Strychnos henningsii

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Internal ID UUID644004eaa6a2b269006809
Scientific name Strychnos henningsii
Authority Gilg
First published in Bot. Jahrb. Syst. 15: 569 (1893)

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.

Ethnobotanical Uses

In southern and eastern Africa, practitioners have long prepared Strychnos henningsii as a bitter, stimulant decoction from the root bark. Von Koenen’s Medicinal and Poisonous Plants of Southern and Eastern Africa records the Zulu and Xhosa of South Africa, the Venda and Shona of Zimbabwe, and the Nguni and Tsonga of Mozambique preparing a decoction for malaria fevers and associated digestive complaints, describing it as a strong tonic for debility and loss of appetite. Studies of South African herbal practice by Van Wyk and Van Oudtshoorn and the Africa Centre for Biodiversity and Traditional Knowledge confirm the same bark decoction for fever and indigestion, noting its bitter reputation. The Southern African Commercial Crops, Herbs and Aromatics (SACCHA) report further documents the root bark as a traditional remedy for fever and digestive upset, with the bitter principle used to stimulate digestion, and confirms concurrent medicinal use of the leaves and seed kernel (macere) in localized communities.

The bark’s bitter activity is well supported by modern analyses: whereas seeds and the macere are high in strychnine and related indole alkaloids, the bark contains a distinct alkaloidal profile dominated by bisindole alkaloids such as diaboline together with iridoid glycosides such as loganin and loganic acid, alongside phenolics and triterpenoids that contribute bitter flavor and irritant toxicity (Bello et al., African Journal of Traditional, Complementary and Alternative Medicines). Contemporary pharmacology links S. henningsii bark extracts to analgesic and antimalarial effects in laboratory studies, though the same chemistry underscores caution when using decoctions due to low‑dose neurotoxicity (Ojewole, Journal of Ethnopharmacology; ECDOH, African Herbal Pharmacopoeia).

Practical preparation: for a mild bark decoction, simmer 5–10 g of dried root bark in 500 ml water for 20 minutes; cool, strain, and sip one cup once or twice daily for fevers or digestive sluggishness. Do not exceed 3–5 g bark per day without supervision. Avoid seed, kernel, or bark preparations during pregnancy and lactation; neurotoxic symptoms (muscle stiffness, respiratory depression) require immediate medical care (ECDOH, African Herbal Pharmacopoeia).

Modern relevance: ongoing chemical and pharmacological work on the bark’s bisindole and iridoid constituents continues to inform conservation and quality control as community practitioners and a small traditional-products industry keep decoctions in current use.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Strychnos utilis Sim Forest Fl. Cape : 273 (1907)
Strychnos ligustroides Gossw. & Mendonça Carta Fitogeogr. Angola 120 (1939), sine descr. lat.
Strychnos holstii Gilg ex Engl. Abh. Königl. Akad. Wiss. Berlin 1894: 36. ; et in Engl. Pflanzenw. Ost-Afr. C (1895) 310
Strychnos sennensis Baker Bull. Misc. Inform. Kew 1895: 97 (1895)
Strychnos pauciflora Gilg Bot. Jahrb. Syst. 28: 121 (1899)
Strychnos procera Gilg & Busse Bot. Jahrb. Syst. 36: 97 (1905)
Strychnos albersii Gilg & Busse Bot. Jahrb. Syst. 36: 99 (1905)
Strychnos elliottii Gilg & Busse Bot. Jahrb. Syst. 36: 99 (1905)
Strychnos myrcioides S.Moore J. Bot. 45: 52 (1907)
Strychnos reticulata Burtt Davy & Honore Bull. Misc. Inform. Kew 1932: 270 (1932)
Strychnos barbata Chiov. Fl. Somala 2: 305. 1932
Strychnos holstii var. reticulata (Burtt Davy & Honoré) J.Duvign. Bull. Inst. Roy. Col. Belg. 20: 588 1949
