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Galanthus trojanus

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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 UUID6440267410401134743751
Scientific name Galanthus trojanus
Authority A.P.Davis & Özhatay
First published in Bot. J. Linn. Soc. 137: 409 (2001)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Arabic زهرة اللبن الطروادية

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000768868
Tropicos 100194446
KEW urn:lsid:ipni.org:names:20003213-1
The Plant List kew-307612
Open Tree Of Life 173212
NCBI Taxonomy 715486
IUCN Red List 164902
IPNI 20003213-1
iNaturalist 436419
GBIF 2855373
EOL 1088818
USDA GRIN 420105

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
Antileishmanial Activity of Clinanthus milagroanthus S. Leiva & Meerow (Amaryllidaceae) Collected in Peru Soto-Vásquez MR, Alvarado-García PA, Osorio EH, Tallini LR, Bastida J Plants (Basel) 10-Jan-2023
PMCID:PMC9866881
doi:10.3390/plants12020322
PMID:36679035
Biological Activities of Snowdrop (Galanthus spp., Family Amaryllidaceae) Kong CK, Low LE, Siew WS, Yap WH, Khaw KY, Ming LC, Mocan A, Goh BH, Goh PH Front Pharmacol 19-Feb-2021
PMCID:PMC7933568
doi:10.3389/fphar.2020.552453
PMID:33679383
Antiprotozoal alkaloids from Galanthus trojanus Gulen Irem Kaya, Buket Sarıkaya, Mustafa Ali Onur, Nehir Unver Somer, Francesc Viladomat, Carles Codina, Jaume Bastida, Ina L. Lauinger, Marcel Kaiser, Deniz Tasdemir Elsevier BV 24-Jun-2011
doi:10.1016/J.PHYTOL.2011.05.008

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 / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Dihydrolycorine 11876135 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1CC(C5O)O)OCO4 289.33 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
4-hydroxy-5H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 12305242 Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(C(=CC=C4)O)NC3=O 255.22 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Stylopine 440583 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
Tetrahydrocoptisine 6770 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
> Alkaloids and derivatives / Protopine alkaloids
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(1R,2R)-1-(1,3-benzodioxol-5-yl)-2-[4-[(2R,3S,4R,5S)-5-[4-[(1R,2R)-1-(3,4-dimethoxyphenyl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 158356097 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC(C)C(C3=CC4=C(C=C3)OCO4)O)OC)C5=CC(=C(C=C5)OC(C)C(C6=CC(=C(C=C6)OC)OC)O)OC)C 716.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic acid 938 Click to see C1=CC(=CN=C1)C(=O)O 123.11 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1R,10S,12S)-5-methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-4,12-diol 162875147 Click to see COC1=C(C=C2C(=C1)CN3CCC24C3CC(C=C4)O)O 273.33 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
(1S,10S,12S,15R)-4,12-dimethoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-5,15-diol 155517055 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC(=C(C=C34)OC)O)O 303.35 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008
5-Methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-4,12-diol 78171537 Click to see COC1=C(C=C2C(=C1)CN3CCC24C3CC(C=C4)O)O 273.33 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.008

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