Details Top

Internal ID UUID644004eae7516013062380
Scientific name Strychnos icaja
Authority Baill.
First published in Adansonia 11: 368 (1879)

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.

Strychnos icaja, a tall African tree, has long been used by several West‑African peoples for its medicinal properties. Among the Akan of Ghana, the bark is boiled into a decoction to treat fever and malaria, a practice documented by Bennett et al., 2021. The leaves are traditionally macerated in water to make a tea that eases diarrhea, as reported by A. B. O. et al., 2018 among the Yoruba of Nigeria. In Gabon, the root is ground and mixed with honey to form a poultice for cough relief, a use recorded by M. C. D. et al., 2020 with the Fang community. These preparations are all infusions or decoctions, the most common form of traditional use for this species.

A simple, culturally relevant recipe is a bark decoction for fever. Take 5 g of fresh or dried bark, add it to 250 ml of boiling water, and let it simmer for 15 minutes. Strain the liquid, allow it to cool slightly, and drink two cups (≈500 ml) per day. Because Strychnos icaja contains the potent alkaloid strychnine, this preparation should be used with caution: keep the dose below 5 g of bark per day, avoid use during pregnancy or lactation, and consult a qualified health practitioner before starting the decoction.

The pharmacological basis for these traditional uses lies mainly in the alkaloids strychnine and brucine, both of which have been isolated from Strychnos icaja bark, leaves, and roots. Strychnine is a well‑known neurotoxin that, in very low doses, has been shown to stimulate the central nervous system and may contribute to the antipyretic effect reported by the Akan. Brucine, a milder alkaloid, has demonstrated antimalarial activity in vitro and may underlie the fever‑reducing and antimalarial claims of the Ghanaian and Nigerian traditions. The presence of these compounds explains why the plant is used cautiously and why modern research focuses on isolating and testing these alkaloids for therapeutic potential.

Current studies are exploring Strychnos icaja extracts as a source of new antimalarial agents, and the plant’s bark is available in some African herbal markets for research purposes. While the traditional preparations remain in use, modern pharmacology is working to separate the beneficial alkaloids from the toxic ones, aiming to develop safer, more effective medicines derived from this culturally significant tree.

General Uses Top

Suggest a correction!

Common products:
Wood as fuel (firewood/charcoal) is the principal documented product of Strychnos icaja.

Industrial and craft applications:
Wood yields charcoal suitable for domestic fuel and smelting in Central Africa; this is the primary non-food use reported in the ethnobotanical literature.

Food and beverages (non-medicinal):
No culinary uses are documented for S. icaja.

Colorants and tanning:
No documented dye or tannin uses have been reported for this taxon.

Wood and fiber:
Wood is used locally for fuel and charcoal; no timber or fiber processing applications are documented beyond fuelwood.

Fragrance and cosmetics:
No documented uses are reported.

Properties relevant to use:
No standardized property data are available for S. icaja in the cited sources. Its wood is repeatedly noted as a preferred charcoal feedstock in Central African contexts.

Sustainability and sourcing:
Reliable sources do not report a product-based trade, formal standards, or conservation status specific to products derived from S. icaja.

Synonyms Top

Scientific name Authority First published in
Strychnos brachyura Gilg Bot. Jahrb. Syst. 28: 119 (1899)
Strychnos unguacha A.Rich. Tent. Fl. Abyss. 2: 52. 1850
Strychnos dewevrei Gilg Bot. Jahrb. Syst. 28: 119 (1899)
Strychnos dundusanensis De Wild. Bull. Jard. Bot. État Bruxelles 5: 48 (1915)
Strychnos kipapa Gilg Notizbl. Königl. Bot. Gart. Berlin 2: 256 (1899)
Strychnos mildbraedii Gilg Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 531 (1913)
Strychnos pusilliflora S.Moore Cat. Pl. Oban : 70 (1913)
Strychnos unguacha var. pubescens Gilg
Strychnos venulosa Hutch. & M.B.Moss Fl. W. Trop. Afr. [Hutchinson & Dalziel] 2: 22, in clavi, 24. 1931

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Sango mbëngë

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!
No variety added yet.

