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Catharanthus trichophyllus

Catharanthus trichophyllus - Unknown
Part: Unknown
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
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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)

Description 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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
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
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
Catharanthus alkaloids. XXXVI. Isolation of vincaleukoblastine (VLB) and periformyline from Catharanthus trichophyllus and pericyclivine from Catharanthus roseus. Mukhopadhyay S, Cordell GA J Nat Prod 01-May-1981
doi:10.1021/NP50015A017
PMID:7264682

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
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 CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C 396.50 unknown https://doi.org/10.1016/S0031-9422(00)98066-X
Horhammericine 443358 Click to see CC(C12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC)O 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-(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 COC(=O)C1=C2C3(CCN4C3C(C1)(CCC4)C(=O)CO)C5=CC=CC=C5N2 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 CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C 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/10.1016/S0031-9422(00)98066-X
https://doi.org/10.1002/JPS.2600650312
Minovincine, 16-methoxy- 586568 Click to see CC(=O)C12CCCN3C1C4(CC3)C5=C(C=C(C=C5)OC)NC4=C(C2)C(=O)OC 382.50 unknown https://doi.org/10.1002/JPS.2600650312
Minovincinine 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/10.1016/S0031-9422(00)98066-X
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 CC1C2C3C=CCN4C3C5(C1(C2C(=O)OC)NC6=CC=CC=C65)CC4 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
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
Vidorosine 21304 Click to see CCC12C=CCN3C1C4(CC3)C(C(C2OC(=O)C)O)N(C5=CC=CC(=C45)C(=O)OC)C 426.50 unknown https://doi.org/10.1002/JPS.2600650312
> Alkaloids and derivatives / Strychnos alkaloids
Akuammicine 10314057 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC 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
Vinrosidine 3823887 Click to see CCC1(CC2CC(C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O 811.00 unknown https://doi.org/10.1021/NP50015A017
> Alkaloids and derivatives / Yohimbine alkaloids
Ajmalicine 441975 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
https://doi.org/10.1002/JPS.2600630918
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)97752-5
https://doi.org/10.1016/S0031-9422(00)98066-X
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 CC=C1CN2CCC1C(=C)C3=C(C2)C=C4C=CNC4=C3 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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 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 CC1(CC(=C2C3(CCN(C3=O)CC=C1)C4=CC=CC=C4N2)C(=O)OC)C=O 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 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 (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 CC1C23CC(C14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)C(=O)OC 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 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
https://doi.org/10.1002/JPS.2600630918

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