Alkaloid constituents from flower buds and leaves of sacred lotus (Nelumbo nucifera, Nymphaeaceae) with melanogenesis inhibitory activity in B16 melanoma cells.
暂无分享,去创建一个
Masayuki Yoshikawa | H. Matsuda | M. Yoshikawa | Hisashi Matsuda | Seikou Nakamura | Souichi Nakashima | Yoshimi Oda | Hisako Miki | Genzo Tanabe | Nami Yokota | Katsuyoshi Fujimoto | Takahiro Matsumoto | Rika Sakuma | Tomoe Ohta | Keiko Ogawa | Shino Nishida | Osamu Muraoka | G. Tanabe | O. Muraoka | Takahiro Matsumoto | Seikou Nakamura | Souichi Nakashima | Yoshimi Oda | Hisako Miki | Tomoe Ohta | Keiko Ogawa | Katsuyoshi Fujimoto | N. Yokota | Shino Nishida | R. Sakuma
[1] H. Matsuda,et al. Medicinal flowers. XXXV. Nor-oleanane-type and acylated oleanane-type triterpene saponins from the flower buds of Chinese Camellia japonica and their inhibitory effects on melanogenesis. , 2012, Chemical & pharmaceutical bulletin.
[2] Masayuki Yoshikawa,et al. Melanogenesis inhibitors from the rhizomes of Alpinia officinarum in B16 melanoma cells. , 2009, Bioorganic & medicinal chemistry.
[3] H. Matsuda,et al. Medicinal flowers. XXXVI.1) Acylated oleanane-type triterpene saponins with inhibitory effects on melanogenesis from the flower buds of Chinese Camellia japonica. , 2012, Chemical & pharmaceutical bulletin.
[4] T. Morikawa,et al. [Pharmaceutical food science: search for anti-obese constituents from medicinal foods-anti-hyperlipidemic saponin constituents from the flowers of Bellis perennis]. , 2010, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.
[5] P. Joseph-Nathan,et al. Pronuciferine N-oxide, a proaporphine N-oxide alkaloid from Berberis coletioides. , 2009, Journal of natural products.
[6] N. Blaquière,et al. Aporphine alkaloid synthesis and diversification via direct arylation , 2007 .
[7] J. Toda,et al. A HIGHLY EFFICIENT SYNTHESIS OF 1-METHYL-, 1-BENZYL-, AND 1-PHENYL- 1,2,3,4-THETRAHYDROISOQUINOLINES BY A MODIFIED PUMMERER REACTION , 1997 .
[8] H. Matsuda,et al. Medicinal flowers. XIV. New acylated oleanane-type triterpene oligoglycosides with antiallergic activity from flower buds of chinese tea plant (Camellia sinensis). , 2007, Chemical & pharmaceutical bulletin.
[9] H. Elsohly,et al. New sesquiterpenoids from the root of Guatteria multivenia. , 2002, Journal of natural products.
[10] M. Kozuka,et al. [ALKALOIDS OF ASIMINA TRILOBA DUNAL]. , 1965, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.
[11] G. Prota. Progress in the chemistry of melanins and related metabolites , 1988, Medicinal research reviews.
[12] M. Cava,et al. Dehydroaporphines: A protonation study , 1976 .
[13] H. Matsuda,et al. Medicinal flowers. XV. The structures of noroleanane- and oleanane-type triterpene oligoglycosides with gastroprotective and platelet aggregation activities from flower buds of Camellia japonica. , 2007, Chemical & pharmaceutical bulletin.
[14] H. Matsuda,et al. Medicinal flowers. XXI. Structures of perennisaponins A, B, C, D, E, and F, acylated oleanane-type triterpene oligoglycosides, from the flowers of Bellis perennis. , 2008, Chemical & pharmaceutical bulletin.
[15] R. Buscà,et al. Different cis-Acting Elements Are Involved in the Regulation of TRP1 and TRP2 Promoter Activities by Cyclic AMP: Pivotal Role of M Boxes (GTCATGTGCT) and of Microphthalmia , 1998, Molecular and Cellular Biology.
[16] Li‐jun Wu,et al. Medicinal flowers. XXX. Eight new glycosides, everlastosides F-M, from the flowers of Helichrysum arenarium. , 2009, Chemical & pharmaceutical bulletin.
[17] V. Hearing,et al. Mammalian tyrosinase--the critical regulatory control point in melanocyte pigmentation. , 1987, The International journal of biochemistry.
[18] P. Mukherjee,et al. The sacred lotus (Nelumbo nucifera)– phytochemical and therapeutic profile , 2009 .
[19] T. Mabry,et al. Carbon-13 NMR studies of flavonoids. III. Naturally occurring flavonoid glycosides and their acylated derivatives , 1978 .
[20] Masayuki Yoshikawa,et al. Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells. , 2010, Bioorganic & medicinal chemistry.
[21] M. Cava,et al. Regioselective O-demethylation in the aporphine alkaloid series. , 1977, The Journal of organic chemistry.