Strychnos holstii f. condensata Duvign Bull. Inst. Roy. Col. Belg. 20: 588 1949
Strychnos holstii f. laxiuscula Duvign Bull. Inst. Roy. Col. Belg. 20: 588 1949
Strychnos holstii var. procera (Gilg & Busse) J.Duvign. Bull. Mus. Roy. Hist. Nat. Belgique 20: 587 (1949)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Zaïre
    • Western Indian Ocean
      • Madagascar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000502962
Tropicos 19000122
KEW urn:lsid:ipni.org:names:547225-1
The Plant List kew-2598256
Open Tree Of Life 420772
NCBI Taxonomy 1040887
IUCN Red List 146213463
IPNI 547225-1
iNaturalist 340252
GBIF 5645835
CMAUP NPO17344

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
A Review of Ethnomedicinal Plants as Potential Anthelmintic Agents to Alternatively Control Gastrointestinal Nematodes of Ruminants in South Africa Mhlongo LC, Mseleku C, Tenza T, Fomum SW, McGaw LJ, Hassen A, Nsahlai IV J Parasitol Res 16-Jan-2024
PMCID:PMC10805549
doi:10.1155/2024/7955692
PMID:38268708
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
Diversity of woody species in traditional agroforestry practices in Wondo district, south-central Ethiopia Molla T, Asfaw Z, Muluneh MG, Worku BB Heliyon 07-Feb-2023
PMCID:PMC9941991
doi:10.1016/j.heliyon.2023.e13549
PMID:36825171
Antihyperglycemic and hepatoprotective effects of Salvia tebesana Bunge in diabetic rats Aramjoo H, Kiani Z, Eghbali S Res Pharm Sci 14-Jul-2022
PMCID:PMC9400469
doi:10.4103/1735-5362.350241
PMID:36034081
Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa Aremu AO, Pendota SC Front Pharmacol 22-Oct-2021
PMCID:PMC8569556
doi:10.3389/fphar.2021.758583
PMID:34744737
A Review of Ethnoveterinary Knowledge, Biological Activities and Secondary Metabolites of Medicinal Woody Plants Used for Managing Animal Health in South Africa Selogatwe KM, Asong JA, Struwig M, Ndou RV, Aremu AO Vet Sci 12-Oct-2021
PMCID:PMC8537377
doi:10.3390/vetsci8100228
PMID:34679058
Ethnobotanical Documentation, Phytochemical Screening, and Cytotoxicity Evaluation of Medicinal Plants Used to Manage Snakebite Envenomation in Mwingi West Subcounty, Kenya Mokua SK, Mbaria JM, Maitho TE, Moriasi GA Evid Based Complement Alternat Med 27-Sep-2021
PMCID:PMC8490041
doi:10.1155/2021/4167296
PMID:34616476
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
South Africa’s Best BARK Medicines Prescribed at the Johannesburg Muthi Markets for Skin, Gut, and Lung Infections: MIC’s and Brine Shrimp Lethality Khumalo GP, Sadgrove NJ, Van Vuuren SF, Van Wyk BE Antibiotics (Basel) 07-Jun-2021
PMCID:PMC8227155
doi:10.3390/antibiotics10060681
PMID:34200286
Ethnobotanical study of plants used by the traditional healers to treat malaria in Mogovolas district, northern Mozambique Manuel L, Bechel A, Noormahomed EV, Hlashwayo DF, Madureira MD Heliyon 18-Dec-2020
PMCID:PMC7753128
doi:10.1016/j.heliyon.2020.e05746
PMID:33364508
Conservation of Wild Food Plants and Their Potential for Combatting Food Insecurity in Kenya as Exemplified by the Drylands of Kitui County Mutie FM, Rono PC, Kathambi V, Hu GW, Wang QF Plants (Basel) 12-Aug-2020
PMCID:PMC7464302
doi:10.3390/plants9081017
PMID:32806636
Antimalarial Plants Used across Kenyan Communities Omara T Evid Based Complement Alternat Med 12-Jun-2020
PMCID:PMC7306085
doi:10.1155/2020/4538602
PMID:32617107
The Potential Therapeutic Value of Medicinal Plants in the Management of Metabolic Disorders Nyakudya TT, Tshabalala T, Dangarembizi R, Erlwanger KH, Ndhlala AR Molecules 09-Jun-2020
PMCID:PMC7321241
doi:10.3390/molecules25112669
PMID:32526850
An Ethnobotanical Survey of a Dryland Botanical Garden and Its Environs in Kenya: The Mutomo Hill Plant Sanctuary Mutie FM, Gao LL, Kathambi V, Rono PC, Musili PM, Ngugi G, Hu GW, Wang QF Evid Based Complement Alternat Med 17-Mar-2020
