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Internal ID UUID643fee7eb068c547101149
Scientific name Tabernaemontana eglandulosa
Authority Stapf
First published in Bull. Misc. Inform. Kew 1894: 24 (1894)

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Synonyms Top

Scientific name Authority First published in
Tabernaemontana brachypoda K.Schum. Bot. Jahrb. Syst. 23: 223 (1896)
Tabernaemontana chartacea Pichon Notul. Syst. (Paris) 13: 253 (1948)
Tabernaemontana crispiflora K.Schum. Nat. Pflanzenfam. 4(2): 148 (1895)
Gabunia brachypoda Stapf Fl. Trop. Afr. 4(1): 137 (1902)
Gabunia crispiflora Stapf Fl. Trop. Afr. 4(1): 139 (1902)
Gabunia eglandulosa Stapf Fl. Trop. Afr. 4(1): 138 (1902)
Gabunia eglandulosa var. macrocalyx Stapf Fl. Trop. Afr. 4(1): 138 1902
Gabunia latifolia Stapf Fl. Trop. Afr. 4(1): 137 (1902)
Gabunia longiflora Stapf Fl. Trop. Afr. 4(1): 138 (1902)
Gabunia macrocalyx (Stapf) Boiteau Bull. Mus. Natl. Hist. Nat., B, Adansonia 1981: 224 (1981)
Gabunia macrocarpa Boiteau Bull. Mus. Natl. Hist. Nat., B, Adansonia 1981: 224 (1981)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Nigeria
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000319845
Tropicos 1800046
KEW urn:lsid:ipni.org:names:82107-1
The Plant List kew-200684
Open Tree Of Life 312297
NCBI Taxonomy 761067
IPNI 82107-1
GBIF 3617625
Freebase /m/012dtdpm
Wikipedia Tabernaemontana_eglandulosa

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Recent Advances in the Synthesis of β-Carboline Alkaloids Szabó T, Volk B, Milen M Molecules 27-Jan-2021
PMCID:PMC7866041
doi:10.3390/molecules26030663
PMID:33513936
Study on the total synthesis of velbanamine: Chemoselective dioxygenation of alkenes with PIFA via a stop-and-flow strategy Liu H, Zheng K, Lu X, Wang X, Hong R Beilstein J Org Chem 23-May-2013
PMCID:PMC3678578
doi:10.3762/bjoc.9.113
PMID:23766815
Identification of Novel Human Dipeptidyl Peptidase-IV Inhibitors of Natural Origin (Part II): In Silico Prediction in Antidiabetic Extracts Guasch L, Sala E, Ojeda MJ, Valls C, Bladé C, Mulero M, Blay M, Ardévol A, Garcia-Vallvé S, Pujadas G PLoS One 21-Sep-2012
PMCID:PMC3448616
doi:10.1371/journal.pone.0044972
PMID:23028712
Alkaloids of Tabernaemontana eglandulosa Teris A. Van Beek, Robert Verpoorte, Anders Baerheim Svendsen Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)91102-0
Dichomine, a novel type of iboga alkaloid*,**. Perera P, van Beek TA, Verpoorte R Planta Med 01-Dec-1983
doi:10.1055/S-2007-969857
PMID:17405059
Alkaloid studies. 8. Isolation and characterization of alkaloids of Tabernaemontana heyneana Wall and antifertility properties of coronaridine. Meyer WE, Coppola JA, Goldman L J Pharm Sci 01-Jul-1973
doi:10.1002/JPS.2600620733
PMID:4714135