[22] Robin S. Dothager,et al. Synthesis and identification of small molecules that potently induce apoptosis in melanoma cells through G1 cell cycle arrest. , 2005, Journal of the American Chemical Society.
[23] R. Sheldon,et al. Synthesis of benzyl substituted tetrahydropyridines and 1,2,3,4-tetrahydroisoquinolines via acid catalyzed cyclization of γ,δ-unsaturated N-formyl-N-styryl amines , 1999 .
[24] V. Hearing,et al. New regulators of melanogenesis are associated with purified tyrosinase isozymes. , 1982, The Journal of investigative dermatology.
[25] Gang Chen,et al. Brazilian natural medicines. IV. New noroleanane-type triterpene and ecdysterone-type sterol glycosides and melanogenesis inhibitors from the roots of Pfaffia glomerata. , 2010, Chemical & pharmaceutical bulletin.
[26] H. Matsuda,et al. Medicinal flowers. XXIV. Chemical structures and hepatoprotective effects of constituents from flowers of Hedychium coronarium. , 2008, Chemical & pharmaceutical bulletin.
[27] T. Hayakawa,et al. Medicinal Flowers. XXXII. , 2011 .
[28] D. Yuan,et al. Medicinal flowers. XXIII. New taraxastane-type triterpene, punicanolic acid, with tumor necrosis factor-alpha inhibitory activity from the flowers of Punica granatum. , 2008, Chemical & pharmaceutical bulletin.
[29] R. Stephens,et al. The Carbon-13 NMR Spectra of Aporphine Alkaloids , 1979 .
[30] W. Xiao,et al. Preparative separation of alkaloids from Nelumbo nucifera leaves by conventional and pH-zone-refining counter-current chromatography , 2010 .
[31] H. Matsuda,et al. Melanogenesis inhibitory and fibroblast proliferation accelerating effects of noroleanane- and oleanane-type triterpene oligoglycosides from the flower buds of Camellia japonica. , 2012, Journal of natural products.
[32] K. Wakamatsu,et al. Eumelanin biosynthesis is regulated by coordinate expression of tyrosinase and tyrosinase-related protein-1 genes. , 1993, Experimental cell research.
[33] H. Furukawa,et al. [On the alkaloids of Nelumbo nucifera Gaertn. IV. Isolation of dl-armepavine]. , 1961, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.
[34] Synthesis and binding studies of 2-O- and 11-O-substituted N-alkylnoraporphines. , 2008, Bioorganic & medicinal chemistry letters.
[35] H. Matsuda,et al. Medicinal Flowers. XXXI. Acylated oleanane-type triterpene saponins, Sasanquasaponins I-V, with antiallergic activity from the flower buds of Camellia sasanqua. , 2010, Chemical and pharmaceutical bulletin.
[36] G. Cuny. Intramolecular ortho-arylation of phenols utilized in the synthesis of the aporphine alkaloids (′)-lirinidine and (′)-nuciferine , 2003 .
[37] J. Toda,et al. Aporphine glycosides from Stephania cepharantha seeds. , 2000, Journal of natural products.
[38] H. Matsuda,et al. Medicinal flowers. XII.(1)) New spirostane-type steroid saponins with antidiabetogenic activity from Borassus flabellifer. , 2007, Chemical & pharmaceutical bulletin.
[39] I. Ugi,et al. Flavonol glycosides of Warburgia ugandensis leaves. , 2003, Phytochemistry.
[40] Sanghyun Lee,et al. Inhibitory effects of isorhamnetin-3-O-beta-D-glucoside from Salicornia herbacea on rat lens aldose reductase and sorbitol accumulation in streptozotocin-induced diabetic rat tissues. , 2005, Biological & pharmaceutical bulletin.
[41] N. Blaquière,et al. Direct intramolecular arylation of unactivated arenes: application to the synthesis of aporphine alkaloids. , 2004, Chemical communications.
[42] K. Oh,et al. Antibacterial compounds from the leaves ofAcanthopanax senticosus , 2003, Archives of pharmacal research.
[43] Li‐jun Wu,et al. Medicinal flowers. XXVII. New flavanone and chalcone glycosides, arenariumosides I, II, III, and IV, and tumor necrosis factor-alpha inhibitors from everlasting, flowers of Helichrysum arenarium. , 2009, Chemical & pharmaceutical bulletin.
[44] 古川 宏. ハスNelumbo nucifera Gaertn.のアルカロイド研究 , 1961 .
[45] Mi Yan,et al. Racemization of (S)-(+)-10,11-dimethoxyaporphine and (S)-(+)-aporphine: efficient preparations of (R)-(−)-apomorphine and (R)-(−)-aporphine via a recycle process of resolution , 2006 .
[46] P. Sokoloff,et al. Development of Novel 1,2,3,4‐Tetrahydroisoquinoline Derivatives and Closely Related Compounds as Potent and Selective Dopamine D3 Receptor Ligands , 2004, Chembiochem : a European journal of chemical biology.
[47] Y. Wu,et al. The Oxidation of Isoquinoline Alkaloids with m‐Chloroperbenzoic Acid , 1987 .