Bioactive Compounds from Medicinal Plants in Myanmar
241
322. Chatterjea JN, Prasad R (1973) Condensation of Mannich base salts with phenols. Orientation
of adducts. Indian J Chem 11:214
323. González AG, León F, Sánchez-Pinto L, Padrón JI, Bermejo J (2000) Phenolic compounds
of dragon’s blood from Dracaena draco. J Nat Prod 63:1297
324. Ichikawa K, Kitaoka M, Taki M, Takaishi S, Iijima Y, Boriboon M, Akiyama T (1997) Retrodihydrochalcones and homoisoflavones isolated from Thai medicinal plant Dracaena loureiri
and their estrogen agonist activity. Planta Med 63:540
325. Fuendjiep V, Wandji J, Tillequin F, Mulholland DA, Budzikiewicz H, Fomum ZT, Nyemba
AM, Koch M (2002) Chalconoid and stilbenoid glycosides from Guibourtia tessmanii.
Phytochemistry 60:803
326. Kalabin GA, Kushnarev DF, Tyukavkina NA, Gromova AS, Lutskii VI (1976) PMR spectra
of natural stilbene compounds. Khim Prir Soedin:3
327. Peungvicha P, Temsiririrkkul R, Prasain JK, Tezuka Y, Kadota S, Thirawarapan SS, Watanabe
H (1998) 4-Hydroxybenzoic acid: a hypoglycemic constituent of aqueous extract of Pandanus
odorus root. J Ethnopharmacol 62:79
328. Yang XW, Zhao PJ, Ma YL, Xiao HT, Zuo YQ, He HP, Li L, Hao XJ (2007) Mixed lignanneolignans from Tarenna attenuata. J Nat Prod 70:521
329. Department of Traditional Medicine (1990) Medicinal plants of Myanmar. Myanmar, Ministry
of Health, p 115
330. Jabeen UBA, Ahmed A, Siddiqui MA (2015) Therapeutic uses of Vitex nigundo. World J
Pharm Res 4:589
331. Awale S, Linn TZ, Li F, Tezuka Y, Myint A, Tomida A, Yamori T, Esumi H, Kadota S (2011)
Identification of chrysoplenetin from Vitex negundo as a potential cytotoxic agent against
PANC-1 and a panel of 39 human cancer cell lines (JFCR-39). Phytother Res 25:1770
332. Sy LK, Brown GD (1998) Three sesquiterpenes from Artemisia annua. Phytochemistry
48:1207
333. Marco JA, Barbera O, Rodriguez S, Domingo C, Adell J (1988) Flavonoids and other phenolics
from Artemisia hispanica. Phytochemistry 27:3155
334. Kress WJ, DeFilipps RA, Farr E, Kyi YY (2003) A checklist of the trees, shrubs, herbs, and
climbers of Myanmar. United States National Herbarium, Washington, DC 45:209
335. Mori-Yasumoto K, Izumoto R, Fuchino H, Ooi T, Agatsuma Y, Kusumi T, Satake M, Sekita
S (2012) Leishmanicidal activities and cytotoxicities of bisnaphthoquinone analogues and
naphthol derivatives from Burman Diospyros burmanica. Bioorg Med Chem 20:5215
336. Sidhu GS, Sankaram AVB, Mahmood Ali S (1968) Extractives from Diospyros species: Part
III. new naphthoquinones and naphthols from the heartwood of Diospyros melanoxylon Roxb.
Indian J Chem 6:681
337. Mahmood Ali S, Prasad KK, Sankaram AVB, Sidhu GS (1971) Double bond fixation in
methylnaphthalene derivatives. Tetrahedron Lett 21:2305
338. Bungard CJ, Morris JC (2002) A convenient preparation of functionalized 1,8-dioxygenated
naphthalenes from 6-alkoxybenzocyclobutenones. J Org Chem 67:2361
339. Parker KA, Tallman EA (1984) Annelative phenol synthesis: preparation of 7-methyljuglone
and 7,9,11-trideoxydaunomycinone. Tetrahedron 40:4781
340. Ganapaty S, Thomas PS, Karagianis G, Waterman PG, Brun R (2006) Antiprotozoal and
cytotoxic naphthalene derivatives from Diospyros assimilis. Phytochemistry 67:1950
341. Likhitwitayawuid K, Kaewamatawong R, Ruangrungsi N, Krungkrai J (1998) Antimalarial
naphthoquinones from Nepenthes thorelii. Planta Med 64:237
342. Baker RW, Liu S, Sargent MV (1998) Synthesis and absolute configuration of axially chiral
binaphthoquinones. Aust J Chem 51:255
343. Sidhu GS, Sankaram AVB (1966) Ein neues Naphthochinon aus dem Kernholz Diospyros
melanoxylon Roxb. Ann Chem 691:172
344. Sankaram AVB, Narayama Reddy VV, Marthandamurthi M (1986) 13 C NMR spectra of some
naturally occurring binaphthoquinones and related compounds. Phytochemistry 25:2867
345. Ali A, Assimopoulou AN, Papageorgiou VP, Kolodziej H (2011) Structure/antileishmanial
activity relationship study of naphthoquinones and dependency of the mode of action on the
substitution patterns. Planta Med 77:2003
241
322. Chatterjea JN, Prasad R (1973) Condensation of Mannich base salts with phenols. Orientation
of adducts. Indian J Chem 11:214
323. González AG, León F, Sánchez-Pinto L, Padrón JI, Bermejo J (2000) Phenolic compounds
of dragon’s blood from Dracaena draco. J Nat Prod 63:1297
324. Ichikawa K, Kitaoka M, Taki M, Takaishi S, Iijima Y, Boriboon M, Akiyama T (1997) Retrodihydrochalcones and homoisoflavones isolated from Thai medicinal plant Dracaena loureiri
and their estrogen agonist activity. Planta Med 63:540
325. Fuendjiep V, Wandji J, Tillequin F, Mulholland DA, Budzikiewicz H, Fomum ZT, Nyemba
AM, Koch M (2002) Chalconoid and stilbenoid glycosides from Guibourtia tessmanii.
