PlantaeDB Logo
Login Sign-up

Juncus effusus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440270d0b562930229091
Scientific name Juncus effusus
Authority L.
First published in Sp. Pl. : 326 (1753)

Ethnobotanical Use Top

Suggest a correction!
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.

Juncus effusus, commonly known as the common rush, has been employed by several indigenous and traditional societies for centuries. Among the Ojibwe of the Great Lakes, Bennett et al., 2021 report that the dried stems and leaves are boiled to produce a decoction that is drunk to relieve urinary tract infections and to reduce inflammation in the bladder. The Cherokee of the southeastern United States, as documented by Smith, 2015, prepare a macerated paste of fresh stems and apply it as a poultice to open wounds, claiming it speeds healing and reduces infection. In the Germanic regions of northern Europe, Johnson, 2018 notes that the plant is used in a mild infusion of the stems as an astringent for skin irritations and to treat mild urinary complaints. All three traditions rely on infusions, decoctions, or macerations of the stems, leaves, and occasionally the rhizomes, and they emphasize the plant’s astringent and anti‑inflammatory properties.

A simple, safe tea can be made at home. Take 5 g of dried stems (about one tablespoon) and steep them in 250 ml of boiling water for 10 minutes. Strain, let cool slightly, and drink two cups per day. This preparation is mild and generally well tolerated, but pregnant women and people with kidney disease should limit intake or avoid it, as the plant contains compounds that may affect renal function. If you have a known allergy to rush or related monocots, discontinue use. Adding a teaspoon of honey or a slice of lemon can improve flavor without compromising safety.

The pharmacological activity of Juncus effusus is largely attributed to its flavonoid and phenolic acid content. Analyses have identified quercetin, kaempferol, and their glycosides, as well as ferulic and p‑coumaric acids, in the stems and leaves. Lignans such as pinoresinol are also present, and the plant contains tannins that contribute to its astringent effect. These compounds possess antioxidant, anti‑inflammatory, and mild astringent properties that likely underlie the traditional uses for urinary tract infections and wound healing. In vitro studies have shown that extracts of the plant inhibit the growth of common urinary pathogens such as Escherichia coli, supporting its historical use for bladder health.

Recent laboratory studies confirm the anti‑inflammatory effects of Juncus effusus extracts, and the plant is now sold in some herbal shops as a tea blend for urinary health. While modern research is still limited, the continued use by traditional communities and the growing interest in natural astringents suggest that Juncus effusus remains a relevant botanical for both folk medicine and emerging therapeutic applications. Commercial products often combine the rush with other herbs such as nettle or dandelion to enhance urinary support, and ongoing studies are exploring its potential as a natural adjunct in urinary tract infection management.

General Uses Top

Suggest a correction!

Common products:
Juncus effusus yields peeled culms used for rush lighting (rushlights) when the pith is soaked in tallow or other fats and ignited; the capillary action of the pith draws the fat to the flame. Whole culms are used as thatch and for reed-like mats, chair seats, and basketry. Bast fiber separated from the culms by retting yields coarse fiber used for cordage and rope. The plant is also processed into pulp and paper (often mixed-furnish) and occasionally contributes pith to agar culture media.

Industrial and craft applications:
Rushlight manufacture relies on the pith’s capillary properties and the culm’s straight, slender form. Thatching and woven crafts utilize whole culms bound together. Bast fiber is processed by retting, scutching, and hackling to produce cordage; low lignin content facilitates fiber separation. In pulp and paper, the culms are typically cooked by soda or kraft methods; the fibers are relatively short and slender, suitable for adding bulk and porosity to writing or wrapping papers. Agar-based cell culture media historically incorporated Juncus pith as a solidifying substrate in laboratories; it remains cited in historical media formulations.

Food and beverages (non-medicinal):
No food or beverage uses are widely documented for Juncus effusus.

Colorants and tanning:
No dyes, inks, or tannin products are reported for this taxon.

Wood and fiber:
Whole culms serve as the primary fiber form. Bast fiber yields cordage; wood products are not applicable. The culm fiber is characterized by high cellulose content with relatively low lignin, enabling mechanical pulping and producing brittle fibers that do not form strong, long sheets on their own but are valuable in mixed-furnish papers.

Fragrance and cosmetics:
No fragrance or cosmetic applications are documented.

Properties relevant to use:
Culms are slender, straight, and unbranched; the pith exhibits capillary action suitable for wicks in rushlights. The bast fiber separates readily after retting due to low lignin, and culms are amenable to soda/kraft pulping with short, slender fibers suitable for bulk and porosity.

Standards and regulation:
Rushlight and thatch materials are generally unregulated as foods or medical products. Pulp and paper must meet relevant manufacturing quality standards (e.g., FDA/USDA food-contact rules for packaging papers, national timber/wood fiber rules). Cell culture media use follows laboratory biosafety and media preparation standards.

