Convolvulus scammonia - Unknown
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Details Top

Internal ID UUID64405bd0ba70f555571167
Scientific name Convolvulus scammonia
Authority L.
First published in Sp. Pl. : 153 (1753)

Description Top

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Convolvulus scammonia, also known as scammony, is a perennial plant found in the eastern Mediterranean region. It has arrow-shaped leaves and produces flowers similar to Convolvulus arvensis. The dried juice, obtained from the root, has been used in traditional medicine as a purgative. However, due to the inconsistent quality of the drug, a resin called scammoniae resina is now commonly used. This resin is converted into a powerful purgative when it reacts with bile in the small intestine. Scammony has been used as an anthelmintic, particularly effective against roundworms. Its main active component is a glucoside called scammonin, also known as jalapin.

Synonyms Top

Scientific name Authority First published in
Calystegia scammonia Pritz. Icon. Bot. Index 2: 58 (1855)
Convolvulus elongatus Salisb. Prodr. Stirp. Chap. Allerton : 123 (1796)

Common names Top

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Language Common/alternative name
English scammony
Spanish escamonia
Arabic سقمونيا
Arabic محموده
Arabic محمودة
Azerbaijani oxyarpaq sarmaşıq
Catalan glòria de matí
German skammonium
German orientalische purgierwinde
Persian گیاه سمقونیا
Persian سمقونیا
French diagrède
French scammonée
French scammonee
io skamoneo
Russian Вьюнок смолоносный
Turkish mahmude otu

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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
    • Western Asia
      • East Aegean Islands
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001298534
UNII RI13X61R6E
USDA Plants COSC10
KEW urn:lsid:ipni.org:names:266929-1
Open Tree Of Life 3870489
Observations.org 142746
NCBI Taxonomy 1428931
IPNI 266929-1
iNaturalist 494311
GBIF 2928397
Freebase /m/04ygnx
EPPO CONSC
Elurikkus 336346
USDA GRIN 11319
Wikipedia Convolvulus_scammonia
CMAUP NPO10164

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
Mass Defect Filtering-Oriented Identification of Resin Glycosides from Root of Convolvulus scammonia Based on Quadrupole-Orbitrap Mass Spectrometer Yin Q, Abdulla R, Kahar G, Aisa HA, Li C, Xin X Molecules 06-Jun-2022
PMCID:PMC9182046
doi:10.3390/molecules27113638
PMID:35684574
Ca’ Granda, Hortus simplicium: Restoring an Ancient Medicinal Garden of XV–XIX Century in Milan (Italy) Bottoni M, Milani F, Galimberti PM, Vignati L, Romanini PL, Lavezzo L, Martinetti L, Giuliani C, Fico G Molecules 17-Nov-2021
PMCID:PMC8620247
doi:10.3390/molecules26226933
PMID:34834025
