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Family Verbenaceae / Lamiaceae
Pelegrina
Clerodendrum fragrans Vent.
FRAGRANT GLORY BOWER

Chong ban xiu mo li

Scientific names Common names
Clerodendrum fragrans Vent. Higantong (Bis.)
Clerodendrum philippinum Schauer Mil flores (Span.)
Clerodendrum chinense (Osbeck) Mabb. Pelegrina (Bik., Tag.)
  Peregrino (Span.)
  Sabuka (Ig.)
  Chinese glory bower (Engl.)
  Fragrant glory bower (Engl.)
  Stickbush (Engl.)
  Chong ban xiu mo li (Engl.)

Botany
Pelegrina is an erect, branched, somewhat hairy shrub, 1 to 2 meters in height. Leaves are broadly ovate, up to 25 centimeters long, pointed at the tip and blunt at the base. The inflorescences (cymes) are short-stalked and terminal, 6 to 12 centimeters in diameter, densely crowded with flowers. Flowers are fragrant, in stalks 1 to 2 centimeters long. The calyx-tube is rather slender below and enlarged above, with five to six lanceolate lobes which are reddish-purple and about 1.5 centimeters long. Corrola is white, 3 to 3.5 centimeters in diameter and 1 to 1.5 centimeters long in the tube.

Distribution
- Cultivated in and near towns throughout the Philippines.
- Occasionally, an escape plant.

- Native of southeastern Asia, from southern China and northern Viet Nam.
- Now pantropic.

Constituents
- Yields (24S)-ethylcholestra-5, 22,25-triene-3ß-ol.
- Petroleum ether extracts yielded steroids - clerosterol and deucosterol.
- Yields phenolic compounds acetoside, leucosceptoside A, isoacteoside, methyl and ethyl esters of caffeic acid, jinoside.
- Leaves yield flavonoids, kaempferol.

- Aerial parts yielded a new iridoid diglucoside, 5-O-ß-glycopyranosyl-harpagide with three known iridoid glucosides and six known cyclohexylethanoids.
- Study isolated two minor sterols: 24β-methylcholesta-5,22E,25-trien-3β-ol and 24α-ethyl-5α-cholest-22E-en-3β-ol.

Uses
Folkloric
- The Malays use the plant externally as a poultice, for rheumatism and ague; or mixed with other substances, for skin ailments.
- In the Guianas, decoction of leaves used for scabies.

Studies
Phytochemicals:
Study yielded beta-sitosterol, clerosterol, daucosterol, caffeic acid, kaempferol, 5,4'-dihydroxy-kaempferol-7-O-beta-rutinoside, acteoside and leucoseceptoside A.
Anti-Leukemic: Study showed promyelocytic cell liine HL-60 could be induced to differentiate into morphologically and functionally mature monocytoid cells (up to 20%) after dose-dependent exposure to Clerodendron fragrans working in synergism with interferon-r. Results suggest a potential therapeutic value for the treatment of certain acute myelocytic leukemia.

Availability
Seasonal fruiting and ubiquitoous market produce.

Last Update April 2012

IMAGE SOURCE / Public Domain / File:Clerodendrum chinense Blanco1.222.png / Flora de Filipinas / Franciso Manuel Blanco (OSA), 1880-1883 / Modifications by Carol Spears / Wikimedia Commons

Additional Sources and Suggested Readings
(1)
Studies on chemical constituents in leafs of Clerodendron fragrans / Gao LM, Wei XM, He YQ. / Zhongguo Zhong Yao Za Zhi. 2003 Oct;28(10):948-51.
(2)
Flavonoid with antioxidant effects extracted recently from leaves of Clerodendron fragrans / Tap Chi Duoc Hoc, 2000, 3, 10-12. / Hoang, T. H.; Ha, V. H.; Nguyen, H. K.; Pyne, S. G.
(3)
In Vitro Induction of Differentiation in HL-60 Leukemic Cell Line by Clerodendron Fragrans / Po-min Chen et al / The American Journal of Chinese Medicine • Volume: 16, Issues: 3-4 (1988) pp. 139-144 / DOI: 10.1142/S0192415X88000200
(4)
Clerodendrum and Healthcare: An Overview / B V Patel et al / Medicinal and Aromatic Plant Science and Biotechnology • 1(1), 142-150
(5)
Medicinal Plants of the Guianas (Guyana, Surinam, French Guiana)
(6)
Clerodendrum and Healthcare: An Overview - Part II / Phytochemistry and Biotechnology / Neeta Shrivastava, Tejas Patel / Medicinal and Aromatic Plant Science and Biotechnology 1(2), 209-223
(7)
A New Iridoid Diglycoside from Clerodendron chinense / Tripetch Kanchanapoom et al / Journal of Asian Natural Products Research, Vol 7, No 5, June 2005, Pp 269-272.
(8)
24β-methylcholesta-5,22E,25-trien-3β-ol and 24α-ethyl-5α-cholest-22E-en-3β-ol from Clerodendrumfragrans
/ Toshihiro Akihisab, Parthasarathi Ghosha, Swapnadip Thakura et al / Phytochemistry, Volume 27, Issue 1, 1988, Pages 241–244


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