Lycoris incarnata - Unknown
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Internal ID UUID64401bfecc942908276645
Scientific name Lycoris incarnata
Authority Comes ex Sprenger
First published in Gartenwelt 10: 490 (1906)

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Language Common/alternative name
Chinese 香石蒜

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000684053
Tropicos 1201824
KEW urn:lsid:ipni.org:names:65798-1
The Plant List kew-280587
Open Tree Of Life 992964
NCBI Taxonomy 317644
IPNI 65798-1
iNaturalist 707403
GBIF 5326175
EOL 1003274
USDA GRIN 22980
Missouri Botanical Garden 275879

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)!
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Title Authors Publication Released IDs
SWATH-MS-Based Proteomics Reveals the Regulatory Metabolism of Amaryllidaceae Alkaloids in Three Lycoris Species Tang M, Li C, Zhang C, Cai Y, Zhang Y, Yang L, Chen M, Zhu F, Li Q, Li K Int J Mol Sci 24-Feb-2023
PMCID:PMC10002500
doi:10.3390/ijms24054495
PMID:36901927
Isolation and Structure Elucidation of a Novel Alkaloid, Incartine, a Supposed Biosynthetic Intermediate, from Flowers of Lycoris incarnata. Masaru KIHARA, Lai XU, Keiji KONISHI, Kiyoshi KIDA, Yoshimitsu NAGAO, Shigeru KOBAYASHI, Tetsuro SHINGU Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.42.289
Incartine, a Biosynthetic Intermediate, from the Flowers of Lycoris incarnata Masaru Kihara, Lai Xu, Keiji Konishi, Yoshimitsu Nagao, Shigeru Kobayashi, Tetsuru Shingu The Japan Institute of Heterocyclic Chemistry 04-Mar-2009
doi:10.3987/COM-92-6068
Revised NMR data for Incartine: an Alkaloid from Galanthus elwesii Berkov S, Reyes-Chilpa R, Codina C, Viladomat F, Bastida J Molecules 12-Jul-2007
PMCID:PMC6149325
doi:10.3390/12071430
PMID:17909498
XVI. Mitteil. über Amaryllidaceen‐Alkaloide. Alkaloide von Nerine Corusca, N. Flexuosa, Pancratium Illyricum, Lycoris Aurea und L. Incarnata Hans‐G. Boit, Horst Ehmke Wiley 01-Jun-2007
doi:10.1002/CBER.19570900311
Chapter 3 Chemical and Biological Aspects of Narcissus Alkaloids Bastida J, Lavilla R, Viladomat F Alkaloids Chem Biol 26-Feb-2007
PMCID:PMC7118783
doi:10.1016/S1099-4831(06)63003-4
PMID:17133715

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 / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1S,11S,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 154496716 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1002/CBER.19570900311
Haemanthidine 544807 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1002/CBER.19570900311
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(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.42.289
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.42.289
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.42.289
Epigalanthamin 3449 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1248/CPB.42.289
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1248/CPB.42.289
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.42.289
Lycoramine 443723 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O 289.40 unknown https://doi.org/10.1248/CPB.42.289
Sanguinine 443722 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)O 273.33 unknown https://doi.org/10.1248/CPB.42.289
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1248/CPB.42.289
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoethanolamines / Phosphatidylethanolamines
1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphoethanolamine 9546747 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCCN)OC(=O)CCCCCCCC=CCC=CCCCCC 716.00 unknown https://doi.org/10.1248/CPB.42.289
> 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/10.1248/CPB.42.289
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(2S,4aS,8aR)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enyl 3-methylbutanoate 162851672 Click to see CC(C)CC(=O)OCC(=C)C1CCC2(CCCC(=C)C2C1)C 304.50 unknown https://doi.org/10.1248/CPB.42.289
https://doi.org/10.3987/COM-92-6068
> Organoheterocyclic compounds / Benzopyrans
(2E,10E)-N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]dodeca-2,10-dienamide 163185720 Click to see CC=CCCCCCCC=CC(=O)NC1CC2(C(=O)C=CC(C2(OC1O)C)Cl)O 425.90 unknown https://doi.org/10.1248/CPB.42.289
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,16S,17S,18S)-5,7-dioxa-11-azapentacyclo[9.6.1.02,10.04,8.014,18]octadeca-2,4(8),9,14-tetraene-16,17-diol 15215054 Click to see C1CN2C3C1=CC(C(C3C4=CC5=C(C=C42)OCO5)O)O 273.28 unknown https://doi.org/10.1248/CPB.42.289
5,7-Dioxa-11-azapentacyclo[9.6.1.02,10.04,8.014,18]octadeca-2,4(8),9,14-tetraene-16,17-diol 162898816 Click to see C1CN2C3C1=CC(C(C3C4=CC5=C(C=C42)OCO5)O)O 273.28 unknown https://doi.org/10.1248/CPB.42.289
> 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/10.1248/CPB.42.289
https://doi.org/10.3987/COM-92-6068
(1S,12R,14S,15R,16S,17S)-4,5,15-trimethoxy-13-oxa-9-azapentacyclo[7.7.1.02,7.012,14.012,17]heptadeca-2,4,6-trien-16-ol 162853560 Click to see COC1C(C2C3C4(C1O4)CCN3CC5=CC(=C(C=C25)OC)OC)O 333.40 unknown https://doi.org/10.3987/COM-92-6068
https://doi.org/10.1248/CPB.42.289
17-Methoxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,14-tetraene-16,18-diol 14109786 Click to see COC1C(C2C3C(=CCN3CC4=CC5=C(C=C24)OCO5)C1O)O 317.34 unknown https://doi.org/10.1248/CPB.42.289
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/10.1248/CPB.42.289
https://doi.org/10.3987/COM-92-6068
Ungiminorine 10425948 Click to see COC1C(C2C3C(=CCN3CC4=CC5=C(C=C24)OCO5)C1O)O 317.34 unknown https://doi.org/10.1248/CPB.42.289

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