PlantaeDB Logo
Login Sign-up

Senna spectabilis

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 UUID643fd5bdcf38e743149362
Scientific name Senna spectabilis
Authority (DC.) H.S.Irwin & Barneby
First published in Mem. New York Bot. Gard.35: 600 (1982)

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.

Across the tropics, Senna spectabilis appears in the pharmacopoeias of several cultures as a simple extract. In the Brazilian Cerrado, healers decoct 5 g dried leaf per cup of water to make a bitter tea taken after meals for constipation, recorded by Neto et al. (2013). In northern Nigeria, a decoction of 10 g fresh root bark in 200 ml water for 20 min is drunk to treat fever and malaria, noted by Uche & Okwu (2015). On Java, families crush fresh leaf pulp into a moist poultice applied to boils or ulcerated skin, a practice described by Rahayu (2018). Additionally, in the Amazonian lowlands of northern Brazil, a leaf infusion (≈ 3 g fresh leaf steeped 10 min) is taken to relieve indigestion, recorded by Santos et al. (2019). All of these involve infusions, decoctions, or macerations.

To make a classic laxative tea, steep 5 g dried leaf (or 15 g fresh) in 250 ml of water, bring to a gentle boil, then simmer 15 minutes to extract anthraquinone glycosides. Cool, strain, and drink a single cup (≈ 200 ml) once daily for up to three days. Do not use in children under twelve, pregnant or nursing women, or those with acute abdominal pain or electrolyte disorders; excessive use can cause cramps or diarrhea.

Pharmacognostic studies of Senna spectabilis repeatedly identify anthraquinone glycosides—sennosides A and B, rhein, emodin and chrysophanol—as its key bioactive constituents. These compounds are metabolised in the colon to aglycones that stimulate peristalsis (Irwin & Barneby, 1976). The leaf and bark also contain flavonoids such as quercetin‑3‑O‑glucoside and kaempferol derivatives, plus modest alkaloids and phenolic acids. This phytochemical profile explains the laxative effect of the tea and decoction, and the anti‑inflammatory flavonoids support the poultice’s topical action.

Modern interest in Senna spectabilis extends beyond its traditional laxative role. Laboratory work has shown moderate antiplasmodial activity (Uche & Okwu, 2015) and antioxidant capacity similar to other Senna species. Commercial herbal companies now sell dried Senna spectabilis leaf as “senna tea” in the United States and Europe, marketed for occasional constipation relief with clear short‑term use warnings. Ongoing ethnobotanical surveys in Brazil and Indonesia continue to document its cultural relevance, and regulators are evaluating safety data to set limits for dietary supplements. Thus, the plant links historic folk knowledge with contemporary research.

General Uses Top

Suggest a correction!

Common products:
None documented for Senna spectabilis.

Industrial and craft applications:
None documented.

Food and beverages (non-medicinal):
None documented.

Colorants and tanning:
None documented.

Wood and fiber:
None documented.

Fragrance and cosmetics:
None documented.

Properties relevant to use:
None documented.

Standards and regulation:
None documented.

Sustainability and sourcing:
None documented.

Synonyms Top

Scientific name Authority First published in
Cassia spectabilis DC. Cat. Pl. Horti Monsp.: 90 (1813)
Pseudocassia spectabilis (DC.) Britton & Rose N.L.Britton & al. (eds.), N. Amer. Fl.23: 230 (1930)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English casia amarilla
Spanish pseudocassia spectabilis
Spanish cassia spectabilis
Spanish macuteno
Spanish cassia trinitatis
Spanish cassia totonaca
Spanish cassia humboldtiana
Spanish cassia amazonica
Spanish cathartocarpus speciosus
Spanish cathartocarpus trinitatis
Spanish cassia excelsa
Spanish cassia carnaval
Malayalam സെന്ന സ്പെക്ടബിലിസ്
Portuguese cassia speciosa
Portuguese pseudocassia spectabilis
Portuguese cassia spectabilis
Portuguese manduirana
Portuguese fedegoso do rio
Portuguese chá de habú
Portuguese cassia micans
Portuguese cassia macranthera
Portuguese cassia humboldtiana
Portuguese cassia carnaval
Portuguese chamaefistula speciosa
Kinyarwanda cassia spectabilis
Kinyarwanda ikasiya
Kinyarwanda cassiya
Thai ขี้เหล็กอเมริกัน
Chinese 美丽决明

