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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

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
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
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
Recent ecophysiological, biochemical and evolutional insights into plant carnivory Adamec L, Matušíková I, Pavlovič A Ann Bot 10-Jun-2021
PMCID:PMC8389183
doi:10.1093/aob/mcab071
PMID:34111238
Metabolomic analysis reveals reliance on secondary plant metabolites to facilitate carnivory in the Cape sundew, Drosera capensis Hatcher CR, Sommer U, Heaney LM, Millett J Ann Bot 02-Jun-2021
PMCID:PMC8389465
doi:10.1093/aob/mcab065
PMID:34077503
Multiple Myeloma Inhibitory Activity of Plant Natural Products Jöhrer K, Ҫiҫek SS Cancers (Basel) 29-May-2021
PMCID:PMC8198565
doi:10.3390/cancers13112678
PMID:34072312
Therapeutic Potentials of Antiviral Plants Used in Traditional African Medicine With COVID-19 in Focus: A Nigerian Perspective Attah AF, Fagbemi AA, Olubiyi O, Dada-Adegbola H, Oluwadotun A, Elujoba A, Babalola CP Front Pharmacol 26-Apr-2021
PMCID:PMC8108136
doi:10.3389/fphar.2021.596855
PMID:33981214
Alkaloids and flavonoids from African phytochemicals as potential inhibitors of SARS-Cov-2 RNA-dependent RNA polymerase: an in silico perspective Ogunyemi OM, Gyebi GA, Elfiky AA, Afolabi SO, Ogunro OB, Adegunloye AP, Ibrahim IM Antivir Chem Chemother 29-Dec-2020
PMCID:PMC7783895
doi:10.1177/2040206620984076
PMID:33372806
Rapid metabolite response in leaf blade and petiole as a marker for shade avoidance syndrome Sng BJ, Singh GP, Van Vu K, Chua NH, Ram RJ, Jang IC Plant Methods 27-Oct-2020
PMCID:PMC7590806
doi:10.1186/s13007-020-00688-0
PMID:33117429

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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