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Triphyophyllum peltatum

Triphyophyllum peltatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440540489ed2664186140
Scientific name Triphyophyllum peltatum
Authority (Hutch. & Dalziel) Airy Shaw
First published in Kew Bull. 7: 342 (1952)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Spanish dioncophyllum peltatum
German dreifaltigblatt
German hakenblatt
Estonian Õgiköis
Persian سهگونبرگ
Italian dioncophyllum peltatum
Italian ouratea glomerata
Japanese トリフィオフィルム・ペルタトゥム
Chinese 盾籽穗葉藤
Chinese 穗叶藤属
Chinese 穗葉藤屬
Chinese 露松藤

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
    • West Tropical Africa
      • Guinea
      • Ivory Coast
      • Liberia
      • Sierra Leone

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001224123
Tropicos 50040755
KEW urn:lsid:ipni.org:names:317595-1
The Plant List tro-50040755
Open Tree Of Life 416255
NCBI Taxonomy 63090
IPNI 317595-1
iNaturalist 317889
GBIF 4161362
Freebase /m/03kbg2
EOL 6875223
USDA GRIN 417582
Wikipedia Triphyophyllum

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
Recent advances in research on phosphate starvation signaling in plants Puga MI, Poza-Carrión C, Martinez-Hevia I, Perez-Liens L, Paz-Ares J J Plant Res 26-Apr-2024
PMCID:PMC11081996
doi:10.1007/s10265-024-01545-0
PMID:38668956
Naphthylisoquinoline alkaloids: novel agents against the causative pathogens of eumycetoma and actinomycetoma—en route to broad-spectrum antimycetomal drugs Khalid SA, Abd Algaffar S, Tajuddeen N, Lombe BK, Bringmann G Antimicrob Agents Chemother 11-Apr-2024
PMCID:PMC11064494
doi:10.1128/aac.01612-23
PMID:38602413
Distinctive plastome evolution in carnivorous angiosperms Fu CN, Wicke S, Zhu AD, Li DZ, Gao LM BMC Plant Biol 20-Dec-2023
PMCID:PMC10731798
doi:10.1186/s12870-023-04682-1
PMID:38124058
Phytochemicals as Immunomodulatory Molecules in Cancer Therapeutics Paudel S, Mishra N, Agarwal R Pharmaceuticals (Basel) 26-Nov-2023
PMCID:PMC10746110
doi:10.3390/ph16121652
PMID:38139779
Differences in the Occurrence of Cell Wall Components between Distinct Cell Types in Glands of Drosophyllum lusitanicum Płachno BJ, Kapusta M, Stolarczyk P, Świątek P, Lichtscheidl I Int J Mol Sci 10-Oct-2023
PMCID:PMC10606540
doi:10.3390/ijms242015045
PMID:37894725
Ancistrocladinium A Induces Apoptosis in Proteasome Inhibitor-Resistant Multiple Myeloma Cells: A Promising Therapeutic Agent Candidate Brünnert D, Seupel R, Goyal P, Bach M, Schraud H, Kirner S, Köster E, Feineis D, Bargou RC, Schlosser A, Bringmann G, Chatterjee M Pharmaceuticals (Basel) 18-Aug-2023
PMCID:PMC10459547
doi:10.3390/ph16081181
PMID:37631095
Biological Potential of Carnivorous Plants from Nepenthales Wójciak M, Feldo M, Stolarczyk P, Płachno BJ Molecules 21-Apr-2023
PMCID:PMC10146735
doi:10.3390/molecules28083639
PMID:37110873
Defensive functions and potential ecological conflicts of floral stickiness Chautá A, Kumar A, Mejia J, Stashenko EE, Kessler A Sci Rep 18-Nov-2022
PMCID:PMC9674602
doi:10.1038/s41598-022-23261-2
PMID:36400941
Demystifying racemic natural products in the homochiral world Bitchagno GT, Nchiozem-Ngnitedem VA, Melchert D, Fobofou SA Nat Rev Chem 14-Oct-2022
PMCID:PMC9562063
doi:10.1038/s41570-022-00431-4
PMID:36259059
Naphthylisoindolinone alkaloids: the first ring-contracted naphthylisoquinolines, from the tropical liana Ancistrocladus abbreviatus, with cytotoxic activity Fayez S, Bruhn T, Feineis D, Assi LA, Kushwaha PP, Kumar S, Bringmann G RSC Adv 12-Oct-2022
PMCID:PMC9555057
doi:10.1039/d2ra05758a
PMID:36320727
Potential of Triterpenic Natural Compound Betulinic Acid for Neglected Tropical Diseases New Treatments Rocha V, Quadros H, Meira C, Silva L, Carvalho D, Hodel K, Moreira D, Soares M Biomedicines 01-Apr-2022
PMCID:PMC9027248
doi:10.3390/biomedicines10040831
PMID:35453582
Carnivorous Nepenthes x ventrata plants use a naphthoquinone as phytoanticipin against herbivory Dávila-Lara A, Rahman-Soad A, Reichelt M, Mithöfer A PLoS One 22-Oct-2021
PMCID:PMC8535358
doi:10.1371/journal.pone.0258235
PMID:34679089
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782
Betulinic acid induces autophagy-dependent apoptosis via Bmi-1/ROS/AMPK-mTOR-ULK1 axis in human bladder cancer cells Zhang Y, He N, Zhou X, Wang F, Cai H, Huang SH, Chen X, Hu Z, Jin X Aging (Albany NY) 12-Sep-2021
PMCID:PMC8457576
doi:10.18632/aging.203441
PMID:34510030
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

