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Catharanthus ovalis

Catharanthus ovalis - 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 UUID64402b4bab800422150210
Scientific name Catharanthus ovalis
Authority Markgr.
First published in Adansonia , n.s., 10: 24 (1970)

Description Top

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Catharanthus ovalis is a flowering plant belonging to the dogbane family and is found only in Madagascar. It was first identified as a species in 1970, and although there have been suggestions of different subspecies or varieties, none have been officially recognized.

Synonyms Top

Scientific name Authority First published in
Catharanthus ovalis subsp. grandiflorus Markgr. Adansonia n.s., 10: 24. 1970 (1970)
Catharanthus ovalis var. tomentellus Markgr. Adansonia n.s., 10: 24. 1970

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-0000819398
Tropicos 1803432
KEW urn:lsid:ipni.org:names:77878-1
The Plant List kew-35715
Open Tree Of Life 871031
NCBI Taxonomy 1167200
IPNI 77878-1
iNaturalist 469129
GBIF 3618574
Freebase /m/011snx9c
USDA GRIN 102191
Wikipedia Catharanthus_ovalis

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 7-Deoxyloganetic Acid Glucosyltransferase Contributes a Key Step in Secologanin Biosynthesis in Madagascar Periwinkle Asada K, Salim V, Masada-Atsumi S, Edmunds E, Nagatoshi M, Terasaka K, Mizukami H, De Luca V Plant Cell 08-Oct-2013
PMCID:PMC3877786
doi:10.1105/tpc.113.115154
PMID:24104568
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
Tetra­hydro­alstonine Cachet X, Porée FH, Michel S, Lemoine P Acta Crystallogr Sect E Struct Rep Online 07-Aug-2013
PMCID:PMC3884471
doi:10.1107/S1600536813021168
PMID:24427031
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
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
Alcaloïdes mono-indoliques de Catharanthus ovalis Nicole Langlois, Luc Diatta, Ratremaniaina Z. Andriamialisoa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81889-0

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 / Aspidofractine alkaloids
methyl (1S,2R,4S,9R,17R,18R,22R)-3-oxa-6,16-diazaheptacyclo[15.2.2.11,6.02,4.09,17.010,15.09,22]docosa-10,12,14-triene-18-carboxylate 101306780 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC6C3O6)C7=CC=CC=C7N4 352.40 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
methyl (1S,9S,16S,18R,21R)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7,14-tetraene-18-carboxylate 162124618 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4 336.40 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
methyl (1R,12S,13R,15S,20R)-12-[(1S)-1-hydroxyethyl]-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate 162995586 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)81889-0
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/S0031-9422(00)81889-0
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/S0031-9422(00)81889-0
methyl (1R,9R,10S,11S,12R,13R,19R)-12-ethyl-11-hydroxy-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 162873025 Click to see CCC12C3CCN4C1C5(CC4)C(C(C2O)(O3)C(=O)OC)N(C6=CC=CC=C56)C 384.50 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
methyl (1R,9R,10S,11S,12S,13S,14S,19R)-11-acetyloxy-12-ethyl-14-hydroxy-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 163058109 Click to see CCC12C3C(CN4C1C5(CC4)C(C(C2OC(=O)C)(O3)C(=O)OC)N(C6=CC=CC=C56)C)O 442.50 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
methyl (1R,9R,11S,14S,19R)-11-acetyloxy-12-ethyl-14-hydroxy-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 163187996 Click to see CCC12C3C(CN4C1C5(CC4)C(C(C2OC(=O)C)(O3)C(=O)OC)N(C6=CC=CC=C56)C)O 442.50 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
> Alkaloids and derivatives / Plumeran-type alkaloids
methyl (1R,12S,19R)-12-[(1R)-1-hydroxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate 57506202 Click to see CC(C12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC)O 352.40 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
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)81889-0
Vindoline 260535 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/10.1016/S0031-9422(00)81889-0
Vindorosine 11618751 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/10.1016/S0031-9422(00)81889-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,7,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate 163031916 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
> 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)81889-0
methyl (1R,9S,10S,12R,13R,20S)-9-methoxy-12-methyl-11-oxa-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2,4,6,14-tetraene-10-carboxylate 162956130 Click to see CC1C23CC(O1)(C4(C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)OC)C(=O)OC 382.50 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
methyl (1R,9S,10S,12S,13R,20S)-9-methoxy-12-methyl-11-oxa-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2,4,6,14-tetraene-10-carboxylate 162956131 Click to see CC1C23CC(O1)(C4(C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)OC)C(=O)OC 382.50 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
methyl (1R,9S,12S,13R,20S)-9-methoxy-12-methyl-11-oxa-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2,4,6,14-tetraene-10-carboxylate 163193472 Click to see CC1C23CC(O1)(C4(C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)OC)C(=O)OC 382.50 unknown https://doi.org/10.1016/S0031-9422(00)81889-0
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)81889-0

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