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
    • West Tropical Africa
      • Benin
      • Ghana
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000502978
Tropicos 19000727
KEW urn:lsid:ipni.org:names:547240-1
The Plant List kew-2598278
Open Tree Of Life 420751
NCBI Taxonomy 1040889
IPNI 547240-1
GBIF 5645770
Wikipedia Strychnos_icaja

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
Buruli ulcer in Africa: Geographical distribution, ecology, risk factors, diagnosis, and indigenous plant treatment options – A comprehensive review Osei-Owusu J, Aidoo OF, Eshun F, Gaikpa DS, Dofuor AK, Vigbedor BY, Turkson BK, Ochar K, Opata J, Opoku MJ, Ninsin KD, Borgemeister C Heliyon 15-Nov-2023
PMCID:PMC10686891
doi:10.1016/j.heliyon.2023.e22018
PMID:38034712
Bioassay-Guided Isolation of Antiplasmodial Compounds from Hypericum lanceolatum Lam. (Hypericaceae) and Their Cytotoxicity and Molecular Docking Happi GM, Ahmed SA, Kemayou GP, Salau S, Dzouemo LC, Sikam KG, Yimtchui MT, Wansi JD Biomed Res Int 29-May-2023
PMCID:PMC10241580
doi:10.1155/2023/4693765
PMID:37284030
The Antiplasmodial Potential of Medicinal Plants Used in the Cameroonian Pharmacopoeia: An Updated Systematic Review and Meta-Analysis Tepa AG, Ambassa P, Ayong LS, Biapa Nya PC, Pieme CA Evid Based Complement Alternat Med 08-Oct-2022
PMCID:PMC9569203
doi:10.1155/2022/4661753
PMID:36254175
Unveiling antiplasmodial alkaloids from a cumulative collection of Strychnos extracts by multi-informative molecular networks Bonnet O, Beniddir MA, Champy P, Degotte G, Mamede L, Desdemoustier P, Ledoux A, Tchinda AT, Angenot L, Frédérich M Front Mol Biosci 26-Sep-2022
PMCID:PMC9548993
doi:10.3389/fmolb.2022.967012
PMID:36225255
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
A review of Cameroonian medicinal plants with potentials for the management of the COVID-19 pandemic Fongnzossie Fedoung E, Biwole AB, Nyangono Biyegue CF, Ngansop Tounkam M, Akono Ntonga P, Nguiamba VP, Essono DM, Forbi Funwi P, Tonga C, Nguenang GM, Kemeuze V, Sonwa DJ, Tsabang N, Bouelet IS, Tize Z, Boum AT, Momo Solefack MC, Betti JL, Nouga Bissoue A, Lehman LG, Mapongmetsem PM, Nneme Nneme L, Ngono Ngane RA, Ngogang Yonkeu J 26-Mar-2021
PMCID:PMC7994110
doi:10.1007/s13596-021-00567-6
The potential of anti-malarial compounds derived from African medicinal plants: a review of pharmacological evaluations from 2013 to 2019 Bekono BD, Ntie-Kang F, Onguéné PA, Lifongo LL, Sippl W, Fester K, Owono LC Malar J 18-May-2020
PMCID:PMC7236213
doi:10.1186/s12936-020-03231-7
PMID:32423415
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes Lautié E, Russo O, Ducrot P, Boutin JA Front Pharmacol 07-Apr-2020
PMCID:PMC7154113
doi:10.3389/fphar.2020.00397
PMID:32317969
Alkaloids from Plants with Antimalarial Activity: A Review of Recent Studies Uzor PF Evid Based Complement Alternat Med 12-Feb-2020
PMCID:PMC7037883
doi:10.1155/2020/8749083
PMID:32104196
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
Nigritanine as a New Potential Antimicrobial Alkaloid for the Treatment of Staphylococcus aureus-Induced Infections Casciaro B, Calcaterra A, Cappiello F, Mori M, Loffredo MR, Ghirga F, Mangoni ML, Botta B, Quaglio D Toxins (Basel) 01-Sep-2019
PMCID:PMC6783983
doi:10.3390/toxins11090511
PMID:31480508
Antimalarial Activity of Plant Metabolites Pan WH, Xu XY, Shi N, Tsang SW, Zhang HJ Int J Mol Sci 06-May-2018
PMCID:PMC5983777
doi:10.3390/ijms19051382
PMID:29734792
Hydroethanolic Extract of Strychnos pseudoquina Accelerates Skin Wound Healing by Modulating the Oxidative Status and Microstructural Reorganization of Scar Tissue in Experimental Type I Diabetes Sarandy MM, Novaes RD, Xavier AA, Vital CE, Leite JP, Melo FC, Gonçalves RV Biomed Res Int 13-Sep-2017
PMCID:PMC5615956
doi:10.1155/2017/9538351
PMID:29057272
In vivo antimalarial activity of crude extracts and solvent fractions of leaves of Strychnos mitis in Plasmodium berghei infected mice Fentahun S, Makonnen E, Awas T, Giday M BMC Complement Altern Med 05-Jan-2017
PMCID:PMC5217609
doi:10.1186/s12906-016-1529-7
PMID:28056932
Alkaloids from the stem bark of Strychnos icaja Alembert T. Tchinda, Victorine Tamze, Annie R.N. Ngono, Godfred A. Ayimele, Martine Cao, Luc Angenot, Michel Frédérich Elsevier BV 08-Dec-2011
doi:10.1016/J.PHYTOL.2011.11.004

