240
N. N. Win and H. Morita
298. Brodowsky ID, Hamberg M, Oliw EH (1992) A linoleic acid (8R)-dioxygenase and
hydroperoxide isomerase of the fungus Gaeumannomyces graminis. Biosynthesis of (8R)hydroxylinoleic acid and (7S,8S)-dihydroxylinoleic acid from (8R)-hydroperoxylinoleic acid.
J Biol Chem 267:14738
299. Chang HW, Jang KH, Lee D, Kang HR, Kim TY, Lee BH, Choi BW, Kim S, Shin J
(2008) Monoglycerides from the brown alga Sargassum sagamianum: isolation, synthesis,
and biological activity. Bioorg Med Chem Lett 18:3589
300. Iadecola C (1997) Bright and dark sides of nitric oxide in ischemic brain injury. Trends
Neurosci 20:132
301. Lwin T (1982) A manual of traditional medicine practitioners (Myanmar version), 3rd edn.
Phoeyarzar Publishing House, Yangon 51, 53, 55, 85, 97
302. Chopra RN, Nayar SL, Chopra IC (1956) Glossary of Indian medicinal plants CSIR, New
Delhi, p 232
303. Diwan PV, Singh AK (1993) Anti-inflammatory activity of “Soymida febrifuga” (Mansa
rohini) in rats and mice. Phytother Res 7:255
304. Karunasree V, Veeresham C, Rao KRSS, Asres K (2012) Antioxidant, 5-lipoxygenase
inhibitory and anticancer activities of Soymida febrifuga A. Juss. Mol Clin Pharmacol 3:134
305. Yadav PA, Suresh G, Prasad KR, Rao MSA, Babu KS (2012) New phragmalin-type limonoids
from Soymida febrifuga. Tetrahedron Lett 53:773
306. Yadav PA, Suresh G, Rao MSA, Shankaraiah G, Rani PU, Babu KS (2014) Limonoids from
the leaves of Soymida febrifuga and their insect antifeedant activities. Bioorg Med Chem Lett
24:888
307. Ambaye RY, Indap MA, Panse TB (1971) Identification of methyl angolensate in the bark of
Soymida febrifuga (Roxb.) A. Juss. Curr Sci 158:7
308. Adesida GA, Taylor DAH (1972) Extractives from Soymida febrifuga. Phytochemistry
11:1520
309. Purushothaman KK, Chandrasekharan S (1974) Occurrence of methyl angolensate and
deoxyandirobin in Soymida febrifuga A. Juss. Indian J Chem 12:207
310. Purushothaman KK, Chandrasekharan S, Connolly JD, Rycroft DS (1977) Tetranortriterpenoids and related substances. Part 18. Two new tetranortriterpenoids with a modified furan
ring from the bark of Soymida febrifuga A. Juss. (Meliaceae). J Chem Soc Perkin Trans 1:1873
311. Awale S, Miyamoto T, Linn TZ, Li F, Win NN, Tezuka Y, Esumi H, Kadota S (2009) Cytotoxic
constituents of Soymida febrifuga from Myanmar. J Nat Prod 72:1631
312. Zheng QA, Li HZ, Zhang YJ, Yang CR (2004) Flavonoids from the resin of Dracaena
cochinchinensis. Helv Chim Acta 87:1167
313. Camarda L, Merlini L, Nasini G (1983) Dragon’s blood from Dracaena draco, structure of
novel homoisoflavanoids. Heterocycles 20:39
314. Mutanyatta J, Matapa BG, Shushu DD, Abegaz BM (2003) Homoisoflavonoids and xanthones
from the tubers of wild and in vitro regenerated Ledebouria graminifolia and cytotoxic
activities of some of the homoisoflavonoids. Phytochemistry 62:797
315. Ioset JR, Marston A, Gupta MP, Hostettmann K (2001) A methylflavan with free radical
scavenging properties from Pancratium littorale. Fitoterapia 72:35
316. Pan WB, Chang FR, Wei LM, Wu YC (2003) New flavans, spirostanol sapogenins, and a
pregnane genin from Tupistra chinensis and their cytotoxicity. J Nat Prod 66:161
317. Achenbach H, Stöcker M, Constenla MA (1988) Flavonoid and other constituents of Bauhinia
manca. Phytochemistry 27:1835
318. Ma XM, Liu Y, Shi YP (2007) Phenolic derivatives with free-radical-scavenging activities
from Ixeridium gracile (DC.) Shih. Chem Biodivers 4:2172
319. Tanaka S, Kuwai Y, Tabata M (1987) Isolation of monoamine oxidase inhibitors from
Glycyrrhiza uralensis roots and the structure-activity relationship. Planta Med 53:5
320. Carlson RE, Dolphin DH (1982) Pisum sativum stress metabolites: two cinnamylphenols and
a 2 -methoxychalcone. Phytochemistry 21:1733
321. Meksuriyen D, Cordell GA (1988) Retrodihydrochalcones from Dracaena loureiri. J Nat
Prod 51:1129
N. N. Win and H. Morita
298. Brodowsky ID, Hamberg M, Oliw EH (1992) A linoleic acid (8R)-dioxygenase and
hydroperoxide isomerase of the fungus Gaeumannomyces graminis. Biosynthesis of (8R)hydroxylinoleic acid and (7S,8S)-dihydroxylinoleic acid from (8R)-hydroperoxylinoleic acid.
