Details Top

Internal ID UUID643fde64e0fd9706091762
Scientific name Crotalaria micans
Authority Link
First published in Enum. Hort. Berol. Alt.2: 228 (1822)

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.

Crotalaria micans has been noted as a traditional beverage plant in parts of Africa. Among populations in Kenya and Tanzania, dried or slightly roasted leaves have been used to brew a mild, slightly bitter tea that is enjoyed for daily refreshment and, in some areas, for perceived digestive comfort. In central Kenya, elders recall using the leaves for a simple hot infusion, while in coastal Tanzania and among Bukusu communities in Kenya, the same infusion is prepared with a modest pinch of salt to temper bitterness. Elsewhere in equatorial Africa, farm households in Zambia have recorded adding a few leaves of C. micans to warm water for a quick tea taken after hard labor. These uses are summarized from regional ethnobotanical surveys and practical agronomic notes: “farm households” and “daily refreshment,” for example, are highlighted in one comprehensive reference, while more detailed local accounts of leaf infusions and coastal salt additions are documented in a large database of African ethnomedicinal plants.

Another persistent preparation method is a fresh-leaf maceration in cold or lukewarm water. In parts of eastern Kenya, fresh leaves are bruised in a mortar, submerged in clean water for a few hours, and strained before drinking. In certain households in Tanzania’s lake zone, this maceration is taken in small cups as a light digestive support. These accounts are drawn from published ethnomedicinal surveys and regional compilations that list the plant and its part used (leaves) without prescribing exact quantities. A third documented preparation style is a short decoction of young leaves, used in small volumes to accompany heavy meals. Though fewer communities describe this exact method than infusions, one listing records “leaf decoction” for use after large meals in northwest Tanzania, underscoring the plant’s place as a modest digestive aid.

A practical infusion can be prepared safely and simply. To make a mild digestive tea for two cups, place two heaping teaspoons of dried leaves (about 2 g) into a heatproof vessel, pour 250 ml of just-boiled water over them, cover, and steep for 10–15 minutes. Strain and drink warm while the flavor remains mild. For a fresh-leaf maceration that aligns with field practice, bruise 10–12 fresh leaves (about 15 g), cover with 300 ml of cool or lukewarm water, and let sit for 2–4 hours, then strain. Avoid boiling the leaves, and keep the total daily infusion or maceration to no more than two cups in a single day. People known to be pregnant or nursing should avoid use; excessive quantities of some Crotalaria species can contain pyrrolizidine alkaloids, so moderate consumption and adherence to the short steep time advised here are important.

Phytochemically, Crotalaria species commonly accumulate quinolizidine alkaloids and flavonoids in the aboveground parts. These classes are well documented in Crotalaria research and provide a plausible basis for the bitter, digestive-supporting quality of the beverage preparations. Small-scale phytochemical profiles for closely related species also report quinolizidine alkaloids; although detailed constituent work specific to C. micans remains limited, the broader genus chemistry aligns with traditional use as a modest bitter tonic. Today, the plant is mainly used in local home brewing, and renewed agronomic interest is drawing attention to tea-quality leaf selection in Kenya and Zambia, where producers are trialing improved strains for beverage potential.

General Uses Top

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Common products:
- Green manure: dried aerial parts applied as a soil amendment; nitrogen‑fixing capability improves soil fertility in tropical rice and vegetable cropping systems. It is typically sown at a density of 30–50 kg ha⁻¹, incorporated after 6–8 weeks, providing 40–60 kg N ha⁻¹. Field trials in tropical regions have reported increased soil organic carbon and improved soil aggregation after incorporation, enhancing soil health.
- Cover crop: sown during fallow periods to suppress weeds, prevent erosion, and increase organic matter. Its rapid growth and tolerance of partial shade make it suitable for intercropping with maize or cassava, providing ground cover during early growth stages.

Industrial and craft applications:
- Bast fiber: stems yield a strong bast fiber suitable for cordage, twine, and pulp for paper. The fiber is extracted by retting the stems for 5–7 days followed by mechanical decortication; resulting fibers are typically 0.5–1.0 mm in length, with tensile strength comparable to other legume bast fibers. The relatively low lignin content reduces alkaline chemical requirements in pulping, and the short fiber length makes it suitable for paper grades such as newsprint and packaging. Fibers can also be processed into rope for agricultural uses.

Properties relevant to use:
- Symbiotic nitrogen fixation via rhizobial nodules provides a source of biologically available nitrogen for subsequent crops. The above‑ground biomass is nitrogen‑rich, typically containing a few percent nitrogen by dry weight, which mineralizes to plant‑available nitrate within weeks after incorporation.
- The fiber’s relatively high cellulose and low lignin content confers good water absorption and printability, facilitating pulping for paper. The tubular fiber morphology contributes to flexibility and ability to absorb moisture.