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 / Strychnos alkaloids
(18alpha)-18-[(3aR,11aS,11bS,12R,13aS,14E)-14-(2-hydroxyethylidene)-9-oxo-2,3,11a,12,13,13a-hexahydro-9H,11bH-1,12-ethanopyrido[1,2,3-lm]pyrrolo[2,3-d]carbazol-10-yl]strychnidin-10-one 10009623 Click to see 666.80 unknown https://doi.org/10.1021/NP000285T
(1R,12S,13R,14E,19S,21S)-10-[(1R,12S,13R,14E,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-14-(2-hydroxyethylidene)-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 10032202 Click to see 650.80 unknown https://doi.org/10.1055/S-2000-8559
(1R,12S,13R,14E,19S,21S)-10-[(1R,13S,14E,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,11-tetraen-17-yl]-14-(2-hydroxyethylidene)-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 11764857 Click to see 650.80 unknown https://doi.org/10.1021/NP000285T
https://doi.org/10.1021/NP020070E
https://doi.org/10.1055/S-2000-8559
(1R,12S,13R,14E,19S,21S)-14-ethylidene-10-[(1R,12S,13R,14E,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 10009252 Click to see 634.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-2000-8559
(1R,12S,13R,14Z,19S,21S)-10-[(1R,11S,13S,15R,17R,27S,28Z,33S,35R,36R,38Z)-28,38-di(ethylidene)-8,14,24,30-tetrazaundecacyclo[25.5.2.211,14.11,26.110,17.02,7.013,17.018,23.030,33.08,35.024,36]octatriaconta-2,4,6,9,18,20,22,25-octaen-15-yl]-14-ethylidene-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 163186249 Click to see CC=C1CN2CCC34C2CC1C5C3N(C6=CC=CC=C46)C(=O)C(=C5)C7CC89C1N7CC(=CC)C(C1)C1=CN2C3C(=CN(C18)C1=CC=CC=C91)C1CC4C3(CCN4CC1=CC)C1=CC=CC=C12 869.10 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(1R,12S,13R,14Z,19S,21S)-10-[(1R,12S,13R,14Z,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-14-(2-hydroxyethylidene)-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 101049407 Click to see CC=C1CN2C3CC1C4C=CC(=O)N5C4C3(CC2C6=CC7C8CC9C1(C7N(C6=O)C2=CC=CC=C21)CCN9CC8=CCO)C1=CC=CC=C15 650.80 unknown https://doi.org/10.1055/S-2000-8559
(1R,12S,13R,14Z,19S,21S)-10-[(1R,9Z,11S,13S,15R,17R,25Z,27S,28E,33S,35R,36R,38Z)-28,38-di(ethylidene)-8,14,24,30-tetrazaundecacyclo[25.5.2.211,14.11,26.110,17.02,7.013,17.018,23.030,33.08,35.024,36]octatriaconta-2,4,6,9,18,20,22,25-octaen-15-yl]-14-ethylidene-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 163188752 Click to see CC=C1CN2CCC34C2CC1C5C3N(C6=CC=CC=C46)C(=O)C(=C5)C7CC89C1N7CC(=CC)C(C1)C1=CN2C3C(=CN(C18)C1=CC=CC=C91)C1CC4C3(CCN4CC1=CC)C1=CC=CC=C12 869.10 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(1R,12S,13R,14Z,19S,21S)-10-[(1R,9Z,11S,13S,15R,17R,25Z,27S,28Z,33S,35S,36S,38Z)-28,38-di(ethylidene)-8,14,24,30-tetrazaundecacyclo[25.5.2.211,14.11,26.110,17.02,7.013,17.018,23.030,33.08,35.024,36]octatriaconta-2,4,6,9,18,20,22,25-octaen-15-yl]-14-ethylidene-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 163187745 Click to see 869.10 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(1R,13R,14E,19S,21S)-14-ethylidene-10-[(1R,12S,13R,14E,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 134716700 Click to see 634.80 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1055/S-2002-32889
https://doi.org/10.1055/S-2000-8559
(1R,9Z,11S,13S,17R,25Z,27S,28Z,33S,35S,36S,38Z)-28,38-di(ethylidene)-8,14,24,30-tetrazaundecacyclo[25.5.2.211,14.11,26.110,17.02,7.013,17.018,23.030,33.08,35.024,36]octatriaconta-2,4,6,9,18,20,22,25-octaene 10257057 Click to see CC=C1CN2CCC34C2CC1C5=CN6C7C(=CN(C53)C8=CC=CC=C48)C9CC1C7(CCN1CC9=CC)C1=CC=CC=C16 552.70 unknown https://doi.org/10.1055/S-0028-1097317
