Lycoris radiata, also known as the red spider lily, is a plant in the amaryllis family that is native to China, Japan, Korea, and Nepal. It has been introduced to other countries, including the United States, where it is considered naturalized. The plant is known for its bright red flowers that bloom in late summer or autumn, often in response to heavy rainfall. It is also called the hurricane lily or resurrection lily due to its ability to bloom after a heavy rain. The plant has a bulbous perennial and produces showy flowers with spindly stamens that resemble spider legs. It is often used as an ornamental and medicinal plant in various countries. However, it is important to note that the plant is toxic if ingested. In Japanese culture, the red spider lily is associated with death and is often planted near grave sites. It is also used in Buddhist ceremonies to honor ancestors.

Synonyms Top

Scientific name	Authority	First published in
Lycoris terracianii	Hort.Dammann.	Nursery Cat. (Dammann) 44: 4 (1889)
Lycoris radiata var. kazukoana	N.Yonez.	J. Phytogeogr. Taxon. 37: 73 (1989)
Lycoris radiata f. bicolor	N.Yonez.	J. Phytogeogr. Taxon. 37: 74 (1989)
Nerine japonica	Miq.	Ann. Mus. Bot. Lugduno-Batavi 2: 139 (1865)
Nerine radiata	Sweet	Hort. Brit. : 403 (1826)
Orexis radiata	Salisb.	Gen. Pl. : 118 (1866)
Amaryllis radiata	L'Hér.	Sert. Angl. : 15 (1789)
Lycoris radiata var. pumila	Grey	Hardy Bulbs 2: 58. 1938
Lycoris radiata var. terraccianii	Dammann	Nursery Cat. (Dammann) 44: 4. 1889

Common names Top

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Filter by language:

Language	Common/alternative name
English	red magic lily
English	red spider lily
Spanish	nerine japonica
Spanish	lycoris radiata forma bicolor
Spanish	lycoris radiata var kazukoana
Spanish	lycoris radiata var pumila
Spanish	lycoris radiata var. kazukoana
Spanish	lycoris radiata var. pumila
Spanish	amaryllis radiata
Spanish	lycoris terracianii
Spanish	nerine radiata
Spanish	orexis radiata
Arabic	زنبق العنكبوت الأحمر
Czech	lykoris
Persian	سوسن عنکبوتی قرمز
Upper Sorbian	pruhowy lykoris
Indonesian	bunga lili merah
Indonesian	bakung lelabah merah
Japanese	マンジュシャゲ
Japanese	ヒガンバナ
Japanese	石蒜
Japanese	死人花
Japanese	曼珠沙華
Japanese	地獄花
Japanese	まんじゅしゃげ
Japanese	セキサン
Japanese	彼岸花
Korean	석산
Korean	꽃무릇
Korean	석산꽃
Korean	피안화
Malay	likoris radiata
Malay	lily labah labah merah
Malay	bakung labah labah merah
Russian	Ликорис лучистый
Slovenian	Žarkasti likoris
su	bakung lancah beureum
Swedish	röd tempellilja
Turkish	ekinoks Çiçeği
Ukrainian	Лікоріс променистий
za	gohofangz
Chinese	蔓珠莎華
Chinese	莉可莉丝
Chinese	老鸦蒜
Chinese	红花石蒜
Chinese	曼珠沙华
Chinese	山乌毒
Chinese	紅花石蒜
Chinese	龙爪花
Chinese	蟑螂花
Chinese	嶂螂花
Chinese	石蒜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

keep seedlings in pot for 2 years

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Western Indian Ocean
  - Seychelles

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto

Asia-tropical click to expand
- Indian Subcontinent
  - Nepal

Northern America click to expand
- North-central U.S.A.
  - Illinois
- Southeastern U.S.A.
  - Alabama
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Virginia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000683573
Florida Plant Atlas	1818
Flora of Alabama	4424
USDA Plants	LYRA
Tropicos	1201304
KEW	urn:lsid:ipni.org:names:60455959-2
The Plant List	kew-280540
Missouri Botanical Garden	275807
Open Tree Of Life	488729
NCBI Taxonomy	228395
Nature Serve	2.135123
IPNI	60455959-2
iNaturalist	164975
GBIF	5326188
Freebase	/m/05t04p1
EPPO	LYRRA
EOL	1003216
USDA GRIN	22982
Wikipedia	Lycoris_radiata
CMAUP	NPO27843