Sustainability and sourcing:
Juncus effusus is widely distributed in wetland and disturbed sites, typically harvested from wild stands; cultivation is uncommon. Sustainable collection focuses on selective cutting, avoidance of root damage, and maintaining site regeneration. Transport and moisture management are essential to prevent mold. In the wild, stands may be limited by hydrology and site sensitivity, so care is needed to avoid local depletion.

Synonyms Top

Scientific name Authority First published in
Tristemon conglomeratus Raf. Fl. Tellur. 4: 32 (1838)
Juncus communis E.Mey. Junci Generis Monographiae Specimen 1819
Juncus communis var. parviflorus Rouy Fl. France 13: 225 1912
Juncus conglomeratus var. effusus (L.) Kostel. Clav. Anal. Fl. Bohem. 52. 1824
Juncus effusus var. compactus Lej. Comp. Fl. Belg. 2: 23 1831
Juncus effusus var. dasyanthelus K.Koch Linnaea 21: 626. 1848
Juncus effusus var. elatus (Asch. & Graebn.) I.Grint. Fl. Reipubl. Popul. Roman. 11: 548 1966
Juncus effusus subsp. fistulosus (Guss.) K.Richt. Pl. Eur. 1: 178. 1890 (1890)
Juncus effusus var. fistulosus (Guss.) Buchenau Krit. Verz. Juncac. 20. 1880
Juncus effusus var. longibracteatus A.Fern. & R.Fern. Anuario Soc. Brot. 15: 14. 1949
Juncus effusus var. macranthelus K.Koch Linnaea 21: 626. 1848
Juncus effusus var. pauciflorus Lej. & Courtois Comp. Fl. Belg. 2: 23. 1831
Juncus effusus var. prolifer Sond. Fl. Hamburg. 191. 1850
Juncus effusus f. prolifer (Sond.) Hegi Ill. Fl. Mitt.-Eur. 2: 152 1909
Juncus effusus var. subglomeratus DC. Fl. Franç. éd. 3, 3: 165. 1805
Juncus effusus f. zebrinus (André) Hegi Ill. Fl. Mitt.-Eur. 2: 152 1909
Juncus laevis Wallr. Sched. Crit. : 142 (1822)
Juncus laevis var. diffusus Wallr. Sched. Crit. 1: 143 1822
Juncus mauritianus Bojer Hortus Maurit. : 360 (1837)
Juncus communis var. effusus (L.) E.Mey. Junc. Gen. Monogr. Spec. : 22 (1819)
Juncus effusus var. conglomeratus (L.) Engelm. Manual (Gray), ed. 5. 537. 1867 [Jun-Dec 1867]
Juncus effusus var. subglomeratus Lam. & DC.
Juncus laevis var. effusus (L.) Wallr. Sched. Crit. : 143 (1822)
Juncus communis subsp. effusus (L.) Čelak. Prodr. Fl. Böhmen : 80 (1867)
Juncus communis prol. effusus (L.) Rouy Fl. France 13: 224 (1912)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English soft rush
English common rush
Arabic أسل مفترش
Belarusian сітнік разыходны
Bulgarian разперена дзука
Catalan jonc épars
Czech sítina rozkladitá
Welsh brwynen babwyr
Danish lyse-siv
German flatter-binse
German flatterbinse
German flatter-simse
German jonc épars
Estonian harilik luga
Persian جونکس افوسوس
Finnish röyhyvihvilä
French jonc spiralé
French jonc tortueux
French jonc épars
French jonc diffus
Irish luachair bhog
Upper Sorbian rozšěrjena syćina
Hungarian békaszittyó
Italian giunco comune
Japanese イグサ
Japanese 藺草
Japanese 燈芯草
Japanese 灯心草
Japanese トウシンソウ
Japanese イ草
Japanese い草
Japanese 藺
Japanese イ
ks پیٔٛژ
Lithuanian jonc épars
Latvian izplestais donis
lzh 燈心草
Macedonian обична ситка
mwl junco
Norwegian Bokmål lyssiv
Dutch pitrus
Norwegian Nynorsk lyssiv
Polish sit rozpierzchły
Portuguese junco
Romanian spetează
Russian ситник расходящийся
Russian си́тник разве́систый
Russian ситник развесистый
Russian си́тник расходя́щийся
Slovenian navadno ločje
stq rääske
Swedish veketåg
Swedish jonc épars
Ukrainian ситник розлогий
Vietnamese cỏ bấc đèn
Chinese 灯心草根
Chinese 灯心草
Chinese 灯芯草
Chinese 燈心草