PMCID:PMC7103046
doi:10.1155/2020/1543831
PMID:32256635
Medicinal plants sold for treatment of bacterial and parasitic diseases in humans in Maputo city markets, Mozambique Barbosa F, Hlashwayo D, Sevastyanov V, Chichava V, Mataveia A, Boane E, Cala A BMC Complement Med Ther 23-Jan-2020
PMCID:PMC7076832
doi:10.1186/s12906-019-2809-9
PMID:32020866

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
> Alkaloids and derivatives / Strychnos alkaloids
(12R,16R,17S,18S)-11-(2-hydroxyacetyl)-16-methyl-15-oxa-1,11-diazapentacyclo[15.3.1.04,12.05,10.013,18]henicosa-5,7,9,13-tetraen-20-one 101615147 Click to see CC1C2CN3CCC4C(C(=CO1)C2CC3=O)N(C5=CC=CC=C45)C(=O)CO 368.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
(16R,17S,18R)-11-(2-hydroxyacetyl)-16-methyl-15-oxa-1,11-diazapentacyclo[15.3.1.04,12.05,10.013,18]henicosa-4(12),5,7,9,13-pentaen-20-one 163190497 Click to see 366.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
(16R,17S,18R)-16-methyl-15-oxa-1,11-diazapentacyclo[15.3.1.04,12.05,10.013,18]henicosa-4(12),5,7,9,13-pentaen-20-one 163186265 Click to see 308.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
(17R)-1-Acetyl-19,20-didehydro-17,18-epoxycuran-17-ol 321983 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=CC=CC=C61 352.40 unknown https://doi.org/10.1002/JLAC.19687120122
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(17R)-1-Acetyl-19,20-didehydro-17,18-epoxycuran-17-ol 12312946 Click to see 352.40 unknown https://doi.org/10.1002/JLAC.19687120122
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(1R,5S,7S,8S,9R,11S,12R,22S)-11-hydroxy-9-methyl-10-oxa-4,15-diazaheptacyclo[10.9.1.14,8.01,5.07,12.015,22.016,21]tricosa-16,18,20-trien-14-one 162867693 Click to see CC1C2CN3CCC45C3CC2C6(C4N(C(=O)C6)C7=CC=CC=C57)C(O1)O 352.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
(1S,10R,13S,14S,20R,22R)-15-ethylidene-10-hydroxy-4-methoxy-11-oxa-8,17-diazahexacyclo[12.5.2.11,8.02,7.017,20.013,22]docosa-2(7),3,5-trien-9-one 163101756 Click to see 382.50 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
(2Z)-2-[(1S,9S,10S,11R,17S)-10-(hydroxymethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-12-ylidene]ethanol 163190295 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(00)89013-5
(4aR,5aR,8aS,13aS,15aR,15bS)-15a-hydroxy-5a,10-dimethoxy-4a,5,7,8,13a,15,15b,16-octahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 162957444 Click to see 410.50 unknown https://doi.org/10.1002/JLAC.19687120122
(4aR,5aR,8aS,13aS,15aS,15bR)-15a-hydroxy-5a-methoxy-4a,5,7,8,13a,15,15b,16-octahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 163093000 Click to see COC12CC3C4C5C16CCN2CC3=CCOC4(CC(=O)N5C7=CC=CC=C67)O 380.40 unknown https://doi.org/10.1002/JLAC.19687120122
(4S,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraene 162910221 Click to see 294.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
[(1S,9S,10S,11R,12Z,17S)-12-(2-hydroxyethylidene)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-10-yl]methyl acetate 163185660 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(00)89013-5
[(1S,9S,10S,11R,17S)-12-(2-hydroxyethylidene)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-10-yl]methyl acetate 162936920 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(00)89013-5
[(4R,12S,13R,14R,19R,21S)-11-acetyl-9-hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-14-yl] acetate 163194649 Click to see 440.50 unknown https://doi.org/10.1080/00359193609518904
[2-(16-Methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraen-11-yl)-2-oxoethyl] acetate 163032302 Click to see CC1C2CN3CCC45C3CC2C(=CO1)C4N(C6=CC=CC=C56)C(=O)COC(=O)C 394.50 unknown https://doi.org/10.1016/0031-9422(91)83227-C