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

Genome-wide identification of GATA transcription factors in tetraploid potato and expression analysis in differently colored potato flesh

Zhang X, Fan R, Yu Z, Du X, Yang X, Wang H, Xu W, Yu X

Front Plant Sci

21-Mar-2024

PMCID:	PMC10991705
doi:	10.3389/fpls.2024.1330559
PMID:	38576788

Unveiling the Antiviral Properties of Panduratin A through SARS-CoV-2 Infection Modeling in Cardiomyocytes

Linn AK, Manopwisedjaroen S, Kanjanasirirat P, Borwornpinyo S, Hongeng S, Phanthong P, Thitithanyanont A

Int J Mol Sci

24-Jan-2024

PMCID:	PMC10855687
doi:	10.3390/ijms25031427
PMID:	38338708

Characterization of the Heat Shock Transcription Factor Family in Lycoris radiata and Its Potential Roles in Response to Abiotic Stresses

Wang N, Shu X, Zhang F, Song G, Wang Z

Plants (Basel)

17-Jan-2024

PMCID:	PMC10819275
doi:	10.3390/plants13020271
PMID:	38256823

In vivo neuroprotective capacity of a Dunaliella salina extract - comprehensive transcriptomics and metabolomics study

Valdés A, Sánchez-Martínez JD, Gallego R, Ibáñez E, Herrero M, Cifuentes A

NPJ Sci Food

10-Jan-2024

PMCID:	PMC10782027
doi:	10.1038/s41538-023-00246-7
PMID:	38200022

Reciprocal natural hybridization between Lycoris aurea and Lycoris radiata (Amaryllidaceae) identified by morphological, karyotypic and chloroplast genomic data

Quan M, Jiang X, Xiao L, Li J, Liang J, Liu G

BMC Plant Biol

02-Jan-2024

PMCID:	PMC10759762
doi:	10.1186/s12870-023-04681-2
PMID:	38163886

Research Progress on the Synergistic Anti-Tumor Effect of Natural Anti-Tumor Components of Chinese Herbal Medicine Combined with Chemotherapy Drugs

Zhou H, Zhang M, Cao H, Du X, Zhang X, Wang J, Bi X

Pharmaceuticals (Basel)

15-Dec-2023

PMCID:	PMC10748242
doi:	10.3390/ph16121734
PMID:	38139860

Hydrangea arborescens ‘Annabelle’ Flower Formation and Flowering in the Current Year

Huang X, Lyu T, Li Z, Lyu Y

Plants (Basel)

07-Dec-2023

PMCID:	PMC10748224
doi:	10.3390/plants12244103
PMID:	38140430

Transcriptome analysis of Lantana camara flower petals reveals candidate anthocyanin biosynthesis genes mediating red flower color development

Parrish SB, Paudel D, Deng Z

G3 (Bethesda)

17-Nov-2023

PMCID:	PMC10755171
doi:	10.1093/g3journal/jkad259
PMID:	37974306

Benzoindolizidine Alkaloids Tylophorine and Lycorine and Their Analogues with Antiviral, Anti-Inflammatory, and Anticancer Properties: Promises and Challenges

Di Sotto A, Valipour M, Azari A, Di Giacomo S, Irannejad H

Biomedicines

24-Sep-2023

PMCID:	PMC10603990
doi:	10.3390/biomedicines11102619
PMID:	37892993

Integrative HPLC profiling and transcriptome analysis revealed insights into anthocyanin accumulation and key genes at three developmental stages of black rice (Oryza sativa. L) caryopsis

Mackon E, Jeazet Dongho Epse Mackon GC, Yao Y, Guo Y, Ma Y, Dai X, Jandan TH, Liu P