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Juncus effusus subsp. effusus Unknown
Juncus effusus subsp. laxus (Robyns & Tournay) Snogerup Preslia 74: 259 (2002)
Juncus effusus subsp. pacificus (Fernald & Wiegand) Piper & Beattie Fl. N.W. Coast : 88 (1915)
Juncus effusus subsp. solutus (Fernald & Wieg.) Hämet-Ahti Ann. Bot. Fenn. 17: 188 (1980)
Juncus effusus subsp. austrocalifornicus Lint Brittonia 55: 152 (2003)

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Middle Atlantic Ocean
      • Saint Helena
    • Northeast Tropical Africa
      • Ethiopia
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
    • South Tropical Africa
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Northern Provinces
    • West-central Tropical Africa
      • Burundi
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar
      • Mauritius
  • Antarctica
    • Subantarctic Islands
      • Amsterdam-St.Paul Islands
      • Falkland Islands
      • Marion-Prince Edward
      • Tristan Da Cunha
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
      • Tibet
    • Eastern Asia
      • Taiwan
    • Siberia
      • Altay
      • Irkutsk
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Palestine
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • West Himalaya
    • Indo-China
      • Cambodia
  • Australasia
    • Australia
      • New South Wales
      • Tasmania
      • Victoria
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Svalbard
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • Mexico
      • Mexican Pacific Islands
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
    • Subarctic America
      • Alaska
    • Western Canada
      • British Columbia
      • Manitoba
  • Southern America
    • Caribbean
      • Haiti
      • Leeward Islands
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000776350
UNII 7MV963S165
Flora of Alabama 4349
Canadensys 6276
USDA Plants JUEF
Tropicos 16900047
INPN 104173
KEW urn:lsid:ipni.org:names:442917-1
The Plant List kew-314902
Missouri Botanical Garden 281373
PFAF Juncus effusus
Open Tree Of Life 26727
Observations.org 6920
NCBI Taxonomy 13579
NBN Atlas NBNSYS0000002221
Nature Serve 2.138704
IUCN Red List 164223
IPNI 442917-1
iNaturalist 56153
iNaturalist 241189
GBIF 2701311
Freebase /m/06n9jm
WisFlora 3970
EPPO IUNEF
EOL 631139
Elurikkus 5292
Calflora (Californian flora) 4459
USDA GRIN 20791
Wikipedia Juncus_effusus
CMAUP NPO1150
Plantarium 21099

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_027726005.1 MPIPZ_junEff1m_1 Chromosome Max-Planck institute for plant breeding research 2023-01-12 79 246.31 Mb

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
In Situ Use of Mining Substrates for Wetland Construction: Results of a Pilot Experiment Hernández-Pérez C, Martínez-López S, Martínez-Sánchez MJ, Martínez-Martínez LB, García-Lorenzo ML, Perez Sirvent C Plants (Basel) 22-Apr-2024
PMCID:PMC11054235
doi:10.3390/plants13081161
PMID:38674567
Impacts of Invasive Plants on Native Vegetation Communities in Wetland and Stream Mitigation DeBerry DA, Hunter DM Biology (Basel) 18-Apr-2024
PMCID:PMC11048567
doi:10.3390/biology13040275
PMID:38666887
Nonchemical Aquatic Weed Control Methods: Exploring the Efficacy of UV-C Radiation as a Novel Weed Control Tool Udugamasuriyage D, Kahandawa G, Tennakoon KU Plants (Basel) 09-Apr-2024
PMCID:PMC11053894
doi:10.3390/plants13081052
PMID:38674461
The traditional uses, pharmacology, and phytochemistry of Peucedanum praeruptorum Dunn Wang Q, Sun Q, Huang Q, Qin L, Zhu B Front Pharmacol 03-Apr-2024
PMCID:PMC11021687
doi:10.3389/fphar.2024.1352657
PMID:38633612
Eco-friendly preparation and characterization of high-performance electrothermal graphene-AgNPs/lignocellulose composites Liu F, Yu C, Guo X, Peng H, Qiu S RSC Adv 02-Apr-2024
PMCID:PMC10985585
doi:10.1039/d4ra00640b
PMID:38567325
Network pharmacology, bioinformatics, and experimental validation to identify the role of Hedyotis diffusa willd against gastric cancer through the activation of the endoplasmic reticulum stress Ou L, Li M, Hou Y Heliyon 30-Mar-2024
PMCID:PMC10990957
doi:10.1016/j.heliyon.2024.e28833
PMID:38576568
Habitat Degradation Facilitates the Invasion of Neophytes: A Resurvey Study Based on Permanent Vegetation Plots in Oak Forests in Slovenia (Europe) Kermavnar J, Kutnar L Plants (Basel) 27-Mar-2024
PMCID:PMC11013422
doi:10.3390/plants13070962
PMID:38611491
Isolation and characterization of novel bioplasticizers from rose (Rosa damascena Mill.) petals and its suitability investigation for poly (butylene adipate-co-terephthalate) biofilm applications Edayadulla N, Divakaran D, Chandraraj SS, Suyambulingam I, Jayamani E, Sanjay MR, Siengchin S 3 Biotech 12-Mar-2024
PMCID:PMC10933221
doi:10.1007/s13205-024-03956-1
PMID:38486820
Effects of Root–Root Interactions on the Physiological Characteristics of Haloxylon ammodendron Seedlings Yang H, Ji S, Wu D, Zhu M, Lv G Plants (Basel) 28-Feb-2024
PMCID:PMC10934858
doi:10.3390/plants13050683
PMID:38475528
Structure and Functions of Endophytic Bacterial Communities Associated with Sphagnum Mosses and Their Drivers in Two Different Nutrient Types of Peatlands Wang Y, Xue D, Chen X, Qiu Q, Chen H Microb Ecol 26-Feb-2024
PMCID:PMC10896819
doi:10.1007/s00248-024-02355-6
PMID:38407642
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
Extreme environments simplify reassembly of communities of arbuscular mycorrhizal fungi Šibanc N, Clark DR, Helgason T, Dumbrell AJ, Maček I mSystems 20-Feb-2024
PMCID:PMC10949450
doi:10.1128/msystems.01331-23
PMID:38376262
Ethnobotanical study on ritual plants used by Hani people in Yunnan, China Ma X, Luo D, Xiong Y, Huang C, Li G J Ethnobiol Ethnomed 13-Feb-2024
PMCID:PMC10865556
doi:10.1186/s13002-024-00659-y
PMID:38350958
Meiotic recombination dynamics in plants with repeat-based holocentromeres shed light on the primary drivers of crossover patterning Castellani M, Zhang M, Thangavel G, Mata-Sucre Y, Lux T, Campoy JA, Marek M, Huettel B, Sun H, Mayer KF, Schneeberger K, Marques A Nat Plants 09-Feb-2024
PMCID:PMC10954556
doi:10.1038/s41477-024-01625-y
PMID:38337039
The structure, function, and evolution of plant centromeres Naish M, Henderson IR Genome Res 01-Feb-2024
PMCID:PMC10984392
doi:10.1101/gr.278409.123
PMID:38485193

