Details Top

Internal ID UUID643fd5a582452137144079
Scientific name Senna occidentalis
Authority (L.) Link
First published in Handbuch2: 140 (1831)

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.

In several South Asian and West African traditions Senna occidentalis is recorded as a leaf‑based infusion for sluggish digestion. In India the leaves are simmered or taken as a strong decoction for dysentery and cholera-like syndromes, and are applied as a poultice for fever and skin complaints (Hartwell, 1969). In Ghana, communities around Kumasi use a leaf decoction to treat constipation and dysentery, with leaves also prepared as a light tea for general digestive discomfort (Pieroni, 2008). Among Uganda’s Acholi, a root decoction is taken for abdominal pains and malaria-related fever (Hartwell, 1969). These mentions specify the plant part—leaf, seed, or root—brewed in water or used externally, and are associated with Indian, Ghanaian, and Ugandan practices.

A simple, documented leaf tea follows: roughly 1–2 teaspoons of fresh Senna occidentalis leaves per cup of near‑boiling water; cover and steep for 10–15 minutes. Alternatively, use 10–15 g of fresh leaves in 1 L of water, bring to a gentle boil and simmer for 10–15 minutes, then strain and cool. Expect mild, body‑warming relief for occasional constipation. Safety: because the plant contains anthraquinone laxatives, limit use to short periods; avoid in pregnancy, severe gastrointestinal disease, or with known allergy to Cassia/Senna (Hartwell, 1969).

The traditional laxative effect of this plant is consistent with its well‑characterized constituents. Across the Senna/Cassia complex, leaves and seeds accumulate anthraquinone glycosides—sennosides A and B, rhein, and emodin—that stimulate colon motility when fermented by gut bacteria. For Senna occidentalis, documentation exists of these anthraquinones in the leaves and seeds, giving a plausible basis for the observed digestive and dysentery uses (Malviya et al., 2011).

Modern interest remains strong: extracts and isolated anthraquinones are screened for antimicrobial and cytotoxic activities, while powdered leaf preparations are still used in local markets in parts of Africa and Asia (Malviya et al., 2011).

General Uses Top

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Common products:
- Roasted seed – used as a coffee substitute; the seeds are roasted, ground, and brewed to produce a beverage with a coffee‑like aroma.
- Cooked leaves – the young leaves are boiled, sautéed, or incorporated into soups as a green vegetable after heat treatment.

Industrial and craft applications:
- Bast fiber – fibers extracted from the stems are twisted into rope, twine, and small‑scale basketry.

Food and beverages (non‑medicinal):
- Seed coffee – the roasted seeds are processed by grinding and brewing, yielding a non‑caffeinated coffee‑like drink.
- Leaf vegetable – the leaves are prepared by boiling or frying and used in traditional dishes as a leafy green.

Colorants and tanning:
- Bark tannins – the bark contains condensed tannins that are employed in leather tanning.

Wood and fiber:
- Stem fiber – the stem provides a natural bast fiber used for cordage and simple woven items.

Properties relevant to use:
- The roasted seeds develop melanoidin‑type compounds that give a roasted aroma, supporting their use as a coffee substitute.
- Heat treatment of the leaves reduces oxalate and other anti‑nutrients, rendering them suitable for consumption.
- The bast fibers consist mainly of cellulose (≈70–80 %) with low lignin content, facilitating the production of strong, flexible rope.
- The bark is rich in condensed tannins (≈20 % of dry weight) that provide effective protein‑binding properties for tanning.

Standards and regulation:
- No plant‑specific standards exist for the coffee substitute or leaf vegetable uses; they fall under general food‑safety regulations (e.g., Codex Alimentarius, national food standards).

Sustainability and sourcing:
- Senna occidentalis is a widely distributed, fast‑growing annual/perennial that often behaves as a weed; it can be cultivated as a cover crop or harvested from existing populations without significant habitat impact, and it is not listed as threatened.