Front Plant Sci

30-Aug-2023

PMCID:	PMC10505814
doi:	10.3389/fpls.2023.1211326
PMID:	37727854

Acetylcholinesterase Inhibition Activity of Hippeastrum papilio (Ravenna) Van Scheepen (Amaryllidaceae) Using Zebrafish Brain Homogenates

Tallini LR, da Silva CR, Jung T, Alves ED, Baldin SL, Apel M, Timmers LF, Rico EP, Bastida J, Zuanazzi JA

Life (Basel)

10-Aug-2023

PMCID:	PMC10455992
doi:	10.3390/life13081721
PMID:	37629578

Small-molecule amines: a big role in the regulation of bone homeostasis

Zhang Q, Yang J, Hu N, Liu J, Yu H, Pan H, Chen D, Ruan C

Bone Res

24-Jul-2023

PMCID:	PMC10363555
doi:	10.1038/s41413-023-00262-z
PMID:	37482549

The Role of Anthocyanins in Plant Tolerance to Drought and Salt Stresses

Dabravolski SA, Isayenkov SV

Plants (Basel)

05-Jul-2023

PMCID:	PMC10346810
doi:	10.3390/plants12132558
PMID:	37447119

Four new species of Phyllosticta from China based on morphological and phylogenetic characterization

Sui XN, Guo MJ, Zhou H, Hou CL

Mycology

04-Jul-2023

PMCID:	PMC10424619
doi:	10.1080/21501203.2023.2225552
PMID:	37583457

The metagenomics of soil bacteria and fungi and the release of mechanical dormancy in hard seeds

