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Tabernaemontana calcarea

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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
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Details Top

Internal ID UUID643fee7c3a7bd073601653
Scientific name Tabernaemontana calcarea
Authority Pichon
First published in Notul. Syst. (Paris) 13: 241 (1948)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pandaca affinis Markgr. Adansonia , n.s., 10: 513 (1971)
Pandaca caducifolia Markgr. Adansonia , n.s., 10: 31 (1970)
Pandaca calcarea (Pichon) Markgr. Adansonia , n.s., 10: 32 (1970)
Pandaca minutiflora (Pichon) Markgr. Adansonia , n.s., 10: 33 (1970)
Tabernaemontana minutiflora Pichon Notul. Syst. (Paris) 13: 248 (1948)
Hazunta decaryi Markgr. Adansonia , n.s., 10: 28 (1970)

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-0000319757
Tropicos 1803492
KEW urn:lsid:ipni.org:names:82035-1
The Plant List kew-200603
Open Tree Of Life 886967
NCBI Taxonomy 761054
IUCN Red List 70102703
IPNI 82035-1
iNaturalist 541920
GBIF 3618579
Freebase /m/012cdzm6
Wikipedia Tabernaemontana_calcarea
CMAUP NPO32495

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
Recycling Upstream Redox Enzymes Expands the Regioselectivity of Cycloaddition in Pseudo-Aspidosperma Alkaloid Biosynthesis Kamileen MO, DeMars MD II, Hong B, Nakamura Y, Paetz C, Lichman BR, Sonawane PD, Caputi L, O’Connor SE J Am Chem Soc 14-Oct-2022
PMCID:PMC9634793
doi:10.1021/jacs.2c08107
PMID:36240425
Biodiversity conservation and drug discovery: Can they be combined? The Suriname and Madagascar experiences Cao S, Kingston DG Pharm Biol 01-Aug-2009
PMCID:PMC2746688
doi:10.1080/13880200902988629
PMID:20161050
New Cytotoxic Indole Alkaloids from <i>Tabernaemontana calcarea</i> from the Madagascar Rainforest. V. S. Prakash Chaturvedula, S. Sprague, J. K. Schilling, D. G. I. Kingston American Chemical Society (ACS) 23-Sep-2005
doi:10.1021/NP058092Z
Bisindole Alkaloids of Pandaca caducifolia Monique Zeches, Gabor Lukacs, Georges Massiot Louisette Le Men-Olivier, Maurice-Marie Debray American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50024A011
16-epi-silicine, an alkaloid of the ervatamine-type from Pandaca caducifolia Pascale Clivio, Bernard Richard, Jean-Marc Nuzillard, Monique Zèches-Hanrot Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00271-8
New cytotoxic indole alkaloids from Tabernaemontana calcarea from the Madagascar rainforest. Prakash Chaturvedula VS, Sprague S, Schilling JK, Kingston DG J Nat Prod 01-Apr-2003
doi:10.1021/NP020548E
PMID:12713407
Morphological and Ultrastructural Diversity of Orbicules in Relation to Evolutionary Tendencies in Apocynaceae s.l. VINCKIER S, SMETS E Ann Bot 01-Nov-2002
PMCID:PMC4240458
doi:10.1093/aob/mcf243
PMID:12466106
Alcaloïdes du Pandaca calcarea et Pandaca debrayi M.J. Hoizey, M.-M. Debray, L. Le Men-Olivier, J. Le Men Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(74)85136-8