J Biol Chem 267:14738
299. Chang HW, Jang KH, Lee D, Kang HR, Kim TY, Lee BH, Choi BW, Kim S, Shin J
(2008) Monoglycerides from the brown alga Sargassum sagamianum: isolation, synthesis,
and biological activity. Bioorg Med Chem Lett 18:3589
300. Iadecola C (1997) Bright and dark sides of nitric oxide in ischemic brain injury. Trends
Neurosci 20:132
301. Lwin T (1982) A manual of traditional medicine practitioners (Myanmar version), 3rd edn.
Phoeyarzar Publishing House, Yangon 51, 53, 55, 85, 97
302. Chopra RN, Nayar SL, Chopra IC (1956) Glossary of Indian medicinal plants CSIR, New
Delhi, p 232
303. Diwan PV, Singh AK (1993) Anti-inflammatory activity of “Soymida febrifuga” (Mansa
rohini) in rats and mice. Phytother Res 7:255
304. Karunasree V, Veeresham C, Rao KRSS, Asres K (2012) Antioxidant, 5-lipoxygenase
inhibitory and anticancer activities of Soymida febrifuga A. Juss. Mol Clin Pharmacol 3:134
305. Yadav PA, Suresh G, Prasad KR, Rao MSA, Babu KS (2012) New phragmalin-type limonoids
from Soymida febrifuga. Tetrahedron Lett 53:773
306. Yadav PA, Suresh G, Rao MSA, Shankaraiah G, Rani PU, Babu KS (2014) Limonoids from
the leaves of Soymida febrifuga and their insect antifeedant activities. Bioorg Med Chem Lett
24:888
307. Ambaye RY, Indap MA, Panse TB (1971) Identification of methyl angolensate in the bark of
Soymida febrifuga (Roxb.) A. Juss. Curr Sci 158:7
308. Adesida GA, Taylor DAH (1972) Extractives from Soymida febrifuga. Phytochemistry
11:1520
309. Purushothaman KK, Chandrasekharan S (1974) Occurrence of methyl angolensate and
deoxyandirobin in Soymida febrifuga A. Juss. Indian J Chem 12:207
310. Purushothaman KK, Chandrasekharan S, Connolly JD, Rycroft DS (1977) Tetranortriterpenoids and related substances. Part 18. Two new tetranortriterpenoids with a modified furan
ring from the bark of Soymida febrifuga A. Juss. (Meliaceae). J Chem Soc Perkin Trans 1:1873
311. Awale S, Miyamoto T, Linn TZ, Li F, Win NN, Tezuka Y, Esumi H, Kadota S (2009) Cytotoxic
constituents of Soymida febrifuga from Myanmar. J Nat Prod 72:1631
312. Zheng QA, Li HZ, Zhang YJ, Yang CR (2004) Flavonoids from the resin of Dracaena
cochinchinensis. Helv Chim Acta 87:1167
313. Camarda L, Merlini L, Nasini G (1983) Dragon’s blood from Dracaena draco, structure of
novel homoisoflavanoids. Heterocycles 20:39
314. Mutanyatta J, Matapa BG, Shushu DD, Abegaz BM (2003) Homoisoflavonoids and xanthones
from the tubers of wild and in vitro regenerated Ledebouria graminifolia and cytotoxic
activities of some of the homoisoflavonoids. Phytochemistry 62:797
315. Ioset JR, Marston A, Gupta MP, Hostettmann K (2001) A methylflavan with free radical
scavenging properties from Pancratium littorale. Fitoterapia 72:35
316. Pan WB, Chang FR, Wei LM, Wu YC (2003) New flavans, spirostanol sapogenins, and a
pregnane genin from Tupistra chinensis and their cytotoxicity. J Nat Prod 66:161
317. Achenbach H, Stöcker M, Constenla MA (1988) Flavonoid and other constituents of Bauhinia
manca. Phytochemistry 27:1835
318. Ma XM, Liu Y, Shi YP (2007) Phenolic derivatives with free-radical-scavenging activities
from Ixeridium gracile (DC.) Shih. Chem Biodivers 4:2172
319. Tanaka S, Kuwai Y, Tabata M (1987) Isolation of monoamine oxidase inhibitors from
Glycyrrhiza uralensis roots and the structure-activity relationship. Planta Med 53:5
320. Carlson RE, Dolphin DH (1982) Pisum sativum stress metabolites: two cinnamylphenols and
a 2 -methoxychalcone. Phytochemistry 21:1733
321. Meksuriyen D, Cordell GA (1988) Retrodihydrochalcones from Dracaena loureiri. J Nat
Prod 51:1129