[2-(16-Methyl-20-oxo-15-oxa-1,11-diazapentacyclo[15.3.1.04,12.05,10.013,18]henicosa-4(12),5,7,9,13-pentaen-11-yl)-2-oxoethyl] acetate 162982261 Click to see CC1C2CN3CCC4=C(C(=CO1)C2CC3=O)N(C5=CC=CC=C45)C(=O)COC(=O)C 408.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
[2-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl] acetate 163191358 Click to see 394.50 unknown https://doi.org/10.1016/0031-9422(91)83227-C
1-(14-Hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,12,17-pentaen-11-yl)ethanone 163011171 Click to see CC(=O)N1C2=C(C=CC(=C2)OC)C34C1=C5C6CC3N(CC4)CC6=CCOC5O 380.40 unknown https://doi.org/10.1002/JLAC.19687120122
1-(14-Hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-11-yl)ethanone 13994711 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=C1C=C(C=C6)OC 382.50 unknown https://doi.org/10.1002/JLAC.19687120122
1-(19-Methyl-16,17-dihydro-2,16-cycloformosanan-1-yl)ethan-1-one 120759 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
1-(9,14-Dihydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,12,17-pentaen-11-yl)ethanone 162934436 Click to see CC(=O)N1C2=C(C=CC(=C2O)OC)C34C1=C5C6CC3N(CC4)CC6=CCOC5O 396.40 unknown https://doi.org/10.1002/JLAC.19687120122
1-[(1R,9S,10S,11R,12Z,17S)-12-(2-hydroxyethylidene)-10-(hydroxymethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-8-yl]ethanone 163187992 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(00)89013-5
1-[(4R,12R,13R,14S,19R,21S)-9,14-dihydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-11-yl]ethanone 163187841 Click to see 398.50 unknown https://doi.org/10.1002/JLAC.19687120122
1-[(4R,12S,13R,16R,17S,18R,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-11-yl]ethanone 162902841 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
1-[(4R,14R,19R,21R)-14-hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,12,17-pentaen-11-yl]ethanone 163193917 Click to see 380.40 unknown https://doi.org/10.1002/JLAC.19687120122
1-[(4R,14R,19R,21R)-9,14-dihydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,12,17-pentaen-11-yl]ethanone 162934437 Click to see CC(=O)N1C2=C(C=CC(=C2O)OC)C34C1=C5C6CC3N(CC4)CC6=CCOC5O 396.40 unknown https://doi.org/10.1002/JLAC.19687120122
1-[(9S,10S,11R,12Z,17S)-12-ethylidene-10-(hydroxymethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-8-yl]ethanone 101297638 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
1-[12-(2-Hydroxyethylidene)-10-(hydroxymethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-8-yl]ethanone 162971909 Click to see CC(=O)N1C2C(C3CC4C2(CCN4CC3=CCO)C5=CC=CC=C51)CO 354.40 unknown https://doi.org/10.1016/S0031-9422(00)89013-5
11-(2-Hydroxyacetyl)-16-methyl-15-oxa-1,11-diazapentacyclo[15.3.1.04,12.05,10.013,18]henicosa-4(12),5,7,9,13-pentaen-20-one 162925124 Click to see 366.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
11-Hydroxy-9-methyl-10-oxa-4,15-diazaheptacyclo[10.9.1.14,8.01,5.07,12.015,22.016,21]tricosa-16,18,20-trien-14-one 162867692 Click to see 352.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
11-Methoxydiaboline 13994712 Click to see 382.50 unknown https://doi.org/10.1002/JLAC.19687120122
15-Ethylidene-10-hydroxy-11-oxa-8,17-diazahexacyclo[12.5.2.11,8.02,7.017,20.013,22]docosa-2,4,6-trien-9-one 162865927 Click to see 352.40 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
15a-hydroxy-5a-methoxy-4a,5,7,8,13a,15,15b,16-octahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 163092999 Click to see 380.40 unknown https://doi.org/10.1002/JLAC.19687120122
15a-hydroxy-5a,10-dimethoxy-4a,5,7,8,13a,15,15b,16-octahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 12314973 Click to see 410.50 unknown https://doi.org/10.1002/JLAC.19687120122
16-Methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraene 162910220 Click to see 294.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
