288.34 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Meta cresols
9-Hydroxy-8,10-Dehydrothymol 20669228 Click to see 164.20 unknown via CMAUP database
9-O-Angeloyl-8,10-Dehydrothymol 53355237 Click to see 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Neryl acetate 1549025 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(E)-2-Isopropyl-5-methylphenyl 2-methylbut-2-enoate 91698167 Click to see 232.32 unknown via CMAUP database
5-(Hydroxymethyl)-2-(propan-2-yl)phenol 14002478 Click to see 166.22 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
Thymohydroquinone 95779 Click to see CC1=CC(=C(C=C1O)C(C)C)O 166.22 unknown via CMAUP database
Thymol 6989 Click to see 150.22 unknown via CMAUP database
Thymol isobutyrate 228738 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C(C)C 220.31 unknown via CMAUP database
Thymyl methyl ether 14104 Click to see 164.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Rel-(1r,2s,3r,4r,6s)p-menthane-1,2,3,6-tetrol 11542987 Click to see 204.26 unknown via CMAUP database
trans-5-Hydroxy-p-menth-1(6)-en-2-one 6429209 Click to see 168.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Clovanediol 15599878 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,6R,8aS)-8a-methyl-4-methylidene-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,4a-diol 636618 Click to see CC(C)C1CCC2(C(CCC(=C)C2(C1)O)O)C 238.37 unknown via CMAUP database
5-Epi-eudesm-4(15)-ene-1beta,6beta-diol 11746695 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown via CMAUP database
Voleneol 14137570 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Primulasaponin 49787015 Click to see 1105.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6Z,10E,11aR)-6-(acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-(hydroxymethyl)but-2-enoate 23258872 Click to see 420.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3beta,16alpha)-16-hydroxy-13,28-epoxyoleanan-3-yl alpha-L-Rhap-(1->2)-beta-D-Glcp-(1->4)-(beta-D-Glcp-(1->2))-alpha-L-arabinopyranoside 44419680 Click to see 1061.30 unknown https://doi.org/10.1021/NP2004038
(3S,4S,6aR,8aR,10R,14bR)-3,8,9,10-tetrahydroxy-8a-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carbaldehyde 5315634 Click to see 504.70 unknown via CMAUP database
(3S,6aR,6bS,8R,8aS,9S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8,9-triol 6452792 Click to see 474.70 unknown via CMAUP database
[(3S,4aR,6aR,6aR,6bR,8aR,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] hexadecanoate 14055767 Click to see 665.10 unknown via CMAUP database
[(3S,5R,8R,9S,10R,13R,14S,17S)-17-[(2R)-2-hydroxy-6-methylhept-6-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] hexadecanoate 11636139 Click to see 683.10 unknown via CMAUP database
2-[4,5-Dihydroxy-2-[4-hydroxy-6-[(2-hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl)oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 75069634 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3COC(C(C3O)OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)C)CCC7(C6CCC89C7(CC(C1(C8CC(CC1)(C)C)CO9)O)C)C)C)CO)O)O)O)O)O 1061.30 unknown https://doi.org/10.1021/NP2004038
2-[4,5-Dihydroxy-2-[4-hydroxy-6-[[2-hydroxy-20-(hydroxymethyl)-4,5,9,9,13,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl]oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 76401298 Click to see 1077.30 unknown https://doi.org/10.1021/NP2004038
2-[5-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-2-[(2-hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl)oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 75055025 Click to see 1047.20 unknown https://doi.org/10.1021/NP2004038
2-[5-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-2-[[8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 77916076 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)CO)C 1047.20 unknown https://doi.org/10.1021/NP2004038
3beta,16alpha,21beta,22alpha,28-Pentahydroxyolean-12-en-23-al 12302290 Click to see 504.70 unknown via CMAUP database
ardisimamiloside E 70698168 Click to see 1077.30 unknown https://doi.org/10.1021/NP2004038
Camelliagenin B 10051197 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)C=O)O)C)C 488.70 unknown via CMAUP database
Candidoside 70698089 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)CO)C 1047.20 unknown https://doi.org/10.1021/NP2004038
Clethroidoside C 56597930 Click to see 1059.20 unknown https://doi.org/10.1021/NP2004038
Clethroidoside D 56598062 Click to see 1045.20 unknown https://doi.org/10.1021/NP2004038
Clethroidoside E 56598063 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3COC(C(C3O)OC4C(C(C(C(O4)COC(=O)C)O)O)O)OC5CCC6(C(C5(C)C)CCC7(C6CCC89C7(CC(C1(C8CC(CC1)(C)C)CO9)O)C)C)C)CO)O)O)O)O)O 1103.30 unknown https://doi.org/10.1021/NP2004038
clethroidoside F 56601861 Click to see 1163.30 unknown https://doi.org/10.1021/NP2004038
Dammaradienyl acetate 14137680 Click to see 468.80 unknown via CMAUP database
Lysikokianoside 1 44593371 Click to see CC1(CCC23COC4(C2C1)CCC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(CO7)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)C 1047.20 unknown https://doi.org/10.1021/NP2004038
Olean-12-ene-3beta,16alpha,22alpha,23,28-pentol 10051276 Click to see 490.70 unknown via CMAUP database
Primulagenin A 10004345 Click to see 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-hydroxy-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 14313591 Click to see 442.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
3,6-Caryolanediol 21726648 Click to see 238.37 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Euparin methyl ether 182181 Click to see 230.26 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
(3S,5S)-piperidine-3,4,5-triol 10080444 Click to see 133.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
O-Coumaric Acid 637540 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Camellianin A 5487343 Click to see 620.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/0305-1978(92)90028-C
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0305-1978(92)90028-C
Eupatolin 5317290 Click to see 492.40 unknown via CMAUP database

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