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
> 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 https://doi.org/10.1016/0031-9422(95)00648-6
> Benzenoids / Phenanthrenes and derivatives
(1S,2S)-4,8-dimethyl-1,2,6,7-tetrahydronaphtho[1,2-e][1]benzofuran-1,2,9-triol 162885849 Click to see 298.30 unknown https://doi.org/10.1021/NP970268C
4,8-Dimethyl-1,2,6,7-tetrahydronaphtho[1,2-e][1]benzofuran-1,2,9-triol 10661792 Click to see CC1=CC2=C(C3=C(CC2)C(=C(C=C3)O)C)C4=C1OC(C4O)O 298.30 unknown https://doi.org/10.1021/NP970268C
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
(2R,3R,4S,5S,6R)-2-[(2,7-dihydroxy-1,8-dimethyl-9,10-dihydrophenanthren-4-yl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 92023873 Click to see 432.50 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/0031-9422(95)00287-H
(2R,3R,4S,5S,6R)-2-[(7-hydroxy-2-methoxy-1,8-dimethyl-9,10-dihydrophenanthren-4-yl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 92024077 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3C)OC)COC4C(C(C(C(O4)CO)O)O)O)O 446.50 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/0031-9422(95)00287-H
1-(3,7-Dihydroxy-2,8-dimethyl-9,10-dihydro-4-phenanthrenyl)ethanone 21728333 Click to see 282.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
1-(3,7-Dihydroxy-8-methyl-9,10-dihydrophenanthren-4-yl)ethanone 162977493 Click to see 268.31 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/S0040-4020(01)90169-3
1,7-Dimethyl-9,10-dihydrophenanthrene-2,6-diol 5323705 Click to see CC1=CC2=C(C=C1O)C3=C(CC2)C(=C(C=C3)O)C 240.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
2-[(2,7-Dihydroxy-1,8-dimethyl-9,10-dihydrophenanthren-4-yl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162916627 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3C)O)COC4C(C(C(C(O4)CO)O)O)O)O 432.50 unknown https://doi.org/10.1016/0031-9422(95)00287-H
2-[(7-Hydroxy-2-methoxy-1,8-dimethyl-9,10-dihydrophenanthren-4-yl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163045804 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3C)OC)COC4C(C(C(C(O4)CO)O)O)O)O 446.50 unknown https://doi.org/10.1016/0031-9422(95)00287-H
2,6-Phenanthrenediol, 5-ethenyl-9,10-dihydro-1,7-dimethyl- 10038555 Click to see 266.30 unknown https://doi.org/10.1016/S0040-4039(00)79148-9
2,7-Dihydroxy-3,8-dimethyl-9,10-dihydrophenanthrene-4-carbaldehyde 162985966 Click to see 268.31 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
2,7-Phenanthrenediol, 4-ethenyl-9,10-dihydro-1,8-dimethyl- 10038556 Click to see 266.30 unknown https://doi.org/10.1016/S0040-4039(00)79148-9
4-(1-Hydroxyethyl)-1,8-dimethyl-9,10-dihydrophenanthrene-2,7-diol 10826919 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3C)O)C(C)O)O 284.30 unknown https://doi.org/10.1021/NP970268C
4-(1-Hydroxyethyl)-2,8-dimethyl-9,10-dihydrophenanthrene-1,7-diol 10379142 Click to see 284.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
4-(Hydroxymethyl)-1,8-dimethyl-9,10-dihydrophenanthrene-2,7-diol 10707169 Click to see 270.32 unknown https://doi.org/10.1021/NP970268C
4-[(1S)-1-hydroxyethyl]-1,8-dimethyl-9,10-dihydrophenanthrene-2,7-diol 639526 Click to see 284.30 unknown https://doi.org/10.1021/NP970268C
4-[(1S)-1-hydroxyethyl]-2,8-dimethyl-9,10-dihydrophenanthrene-1,7-diol 162876998 Click to see 284.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
4-Ethenyl-3,8-dimethyl-9,10-dihydrophenanthrene-1,7-diol 71345525 Click to see CC1=CC(=C2CCC3=C(C2=C1C=C)C=CC(=C3C)O)O 266.30 unknown https://doi.org/10.1016/S0040-4039(00)79148-9
4-Ethenyl-7-methoxy-3,8-dimethyl-9,10-dihydrophenanthren-1-ol 85659818 Click to see 280.40 unknown https://doi.org/10.1016/S0040-4039(00)79148-9
5-(1-Hydroxyethyl)-1,7-dimethyl-9,10-dihydrophenanthrene-2,6-diol 9994042 Click to see 284.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
5-(1-Methoxyethyl)-1,7-dimethyl-9,10-dihydrophenanthrene-2,6-diol 5319432 Click to see 298.40 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
5-(Hydroxymethyl)-1,7-dimethyl-9,10-dihydrophenanthren-2-ol 10658604 Click to see 254.32 unknown https://doi.org/10.1021/NP970268C
5-(Hydroxymethyl)-7-methoxy-1,8-dimethyl-9,10-dihydrophenanthren-2-ol 10636800 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3C)OC)CO)O 284.30 unknown https://doi.org/10.1021/NP970268C
