Galanthus gracilis - Unknown
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Internal ID UUID644026722eddb216422203
Scientific name Galanthus gracilis
Authority Čelak.
First published in Sitzungsber. Königl. Böhm. Ges. Wiss., Math.-Naturwiss. Cl. 1891(1): 195 (1891)

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Synonyms Top

Scientific name Authority First published in
Galanthus elwesii subsp. minor D.A.Webb Bot. J. Linn. Soc. 76: 312 (1978)
Galanthus elwesii var. stenophyllus Kamari Bot. Jahrb. Syst. 103: 122 (1982)
Galanthus reflexus Herb. ex Lindl. Edwards's Bot. Reg. 31(Misc.): 35. 1845
Galanthus nivalis subsp. reflexus (Lindl.) K.Richt. Pl. Eur. 1: 234. 1890 (1890)

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Language Common/alternative name
English snowdrop
German zierliches schneeglöckchen

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Ukraine
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Romania

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000768799
Tropicos 100194400
KEW urn:lsid:ipni.org:names:64482-1
The Plant List kew-307547
Open Tree Of Life 855278
NCBI Taxonomy 197690
IUCN Red List 164897
IPNI 64482-1
iNaturalist 436414
GBIF 2855425
EPPO GAXGR
EOL 1088806
USDA GRIN 410779

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Vicinal ketoesters – key intermediates in the total synthesis of natural products Beller MP, Koert U Beilstein J Org Chem 15-Sep-2022
PMCID:PMC9490073
doi:10.3762/bjoc.18.129
PMID:36158171
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
The Gracilines: A Novel Subgroup of the Amaryllidaceae Alkaloids Manfred Hesse, Seda Noyan, Gudrun Hopp Rentsch, Mustafa Ali Önür, Tekant Gözler, Belkis Gözler The Japan Institute of Heterocyclic Chemistry 24-Mar-2009
doi:10.3987/COM-98-8201
Four New Amaryllidaceae Alkaloids from Galanthus gracilis andÅ@Galanthus plicatus Subsp. byzantinus Manfred Hesse, Nehir Ünver, Seda Noyan, Belkis Gözler, Takant Gözler, Christa Werner The Japan Institute of Heterocyclic Chemistry 09-Mar-2009
doi:10.3987/COM-00-9132
Three New Tazettine-Type Alkaloids from Galanthus gracilis and Galanthus plicatus Subsp. byzantinus. Unver N, Noyan S, Gözler T, Onür MA, Gözler B, Hesse M Planta Med 01-May-1999
doi:10.1055/S-1999-14062
PMID:17260261

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 / Gracilline-type amaryllidaceae alkaloids
(1R,13R,15R)-20-methyl-5,7,12-trioxa-20-azapentacyclo[11.4.3.01,13.02,10.04,8]icosa-2,4(8),9,16-tetraen-15-ol 15384999 Click to see CN1CCC23C1(CC(C=C2)O)OCC4=CC5=C(C=C34)OCO5 301.34 unknown https://doi.org/10.3987/COM-00-9132
(1R,13R)-20-methyl-5,7,12-trioxa-20-azapentacyclo[11.4.3.01,13.02,10.04,8]icosa-2,4(8),9,14,16-pentaene 15384996 Click to see CN1CCC23C1(C=CC=C2)OCC4=CC5=C(C=C34)OCO5 283.32 unknown https://doi.org/10.3987/COM-98-8201
20-Methyl-5,7,12-trioxa-20-azapentacyclo[11.4.3.01,13.02,10.04,8]icosa-2,4(8),9,16-tetraen-15-ol 73193544 Click to see CN1CCC23C1(CC(C=C2)O)OCC4=CC5=C(C=C34)OCO5 301.34 unknown https://doi.org/10.3987/COM-00-9132
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(+)-3-O-demethylcriwelline 12304582 Click to see CN1CC2(C3(C1CC(C=C3)O)C4=CC5=C(C=C4CO2)OCO5)O 317.34 unknown https://doi.org/10.1055/S-1999-14062
(1S,13R,16S,18R)-18-hydroxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-11-one 101035658 Click to see CN1CC2C3(C1CC(C=C3)O)C4=CC5=C(C=C4C(=O)O2)OCO5 315.32 unknown https://doi.org/10.1055/S-1999-14062
18-Hydroxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-11-one 162934310 Click to see CN1CC2C3(C1CC(C=C3)O)C4=CC5=C(C=C4C(=O)O2)OCO5 315.32 unknown https://doi.org/10.1055/S-1999-14062
Isotazettinol 535745 Click to see CN1CC2(C3(C1CC(C=C3)O)C4=CC5=C(C=C4CO2)OCO5)O 317.34 unknown https://doi.org/10.1055/S-1999-14062
> Organoheterocyclic compounds / Naphthopyrans
34,38-Dimethyl-8,10,15,22,27,29-hexaoxa-34,38-diazaundecacyclo[19.11.3.34,16.23,17.01,21.02,18.04,16.05,13.07,11.024,32.026,30]tetraconta-5,7(11),12,19,24,26(30),31,36-octaene 163192467 Click to see CN1CCC23C1(C4C=CC2C5C4C=CC67C5(CN(C6)C)C8=CC9=C(C=C8CO7)OCO9)OCC1=CC2=C(C=C31)OCO2 566.60 unknown https://doi.org/10.3987/COM-98-8201
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Trisphaeridine 443684 Click to see C1OC2=C(O1)C=C3C4=CC=CC=C4N=CC3=C2 223.23 unknown https://doi.org/10.1055/S-1999-14062

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