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Tabernaemontana polyneura

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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 UUID644029c24f60b801345268
Scientific name Tabernaemontana polyneura
Authority (King & Gamble) D.J.Middleton
First published in Taxon 55: 503 (2006)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ervatamia coriacea Ridl. J. Straits Branch Roy. Asiat. Soc. 61: 29 (1912)
Ervatamia polyneura King & Gamble J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 74: 454 (1908)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000806630
Tropicos 100264915
KEW urn:lsid:ipni.org:names:77074605-1
The Plant List kew-344891
Open Tree Of Life 6068029
IUCN Red List 31730
IPNI 77074605-1
iNaturalist 444196
GBIF 3614955
Freebase /m/02y_r5j
Wikipedia Tabernaemontana_polyneura

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
Two bis-indole alkaloids from leaves of Ervatamia polyneura Pascale Clivio, Dominique Guillaume, Joseph Vercauteren, Bernard Richard, Jean-Marc Nuzillard, Monique Zèches-Hanrot, Louisette Le Men-Olivier Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00392-K
Alkaloids from leaves and stem bark of Ervatamia polyneura Pascale Clivio, Bernard Richard, Hamid A. Hadi, Bruno David, Thierry Sevenet, Monique Zeches, Louisette Le Men-Olivier Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)87124-D

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
Dimethyl 14,25-diethyl-24,32-dihydroxy-31-methoxy-33-oxo-12,22-dioxa-1,9,18,29-tetrazadodecacyclo[23.13.1.16,9.02,23.03,21.05,19.06,17.011,13.028,36.030,35.036,39.014,40]tetraconta-3,5(19),16,20,27,29,31,34-octaene-16,27-dicarboxylate 162924351 Click to see CCC12CC(=C3C4(C1N(CC4)C5C(C2O)OC6=CC7=C(C=C56)C89CCN1C8C(CC(=C9N7)C(=O)OC)(C2C(C1)O2)CC)C1=CC(=O)C(=C(C1=N3)OC)O)C(=O)OC 778.80 unknown https://doi.org/10.1016/0031-9422(95)00392-K
> Alkaloids and derivatives / Ibogan-type alkaloids
(1S)-1-[(1R,15R,17R,18R)-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-17-yl]ethanol 44566758 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
19-Epi-heyneanine 44566759 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
Ibogamine-18-carboxylic acid, 12-methoxy-, methyl ester 363270 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1016/0031-9422(90)87124-D
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/10.1016/0031-9422(90)87124-D
methyl (1R,15S,17R,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 134688048 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1016/0031-9422(90)87124-D
methyl (1S,11R,13R,15S,16S,18S)-15-ethyl-19-oxa-9,17-diazahexacyclo[15.2.1.02,10.03,8.011,16.013,18]icosa-2(10),3,5,7-tetraene-11-carboxylate 102239678 Click to see CCC1CC2CC3(C1N4C2OC(C4)C5=C3NC6=CC=CC=C65)C(=O)OC 352.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
methyl (1S,15R,17S,18S)-17-ethyl-11-hydroxy-14-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 102239681 Click to see CCC1CC2CC3(C1N(C2=O)CC(C4=C3NC5=CC=CC=C54)O)C(=O)OC 368.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
> Alkaloids and derivatives / Macroline alkaloids
methyl (12R,14R)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 129317237 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
methyl (1S,14S,15E)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 6436185 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
> 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/10.1016/0031-9422(90)87124-D
> 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/10.1016/0031-9422(90)87124-D
Tubotaiwin 78358510 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
> Alkaloids and derivatives / Vallesaman alkaloids
CID 6912322 6912322 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
> Alkaloids and derivatives / Vobasan alkaloids
Dregamine 99108 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
methyl (15E)-15-ethylidene-10,17-dimethyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 6912202 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)N(C4=CC=CC=C34)C)C 366.50 unknown https://doi.org/10.1016/0031-9422(90)87124-D
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/10.1016/0031-9422(90)87124-D
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/10.1016/0031-9422(90)87124-D
methyl (1S,14R,18R)-15-formyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8,15-pentaene-18-carboxylate 102061537 Click to see CN1C=C(C2CC(=O)C3=C(CC1C2C(=O)OC)C4=CC=CC=C4N3)C=O 352.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
methyl (1S,14R,18S)-15-formyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8,15-pentaene-18-carboxylate 102061536 Click to see CN1C=C(C2CC(=O)C3=C(CC1C2C(=O)OC)C4=CC=CC=C4N3)C=O 352.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
methyl (1S,14S,15S)-15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 20056338 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
Perivine 6473766 Click to see CC=C1CNC2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34 338.40 unknown https://doi.org/10.1016/0031-9422(90)87124-D
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/10.1016/0031-9422(90)87124-D

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