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Vinca herbacea

Vinca herbacea - 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 UUID643ff08954f73737223294
Scientific name Vinca herbacea
Authority Waldst. & Kit.
First published in Descr. Icon. Pl. Hung. 1: 8 (1799)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vinca bottae Jaub. & Spach Ill. Pl. Orient. 2: 104 (1847)
Vinca haussknechtii Bornm. & Sint. ex Bornm. Mitth. Thüring. Bot. Vereins , n.f., 6: 66 (1894)
Vinca herbacea subsp. libanotica (Zucc.) Bornm. Beih. Bot. Centralbl. 31(2): 239. 1914 (1914)
Vinca herbacea subsp. mixta Velen. Fl. Bulg. 380. 1891 (1891)
Vinca libanotica Zucc. Denkschr. Königl. Akad. Wiss. München 2: 247 (1840)
Vinca mixta Velen. Fl. Bulg. : 646 (1891)
Vinca pumila E.D.Clarke Trav. 4: 555 (1818)
Vinca semidesertorum Ponert Feddes Repert. 82: 581 (1971)
Vinca sessilifolia A.DC. Prodr. 8: 383 (1844)

Common names Top

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Language Common/alternative name
English herbaceous periwinkle
Arabic الونكا
Azerbaijani otvari qıfotu
Belarusian Барвенак травяністы
Bulgarian тревист зимзелен
Danish asiatisk singrøn
German krautiges immergrün
Persian پیچتلگرافی ایرانی
Hebrew וינקה עשבונית
Hungarian pusztai meténg
Georgian ბალახოვანი გველის სურო
Polish barwinek zielny
Russian Барвинок травяной
Russian Барвинок травянистый
Swedish girlandvintergröna
Ukrainian Барвінок трав'янистий
Ukrainian барвінок трав'янистий
Ukrainian барвінок трав'яний

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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Eastern Europe
      • Central European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
    • Southeastern Europe
      • Bulgaria
      • Romania
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000332775
USDA Plants VIHE3
Tropicos 1800052
KEW urn:lsid:ipni.org:names:82691-1
The Plant List kew-213157
Open Tree Of Life 3870714
Observations.org 127837
NBN Atlas NBNSYS0000003955
Nature Serve 2.157348
IPNI 82691-1
iNaturalist 170230
GBIF 3169710
Freebase /m/0gjpfb
EPPO VINHE
EOL 585621
Wikipedia Vinca_herbacea

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
Die Struktur des Herbalins — eines Oxindol‐Alkaloids aus <i>Vinca herbacea</i> W. K. Iliya Ognyanov Wiley 08-Jun-2007
doi:10.1002/CBER.19660990636
d,l-Vincadifformine, 11-methoxyvincadifformine, and ervine from the herbVinca herbacea G. V. Chkhikvadze, V. Yu. Vachnadze Springer Science and Business Media LLC 09-Dec-2004
doi:10.1007/BF00598334
Isoreserpinine fromVinca herbacea �. Z. Dzhakeli Springer Science and Business Media LLC 01-Dec-2004
doi:10.1007/BF00713359
Method for the quantitative determination of vincarine, herbadine, and herbamine in the herbage of Vinca herbacea G. V. Chkhikvadze Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574608
The structure of vincarine P. Kh. Yuldashev, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568730
Structure of herboxine G. V. Chkhikvadze, M. M. Khalmirzaev, V. Yu. Vachnadze, V. M. Malikov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00566344
A study of the alkaloids of Vinca herbaceae V. Yu. Vachnadze, V. M. Malikov, K. S. Mudzhiri, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568445
Alkaloids of Vinca major cv. Variegata. Balsevich J, Constabel F, Kurz WG Planta Med 01-Feb-1982
doi:10.1055/S-2007-971409
PMID:17402086
Alkaloids of Vinca species V: structure elucidation of herbadine, an alkaloid isolated from Vinca libanotica. Aynilian GH, Bell CL, Farnsworth NR J Pharm Sci 01-Feb-1975
doi:10.1002/JPS.2600640236
PMID:1127594
Catharanthus alkaloids. XXIX. Isolation and structure elucidation of vincoline. Aynilian GH, Weiss SG, Cordell GA, Abraham DJ, Crane FA, Farnsworth NR J Pharm Sci 01-Apr-1974
doi:10.1002/JPS.2600630409
PMID:4828700

