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Triclisia gilletii

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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
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Details Top

Internal ID UUID643ffec47b93e747105070
Scientific name Triclisia gilletii
Authority (De Wild.) Staner
First published in Bull. Inst. Roy. Congo Belg. 4: 430 (1933)

Description Top

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Synonyms Top

Scientific name Authority First published in
Triclisia flava Exell J. Bot. 64(Suppl.): 12 (1926)
Tiliacora gilletii De Wild. Bull. Jard. Bot. État Bruxelles 3: 255 (1911)

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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-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000456505
Tropicos 20600275
KEW urn:lsid:ipni.org:names:581668-1
The Plant List kew-2516835
Open Tree Of Life 7591038
IPNI 581668-1
iNaturalist 186665
GBIF 3829906

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)!
Title Authors Publication Released IDs
Gilletine, a New Bisbenzylisoquinoline Alkaloid from Triclisia gilletii Paul L. Schiff, Jr., Daniel Dwuma-Badu, John S. K. Ayim, Albert N. Tackie, Philip D. Owusu, Joseph E. Knapp, David J. Slatkin The Japan Institute of Heterocyclic Chemistry 27-Mar-2009
doi:10.3987/R-1978-08-0995
Trigilletimine: A newBisbenzylisoquinoline alkaloid fromTriclisia species D. Dwuma-Badu, J. S. K. Ayim, A. N. Tackie, M. A. El Sohly, J. E. Knapp, D. J. Slatkin, P. L. Schiff Springer Science and Business Media LLC 27-Jul-2005
doi:10.1007/BF01945760
Constituents of West African Medicinal Plants. XXVIII. Additional Alkaloids of Triclisia gilletti P. D. Owusu, D. J. Slatkin, J. E. Knapp, P. L. Schiff American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50013A011
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

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
(1R,14S,15S)-9,20-dimethoxy-15-methyl-15-oxido-7,23,33-trioxa-30-aza-15-azoniaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaen-25-ol 163186339 Click to see C[N+]1(CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O3)C(=C(C=C8CCN7)O)O4)C=C6)OC)[O-] 594.70 unknown https://doi.org/10.3987/R-1978-08-0995
(1R,14S)-9,20-dimethoxy-15-methyl-15-oxido-7,23,33-trioxa-30-aza-15-azoniaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaen-25-ol 163187973 Click to see C[N+]1(CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O3)C(=C(C=C8CCN7)O)O4)C=C6)OC)[O-] 594.70 unknown https://doi.org/10.3987/R-1978-08-0995
(1S,14S)-9,20-dimethoxy-15-methyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaen-25-ol 102090441 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O3)C(=C(C=C8CCN7)O)O4)C=C6)OC 578.70 unknown https://doi.org/10.3987/R-1978-08-0995
27-Methoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol 10099394 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)OC 562.70 unknown https://doi.org/10.1016/0031-9422(73)80465-0
Alkaloid TGL 4,from Triclisia gilletii 99954 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O3)C(=C(C=C8CCN7)O)O4)C=C6)OC 578.70 unknown https://doi.org/10.1021/NP50013A011
https://doi.org/10.3987/R-1978-08-0995
Obamegine 441064 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown https://doi.org/10.3987/R-1978-08-0995
https://doi.org/10.1021/NP50013A011
Oxyacanthan-12'-ol, 6',7-epoxy-6-methoxy-2,2'-dimethyl-, (1'alpha)- 21579625 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)OC 562.70 unknown https://doi.org/10.1016/0031-9422(73)80465-0
Stebisimine 3083913 Click to see COC1=C2C=C(CC3=NCCC4=CC(=C(C=C43)OC5=C6C(=CC(=C5OC)OC)CCN=C6CC7=CC=C(O2)C=C7)OC)C=C1 590.70 unknown https://doi.org/10.1021/NP50013A011
> Organoheterocyclic compounds / Benzodioxins / Benzo-p-dioxins / Dibenzo-p-dioxins
Alkaloid TGS 1 179594 Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7=NC=CC8=CC(=C(O3)C(=C78)O4)OC)C=C6 558.60 unknown https://doi.org/10.1007/BF01945760

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