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Internal ID UUID643fee8535cc9354174947
Scientific name Tabernaemontana solanifolia
Authority A.DC.
First published in Prodr. 8: 365 (1844)

Description Top

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Tabernaemontana solanifolia is a type of plant belonging to the Apocynaceae family, commonly found in Brazil.

Synonyms Top

Scientific name Authority First published in
Peschiera affinis var. campestris Rizzini Simpos. Cerrado Univ. S. Paulo : 165 (1963)
Peschiera campestris (Rizzini) Rizzini Rodriguésia 32(52): 29 (1980):.
Peschiera fallax Miers Apocyn. S. Amer. : 40 (1878)
Peschiera solanifolia Miers Apocyn. S. Amer. : 46 (1878)
Peschiera solanifolia var. fallax (Müll.Arg.) L.Allorge Mém. Mus. Natl. Hist. Nat., B, Bot. 30: 138 (1985)
Tabernaemontana accedens Müll.Arg. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1869: 107 (1869)
Tabernaemontana fallax Müll.Arg. Fl. Bras. 6(1): 84 (1860)
Tabernaemontana nervosa Glaz. Mém. Soc. Bot. France 3: 453 (1910)
Tabernaemontana warmingii Müll.Arg. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1869: 107 (1869)
Tabernaemontana affinis var. campestris Rizzini Simpos. Cerrado Univ. S. Paulo 165. 1963

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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 Northeast
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000320121
Tropicos 1800634
KEW urn:lsid:ipni.org:names:82334-1
The Plant List kew-200936
Open Tree Of Life 94072
NCBI Taxonomy 761098
IUCN Red List 148765919
IPNI 82334-1
GBIF 3621909
Freebase /m/012dtdg5
Wikipedia Tabernaemontana_solanifolia

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
Plants from Brazilian Cerrado with Potent Tyrosinase Inhibitory Activity Souza PM, Elias ST, Simeoni LA, de Paula JE, Gomes SM, Guerra EN, Fonseca YM, Silva EC, Silveira D, Magalhães PO PLoS One 16-Nov-2012
PMCID:PMC3500240
doi:10.1371/journal.pone.0048589
PMID:23173036
Identity and relationships of the Arboreal Caatinga among other floristic units of seasonally dry tropical forests (SDTFs) of north-eastern and Central Brazil Santos RM, Oliveira-Filho AT, Eisenlohr PV, Queiroz LP, Cardoso DB, Rodal MJ Ecol Evol 01-Feb-2012
PMCID:PMC3298952
doi:10.1002/ece3.91
PMID:22423333
Alkaloide in Tabernaemontana‐Arten, VII. Über einige Bisindolalkaloide aus Tabernaemontana accedens Hans Achenbach, Enmont Schaller Wiley 29-Jun-2007
doi:10.1002/CBER.19761091103
Alkaloide in <i>Tabernaemontana</i>‐Arten, V. Accedin und <i>N</i><sub>(a)</sub>‐Methyl‐epi‐affinin, zwei neue Alkaloide aus <i>Tabernaemontana accedens</i> Hans Achenbach, Egmont Schaller Wiley 29-Jun-2007
doi:10.1002/CBER.19751081217
Indole alkaloids from Peschiera campestris Adriana E. Gower, Benedito Da S. Pereira, Anita J. Marsaioli Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83770-X

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
(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/S0031-9422(00)83770-X
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(00)83770-X
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/S0031-9422(00)83770-X
Isovoacangine 44393473 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1016/S0031-9422(00)83770-X
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/S0031-9422(00)83770-X
methyl (1R,15R,17S,18S)-17-ethyl-8-[(1R,12R,14S,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]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 163106921 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=CC(=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/10.1002/CBER.19761091103
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/S0031-9422(00)83770-X
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/10.1016/S0031-9422(00)83770-X
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/10.1016/S0031-9422(00)83770-X
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/10.1016/S0031-9422(00)83770-X
> Alkaloids and derivatives / Macroline alkaloids
(1R,12S,13R,14R,15E)-15-ethylidene-13-(hydroxymethyl)-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-1-ol 162858937 Click to see CC=C1CN2C3CC4=C(C2(CC1C3CO)O)N(C5=CC=CC=C45)C 324.40 unknown https://doi.org/10.1002/CBER.19751081217
Methyl (12S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 134716706 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)(CO)C(=O)OC 366.50 unknown https://doi.org/10.1016/S0031-9422(00)83770-X
methyl (1R,12S,14S,15E,18S)-15-ethylidene-12-[(1R,12R,13S,14S,15E)-15-ethylidene-1-hydroxy-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 163185475 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)C4=CC5=C(C=C4)N(C6=C5CC7C(C8CC6(N7CC8=CC)O)CO)C)NC9=CC=CC=C39)C 660.80 unknown https://doi.org/10.1002/CBER.19761091103
methyl (1R,12S,14S,15E,18S)-15-ethylidene-12-[(1S,12S,13S,14R,15E)-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 163186251 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/10.1002/CBER.19761091103
> 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/10.1016/S0031-9422(00)83770-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(5Z)-2-(5-bromo-1H-indole-3-carbonyl)-5-[(6-hydroxy-1H-indol-3-yl)methylidene]-1H-imidazol-4-one 10456352 Click to see C1=CC2=C(C=C1O)NC=C2C=C3C(=O)N=C(N3)C(=O)C4=CNC5=C4C=C(C=C5)Br 449.30 unknown https://doi.org/10.1016/S0031-9422(00)83770-X

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