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Dioncophyllum thollonii

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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 UUID64401729b456f595474681
Scientific name Dioncophyllum thollonii
Authority Baill.
First published in Bull. Mens. Soc. Linn. Paris 2: 870 (1890)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Japanese ディオンコフィルム・トロニイ
Chinese 托倫雙鉤葉
Chinese 雙鉤葉屬
Chinese 双钩叶属
Chinese 雙鈎葉屬

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000648032
Tropicos 3800013
KEW urn:lsid:ipni.org:names:111557-1
The Plant List kew-2768927
Open Tree Of Life 992157
NCBI Taxonomy 122299
IPNI 111557-1
iNaturalist 317897
GBIF 4161357
EPPO DNKTH
EOL 6875218
USDA GRIN 450336
Wikipedia Dioncophyllum_thollonii

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
Proteomics of Salt Gland–Secreted Sap Indicates a Pivotal Role for Vesicle Transport and Energy Metabolism in Plant Salt Secretion Lu C, Zhang Y, Mi P, Guo X, Wen Y, Han G, Wang B Int J Mol Sci 11-Nov-2022
PMCID:PMC9693062
doi:10.3390/ijms232213885
PMID:36430364
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Compounds from African Medicinal Plants with Activities Against Selected Parasitic Diseases: Schistosomiasis, Trypanosomiasis and Leishmaniasis Simoben CV, Ntie-Kang F, Akone SH, Sippl W Nat Prod Bioprospect 09-May-2018
PMCID:PMC5971035
doi:10.1007/s13659-018-0165-y
PMID:29744736
Paliurus Fruits from the Oligocene of South China and Their Phytogeographic Implications Dong JL, Sun BN, Ma FJ, Wang QJ, Jin PH, Wang WJ, Deng P, Yang Y, Li XJ PLoS One 04-Nov-2015
PMCID:PMC4633219
doi:10.1371/journal.pone.0140653
PMID:26536607
The potential of anti-malarial compounds derived from African medicinal plants, part I: a pharmacological evaluation of alkaloids and terpenoids Amoa Onguéné P, Ntie-Kang F, Lifongo LL, Ndom JC, Sippl W, Mbaze LM Malar J 13-Dec-2013
PMCID:PMC3878730
doi:10.1186/1475-2875-12-449
PMID:24330395
Cis- and trans-isoshinanolone from Dioncophyllum thollonii: absolute configuration of two `known', wide-spread natural products1Part 127 in the series `Acetogenic isoquinoline alkaloids'. For part 126, see Bringmann et al., submitted for publication (a).1 Gerhard Bringmann, Miriam Münchbach, Kim Messer, Dagmar Koppler, Manuela Michel, Olaf Schupp, Matthias Wenzel, Adriaan M Louis Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00080-1
Dioncophylline E from Dioncophyllum thollonii, the first 7,3'-coupled dioncophyllaceous naphthylisoquinoline alkaloid. Bringmann G, Messer K, Wolf K, Mühlbacher J, Grüne M, Brun R, Louis AM Phytochemistry 01-Jun-2002
doi:10.1016/S0031-9422(02)00109-7
PMID:12031431
The absolute configuration of (+)-isoshinanolone and in situ LC-CD analysis of its stereoisomers from crude extracts. Bringmann G, Messer K, Saeb W, Peters EM, Peters K Phytochemistry 01-Feb-2001
doi:10.1016/S0031-9422(00)00386-1
PMID:11249107

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
> Benzenoids / Benzene and substituted derivatives / Benzenesulfonyl compounds
Methylthiomethyl phenyl sulfone 643313 Click to see CSCS(=O)(=O)C1=CC=CC=C1 202.30 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
> Benzenoids / Tetralins
(3R,4S)-4,8-dihydroxy-3-methyl-3,4-dihydro-2H-naphthalen-1-one 71423441 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/S0031-9422(99)00080-1
4,8-dihydroxy-3-methyl-3,4-dihydro-2H-naphthalen-1-one 71329296 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/S0031-9422(99)00080-1
Isoshinanolone 443777 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/S0031-9422(00)00386-1
https://doi.org/10.1016/S0031-9422(99)00080-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2S,6R,7S,8R,12R,14S,15S,19S,20R)-7,10-dihydroxy-17-methoxy-7,15,19,20-tetramethyl-3,5,11-trioxapentacyclo[10.7.1.02,6.08,20.014,19]icos-16-en-18-one 101921953 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C5C(C(C4CC(O3)O)(C)O)OCO5)C)C)OC 408.50 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 14844756 Click to see CC1CC2=C(C(N1C)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 391.50 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
(1R,3R)-7-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 10384109 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/10.1016/S0031-9422(02)00109-7
(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(02)00109-7
7-(1-Hydroxy-8-methoxy-3-methylnaphthalen-2-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 22297235 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=CC=C4OC)C=C3C)O)O 363.40 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
7-(5-Hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 85127983 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/10.1016/S0031-9422(02)00109-7
Ancistrocladidine 193880 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 405.50 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
Ancistrotectorine 179169 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 421.50 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
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(02)00109-7
Dioncophylline E 636569 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=CC=C4OC)C=C3C)O)O 363.40 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
N-Methyldioncophyllin a 633164 Click to see CC1CC2=C(C(N1C)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 391.50 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
> Organosulfur compounds / Sulfonyls
2,4,5,7-Tetrathiaoctane 4,4-dioxide 10082131 Click to see CSCSS(=O)(=O)CSC 218.40 unknown https://doi.org/10.1016/S0031-9422(02)00109-7
> Organosulfur compounds / Sulfonyls / Sulfones
Methylsulfanyl(methylsulfanylmethylsulfonyl)methane 15326856 Click to see CSCS(=O)(=O)CSC 186.30 unknown https://doi.org/10.1016/S0031-9422(02)00109-7

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