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Triclisia subcordata

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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 UUID643ffec428158636151534
Scientific name Triclisia subcordata
Authority Oliv.
First published in Fl. Trop. Afr. 1: 49 (1868)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tiliacora subcordata (Oliv.) A.Chev. Explor. Bot. Afrique Occ. Franç. 1: 17 (1920)
Triclisia dielsii Hutch. & Dalziel ex Exell J. Bot. 64(Suppl. 1): 13, in obs., nomen. 1926 ; Hutchinson & Dalziel in Kew Bull. 1927, 155. descr.

Common names Top

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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
  • Africa
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Ivory Coast
      • Nigeria
      • Togo

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000456503
Tropicos 20600277
KEW urn:lsid:ipni.org:names:581682-1
The Plant List kew-2516833
Open Tree Of Life 1051373
NCBI Taxonomy 461646
IPNI 581682-1
iNaturalist 506929
GBIF 3829770
EOL 5518251
CMAUP NPO10447

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
First report on the presence of huanglongbing vectors (Diaphorina citri and Trioza erytreae) in Ghana Aidoo OF, Ablormeti FK, Ninsin KD, Antwi-Agyakwa AK, Osei-Owusu J, Heve WK, Dofuor AK, Soto YL, Edusei G, Osabutey AF, Sossah FL, Aryee CO, Alabi OJ, Sétamou M Sci Rep 13-Jul-2023
PMCID:PMC10344884
doi:10.1038/s41598-023-37625-9
PMID:37443168
The Role of Natural and Semi-Synthetic Compounds in Ovarian Cancer: Updates on Mechanisms of Action, Current Trends and Perspectives Islam MR, Rahman MM, Dhar PS, Nowrin FT, Sultana N, Akter M, Rauf A, Khalil AA, Gianoncelli A, Ribaudo G Molecules 22-Feb-2023
PMCID:PMC10004182
doi:10.3390/molecules28052070
PMID:36903316
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Which Plants for What Ailments: A Quantitative Analysis of Medicinal Ethnobotany of Ile-Ife, Osun State, Southwestern Nigeria Mukaila YO, Oladipo OT, Ogunlowo I, Ajao AA, Sabiu S Evid Based Complement Alternat Med 03-Aug-2021
PMCID:PMC8355999
doi:10.1155/2021/5711547
PMID:34394387
In Vivo Efficacy and Metabolism of the Antimalarial Cycleanine and Improved In Vitro Antiplasmodial Activity of Semisynthetic Analogues Uche FI, Guo X, Okokon J, Ullah I, Horrocks P, Boateng J, Huang C, Li WW Antimicrob Agents Chemother 20-Jan-2021
PMCID:PMC7848973
doi:10.1128/AAC.01995-20
PMID:33257443
Emerging Cytotoxic Alkaloids in the Battle against Cancer: Overview of Molecular Mechanisms Habli Z, Toumieh G, Fatfat M, Rahal ON, Gali-Muhtasib H Molecules 08-Feb-2017
PMCID:PMC6155614
doi:10.3390/molecules22020250
PMID:28208712
Trigilletine and tricordatine: Two new bisbenzylisoquinoline alkaloids from Triclisia species Albert N. Tackie, D. Dwuma-Badu, Temple Okarter, Joseph E. Knapp, David J. Slatkin, Paul L. Schiff Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)80465-0
Additional alkaloids of Triclisia patens and Triclisia subcordata D. Dwuma-Badu, J.S.K. Ayim, A.N. Tackie, J.E. Knapp, D.J. Slatkin, P.L. Schiff Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)80390-6

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
> Lignans, neolignans and related compounds
(+)-Tricordatine 44559017 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)O 548.60 unknown https://doi.org/10.1016/0031-9422(73)80465-0
Isotetrandrine 5422 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1016/0031-9422(75)80390-6
Macolidine 5320261 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)O)OC 594.70 unknown https://doi.org/10.1016/0031-9422(75)80390-6
Tricordatine 301928 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)O 548.60 unknown https://doi.org/10.1016/0031-9422(73)80465-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Kaempferol-3-O-rutinoside 5318767 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)O)O)O)O)O 594.50 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Isorhamnetin 3-glucoside-7-rhamnoside 72188972 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 624.50 unknown via CMAUP database
Robinin 5281693 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 14057197 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Melilitocarpan B 23259931 Click to see COC1=C(C2=C(C=C1)C3C(CO2)C4=C(O3)C=C(C=C4)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(3-hydroxy-2,4-dimethoxyphenyl)-, (3R)- 13873811 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O 302.32 unknown via CMAUP database
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown via CMAUP database
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
4',7-Dimethoxyisoflavone 136419 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(2,3-dimethoxyphenyl)prop-2-en-1-one 622927 Click to see COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2)O)O 300.30 unknown via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one 165210 Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)OC 300.30 unknown via CMAUP database
2',4'-Dihydroxy-4-methoxychalcone 5711223 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 270.28 unknown via CMAUP database
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 193568 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown via CMAUP database

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