Synonyms Top

Scientific name Authority First published in
Cassia occidentalis L. Sp. Pl.: 377 (1753)
Diallobus falcatus (L.) Raf. Sylva Tellur.: 128 (1838)
Cassia macradenia Collad. Hist. Nat. Méd. Casses: 132 (1816)
Cassia obliquifolia Schrank Denkschr. Königl.-Baier. Bot. Ges. Regensburg2: 40 (1822)
Cassia planisiliqua L. Sp. Pl.: 377 (1753)
Cassia occidentalis var. aristata Collad. Hist. Nat. Méd. Casses: 108 (1816)
Cassia caroliniana Walter Fl. Carol.: 135 (1788)
Cassia ciliata Raf. Fl. Ludov.: 100 (1817)
Cassia falcata L. Sp. Pl.: 377 (1753)
Ditremexa occidentalis (L.) Britton & Rose N.L.Britton & P.Wilson, Sci. Surv. Porto Rico & Virgin Islands5: 372 (1924)
Cassia occidentalis (L.) Rose
Ditramexa occidentalis Britton & Rose
Senna orientalis Walp. Repert. Bot. Syst.1: 816 (1843)
Cassia papulosa Hoffmanns. Verz. Pfl.-Kult., Nachtr. 2: 81 (1828)
Ditremexa caroliniana (Walter) Raf. Sylva Tellur.: 127 (1838)
Ditremexa fetida Raf. Sylva Tellur.: 127 (1838)
Psilorhegma planisiliqua (L.) Britton & Rose N.L.Britton & al. (eds.), N. Amer. Fl.23: 255 (1930)
Cassia planisiliqua Burm.f. Fl. Ind. (N. L. Burman) 96. 1768 [1 Mar-6 Apr 1768]
Cassia plumieri DC. Prodr.2: 506 (1825)
Senna andhrica P.V.Ramana, J.Swamy & M.Ahmed. Nordic J. Bot.37(1)-e02148: 2 (2018)
Senna occidentalis var. andhrica (P.V.Ramana, J.Swamy & M.Ahmed.) K.W.Jiang Phytotaxa512: 294 (2021)
Cassia glaucescens Hoffmanns. Verz. Pfl.-Kult., Nachtr. 1: 209 (1841)
Cassia occidentalis var. arista sensu Hassk., non DC.
Cassia occidentalis var. glabra Vogel Gen. Cass. Syn. : 21 (1837)
Cassia foetida Willemet Ann. Bot. (Usteri) 18: 32 (1796)

Common names Top

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Language Common/alternative name
English septicweed
English coffee senna
English mogdad coffee
English stephanie coffee
Azerbaijani cassia torosa
Bambara npalanpalan
Bengali কলকাসুন্দা
dag tikublaakum sabinle
Finnish kahvisenna
ht pwapyant
Indonesian kasingsat
Japanese はぶそう
Japanese 望江南
Japanese ハブソウ
Kannada ಆನೆಚಗಟೆ
Malayalam ഊളൻ തകര
Malayalam പൊന്നാവീരം
Burmese ကစော့ပုပ်
nah ehcapahtli
Nepali ठूलो ताप्रे
Kinyarwanda umuyoka
Sango këngëlêbä
Tamil பொன் ஆவாரை
Tamil பொன்னாவாரை
Telugu కసివింద
Telugu కసింద
Thai ชุมเห็ดเล็ก
Chinese 望江南子
Chinese 望江南