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
(-)-Voacangine 10361692 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1021/NP020548E
(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/10.1021/NP058092Z
(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/10.1021/NP058092Z
1-(3,13-Diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-17-yl)ethanol 73009182 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1021/NP058092Z
10-Methoxyibogamine 442108 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1021/NP058092Z
11-Hydroxycoronaridine 44566751 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)O)C(=O)OC 354.40 unknown https://doi.org/10.1021/NP058092Z
11-Methoxyibogamine 44566754 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC 310.40 unknown https://doi.org/10.1021/NP058092Z
19-Epi-heyneanine 44566759 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1021/NP058092Z
19-Epivoacristine 56842093 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP020548E
https://doi.org/10.1021/NP058092Z
19(S)-Heyneanine 44566752 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown via CMAUP database
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/10.1021/NP058092Z
https://doi.org/10.1021/NP020548E
Coronardine 278173 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1021/NP058092Z
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1021/NP020548E
https://doi.org/10.1021/NP058092Z
Ibogamine 100217 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1021/NP020548E
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/10.1021/NP058092Z
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/10.1021/NP020548E
Ibogamine-18-carboxylic acid, 13-methoxy-, methyl ester 99199 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1021/NP020548E
Ibogamine, 12-methoxy- 363272 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1021/NP058092Z
Isovoacangine 44393473 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1021/NP058092Z
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/10.1021/NP058092Z
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/10.1021/NP058092Z
methyl (1S,15R,17R,18S)-17-[(1R)-1-hydroxyethyl]-7-methoxy-14-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 5323585 Click to see CC(C1CC2CC3(C1N(C2=O)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 398.50 unknown https://doi.org/10.1021/NP058092Z
methyl (1S,15R,17R,18S)-17-[(1S)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 102067253 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O 354.40 unknown https://doi.org/10.1021/NP020548E
methyl (1S,15R,17S,18S)-17-[(1R)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 15559733 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O 354.40 unknown https://doi.org/10.1021/NP020548E
methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101243095 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP020548E
https://doi.org/10.1021/NP058092Z
methyl (1S,17S,18S)-17-[(1S)-1-hydroxyethyl]-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 163187265 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP020548E
methyl (1S,17S,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 163188392 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1021/NP020548E
Methyl 17-(1-hydroxyethyl)-7-methoxy-14-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 73746337 Click to see CC(C1CC2CC3(C1N(C2=O)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 398.50 unknown https://doi.org/10.1021/NP058092Z
Methyl 17-ethyl-6-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 14108845 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)O)C(=O)OC 354.40 unknown https://doi.org/10.1021/NP058092Z
Tabernanthine 5089292 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC 310.40 unknown https://doi.org/10.1021/NP058092Z
Voacangine 73255 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown via CMAUP database
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/10.1021/NP058092Z
https://doi.org/10.1021/NP020548E
> Alkaloids and derivatives / Plumeran-type alkaloids
Ervafolidene 158704 Click to see CCC12CC3C4C(CC56N4CCC7(C5O)C8=CC=CC=C8NC7=C(C6)C(=O)OC)(OC39C3(C1N(CC3)CC=C2)C1=CC=CC=C1N9)CC 646.80 unknown https://doi.org/10.1021/NP50024A011
methyl (1S,12S,14R,19R)-14-ethyl-14-hydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 21589059 Click to see CCC1(CC2CC(=C3C4(C2N(C1)CC4)C5=CC=CC=C5N3)C(=O)OC)O 354.40 unknown https://doi.org/10.1016/0031-9422(74)85136-8
methyl (1S,2R,10R,17S,19S,20R,22S,23S,27R,39S)-17,22-diethyl-21-oxa-3,13,24,34-tetrazadodecacyclo[20.15.1.110,13.01,24.02,27.03,20.04,9.010,20.019,23.027,35.028,33.017,39]nonatriaconta-4,6,8,15,28,30,32,35-octaene-36-carboxylate 102274015 Click to see CCC12CC3C4C5(CC67N4CCC8(C6N9C3(O5)C3(C1N(CC3)CC=C2)C1=CC=CC=C19)C1=CC=CC=C1NC8=C(C7)C(=O)OC)CC 628.80 unknown https://doi.org/10.1021/NP50024A011
> Alkaloids and derivatives / Vallesaman alkaloids
Apparicine 5281349 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1016/0031-9422(74)85136-8
> Alkaloids and derivatives / Vobasan alkaloids
(-)-Dregamine 6711192 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(74)85136-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4E,8E,12E,16R)-1-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,9,13,17-tetramethyloctadeca-4,8,12-triene-1,16,17-triol 24801427 Click to see CC(=CCCC=C(C)CCC(C1(CCC(O1)C(C)(C)O)C)O)CCC=C(C)CCC(C(C)(C)O)O 494.70 unknown https://doi.org/10.1016/0031-9422(74)85136-8
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
methyl (1S,5R,6R,8R)-8-ethyl-8-hydroxy-4,13-diazahexacyclo[10.7.0.01,5.04,9.06,10.014,19]nonadeca-11,14,16,18-tetraene-11-carboxylate 101650350 Click to see CCC1(CC2C3C1N4C2C5(CC4)C6=CC=CC=C6NC5=C3C(=O)OC)O 352.40 unknown https://doi.org/10.1016/0031-9422(74)85136-8
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
16-Episilicine 44126867 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 296.40 unknown https://doi.org/10.1016/0031-9422(95)00271-8
Silicine 21586678 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 296.40 unknown https://doi.org/10.1016/0031-9422(95)00271-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Salvianolic acid C 13991590 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C=C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)O)O 492.40 unknown https://doi.org/10.1021/NP058092Z

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