Lycoris squamigera - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID64401bf8a73a2392343050
Scientific name Lycoris squamigera
Authority Maxim.
First published in Bot. Jahrb. Syst. 6: 79 (1884)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Hippeastrum squamigerum H.Lév. Liliac. & C.Chine : 21 (1905)
Amaryllis hallii hort. ex Baker Bot. Mag. 123: t. 7547 (1897)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English resurrection lily
English magic lily
English surprise lily
Japanese ナツズイセン
Korean 상사화
lzh 鹿蔥
Swedish tempellilja
Chinese 鹿葱
Chinese 夏水仙
Chinese 鹿蔥

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northeastern U.S.A.
      • Ohio
    • Southeastern U.S.A.
      • Tennessee

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000683542
Flora of Alabama 5483
USDA Plants LYSQ
Tropicos 1200144
KEW urn:lsid:ipni.org:names:65810-1
The Plant List kew-280535
Missouri Botanical Garden 275706
Open Tree Of Life 859701
NCBI Taxonomy 112568
IPNI 65810-1
iNaturalist 446794
GBIF 5326179
Freebase /m/03d1kkh
EOL 1003205
USDA GRIN 22986
Wikipedia Lycoris_squamigera

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
Phytoconstituents and Ergosterol Biosynthesis-Targeting Antimicrobial Activity of Nutmeg (Myristica fragans Houtt.) against Phytopathogens Cruz A, Sánchez-Hernández E, Teixeira A, Oliveira R, Cunha A, Martín-Ramos P Molecules 18-Jan-2024
PMCID:PMC10819938
doi:10.3390/molecules29020471
PMID:38257384
Effective inhibition of HCoV-OC43 and SARS-CoV-2 by phytochemicals in vitro and in vivo. Ojha D, Jessop F, Bosio CM, Peterson KE Int J Antimicrob Agents 18-Jun-2023
PMCID:PMC10277159
doi:10.1016/j.ijantimicag.2023.106893
PMID:37339711
Comparative Plastome Analysis of Three Amaryllidaceae Subfamilies: Insights into Variation of Genome Characteristics, Phylogeny, and Adaptive Evolution Cheng RY, Xie DF, Zhang XY, Fu X, He XJ, Zhou SD Biomed Res Int 24-Mar-2022
PMCID:PMC8970886
doi:10.1155/2022/3909596
PMID:35372568
Comparative plastomics of Amaryllidaceae: inverted repeat expansion and the degradation of the ndh genes in Strumaria truncata Jacq. Könyves K, Bilsborrow J, Christodoulou MD, Culham A, David J PeerJ 12-Nov-2021
PMCID:PMC8592052
doi:10.7717/peerj.12400
PMID:34824912
Jeopardy of COVID-19: Rechecking the Perks of Phytotherapeutic Interventions Saha P, Bose S, Srivastava AK, Chaudhary AA, Lall R, Prasad S Molecules 10-Nov-2021
PMCID:PMC8621307
doi:10.3390/molecules26226783
PMID:34833873
Gene Loss, Pseudogenization in Plastomes of Genus Allium (Amaryllidaceae), and Putative Selection for Adaptation to Environmental Conditions Scobeyeva VA, Artyushin IV, Krinitsina AA, Nikitin PA, Antipin MI, Kuptsov SV, Belenikin MS, Omelchenko DO, Logacheva MD, Konorov EA, Samoilov AE, Speranskaya AS Front Genet 08-Jul-2021
PMCID:PMC8296844
doi:10.3389/fgene.2021.674783
PMID:34306019
The complete chloroplast genome sequence of Heteropolygonatum ginfushanicum (Asparagaceae) and phylogenetic analysis Gu L, Su T, Luo GL, Hu GX Mitochondrial DNA B Resour 31-May-2021
PMCID:PMC8168753
doi:10.1080/23802359.2021.1933636
PMID:34104777
Human respiratory viral infections: Current status and future prospects of nanotechnology-based approaches for prophylaxis and treatment Dawre S, Maru S Life Sci 26-Apr-2021
PMCID:PMC8074533
doi:10.1016/j.lfs.2021.119561
PMID:33915132
In Vitro Screening of East Asian Plant Extracts for Potential Use in Reducing Ruminal Methane Production Bharanidharan R, Arokiyaraj S, Baik M, Ibidhi R, Lee SJ, Lee Y, Nam IS, Kim KH Animals (Basel) 04-Apr-2021
PMCID:PMC8066825
doi:10.3390/ani11041020
PMID:33916571
In silico validation of potent phytochemical orientin as inhibitor of SARS-CoV-2 spike and host cell receptor GRP78 binding Bhowmik A, Biswas S, Hajra S, Saha P Heliyon 11-Jan-2021
PMCID:PMC7799170
doi:10.1016/j.heliyon.2021.e05923
PMID:33458435
The complete chloroplast genome of Clivia miniata Wang W, Zhang F, Li C, Zhou X Mitochondrial DNA B Resour 03-Feb-2020
PMCID:PMC7748490
doi:10.1080/23802359.2020.1721033
PMID:33366851
The complete chloroplast genome of Lycoris aurea (L’Hér.) Herb Peng Y, Wei J, Yang L Mitochondrial DNA B Resour 24-Jan-2020
PMCID:PMC7748574
doi:10.1080/23802359.2020.1715296
PMID:33366751
Characterisation of the complete chloroplast genome of Lycoris longituba (Amaryllidaceae) Zhang F, Tong H, Yang H, Wang T, Zhuang W, Shu X, Wang Z Mitochondrial DNA B Resour 25-Oct-2019
PMCID:PMC7707485
doi:10.1080/23802359.2019.1681324
PMID:33366189
Characterization of the complete chloroplast genome of Asparagus setaceus Li JR, Li SF, Wang J, Dong R, Zhu HW, Li N, Deng CL, Gao WJ Mitochondrial DNA B Resour 18-Jul-2019
PMCID:PMC7706555
doi:10.1080/23802359.2019.1643798
PMID:33365661
The complete chloroplast genome sequence of Magic Lily (Lycoris squamigera) Jin SW, Park JY, Kang SJ, Park HS, Shim H, Lee TJ, Kang JH, Sung SH, Yang TJ Mitochondrial DNA B Resour 26-Oct-2018
PMCID:PMC7799502
doi:10.1080/23802359.2018.1527193
PMID:33474468