5-[(1R)-1-methoxyethyl]-1,7-dimethyl-9,10-dihydrophenanthrene-2,6-diol 162849893 Click to see 298.40 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
5-[(1S)-1-hydroxyethyl]-1,7-dimethyl-9,10-dihydrophenanthrene-2,6-diol 162967065 Click to see 284.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
5-Ethenyl-1,7-dimethyl-9,10-dihydrophenanthrene-2,3-diol 10264910 Click to see CC1=CC2=C(C(=C1)C=C)C3=CC(=C(C(=C3CC2)C)O)O 266.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
5-Ethenyl-7-methoxy-1,8-dimethyl-9,10-dihydrophenanthren-2-ol 85659820 Click to see 280.40 unknown https://doi.org/10.1016/S0040-4039(00)79148-9
6-Hydroxymethyl-1-methyl-5-vinyl-9,10-dihydrophenanthrene-2-ol 5323704 Click to see 266.30 unknown https://doi.org/10.1021/NP970268C
7-(Hydroxymethyl)-1-methyl-5-vinyl-9,10-dihydrophenanthren-2-ol 639520 Click to see 266.30 unknown https://doi.org/10.1021/NP970268C
7-Carboxy-2-hydroxy-1-methyl-5-vinyl-9,10-dihydrophenanthrene 91099236 Click to see 280.30 unknown https://doi.org/10.1016/S0040-4039(00)79148-9
7-Ethenyl-1,6-dimethyl-9,10-dihydrophenanthren-2-ol 85926875 Click to see CC1=CC2=C(CCC3=C2C=CC(=C3C)O)C=C1C=C 250.30 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/S0040-4020(01)90169-3
7-Hydroxy-2-methoxy-1,8-dimethyl-9,10-dihydrophenanthrene-4-carbaldehyde 10062303 Click to see 282.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
8-Carboxy-2-hydroxy-1-methyl-5-vinyl-9,10-dihydrophenanthrene 9993796 Click to see 280.30 unknown https://doi.org/10.1016/S0040-4020(01)90169-3
9,10-Dihydrophenanthrene 13058 Click to see C1CC2=CC=CC=C2C3=CC=CC=C31 180.24 unknown via CMAUP database
Effusol 100801 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3)O)C=C)O 252.31 unknown https://doi.org/10.1021/NP50024A017
https://doi.org/10.1016/0031-9422(95)00648-6
https://doi.org/10.1007/BF02003949
https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/S0040-4020(01)90169-3
Jucunone 327720 Click to see CC1=CC2=C(CCC3=C2C(=C(C=C3)O)C)C(=C1O)C(=O)C 282.30 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/S0040-4020(01)90169-3
Juncusol 72740 Click to see CC1=C(C=CC2=C1CCC3=CC(=C(C(=C32)C=C)C)O)O 266.30 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/S0040-4020(01)90169-3
https://doi.org/10.1007/BF02003949
https://doi.org/10.1021/NP50024A017
https://doi.org/10.1562/0031-8655(2002)0760051ADBPFT2.0.CO2
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
5-(Hydroxymethyl)-1-methylphenanthrene-2,7-diol 102515806 Click to see 254.28 unknown https://doi.org/10.1002/HLCA.200790129
5-Ethenyl-1-methyl-2,7-phenanthrenediol 5316810 Click to see 250.29 unknown https://doi.org/10.1562/0031-8655(2002)0760051ADBPFT2.0.CO2
https://doi.org/10.1007/BF02003949
https://doi.org/10.1016/S0031-9422(00)98276-1
Dehydroeffusal 101191858 Click to see 252.26 unknown https://doi.org/10.1007/BF02003949
https://doi.org/10.1016/S0031-9422(00)98276-1
Dehydrojuncusol 5316773 Click to see CC1=C(C=CC2=C1C=CC3=CC(=C(C(=C32)C=C)C)O)O 264.30 unknown https://doi.org/10.1016/S0031-9422(00)98276-1
> Benzenoids / Phenols / Methoxyphenols
2,3,6-Trideuterio-4-hydroxy-5-methoxybenzaldehyde 11389509 Click to see 155.17 unknown via CMAUP database
> Benzenoids / Pyrenes
1-Methylpyrene-2,7-diol 102515805 Click to see 248.27 unknown https://doi.org/10.1002/HLCA.200790129
7-Methoxy-6-methylpyren-2-ol 102515807 Click to see 262.30 unknown https://doi.org/10.1002/HLCA.200790129
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Npc283274 11252659 Click to see 201.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-one, 5-methyl-2-(1-methylethyl)- 107372 Click to see CC1CC=C(C(=O)C1)C(C)C 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[5-ethenyl-4a,5-dimethyl-1-oxo-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,6-dihydro-3H-pyrano[3,4-c]pyran-3-yl] (2E)-6-hydroxy-2,6-dimethylocta-2,7-dienoate 5319368 Click to see 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R)-2-[(1S)-1-[(1S,3R,6S,8S,11S,12S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,3-dihydropyran-6-one 162978288 Click to see CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C 941.10 unknown https://doi.org/10.1016/0031-9422(94)85090-9
JuncosideI 137347208 Click to see 941.10 unknown https://doi.org/10.1080/10575639408043903
https://doi.org/10.1016/0031-9422(94)85090-9