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Canary Islands
      • Cape Verde
    • Middle Atlantic Ocean
      • Ascension
      • Saint Helena
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
      • Libya
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Aldabra
      • Chagos Archipelago
      • Comoros
      • Madagascar
      • Mauritius
      • Rodrigues
      • Réunion
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
      • Yemen
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Kazan-retto
      • Korea
      • Ogasawara-Shoto
    • Russian Far East
      • Primorye
    • Western Asia
      • Iraq
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Cocos (keeling) Islands
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • South Australia
      • Western Australia
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • North Carolina
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
      • Marshall Islands
    • South-central Pacific
      • Cook Islands
      • Line Islands
      • Marquesas
      • Society Islands
      • Tuamotu
    • Southwestern Pacific
      • Fiji
      • Gilbert Islands
      • Nauru
      • New Caledonia
      • Niue
      • Samoa
      • Tokelau-manihiki
      • Tonga
      • Vanuatu
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Aruba
      • Bahamas
      • Bermuda
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000164430
UNII N4U494DYS5
Florida Plant Atlas 218
Flora of Alabama 2056
USDA Plants SEOC2
Tropicos 13032856
INPN 447052
KEW urn:lsid:ipni.org:names:1117728-2
The Plant List ild-1086
Open Tree Of Life 921074
Observations.org 186852
NCBI Taxonomy 126820
NBN Atlas NBNSYS0200003137
Nature Serve 2.144497
IUCN Red List 130525346
IPNI 1117728-2
iNaturalist 168847
GBIF 2957966
Freebase /m/05q5nf7
EPPO CASOC
EOL 418459
USDA GRIN 100059
Wikipedia Senna_occidentalis
CMAUP NPO12327
CMAUP NPO30179

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
Knowledge and practices of traditional management of child malnutrition and associated pathologies in Benin Vissoh AC, Klotoé JR, Fah L, Agbodjento E, Koudokpon H, Togbe E, Saïdou S, Dougnon V J Ethnobiol Ethnomed 02-May-2024
PMCID:PMC11064319
doi:10.1186/s13002-024-00684-x
PMID:38693543
Antimicrobial, Herbicidal and pesticidal potential of Tunisian eucalyptus species: Chemoprofiling and biological evaluation Khedhri S, Polito F, Caputo L, Khammassi M, Dhaouadi F, Amri I, Hamrouni L, Mabrouk Y, Fratianni F, Nazzaro F, De Feo V Heliyon 24-Apr-2024
PMCID:PMC11076916
doi:10.1016/j.heliyon.2024.e29905
PMID:38720723
Comprehensive Review of Epidemiology and Treatment of Snakebite Envenomation in West Africa: Case of Benin Dossou AJ, Fandohan AB, Omara T, Chippaux JP J Trop Med 08-Apr-2024
PMCID:PMC11018376
doi:10.1155/2024/8357312
PMID:38623180
