Scientific name	Authority	First published in
Peschiera fuchsiifolia	Miers	Apocyn. S. Amer. : 34 (1878)
Peschiera gaudichaudii	Miers	Apocyn. S. Amer. : 40 (1878)
Peschiera gracillima	Miers	Apocyn. S. Amer. : 41 (1878)
Peschiera granulosa	Miers	Apocyn. S. Amer. : 37 (1878)
Peschiera hystrix	A.DC.	Prodr. 8: 360 (1844)
Peschiera lundii	Miers	Apocyn. S. Amer. : 36 (1878)
Peschiera solandri	Miers	Apocyn. S. Amer. : 46 (1878)
Tabernaemontana bracteolaris	Mart. ex Müll.Arg.	Fl. Bras. 6(1): 83 (1860)
Tabernaemontana collina	Gardner	London J. Bot. 1: 178 (1842)
Tabernaemontana echinata	Vell.	Fl. Flumin. 3: 105, t. 17 (1829)
Tabernaemontana fuchsiifolia	A.DC.	Prodr. 8: 365 (1844)
Tabernaemontana gaudichaudii	A.DC.	Prodr. 8: 365 (1844)
Tabernaemontana gracillima	(Miers) Pichon	Notul. Syst. (Paris) 13: 237 (1948)
Tabernaemontana lundii	A.DC.	Prodr. 8: 365 (1844)
Peschiera fuchsiaefolia	(A.DC.) Miers

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

Southern America click to expand
- Brazil
  - Brazil Northeast
  - Brazil Southeast
  - Brazil West-central

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000319903
Tropicos	1802046
KEW	urn:lsid:ipni.org:names:82157-1
The Plant List	kew-200737
PFAF	Tabernaemontana hystrix
Open Tree Of Life	836904
NCBI Taxonomy	761074
IUCN Red List	148766296
IPNI	82157-1
GBIF	3616928
Freebase	/m/012g432d
Wikipedia	Tabernaemontana_hystrix

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

Bark production of generalist and specialist species across savannas and forests in the Cerrado

Chiminazzo MA, Bombo AB, Charles-Dominique T, Fidelis A

Ann Bot

18-Jan-2023

PMCID:	PMC10147323
doi:	10.1093/aob/mcad014
PMID:	36651635

An insight into the recent developments in anti-infective potential of indole and associated hybrids

Mathada BS, Somappa SB

J Mol Struct

11-Mar-2022

PMCID:	PMC8913251
doi:	10.1016/j.molstruc.2022.132808
PMID:	35291692

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

Screening of plants from the Brazilian Atlantic Forest led to the identification of Athenaea velutina (Solanaceae) as a novel source of antimetastatic agents

Almeida AA, Lima GD, Simão MV, Moreira GA, Siqueira RP, Zanatta AC, Vilegas W, Machado‐Neves M, Bressan GC, Leite JP

Int J Exp Pathol

26-May-2020

PMCID:	PMC7370850
doi:	10.1111/iep.12351
PMID:	32452573

Prenylated flavonoid-enriched fraction from Maclura tinctoria shows biological activity against Staphylococcus aureus and protects Galleria mellonella larvae from bacterial infection

das Chagas Almeida A, Azevedo Rodrigues L, dos Santos Paulino G, Pereira Aguilar A, Andrade Almeida A, Olavo Ferreira S, Brandão GC, Viana Leite JP, de Oliveira Barros Ribon A

BMC Complement Altern Med

29-Jul-2019

PMCID:	PMC6664575
doi:	10.1186/s12906-019-2600-y
PMID:	31357964

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

Sarpagine and related alkaloids

Namjoshi OA, Cook JM

Alkaloids Chem Biol

09-Oct-2015

PMCID:	PMC4864735
doi:	10.1016/bs.alkal.2015.08.002
PMID:	26827883

Quaternary alkaloids from Peschiera fuchsiaefolia

Raquel M. Braga, Francisco De A.M. Reis

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)84797-4

13C NMR analysis of alkaloids from peschiera fuchsiaefolia

Raquel M. Braga, Hermogenes F. Leitáo Filho, Francisco De A.M. Reist

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(84)83102-7

Liquid chromatographic/mass spectrometric determination of biologically active alkaloids in extracts of Peschiera fuschiaefolia.

