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Tabernaemontana heterophylla

Tabernaemontana heterophylla - Unknown
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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 UUID643fee80147ca821139442
Scientific name Tabernaemontana heterophylla
Authority Vahl
First published in Eclog. Amer. 2: 22 (1798)

Description Top

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Synonyms Top

Scientific name Authority First published in
Peschiera cuspidata Miers Apocyn. S. Amer. : 37 (1878)
Peschiera diversifolia Miq. Stirp. Surinam. Select. : 164 (1851)
Peschiera heterophylla Miers Apocyn. S. Amer. : 38 (1878)
Peschiera laevifructa L.Allorge Bull. Soc. Bot. France, Lett. Bot. 130(4-5): 344. 1984 [1983 publ. 1984]
Peschiera stenoloba Miers Apocyn. S. Amer. : 38 (1878)
Peschiera tenuiflora Poepp. & Endl. Nov. Gen. Sp. Pl. 3: 70 (1845)
Stenosolen eggersii Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 14: 177 (1938)
Stenosolen grandifolius Markgr. Acta Bot. Venez. 10: 250 (1975)
Stenosolen heterophyllus (Vahl) Markgr. in Pulle Meded. Afd. Handelsmus. Kolon. Inst. 30: 455 (1937)
Stenosolen holothuria Markgr. ex A.H.Gentry Ann. Missouri Bot. Gard. 61: 899 (-900). 1974
Stenosolen stenolobus (Müll.Arg.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 14: 177 (1938)
Tabernaemontana holothuria (Markgr.) Leeuwenb. Agric. Univ. Wageningen Pap. 87(5): 12. 1988 [1987 publ. 1988]
Tabernaemontana stenoloba Müll.Arg. Linnaea 30: 407 (1860)
Tabernaemontana tenuiflora Müll.Arg. Fl. Bras. 6(1): 76 (1860)
Tabernaemontana urguiculata Rusby Mem. New York Bot. Gard. 7: 324 (1927)
Stenosolen eggersii f. glabra Mez Notizbl. Bot. Gart. Berlin-Dahlem 14: 184. 1938
Stenosolen eggersii f. pubescens Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 14: 184 (1938)

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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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
    • Brazil
      • Brazil North
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000319891
Tropicos 1800047
INPN 732636
KEW urn:lsid:ipni.org:names:82146-1
The Plant List kew-200726
Open Tree Of Life 836890
NCBI Taxonomy 761072
IUCN Red List 150015608
IPNI 82146-1
iNaturalist 743041
GBIF 3617122
Freebase /m/012dtc7q
Wikipedia Tabernaemontana_heterophylla

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
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
ALCALÓIDES DE TABERNAEMONTANA HETEROPHYLLA VAHL. (APOCYNACEAE) Wilson Wolter Filho, , Maria Lúcia Belém Pinheiro, Arnaldo Imbiriba da Rocha, FapUNIFESP (SciELO) 29-Oct-2016
doi:10.1590/1809-43921983132409
Cholinesterase Enzymes Inhibitors from the Leaves of Rauvolfia Reflexa and Their Molecular Docking Study Fadaeinasab M, Hadi AH, Kia Y, Basiri A, Murugaiyah V Molecules 25-Mar-2013
PMCID:PMC6270359
doi:10.3390/molecules18043779
PMID:23529036
Determination of Structures by 1H NMR at 400 MHz: Alkaloids of Stenosolen heterophyllus. Amelia Henriques, Christiane Kan, Henri-Philippe Husson, Siew-Kwong Kan, Mauri Lounasmaa Danish Chemical Society 19-Jun-2008
doi:10.3891/ACTA.CHEM.SCAND.34B-0509
Alcaloïdes Indoliques de Stenosolen heterophyllus Tabernamine et Isotabernamine Christiane Kan, Amélia Henriquès, Yves Jasor, Christian Moretti, Henri-Philippe Husson American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50033A014

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/10.1590/1809-43921983132409
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/10.1590/1809-43921983132409
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/10.1590/1809-43921983132409
> 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/10.1590/1809-43921983132409
[(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/10.1590/1809-43921983132409
> Alkaloids and derivatives / Plumeran-type alkaloids
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/10.3891/ACTA.CHEM.SCAND.34B-0509
> 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/10.1021/NP50033A014
> Alkaloids and derivatives / Vobasan alkaloids
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/10.1590/1809-43921983132409
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1590/1809-43921983132409
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1590/1809-43921983132409
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1590/1809-43921983132409
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1590/1809-43921983132409
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1590/1809-43921983132409
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
7-methoxy-6-[(1R)-1-methoxyethyl]-2,2-dimethylchromene 162953649 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC)OC 248.32 unknown https://doi.org/10.1590/1809-43921983132409
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
1,5-dimethyl-6H-pyrido[4,3-b]carbazole 5281407 Click to see CC1=C2C=CN=C(C2=CC3=C1NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.1590/1809-43921983132409
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/NP50033A014
Olivacine 96364 Click to see CC1=C2C=CNC(=C2C=C3C1=NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.1590/1809-43921983132409

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