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Colchicum szovitsii subsp. brachyphyllum

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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 UUID64402a7781125213282163
Scientific name Colchicum szovitsii subsp. brachyphyllum
Authority (Boiss. & Hausskn.) K.Perss.
First published in Bot. Jahrb. Syst. 127: 221 (2007)

Description Top

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Common names Top

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000810885
Tropicos 100170747
KEW urn:lsid:ipni.org:names:77087130-1
The Plant List kew-349129
Open Tree Of Life 685386
NCBI Taxonomy 1094123
IPNI 77087130-1
iNaturalist 494125
GBIF 2739959
CMAUP NPO24146

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
New colchicinoids from a native Jordanian meadow saffron, colchicum brachyphyllum: isolation of the first naturally occurring dextrorotatory colchicinoid. Alali FQ, El-Elimat T, Li C, Qandil A, Alkofahi A, Tawaha K, Burgess JP, Nakanishi Y, Kroll DJ, Navarro HA, Falkinham JO 3rd, Wani MC, Oberlies NH J Nat Prod 01-Feb-2005
doi:10.1021/NP0496587
PMID:15730238

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 / Allocolchicine alkaloids
(-)-Androbiphenyline 10927179 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=C1C(=C(C=C3)OC)O)OC)OC)OC 387.40 unknown https://doi.org/10.1021/NP0496587
> Alkaloids and derivatives / Lumicolchicine alkaloids
gamma-Lumicolchicine 244898 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=C1C4C3C=C(C4=O)OC)OC)OC)OC 399.40 unknown https://doi.org/10.1021/NP0496587
gamma-Lumicolchicine 110937 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=C1C4C3C=C(C4=O)OC)OC)OC)OC 399.40 unknown https://doi.org/10.1021/NP0496587
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones
(7S)-2,3-dihydroxy-1,10-dimethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 11393749 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)O 343.40 unknown via CMAUP database
1,2,3,10-tetramethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 2832 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1021/NP0496587
2-hydroxy-1,3,10-trimethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 14413735 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 357.40 unknown https://doi.org/10.1021/NP0496587
3-Demethyldemecolcine 14413737 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 357.40 unknown https://doi.org/10.1021/NP0496587
3-Desmethylcolchicine 299664 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 385.40 unknown https://doi.org/10.1021/NP0496587
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/10.1021/NP0496587
Demecolcine 220401 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1021/NP0496587
Demecolcinone 44583926 Click to see CC12CC3N1C24C=C(C(=O)C(=C4C5=CC=C(C(=O)C=C35)OC)OC)O 339.30 unknown via CMAUP database
N-(1,2,3,10-Tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)acetamide 2833 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/10.1021/NP0496587
N-(3-hydroxy-1,2,10-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl)acetamide 494161 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 385.40 unknown https://doi.org/10.1021/NP0496587
> Organoheterocyclic compounds / Benzodioxoles
(-)-Cornigerine 10000015 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=CC=C(C(=O)C=C14)OC)OC)OCO3 383.40 unknown https://doi.org/10.1021/NP0496587
Cornigerine 100188 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=CC=C(C(=O)C=C14)OC)OC)OCO3 383.40 unknown https://doi.org/10.1021/NP0496587

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