Chlidanthus fragrans - Unknown
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Internal ID UUID644025851495f881255511
Scientific name Chlidanthus fragrans
Authority Herb.
First published in Appendix : 46 (1821)

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Synonyms Top

Scientific name Authority First published in
Clitanthes lutea Herb. Edwards's Bot. Reg. 25(Misc.): 87 (1839)
Coleophyllum ehrenbergii Klotzsch Allg. Gartenzeitung 8: 185 (1840)
Hippeastrum marginatum R.E.Fr. Nova Acta Regiae Soc. Sci. Upsal. , ser. 4, 1(1): 161 (1905)
Pancratium luteum Poir. ex Spreng. Syst. Veg. 2: 48 (1825)
Sanmartina marginata (R.E.Fr.) Traub Pl. Life 7: 41 (1951)
Castellanoa marginata (R.E.Fr.) Traub Pl. Life 9: 69 (1953)
Chlidanthus ehrenbergii Kunth Enum. Pl. 5: 654 (1850)
Chlidanthus marginatus (R.E.Fr.) Ravenna Pl. Life 30: 73 (1974)

Common names Top

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Language Common/alternative name
Chinese 黛玉花

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Varieties (abbr. var.) 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
  • Southern America
    • Southern South America
      • Argentina Northwest
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000763183
Tropicos 1200542
KEW urn:lsid:ipni.org:names:63594-1
The Plant List kew-302157
Open Tree Of Life 564148
NCBI Taxonomy 82222
IPNI 63594-1
iNaturalist 371532
GBIF 2854008
EPPO CKEFR
EOL 1086705
USDA GRIN 411934

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
Interactions of Isoquinoline Alkaloids with Transition Metals Iron and Copper Parvin MS, Chlebek J, Hošťálková A, Catapano MC, Lomozová Z, Macáková K, Mladěnka P Molecules 29-Sep-2022
PMCID:PMC9572997
doi:10.3390/molecules27196429
PMID:36234964
Recent Progress on Biological Activity of Amaryllidaceae and Further Isoquinoline Alkaloids in Connection with Alzheimer’s Disease Cahlíková L, Vrabec R, Pidaný F, Peřinová R, Maafi N, Mamun AA, Ritomská A, Wijaya V, Blunden G Molecules 29-Aug-2021
PMCID:PMC8434202
doi:10.3390/molecules26175240
PMID:34500673
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors Hulcová D, Breiterová K, Siatka T, Klímová K, Davani L, Šafratová M, Hošťálková A, De Simone A, Andrisano V, Cahlíková L Molecules 21-Mar-2018
PMCID:PMC6017564
doi:10.3390/molecules23040719
PMID:29561817
Acetylcholinesterase-inhibiting Alkaloids from Zephyranthes concolor Reyes-Chilpa R, Berkov S, Hernández-Ortega S, Jankowski CK, Arseneau S, Clotet-Codina I, Esté JA, Codina C, Viladomat F, Bastida J Molecules 15-Nov-2011
PMCID:PMC6264317
doi:10.3390/molecules16119520
PMID:22086403
Alkaloide von <i>Chlidanthus fragrans</i>, <i>Vallota purpurea</i>, <i>Nerine undulata</i> und <i>Hippeastrum vittatum</i> (XI. Mitteil. über Amaryllidaceen‐Alkaloide) Hans‐G. Boit Wiley 20-May-2007
doi:10.1002/CBER.19560890509
First Nuclear DNA Amounts in more than 300 Angiosperms ZONNEVELD BJ, LEITCH IJ, BENNETT MD Ann Bot 19-May-2005
PMCID:PMC4246870
doi:10.1093/aob/mci170
PMID:15905300

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 / Galanthamine-type amaryllidaceae alkaloids
(1S,12S,14R)-14-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-9-ol 9814447 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)OC 287.35 unknown https://doi.org/10.1002/CBER.19560890509
14-Methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-9-ol 12303005 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)OC 287.35 unknown https://doi.org/10.1002/CBER.19560890509

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