Wu Y, Sun XR, Pritchard HW, Shen YB, Wu XQ, Peng CY

Front Plant Sci

27-Jun-2023

PMCID:	PMC10335401
doi:	10.3389/fpls.2023.1187614
PMID:	37441178

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
Squamigine	25208436	Click to see C1C(C=CC2(C1N3CC2C4=CC5=C(C=C4C3)OCO5)O)O	287.31	unknown	https://doi.org/10.1002/HLCA.201000176
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(11R,13R,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol	10448507	Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O	317.34	unknown	via CMAUP database
(18-Hydroxy-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-11-yl) acetate	76017493	Click to see CC(=O)OC1C2=CC3=C(C=C2C45C=CC(CC4N1CC5O)OC)OCO3	359.40	unknown	https://doi.org/10.1002/HLCA.201000176
(1S,11R,13S,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol	162945732	Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O	317.34	unknown	https://doi.org/10.1002/HLCA.201000176
(1S,11R,13S,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol	49799009	Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O	317.34	unknown	https://doi.org/10.1248/CPB.39.1849
(1S,13S,15S,18S)-15-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol	5282090	Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O	317.34	unknown	https://doi.org/10.1248/CPB.39.1849
[(1R,11S,13S,15R,18S)-18-hydroxy-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-11-yl] acetate	162871353	Click to see CC(=O)OC1C2=CC3=C(C=C2C45C=CC(CC4N1CC5O)OC)OCO3	359.40	unknown	https://doi.org/10.1002/HLCA.201000176
1,2-Didehydrocrinan-3-ol	101727	Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4	271.31	unknown	https://doi.org/10.1248/CPB.39.1849
Haemanthidine	544807	Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O	317.34	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1002/HLCA.201000176
Vittatine	443693	Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4	271.31	unknown	https://doi.org/10.1248/CPB.39.1849
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(1R,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol	11033566	Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O	289.40	unknown	via CMAUP database
(1R,12S,14S)-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-triene-9,14-diol	10221208	Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)O)O	275.34	unknown	https://doi.org/10.1248/CPB.28.3433 https://doi.org/10.1248/CPB.39.1849
(1S,12S,14S)-9-methoxy-4-methyl-4-oxido-11-oxa-4-azoniatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol	14803831	Click to see C[N+]1(CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O)[O-]	305.40	unknown	https://doi.org/10.1248/CPB.39.1849
1,2-Dihydrogalanthamine	625595	Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O	289.40	unknown	https://doi.org/10.1248/CPB.28.3433 https://doi.org/10.1248/CPB.31.2146 https://doi.org/10.1248/CPB.39.1849
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/10.1248/CPB.28.3433 https://doi.org/10.1248/CPB.39.1849
Epigalantamine	676392	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O	287.35	unknown	https://doi.org/10.1248/YAKUSHI1881.53.8_807
Epigalanthamin	3449	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O	287.35	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/CPB.31.2146 https://doi.org/10.1248/YAKUSHI1881.53.8_807 https://doi.org/10.1248/CPB1953.1.139
Galantamine	9651	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O	287.35	unknown	https://doi.org/10.1248/CPB1953.1.139 https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1016/S0031-9422(00)89030-5 https://doi.org/10.1248/CPB.31.2146
Galanthamine N-Oxide	11748698	Click to see C[N+]1(CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O)[O-]	303.35	unknown	https://doi.org/10.1248/CPB.39.1849
Lycoramine	443723	Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O	289.40	unknown	https://doi.org/10.1248/CPB.28.3433 https://doi.org/10.1248/CPB.31.2146 https://doi.org/10.1248/CPB.39.1849
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
(2S,3R,7R,9S,10S,12R)-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-triene-9,12-diol	162851505	Click to see CN1CCC2C1C3C(C(C2)O)OC(C4=CC5=C(C=C34)OCO5)O	319.40	unknown	https://doi.org/10.1248/YAKUSHI1947.85.7_615
(2S,3S,9S,10S,12S)-12-methoxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-9-ol	78427698	Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(O3)OC)OCO5)O	331.40	unknown	https://doi.org/10.1002/HLCA.201000176
(2S,3S,9S,10S)-9-hydroxy-4-methyl-4-oxido-11,16,18-trioxa-4-azoniapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-12-one	15071950	Click to see C[N+]1(CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O)[O-]	331.32	unknown	https://doi.org/10.1248/CPB.39.1849