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
> Alkaloids and derivatives / Ibogan-type alkaloids
(1R,15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene 51055165 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
11-Hydroxycoronaridine 44566751 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)O)C(=O)OC 354.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
6,9-Methano-5H-pyrido[1',2':1,2]azepino[4,5-b]indole, 7-ethyl-6,6a,7,8,9,10,12,13-octahydro-, [6R-(6alpha,6abeta,7beta,9alpha)]- 500053 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
Ibogamine-18-carboxylic acid, 13-hydroxy-, methyl ester 156675 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)O)C(=O)OC 354.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 137628478 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
> Alkaloids and derivatives / Plumeran-type alkaloids
(1S,12S,14S,19R)-14-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,8-tetraen-14-ol 163090373 Click to see CCC1(CC2CCC3=NC4=CC=CC=C4C35C2N(C1)CC5)O 296.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (1R,12S,14S,19S)-14-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 10593117 Click to see CCC1CC2CC(=C3C4(C2N(C1)CC4)C5=CC=CC=C5N3)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (1S,12R,14R,19R)-14-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 13018303 Click to see CCC1CC2CC(=C3C4(C2N(C1)CC4)C5=CC=CC=C5N3)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
> Alkaloids and derivatives / Quebrachamine alkaloids
Voaphylline 10469868 Click to see CCC12CCC3=C(CCN(C1)CC4C2O4)C5=CC=CC=C5N3 296.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
> Alkaloids and derivatives / Strychnos alkaloids
Dihydrocondylocarpine 100004 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (1S,17R,18S)-18-ethyl-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 134716702 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
Norfluorocurarine 5581319 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C=O 292.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
> Alkaloids and derivatives / Tacaman alkaloids
(13R,15R,17R,19R)-13-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-ol 162876613 Click to see CCC1CC2CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)O 296.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
(13R,15R,17S,19R)-13-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-ol 162876614 Click to see CCC1CC2CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)O 296.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
(13R,15S,16S,19R)-13-ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-one 10924954 Click to see CCC1CC2C3C4=C(CCN3C1)C5=CC=CC=C5N4C(=O)C2O 310.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
13-Ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-one 85317663 Click to see CCC1CC2C3C4=C(CCN3C1)C5=CC=CC=C5N4C(=O)C2O 310.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (13R,15R,17R,19R)-13-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate 11024649 Click to see CCC1CC2CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)(C(=O)OC)O 354.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (13R,15R,17R,19R)-17-hydroxy-13-[(1S)-1-hydroxyethyl]-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate 11089992 Click to see CC(C1CC2CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)(C(=O)OC)O)O 370.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (13R,15R,17S,19R)-13-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate 21724535 Click to see CCC1CC2CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)(C(=O)OC)O 354.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
methyl (13R,15R,19R)-13-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate 11142284 Click to see CCC1CC2C=C(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)C(=O)OC 336.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
Methyl 13-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate 73810576 Click to see CCC1CC2CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)(C(=O)OC)O 354.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
Tacamonine 9971698 Click to see CCC1CC2CC(=O)N3C4=CC=CC=C4C5=C3C2N(C1)CC5 294.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(15R,17R)-17-ethyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraene 101749635 Click to see CCC1CC2CCC3=C(CCN(C2)C1)C4=CC=CC=C4N3 282.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
(15R,17S)-17-ethyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraene 101749634 Click to see CCC1CC2CCC3=C(CCN(C2)C1)C4=CC=CC=C4N3 282.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
> Organoheterocyclic compounds / Indolizidines
(1S,9R,13R,14R,16S)-14-ethyl-19-oxa-2,12-diazahexacyclo[12.4.1.112,16.01,9.03,8.09,13]icosa-3,5,7-triene 163105848 Click to see CCC12CC3CCC4(O1)C5(C2N(C3)CC5)C6=CC=CC=C6N4 296.40 unknown https://doi.org/10.1016/S0040-4020(01)91102-0
Dichomine 5491776 Click to see CCC12CC3CCC4(O1)C5(C2N(C3)CC5)C6=CC=CC=C6N4 296.40 unknown https://doi.org/10.1055/S-2007-969857
> Organoheterocyclic compounds / Quinolizidines
methyl (1'S,2R,7'R,8'R,9'R)-9'-ethyl-5-methoxy-3-oxospiro[1H-indole-2,6'-3-azatricyclo[5.3.1.03,8]undecane]-7'-carboxylate 101593056 Click to see CCC1CC2CC3(C1N(C2)CCC34C(=O)C5=C(N4)C=CC(=C5)OC)C(=O)OC 384.50 unknown https://doi.org/10.1002/JPS.2600620733

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