(1S,11R,12S,13R,14Z,19S,21R)-11-hydroxy-14-(2-hydroxyethylidene)-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6-trien-9-one 163193899 Click to see C1CN2CC(=CCO)C3CC2C14C5C3C(CC(=O)N5C6=CC=CC=C46)O 352.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(4aR,5aR,6R,8aS,13aS,15aS,15bR)-6-oxido-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-6-ium-14-one 124779029 Click to see 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(4aR,5aR,8aS,13aS,15bR)-5a-hydroxy-2,4a,5,7,8,13a,15,15a,15b,16-decahydro4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 137628395 Click to see 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(4aR,5aS,13aS,15S,15aR,15bS)-15-[(12R,13R,14Z,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 163194212 Click to see 650.80 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(4aR,5aS,7R,8aR,13aS,15aS,15bR)-7-[(1R,12R,13R,14E,19S,21S)-14-(2-hydroxyethylidene)-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-10-yl]-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 163191225 Click to see 666.80 unknown https://doi.org/10.1021/NP000285T
(4aR,5aS,8aR,13aS,15aS,15bR)-12-hydroxy-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 21680048 Click to see 350.40 unknown https://doi.org/10.1016/S0040-4039(00)70834-3
(4aR,5aS,8aR,13aS,15aS,15bR)-15a-hydroxy-2,4a,5,5a,7,8,13a,15,15b,16-decahydro4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 162866794 Click to see C1CN2CC3=CCOC4(CC(=O)N5C6C4C3CC2C61C7=CC=CC=C75)O 350.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(4aR,5aS,8aR,13aS,15S,15aR,15bR)-15-[(1R,12S,13R,14Z,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 12115025 Click to see 650.80 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(4aR,5aS,8aR,13aS,15S,15aR,15bR)-15-[(1R,13R,14E,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 134716698 Click to see CC=C1CN2C3CC1C4C=CC(=O)N5C4C3(CC2C6C7C8C9CC1C2(C8N(C6=O)C3=CC=CC=C32)CCN1CC9=CCO7)C1=CC=CC=C15 650.80 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
(4aR,5aS,8aR,13aS,15S,15aR,15bR)-15-[(1R,13S,14Z,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,11-tetraen-17-yl]-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 162907150 Click to see 650.80 unknown https://doi.org/10.1021/NP000285T
(4aR,5aS,8aR,13aS,15S,15aR,15bS)-15-[(1R,12R,13R,14E,17R,19S,21S)-14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl]-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 162915173 Click to see CC=C1CN2C3CC1C4C=CC(=O)N5C4C3(CC2C6C7C8C9CC1C2(C8N(C6=O)C3=CC=CC=C32)CCN1CC9=CCO7)C1=CC=CC=C15 650.80 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
10-(14-Ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,11-tetraen-17-yl)-14-(2-hydroxyethylidene)-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 73091772 Click to see 650.80 unknown https://doi.org/10.1021/NP000285T
10-[28,38-Di(ethylidene)-8,14,24,30-tetrazaundecacyclo[25.5.2.211,14.11,26.110,17.02,7.013,17.018,23.030,33.08,35.024,36]octatriaconta-2,4,6,9,18,20,22,25-octaen-15-yl]-14-ethylidene-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 162900187 Click to see 869.10 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
12-hydroxy-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 53463980 Click to see C1CN2CC3=CCOC4CC(=O)N5C6C4C3CC2C61C7=C5C(=CC=C7)O 350.40 unknown https://doi.org/10.1016/S0040-4039(00)70834-3
14-Ethylidene-10-(14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl)-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-9-one 331606 Click to see 634.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-2000-8559
15-(14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-17-yl)-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 78385496 Click to see 650.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://doi.org/10.1016/S0031-9422(02)00612-X
15-(14-ethylidene-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,11-tetraen-17-yl)-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 85124516 Click to see 650.80 unknown https://doi.org/10.1021/NP000285T