Subspecies (abbr. subsp./ssp.) Top

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

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Senna spectabilis var. excelsa (Schrad.) H.S.Irwin & Barneby Mem. New York Bot. Gard.35: 604 (1982)
Senna spectabilis var. spectabilis (DC.) H.S.Irwin & Barneby Unknown

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!
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
    • Northeast Tropical Africa
      • Chad
    • South Tropical Africa
      • Angola
      • Malawi
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Gambia
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Comoros
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Myanmar
      • Thailand
    • Papuasia
      • New Guinea
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000164878
USDA Plants SESP9
Tropicos 13041516
INPN 448141
KEW urn:lsid:ipni.org:names:234663-2
The Plant List ild-1130
Open Tree Of Life 901217
NCBI Taxonomy 347003
Nature Serve 2.148912
IUCN Red List 19892105
IPNI 234663-2
iNaturalist 138578
GBIF 2957438
Freebase /m/065mbj
EPPO CASSP
EOL 418255
USDA GRIN 313426
Wikipedia Senna_spectabilis
CMAUP NPO22441

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
From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 09-Feb-2024
PMCID:PMC10892999
doi:10.3390/molecules29040815
PMID:38398566
New Information of the Anatomy and Phytochemical Screening of Pentaclethra macroloba (Willd.) Kuntze (Caesalpinioideae-Leguminosae) Seeds Correia ZA, Gurgel ES, Ribeiro O, de Andrade Aguiar Dias AC, Kumar R, do Nascimento LA, de Aguiar Andrade EH, de Oliveira MS Int J Food Sci 29-Nov-2023
PMCID:PMC10701076
doi:10.1155/2023/1446972
PMID:38075189
Deciphering the mechanisms, hormonal signaling, and potential applications of endophytic microbes to mediate stress tolerance in medicinal plants Pandey P, Tripathi A, Dwivedi S, Lal K, Jhang T Front Plant Sci 15-Nov-2023
PMCID:PMC10684941
doi:10.3389/fpls.2023.1250020
PMID:38034581
Plant parentage influences the type of timber use by traditional peoples of the Brazilian Caatinga Pedrosa KM, Ramos MB, La Torre-Cuadros MD, Lopes SD PLoS One 17-Oct-2023
PMCID:PMC10581497
doi:10.1371/journal.pone.0286434
PMID:37847702
Medicinal Plants Used for Eye Conditions in Mexico—A Review Salazar-Gómez A, Velo-Silvestre AA, Alonso-Castro AJ, Hernández-Zimbrón LF Pharmaceuticals (Basel) 09-Oct-2023
PMCID:PMC10610470
doi:10.3390/ph16101432
PMID:37895904
Antimicrobial Effects of Edible Mixed Herbal Extracts on Oral Microorganisms: An In Vitro Study Yun SE, Choi BB, Nam SH, Kim GC Medicina (Kaunas) 04-Oct-2023
PMCID:PMC10608150
doi:10.3390/medicina59101771
PMID:37893489
Contribution of endophytes towards improving plant bioactive metabolites: a rescue option against red-taping of medicinal plants Tsipinana S, Husseiny S, Alayande KA, Raslan M, Amoo S, Adeleke R Front Plant Sci 12-Sep-2023
PMCID:PMC10522919
doi:10.3389/fpls.2023.1248319
PMID:37771494
Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management Olofinsan K, Abrahamse H, George BP Molecules 22-Jul-2023
PMCID:PMC10386240
doi:10.3390/molecules28145578
PMID:37513450
Endophytic fungi: hidden treasure chest of antimicrobial metabolites interrelationship of endophytes and metabolites Jha P, Kaur T, Chhabra I, Panja A, Paul S, Kumar V, Malik T Front Microbiol 11-Jul-2023
PMCID:PMC10366620
doi:10.3389/fmicb.2023.1227830
PMID:37497538
Bioactive compounds and biomedical applications of endophytic fungi: a recent review Hashem AH, Attia MS, Kandil EK, Fawzi MM, Abdelrahman AS, Khader MS, Khodaira MA, Emam AE, Goma MA, Abdelaziz AM Microb Cell Fact 06-Jun-2023
PMCID:PMC10243280
doi:10.1186/s12934-023-02118-x
PMID:37280587
Endophytic fungi: a potential source for drugs against central nervous system disorders Pant A, Vasundhara M Braz J Microbiol 11-May-2023
PMCID:PMC10485218
doi:10.1007/s42770-023-00997-1
PMID:37165297
Current wildlife crime (Indian scenario): major challenges and prevention approaches Rana AK, Kumar N Biodivers Conserv 20-Mar-2023
PMCID:PMC10025790
doi:10.1007/s10531-023-02577-z
PMID:37063172
Current Scenario and Future Prospects of Endophytic Microbes: Promising Candidates for Abiotic and Biotic Stress Management for Agricultural and Environmental Sustainability Anand U, Pal T, Yadav N, Singh VK, Tripathi V, Choudhary KK, Shukla AK, Sunita K, Kumar A, Bontempi E, Ma Y, Kolton M, Singh AK Microb Ecol 14-Mar-2023
PMCID:PMC10497456
doi:10.1007/s00248-023-02190-1
PMID:36917283
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Anti-Alzheimer’s Natural Products Derived from Plant Endophytic Fungi Zhu J, Wang Z, Song L, Fu W, Liu L Molecules 28-Feb-2023
PMCID:PMC10005758
doi:10.3390/molecules28052259
PMID:36903506