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
(-)-Montanine 11087935 Click to see COC1C=C2C(CC1O)N3CC2C4=CC5=C(C=C4C3)OCO5 301.34 unknown https://doi.org/10.3987/COM-08-S(F)92
Squamigine 25208436 Click to see C1C(C=CC2(C1N3CC2C4=CC5=C(C=C4C3)OCO5)O)O 287.31 unknown https://doi.org/10.3987/COM-08-S(F)92
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(1S,12S,14S)-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-triene-9,14-diol 162965349 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)O)O 275.34 unknown https://doi.org/10.3987/COM-08-S(F)92
(1S,12S,14S)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol 12312560 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O 289.40 unknown https://doi.org/10.3987/COM-08-S(F)92
1,2-Dihydrogalanthamine 625595 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O 289.40 unknown https://doi.org/10.3987/COM-08-S(F)92
4-Methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-triene-9,14-diol 162965348 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)O)O 275.34 unknown https://doi.org/10.3987/COM-08-S(F)92
9-Methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-ol 11357792 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown https://doi.org/10.3987/COM-08-S(F)92
Epigalanthamin 3449 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.3987/COM-08-S(F)92
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.3987/COM-08-S(F)92
Norgalanthamine 9838394 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown https://doi.org/10.3987/COM-08-S(F)92
Sanguinine 443722 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)O 273.33 unknown https://doi.org/10.3987/COM-08-S(F)92
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Norbelladine-type amaryllidaceae alkaloids
(alphaR)-4-Hydroxy-alpha-[[[(3-hydroxy-4-methoxyphenyl)methyl]methylamino]methyl]benzenemethanol 102038797 Click to see CN(CC1=CC(=C(C=C1)OC)O)CC(C2=CC=C(C=C2)O)O 303.35 unknown https://doi.org/10.3987/COM-08-S(F)92
5-[[[2-Hydroxy-2-(4-hydroxyphenyl)ethyl]-methylamino]methyl]-2-methoxyphenol 163055676 Click to see CN(CC1=CC(=C(C=C1)OC)O)CC(C2=CC=C(C=C2)O)O 303.35 unknown https://doi.org/10.3987/COM-08-S(F)92
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
2,3,4-trihydroxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 434381 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O 291.26 unknown https://doi.org/10.3987/COM-08-S(F)92
Ismine 188957 Click to see CNC1=CC=CC=C1C2=CC3=C(C=C2CO)OCO3 257.28 unknown https://doi.org/10.3987/COM-08-S(F)92
Lycoricidin-A 619061 Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O)O 307.25 unknown https://doi.org/10.3987/COM-08-S(F)92
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(3S,13bS)-3,8beta-Dimethoxy-5-methyl-3,4,4abeta,5,6,6abeta-hexahydro-8H-[1,3]dioxolo[6,7][2]benzopyrano[3,4-c]indole 10926024 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)OC)OCO5 345.40 unknown https://doi.org/10.3987/COM-08-S(F)92
o-Methylprecriwelline 550913 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)OC)OCO5 345.40 unknown https://doi.org/10.3987/COM-08-S(F)92
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.3987/COM-08-S(F)92
Tazettine 271607 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.3987/COM-08-S(F)92
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
3-[(4S,5S,8S,9R,10S,13R,14R,17R)-5,8,9,13-tetramethyl-3-oxo-17-propan-2-yl-1,2,4,6,7,10,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-4-yl]propanoic acid 163007975 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC(=O)C4CCC(=O)O)C)C)C)C 416.60 unknown https://doi.org/10.3987/COM-08-S(F)92
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,12S)-16-methoxy-1,5,5,15,17,17-hexamethyl-8-methylidene-12-propan-2-yl-19-oxatetracyclo[9.8.0.04,7.013,18]nonadeca-13(18),15-dien-14-one 162818693 Click to see CC1=C(C(C2=C(C1=O)C(C3CCC(=C)C4CC(C4CCC3(O2)C)(C)C)C(C)C)(C)C)OC 440.70 unknown https://doi.org/10.3987/COM-08-S(F)92
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
N-[1-(5-hydroxy-6-methyloxan-2-yl)-2-oxopyrimidin-4-yl]-3-methylbut-2-enamide 163061909 Click to see CC1C(CCC(O1)N2C=CC(=NC2=O)NC(=O)C=C(C)C)O 307.34 unknown https://doi.org/10.3987/COM-08-S(F)92
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Lycoricidine 73065 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O 291.26 unknown https://doi.org/10.3987/COM-08-S(F)92
Narciclasine 72376 Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O)O 307.25 unknown https://doi.org/10.3987/COM-08-S(F)92

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.