Catharanthus trichophyllus

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Ethnobotanical Use

General Uses

Synonyms

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Details Top

Internal ID	UUID64402b5312fb7140117428
Scientific name	Catharanthus trichophyllus
Authority	(Baker) Pichon
First published in	Mém. Mus. Natl. Hist. Nat. 27: 238 (1948)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Lochnera trichophylla	(Baker) Pichon	Notul. Syst. (Paris) 13: 207 (1948)
Vinca trichophylla	Baker	J. Linn. Soc., Bot. 20: 204 (1883)

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

Africa click to expand
- Western Indian Ocean
  - Madagascar

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000819497
Tropicos	1803427
KEW	urn:lsid:ipni.org:names:77882-1
The Plant List	kew-35724
Open Tree Of Life	568438
NCBI Taxonomy	319559
IPNI	77882-1
iNaturalist	446827
GBIF	3618529
Freebase	/m/0wg04b2
EOL	5325288
Wikipedia	Catharanthus_trichophyllus

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

Chemico-pharmacological evaluation of the methanolic leaf extract of Catharanthus ovalis: GC–MS/MS, in vivo, in vitro, and in silico approaches

Shahriar S, Shermin SA, Hasnat H, Hossain F, Han A, Geng P, Alam S, Mamun AA

Front Pharmacol

01-Mar-2024

PMCID:	PMC10940508
doi:	10.3389/fphar.2024.1347069
PMID:	38495091

A review on efforts for improvement in medicinally important chemical constituents inAconitum through biotechnological interventions

Tiwari S, Acharya P, Solanki B, Sharma AK, Rawat S

3 Biotech

13-May-2023

PMCID:	PMC10183062
doi:	10.1007/s13205-023-03578-z
PMID:	37193333

Virtual Screening of Alkaloid and Terpenoid Inhibitors of SMT Expressed in Naegleria sp.

Abraham J, Chauhan N, Ray S

Molecules

05-Sep-2022

PMCID:	PMC9457665
doi:	10.3390/molecules27175727
PMID:	36080504

Plant tissue culture as a perpetual source for production of industrially important bioactive compounds

Chandran H, Meena M, Barupal T, Sharma K

Biotechnol Rep (Amst)

20-Apr-2020

PMCID:	PMC7193120
doi:	10.1016/j.btre.2020.e00450
PMID:	32373483

Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention)

Alamgir AN

Therapeutic Use of Medicinal Plants and their Extracts: Volume 2

24-Jun-2018

PMCID:	PMC7123938
doi:	10.1007/978-3-319-92387-1_7

Efficient delivery of ursolic acid by poly(N-vinylpyrrolidone)-block-poly (ε-caprolactone) nanoparticles for inhibiting the growth of hepatocellular carcinoma in vitro and in vivo

Zhang H, Zheng D, Ding J, Xu H, Li X, Sun W

Int J Nanomedicine

11-Mar-2015

PMCID:	PMC4362907
doi:	10.2147/IJN.S77125
PMID:	25792825

ATP-binding cassette transporter controls leaf surface secretion of anticancer drug components in Catharanthus roseus

Yu F, De Luca V

Proc Natl Acad Sci U S A

09-Sep-2013

PMCID:	PMC3785729
doi:	10.1073/pnas.1307504110
PMID:	24019465

Influence of abiotic stress signals on secondary metabolites in plants

Ramakrishna A, Ravishankar GA

Plant Signal Behav

01-Nov-2011

PMCID:	PMC3329344
doi:	10.4161/psb.6.11.17613
PMID:	22041989

Vinca drug components accumulate exclusively in leaf exudates of Madagascar periwinkle

Roepke J, Salim V, Wu M, Thamm AM, Murata J, Ploss K, Boland W, De Luca V

Proc Natl Acad Sci U S A

09-Aug-2010

PMCID:	PMC2930567
doi:	10.1073/pnas.0911451107
PMID:	20696903

Phytochemistry of Cimicifugic Acids and Associated Bases in Cimicifuga racemosa Root Extracts

GÖdecke T, Nikolic D, Lankin DC, Chen SN, Powell SL, Dietz B, Bolton JL, Van Breemen RB, Farnsworth NR, Pauli GF

Phytochem Anal

01-Mar-2009

PMCID:	PMC2715282
doi:	10.1002/pca.1106
PMID:	19140115

Production of indole alkaloids by in vitro root cultures from Catharanthus trichophyllus

Elisabeth Davioud, Christiane Kan, Janine Hamon, Jacques Tempé, Henri-Philippe Husson

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)98066-X

Epiallo-yohimbine derivatives isolated from in vitro hairy-root cultures of Catharanthus trichophyllus

Elisabeth Davioud, Christiane Kan, Jean-Charles Quirion, Bhupesh C. Das, Henri-Philippe Husson

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)97752-5

Catharanthus alkaloids—XXXIX

Sibabrata Mukhopadhyay, Geoffrey A. Cordell, George A. Sim, Philip J. Cox

Elsevier BV

25-Jul-2002

doi:	10.1016/S0040-4020(01)88602-6

Molecular and Biochemical Analysis of a Madagascar Periwinkle Root-Specific Minovincinine-19-Hydroxy-O-Acetyltransferase