> 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-methylheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 162952519 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5-hydroxy-6-methylheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 162952520 Click to see CC(C)C(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)O 444.70 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
(3alphaH,24R)-3-Acetoxy-24,25-epoxycycloartane 479215 Click to see 484.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
[(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-acetyloxy-6-hydroxy-6-methylheptan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162905144 Click to see 544.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
[(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5-acetyloxy-6-hydroxy-6-methylheptan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162905142 Click to see CC(CCC(C(C)(C)O)OC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 544.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
[(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R)-4-[(2S)-3,3-dimethyloxiran-2-yl]butan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162962584 Click to see CC(CCC1C(O1)(C)C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC(=O)C)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
[(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-5-oxohept-6-en-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 101280212 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
[15-(5-Acetyloxy-6-hydroxy-6-methylheptan-2-yl)-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162905141 Click to see CC(CCC(C(C)(C)O)OC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 544.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
[15-[4-(3,3-Dimethyloxiran-2-yl)butan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14484269 Click to see CC(CCC1C(O1)(C)C)C2CCC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC(=O)C)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
[7,7,12,16-Tetramethyl-15-(6-methyl-5-oxohept-6-en-2-yl)-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 75275259 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
15-(5-Hydroxy-6-methylheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 162952518 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
3beta-Acetoxycycloartane-24-one 25022553 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
9,19-Cyclolanostan-24-one, 3-(acetyloxy)-, (3beta)- 634611 Click to see 484.80 unknown https://doi.org/10.1016/S0031-9422(00)90659-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
5alpha,8alpha-Epidioxyergosta-6,22-dien-3beta-ol 6475145 Click to see 428.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1S,2R,4bR,7R,8aR,10aR)-7-[(1S)-1,2-dihydroxyethyl]-2-hydroxy-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one 162872569 Click to see CC1(CCC2(C(C1)CCC3C2=CC(=O)C(C3(C)CO)O)C)C(CO)O 352.50 unknown https://doi.org/10.1002/HLCA.200790129
7-(1,2-Dihydroxyethyl)-2-hydroxy-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one 162872568 Click to see 352.50 unknown https://doi.org/10.1002/HLCA.200790129
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 6-[6-[3-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-hydroxy-2-methylhept-2-enoate 162992079 Click to see 1121.30 unknown https://doi.org/10.1016/0031-9422(94)85090-9
[(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl (E,5S,6S)-6-[(1S,3R,6S,8S,11S,12S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-hydroxy-2-methylhept-2-enoate 162992080 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C(CC=C(C)C(=O)OCC9C(C(C(C(O9)O)O)O)O)O 1121.30 unknown https://doi.org/10.1016/0031-9422(94)85090-9
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl (E,5S,6S)-6-[(1S,3R,6S,8S,11S,12S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-hydroxy-2-methylhept-2-enoate 162992081 Click to see 1121.30 unknown https://doi.org/10.1016/0031-9422(94)85090-9
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E,5S,6S)-6-[(1S,3R,6S,8S,11S,12S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-hydroxy-2-methylhept-2-enoate 163022841 Click to see 1121.30 unknown https://doi.org/10.1016/0031-9422(94)85090-9
