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Family Annonaceae
Duhat-matsing
Polyalthia suberosa (Roxb.) Thwaites.

CORKY DEBBAR TREE

Scientific names Common names 
Polyalthia suberosa Roxb. Baling-manok (Tag.) 
Guatteria suberosa (Roxb.) Dunal Duhat-duhatan (Tag.,)
Uvaria suberosa Roxb. Duhat-matsing (Tag.)
Phaeanthus cumingii Vidal Duyat-nasi (Pamp.)
Phaeanthus malabaricus Naves Lanutan (Tag.)
  Tagputagpuan (Tag.)
  Munat (Ilk.) 
  Polyalthia (Engl.)
  Corky debbar tree (Engl.)
Lanutan is a common name shared by: (1) Kalai, Alphonsea arborea (2) Malaatis, Dasymaschalon clusiflorum (3) Kalimatas, Phaenthus ebracteolatus, and (4) Duhat-matsing, Polyalthia suberosa.

Botany
Duhat-matsing is a shrub or small tree growing to a height of 2 to 4 meters. Leaves are oblong to narrowly oblong-obovate, 5 to 11 centimeters long. Flowers are solitary, pale-yellow, about 1 centimeter long or less, on slender pedicels 1 to 2 centimeters long. Sepals and petals are slightly hairy. Fruits are numerous, ovoid or globose, 4 to 5 millimeters long, purple, fleshy and edible.

Distribution
- In the Philippines, common in thickets at low and medium altitudes in Luzon (Cagayan to Laguna) and Mindanao.
- Also occurs in India, China, Malaysia, Myanmar, Sri Lanka, Thailand and Vietnam.

Parts utilized
Fresh roots.

Constituents
• Study yielded an azaanthracene alkaloid, kalasinamide, from the stems of P. suberosa., together with the known N-trans-feruloyltyramine and N-trans-coumaroyltyramine.
• Study isolated two new 2-substituted furans from the stems of P. suberosa.

• Leaves contain alpha- and beta-amyrin, lupeol, beta-sitosterol, stigmasterol and campesterol. Stems and leaves contain triterpene, suberosol, which have shown anti-HIV replication activity. Stem bark yields alkaloids, oxostephanine and lanuginosine, which has shown antibacterial activity.

Properties
• Anti-HIV replication activity and antibacterial activity.
• Adaptogenic.

Uses
Folkloric
Decoction of fresh roots used as abortifacient.

Studies
Furans / Antiviral Activity: 2-substituted furans from Polyalthia suberosa: Two new 2-substituted furans, 1-(2-furyl)pentacosa16,18-diyne and 23-(2-furyl)tricosa-5,7-diynoic acid, were isolated from the stems of P. suberosa. These compounds, with kalasinamide, N-trans-feruloyltyramine and N-trans-coumaroyltyramine showed anti-HIV activities.
Anti-HIV Activity: Anti-AIDS Agents, 9. Suberosol, a New C31 Lanostane-Type Triterpene and Anti-HIV Principle from Polyalthia suberosa: In the course of searching for anti-HIV agents, a new triterpene, suberosol, was isolated and studied for anti-HIV activity. (Publ.1993)
Cytotoxic: Study isolated four new styryl-lactones, crassalactones A-D together with seven known compounds from an extract of leaves and twigs of PC. Cytotoxic evaluation against mammalian cancer lines were done on all the new isolates.
Natural Excipient: Study showed the extracted mucilage from the leaves of Polyalthia suberosa is non-toxic, with a potential as a suspending agent, binding agent and pharmaceutical adjuvant.

Availability
Wild-crafted. 

Last Update July 2011

IMAGE SOURCE: Public Domain / File:Phaeanthus malabaricus Blanco1.193-original.png / Flora de Filipinas / Francisco Manuel Blanco (O.S.A.) / 1880-1883 / Wikipedia

Additional Sources and Suggested Readings
(1)
An azaanthracene alkaloid from Polyalthia suberosa. / Tuchinda P et al / Phytochemistry. 2000 Apr;53(8):1079-82.
(2)
2-substituted furans from Polyalthia suberosa / Planta medica / 2001, vol. 67, no6, pp. 572-575
(3)
Anti-AIDS Agents, 9. Suberosol, a New C31 Lanostane-Type Triterpene and Anti-HIV Principle from Polyalthia suberosa / Hui-Ying Li, Nan-Jun Sun et al / J. Nat. Prod., 1993, 56 (7), pp 1130–1133 /
DOI: 10.1021/np50097a017
(4)
Cytotoxic Styryl-Lactones from the Leaves and Twigs of Polyalthia crassa / J. Nat. Prod., 2006, 69 (12), pp 1728–1733 / DOI: 10.1021/np060323u
(5)
Indian Medicinal Plants: An Illustrated Dictionary / C. P. Khare
(6)
Isolation, Characterization and Pharmaceutical evaluation of the mucilage from Polyalthia suberosa leaves / Sunil Mistry, P.K.Biswal, B.Mishra, S.Sahoo / International Journal of PharmTech Research, Vol.2, No.2, pp 1455-1459, April-June 2010


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