16-Methyl-15-oxa-1,11-diazapentacyclo[15.3.1.04,12.05,10.013,18]henicosa-4(12),5,7,9,13-pentaen-20-one 163000396 Click to see 308.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-[(1S,9S,10S,11R,17S)-10-(hydroxymethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-12-ylidene]ethanol 162950036 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(00)89013-5
2-Hydroxy-1-(14-hydroxy-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-11-yl)ethanone 163041490 Click to see 370.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-Hydroxy-1-(16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-11-yl)ethanone 163090209 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-Hydroxy-1-(16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraen-11-yl)ethanone 162910828 Click to see CC1C2CN3CCC45C3CC2C(=CO1)C4N(C6=CC=CC=C56)C(=O)CO 352.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-Hydroxy-1-(20-hydroxy-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-11-yl)ethanone 12304544 Click to see 370.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-Hydroxy-1-(20-hydroxy-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraen-11-yl)ethanone 162988151 Click to see 368.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-hydroxy-1-[(12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraen-11-yl]ethanone 101615145 Click to see 352.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-hydroxy-1-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraen-11-yl]ethanone 162910829 Click to see 352.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-hydroxy-1-[(4R,12S,13R,14S,16R,17S,18S,20S)-14-hydroxy-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-11-yl]ethanone 163041491 Click to see CC1C2CN3CCC45C3CC2C(C4N(C6=CC=CC=C56)C(=O)CO)C(O1)O 370.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-hydroxy-1-[(4R,12S,13R,16R,17S,18R,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-11-yl]ethanone 163090211 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-hydroxy-1-[(4R,12S,13R,16S,17S,18R,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-11-yl]ethanone 163090210 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
2-hydroxy-1-[(4S,12S,16R,17S,18S,20R)-20-hydroxy-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9,13-tetraen-11-yl]ethanone 163194711 Click to see CC1C2CN3CCC45C3(CC2C(=CO1)C4N(C6=CC=CC=C56)C(=O)CO)O 368.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
Henningsoline 321985 Click to see 398.50 unknown https://doi.org/10.1002/JLAC.19687120122
Henningsoline, acetate (ester) 633272 Click to see 440.50 unknown https://doi.org/10.1080/00359193609518904
Splendoline 134716697 Click to see 370.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
methyl 7-[(9S)-2,5-dihydroxy-3-methoxycarbonyl-4-methyl-9-[(2R)-2-methylbutanoyl]oxy-10-oxoanthracen-9-yl]-3,8-dihydroxy-1-methyl-9,10-dioxoanthracene-2-carboxylate 163071499 Click to see CCC(C)C(=O)OC1(C2=C(C(=CC=C2)O)C(=O)C3=C(C(=C(C=C31)O)C(=O)OC)C)C4=C(C5=C(C=C4)C(=O)C6=CC(=C(C(=C6C5=O)C)C(=O)OC)O)O 708.70 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
> 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 / Methoxybenzenes / Dimethoxybenzenes
8-[4-(3-Hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]-2,6-dimethylocta-3,6-dien-2-ol 162990839 Click to see 362.50 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
[3-(acetyloxymethyl)-5-(1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)pent-3-enyl] acetate 73826392 Click to see 390.60 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylated hydroquinones