Phytochemistry 60:803
326. Kalabin GA, Kushnarev DF, Tyukavkina NA, Gromova AS, Lutskii VI (1976) PMR spectra
of natural stilbene compounds. Khim Prir Soedin:3
327. Peungvicha P, Temsiririrkkul R, Prasain JK, Tezuka Y, Kadota S, Thirawarapan SS, Watanabe
H (1998) 4-Hydroxybenzoic acid: a hypoglycemic constituent of aqueous extract of Pandanus
odorus root. J Ethnopharmacol 62:79
328. Yang XW, Zhao PJ, Ma YL, Xiao HT, Zuo YQ, He HP, Li L, Hao XJ (2007) Mixed lignanneolignans from Tarenna attenuata. J Nat Prod 70:521
329. Department of Traditional Medicine (1990) Medicinal plants of Myanmar. Myanmar, Ministry
of Health, p 115
330. Jabeen UBA, Ahmed A, Siddiqui MA (2015) Therapeutic uses of Vitex nigundo. World J
Pharm Res 4:589
331. Awale S, Linn TZ, Li F, Tezuka Y, Myint A, Tomida A, Yamori T, Esumi H, Kadota S (2011)
Identification of chrysoplenetin from Vitex negundo as a potential cytotoxic agent against
PANC-1 and a panel of 39 human cancer cell lines (JFCR-39). Phytother Res 25:1770
332. Sy LK, Brown GD (1998) Three sesquiterpenes from Artemisia annua. Phytochemistry
48:1207
333. Marco JA, Barbera O, Rodriguez S, Domingo C, Adell J (1988) Flavonoids and other phenolics
from Artemisia hispanica. Phytochemistry 27:3155
334. Kress WJ, DeFilipps RA, Farr E, Kyi YY (2003) A checklist of the trees, shrubs, herbs, and
climbers of Myanmar. United States National Herbarium, Washington, DC 45:209
335. Mori-Yasumoto K, Izumoto R, Fuchino H, Ooi T, Agatsuma Y, Kusumi T, Satake M, Sekita
S (2012) Leishmanicidal activities and cytotoxicities of bisnaphthoquinone analogues and
naphthol derivatives from Burman Diospyros burmanica. Bioorg Med Chem 20:5215
336. Sidhu GS, Sankaram AVB, Mahmood Ali S (1968) Extractives from Diospyros species: Part
III. new naphthoquinones and naphthols from the heartwood of Diospyros melanoxylon Roxb.
Indian J Chem 6:681
337. Mahmood Ali S, Prasad KK, Sankaram AVB, Sidhu GS (1971) Double bond fixation in
methylnaphthalene derivatives. Tetrahedron Lett 21:2305
338. Bungard CJ, Morris JC (2002) A convenient preparation of functionalized 1,8-dioxygenated
naphthalenes from 6-alkoxybenzocyclobutenones. J Org Chem 67:2361
339. Parker KA, Tallman EA (1984) Annelative phenol synthesis: preparation of 7-methyljuglone
and 7,9,11-trideoxydaunomycinone. Tetrahedron 40:4781
340. Ganapaty S, Thomas PS, Karagianis G, Waterman PG, Brun R (2006) Antiprotozoal and
cytotoxic naphthalene derivatives from Diospyros assimilis. Phytochemistry 67:1950
341. Likhitwitayawuid K, Kaewamatawong R, Ruangrungsi N, Krungkrai J (1998) Antimalarial
naphthoquinones from Nepenthes thorelii. Planta Med 64:237
342. Baker RW, Liu S, Sargent MV (1998) Synthesis and absolute configuration of axially chiral
binaphthoquinones. Aust J Chem 51:255
343. Sidhu GS, Sankaram AVB (1966) Ein neues Naphthochinon aus dem Kernholz Diospyros
melanoxylon Roxb. Ann Chem 691:172
344. Sankaram AVB, Narayama Reddy VV, Marthandamurthi M (1986) 13 C NMR spectra of some
naturally occurring binaphthoquinones and related compounds. Phytochemistry 25:2867
345. Ali A, Assimopoulou AN, Papageorgiou VP, Kolodziej H (2011) Structure/antileishmanial
activity relationship study of naphthoquinones and dependency of the mode of action on the
substitution patterns. Planta Med 77:2003