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Tabernaemontana vanheurckii

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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
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Details Top

Internal ID UUID643fee85da88f428983166
Scientific name Tabernaemontana vanheurckii
Authority Müll.Arg.
First published in Observ. Bot. Descript. Pl. Nov. Herb. Van Heurckiani 2: 168 (1871)

Description Top

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Synonyms Top

Scientific name Authority First published in
Peschiera lingulata Miers Apocyn. S. Amer. : 42 (1878)
Peschiera vanheurckii (Müll.Arg.) L.Allorge Mém. Mus. Natl. Hist. Nat., B, Bot. 30: 154 (1985)
Stenosolen macrosiphon (Herzog) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 14: 177. 1938
Stenosolen vanheurckii (Müll.Arg.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 14: 177 (1938)
Tabernaemontana macrosiphon Herzog Repert. Spec. Nov. Regni Veg. 7: 66 (1909)

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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
  • Southern America
    • Brazil
      • Brazil North
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000320163
Tropicos 1800647
INPN 921109
KEW urn:lsid:ipni.org:names:285821-2
The Plant List kew-200977
Open Tree Of Life 483481
Observations.org 278428
NCBI Taxonomy 761102
IUCN Red List 189173892
IPNI 285821-2
GBIF 3621315
Freebase /m/012dvhb7
Elurikkus 385395
Wikipedia Tabernaemontana_vanheurckii

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
Systematically Significant Indole Alkaloids from Peschiera van heurckii. Tournon J, Gastiger V, Forgacs P, Kan C, Husson HP Planta Med 01-Oct-1994
doi:10.1055/S-2006-959554
PMID:17236078
Isolation of bis-indole alkaloids with antileishmanial and antibacterial activities from Peschiera van heurkii (syn. Tabernaemontana van heurkii). Muñoz V, Moretti C, Sauvain M, Caron C, Porzel A, Massiot G, Richard B, Le Men-Olivier L Planta Med 01-Oct-1994
doi:10.1055/S-2006-959531
PMID:7997477

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 / Aspidospermatan-type alkaloids
Apodine 441984 Click to see COC(=O)C1=C2C3(CCN4C3C5(C1)CC(=O)OC5CC4)C6=CC=CC=C6N2 366.40 unknown https://doi.org/10.1055/S-2006-959531
methyl (1R,12R,14R,16S,22R)-14-hydroxy-15-oxa-8,19-diazahexacyclo[10.9.1.01,9.02,7.012,16.019,22]docosa-2,4,6,9-tetraene-10-carboxylate 12310395 Click to see COC(=O)C1=C2C3(CCN4C3C5(C1)CC(OC5CC4)O)C6=CC=CC=C6N2 368.40 unknown https://doi.org/10.1055/S-2006-959531
> 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/10.1055/S-2006-959554
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/10.1055/S-2006-959554
Conodurine B640243K102 5477056 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1055/S-2006-959531
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1055/S-2006-959531
https://doi.org/10.1055/S-2006-959554
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/10.1055/S-2006-959554
https://doi.org/10.1055/S-2006-959531
methyl (1S,15R,17S,18S)-17-ethyl-6-[(1R,15E,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 137628555 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC 704.90 unknown https://doi.org/10.1055/S-2006-959554
methyl (1S,15R,17S,18S)-17-ethyl-7-[(1S,12R,14R,15Z,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 101603227 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1055/S-2006-959531
methyl (1S,15R,17S,18S)-17-ethyl-8-[(1S,12R,14R,15E,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 102079827 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C(=C(C=C5)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC 704.90 unknown https://doi.org/10.1055/S-2006-959554
methyl (1S,15S,17S,18S)-17-ethyl-5-[(1S,12R,14S,15E)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 134714950 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1055/S-2006-959531
Voacamine 11953931 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC 704.90 unknown https://doi.org/10.1055/S-2006-959554
Voacangarine 328231 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1055/S-2006-959554
Voacristine 196982 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1055/S-2006-959554
> Alkaloids and derivatives / Macroline alkaloids
(+)-Affinisine 5281346 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO 308.40 unknown https://doi.org/10.1055/S-2006-959554
https://doi.org/10.1055/S-2006-959531
[(1S,14R,15Z)-15-ethylidene-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol 101286222 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO 308.40 unknown https://doi.org/10.1055/S-2006-959554
https://doi.org/10.1055/S-2006-959531
methyl (1S,14R,15Z,18S)-15-ethylidene-12-[(1S,14R,15Z)-15-ethylidene-13-(hydroxymethyl)-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-7-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101927008 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)C4=CC5=C(C=C4)N(C6=C5CC7C(C8CC6N7CC8=CC)CO)C)NC9=CC=CC=C39)C 644.80 unknown https://doi.org/10.1055/S-2006-959531
Normacusine B 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1055/S-2006-959531
> Alkaloids and derivatives / Vobasan alkaloids
(1S,14R,15Z,18R)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one 101926661 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C 324.40 unknown https://doi.org/10.1055/S-2006-959531
methyl (1S,12R,14R,15Z,18S)-15-ethylidene-12-hydroxy-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 102240003 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)O)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.1055/S-2006-959531
methyl (1S,14R,15Z,18S)-15-ethylidene-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101281359 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 352.40 unknown https://doi.org/10.1055/S-2006-959554
https://doi.org/10.1055/S-2006-959531
Perivine 6473766 Click to see CC=C1CNC2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34 338.40 unknown https://doi.org/10.1055/S-2006-959531
Vobasinol 5374872 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)O)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.1055/S-2006-959531
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Penipacid A 139585900 Click to see CC(=NCC(C)(C)O)NC1=CC=CC=C1C(=O)O 250.29 unknown https://doi.org/10.1055/S-2006-959531
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2-[(2R,3Z,12bS)-3-ethylidene-9-methoxy-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 101630448 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=C3C=C(C=C4)OC 326.40 unknown https://doi.org/10.1055/S-2006-959554

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