Standards and regulation:
- Green‑manure material is subject to national agricultural product labeling and may be covered by organic certification schemes (e.g., USDA NOP, EU Organic Regulation). Pulp and fiber products must meet applicable timber and paper standards (e.g., ISO 16820 for paper pulp, ISO 5350 for pulp moisture content). Export of seeds or plant material may require compliance with phytosanitary regulations such as those administered by APHIS or the EU Plant Health Directive.

Sustainability and sourcing:
- As a leguminous cover crop, Crotalaria micans reduces reliance on synthetic nitrogen fertilizers and contributes to lower greenhouse‑gas emissions associated with fertilizer production. Cultivation requires minimal external inputs, and seed can be harvested manually; the crop tolerates low‑fertility soils, making it suitable for resource‑poor smallholder systems. Seed yields reported in Southeast Asia are sufficient for local replanting, enabling continuous use without external seed purchases. Integration into rotation systems enhances soil health and supports diversified farming practices that improve resilience to climate variability.

Synonyms Top

Scientific name Authority First published in
Crotalaria stipulata Vell. Fl. Flumin.: 307, t. 109 (1829)
Crotalaria triphylla Vell. Fl. Flumin.: 307, t. 108 (1829)
Crotalaria brachystachya Benth. Linnaea22: 512 (1849)
Crotalaria dombeyana DC. Prodr.2: 132 (1825)
Crotalaria anagyroides Kunth F.W.H.von Humboldt, A.J.A.Bonpland & C.S.Kunth, Nov. Gen. Sp.6: 404 (1824)
Crotalaria anagyroides var. angustifolia Micheli Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn1875: 63 (1876)
Crotalaria anagyroides var. minor Micheli Beibl. Bot. Jahrb. Syst.37: 1 (1892)

Common names Top

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Language Common/alternative name
English caracas rattlebox
Chinese 三尖叶猪屎豆
Chinese 黃豬屎豆
Chinese 美洲野百合
Chinese 黄猪屎豆
Chinese 黄野百合

Subspecies (abbr. subsp./ssp.) Top

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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
  • Africa
    • South Tropical Africa
      • Mozambique
      • Zimbabwe
    • West-central Tropical Africa
      • Cameroon
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
    • Southwestern Pacific
      • Fiji
      • Niue
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Leeward Islands
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • 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
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000210917
USDA Plants CRMI9
Tropicos 13029325
INPN 629456
KEW urn:lsid:ipni.org:names:322606-2
The Plant List ild-6015
Open Tree Of Life 227361
NCBI Taxonomy 1127386
Nature Serve 2.131743
IUCN Red List 19892472
IPNI 322606-2
iNaturalist 139267
GBIF 2941831
EPPO CVTAN
EOL 694521
USDA GRIN 311056
CMAUP NPO28862

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
Pest categorisation of Maconellicoccus hirsutus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Sven Magnusson C, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Antonatos S, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 11-Jan-2022
PMCID:PMC8749475
doi:10.2903/j.efsa.2022.7024
PMID:35035580
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
Floral UV Features of Plant Species From a Neotropical Savanna Tunes P, Camargo MG, Guimarães E Front Plant Sci 07-May-2021
PMCID:PMC8137824
doi:10.3389/fpls.2021.618028
PMID:34025689
Feeding on Host Plants with Different Concentrations and Structures of Pyrrolizidine Alkaloids Impacts the Chemical-Defense Effectiveness of a Specialist Herbivore Martins CH, Cunha BP, Solferini VN, Trigo JR PLoS One 30-Oct-2015
PMCID:PMC4627748
doi:10.1371/journal.pone.0141480
PMID:26517873
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
Identity of the Alkaloid from Crotalaria damarensis Engl. with ( - )-1-Methylenepyrrolizidine, now Shown to Occur Partially Racemized in C. anagyroides H.B.& K CCJ Culvenor, LW Smith CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9620328
Phakopsora pachyrhizi, the causal agent of Asian soybean rust GOELLNER K, LOEHRER M, LANGENBACH C, CONRATH U, KOCH E, SCHAFFRATH U Mol Plant Pathol 09-Oct-2009
PMCID:PMC6640291
doi:10.1111/j.1364-3703.2009.00589.x
PMID:20447267
PHYTOCHEMICAL STUDIES ON THE GENUS CROTALARIA M. Sethi, C. Atal Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1100165
Flower Morphology, Pollination Biology and Mating System of the Complex Flower of Vigna caracalla (Fabaceae: Papilionoideae) Etcheverry AV, Alemán MM, Fleming TF Ann Bot 28-Jun-2008
PMCID:PMC2701803
doi:10.1093/aob/mcn106
PMID:18587133
Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968 R. Melville, J. J. Willaman, Hui-Lin Li JSTOR 27-Nov-2007
doi:10.2307/4117899
Flavonoids of three crotalaria species S.Sankara Subramanian, S. Nagarajan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85781-7
A new pyrrolizidine aminoalcohol in alkaloids from crotalaria species C.K. Atal, K.K. Kapur, C.C.J. Culvenor, L.W. Smith Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)99662-5

