Hymenocallis speciosa - Unknown
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Internal ID UUID644019ba69560686918785
Scientific name Hymenocallis speciosa
Authority Salisb.
First published in Trans. Hort. Soc. London i. (1812) 340.

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Synonyms Top

Scientific name Authority First published in
Hymenocallis speciosa var. angustifolia Herb. Appendix : 43 (1821)
Hymenocallis speciosa var. humilis Herb. Appendix : 43 (1821)
Hymenocallis speciosa var. longipetiolata Herb. Amaryllidaceae : 209 (1837)
Nemepiodon speciosum (L.f. ex Salisb.) Raf. Fl. Tellur. 4: 22 (1838)
Pancratium formosum hort. ex M.Roem. Fam. Nat. Syn. Monogr. 4: 167 (1847)
Pancratium speciosum L.f. ex Salisb. Trans. Linn. Soc. London 2: 73 (1794)
Hymenocallis erosa Salisb. Gen. Pl. : 110 (1866)

Common names Top

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Language Common/alternative name
English green-tinge spiderlily
Danish kejserindelilje
Estonian kaunis ämblikliilia
Japanese ヒメノカリス・スペキオサ
Japanese 笹蟹百合
Japanese ササガニユリ
Chinese 螫蟹百合
Chinese 美丽水鬼蕉

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000667858
USDA Plants HYSP10
Tropicos 50196709
INPN 629881
KEW urn:lsid:ipni.org:names:30010600-2
The Plant List kew-278909
Open Tree Of Life 591380
NCBI Taxonomy 146442
IPNI 65317-1
iNaturalist 345577
GBIF 2860247
Freebase /m/03cdg67
EPPO HMJSP
EOL 1001661
USDA GRIN 19514
Wikipedia Hymenocallis_speciosa
CMAUP NPO24554

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
Genera of phytopathogenic fungi: GOPHY 4 Chen Q, Bakhshi M, Balci Y, Broders KD, Cheewangkoon R, Chen SF, Fan XL, Gramaje D, Halleen F, Jung MH, Jiang N, Jung T, Májek T, Marincowitz S, Milenković I, Mostert L, Nakashima C, Nurul Faziha I, Pan M, Raza M, Scanu B, Spies CF, Suhaizan L, Suzuki H, Tian CM, Tomšovský M, Úrbez-Torres JR, Wang W, Wingfield BD, Wingfield MJ, Yang Q, Yang X, Zare R, Zhao P, Groenewald JZ, Cai L, Crous PW Stud Mycol 02-Jun-2022
PMCID:PMC9365048
doi:10.3114/sim.2022.101.06
PMID:36059898
Phylogenomics of the Andean Tetraploid Clade of the American Amaryllidaceae (Subfamily Amaryllidoideae): Unlocking a Polyploid Generic Radiation Abetted by Continental Geodynamics Meerow AW, Gardner EM, Nakamura K Front Plant Sci 05-Nov-2020
PMCID:PMC7674842
doi:10.3389/fpls.2020.582422
PMID:33250911
TOTAL SYNTHESES OF PANCRATISTATIN. A REVIEW Manpadi M, Kornienko A Org Prep Proced Int 18-Feb-2009
PMCID:PMC5115790
doi:10.1080/00304940809458083
PMID:27867225
Alkaloide aus Urceolina‐, Hymenocallis‐, Elisena‐, Calostemma‐, Eustephia‐ und Hippeastrum‐Arten Hans‐G. Boit, Werner Döpke Wiley 21-May-2007
doi:10.1002/CBER.19570900920
Antineoplastic agents, 301. An investigation of the Amaryllidaceae genus Hymenocallis. Pettit GR, Pettit GR 3rd, Groszek G, Backhaus RA, Doubek DL, Barr RJ, Meerow AW J Nat Prod 01-May-1995
doi:10.1021/NP50119A017
PMID:7623049

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 / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Pancratistatin 441597 Click to see C1OC2=C(O1)C(=C3C(=C2)C4C(C(C(C(C4O)O)O)O)NC3=O)O 325.27 unknown https://doi.org/10.1021/NP50119A017
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxylup-20(29)-en-28-amide 10161414 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)N 455.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
5,6,6-Trimethoxy-2-prop-2-enylcyclohexa-1,3-diene 163192813 Click to see COC1C=CC(=CC1(OC)OC)CC=C 210.27 unknown https://doi.org/10.1002/CBER.19570900920
> Organoheterocyclic compounds / Indoles and derivatives
6-[(6R,7S,7aS)-6-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydroindol-7-yl]-2,3,4-trimethoxybenzaldehyde 163062045 Click to see CN1CCC2=CCC(C(C21)C3=CC(=C(C(=C3C=O)OC)OC)OC)O 347.40 unknown https://doi.org/10.1002/CBER.19570900920
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-hydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 22524175 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database

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