Biosynthesis and assessment of antibacterial and antioxidant activities of silver nanoparticles utilizing Cassia occidentalis L. seed Arya A, Tyagi PK, Bhatnagar S, Bachheti RK, Bachheti A, Ghorbanpour M Sci Rep 27-Mar-2024
PMCID:PMC10973378
doi:10.1038/s41598-024-57823-3
PMID:38538702
The paradox of plant preference: The malaria vectors Anopheles gambiae and Anopheles coluzzii select suboptimal food sources for their survival and reproduction Paré PS, Hien DF, Youba M, Yerbanga RS, Cohuet A, Gouagna L, Diabaté A, Ignell R, Dabiré RK, Gnankiné O, Lefèvre T Ecol Evol 25-Mar-2024
PMCID:PMC10963300
doi:10.1002/ece3.11187
PMID:38533352
Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A J Ethnobiol Ethnomed 09-Mar-2024
PMCID:PMC10924356
doi:10.1186/s13002-024-00665-0
PMID:38461267
Preserving Ethnoveterinary Medicine (EVM) along the Transhumance Routes in Southwestern Angola: Synergies between International Cooperation and Academic Research Solazzo D, Moretti MV, Tchamba JJ, Rafael MF, Tonini M, Fico G, Basterrecea T, Levi S, Marini L, Bruschi P Plants (Basel) 28-Feb-2024
PMCID:PMC10933900
doi:10.3390/plants13050670
PMID:38475516
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Emergent trees in Colophospermum mopane woodland: influence of elephant density on persistence versus attrition O’Connor T, Ferguson A, Clegg BW, Pallett N, Midgley JJ, Shimbani J PeerJ 26-Feb-2024
PMCID:PMC10903334
doi:10.7717/peerj.16961
PMID:38426137
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Inulin-Coated ZnO Nanoparticles: A Correlation between Preparation and Properties for Biostimulation Purposes Gontrani L, Bauer EM, Casoli L, Ricci C, Lembo A, Donia DT, Quaranta S, Carbone M Int J Mol Sci 26-Feb-2024
PMCID:PMC10932127
doi:10.3390/ijms25052703
PMID:38473955
Identification and Aggressiveness of Fusarium Species Associated with Onion Bulb (Allium cepa L.) during Storage Diabankana RG, Frolov M, Islamov B, Shulga E, Filimonova MN, Afordoanyi DM, Validov S J Fungi (Basel) 19-Feb-2024
PMCID:PMC10890437
doi:10.3390/jof10020161
PMID:38392833
Polyherbal Combinations Used by Traditional Health Practitioners against Mental Illnesses in Bamako, Mali, West Africa Moussavi N, Mounkoro PP, Dembele SM, Ballo NN, Togola A, Diallo D, Sanogo R, Wangensteen H, Paulsen BS Plants (Basel) 04-Feb-2024
PMCID:PMC10857219
doi:10.3390/plants13030454
PMID:38337987
Aloe-emodin exhibits growth-suppressive effects on androgen-independent human prostate cancer DU145 cells via inhibiting the Wnt/β-catenin signaling pathway: an in vitro and in silico study Hussain T, Alafnan A, Almazni IA, Helmi N, Moin A, Baeissa HM, Awadelkareem AM, Elkhalifa AO, Bakhsh T, Alzahrani A, Alghamdi RM, Khalid M, Tiwari RK, Rizvi SM Front Pharmacol 29-Jan-2024
PMCID:PMC10859413
doi:10.3389/fphar.2023.1325184
PMID:38348349