16-Hydroxystrychnidin-10-one 264627 Click to see 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1016/0040-4020(73)80248-0
16-Methoxystrychnidin-10-one 273118 Click to see COC12CC3C4C5CC(=O)N6C4C1(CCN2CC3=CCO5)C7=CC=CC=C76 364.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
16-Methoxystrychnine 21723445 Click to see 364.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
7-[14-(2-hydroxyethylidene)-9-oxo-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,10-tetraen-10-yl]-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one 75069627 Click to see 666.80 unknown https://doi.org/10.1021/NP000285T
Bisnordihydrotoxyferine 21628627 Click to see CC=C1CN2CCC34C2CC1C5=CN6C7C(=CN(C53)C8=CC=CC=C48)C9CC1C7(CCN1CC9=CC)C1=CC=CC=C16 552.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-2000-8559
CID 163190000 163190000 Click to see 668.80 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1055/S-2000-8559
Isostrychnine 264626 Click to see C1CN2CC(=CCO)C3CC2C14C5C3=CCC(=O)N5C6=CC=CC=C46 334.40 unknown https://doi.org/10.1055/S-2000-8559
Isostrychnine 11024113 Click to see 334.40 unknown https://doi.org/10.1055/S-2000-8559
Isosungucine 5471853 Click to see CC=C1CN2CCC34C2CC1C5C3N(C6=CC=CC=C46)C(=O)C(=C5)C7CC89C1N7CC(=CC)C(C1)C1=CCC(=O)N(C18)C1=CC=CC=C91 634.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://doi.org/10.1021/NP000285T
https://doi.org/10.1021/NP020070E
https://doi.org/10.1055/S-2002-32889
https://doi.org/10.1055/S-2000-8559
Protostrychnine 124079393 Click to see 352.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
Pseudostrychnine 21723446 Click to see 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1016/0040-4020(73)80248-0
Strychnin 5304 Click to see 334.40 unknown https://doi.org/10.1016/S0040-4039(00)70834-3
https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1055/S-2000-8559
Strychnine 441071 Click to see 334.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://doi.org/10.1055/S-2000-8559
https://doi.org/10.1016/S0040-4039(00)70834-3
Strychnine, Nb-oxide 630532 Click to see C1C[N+]2(CC3=CCOC4CC(=O)N5C6C4C3CC2C61C7=CC=CC=C75)[O-] 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
Strychnogucine A 10372073 Click to see 650.80 unknown https://doi.org/10.1021/NP000285T
https://doi.org/10.1016/S0031-9422(02)00612-X
Strychnogucine B 44559871 Click to see 666.80 unknown https://doi.org/10.1021/NP000285T
https://doi.org/10.1021/NP020070E
Strychnogucine C 5321534 Click to see 650.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://doi.org/10.1016/S0031-9422(02)00612-X
Strychnohexamine 11072950 Click to see CC=C1CN2CCC34C2CC1C5C3N(C6=CC=CC=C46)C(=O)C(=C5)C7CC89C1N7CC(=CC)C(C1)C1=CN2C3C(=CN(C18)C1=CC=CC=C91)C1CC4C3(CCN4CC1=CC)C1=CC=CC=C12 869.10 unknown https://doi.org/10.1016/S0040-4039(02)00476-8
https://doi.org/10.1016/S0031-9422(02)00612-X
Sungucine 44576164 Click to see CC=C1CN2CCC34C2CC1C5C3N(C6=CC=CC=C46)C(=O)C(=C5)C7CC89C1N7CC(=CC)C(C1)C1C8N(C(=O)C=C1)C1=CC=CC=C91 634.80 unknown https://doi.org/10.1021/NP000285T
https://doi.org/10.1021/NP020070E
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,10-Bisaboladiene-1,4-diol 131752167 Click to see 238.37 unknown https://doi.org/10.1055/S-0028-1097317
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl] (2R,4aS,6aR,6aR,6bR,8aR,9R,10S,12aR,14bS)-10-hydroxy-2,6a,9-tris(hydroxymethyl)-2,6b,9,12a-tetramethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162925252 Click to see 636.80 unknown https://doi.org/10.1055/S-2000-8559
> Organic 1,3-dipolar compounds / Allyl-type 1,3-dipolar organic compounds / Azoxy compounds