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
methyl (1R,12R,18R,19S)-12-ethyl-18-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 162889408 Click to see CCC12CCCN3C1C4(C(C3)OC)C5=CC=CC=C5NC4=C(C2)C(=O)OC 368.50 unknown https://doi.org/10.1007/BF00598334
methyl (1S,12R,19S)-12-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 6341288 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1007/BF00598334
methyl (1S,12S,18S,19S)-12-ethyl-18-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 154495947 Click to see CCC12CCCN3C1C4(C(C3)OC)C5=CC=CC=C5NC4=C(C2)C(=O)OC 368.50 unknown https://doi.org/10.1007/BF00574608
Methyl 12-ethyl-18-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 162889407 Click to see CCC12CCCN3C1C4(C(C3)OC)C5=CC=CC=C5NC4=C(C2)C(=O)OC 368.50 unknown https://doi.org/10.1007/BF00598334
Methyl 2,3-didehydroaspidospermidine-3-carboxylate 579873 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1007/BF00598334
> Alkaloids and derivatives / Corynanthean-type alkaloids
Akuammine 13491909 Click to see CC=C1CN2CCC34C5=C(C=CC(=C5)O)N(C36C2CC1C4(CO6)C(=O)OC)C 382.50 unknown https://doi.org/10.1002/JPS.2600640236
Herbamine 5476088 Click to see CC=C1C2CC3C4(C5(CC(C2(C5)C(=O)OC)N3C1O)C6=CC=CC=C6N4C)O 382.50 unknown https://doi.org/10.1007/BF00574608
methyl (13E)-13-ethylidene-9,14-dihydroxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate 5476087 Click to see CC=C1C2CC3C4(C5(CC(C2(C5)C(=O)OC)N3C1O)C6=CC=CC=C6N4)O 368.40 unknown https://doi.org/10.1007/BF00574608
https://doi.org/10.1002/JPS.2600640236
methyl (14E,16S,19S)-14-ethylidene-6-hydroxy-2-methyl-18-oxa-2,12-diazahexacyclo[13.3.2.01,9.03,8.09,16.012,19]icosa-3(8),4,6-triene-16-carboxylate 6441511 Click to see CC=C1CN2CCC34C5=C(C=CC(=C5)O)N(C36C2CC1C4(CO6)C(=O)OC)C 382.50 unknown https://doi.org/10.1002/JPS.2600640236
methyl (1R,9R,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate 44592588 Click to see CC=C1CN2C3CC1C4(C2CC5(C3NC6=CC=CC=C65)C4O)C(=O)OC 352.40 unknown https://doi.org/10.1007/BF00568730
> Alkaloids and derivatives / Eburnan-type alkaloids
Vincamine 15376 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)(C(=O)OC)O 354.40 unknown https://doi.org/10.1002/JPS.2600640236
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
10-Hydroxycanthin-6-one 158929 Click to see C1=CC2=C(C=C1O)C3=C4N2C(=O)C=CC4=NC=C3 236.22 unknown https://doi.org/10.1007/BF00598334
> Alkaloids and derivatives / Plumeran-type alkaloids
Tabersonine 20485 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC 336.40 unknown https://doi.org/10.1002/JPS.2600640236
> Alkaloids and derivatives / Strychnos alkaloids
methyl (1R,11R,12E,17S)-12-ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 162899063 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1002/JPS.2600640236
Methyl 12-ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 5087855 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1055/S-2007-971409
> Alkaloids and derivatives / Yohimbine alkaloids
19-epi-Ajmalicine 179460 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1007/BF00598334
Isoreserpinine 251563 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=CC(=C5)OC 382.50 unknown https://doi.org/10.1007/BF00713359
Lamuran 251561 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1007/BF00598334
methyl (1S,4S,4aR,5aS,6R,10aS)-5',6'-dimethoxy-1-methyl-2'-oxospiro[1,3,4,4a,5,5a,7,8,10,10a-decahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 162937867 Click to see CC1C2CN3CCC4(C3CC2C(CO1)C(=O)OC)C5=CC(=C(C=C5NC4=O)OC)OC 430.50 unknown https://doi.org/10.1002/CBER.19660990636
Methyl 11-methoxy-19-methyl-16,17-didehydro-18-oxayohimban-16-carboxylate 95501 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=CC(=C5)OC 382.50 unknown https://doi.org/10.1007/BF00713359
methyl 5',6'-dimethoxy-1-methyl-2'-oxospiro[1,3,4,4a,5,5a,7,8,10,10a-decahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 12310419 Click to see CC1C2CN3CCC4(C3CC2C(CO1)C(=O)OC)C5=CC(=C(C=C5NC4=O)OC)OC 430.50 unknown https://doi.org/10.1002/CBER.19660990636
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / 1,3-dicarbonyl compounds / Beta-diketones
2-(4-Butanoyl-3,5-dioxooxolan-2-yl)acetic acid 163037595 Click to see CCCC(=O)C1C(=O)C(OC1=O)CC(=O)O 228.20 unknown https://doi.org/10.1007/BF00574608
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
Vincoline 3032566 Click to see CC1C23CC(O1)(C4(C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)O)C(=O)OC 368.40 unknown https://doi.org/10.1002/JPS.2600630409
> Organoheterocyclic compounds / Indolizidines
Majdine 21627963 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=C(C(=C(C=C5)OC)OC)NC4=O 428.50 unknown https://doi.org/10.1002/JPS.2600640236
methyl (1S,6R)-6',7'-dimethoxy-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 139292077 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=C(C(=C(C=C5)OC)OC)NC4=O 428.50 unknown https://doi.org/10.1007/BF00566344
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1002/JPS.2600640236
https://doi.org/10.1007/BF00568445

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