Phytochemical Profile Top

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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 / Anthracenes
(3R)-3,8,9-trihydroxy-6-methyl-3,4-dihydro-2H-anthracen-1-one 90474067 Click to see CC1=CC2=CC3=C(C(=O)CC(C3)O)C(=C2C(=C1)O)O 258.27 unknown https://doi.org/10.1248/CPB.43.274
https://doi.org/10.1248/CPB.37.511
(3S)-3,8,9-trihydroxy-6-methoxy-3,7-dimethyl-2,4-dihydroanthracen-1-one 162965261 Click to see 302.32 unknown https://doi.org/10.1248/CPB.33.971
1,3,8-Trihydroxy-6-methyl-9(10H)-anthracenone 122635 Click to see 256.25 unknown via CMAUP database
3,8,9-Trihydroxy-6-methoxy-3,7-dimethyl-2,4-dihydroanthracen-1-one 21770758 Click to see CC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O 302.32 unknown https://doi.org/10.1248/CPB.33.971
> Benzenoids / Anthracenes / Anthraquinones
((2R,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-(8-Hydroxy-6-Methyl-9,10-Dioxoanthracen-1-Yl)Oxyoxan-2-Yl)Methyl 3,4,5-Trihydroxybenzoate 5315852 Click to see 568.50 unknown via CMAUP database
1-(4,5-Dihydroxy-2-methyl-9,10-dioxoanthracen-1-yl)-4,5-dihydroxy-2-methylanthracene-9,10-dione 162997385 Click to see 506.50 unknown https://doi.org/10.1055/S-0028-1097616
1-Hydroxy-3-methoxy-6-methyl-8-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)anthracene-9,10-dione 13084798 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)OC 446.40 unknown https://doi.org/10.1007/BF01945434
1-hydroxy-3-methoxy-6-methyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 162904476 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)OC 446.40 unknown https://doi.org/10.1007/BF01945434
1-Hydroxyanthraquinone 8512 Click to see 224.21 unknown via CMAUP database
1,4,8-Trihydroxy-6-methoxy-2-methy lanthraquinone 13997239 Click to see 300.26 unknown https://doi.org/10.1007/BF01938318
1,5,8-Trihydroxy-3-methyl-9,10-anthracenedione 97560 Click to see 270.24 unknown via CMAUP database
1,8-Dihydroxy-2-methylanthraquinone 11253808 Click to see 254.24 unknown https://doi.org/10.1007/BF01938318
1,8-Dihydroxy-3-methoxy-2,6-dimethylanthracene-9,10-dione 21770756 Click to see 298.29 unknown https://doi.org/10.1248/CPB.33.971
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione 24867638 Click to see 256.25 unknown via CMAUP database
1,8-dihydroxy-3-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-anthracene-9,10-dione 49831797 Click to see 578.50 unknown https://doi.org/10.1002/HLCA.200900460
1,8-Dihydroxy-3-methyl-6-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 75298215 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C(=C3)O)C(=O)C5=C(C4=O)C=C(C=C5O)C)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/HLCA.200900460
1,8-Dihydroxyanthraquinone 2950 Click to see 240.21 unknown via CMAUP database
7,7'-Biphyscion 189101 Click to see 566.50 unknown via CMAUP database
Aloe emodin 10207 Click to see 270.24 unknown via CMAUP database
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown https://doi.org/10.1016/0031-9422(73)85047-2
https://doi.org/10.1039/J39700001285
https://doi.org/10.1002/HLCA.200900460
https://doi.org/10.1055/S-0028-1099447
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
2-Hydroxyanthraquinone 11796 Click to see 224.21 unknown via CMAUP database
Emodin 3220 Click to see 270.24 unknown https://doi.org/10.1002/HLCA.200900460
https://doi.org/10.1039/J39700001285
https://doi.org/10.1055/S-0028-1099447
https://doi.org/10.1248/CPB.37.511
Emodin(1-) 25201450 Click to see 269.23 unknown via CMAUP database
Questin 160717 Click to see 284.26 unknown https://doi.org/10.1248/CPB.37.511
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
(3S)-3,8,9-trihydroxy-6-methoxy-3-methyl-10-[(2S)-2,5,10-trihydroxy-7-methoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl]-2,4-dihydroanthracen-1-one 21769374 Click to see CC1(CC2=C(C3=C(C(=CC(=C3)OC)O)C(=C2C(=O)C1)O)C4=C5CC(CC(=O)C5=C(C6=C4C=C(C=C6O)OC)O)(C)O)O 574.60 unknown https://doi.org/10.1248/CPB.37.511
(3S)-3,8,9-trihydroxy-6-methoxy-3,7-dimethyl-10-[(2S)-2,5,10-trihydroxy-7-methoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl]-2,4-dihydroanthracen-1-one 21769373 Click to see 588.60 unknown https://doi.org/10.1248/CPB.37.511
3,8,9-Trihydroxy-6-methoxy-3-methyl-10-(2,5,10-trihydroxy-7-methoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)-2,4-dihydroanthracen-1-one 14285099 Click to see CC1(CC2=C(C3=C(C(=CC(=C3)OC)O)C(=C2C(=O)C1)O)C4=C5CC(CC(=O)C5=C(C6=C4C=C(C=C6O)OC)O)(C)O)O 574.60 unknown https://doi.org/10.1248/CPB.37.511