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Naphthalenes / Naphthoquinones
Droserone 442739 Click to see CC1=C(C2=C(C(=CC=C2)O)C(=O)C1=O)O 204.18 unknown https://doi.org/10.1016/S0031-9422(99)00543-9
Plumbagin 10205 Click to see CC1=CC(=O)C2=C(C1=O)C=CC=C2O 188.18 unknown https://doi.org/10.1016/S0031-9422(99)00543-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
[(1R,2S,3S,4S,5S,8R,9S,10R,11R,14R,16S,17R,18R,19R)-2,19-diacetyloxy-3-hydroxy-5-methyl-12-methylidene-4-(2-methylpropanoyloxy)-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-10-yl] benzoate 163104266 Click to see CC(C)C(=O)OC1C(C(C23C4C1(CN5C4CC67C2C(C(C(C6C35)OC(=O)C8=CC=CC=C8)C(=C)C7)OC(=O)C)C)OC(=O)C)O 619.70 unknown https://doi.org/10.1016/0031-9422(91)80135-N
https://doi.org/10.1016/S0031-9422(00)86875-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5R)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101918991 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)O)O)O)OC9C(C(C(CO9)O)O)O 1045.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 76141271 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/S0031-9422(99)00543-9
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-2006-957666
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-2006-957666
> Organoheterocyclic compounds / Azolidines / Oxazolidines
DL-Goitrin 3034683 Click to see C=CC1CNC(=S)O1 129.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
2-amino-7-hydroxy-3H-purin-6-one 73069 Click to see C1=NC2=C(N1O)C(=O)N=C(N2)N 167.13 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R,4R)-7-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-4,8-diol 10667425 Click to see CC1C(C2=C(C(N1)C)C(=C(C=C2)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)O)O 379.40 unknown https://doi.org/10.3987/COM-97-S(N)62
(1R,3R)-7-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 9799110 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)O 363.40 unknown https://doi.org/10.1016/S0031-9422(98)00070-3
(1R,3R)-7-[2-(hydroxymethyl)-4,5-dimethoxynaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 156696 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)OC)O 393.50 unknown https://doi.org/10.1016/S0031-9422(02)00547-2
(1R,3S)-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 162863866 Click to see CC1CC2=C(C=CC(=C2C(N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)O 363.40 unknown https://doi.org/10.1016/S0031-9422(00)97576-9
(1S,3R)-7-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 163076801 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)O)O 363.40 unknown https://doi.org/10.3987/COM-97-S(N)62
(1S,3R)-7-[5-hydroxy-2-(hydroxymethyl)-4-methoxynaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 162931708 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1016/0031-9422(91)84235-K
(1S,3S)-7-[2-(hydroxymethyl)-4,5-dimethoxynaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 163094318 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)OC)O 393.50 unknown https://doi.org/10.1016/S0031-9422(02)00547-2
(1S)-5-[3-[4-[(1S)-6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol 5459215 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O 756.90 unknown https://doi.org/10.1006/ABBI.1997.0494
(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375943 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1016/S0031-9422(00)86875-2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164157/
https://doi.org/10.1007/S004360050318
https://doi.org/10.1021/AC061526Q
(3R)-7-[5-hydroxy-2-(hydroxymethyl)-4-methoxynaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375947 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1016/S0031-9422(00)86875-2
https://doi.org/10.1016/0031-9422(91)84235-K
5-(5-Hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 3956689 Click to see CC1CC2=C(C=CC(=C2C(N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)O 363.40 unknown https://doi.org/10.1016/S0031-9422(00)97576-9
7-(1-Hydroxy-8-methoxy-6-methylnaphthalen-2-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-4,8-diol 78183236 Click to see CC1C(C2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)O)O 379.40 unknown https://doi.org/10.1016/S0031-9422(00)00107-2