Lépine F, Milot S, Zamir L, Morel R

J Mass Spectrom

01-Feb-2002

doi:	10.1002/JMS.277
PMID:	11857766

Antiplasmodial activity of the alkaloids of Peschiera fuchsiaefolia.

Federici E, Palazzino G, Nicoletti M, Galeffi C

Planta Med

01-Feb-2000

doi:	10.1055/S-0029-1243122
PMID:	10705750

Phytochemical Profile Top

Add a new one!

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 / Ibogan-type alkaloids
(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/10.1055/S-0029-1243122
(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/10.1055/S-0029-1243122
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/10.1055/S-0029-1243122
Coronaridine	73489	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC	338.40	unknown	https://doi.org/10.1055/S-0029-1243122
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(84)83102-7 https://doi.org/10.1055/S-0029-1243122
methyl (12R,15E)-12-[(1R,15S,17S,18S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-6-yl]-15-ethylidene-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate	118701524	Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC	616.80	unknown	https://doi.org/10.1055/S-0029-1243122
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/10.1055/S-0029-1243122
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/10.1055/S-0029-1243122 https://doi.org/10.1016/0031-9422(84)83102-7
methyl (1S,15R,17R,18S)-17-ethyl-16-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	102428240	Click to see CCC1C(C2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O	354.40	unknown	https://doi.org/10.1055/S-0029-1243122
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/10.1055/S-0029-1243122 https://doi.org/10.1016/0031-9422(84)83102-7 https://doi.org/10.1002/JMS.277
methyl (1S,15R,17S,18S)-17-ethyl-6-[(1S,12R,14R,15Z,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]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate	101254412	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC	674.90	unknown	https://doi.org/10.1055/S-0029-1243122
methyl (1S,15R,17S,18S)-17-ethyl-8-[(1S,12R,14R,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(9),5,7-tetraene-1-carboxylate	102079827	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C(=C(C=C5)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC	704.90	unknown	https://doi.org/10.1002/JMS.277 https://doi.org/10.1055/S-0029-1243122 https://doi.org/10.1016/0031-9422(84)83102-7
methyl (1S,15R,18S)-17-ethyl-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	137706033	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)OC)C(=O)OC	398.50	unknown	https://doi.org/10.1055/S-0029-1243122
Methyl 17-ethyl-5-(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(9),5,7-tetraene-1-carboxylate	431073	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC	704.90	unknown	https://doi.org/10.1016/0031-9422(84)83102-7
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/10.1016/0031-9422(84)83102-7 https://doi.org/10.1002/JMS.277 https://doi.org/10.1055/S-0029-1243122
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/10.1055/S-0029-1243122
> Alkaloids and derivatives / Macroline alkaloids
(-)-Fuchsiaefoline	163184393	Click to see CCOC(=O)C1C2CC3C4=C(CC1[N+]3(CC2=CC)C)C5=C(N4C)C(=CC=C5)OC	395.50	unknown	https://doi.org/10.1016/S0031-9422(00)84797-4
(+)-Affinisine	5281346	Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO	308.40	unknown	https://doi.org/10.1055/S-0029-1243122 https://doi.org/10.1016/0031-9422(84)83102-7
(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	5087854	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/10.1055/S-0029-1243122 https://doi.org/10.1016/0031-9422(84)83102-7
ethyl (1S,14R,15Z)-15-ethylidene-5-methoxy-3,17-dimethyl-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraene-13-carboxylate	102357237	Click to see CCOC(=O)C1C2CC3C4=C(CC1[N+]3(CC2=CC)C)C5=C(N4C)C(=CC=C5)OC	395.50	unknown	https://doi.org/10.1016/S0031-9422(00)84797-4
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/10.1055/S-0029-1243122 https://doi.org/10.1002/JMS.277
> Alkaloids and derivatives / Vobasan alkaloids
(1S,14R,15Z,18R)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one	101926661	Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C	324.40	unknown	https://doi.org/10.1055/S-0029-1243122 https://doi.org/10.1016/0031-9422(84)83102-7
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/10.1055/S-0029-1243122
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/10.1002/JMS.277 https://doi.org/10.1055/S-0029-1243122
Perivine	6473766	Click to see CC=C1CNC2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34	338.40	unknown	https://doi.org/10.1055/S-0029-1243122 https://doi.org/10.1016/0031-9422(84)83102-7
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/10.1055/S-0029-1243122
> 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/10.1002/JMS.277 https://doi.org/10.1055/S-0029-1243122

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Tabernaemontana hystrix

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top