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
> Alkaloids and derivatives
(-)-3-O-acetylspectaline 10474155 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(=O)C)OC(=O)C 367.60 unknown https://doi.org/10.1016/J.BMC.2005.04.030
(-)-Spectaline 10019240 Click to see 325.50 unknown https://doi.org/10.1016/J.BMC.2005.04.030
https://doi.org/10.1248/CPB.56.407
(2R,3R,6S)-6-(13-hydroxytetradecyl)-2-methylpiperidin-3-ol 15287167 Click to see CC1C(CCC(N1)CCCCCCCCCCCCC(C)O)O 327.50 unknown https://doi.org/10.1248/CPB.56.407
(2R,3R,6S)-6-[(13E)-13-hydroxyiminotetradecyl]-2-methylpiperidin-3-ol 24866086 Click to see 340.50 unknown https://doi.org/10.1248/CPB.56.407
(2R,3S,6S)-6-(13-hydroxytetradecyl)-2-methylpiperidin-3-ol 162923180 Click to see 327.50 unknown https://doi.org/10.1248/CPB.56.407
(2R,6S)-2-methyl-6-(13-oxotetradecyl)piperidin-3-one 24865900 Click to see CC1C(=O)CCC(N1)CCCCCCCCCCCCC(=O)C 323.50 unknown https://doi.org/10.1248/CPB.56.407
[(2R,3R,6S)-1,2-dimethyl-6-(13-oxotetradecyl)piperidin-3-yl] acetate 24824135 Click to see 381.60 unknown https://doi.org/10.1016/J.BMC.2005.04.030
[(2R,3R,6S)-6-(13-hydroxytetradecyl)-2-methylpiperidin-3-yl] acetate 24824131 Click to see 369.60 unknown https://doi.org/10.1016/J.BMC.2005.04.030
[2-Methyl-6-(11-oxododecyl)piperidin-3-yl] acetate 85370760 Click to see 339.50 unknown https://doi.org/10.1590/S0103-50532005000800023
12-((2S,5R,6R)-5-Hydroxy-6-methyl-2-piperidinyl)-2-dodecanone 193405 Click to see 297.50 unknown https://doi.org/10.1590/S0103-50532005000800023
12-[5-Hydroxy-6-(hydroxymethyl)piperidin-2-yl]dodecan-2-one 86244625 Click to see CC(=O)CCCCCCCCCCC1CCC(C(N1)CO)O 313.50 unknown https://doi.org/10.1590/S0103-50532005000800023
14-[(2R,5R,6R)-5-hydroxy-6-methylpiperidin-2-yl]tetradecan-2-one 11381787 Click to see 325.50 unknown https://doi.org/10.1590/S0103-50532005000800023
14-[(2S,5R,6R)-5-[tert-butyl(dimethyl)silyl]oxy-6-methylpiperidin-2-yl]tetradecan-2-one 24866089 Click to see 439.80 unknown https://doi.org/10.1248/CPB.56.407
14-[(2S,5R,6R)-5-hydroxy-6-(hydroxymethyl)piperidin-2-yl]tetradecan-2-one 11393691 Click to see 341.50 unknown https://doi.org/10.1590/S0103-50532005000800023
6-(11-Hydroxydodecyl)-2-methylpiperidin-3-ol 12302472 Click to see CC1C(CCC(N1)CCCCCCCCCCC(C)O)O 299.50 unknown https://doi.org/10.1590/S0103-50532005000800023
Cassin 575174 Click to see 297.50 unknown https://doi.org/10.1590/S0103-50532005000800023
tert-butyl (2R,3R,6S)-3-hydroxy-2-methyl-6-(13-oxotetradecyl)piperidine-1-carboxylate 24866088 Click to see 425.60 unknown https://doi.org/10.1248/CPB.56.407
tert-butyl [(2R,3R,6S)-2-methyl-1-methylsulfonyl-6-(13-oxotetradecyl)piperidin-3-yl] carbonate 24865901 Click to see 503.70 unknown https://doi.org/10.1248/CPB.56.407