7-(1-Hydroxy-8-methoxy-6-methylnaphthalen-2-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-4-ol 85242743 Click to see CC1C(C2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)OC)O 393.50 unknown https://doi.org/10.1016/S0031-9422(00)00107-2
7-(4-Hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-4,8-diol 85225421 Click to see CC1C(C2=C(C(N1)C)C(=C(C=C2)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)O)O 379.40 unknown https://doi.org/10.3987/COM-97-S(N)62
8-Methoxy-2-(8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-6-methylnaphthalen-1-ol 85189748 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)OC 377.50 unknown https://doi.org/10.1016/S0031-9422(00)00107-2
8-methoxy-2-[(1S,3R)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl]-6-methylnaphthalen-1-ol 10571649 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)OC 377.50 unknown https://doi.org/10.1016/S0031-9422(00)00107-2
8-Methoxy-4-(8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-6-methylnaphthalen-1-ol 85064929 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)OC 377.50 unknown https://doi.org/10.1016/S0031-9422(98)00070-3
8-methoxy-4-[(1R,3R)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl]-6-methylnaphthalen-1-ol 9907741 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)OC 377.50 unknown https://doi.org/10.1016/S0031-9422(98)00070-3
8-methoxy-5-[(1R,3R)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl]-6-methylnaphthalen-1-ol 59095071 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)O)OC 377.50 unknown https://doi.org/10.1016/S0031-9422(00)90491-6
8-O-Methyldioncophyllinol B 10715588 Click to see CC1C(C2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)OC)O 393.50 unknown https://doi.org/10.1016/S0031-9422(00)00107-2
CID 21123501 21123501 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)OC)O 393.50 unknown https://doi.org/10.1016/S0031-9422(02)00547-2
Dioncopeltin a 631460 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1016/0031-9422(91)84235-K
Dioncopeltine A 185971 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1016/0031-9422(91)84235-K
https://doi.org/10.1016/S0031-9422(00)86875-2
Dioncophyllacine A 375955 Click to see CC1=CC(=C2C(=C1C3=C(C4=C(N=C(C(=C4C=C3)OC)C)C)OC)C=CC=C2OC)OC 417.50 unknown https://doi.org/10.1055/S-2006-960376
Dioncophyllin A 3095 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1021/AC061526Q
Dioncophyllin b 631573 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)O 363.40 unknown https://doi.org/10.1055/S-2006-957970
https://doi.org/10.1016/0031-9422(91)80135-N
Dioncophyllin d 631577 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)O 363.40 unknown https://doi.org/10.1016/S0031-9422(98)00070-3
Dioncophylline A 443773 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1016/S0031-9422(00)86875-2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164157/
https://doi.org/10.1007/S004360050318
Dioncophylline B 178558 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)O 363.40 unknown https://doi.org/10.1016/S0031-9422(00)86875-2
https://doi.org/10.1055/S-2006-957970
https://doi.org/10.1016/0031-9422(91)80135-N
Dioncophylline C 443774 Click to see CC1CC2=C(C=CC(=C2C(N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)O 363.40 unknown https://doi.org/10.1016/S0031-9422(00)97576-9
Dioncophyllinol B 443775 Click to see CC1C(C2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)O)O 379.40 unknown https://doi.org/10.1016/S0031-9422(00)00107-2
> Organoheterocyclic compounds / Naphthopyrans
(16R,18R)-7-hydroxy-9-methoxy-16,18-dimethyl-13-oxa-17-azapentacyclo[12.8.0.02,11.03,8.015,20]docosa-1(14),2,4,6,8,10,15(20),21-octaen-12-one 10362108 Click to see CC1CC2=C(C(N1)C)C3=C(C=C2)C4=C5C=CC=C(C5=C(C=C4C(=O)O3)OC)O 375.40 unknown https://doi.org/10.1016/0031-9422(91)84235-K
7-Hydroxy-9-methoxy-16,18-dimethyl-13-oxa-17-azapentacyclo[12.8.0.02,11.03,8.015,20]docosa-1(14),2,4,6,8,10,15(20),21-octaen-12-one 375946 Click to see CC1CC2=C(C(N1)C)C3=C(C=C2)C4=C5C=CC=C(C5=C(C=C4C(=O)O3)OC)O 375.40 unknown https://doi.org/10.1016/0031-9422(91)84235-K

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