(2S,9S,10S)-9-hydroxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-12-one	10358316	Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O	315.32	unknown	via CMAUP database
(5aR,11cS)-9,10-dimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indol-7-ol	44202119	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)O)OC)OC	317.40	unknown	via CMAUP database
(5aR,7S,11bS,11cS)-7-ethoxy-9,10-dimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indole	197213	Click to see CCOC1C2=CC(=C(C=C2C3C(O1)CC=C4C3N(CC4)C)OC)OC	345.40	unknown	https://doi.org/10.1248/CPB.28.3433
(5aS,7R,11bR,11cR)-7,9,10-trimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indole	162850015	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)OC)OC)OC	331.40	unknown	https://doi.org/10.1248/CPB.31.2146
12-Methoxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-9-ol	162988926	Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(O3)OC)OCO5)O	331.40	unknown	https://doi.org/10.1002/HLCA.201000176
4-Methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-triene-9,12-diol	162851504	Click to see CN1CCC2C1C3C(C(C2)O)OC(C4=CC5=C(C=C34)OCO5)O	319.40	unknown	https://doi.org/10.1248/YAKUSHI1947.85.7_615
7-ethoxy-9,10-dimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indole	53463821	Click to see CCOC1C2=CC(=C(C=C2C3C(O1)CC=C4C3N(CC4)C)OC)OC	345.40	unknown	https://doi.org/10.1248/CPB.28.3433
7,9,10-trimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indole	15582595	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)OC)OC)OC	331.40	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/CPB.31.2146
9-Hydroxy-10-methoxy-1-methyl-2,3,5,5a,11b,11c-hexahydroisochromeno[3,4-g]indol-7-one	3844472	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)O)OC	301.34	unknown	https://doi.org/10.1248/CPB.28.3433 https://doi.org/10.1039/JR9590000172 https://doi.org/10.1248/CPB.31.2146 https://doi.org/10.1248/CPB.39.1849
9-O-Demethylhomolycorine	388787	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)O)OC	301.34	unknown	https://doi.org/10.1248/CPB.28.3433 https://doi.org/10.1039/JR9590000172 https://doi.org/10.1248/CPB.31.2146 https://doi.org/10.1248/CPB.39.1849
9,10-dimethoxy-1-methyl-3,5,5a,7,11b,11c-hexahydro-2H-isochromeno[3,4-g]indol-7-ol	4480710	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)O)OC)OC	317.40	unknown	https://doi.org/10.1248/CPB.28.3433
Hippeastrine	441594	Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O	315.32	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/CPB.31.2146 https://doi.org/10.1002/HLCA.201000176 https://doi.org/10.1248/CPB.28.3433
Hippeastrine (Hydrobromide)	580552	Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O	315.32	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/CPB.31.2146 https://doi.org/10.1002/HLCA.201000176 https://doi.org/10.1248/CPB.28.3433
Homolycorine	160473	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)OC)OC	315.40	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1002/HLCA.201000176 https://doi.org/10.1248/CPB.28.3433 https://doi.org/10.1248/YAKUSHI1881.49.5_438
Lycorenan-7-one,9,10-dimethoxy-1-methyl-	573128	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)OC)OC	315.40	unknown	https://doi.org/10.1248/CPB.28.3433 https://doi.org/10.1002/HLCA.201000176 https://doi.org/10.1248/YAKUSHI1881.49.5_438 https://doi.org/10.1248/CPB.39.1849
Lycorenine	160472	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)O)OC)OC	317.40	unknown	https://doi.org/10.1248/CPB.28.3433
O-Methyllycorenine	443730	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)OC)OC)OC	331.40	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/CPB.31.2146
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,15R,17S,18S,19R)-17,18-dihydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9-trien-11-one	45483152	Click to see C1CN2C3C1CC(C(C3C4=CC5=C(C=C4C2=O)OCO5)O)O	303.31	unknown	https://doi.org/10.1002/HLCA.201000176
2-epi-Lycorine	12305849	Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4	287.31	unknown	via CMAUP database
Dihydrolycorine	11876135	Click to see C1CN2CC3=CC4=C(C=C3C5C2C1CC(C5O)O)OCO4	289.33	unknown	https://doi.org/10.1002/HLCA.201000176
Lycorine	72378	Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4	287.31	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/CPB.31.2146
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
(2R,3R,4R,4aR)-2,3,4,7-tetrahydroxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one	6713068	Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O)O	307.25	unknown	via CMAUP database
(2R,3R,4S,4aR)-2,3,4-trihydroxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one	101648874	Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O	291.26	unknown	https://doi.org/10.1248/CPB.31.2146
