Language	Common/alternative name
Japanese	オオキツネノカミソリ
Japanese	キツネノカミソリ
Japanese	ムジナノカミソリ
Japanese	狐の剃刀
Chinese	夏水仙
Chinese	血红石蒜
Chinese	血紅石蒜

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Lycoris sanguinea var. kiushiana	Makino ex T.Koyama	Baileya 7: 5 (1959)
Lycoris sanguinea var. koreana	(Nakai) T.Koyama	Baileya 7: 6 (1959)
Lycoris sanguinea var. sanguinea		Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000683495
Tropicos	1200142
KEW	urn:lsid:ipni.org:names:65807-1
The Plant List	kew-280530
Missouri Botanical Garden	275704
Open Tree Of Life	631072
NCBI Taxonomy	108053
IPNI	65807-1
iNaturalist	447261
GBIF	5326164
EOL	1003203
USDA GRIN	22983

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

Comparative Chloroplast Genomics of Seven Endangered Cypripedium Species and Phylogenetic Relationships of Orchidaceae

Zhang JY, Liao M, Cheng YH, Feng Y, Ju WB, Deng HN, Li X, Plenković-Moraj A, Xu B

Front Plant Sci

22-Jun-2022

PMCID:	PMC9257239
doi:	10.3389/fpls.2022.911702
PMID:	35812969

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

Characterization of the complete chloroplast genome of Zephyranthes phycelloides (Amaryllidaceae, tribe Hippeastreae) from Atacama region of Chile

Contreras-Díaz R, Arias-Aburto M, van den Brink L

Saudi J Biol Sci

22-Oct-2021

PMCID:	PMC8716934
doi:	10.1016/j.sjbs.2021.10.035
PMID:	35002462

The complete chloroplast genome of Chinese medicinal herb Belamcanda chinensis (L.) Redouté (Iridaceae)

Li C, Hu S, Ding Y, Bi G, Su C, Xia Z

Mitochondrial DNA B Resour

08-Feb-2021

PMCID:	PMC7889214
doi:	10.1080/23802359.2020.1866455
PMID:	33628873

Field Experiments of Pollination Ecology: The Case of Lycoris sanguinea var. sanguinea

Yamaji F, Ohsawa TA

J Vis Exp

25-Nov-2016

PMCID:	PMC5226278
doi:	10.3791/54728
PMID:	27911369

Crisis of Japanese Vascular Flora Shown By Quantifying Extinction Risks for 1618 Taxa

Kadoya T, Takenaka A, Ishihama F, Fujita T, Ogawa M, Katsuyama T, Kadono Y, Kawakubo N, Serizawa S, Takahashi H, Takamiya M, Fujii S, Matsuda H, Muneda K, Yokota M, Yonekura K, Yahara T

PLoS One

12-Jun-2014

PMCID:	PMC4055661
doi:	10.1371/journal.pone.0098954
PMID:	24922311

Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes

Chen S, Kim DK, Chase MW, Kim JH

PLoS One

18-Mar-2013

PMCID:	PMC3605904
doi:	10.1371/journal.pone.0059472
PMID:	23544071

Alkaloids of the amaryllidaceae. A new alkaloid, sanguinine, from Lycoris sanguinea Maxim. var. Kiushiana Makino, and pretazettine from Lycoris radiata Herb.

SHIGERU KOBAYASHI, SHIGEKO TAKEDA, HIDEKI ISHIKAWA, HIROSHI MATSUMOTO, MASARU KIHARA, TETSURO SHINGU, ATSUSHI NUMATA, SHOJIRO UYEO

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.24.1537

Endangered vascular plants in Japan: —Present status and a proposal for conservation—

Iwatsuki K

Proc Jpn Acad Ser B Phys Biol Sci

01-Oct-2008

PMCID:	PMC3722017
doi:	10.2183/pjab/84.275
PMID:	18941303

Chemistry, Biology and Medicinal Potential of Narciclasine and its Congeners

Kornienko A, Evidente A

Chem Rev

20-May-2008

PMCID:	PMC2856661
doi:	10.1021/cr078198u
PMID:	18489166

Minor alkaloids from Lycoris sanguinea

O Abdallah

Elsevier BV

30-Apr-2003

doi:	10.1016/0031-9422(94)00929-N

Alkaloid N-oxides from Lycoris sanguinea

Shigeru Kobayashi, Kimihito Satoh, Atsushi Numata, Tetsuro Shingu, Masaru Kihara

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(91)83751-6

[On the constituents of the bulbs of Lycoris sanguinea Maxim (author's transl)].