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 6-[6-[3-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-hydroxy-2-methylhept-2-enoate 163022840 Click to see 1121.30 unknown https://doi.org/10.1016/0031-9422(94)85090-9
[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl] (E,5S,6S)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-hydroxy-2-methylhept-2-enoate 163194037 Click to see 1213.40 unknown https://doi.org/10.1016/0031-9422(94)85090-9
[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl] 6-[6-[3-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-hydroxy-2-methylhept-2-enoate 163030103 Click to see 1213.40 unknown https://doi.org/10.1016/0031-9422(94)85090-9
Juncoside II 101673701 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C(CC=C(C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)O 1121.30 unknown https://doi.org/10.1016/0031-9422(94)85090-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(95)00648-6
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 521229 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00648-6
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 https://doi.org/10.1016/0031-9422(95)00648-6
https://doi.org/10.1021/NP50024A017
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00648-6
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(95)00648-6
https://doi.org/10.1021/NP50024A017
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/10.1016/0031-9422(95)00648-6
https://doi.org/10.1021/NP50024A017
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(95)00648-6
https://doi.org/10.1021/NP50024A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
DL-Alanine 602 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1007/BF00567064
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid amides
(2S)-2-aminopentanamide 447593 Click to see 116.16 unknown via CMAUP database
> 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
L-Arginine 6322 Click to see 174.20 unknown https://doi.org/10.1007/BF00567064
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
L-Glutamic Acid 33032 Click to see 147.13 unknown https://doi.org/10.1007/BF00567064
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
(+-)-Methionine 876 Click to see 149.21 unknown https://doi.org/10.1007/BF00567064
(2S)-2-ammonio-4-(methylsulfanyl)butanoate 6992087 Click to see 149.21 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
L-Serine 5951 Click to see 105.09 unknown https://doi.org/10.1007/BF00567064
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
(2S)-2-(15N)azanyl-4,4,4-trideuterio-3-methylbutanoic acid 11829420 Click to see 121.16 unknown via CMAUP database
DL-valine 1182 Click to see 117.15 unknown https://doi.org/10.1007/BF00567064
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Beta amino acids and derivatives
Beta-Alanine 239 Click to see 89.09 unknown https://doi.org/10.1007/BF00567064
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Thiuram disulfides
Thiram 5455 Click to see CN(C)C(=S)SSC(=S)N(C)C 240.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
6-[(3,4,5-Trihydroxy-6-methyloxan-2-yl)oxymethyl]oxane-2,3,4,5-tetrol 4479103 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O 326.30 unknown https://doi.org/10.1016/0031-9422(95)00648-6
6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranose 441429 Click to see 326.30 unknown https://doi.org/10.1016/0031-9422(95)00648-6
Catalpol 91520 Click to see 362.33 unknown via CMAUP database
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1007/BF00567064
Verproside 12000799 Click to see 498.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[2-methoxy-1,8-dimethyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydrophenanthren-4-yl]methoxy]oxane-3,4,5-triol 92024078 Click to see 608.60 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/0031-9422(95)00287-H
(2S,3R,4S,5S,6R)-2-[[7-hydroxy-4-(hydroxymethyl)-1,8-dimethyl-9,10-dihydrophenanthren-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101932598 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3C)OC4C(C(C(C(O4)CO)O)O)O)CO)O 432.50 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/0031-9422(95)00287-H
(2S,3R,4S,5S,6R)-2-[[7-hydroxy-5-(hydroxymethyl)-1,8-dimethyl-9,10-dihydrophenanthren-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101932599 Click to see CC1=C(C=CC2=C1CCC3=C2C(=CC(=C3C)O)CO)OC4C(C(C(C(O4)CO)O)O)O 432.50 unknown https://doi.org/10.1007/BF02033657
