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Tabernaemontana citrifolia

Tabernaemontana citrifolia - Unknown
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Author: Public Domain - WikiMedia
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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 UUID643fee7d100e2791570380
Scientific name Tabernaemontana citrifolia
Authority L.
First published in Sp. Pl. : 210 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tabernaemontana citrifolia var. lanceolata (Miers) L.Allorge Mém. Mus. Natl. Hist. Nat., B, Bot. 30: 18 (1985)
Tabernaemontana lanceolata Miers Apocyn. S. Amer. 268. t. 7. 1878 [May-June 1878]
Tabernaemontana plumieri E.H.L.Krause Beih. Bot. Centralbl. 32(2): 344 (1914)
Ervatamia citrifolia (L.) M.R.Almeida Fl. Maharashtra 3A: 206 (2001)

Common names Top

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Language Common/alternative name
English milkwood
French bois-lait

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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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Southwest Caribbean
      • Trinidad-Tobago
      • Windward Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000319784
USDA Plants TACI
Tropicos 1800795
INPN 630772
KEW urn:lsid:ipni.org:names:82055-1
The Plant List kew-200629
Open Tree Of Life 536682
NCBI Taxonomy 141615
IPNI 82055-1
iNaturalist 291821
GBIF 3169629
Freebase /m/012dtbx_
EPPO TAECI
USDA GRIN 36162
Wikipedia Tabernaemontana_citrifolia

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
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
A Systematic Review on Comparative Analysis, Toxicology, and Pharmacology of Medicinal Plants Against Haemonchus contortus Ali R, Rooman M, Mussarat S, Norin S, Ali S, Adnan M, Khan SN Front Pharmacol 10-May-2021
PMCID:PMC8141741
doi:10.3389/fphar.2021.644027
PMID:34040520
Plant-Based Indole Alkaloids: A Comprehensive Overview from a Pharmacological Perspective Omar F, Tareq AM, Alqahtani AM, Dhama K, Sayeed MA, Emran TB, Simal-Gandara J Molecules 15-Apr-2021
PMCID:PMC8071433
doi:10.3390/molecules26082297
PMID:33921093
Major Bioactive Alkaloids and Biological Activities of Tabernaemontana Species (Apocynaceae) Naidoo CM, Naidoo Y, Dewir YH, Murthy HN, El-Hendawy S, Al-Suhaibani N Plants (Basel) 05-Feb-2021
PMCID:PMC7915066
doi:10.3390/plants10020313
PMID:33562893
Anthelmintic activity of acetone extracts from South African plants used on egg hatching of Haemonchus contortus Fouche G, Sakong BM, Adenubi OT, Pauw E, Leboho T, Wellington KW, Elof JN Onderstepoort J Vet Res 28-Jul-2016
PMCID:PMC6238697
doi:10.4102/ojvr.v83i1.1164
PMID:27543148
The use of Amerindian charm plants in the Guianas van Andel T, Ruysschaert S, Boven K, Daly L J Ethnobiol Ethnomed 15-Sep-2015
PMCID:PMC4570145
doi:10.1186/s13002-015-0048-9
PMID:26369661
Activity of Cuban Plants Extracts against Leishmania amazonensis García M, Monzote L, Scull R, Herrera P ISRN Pharmacol 15-Mar-2012
PMCID:PMC3316957
doi:10.5402/2012/104540
PMID:22530133
Contribution à l'Étude des Tabemaemontanées Américaines, VI. Alcaloïdes des Feuilles de Tabernaemontana citrifolia J. Abaul, É. Philogène, P. Bourgeois, A. Ahond, C. Poupat, P. Potier American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50066A013
Studies on Natural Products from Cuban Plants. Alkaloids from <i>Tabernaemontana citrifolia</i> James P. Kutney, Ileana Perez Wiley 28-Dec-2004
doi:10.1002/HLCA.19820650729
Antimycobacterial activity of chemically defined natural substances from the Caribbean flora in Guadeloupe. Rastogi N, Abaul J, Goh KS, Devallois A, Philogène E, Bourgeois P FEMS Immunol Med Microbiol 01-Apr-1998
doi:10.1111/J.1574-695X.1998.TB01136.X
PMID:9626931

