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Catharanthus lanceus

Catharanthus lanceus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Catharanthus lanceus - 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
Contributors
Collections

Details Top

Internal ID UUID64402b4a2a03a820605657
Scientific name Catharanthus lanceus
Authority (Bojer ex A.DC.) Pichon
First published in Mém. Mus. Natl. Hist. Nat. 27: 237 (1948)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lochnera lancea K.Schum. Nat. Pflanzenfam. 4(2): 145 (1895)
Vinca lancea Bojer ex A.DC. Prodr. 8: 382 (1844)
Tachiadenus parviflorus Baker Bull. Misc. Inform. Kew 1897: 274 (1897)

Common names Top

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Language Common/alternative name
Persian کاتارانتوس لانسئوس پیچون

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-0000819376
Tropicos 1803425
KEW urn:lsid:ipni.org:names:77876-1
The Plant List kew-35713
Open Tree Of Life 6068060
NCBI Taxonomy 1750993
IPNI 77876-1
iNaturalist 429404
GBIF 3618592
Freebase /m/0wf1m27
Wikipedia Catharanthus_lanceus

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
Phytochemicals from Plant Foods as Potential Source of Antiviral Agents: An Overview Behl T, Rocchetti G, Chadha S, Zengin G, Bungau S, Kumar A, Mehta V, Uddin MS, Khullar G, Setia D, Arora S, Sinan KI, Ak G, Putnik P, Gallo M, Montesano D Pharmaceuticals (Basel) 19-Apr-2021
PMCID:PMC8073840
doi:10.3390/ph14040381
PMID:33921724
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
Two Tabersonine 6,7-Epoxidases Initiate Lochnericine-Derived Alkaloid Biosynthesis in Catharanthus roseus Carqueijeiro I, Brown S, Chung K, Dang TT, Walia M, Besseau S, Dugé de Bernonville T, Oudin A, Lanoue A, Billet K, Munsch T, Koudounas K, Melin C, Godon C, Razafimandimby B, de Craene JO, Glévarec G, Marc J, Giglioli-Guivarc’h N, Clastre M, St-Pierre B, Papon N, Andrade RB, O’Connor SE, Courdavault V Plant Physiol 22-Jun-2018
PMCID:PMC6084683
doi:10.1104/pp.18.00549
PMID:29934299
Designing Second Generation Anti-Alzheimer Compounds as Inhibitors of Human Acetylcholinesterase: Computational Screening of Synthetic Molecules and Dietary Phytochemicals Amat-ur-Rasool H, Ahmed M PLoS One 01-Sep-2015
PMCID:PMC4556483
doi:10.1371/journal.pone.0136509
PMID:26325402
Medicinal plants sold in the markets of Antananarivo, Madagascar Randriamiharisoa MN, Kuhlman AR, Jeannoda V, Rabarison H, Rakotoarivelo N, Randrianarivony T, Raktoarivony F, Randrianasolo A, Bussmann RW J Ethnobiol Ethnomed 28-Jul-2015
PMCID:PMC4517502
doi:10.1186/s13002-015-0046-y
PMID:26216098
Structure Elucidation and Chemistry of Catharanthus Alkaloids II. Isolation and Partial Structure of Catharine, a Dimeric Indole Alkaloid From C. Zanceus and C. Roseus Donald J. Abraham, Norman R. Farnsworth, Ralph N. Blomster, Robert E. Rhodes Elsevier BV 14-Oct-2006
doi:10.1002/JPS.2600560322
Catharanthus alkaloids. XXVII. Cathanneine, a new alkaloid from catharanthus lanceus G.H. Aynilian, M. Tin-Wa, N.R. Farnsworth, M. Gorman Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)84247-7
Anomalous isolation of an active antitumor alkaloid from a fraction of Catharanthus lanceus devoid of anticancer activity. Farnsworth NR J Pharm Sci 01-Nov-1972
doi:10.1002/JPS.2600611137
PMID:4652666
Catharanthus alkaloids. XXVI. Isolation of cathanneine, a new alkaloid from Catharanthus lanceus. Aynilian G, Farnsworth NR, Lyon RL, Fong HH J Pharm Sci 01-Feb-1972
doi:10.1002/JPS.2600610241
PMID:5059809
Catharanthus alkaloids. XV. Isolation of vindolinine from C. lanceus leaves. Maloney EM, Fong HH, Farnsworth NR, Blomster RN, Abraham DJ J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600570629
PMID:5677682
STUDIES ON CATHARANTHUS LANCEUS (VINCA LANCEA). I. ISOLATION OF LEUROSINE, PERIVINE, AND YOHIMBINE. FARNSWORTH NR, LOUB WD, BLOMSTER RN J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600521126
PMID:14079649
PERICYCLIVINE, A NEW CATHARANTHUS ALKALOID. FARNSWORTH NR, LOUB WD, BLOMSTER RN, GORMAN M J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600531238
PMID:14255153
Catharanthus alkaloids. X. Isolation of lanceine and vinosidine from Catharanthus lanceus roots. Blomster RN, Farnsworth NR, Abraham DJ J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600560232
PMID:6025793

