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Family Amaryllidaceae
Spider lily
Hymenocallis littoralis
(Jacq.) Salisb.

BEACH SPIDER LILY

Other scientific names  Common names
Pancratium littorale Jacq. Ajos-ajos nga maputi (Bis.)
Pancratium illyricum Blanco Bakong (Tag..) 
Pancratium maritinum Blanco Lirio (Span.) 
Hymenocallis adnata Herb. Spider lily (Engl.)
Hymenocallis tennuiflora Herb. Beach spiderlily (Engl.)
  Beach hymenocallis (Engl.)
   
Bakong is a local name shared by (1) Crinum asiaticum (2) Crinum latifolium, lirio and (3) Hymenocallis littorale, spider lily.
Spider lily is a shared common name of (1) Hymenocallis littorale, bakong, lirio and (2) Crinum asiaticum
Lirio is a common name shared by (1) Crinum latifolium (2) Hymenocallis littorale.


Botany
Spider lily is a bulbous, herbaceious plant. Leaves are fleshy, dark green and glossy, narrowly lanceolate, 0.5 to 1 meter long, 6 to 7 cm wide. Scape is erect, solid, somewhat compressed, about 0.5 m tall, bearing at its apex few to many sessile, umbellate flowers. The flowers are fragrant with the perianth-tube greenish below and whitish above, about 12 cm long, with white, linear and spreading lobes, 10 cm long and 5 to 7 mm wide. The membranous cup connecting the filaments is white, funnel-shaped, 4 to 5 cm diameter. The anthers are green and erect.

Distribution
Cultivated as hedge in Manila and other large towns.
Grows wild in waste places, through bulb reproduction.
Found in a broad range of growing conditions, from wet and boggy to dry areas.

Constituents and properties
Toxic alkaloid, lycorine is responsible for its emetic property. The roots contain 0.015 per cent of the alkaloid.

Parts utilized
Bulb

Uses
Folkloric
- In the Philippines, the bulb is the only part of the plant used for wound healing.
- In Lao, roots boiled in water, used for testicles too low because of excessive running.

Studies
Methylflavan / Antioxidant: Study isolated 7,4'-dihydroxy-8-methylflavan from the extract of P littorale stem and assessed for its radical scavenging properties.
Cytotoxicity: A 1993 study isolated pancratistatin (PST) from H littoralis which displayed potent cytoxicity against a human tumor cell line. A recent study showed selectivity of PST to cancer cells and sparing of normal cells. This study investigated the anti-cancer efficacy and specificity of two PST-related natural compounds, AMD4 and AMD5. Results showed AMD5 had efficacy and selectivity similar to PST and AMD4 lacked apoptotic activity. The phenanthridone skeleton in natural Amaryllidaceae alkaloids may be a common element for selectivity against cancer cells.
Anti-tumor: The biologic activities of isocarbostyril alkaloids showed excellent in vitro and in vivo cytotoxicity against many tumor cell lines and high selectivity for cancer cells versus normal cells.
Littoraline / Cytotoxicity: Study isolated a new alkaloid, littoraline, with 13 other known lycorine alkaloids and one lignan. Littoraline showed inhibitory activity of HIV reverse transcriptase and lycorine and haemanthamine showed potent in vitro cytotoxicity.
Pancratistatin / Anticancer: (1) The species serves as an effective source of pancratistatin, a powerful anticancer agent. Pancratistatin is primarily produced in the bulbs, to a lesser extent, in the roots. The report describes a method for large-scale production. (2) Narciclasine was employed as precursor for synthetic conversion to natural (+) pancratistatin.
Alkaloids: Phytochemical screening of bulbs and flowers yielded four alkaloids: lycorine, hippeastrine, 11-hydroxyvittatine, and (+)-8-O-demethylmaritidine, plus two flavonoids, quercetin 3-O-glucoside and rutin. Study investigated the antimicrobial activity of a petroleum ether extract of the flowers.
Narcistatin / Antineoplastic: Human cancer cell line inhibitory isocarbostyril precursors were isolated from the buls of Hymenocallis littoralis from the horticultural production or reduction of narciclasine 1a-4 from the same source.

Availability
Cultivated.

Last Update May 2011

Photos © Godofredo Stuart / StuartXchange

Additional Sources and Suggested Readings
(1)
A methylflavan with free radical scavenging properties from Pancratium littorale / Jean-Robert Ioset et al / Fitoterapia Vol 72, Issue 1, January 2001, Pages 35-39 / doi:10.1016/S0367-326X(00)00250-1
(2)
Selective cytotoxicity of Pancratistatin-related natural Amaryllidaceae alkaloids: evaluation of the activity of two new compounds / Carly Griffin, Natasha Sharda et al / Cancer Cell Int. 2007; 7: 10. / doi: 10.1186/1475-2867-7-10.
(3)
Amaryllidaceae Isocarbostyril Alkaloids and Their Derivatives as Promising Antitumor Agents / Laurent Ingrassia, Florence Lefranc et al / Transl Oncol. 2008 March; 1(1): 1–13.
(4)
Lycorine alkaloids from Hymenocallis littoralis / Long-Ze Lin, Shu-Fang Hu et al / Phytochemistry Vol 40, Issue 4, November 1995, Pages 1295-129 / doi:10.1016/0031-9422(95)00372-E
(5)
BIOSYNTHESIS OF THE ANTINEOPLASTIC PANCRATISTATIN FOLLOWING TISSUE CULTURE OF HYMENOCALLIS LITTORALIS (AMARYLLIDACEAE) / R A Backhaus et al / ISHS Acta Horticulturae 306: International Symposium on Medicinal and Aromatic Plants, XXIII IHC
(6)
The role of medicinal plants in the provision of health care in Lao PDR
/ Claudio O Delang / Journal of Medicinal Plants Research Vol. 1(3), pp. 050-059, October 2007
(7)
Antineoplastic Agents. 450. Synthesis of (+)-Pancratistatin from (+)-Narciclasine as Relay / George R Pettit, Noeleen Melody and Delbert Herald / J. Org. Chem., 2001, 66 (8), pp 2583–2587
DOI: 10.1021/jo000710n
(8)
Phytochemical and biological investigation of Hymenocallis littoralis SALISB. / Amina H Abou-Donia, Soad M Toaima et al / Chemistry biodiversity (2008), Volume: 5, Issue: 2, Pages: 332-340 / PubMed ID: 18293433
(9)
Antineoplastic Agents. 527. Synthesis of 7-Deoxynarcistatin, 7-Deoxy-trans-dihydronarcistatin, and trans-Dihydronarcistatin 1 / George Pettit and Noeleen Melody / J. Nat. Prod., 2005, 68 (2), pp 207–211
DOI: 10.1021/np0304518


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