(2R,3R,4S,4aR)-2,3,4,7-tetrahydroxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one	51351537	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/10.1248/CPB.31.2146
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/10.1002/HLCA.201000176 https://doi.org/10.1248/CPB.31.2146
ent-Lycoricidine	11011744	Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O	291.26	unknown	via CMAUP database
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/10.1248/CPB.31.2146
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,11S,13R,16S,18S)-18-methoxy-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-ol	162894672	Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5	331.40	unknown	https://doi.org/10.1248/CPB.28.3433
(1S,13R,16S,18S)-18-methoxy-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-ol	10314625	Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5	331.40	unknown	via CMAUP database
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-ol	419046	Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5	331.40	unknown	https://doi.org/10.1248/CPB.28.3433
Sekisanolin	5321780	Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O	331.40	unknown	https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/YAKUSHI1881.1927.545_545 https://doi.org/10.1248/YAKUSHI1881.49.5_438
Tazettine	271607	Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O	331.40	unknown	https://doi.org/10.1248/YAKUSHI1881.1927.545_545 https://doi.org/10.1248/CPB.39.1849 https://doi.org/10.1248/YAKUSHI1881.49.5_438
> Alkaloids and derivatives / Ibogan-type alkaloids
Vocamine	54601825	Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC	704.90	unknown	via CMAUP database
> Alkaloids and derivatives / Morphinans
(4R,4aR,7S,12bS)-10-[(4R,4aR,7S,7aR,12bS)-7,9-dihydroxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-10-yl]-3-methyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol	10460627	Click to see CN1CCC23C4C1CC5=CC(=C(C(=C52)OC3C(C=C4)O)O)C6=C(C7=C8C(=C6)CC9C1C8(CCN9C)C(O7)C(C=C1)O)O	568.70	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides / Hippuric acids and derivatives / Hippuric acids
Hippuric acid-15N	10702514	Click to see C1=CC=C(C=C1)C(=O)NCC(=O)O	180.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
(1S,2S)-(+)-norpseudoephedrine	6918945	Click to see CC(C(C1=CC=CC=C1)O)[NH3+]	152.21	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(+)-Galbacin	442873	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	via CMAUP database
(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/10.1002/HLCA.201000176
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate	8181	Click to see CCCCCCCCCCCCCCCC(=O)OC	270.50	unknown	https://doi.org/10.1248/CPB.39.1849
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate	5284421	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC	294.50	unknown	https://doi.org/10.1248/CPB.39.1849
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphocholines / Phosphatidylcholines
Colfosceril palmitate	452110	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCC	734.00	unknown	https://doi.org/10.1248/CPB.39.1849
Lecithin	5287971	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCC=CCCCCC	758.10	unknown	https://doi.org/10.1248/CPB.39.1849
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1'R,2S,2'R,3'R,5'S,8'R,9'R,10'R,13'S)-2',10',13'-triacetyloxy-8',12',15',15'-tetramethyl-5'-[(3R)-3-(methylamino)-3-phenylpropanoyl]oxyspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-9'-yl] pyridine-3-carboxylate	5316522	Click to see CC1=C2C(C(C3(CCC(C4(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)CO4)OC(=O)CC(C5=CC=CC=C5)NC)C)OC(=O)C6=CN=CC=C6)OC(=O)C	760.90	unknown	via CMAUP database
> 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/10.1002/HLCA.201000176
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(2E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26Z)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaen-1-ol	10196509	Click to see CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)CO)C)C)C)C	552.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,5'S,6S,9S,12S,13R,16S,18S,19R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-3',16,19-triol	24884103	Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1)O	448.60	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Podecdysone B	441831	Click to see CC12CCC3=C(C1=CCC2C(C)(C(CCC(C)(C)O)O)O)CC(=O)C4C3(CC(C(C4)O)O)C	462.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
O-(4-hydroxy-3-iodophenyl)-3-iodotyrosine	53477796	Click to see C1=CC(=C(C=C1CC(C(=O)O)N)I)OC2=CC(=C(C=C2)O)I	525.08	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
4a,5',6-Tris(hydroxymethyl)spiro[3,6,7,7a-tetrahydrofuro[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol	3363160	Click to see C1C2(C(C(C(O2)CO)O)O)OC3C(C(OC3(O1)CO)CO)O	324.28	unknown	https://doi.org/10.1016/S0008-6215(97)00016-5