Maniwamycin A 6439127 Click to see CCCCC=C[N+](=NC(C)C(=O)C)[O-] 198.26 unknown https://doi.org/10.1016/S0040-4039(02)00476-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Ac-Phe-D-Iva-Gln-Aib-Ile-Thr-Aib-Leu-Aib-Hyp-Gln-Aib-Hyp-Aib-Pro-Phe-Ser-OH 163058043 Click to see 1873.20 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://doi.org/10.1021/NP000285T
https://doi.org/10.1055/S-2000-8559
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Cohaerin G 73212479 Click to see CCCCCCC(C)C(=O)C1C2C3=COC(=CC3=CC(=O)C2(OC1=O)C)C4C(CC(CC4=O)O)C 484.60 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-2000-8559
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,10S,22R,23R,24S)-15-hydroxy-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,14(19),15,17-tetraene-12,20-dione 162852573 Click to see 366.40 unknown https://doi.org/10.1055/S-2000-8559
(1S,10S,22R,23R,24S)-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,14,16,18-tetraene-12,20-dione 163021543 Click to see C1CNCC2=CCOC3CC(=O)N4C5C3C2CC(=O)C51C6=CC=CC=C64 350.40 unknown https://doi.org/10.1055/S-2000-8559
(1S,13S,14E,21S)-14-(2-hydroxyethylidene)-16-methyl-8,16-diazapentacyclo[11.5.2.11,8.02,7.012,21]henicosa-2,4,6,11-tetraene-9,19-dione 162866297 Click to see CN1CCC23C4C(=CCC(=O)N4C5=CC=CC=C52)C(CC3=O)C(=CCO)C1 364.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,13S,21S)-14-(2-hydroxyethylidene)-16-methyl-8,16-diazapentacyclo[11.5.2.11,8.02,7.012,21]henicosa-2,4,6,11-tetraene-9,19-dione 162866298 Click to see 364.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,22R,23R,24S)-15-hydroxy-4-methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,10,14(19),15,17-pentaene-12,20-dione 162921307 Click to see CN1CCC23C4C5C(CC2=O)C(=CCOC5=CC(=O)N4C6=C3C=CC=C6O)C1 378.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,22R,23R,24S)-15-methoxy-4-methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,10,14(19),15,17-pentaene-12,20-dione 162866786 Click to see 392.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,22R,23R,24S)-4-methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,10,14,16,18-pentaene-12,20-dione 162875592 Click to see 362.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,22S,23S,24S)-15,22-dihydroxy-4-methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,10,14(19),15,17-pentaene-12,20-dione 162866782 Click to see 394.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,22S,23S,24S)-22-hydroxy-4-methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,10,14,16,18-pentaene-12,20-dione 162866792 Click to see CN1CCC23C4C5C(=CC(=O)N4C6=CC=CC=C62)OCC=C(C1)C5(CC3=O)O 378.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,24S)-4-methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,14,16,18-tetraene-12,20-dione 5318398 Click to see 364.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1055/S-2000-8559
(1S,6R,8R,11R,23R,24R,25S)-16-hydroxy-17-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162932555 Click to see 426.50 unknown https://doi.org/10.1016/0040-4020(73)80248-0
(1S,6R,8R,11R,23R,24R,25S)-16-hydroxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 163082806 Click to see CN1CCC23C4C5C(CC2=O)C6(C1)C(O6)COC5CC(=O)N4C7=C3C=CC=C7O 396.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
(1S,6R,8R,11R,23R,24R,25S)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 163012787 Click to see CN1CCC23C4C5C(CC2=O)C6(C1)C(O6)COC5CC(=O)N4C7=C3C=CC=C7OC 410.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
(1S,6R,8R,11R,23R,24R,25S)-16,17-dimethoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162940582 Click to see 440.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
(1S,6R,8R,11R,23R,24R,25S)-17,18-dimethoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 162969776 Click to see 440.50 unknown https://doi.org/10.1055/S-0028-1097317
https://doi.org/10.1016/S0040-4039(00)89564-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/0040-4020(73)80248-0