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
Lochnerinine 443417 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC)C(=O)OC 382.50 unknown https://doi.org/10.1002/JPS.2600560322
methyl (1R,9R,10R,11S,12R,13R,19R)-11-acetyloxy-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.110,13.01,9.02,7.016,19]icosa-2,4,6-triene-10-carboxylate 163025794 Click to see CCC12C3CCN4C1C5(CC4)C(C(C2OC(=O)C)(O3)C(=O)OC)N(C6=CC=CC=C56)C 426.50 unknown https://doi.org/10.1016/S0040-4039(01)84247-7
methyl (1R,9R,10R,11S,12R,19R)-11-acetyloxy-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.110,13.01,9.02,7.016,19]icosa-2,4,6-triene-10-carboxylate 163193332 Click to see CCC12C3CCN4C1C5(CC4)C(C(C2OC(=O)C)(O3)C(=O)OC)N(C6=CC=CC=C56)C 426.50 unknown https://doi.org/10.1016/S0040-4039(01)84247-7
Methyl 11-acetyloxy-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.110,13.01,9.02,7.016,19]icosa-2,4,6-triene-10-carboxylate 12302544 Click to see CCC12C3CCN4C1C5(CC4)C(C(C2OC(=O)C)(O3)C(=O)OC)N(C6=CC=CC=C56)C 426.50 unknown https://doi.org/10.1002/JPS.2600610241
> Alkaloids and derivatives / Macroline alkaloids
methyl (12R,14R)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 129317237 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1002/JPS.2600531238
methyl (1S,14S,15E)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 6436185 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1002/JPS.2600531238
> Alkaloids and derivatives / Plumeran-type alkaloids
Catharine 11953924 Click to see CCC1=CN(CCC2=C(C(CC(=O)C1)(C3=C(C=C4C(=C3)C56CCN7C5C(C=CC7)(C(C(C6N4C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)NC8=CC=CC=C28)C=O 822.90 unknown https://doi.org/10.1002/JPS.2600560322
> Alkaloids and derivatives / Vinca alkaloids
Vinleurosine 442111 Click to see CCC12CN3CCC4=C(C(CC(C3)C1O2)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)NC1=CC=CC=C41 809.00 unknown https://doi.org/10.1002/JPS.2600611137
https://doi.org/10.1002/JPS.2600521126
https://doi.org/10.1002/JPS.2600531238
> Alkaloids and derivatives / Vobasan alkaloids
Periformyline 11969538 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C=O 366.40 unknown https://doi.org/10.1002/JPS.2600560322
Perivine 6473766 Click to see CC=C1CNC2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34 338.40 unknown https://doi.org/10.1002/JPS.2600570629
https://doi.org/10.1002/JPS.2600521126
https://doi.org/10.1002/JPS.2600531238
> 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/10.1002/JPS.2600560232
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.2600560322
Yohimbine 8969 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1002/JPS.2600570629
https://doi.org/10.1002/JPS.2600531238
https://doi.org/10.1002/JPS.2600521126
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
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.2600570629
Vindolinine 24148538 Click to see CC1C23CC(C14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)C(=O)OC 336.40 unknown https://doi.org/10.1002/JPS.2600570629

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