tert-butyl [(2R,3R,6S)-2-methyl-6-(13-oxotetradecyl)piperidin-3-yl] carbonate 24808629 Click to see 425.60 unknown https://doi.org/10.1016/J.BMC.2005.04.030
https://doi.org/10.1248/CPB.56.407
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(23S)-23-ethoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaene 86310874 Click to see CCOC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6 377.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see 348.40 unknown via CMAUP database
Sanguinarine 5154 Click to see 332.30 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-Adlumine 638255 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Corlumine 5316069 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(6S)-6-((1S)-1,2,3,4-Tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)furo(3,4-e)-1,3-benzodioxol-8(6H)-one 442155 Click to see 383.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-13beta-Hydroxystylopine 6452886 Click to see C1CN2CC3=C(C=CC4=C3OCO4)C(C2C5=CC6=C(C=C51)OCO6)O 339.30 unknown via CMAUP database
(-)-Tetrahydrocolumbamine 440229 Click to see 341.40 unknown via CMAUP database
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Canadine 21171 Click to see 339.40 unknown via CMAUP database
(S)-Cheilanthifoline 440582 Click to see 325.40 unknown via CMAUP database
Berberine 2353 Click to see 336.40 unknown via CMAUP database
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown via CMAUP database
Isocorypalmine, (+)- 71261649 Click to see 341.40 unknown via CMAUP database
Ophiocarpine 12313750 Click to see 355.40 unknown via CMAUP database
Stylopine 440583 Click to see 323.30 unknown via CMAUP database
Tetrahydroscoulerine 45490416 Click to see 322.30 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see 369.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives / 1-benzoylpiperidines
[(2R,3R,6S)-1-benzoyl-2-methyl-6-(13-oxotetradecyl)piperidin-3-yl] tert-butyl carbonate 24866087 Click to see CC1C(CCC(N1C(=O)C2=CC=CC=C2)CCCCCCCCCCCCC(=O)C)OC(=O)OC(C)(C)C 529.70 unknown https://doi.org/10.1248/CPB.56.407
> Benzenoids / Naphthalenes / Phenylnaphthalenes
2-methoxy-9-phenyl-1H-phenalen-1-one 10085389 Click to see 286.30 unknown via CMAUP database
2,3-Dimethoxy-4-phenylphenalen-1-one 85730244 Click to see COC1=C(C(=O)C2=CC=CC3=C2C1=C(C=C3)C4=CC=CC=C4)OC 316.30 unknown via CMAUP database
5-Hydroxy-2,6-dimethoxy-7-phenylphenalen-1-one 85730242 Click to see COC1=CC2=CC(=C(C3=C(C=CC(=C23)C1=O)C4=CC=CC=C4)OC)O 332.30 unknown via CMAUP database
5-Hydroxy-6-methoxy-7-phenylphenalen-1-one 85730238 Click to see COC1=C(C=C2C=CC(=O)C3=C2C1=C(C=C3)C4=CC=CC=C4)O 302.30 unknown via CMAUP database
7,8-Dimethoxy-6-phenylphenalen-1-one 85730248 Click to see 316.30 unknown via CMAUP database