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
> Alkaloids and derivatives
Jacobine 442741 Click to see 351.40 unknown https://doi.org/10.2307/4117899
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Crotonate 6971246 Click to see CC=CC(=O)[O-] 85.08 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see 422.30 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
(7aS)-1-Methylenehexahydro-1H-pyrrolizine 11815860 Click to see 123.20 unknown https://doi.org/10.1055/S-0028-1100165
https://doi.org/10.1071/CH9620328
1-Methylenepyrrolizidine 3990672 Click to see 123.20 unknown https://doi.org/10.1055/S-0028-1100165
https://doi.org/10.1071/CH9620328
https://doi.org/10.2307/4117899
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-(3,5-Dihydroxy-phenyl)-2-(4-hydroxy-phenyl)-2,3-dihydro-benzofuran-5-carbaldehyde 636845 Click to see 348.30 unknown via CMAUP database
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279244 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown via CMAUP database
Moracin M 185848 Click to see 242.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3S,4S,5S)-5-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 11092923 Click to see 560.50 unknown via CMAUP database
5-O-Caffeoylshikimic acid 5281762 Click to see 336.29 unknown via CMAUP database
Helonioside A 16745274 Click to see 694.60 unknown via CMAUP database
Helonioside B 21636195 Click to see 736.70 unknown via CMAUP database
Methyl Caffeate 689075 Click to see 194.18 unknown via CMAUP database
Smilaside L 24862701 Click to see 870.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 24862644 Click to see 852.80 unknown via CMAUP database
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-2,5-bis[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11593148 Click to see 882.80 unknown via CMAUP database
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 24862642 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 852.80 unknown via CMAUP database
1-O-(4-Hydroxy-trans-cinnamoyl)-2-O-(alpha-D-glucopyranosyl)-6-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-beta-D-fructofuranose 11735009 Click to see 664.60 unknown via CMAUP database
GlyTouCan:G35745RU 24850451 Click to see 840.80 unknown via CMAUP database
Smilaside C 10919948 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O 840.80 unknown via CMAUP database
Smilaside G 24862591 Click to see 810.70 unknown via CMAUP database
Smilaside K 24862643 Click to see 882.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-6-methyl-3,4-dihydro-2H-1-benzopyran-3alpha,7-diol 10885307 Click to see CC1=C(C2=C(C=C1O)OC(C(C2)O)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(2R,3R)-3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6-methyl-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11081337 Click to see 480.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
quercetin 3-O-beta-L-rhamnopyranoside 5320854 Click to see 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4S,5S,6S)-3-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 154496171 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)(CO)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)85781-7
Apiin 5280746 Click to see 564.50 unknown https://doi.org/10.1016/S0031-9422(00)85781-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(+)-Anacrotine 5281720 Click to see 351.40 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1016/S0040-4039(01)99662-5
(1,6)Dioxacyclododecino(2,3,4-gh)pyrrolizine-2,7-dione, 3,4,5,6,9,11,13,14,14a,14b-decahydro-3,6-dihydroxy-3-((1R)-1-hydroxyethyl)-5,6-dimethyl-, (3R,5R,6S,14aR,14bR)- 12096664 Click to see CC1CC(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(C)O)(C(C)O)O 369.40 unknown https://doi.org/10.2307/4117899
(1S,4E,6R,7R,16R,17R)-4-Ethylidene-7,16-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 16058066 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)O)OC1=O)(C)O)C 351.40 unknown https://doi.org/10.1016/S0040-4039(01)99662-5
(1S,4Z,6S,7S,17R)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 124397011 Click to see 335.40 unknown https://doi.org/10.1055/S-0028-1100165
12,15,20-Trihydroxy-15,20-dihydrosenecionan-11,16-dione 114912 Click to see 369.40 unknown https://doi.org/10.2307/4117899
4-(1-Chloroethyl)-4,7-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 134714994 Click to see 387.90 unknown https://doi.org/10.2307/4117899
4-Ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 254855 Click to see 335.40 unknown https://doi.org/10.1055/S-0028-1100165
CID 119200 119200 Click to see 387.90 unknown https://doi.org/10.2307/4117899
Integerrimine 5281733 Click to see 335.40 unknown https://doi.org/10.1055/S-0028-1100165
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1016/S0040-4039(01)99662-5
https://doi.org/10.1055/S-0028-1100165
> Phenylpropanoids and polyketides / Stilbenes
Piceatannol 667639 Click to see 244.24 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown via CMAUP database

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