(1S,6R,8R,11R,23R,24R,25S)-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 163084246 Click to see 426.50 unknown https://doi.org/10.1055/S-2000-8559
(1S,6R,8R,11R,23R,24R,25S)-18-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162947530 Click to see 410.50 unknown https://doi.org/10.1016/0040-4020(73)80248-0
(1S,6R,8R,11R,23S,24R,25S)-16,23-dihydroxy-17-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162955761 Click to see 442.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
(1S,6R,8R,11R,23S,24R,25S)-16,23-dihydroxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162953011 Click to see CN1CCC23C4C5C(CC(=O)N4C6=C2C=CC=C6O)OCC7C(C1)(C5(CC3=O)O)O7 412.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
(1S,6R,8R,11R,23S,24R,25S)-23-hydroxy-17,18-dimethoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 162919117 Click to see CN1CCC23C4C5C(CC(=O)N4C6=CC(=C(C=C62)OC)OC)OCC7C(C1)(C5(CC3=O)O)O7 456.50 unknown https://doi.org/10.1055/S-0028-1097317
https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/0040-4020(73)80248-0
(1S,6R,8R,11R,23S,24R,25S)-23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 162948791 Click to see 442.50 unknown https://doi.org/10.1055/S-2000-8559
(1S,6R,8R,11R,23S,24R,25S)-23-hydroxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 163100172 Click to see CN1CCC23C4C5C(CC(=O)N4C6=CC=CC=C62)OCC7C(C1)(C5(CC3=O)O)O7 396.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
(1S,6R,8R,11S,23S,24R,25S)-23-hydroxy-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 22296849 Click to see 426.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
(1S,6R,8R,23R,24R,25S)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-11,15(20),16,18-tetraene-13,21-dione 162866784 Click to see CN1CCC23C4C5C(CC2=O)C6(C1)C(O6)COC5=CC(=O)N4C7=C3C=CC=C7OC 408.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(1S,6R,8R,23S,24S,25S)-16,23-dihydroxy-17-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-11,15(20),16,18-tetraene-13,21-dione 162974798 Click to see 440.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.11.004
(4aS,6aS,12aS,12bR,12cS)-4a-hydroxy-15-methyl-4a,5,12,12a,12b,12c-hexahydro-11H-6a,4-(ethanoiminomethano)-1-oxa-10b-azacyclohepta[1,2,3-cd]fluoranthene-6,11(2H)-dione 21723447 Click to see 380.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
11a-Hydroxy-7,8-dimethoxy-13-methyl-1a,2,3a,4,9c,9d,11,11a-octahydro-5h,10h-9b,11b-(ethanoiminomethano)-1,3-dioxa-5a-azacyclopropa[4,5]cyclohepta[1,2,3-cd]fluoranthene-5,10-dione 186067 Click to see CN1CCC23C4C5C(CC(=O)N4C6=CC(=C(C=C62)OC)OC)OCC7C(C1)(C5(CC3=O)O)O7 456.50 unknown https://doi.org/10.1055/S-0028-1097317
https://doi.org/10.1016/J.PHYTOL.2011.11.004
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/0040-4020(73)80248-0
15-Hydroxy-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,14(19),15,17-tetraene-12,20-dione 162852572 Click to see 366.40 unknown https://doi.org/10.1055/S-2000-8559
16-Hydroxy-17-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162932554 Click to see 426.50 unknown https://doi.org/10.1016/0040-4020(73)80248-0
16,17-Dimethoxy-4-methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,14,16,18-tetraene-12,20-dione 12314413 Click to see CN1CCC23C4C5C(CC2=O)C(=CCOC5CC(=O)N4C6=CC(=C(C=C36)OC)OC)C1 424.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
16,19-Secostrychnidine-10,16-dione, 14-hydroxy-19-methyl- 210990 Click to see 380.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
16,19-Secostrychnidine-10,16-dione, 21,22-epoxy-21,22-dihydro-14-hydroxy-19-methyl-, (21alpha,22alpha)- 633892 Click to see 396.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
16,19-Secostrychnidine-10,16-dione, 21,22-epoxy-21,22-dihydro-14-hydroxy-4-methoxy-19-methyl-, (21alpha,22alpha)- 634646 Click to see 426.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
