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Vinca erecta

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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 UUID643ff0894085f229812959
Scientific name Vinca erecta
Authority Regel & Schmalh.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada , prepr. 6: 330 (1879)

Description Top

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Vinca erecta is a type of flowering plant that belongs to the Apocynaceae family. It is found naturally in Central Asia and Northeast Afghanistan.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Georgian სწორი გველის სურო
Russian Барвинок прямой
Uzbek boʻrigul
Uzbek bo‘rigul

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
  • Asia-temperate
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Western Asia
      • Afghanistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000332770
Tropicos 1802513
KEW urn:lsid:ipni.org:names:82686-1
The Plant List kew-213152
Open Tree Of Life 6068172
Observations.org 124451
IPNI 82686-1
GBIF 3616629
Elurikkus 384604
Wikipedia Vinca_erecta

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
Isolation of pseudocopsinine methochloride and of minovincinine from Vinca erecta M. M. Khalmirzaev, V. M. Malikov, S. Yu. Yunusov Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570701
Robinin and kaempfereol fromVinca erecta V. Akhmedzhanova Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00599275
10-Methoxyvinorine — A new alkaloid from Vinca erecta M. M. Khalmirzhaev, V. M. Malikov, S. Yu. Yunusov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00564414
Isolation of kopsinilam and ervincine D. A. Rakhimov, V. M. Malikov, S. Yu. Yunusov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00574649
NMR study of alkaloids. V.13C NMR spectra and reconsideration of the structures of 11- and 10-hydroxypleiocarpamines and the structures of new alkaloids fromVinca erecta M. R. Yagudaev, M. M. Khalmirzaev, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00575706
NMR study of alkaloids. VIII.1H and13C NMR spectra and reconsideration of the structures of vincaricine and vincarinine M. R. Yagudaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574281
Alkaloids of Vinca erecta M. R. Sharipov, M. M. Khalmirzaev, V. M. Malikov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567831
Quantitative determination of vincanidine in the roots of Vinca erecta R. A. Mirkina, T. T. Shakirov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568219
Isolation of 6,7-dehydro-8-oxokopsinine, vincanine N-oxide, and venalstonine from Vinca erecta M. Sharipov, V. M. Malikov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563654
The isolation of vincine and N-acetylvinerine V. M. Malikov, Sh. Z. Kasymov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563482
Vinerinine — A new oxindole alkaloid from Vinca erecta M. M. Khalmirzaev, V. M. Malikov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563923

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 / Ajmaline-sarpagine alkaloids
[(12R,13Z,16S,17S,18R)-13-ethylidene-4-methoxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2(7),3,5,8-tetraen-18-yl] acetate 101919850 Click to see CC=C1CN2C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=C5C=C(C=C6)OC 364.40 unknown https://doi.org/10.1007/BF00564414
Ajmalan-17-ol, 19,20-didehydro-10-methoxy-, acetate (ester), (17R,19E)- 162981158 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=C5C=C(C=C6)OC)C)C4OC(=O)C 380.50 unknown https://doi.org/10.1007/BF00567831
> Alkaloids and derivatives / Aspidofractine alkaloids
(-)-Venalstonine 821468 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4 336.40 unknown https://doi.org/10.1007/BF00563654
methyl (1R,9R,16R,18R,21S)-11-oxo-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 21607614 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4=O 352.40 unknown https://doi.org/10.1007/BF00574649
Venalstonine 426061 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4 336.40 unknown https://doi.org/10.1007/BF00563654
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
Ervinceine 13018301 Click to see CCC12CCCN3C1C4(CC3)C5=C(C=C(C=C5)OC)NC4=C(C2)C(=O)OC 368.50 unknown https://doi.org/10.1007/BF00563482
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/10.1007/BF00570701
methyl (1R,9R,10S,12S,19S,20R)-20-methyl-8,16-diazahexacyclo[10.6.1.19,12.01,9.02,7.016,19]icosa-2,4,6-triene-10-carboxylate 1403404 Click to see CC1C23CCCN4C2C5(C1(C(C3)C(=O)OC)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1007/BF00570701
> Alkaloids and derivatives / Corynanthean-type alkaloids
Ercinaminine 56842220 Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(CO)C(=O)OC 352.40 unknown https://doi.org/10.1007/BF00575706
methyl (1R,9S,11S,14Z,15S,19R)-14-ethylidene-19-formyl-4-methoxy-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3(8),4,6-triene-19-carboxylate 101324755 Click to see CC=C1CN2C3CC1C(C45C3(NC6=C4C=CC=C6OC)OC2C5)(C=O)C(=O)OC 396.40 unknown https://doi.org/10.1007/BF00574281
> Alkaloids and derivatives / Eburnan-type alkaloids
methyl (15S,17S,19S)-15-ethyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2(7),3,5,8(18)-tetraene-17-carboxylate 12444841 Click to see CCC12CCCN3C1C4=C(CC3)C5=C(N4C(C2)(C(=O)OC)O)C=C(C=C5)OC 384.50 unknown https://doi.org/10.1007/BF00563482
> Alkaloids and derivatives / Strychnos alkaloids
(11S,12Z,17S)-12-ethylidene-6-hydroxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraene-10-carbaldehyde 101627612 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=C4C=CC=C5O)C=O 308.40 unknown https://doi.org/10.1007/BF00568219
(11S,12Z,17S)-12-ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carbaldehyde 12313539 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C=O 292.40 unknown https://doi.org/10.1007/BF00568219
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5R,9R,10S,13R,14R,17R)-17-[(2S,3E,5S)-5-ethyl-6-methylhepta-3,6-dien-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163007760 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown https://doi.org/10.1007/BF00563482
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
methyl (1R,9R,11S,14Z,15R,19S)-14-ethylidene-6-methoxy-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3(8),4,6-triene-19-carboxylate 101650347 Click to see CC=C1CN2C3CC1C(C45C3(NC6=C4C=C(C=C6)OC)OC2C5)C(=O)OC 368.40 unknown https://doi.org/10.1007/BF00574281
> Organoheterocyclic compounds / Indolizidines
Vinerinine 101277386 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=C(C(=C(C=C5)O)OC)NC4=O 414.50 unknown https://doi.org/10.1007/BF00563923
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00599275
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Robinin 5281693 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1007/BF00599275

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