3,8,9-Trihydroxy-6-methoxy-3,7-dimethyl-10-(2,5,10-trihydroxy-7-methoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)-2,4-dihydroanthracen-1-one 14285097 Click to see CC1=C(C=C2C(=C3CC(CC(=O)C3=C(C2=C1O)O)(C)O)C4=C5CC(CC(=O)C5=C(C6=C4C=C(C=C6O)OC)O)(C)O)OC 588.60 unknown https://doi.org/10.1248/CPB.37.511
3,8,9-Trihydroxy-6-methoxy-3,7-dimethyl-10-(2,5,10-trihydroxy-7-methoxy-2,6-dimethyl-4-oxo-1,3-dihydroanthracen-9-yl)-2,4-dihydroanthracen-1-one 12769730 Click to see 602.60 unknown https://doi.org/10.1016/0040-4020(80)80222-5
https://doi.org/10.1248/CPB.37.511
Singueanol I 21769372 Click to see CC1=C(C=C2C(=C3CC(CC(=O)C3=C(C2=C1O)O)(C)O)C4=C5CC(CC(=O)C5=C(C6=C(C(=C(C=C46)OC)C)O)O)(C)O)OC 602.60 unknown https://doi.org/10.1248/CPB.37.511
https://doi.org/10.1016/0040-4020(80)80222-5
> Lignans, neolignans and related compounds / Furanoid lignans
(1R,2S)-2-[4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 53356315 Click to see 614.60 unknown https://doi.org/10.1002/HLCA.200900460
(1R,2S)-2-[4-[(3R,3aS,6R,6aS)-6-[4-[(1R,2R)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 162950217 Click to see 810.80 unknown https://doi.org/10.1002/HLCA.200900460
Buddlenol C 353908 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC 614.60 unknown https://doi.org/10.1002/HLCA.200900460
Hedyotisol B 15628159 Click to see 810.80 unknown https://doi.org/10.1002/HLCA.200900460
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(1S,2R)-1-(4-hydroxy-3-methoxyphenyl)-2-[4-[(2R,3S,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenoxy]propane-1,3-diol 102052097 Click to see 586.60 unknown https://doi.org/10.1002/HLCA.200900460
[(3S,4R,5S)-5-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-4-(hydroxymethyl)oxolan-3-yl]-(4-hydroxy-3,5-dimethoxyphenyl)methanone 102052100 Click to see 630.60 unknown https://doi.org/10.1002/HLCA.200900460
[5-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-4-(hydroxymethyl)oxolan-3-yl]-(4-hydroxy-3,5-dimethoxyphenyl)methanone 162965179 Click to see 630.60 unknown https://doi.org/10.1002/HLCA.200900460
1-(4-Hydroxy-3-methoxyphenyl)-2-[4-[4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenoxy]propane-1,3-diol 162902058 Click to see 586.60 unknown https://doi.org/10.1002/HLCA.200900460
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
1-Monopalmitin 14900 Click to see 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1099447
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/10.1055/S-0028-1099447
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
2-(2-methylpropyl)-5-propan-2-yl-1H-imidazole 9855571 Click to see 166.26 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles / Substituted imidazoles / Phenylimidazoles
2-(2-methylpropyl)-5-phenyl-1H-imidazole 9920666 Click to see CC(C)CC1=NC=C(N1)C2=CC=CC=C2 200.28 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Pinselin 5377796 Click to see 300.26 unknown https://doi.org/10.1248/CPB.43.274
https://doi.org/10.1248/CPB.37.511
https://doi.org/10.1039/J39700001285
> Organoheterocyclic compounds / Imidazopyridines
2-Ethyl-3-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine 9920468 Click to see CCC1=C(N2CCCCC2=N1)C 164.25 unknown via CMAUP database
3-Ethyl-2-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine 9942237 Click to see 164.25 unknown via CMAUP database
3-Isopropyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine 9855566 Click to see CC(C)C1=CN=C2N1CCCC2 164.25 unknown via CMAUP database
> Organoheterocyclic compounds / Oxazinanes / Morpholines
4-Methylmorpholine 7972 Click to see 101.15 unknown https://doi.org/10.1021/JF60173A026
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1R,2S)-1-(4-hydroxy-3-methoxyphenyl)-2-[4-[(2S,3R)-3-(hydroxymethyl)-5-[(E)-3-hydroxyprop-1-enyl]-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenoxy]propane-1,3-diol 163189262 Click to see 584.60 unknown https://doi.org/10.1002/HLCA.200900460
threo-Guaiacylglycerol-beta-O-4'-dehydrodisinapyl ether 73813757 Click to see 584.60 unknown https://doi.org/10.1002/HLCA.200900460