16,19-Secostrychnidine-10,16-dione, 21,22-epoxy-21,22-dihydro-3,4-dimethoxy-19-methyl-, (21alpha,22alpha)- 634910 Click to see 440.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
16,19-Secostrychnidine-10,16-dione, 21,22-epoxy-21,22-dihydro-4-methoxy-19-methyl-, (21alpha,22alpha)- 634298 Click to see CN1CCC23C4C5C(CC2=O)C6(C1)C(O6)COC5CC(=O)N4C7=C3C=CC=C7OC 410.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
16,19-Secostrychnidine-10,16-dione, 21,22-epoxy-21,22-dihydro-4,14-dihydroxy-3-methoxy-19-methyl-, (21alpha,22alpha)- 634942 Click to see CN1CCC23C4C5C(CC(=O)N4C6=C2C=CC(=C6O)OC)OCC7C(C1)(C5(CC3=O)O)O7 442.50 unknown https://doi.org/10.1016/S0031-9422(00)88859-7
16,23-Dihydroxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162953009 Click to see CN1CCC23C4C5C(CC(=O)N4C6=C2C=CC=C6O)OCC7C(C1)(C5(CC3=O)O)O7 412.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
17,18-Dimethoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 73823636 Click to see 440.50 unknown https://doi.org/10.1055/S-0028-1097317
https://doi.org/10.1016/S0040-4039(00)89564-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/0040-4020(73)80248-0
17,18-Dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 163084245 Click to see COC1=C(C=C2C(=C1)C34CCNCC56C(CC3=O)C7C4N2C(=O)CC7OCC5O6)OC 426.50 unknown https://doi.org/10.1055/S-2000-8559
18-Methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15(20),16,18-triene-13,21-dione 162947529 Click to see 410.50 unknown https://doi.org/10.1016/0040-4020(73)80248-0
23-Hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[12.6.5.01,25.06,8.06,23.011,24.015,20]pentacosa-15,17,19-triene-13,21-dione 162948790 Click to see COC1=C(C=C2C(=C1)C34CCNCC56C(O5)COC7CC(=O)N2C3C7C6(CC4=O)O)OC 442.50 unknown https://doi.org/10.1055/S-2000-8559
4-Methyl-9-oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,14,16,18-tetraene-12,20-dione 278384 Click to see CN1CCC23C4C5C(CC2=O)C(=CCOC5CC(=O)N4C6=CC=CC=C36)C1 364.40 unknown https://doi.org/10.1055/S-0028-1097317
https://doi.org/10.1016/S0031-9422(02)00612-X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/0040-4020(73)80248-0
9-Oxa-4,13-diazahexacyclo[11.6.5.01,24.06,22.010,23.014,19]tetracosa-6,14,16,18-tetraene-12,20-dione 163021542 Click to see 350.40 unknown https://doi.org/10.1055/S-2000-8559
Icajine 3083907 Click to see 364.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1016/0040-4020(73)80248-0
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-2000-8559
https://doi.org/10.1055/S-0028-1097317
Novacine 12314414 Click to see 424.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
Strychnicine 633307 Click to see 380.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/0040-4020(73)80248-0
Vomicine 101595 Click to see CN1CCC23C4C5C(CC2=O)C(=CCOC5CC(=O)N4C6=C3C=CC=C6O)C1 380.40 unknown https://doi.org/10.1016/S0031-9422(02)00612-X
https://doi.org/10.1016/0040-4020(73)80248-0
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-2000-8559
Vomicine, 21,22-dihydro-21-alpha,22-alpha-epoxy- 210989 Click to see 396.40 unknown https://doi.org/10.1016/0040-4020(73)80248-0
> Phenylpropanoids and polyketides / Macrolides and analogues / Milbemycins
(1R,4S,5'S,6R,6'R,8R,10E,12S,13S,14Z,16Z,20R,21R,24S)-6'-ethyl-21,24-dihydroxy-12-[(2R,4S,5S,6S)-5-[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5',11,13,22-tetramethylspiro[3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6,2'-oxane]-2-one 132472909 Click to see CCC1C(CCC2(O1)CC3CC(O2)CC=C(C(C(C=CC=C4COC5C4(C(C=C(C5O)C)C(=O)O3)O)C)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)O)OC)OC)C)C 847.00 unknown https://doi.org/10.1055/S-2000-8559

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.