Colchicum szovitsii - Unknown
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Internal ID UUID644025a986109184760186
Scientific name Colchicum szovitsii
Authority Fisch. & C.A.Mey.
First published in Index Seminum (LE, Petropolitanus) 1: 24 (1835)

Description Top

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Colchicum szovitsii is a flowering plant that belongs to the Colchicaceae family. It is found in eastern Bulgaria, northwestern Jordan, and Iran. It was first described in 1835. There are two recognized subspecies of this plant: Colchicum szovitsii subsp. brachyphyllum, found in Lebanon, Syria, Palestine, and Turkey, and Colchicum szovitsii subsp. szovitsii, found in eastern Bulgaria to Iran.

Synonyms Top

Scientific name Authority First published in
Colchicum acutifolium Siehe ex Stefanoff, Monogr. Colch. (Sborn. B'lghar. Akad. Nauk. xxii.) 34 (1926), inobs.
Colchicum diampolis Delip. & Ceschm. Fl. Reipubl. Popul. Bulgar. ii. 191, 402 (1964).
Colchicum szovitsii var. bifolium (Freyn & Sint.) Bordz. Trudy Tiflissk. Bot. Sada 18: 489. 1919
Colchicum szovitsii var. nivale Boiss. & A.Huet Diagn. Pl. Orient. ser. 2, 4: 122. 1859

Common names Top

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Language Common/alternative name
Arabic لحلاح زوفيتسي
German vorfrühlings-zeitlose
Persian گلحسرت برفدوست
Russian Безвременник Шовица
Turkish katır çiğdemi

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Colchicum szovitsii subsp. brachyphyllum (Boiss. & Hausskn.) K.Perss. Bot. Jahrb. Syst. 127: 221 (2007)
Colchicum szovitsii subsp. szovitsii Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
must have summer heat to germinate; may take 6 years to germinate; grow seedlings @ 4°C x 1 month

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Turkmenistan
    • Western Asia
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764025
Tropicos 18404245
KEW urn:lsid:ipni.org:names:533394-1
The Plant List kew-302956
Open Tree Of Life 998068
Observations.org 146890
NCBI Taxonomy 1094121
IPNI 533394-1
iNaturalist 363505
GBIF 2739945
EOL 1087049
Elurikkus 294036
Wikipedia Colchicum_szovitsii

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
Phenethyisoquinoline Alkaloids from the Leaves of Androcymbium palaestinum El-Elimat T, Alhawarri MB, Rivera-Chávez J, Burdette JE, Czarnecki A, Al-Gharaibeh M, Al Sharie AH, Alhusban A, Alali F, Oberlies NH Fitoterapia 21-Aug-2020
PMCID:PMC7871506
doi:10.1016/j.fitote.2020.104706
PMID:32829012
Phytochemical Profile and Biological Properties of Colchicum triphyllum (Meadow Saffron) Senizza B, Rocchetti G, Okur MA, Zengin G, Yıldıztugay E, Ak G, Montesano D, Lucini L Foods 08-Apr-2020
PMCID:PMC7231061
doi:10.3390/foods9040457
PMID:32276367
Chemical Profiling and Biological Properties of Extracts from Different Parts of Colchicum Szovitsii Subsp. Szovitsii Rocchetti G, Senizza B, Zengin G, Okur MA, Montesano D, Yildiztugay E, Lobine D, Mahomoodally MF, Lucini L Antioxidants (Basel) 11-Dec-2019
PMCID:PMC6943543
doi:10.3390/antiox8120632
PMID:31835669
Structure-Dependent Activity of Natural GABA(A) Receptor Modulators Çiçek SS Molecules 22-Jun-2018
PMCID:PMC6100244
doi:10.3390/molecules23071512
PMID:29932138
Structure of szovitsidine M. K. Yusupov, Kh. A. Aslanov, Din' Tkhi Bik Ngo Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570709
Two Trioxygenated Phenethylisoquinoline Alkaloids from Colchicum szovitsii Emilia Tojo, Mustafa Ali Önür, Alan J. Freyer, Maurice Shamma American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50069A015
Mass-Spectrometric analysis of homoaporphine bases structure of szovitsinine A. K. Kasimov, �. Kh. Timbekov, M. K. Yusupov, Kh. A. Aslanov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00563946
Alkaloids ofColchicum szovitsii. Structure of szovitsamine M. K. Yusupov, Din'Tkhi Ngo, Kh. A. Aslanov, A. S. Sadykov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567063
O-methylkreysigine fromColchicum szovitsii M. K. Yusupov, Din' Tkhi Bik Ngo, Kh. A. Aslanov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00566822

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 / Androcymbine alkaloids
O-methylandrocymbine 15286666 Click to see CN1CCC23C=C(C(=O)C=C2C1CCC4=CC(=C(C(=C34)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1007/BF00570709
> Alkaloids and derivatives / Homoaporphines
(6As)-1,2,10,11,12-pentamethoxy-6-methyl-4,5,6,6a,7,8-hexahydrobenzo[6,7]cyclohepta[1,2,3-ij]isoquinoline 11258064 Click to see CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)OC)OC)OC)OC)OC 399.50 unknown https://doi.org/10.1007/BF00566822
3,4,5,16,17-Pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,6,14,16-hexaene 13943915 Click to see CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)OC)OC)OC)OC)OC 399.50 unknown https://doi.org/10.1007/BF00566822
4,5,16,17-Tetramethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,6,14,16-hexaen-3-ol 14488021 Click to see CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)O)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1007/BF00567063
4,5,17-Trimethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,6,14,16-hexaene-3,16-diol 101967021 Click to see CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)O)OC)OC)OC)O 371.40 unknown https://doi.org/10.1007/BF00563946
> Alkaloids and derivatives / Phenethylisoquinoline alkaloids
(1S)-1-[2-(4-hydroxyphenyl)ethyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 14655880 Click to see CN1CCC2=CC(=C(C=C2C1CCC3=CC=C(C=C3)O)OC)O 313.40 unknown https://doi.org/10.1021/NP50069A015
(1S)-7-methoxy-1-[2-(4-methoxyphenyl)ethyl]-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 14655882 Click to see CN1CCC2=CC(=C(C=C2C1CCC3=CC=C(C=C3)OC)OC)O 327.40 unknown https://doi.org/10.1021/NP50069A015
> Hydrocarbon derivatives / Tropones
2-Demethylcolchicine 23757 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 385.40 unknown https://doi.org/10.1007/BF00566822
https://doi.org/10.1007/BF00567063
Colchicine 6167 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 399.40 unknown https://doi.org/10.1007/BF00566822
https://doi.org/10.1007/BF00567063
> Hydrocarbon derivatives / Tropones / Tropolones
Acetamide, N-(5,6,7,9-tetrahydro-2,10-dihydroxy-1,3-dimethoxy-9-oxobenzo(a)heptalen-7-yl)-, (S)- 453130 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)O)OC)O)OC 371.40 unknown https://doi.org/10.1007/BF00567063
> Organoheterocyclic compounds / Piperidines
(7S,10S,16R,17S)-4,5,16,17-tetramethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,14-tetraen-3-ol 162978893 Click to see CN1CCC2=CC(C(C3=C2C1CCC4C3=C(C(=C(C4)OC)OC)O)OC)OC 389.50 unknown https://doi.org/10.1007/BF00567063
4,5,16,17-Tetramethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,14-tetraen-3-ol 162978892 Click to see CN1CCC2=CC(C(C3=C2C1CCC4C3=C(C(=C(C4)OC)OC)O)OC)OC 389.50 unknown https://doi.org/10.1007/BF00567063

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