Phylobioactive hotspots in plant resources used to treat Chagas disease Salm A, Krishnan SR, Collu M, Danton O, Hamburger M, Leonti M, Almanza G, Gertsch J iScience 15-Mar-2021
PMCID:PMC8040286
doi:10.1016/j.isci.2021.102310
PMID:33870129
Medicinal plants as a fight against murine blood-stage malaria Dkhil MA, Al-Quraishy S, Al-Shaebi EM, Abdel-Gaber R, Thagfan FA, Qasem MA Saudi J Biol Sci 19-Dec-2020
PMCID:PMC7938113
doi:10.1016/j.sjbs.2020.12.014
PMID:33732056
Synthesis of ZnO-NPs Using a Convolvulus arvensis Leaf Extract and Proving Its Efficiency as an Inhibitor of Carbon Steel Corrosion Al-Senani GM Materials (Basel) 17-Feb-2020
PMCID:PMC7079658
doi:10.3390/ma13040890
PMID:32079220
Consequences of Opioid Abuse and their Treatments in Persian Medicine: A Review Study Kamali M, Tajadini H, Mehrabani M, Moghadari M Addict Health 01-Jan-2020
PMCID:PMC7291898
doi:10.22122/ahj.v12i1.250
PMID:32582415
Treatment of liver and spleen illnesses by herbs: Recommendations of Avicenna’s heritage "Canon of Medicine" Ghobadi Pour M, Mirazi N, Seif A Avicenna J Phytomed 01-Mar-2019
PMCID:PMC6448543
PMID:30984575
New candidates for treatment and management of carpal tunnel syndrome based on the Persian Canon of Medicine Setayesh M, Zargaran A, Sadeghifar AR, Salehi M, Rezaeizadeh H Integr Med Res 20-Feb-2018
PMCID:PMC6026351
doi:10.1016/j.imr.2018.02.003
PMID:29984174
Resin glycosides from Convolvulaceae plants Ono M J Nat Med 26-Jul-2017
PMCID:PMC6763574
doi:10.1007/s11418-017-1114-5
PMID:28748432
Historical root of precision medicine: an ancient concept concordant with the modern pharmacotherapy Moeini R, Memariani Z, Pasalar P, Gorji N Daru 04-Apr-2017
PMCID:PMC5379719
doi:10.1186/s40199-017-0173-1
PMID:28372571
Review of Medicinal Remedies on Hand Eczema Based on Iranian Traditional Medicine: A Narrative Review Article MANSOURI P, KHADEMI A, PAHLEVAN D, MEMARIANI Z, ALIASL J, SHIRBEIGII L Iran J Public Health 01-Aug-2016
PMCID:PMC5139979
PMID:27928524
Avicenna’s contribution to mechanisms of cardiovascular drugs Javadi B, Emami SA Iran J Basic Med Sci 01-Aug-2015
PMCID:PMC4633453
PMID:26557959
Avicenna's Canon of Medicine: a review of analgesics and anti-inflammatory substances Mahdizadeh S, Khaleghi Ghadiri M, Gorji A Avicenna J Phytomed 01-May-2015
PMCID:PMC4469963
PMID:26101752
Antiplasmodial Activity and Cytotoxicity of Plants Used in Traditional Medicine of Iran for the Treatment of Fever Esmaeili S, Ghiaee A, Naghibi F, Mosaddegh M Iran J Pharm Res 01-Jan-2015
PMCID:PMC4499432
PMID:26185511
Herbal Remedies Connected to Malaria like Fever in Iranian Ancient Medicinal Books- Brief Review Article GHIAEE A, NAGHIBI F, ESMAEILI S, MOSADDEGH M Iran J Parasitol 01-Oct-2014
PMCID:PMC4345095
PMID:25759737