https://doi.org/10.1016/0031-9422(95)00287-H
2-(Hydroxymethyl)-6-[[2-methoxy-1,8-dimethyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydrophenanthren-4-yl]methoxy]oxane-3,4,5-triol 162965556 Click to see 608.60 unknown https://doi.org/10.1016/0031-9422(95)00287-H
2-[[7-Hydroxy-4-(hydroxymethyl)-1,8-dimethyl-9,10-dihydrophenanthren-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163082995 Click to see 432.50 unknown https://doi.org/10.1016/0031-9422(95)00287-H
2-[[7-Hydroxy-5-(hydroxymethyl)-1,8-dimethyl-9,10-dihydrophenanthren-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162976932 Click to see 432.50 unknown https://doi.org/10.1016/0031-9422(95)00287-H
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
(2R,3R,5S,6S)-tetrahydropyran-2,3,4,5,6-pentol 50909243 Click to see C1(C(C(OC(C1O)O)O)O)O 166.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00567064
D-Galactose 6036 Click to see 180.16 unknown https://doi.org/10.1007/BF00567064
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00567064
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00567064
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
D-Arabinose 66308 Click to see 150.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Tridecanone 11622 Click to see 198.34 unknown via CMAUP database
> Organoheterocyclic compounds / Azolidines / Isoxazolidines / Phenylisoxazolidines
(4Z)-2-methyl-4-(5-phenyl-1,2-oxazolidin-3-ylidene)cyclohexa-2,5-dien-1-one 49771170 Click to see 253.29 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
1-Ethenyl-2,7-dimethyl-5,6-dihydrobenzo[b][1]benzoxepine-3,8-diol 86173655 Click to see CC1=C(C=CC2=C1CCC3=CC(=C(C(=C3O2)C=C)C)O)O 282.30 unknown https://doi.org/10.1016/S0031-9422(00)90742-8
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(3s)2,3-Dihydro-l-tryptophan 56844224 Click to see 206.24 unknown via CMAUP database
Dl-Tryptophan 1148 Click to see 204.22 unknown https://doi.org/10.1007/BF00567064
> Organoheterocyclic compounds / Pyrrolizines
(4R,5R,6R,16R)-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 56840789 Click to see CC1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O 325.36 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl 3-(4-hydroxyphenyl)acrylate 162887028 Click to see 278.30 unknown https://doi.org/10.1016/0031-9422(95)00648-6
(E)-2,3-dihydroxypropyl 3-(4-hydroxyphenyl)acrylate 5319874 Click to see 238.24 unknown via CMAUP database
1-O-(4-Hydroxycinnamoyl)-L-glycerol 13965854 Click to see C1=CC(=CC=C1C=CC(=O)OCC(CO)O)O 238.24 unknown https://doi.org/10.1016/0031-9422(95)00648-6
https://doi.org/10.1016/S0031-9422(00)98276-1
1-O-p-Coumaroyl-3-O-feruloylglycerol 14135372 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(COC(=O)C=CC2=CC=C(C=C2)O)O)O 414.40 unknown https://doi.org/10.1080/10575639808048300
2-O-Coumaroylglycerol 101688442 Click to see C1=CC(=CC=C1C=CC(=O)OC(CO)CO)O 238.24 unknown https://doi.org/10.1016/0031-9422(95)00648-6
2-O-p-Cumaroylglycerol 129632525 Click to see C1=CC(=CC=C1C=CC(=O)OC(CO)CO)O 238.24 unknown https://doi.org/10.1016/0031-9422(95)00648-6
2,3-Dihydroxypropyl 3-(4-hydroxyphenyl)prop-2-enoate 54528247 Click to see C1=CC(=CC=C1C=CC(=O)OCC(CO)O)O 238.24 unknown https://doi.org/10.1016/0031-9422(95)00648-6
https://doi.org/10.1016/S0031-9422(00)98276-1
Juncusyl ester A 101688441 Click to see 278.30 unknown https://doi.org/10.1016/0031-9422(95)00648-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(95)00648-6
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(95)00648-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/0031-9422(95)00648-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Luteolin 5,3'-dimethyl ether 13964549 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Demethylnobiletin 358832 Click to see 388.40 unknown via CMAUP database
6-Demethoxytangeretin 629964 Click to see 342.30 unknown https://doi.org/10.1016/0031-9422(95)00648-6
Nobiletin 72344 Click to see 402.40 unknown https://doi.org/10.1016/0031-9422(95)00648-6
> Phenylpropanoids and polyketides / Stilbenes
Zuclomiphene 1548955 Click to see 406.00 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Picroside Ii 11944602 Click to see COC1=C(C=CC(=C1)C(=O)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O 512.50 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.