Takagi S, Yamaki M

Yakugaku Zasshi

01-May-1974

doi:	10.1248/YAKUSHI1947.94.5_617
PMID:	4473105

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 / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1S,11R,13R,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	162945736	Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O	317.34	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
(1S,13R,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol	38988650	Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O	301.34	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
Crinamine	500027	Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O	301.34	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
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/YAKUSHI1947.94.5_617
> 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	https://doi.org/10.1248/YAKUSHI1947.94.5_617
(1S,12S,14R)-4-methyl-4-oxido-11-oxa-4-azoniatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-9,14-diol	14803829	Click to see C[N+]1(CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)O)[O-]	289.33	unknown	https://doi.org/10.1016/0031-9422(91)83751-6
(1S,14R)-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-9,14-diol	49849700	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)O	273.33	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
(9-Hydroxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl) 3-hydroxybutanoate	162886398	Click to see CC(CC(=O)OC1CC2C3(CCNCC4=C3C(=C(C=C4)O)O2)C=C1)O	345.40	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
[(1S,12S,14R)-9-hydroxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl] (3R)-3-hydroxybutanoate	15214893	Click to see CC(CC(=O)OC1CC2C3(CCNCC4=C3C(=C(C=C4)O)O2)C=C1)O	345.40	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
[(1S,14R)-9-hydroxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl] (3S)-3-hydroxybutanoate	162886399	Click to see CC(CC(=O)OC1CC2C3(CCNCC4=C3C(=C(C=C4)O)O2)C=C1)O	345.40	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
1,2-Dihydrogalanthamine	625595	Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O	289.40	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617 https://doi.org/10.1016/0031-9422(91)83751-6
11-Oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-9,14-diol	73131244	Click to see C1CNCC2=C3C14C=CC(CC4OC3=C(C=C2)O)O	259.30	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
5,6,9,10,11,12-Hexahydro-4aH-[1]benzofuro[3a,3,2-ef][2]benzazepine-3,6-diol	49849704	Click to see C1CNCC2=C3C14C=CC(CC4OC3=C(C=C2)O)O	259.30	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
Epigalantamine	676392	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O	287.35	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
Epigalanthamin	3449	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O	287.35	unknown	https://doi.org/10.1016/0031-9422(94)00929-N https://doi.org/10.1248/YAKUSHI1947.94.5_617
Galantamine	9651	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O	287.35	unknown	https://doi.org/10.1016/0031-9422(94)00929-N https://doi.org/10.1016/0031-9422(91)83751-6
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/10.1016/0031-9422(91)83751-6
Lycoramine	443723	Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O	289.40	unknown	https://doi.org/10.1016/0031-9422(91)83751-6 https://doi.org/10.1248/YAKUSHI1947.94.5_617
Norsanguinine	443739	Click to see C1CNCC2=C3C14C=CC(CC4OC3=C(C=C2)O)O	259.30	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
Sanguinine	443722	Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)O	273.33	unknown	https://doi.org/10.1016/0031-9422(94)00929-N https://doi.org/10.1248/CPB.24.1537 https://doi.org/10.1016/0031-9422(91)83751-6
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,17S,18S,19R)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraene-17,18-diol	7060909	Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4	287.31	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
3,3a-Didehydrolycoran-1alpha,2beta-diol	3978	Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4	287.31	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
Lycorine	72378	Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4	287.31	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
> 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/10.1248/YAKUSHI1947.94.5_617
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/10.1248/YAKUSHI1947.94.5_617
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/YAKUSHI1947.94.5_617
Narciprimine	5387508	Click to see C1OC2=C(O1)C(=C3C(=C2)C4=C(C(=CC=C4)O)NC3=O)O	271.22	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1R,13R,16S,18R)-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-13-ol	163037542	Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O	331.40	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
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/YAKUSHI1947.94.5_617
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/YAKUSHI1947.94.5_617
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
methyl (9E,12Z)-octadeca-9,12-dienoate	5462988	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC	294.50	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
Methyl octadeca-9,12-dienoate	8203	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC	294.50	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162965363	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1R,14R,15R,16R)-4,5,14-trimethoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,12-tetraen-15-ol	133564758	Click to see COC1C=C2CCN3C2C(C1O)C4=CC(=C(C=C4C3)OC)OC	317.40	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
(1S,14S,15S,16R)-5-methoxy-9-azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6,12-tetraene-4,14,15-triol	163072246	Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)O	289.33	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
3,12-Didehydro-2beta,9,10-trimethoxygalanthan-1alpha-ol	97315	Click to see COC1C=C2CCN3C2C(C1O)C4=CC(=C(C=C4C3)OC)OC	317.40	unknown	https://doi.org/10.1016/0031-9422(94)00929-N
Hippadine	100605	Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5	263.25	unknown	https://doi.org/10.1248/YAKUSHI1947.94.5_617
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/10.1248/YAKUSHI1947.94.5_617
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/10.1248/YAKUSHI1947.94.5_617
Pseudolycorine	443689	Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)O	289.33	unknown	https://doi.org/10.1016/0031-9422(94)00929-N

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Lycoris sanguinea

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top