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Catharanthus pusillus

Catharanthus pusillus - 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 UUID64402b4e0a2d8308912706
Scientific name Catharanthus pusillus
Authority G.Don
First published in Gen. Hist. 4: 95 (1837)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lochnera pusilla K.Schum. Nat. Pflanzenfam. 4(2): 145 (1895)
Vinca parviflora Retz. Observ. Bot. 2: 14 (1781)
Vinca pusilla Murray Commentat. Soc. Regiae Sci. Gott. 3: 66 (1772 publ. 1773)

Common names Top

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Language Common/alternative name
English tiny periwinkle

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
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Nepal
      • Sri Lanka
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000819431
Tropicos 1800006
KEW urn:lsid:ipni.org:names:77879-1
The Plant List kew-35718
Open Tree Of Life 6068061
IPNI 77879-1
GBIF 3618565
Freebase /m/011spm25
EPPO CTUPU
USDA GRIN 418426
Wikipedia Catharanthus_pusillus

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)!
Title Authors Publication Released IDs
Vincapusine, a minor indole alkaloid of Vinca pusilla Alok K. Mitra, Amarendra Patra, Apurba K. Mukhopadhyay Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85205-3
Terpenoid indole alkaloid profile changes in Catharanthus pusillus during development. Zárate R, Dirks C, van der Heijden R, Verpoorte R Plant Sci 01-Apr-2001
doi:10.1016/S0168-9452(01)00340-5
PMID:11297794
Catharanthus alkaloids. XXI. Isolation of lochnerinine, one of the cytotoxic principles of C. pusillus. Tin-Wa M, Fong HH, Blomster RN, Farnsworth NR J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600571232
PMID:5708365

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.2600571232
> Alkaloids and derivatives / Ibogan-type alkaloids
Methyl (1R,15R)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8,16-pentaene-1-carboxylate 13993928 Click to see CCC1=CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 336.40 unknown https://doi.org/10.1016/S0168-9452(01)00340-5
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
methyl (1S,15S,16S,18S,20S)-20-ethyl-15-hydroxy-17-oxa-3,13-diazahexacyclo[11.7.0.02,10.03,18.04,9.016,20]icosa-2(10),4,6,8-tetraene-18-carboxylate 11646359 Click to see CCC12CC3(N4C5=CC=CC=C5C6=C4C1N(CC6)CC(C2O3)O)C(=O)OC 368.40 unknown https://doi.org/10.1016/0031-9422(81)85205-3
> 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/10.1016/S0168-9452(01)00340-5
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.2600571232
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.2600571232
> 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.2600571232

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