2,5-dihydroxy-3-(3-methylbut-2-enyl)-6-[2-[11-methyl-3-[[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene]-2,5-dioxo-1,4-diazaspiro[5.5]undec-9-en-8-yl]ethenyl]benzaldehyde 162899841 Click to see CC1C=CC(CC12C(=O)NC(=CC3=C(NC4=CC=CC=C43)C(C)(C)C=C)C(=O)N2)C=CC5=C(C=C(C(=C5C=O)O)CC=C(C)C)O 619.70 unknown https://doi.org/10.1016/0031-9422(91)83227-C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4S,5S)-2-[[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-2-hydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-yl]oxy]oxane-3,4,5-triol 163088565 Click to see 620.80 unknown https://doi.org/10.1016/0031-9422(91)83227-C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
7alpha-Hydroxysitosterol 161816 Click to see 430.70 unknown via CMAUP database
7Beta-hydroxy-beta-sitosterol 12309569 Click to see 430.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 86311182 Click to see 242.22 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 54353627 Click to see 226.23 unknown via CMAUP database
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(15Z)-15-Ethylidene-10-hydroxy-17-methyl-11-oxa-8,17-diazapentacyclo[12.5.2.11,8.02,7.013,22]docosa-2,4,6-triene-9,20-dione 5358759 Click to see CC=C1CN(CCC23C4C(C1CC2=O)COC(C(=O)N4C5=CC=CC=C35)O)C 382.50 unknown https://doi.org/10.1016/0031-9422(91)83227-C
(1S,10R,13R,14R,15Z,22S)-15-ethylidene-4,10-dimethoxy-17-methyl-11-oxa-8,17-diazapentacyclo[12.5.2.11,8.02,7.013,22]docosa-2(7),3,5-triene-9,20-dione 163193803 Click to see 426.50 unknown https://doi.org/10.1080/00359193609518904
(1S,10R,13R,14R,22S)-15-ethylidene-4,10-dimethoxy-17-methyl-11-oxa-8,17-diazapentacyclo[12.5.2.11,8.02,7.013,22]docosa-2(7),3,5-triene-9,20-dione 162866246 Click to see 426.50 unknown https://doi.org/10.1080/00359193609518904
(1S,13R,14R,15E,22S)-15-ethylidene-10-hydroxy-17-methyl-11-oxa-8,17-diazapentacyclo[12.5.2.11,8.02,7.013,22]docosa-2,4,6-triene-9,20-dione 119079924 Click to see 382.50 unknown https://doi.org/10.1016/0031-9422(91)83227-C
11-Hydroxy-4,9-dimethyl-10-oxa-4,15-diazahexacyclo[10.9.1.01,5.07,12.015,22.016,21]docosa-16,18,20-trien-14-one 163192464 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(91)83227-C
15-Ethylidene-10-hydroxy-17-methyl-11-oxa-8,17-diazapentacyclo[12.5.2.11,8.02,7.013,22]docosa-2,4,6-triene-9,20-dione 321984 Click to see 382.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
Holstiine 23278454 Click to see CC=C1CN(CCC23C4C(C1CC2=O)COC(C(=O)N4C5=CC=CC=C35)O)C 382.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] 3,4,5-trihydroxybenzoate 163106439 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O 762.60 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
7-methoxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10366980 Click to see 460.40 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
> Phenylpropanoids and polyketides / Macrolides and analogues
(7E,9R,12R,13R,16E,21R,22S)-12-(hydroxymethyl)-22-[(Z)-[(2R,4Z)-4-(5-methoxypentan-2-ylidene)-2-(2-methylpropyl)oxolan-3-ylidene]methyl]-8,12-dimethyl-17-(2-methylpropyl)-10,14,19,24-tetraoxa-23,25-diazatetracyclo[19.2.1.12,5.09,13]pentacosa-1(23),2,4,7,16-pentaene-11,15,18-trione 163187286 Click to see 736.90 unknown https://doi.org/10.1016/S0031-9422(00)85234-6
> Phenylpropanoids and polyketides / Stilbenes
(2S,3R)-3-Ethoxy-2,3-bis(3-methoxy-4-hydroxyphenyl)propane-1-ol 11759831 Click to see CCOC(C1=CC(=C(C=C1)O)OC)C(CO)C2=CC(=C(C=C2)O)OC 348.40 unknown via CMAUP database
[4-[(4R,5R)-4-(4-acetyloxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenyl] acetate 21591953 Click to see CC(=O)OC1=C(C=C(C=C1)C2COCOC2C3=CC(=C(C=C3)OC(=O)C)OC)OC 416.40 unknown via CMAUP database
4-[(4S,5S)-4-(4-hydroxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenol 10871293 Click to see COC1=C(C=CC(=C1)C2COCOC2C3=CC(=C(C=C3)O)OC)O 332.30 unknown via CMAUP database

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