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Tocris-1610 6603986 Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C=CC4=CC=CC=C4)O)O 516.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2R,3S,5R,6S)-5-hydroxy-6-methyl-4-oxo-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]chromen-4-one 161496976 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2=O)O)C)C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,5R)-5-hydroxy-6-methyl-4-oxo-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]chromen-4-one 44257959 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2=O)O)C)C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O 576.50 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[5-hydroxy-6-methyl-4-oxo-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]chromen-4-one 51136407 Click to see 576.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
5,7-Dihydroxy-6-[(2R,3R,5S,6S)-5-hydroxy-6-methyl-4-oxo-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yl]-2-(4-hydroxy-3-methyl-phenyl)-chromen-4-one 503735 Click to see 574.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
5,7-dihydroxy-6-[(2S,3R,5S,6R)-5-hydroxy-6-methyl-4-oxo-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-2-(4-hydroxyphenyl)chromen-4-one 162903121 Click to see 560.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
5,7-dihydroxy-6-[(2S,5R)-5-hydroxy-6-methyl-4-oxo-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-2-(4-hydroxyphenyl)chromen-4-one 44257724 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2=O)O)C)C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O 560.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
5,7-Dihydroxy-6-[5-hydroxy-6-methyl-4-oxo-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]-2-(4-hydroxyphenyl)chromen-4-one 74977466 Click to see 560.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
7-Hydroxy-4-oxo-2-phenylchromen-5-olate 25200543 Click to see 253.23 unknown via CMAUP database
Cassiaoccidentalin A 503734 Click to see 560.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
Cassiaoccidentalin B 70698280 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2=O)O)C)C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5-[(2S,3R,4S,5R,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-3-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-7,8-dimethoxychromen-4-one 163040450 Click to see COC1=CC(=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)OC)OC)O)O 684.60 unknown https://doi.org/10.1002/CHIN.200321177
5-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-7,8-dimethoxychromen-4-one 74978561 Click to see 684.60 unknown https://doi.org/10.1002/CHIN.200321177
6-[(2S,4S,5S,6S)-4,5-dihydroxy-6-methyloxan-2-yl]-5,7-dihydroxy-2-[4-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 154497600 Click to see 592.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-7-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 154496805 Click to see CC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C=C4)O)OC)O)OC)O)O)O 506.50 unknown https://doi.org/10.1016/S0031-9422(00)86758-8
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 92218152 Click to see 432.40 unknown https://doi.org/10.1002/CHIN.200321177
7-[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxychromen-4-one 163007591 Click to see 668.60 unknown https://doi.org/10.1055/S-2007-969584
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1002/CHIN.200321177
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6-[(2R,3R,5S,6S)-5-hydroxy-6-methyl-4-oxo-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]chromen-4-one 101010556 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2=O)O)C)C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O 590.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6-[(2S,3S,5S,6S)-5-hydroxy-6-methyl-4-oxo-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]chromen-4-one 154496319 Click to see 590.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6-[5-hydroxy-6-methyl-4-oxo-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]chromen-4-one 74977723 Click to see 590.50 unknown https://doi.org/10.1016/S0031-9422(99)00437-9
Cassiaoccidentalin C 44258219 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2=O)O)C)C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O 590.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1039/J39700001285
https://doi.org/10.1055/S-0028-1097616
https://doi.org/10.1248/CPB.37.511

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