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
(5alpha,12R,19alpha)-2,3-Didehydro-6alpha,7alpha-epoxyaspidospermidine-3-carboxylic acid methyl ester 317834 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC 352.40 unknown https://doi.org/10.1002/HLCA.19820650729
Lochnericine 11382599 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC 352.40 unknown https://doi.org/10.1002/HLCA.19820650729
> 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/10.1002/HLCA.19820650729
(1R,15S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene 89578867 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1111/J.1574-695X.1998.TB01136.X
(1S)-1-[(1R,15S,17S,18R)-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-17-yl]ethanol 163193354 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)O 326.40 unknown https://doi.org/10.1002/HLCA.19820650729
10-Methoxyibogamine 442108 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1111/J.1574-695X.1998.TB01136.X
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/10.1002/HLCA.19820650729
CID 3582412 3582412 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1002/HLCA.19820650729
Coronardine 278173 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1002/HLCA.19820650729
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1002/HLCA.19820650729
Ibogamin-20-ol, 12-methoxy-, (4a,20S)- 12310765 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)O 326.40 unknown https://doi.org/10.1002/HLCA.19820650729
Ibogamine 100217 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1002/HLCA.19820650729
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/10.1111/J.1574-695X.1998.TB01136.X
https://doi.org/10.1002/HLCA.19820650729
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/10.1111/J.1574-695X.1998.TB01136.X
methyl (1S,10R,15R,17S,18S)-17-ethyl-10-hydroxy-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2,4(9),5,7-tetraene-1-carboxylate 21604116 Click to see CCC1CC2CC3(C1N(C2)CCC4(C3=NC5=C4C=C(C=C5)OC)O)C(=O)OC 384.50 unknown https://doi.org/10.1002/HLCA.19820650729
methyl (1S,10S,15R,17S,18S)-17-ethyl-10-hydroxy-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2,4(9),5,7-tetraene-1-carboxylate 22296670 Click to see CCC1CC2CC3(C1N(C2)CCC4(C3=NC5=C4C=C(C=C5)OC)O)C(=O)OC 384.50 unknown https://doi.org/10.1002/HLCA.19820650729
methyl (1S,15R,17S,18S)-17-[(1S)-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 163189231 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/10.1002/HLCA.19820650729
methyl (1S,15R,17S,18S)-17-ethyl-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 12110672 Click to see CCC1CC2CC3(C1N(C2=O)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 382.50 unknown https://doi.org/10.1002/HLCA.19820650729
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/10.1002/HLCA.19820650729
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/10.1002/HLCA.19820650729
Methyl 12-methoxy-19-oxoibogamine-18-carboxylate 3083798 Click to see CCC1CC2CC3(C1N(C2=O)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 382.50 unknown https://doi.org/10.1002/HLCA.19820650729
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/10.1002/HLCA.19820650729
Voacangine hydroxyindolenine 633463 Click to see CCC1CC2CC3(C1N(C2)CCC4(C3=NC5=C4C=C(C=C5)OC)O)C(=O)OC 384.50 unknown https://doi.org/10.1002/HLCA.19820650729
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/10.1002/HLCA.19820650729
> Alkaloids and derivatives / Macroline alkaloids
Akuammidine 597842 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC 352.40 unknown https://doi.org/10.1002/HLCA.19820650729
Rhazin 15558574 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC 352.40 unknown https://doi.org/10.1002/HLCA.19820650729
> Alkaloids and derivatives / Plumeran-type alkaloids
(-)-Tabersonine 495253 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC 336.40 unknown https://doi.org/10.1002/HLCA.19820650729
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/10.1021/NP50066A013
methyl (1S,12S,14S,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 21589060 Click to see CCC1(CC2CC(=C3C4(C2N(C1)CC4)C5=CC=CC=C5N3)C(=O)OC)O 354.40 unknown https://doi.org/10.1021/NP50066A013
Tabersonine 20485 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC 336.40 unknown https://doi.org/10.1002/HLCA.19820650729
> Alkaloids and derivatives / Vallesaman alkaloids
19,20-(E)-Vallesamine 13783712 Click to see CC=C1CN2CCC1C(C3=C(C2)C4=CC=CC=C4N3)(CO)C(=O)OC 340.40 unknown https://doi.org/10.1002/HLCA.19820650729
Apparicine 5281349 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1002/HLCA.19820650729
CID 257530 257530 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1002/HLCA.19820650729
methyl (12R,13R,14E)-14-ethylidene-12-(hydroxymethyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate 124356004 Click to see CC=C1CN2CCC1C(C3=C(C2)C4=CC=CC=C4N3)(CO)C(=O)OC 340.40 unknown https://doi.org/10.1002/HLCA.19820650729
methyl (14E)-14-ethylidene-12-(hydroxymethyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate 21599097 Click to see CC=C1CN2CCC1C(C3=C(C2)C4=CC=CC=C4N3)(CO)C(=O)OC 340.40 unknown https://doi.org/10.1002/HLCA.19820650729
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
methyl (1S,5R,6R,8R,9R,10S)-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 131882498 Click to see CCC1(CC2C3C1N4C2C5(CC4)C6=CC=CC=C6NC5=C3C(=O)OC)O 352.40 unknown https://doi.org/10.1021/NP50066A013

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