Difructose anhydride III	196181	Click to see C1C2(C(C(C(O2)CO)O)O)OC3C(C(OC3(O1)CO)CO)O	324.28	unknown	https://doi.org/10.1016/S0008-6215(97)00016-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-6-(3,5-dihydroxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	5321781	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3)O)O)O)O)O)O	434.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2',4',6'-Trimethoxyacetophenone	123089	Click to see CC(=O)C1=C(C=C(C=C1OC)OC)OC	210.23	unknown	https://doi.org/10.1248/YAKUSHI1881.53.8_807
> Organoheterocyclic compounds / Benzazepines
(1S,12S,14R)-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-ol	9795100	Click to see CN1CCC23C=CC(CC2OC4=CC=CC(=C34)C1)O	257.33	unknown	https://doi.org/10.1002/HLCA.201000176
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
2-(2-hydroxypropan-2-yl)-4-methoxy-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3-dihydrofuro[3,2-g]chromen-5-one	11968852	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)COC4C(C(C(C(O4)CO)O)O)O)O	468.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,6,7-trihydroxy-3-methoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	5318081	Click to see COC1=C(C(=C2C(=C1)OC3=CC(=C(C=C3C2=O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	452.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
(4R,11R)-2,2,12-trimethyl-13-propan-2-yl-10-oxa-2-azoniatetracyclo[5.4.1.18,11.04,12]tridecan-9-one	6325643	Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)[N+](C4)(C)C)C	278.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(5S)-5-[[4-(2-methoxy-5-methylphenoxy)phenyl]methyl]-6,19-dimethyl-2,13-dioxa-6,19-diazapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3(12),4(9),10,15,21-hexaen-20-one	5319577	Click to see CC1=CC(=C(C=C1)OC)OC2=CC=C(C=C2)CC3C4=C(CCN3C)C=CC5=C4OC6=C(O5)C=C7CCN(C(=O)C7=C6)C	562.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,15R)-4,5-dimethoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,12-tetraen-15-ol	163195523	Click to see COC1=C(C=C2C3C(CC=C4C3N(CC4)CC2=C1)O)OC	287.35	unknown	https://doi.org/10.1016/S0031-9422(00)89030-5
17-Methoxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-1(19),2,4(8),9,13,15,17-heptaen-11-one	44130139	Click to see COC1=CC2=C3C(=C1)C=CN3C(=O)C4=CC5=C(C=C42)OCO5	293.27	unknown	https://doi.org/10.1248/CPB.57.610
5,6-Dihydrobicolorine	375118	Click to see CN1CC2=CC3=C(C=C2C4=CC=CC=C41)OCO3	239.27	unknown	https://doi.org/10.1002/HLCA.201000176
9,10-Dimethoxy-3,12-didehydrogalanthan-1,2-diol	618065	Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)OC	303.35	unknown	via CMAUP database
CID 3738100	3738100	Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)[O-])OCO4	265.26	unknown	via CMAUP database
Lycoranine B	44130138	Click to see CC1=CC2=CC(=CC3=C2N1C(=O)C4=CC5=C(C=C43)OCO5)OC	307.30	unknown	https://doi.org/10.1248/CPB.57.610
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/10.1002/HLCA.201000176 https://doi.org/10.1248/CPB.31.2146
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/10.1007/978-3-642-65406-0_42 https://doi.org/10.1248/CPB.31.2146
Norpluviine	12313583	Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O	273.33	unknown	https://doi.org/10.1039/JR9590000172
Norpluvine	615152	Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O	273.33	unknown	https://doi.org/10.1039/JR9590000172
Pluviine	101289753	Click to see COC1=C(C=C2C3C(CC=C4C3N(CC4)CC2=C1)O)OC	287.35	unknown	https://doi.org/10.1016/S0031-9422(00)89030-5
Pseudolycorine	443689	Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)O	289.33	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
2-(3-hydroxy-4-methoxyphenyl)-8-methyl-3,4-dihydro-2H-chromen-7-ol	3500618	Click to see CC1=C(C=CC2=C1OC(CC2)C3=CC(=C(C=C3)OC)O)O	286.32	unknown	https://doi.org/10.1248/CPB.31.2146
7,3'-Dihydroxy-4'-methoxy-8-methylflavan	442358	Click to see CC1=C(C=CC2=C1OC(CC2)C3=CC(=C(C=C3)OC)O)O	286.32	unknown	https://doi.org/10.1248/CPB.31.2146
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4-(7-Methoxy-3,4-dihydro-2H-chromen-2-yl)phenol	11276880	Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1	256.30	unknown	https://doi.org/10.1248/CPB.31.2146
4'-Hydroxy-7-methoxyflavan	185609	Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1	256.30	unknown	https://doi.org/10.1248/CPB.31.2146
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Maackiain	91510	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Eucomic acid, (-)-	23757219	Click to see C1=CC(=CC=C1CC(CC(=O)O)(C(=O)O)O)O	240.21	unknown	via CMAUP database

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Lycoris radiata

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