Laflamme P, St-Pierre B, De Luca V

Plant Physiol

01-Jan-2001

PMCID:	PMC61001
doi:	10.1104/pp.125.1.189
PMID:	11154328

High Sensitivity to Auxin is a Common Feature of Hairy Root

Shen WH, Davioud E, David C, Barbier-Brygoo H, Tempé J, Guern J

Plant Physiol

01-Oct-1990

PMCID:	PMC1077268
doi:	10.1104/pp.94.2.554
PMID:	16667748

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 / Aspidospermatan-type alkaloids
Echitoveniline	134714943	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC	548.60	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X
Echitovenine	443402	Click to see	396.50	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X
Horhammericine	443358	Click to see	368.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X https://doi.org/10.1002/JPS.2600650312
Lochnericine	11382599	Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC	352.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X https://doi.org/10.1002/JPS.2600650312
methyl (1R,12R,19R)-12-(1-hydroxyethyl)-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	443401	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)O	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X https://doi.org/10.1002/JPS.2600650312 https://doi.org/10.1016/S0031-9422(00)98066-X
methyl (1R,12R,19R)-12-(2-hydroxyacetyl)-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	101277329	Click to see	368.40	unknown	https://doi.org/10.1002/JPS.2600650312
methyl (1R,12R,19R)-12-[(1R)-1-acetyloxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	101287862	Click to see	396.50	unknown	https://doi.org/10.1002/JPS.2600650312
methyl (1R,12R)-12-(1-hydroxyethyl)-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	118701461	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)O	354.40	unknown	https://doi.org/10.1002/JPS.2600650312 https://doi.org/10.1016/S0031-9422(00)98066-X
Minovincine, 16-methoxy-	586568	Click to see	382.50	unknown	https://doi.org/10.1002/JPS.2600650312
> Alkaloids and derivatives / Plumeran-type alkaloids
(2beta,3beta,4beta,5alpha,12beta,19alpha)-4-(Acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-aspidospermidine-3-carboxylic acid methyl ester	129316872	Click to see CCC12C=CCN3C1C4(CC3)C(C(C2OC(=O)C)(C(=O)OC)O)N(C5=C4C=CC(=C5)OC)C	456.50	unknown	https://doi.org/10.1002/JPS.2600650312
methyl (1R,9R,10S,11R,12S,19S,20S)-20-methyl-8,16-diazahexacyclo[10.6.1.19,11.01,9.02,7.016,19]icosa-2,4,6,13-tetraene-10-carboxylate	154497671	Click to see	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X
methyl (1R,9R,10S,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate	138113920	Click to see CCC12C=CCN3C1C4(CC3)C(C(C2OC(=O)C)(C(=O)OC)O)N(C5=CC=CC=C45)C	426.50	unknown	https://doi.org/10.1002/JPS.2600650312
Methyl 11-acetyloxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate	21304	Click to see	426.50	unknown	https://doi.org/10.1002/JPS.2600650312
Tabersonine	20485	Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X
> Alkaloids and derivatives / Strychnos alkaloids
Akuammicine	10314057	Click to see	322.40	unknown	https://doi.org/10.1002/JPS.2600650312 https://doi.org/10.1016/S0031-9422(00)98066-X
> Alkaloids and derivatives / Vinca alkaloids
Methyl 11-acetyloxy-12-ethyl-4-(17-ethyl-17-hydroxy-13-methoxycarbonyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl)-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate	3823887	Click to see	811.00	unknown	https://doi.org/10.1021/NP50015A017
> Alkaloids and derivatives / Yohimbine alkaloids
Ajmalicine	441975	Click to see	352.40	unknown	https://doi.org/10.1002/JPS.2600630918 https://doi.org/10.1016/S0031-9422(00)98066-X
Akuammigine	1268096	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X
methyl (1R,15S,17R,18R,19S,20S)-17-(2-acetamidobenzoyl)oxy-6,18-dimethoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate	14314388	Click to see CC(=O)NC1=CC=CC=C1C(=O)OC2CC3CN4CCC5=C(C4CC3C(C2OC)C(=O)OC)NC6=C5C=CC(=C6)OC	575.70	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X https://doi.org/10.1016/S0031-9422(00)97752-5
Pseudoyohimbine	251562	Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O	354.40	unknown	https://doi.org/10.1002/JPS.2600650312
Tetrahydroalstonine	72340	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1002/JPS.2600630918
> Benzenoids / Benzene and substituted derivatives / Benzazocines
Pericalline	6436240	Click to see	264.40	unknown	https://doi.org/10.1002/JPS.2600630918 https://doi.org/10.1016/S0031-9422(00)98066-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1002/JPS.2600630918
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Beta amino acids and derivatives
methyl (1S,9Z,12S,13Z)-12-formyl-12-methyl-19-oxo-8,16-diazatetracyclo[14.2.1.01,9.02,7]nonadeca-2,4,6,9,13-pentaene-10-carboxylate	163191165	Click to see	366.40	unknown	https://doi.org/10.1016/S0040-4020(01)88602-6
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
methyl (1R,9S,10R,12S,19S,20S)-20-methyl-8,16-diazahexacyclo[10.6.1.19,12.01,9.02,7.016,19]icosa-2,4,6,13-tetraene-10-carboxylate	163083337	Click to see	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X
methyl (9S,10R,12S,19S,20S)-20-methyl-8,16-diazahexacyclo[10.6.1.19,12.01,9.02,7.016,19]icosa-2,4,6,13-tetraene-10-carboxylate	163185596	Click to see CC1C23CC(C14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)C(=O)OC	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X
Methyl 6,7-didehydro-2,20-cycloaspidospermidine-3-carboxylate	120879	Click to see	336.40	unknown	https://doi.org/10.1002/JPS.2600630918 https://doi.org/10.1016/S0031-9422(00)98066-X
Vindolinine	24148538	Click to see	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)98066-X https://doi.org/10.1002/JPS.2600630918

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Catharanthus trichophyllus

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top