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown via CMAUP database
Betulinic Acid 64971 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
Lupeol 259846 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 / Saccharolipids
(11S)-11-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxyhexadecanoic acid 14704611 Click to see CCCCCC(CCCCCCCCCC(=O)O)OC1C(C(C(C(O1)C)O)O)OC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)C)OC4C(C(C(C(O4)C)O)O)O)O)O 873.00 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[(1S,3R,4S,5S,6R,8S,10R,11S,12S,13R,15R,17S,29R,30S,31S,33R)-30-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(E)-2-methylbut-2-enoyl]oxyoxan-2-yl]oxy-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] (2S)-2-methylbutanoate 162964681 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)CO)OC(=O)C(=CC)C)O)O 1037.20 unknown https://doi.org/10.1016/0031-9422(92)83626-A
[30-[3,4-Dihydroxy-6-(hydroxymethyl)-5-(2-methylbut-2-enoyloxy)oxan-2-yl]oxy-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] 2-methylbutanoate 3083405 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)CO)OC(=O)C(=CC)C)O)O 1037.20 unknown https://doi.org/10.1016/0031-9422(92)83626-A
11-[3-[3-[3,4-Dihydroxy-6-methyl-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxyhexadecanoic acid 14704609 Click to see CCCCCC(CCCCCCCCCC(=O)O)OC1C(C(C(C(O1)C)O)O)OC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)C)OC4C(C(C(C(O4)C)O)O)O)O)O 873.00 unknown https://doi.org/10.1016/0031-9422(91)85287-A
Scammonin viii 6450151 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)CO)OC(=O)C(=CC)C)O)O 1037.20 unknown https://doi.org/10.1016/0031-9422(92)83626-A
> Lipids and lipid-like molecules / Sphingolipids / Ceramides / Phytoceramides
Benjaminamide 56662789 Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(CO)C(C(CCCCCCCC=CCCCCC)O)O)O 682.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(1S,3R,4S,5R,6R,8S,10R,11S,12R,13R,15R,17S,29R,30S,31S,33R)-4,5,11,12-tetraacetyloxy-6-(acetyloxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxy-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] (E)-2-methylbut-2-enoate 163006290 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC5C(C(C(C(O5)C)OC(=O)C)OC(=O)C)OC(=O)C 1273.40 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[(1S,3R,4S,5S,6R,8S,10R,11S,12R,13R,15R,17S,29R,30S,31S,33R)-30-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-methyl-5-[(E)-2-methylbut-2-enoyl]oxyoxan-2-yl]oxy-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] (2S)-2-methylbutanoate 163039359 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1021.20 unknown https://doi.org/10.1016/0031-9422(92)83626-A
[(1S,3R,4S,5S,6R,8S,10R,11S,12S,13R,15R,17S,29R,30S,31S,33R)-30-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-methyl-5-[(E)-2-methylbut-2-enoyl]oxyoxan-2-yl]oxy-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] (2S)-2-methylbutanoate 44593484 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1021.20 unknown https://doi.org/10.1016/0031-9422(90)85277-M
[(1S,3R,4S,5S,6R,8S,10R,11S,12S,13R,15R,17S,29R,30S,31S,33R)-4,5,11,12-Tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] (2S)-2-methylbutanoate 14704606 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)O)O)O 939.10 unknown https://doi.org/10.1016/0031-9422(90)85277-M
[(1S,3R,4S,5S,6R,8S,10R,11S,12S,13R,15R,17S,29R,30S,31S,33R)-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] 2-methylpropanoate 163046580 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)O)O)O 925.10 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-methyl-6-[[(1S,3R,4S,5S,6R,8S,10R,11S,12S,13R,15R,17S,29R,30S,31S,33R)-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-33-(2-methylpropanoyloxy)-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-30-yl]oxy]oxan-3-yl] (E)-2-methylbut-2-enoate 162891946 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1007.20 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-methyl-6-[[(1S,3R,4S,5S,6R,8S,10R,11S,12S,13R,15R,17S,29R,30S,31S,33R)-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-33-[(E)-2-methylbut-2-enoyl]oxy-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-30-yl]oxy]oxan-3-yl] (E)-2-methylbut-2-enoate 162929751 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1019.20 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[30-[3,4-Dihydroxy-6-methyl-5-(2-methylbut-2-enoyloxy)oxan-2-yl]oxy-4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] 2-methylbutanoate 195689 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1021.20 unknown https://doi.org/10.1016/0031-9422(92)83626-A
https://doi.org/10.1016/0031-9422(90)85277-M
[4,5-Dihydroxy-2-methyl-6-[[4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-33-(2-methylbut-2-enoyloxy)-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-30-yl]oxy]oxan-3-yl] 2-methylbut-2-enoate 162929750 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1019.20 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[4,5-Dihydroxy-2-methyl-6-[[4,5,11,12-tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-33-(2-methylpropanoyloxy)-27-oxo-17-pentyl-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-30-yl]oxy]oxan-3-yl] 2-methylbut-2-enoate 162891945 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1007.20 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[4,5,11,12-Tetraacetyloxy-6-(acetyloxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-(3,4,5-triacetyloxy-6-methyloxan-2-yl)oxy-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] 2-methylbut-2-enoate 163006289 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC5C(C(C(C(O5)C)OC(=O)C)OC(=O)C)OC(=O)C 1273.40 unknown https://doi.org/10.1016/0031-9422(91)85287-A
[4,5,11,12-Tetrahydroxy-6-(hydroxymethyl)-13,31-dimethyl-27-oxo-17-pentyl-30-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,7,9,14,16,28,32-heptaoxatetracyclo[27.3.1.03,8.010,15]tritriacontan-33-yl] 2-methylpropanoate 14890556 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)C)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)O)O)O 925.10 unknown https://doi.org/10.1016/0031-9422(91)85287-A
https://doi.org/10.1016/0031-9422(92)83626-A
Scammonin I 6444009 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)OC(=O)C(=CC)C)O)O 1021.20 unknown https://doi.org/10.1016/0031-9422(90)85277-M
https://doi.org/10.1016/0031-9422(92)83626-A
Scammonin II 195688 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(C(C(OC3OC4C(C(C(OC4O1)C)O)O)CO)O)O)C)OC5C(C(C(C(O5)C)O)O)O 939.10 unknown https://doi.org/10.1016/0031-9422(90)85277-M
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydrochromen-2-one 11953803 Click to see COC1=C(C=C2C(=C1)CCC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 356.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database

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