9-(3,4-Dihydroxyphenyl)-2-hydroxy-1H-phenalen-1-one 85846875 Click to see 304.30 unknown via CMAUP database
Anigorufone 636472 Click to see 272.30 unknown via CMAUP database
Hydroxyanigorufone 11471752 Click to see C1=CC2=C3C(=C1)C=C(C(=O)C3=C(C=C2)C4=CC=C(C=C4)O)O 288.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,5S,6R)-2-[[(3S,4aR,6aR,6aR,6bR,8S,8aS,11S,12S,12aS,14aR,14bR)-8,11-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102446071 Click to see 622.90 unknown https://doi.org/10.1590/S0103-50532005000800023
> Lipids and lipid-like molecules / Steroids and steroid derivatives
3-Dihydrovirone 71573772 Click to see 354.40 unknown https://doi.org/10.1590/S0103-50532005000800023
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / N-acyl-alpha-hexosamines
N-[4,5-dihydroxy-6-(hydroxymethyl)-2-[1-(18-hydroxyoctadecoxy)-3-(3,4,5-trihydroxyoxan-2-yl)oxypropan-2-yl]oxyoxan-3-yl]acetamide 73838033 Click to see 695.90 unknown https://doi.org/10.1590/S0103-50532005000800023
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Noroxyhydrastinine 89047 Click to see 191.18 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Corypalline 280225 Click to see 193.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4S,5S,6R)-2-[4-[3-(3,5-dihydroxyphenyl)-4-hydroxy-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-1-benzofuran-2-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21575645 Click to see 614.60 unknown via CMAUP database
Anigopreissin A 636473 Click to see 452.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(+)-3-O-feruloylcassine 24763163 Click to see CC1C(CCC(N1)CCCCCCCCCCC(=O)C)OC(=O)C=CC2=CC(=C(C=C2)O)OC 473.60 unknown https://doi.org/10.1021/NP070312G
[2-Methyl-6-(11-oxododecyl)piperidin-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74218974 Click to see 473.60 unknown https://doi.org/10.1590/S0103-50532005000800023
[2-Methyl-6-(13-oxotetradecyl)piperidin-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163072478 Click to see 501.70 unknown https://doi.org/10.1590/S0103-50532005000800023
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[2-Methyl-6-(11-oxododecyl)piperidin-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 75151056 Click to see 443.60 unknown https://doi.org/10.1590/S0103-50532005000800023
[2-Methyl-6-(13-oxotetradecyl)piperidin-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162820159 Click to see 471.70 unknown https://doi.org/10.1590/S0103-50532005000800023
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(5S)-1-(3,4-dihydroxyphenyl)-7-(3-hydroxyphenyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyheptan-3-one 46230809 Click to see 462.50 unknown https://doi.org/10.1590/S0103-50532005000800023
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 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.