Melanogenesis inhibitors from the desert plant Anastatica hierochuntica 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 | Fengming Xu | Seikou Nakamura | Souichi Nakashima | Yoshimi Oda | Feng-ming Xu
[1] Y. Mishima. Molecular and biological control of melanogenesis through tyrosinase genes and intrinsic and extrinsic regulatory factors. , 1994, Pigment cell research.
[2] H. Matsuda,et al. Structures and Radical Scavenging Activities of Novel Norstilbene Dimer, Longusone A, and New Stilbene Dimers, Longusols A, B, and C, from Egyptian Herbal Medicine Cyperus longus , 2002 .
[3] E. Webb,et al. 3,4-dihydroxybenzaldehyde, a fungistatic substance from green Cavendish bananas , 1969 .
[4] V. Hearing,et al. New regulators of melanogenesis are associated with purified tyrosinase isozymes. , 1982, The Journal of investigative dermatology.
[5] H. S. Mason,et al. Melanoproteins. I. Reactions between enzyme-generated quinones and amino acids. , 1965, Biochimica et biophysica acta.
[6] H. Matsuda,et al. (7R,8S) and (7S,8R) 8-5′ linked neolignans from Egyptian herbal medicine Anastatica hierochuntica and inhibitory activities of lignans on nitric oxide production , 2003 .
[7] M. Steinberg,et al. Stimulation of melanotic expression in a melanoma cell line by theophylline , 1976, Journal of cellular physiology.
[8] Jinhua J. Song,et al. Synthesis of p38 MAP kinase inhibitor BIRB 796 and analogs via copper-mediated N-arylation reaction , 2010 .
[9] C. Chaichantipyuth,et al. Trans-Triacontyl-4-Hydroxy-3-Methoxycinnamate, A New Compound From The Thai Plant Bridelia-Ovata , 1992 .
[10] P. Winterhalter,et al. Isolation and characterization of novel benzoates, cinnamates, flavonoids, and lignans from Riesling wine and screening for antioxidant activity. , 2001, Journal of agricultural and food chemistry.
[11] I. Kubo,et al. Effects of phenolic compounds isolated from Rabdosia japonica on B16‐F10 melanoma cells , 2008, Phytotherapy research : PTR.
[12] H. Achenbach,et al. Flavonoid and other constituents of Bauhinia manca , 1988 .
[13] Jun Sik Lee,et al. Antimelanogenic Activity of 3,4-Dihydroxyacetophenone: Inhibition of Tyrosinase and MITF , 2006, Bioscience, biotechnology, and biochemistry.
[14] Masayuki Yoshikawa,et al. Anastatins A and B, new skeletal flavonoids with hepatoprotective activities from the desert plant Anastatica hierochuntica. , 2003, Bioorganic & medicinal chemistry letters.
[15] S. Arihara,et al. Isolation and absolute structures of enantiomeric 1,2-bis(4-hydroxy-3-methoxyphenyl)-1,3-propanediol 1-O-glucosides from the bark of Hovenia trichocarpa. , 1998, Journal of natural products.
[16] H. Matsuda,et al. Medicinal flowers. VI. Absolute stereostructures of two new flavanone glycosides and a phenylbutanoid glycoside from the flowers of Chrysanthemum indicum L.: their inhibitory activities for rat lens aldose reductase. , 2002, Chemical & pharmaceutical bulletin.
[17] T. Nohara,et al. Tannins and related compounds. LII: Studies on the constituents of the leaves of Thujopsis dolabrata Sieb. et Zucc. , 1987 .
[18] A. Molinaro,et al. Dihydrobenzofuran neolignans from arum italicum , 1994 .
[19] R. Buscà,et al. Cyclic AMP a key messenger in the regulation of skin pigmentation. , 2000, Pigment cell research.
[20] P. Wu,et al. The heartwood constituents of Tetradium glabrifolium , 1995 .
[21] Ute Mühlenbeck,et al. Formation of hydroxycinnamoylamides and α-hydroxyacetovanillone in cell cultures of Solanum khasianum , 1996 .
[22] Keji Miki,et al. Lignans of Larix leptolepis , 1980 .
[23] M. Iinuma,et al. Studies of cuticle drugs from natural sources. IV. Inhibitory effects of some Arctostaphylos plants on melanin biosynthesis. , 1996, Biological & pharmaceutical bulletin.
[24] V. Ferrans,et al. Production of melanocyte-specific antibodies to human melanosomal proteins: expression patterns in normal human skin and in cutaneous pigmented lesions. , 2001, Pigment cell research.
[25] J. Marco,et al. Sesquiterpene lactones and dihydroflavonols from Andryala and Urospermum species , 1994 .
[26] H. Matsuda,et al. Medicinal foodstuffs. XVII. Fenugreek seed. (3): structures of new furostanol-type steroid saponins, trigoneosides Xa, Xb, XIb, XIIa, XIIb, and XIIIa, from the seeds of Egyptian Trigonellafoenum-graecum L. , 2000, Chemical & pharmaceutical bulletin.
[27] T. Mak,et al. On the absolute structure of optically active neolignans containing a dihydrobenzo[b]furan skeleton , 1998 .
[28] M. Yoshikawa,et al. Medicinal flowers. IV. Marigold. (2): Structures of new ionone and sesquiterpene glycosides from Egyptian Calendula officinalis. , 2001, Chemical & pharmaceutical bulletin.
[29] J. Lee,et al. Silibinin prevents TPA-induced MMP-9 expression and VEGF secretion by inactivation of the Raf/MEK/ERK pathway in MCF-7 human breast cancer cells. , 2009, Phytomedicine : international journal of phytotherapy and phytopharmacology.
[30] M. Kato,et al. Absolute Configuration of Dehydrodiconiferyl Alcohol , 1994 .
[31] J. Pezzuto,et al. Plant anticancer agents, XLII. Cytotoxic constituents from Wikstroemia elliptica. , 1986, Journal of natural products.
[32] H. Matsuda,et al. Medicinal flowers. III. Marigold. (1): hypoglycemic, gastric emptying inhibitory, and gastroprotective principles and new oleanane-type triterpene oligoglycosides, calendasaponins A, B, C, and D, from Egyptian Calendula officinalis. , 2001, Chemical & pharmaceutical bulletin.
[33] F. Camacho,et al. Management of Facial Hyperpigmentation , 2000, American journal of clinical dermatology.
[34] H. Matsuda,et al. Structures of new sesquiterpenes and hepatoprotective constituents from the Egyptian herbal medicine Cyperus longus. , 2004, Journal of natural products.
[35] K. Scott. Carbon-13 nuclear magnetic resonance of biologically important aromatic acids. I. Chemical shifts of benzoic acid and derivatives. , 1972, Journal of the American Chemical Society.
[36] B. Gilchrest,et al. Ultraviolet radiation directly induces pigment production by cultured human melanocytes , 1987, Journal of cellular physiology.
[37] A. Thody,et al. Alpha-melanocyte stimulating hormone and its analogue Nle4DPhe7 alpha-MSH affect morphology, tyrosinase activity and melanogenesis in cultured human melanocytes. , 1994, Journal of cell science.
[38] Masayuki Yoshikawa,et al. New crinine-type alkaloids with inhibitory effect on induction of inducible nitric oxide synthase from Crinum yemense. , 2004, Journal of natural products.
[39] H. Ogura,et al. Sterol glucosides from Prunella vulgaris , 1990 .
[40] D. Fisher,et al. MITF: master regulator of melanocyte development and melanoma oncogene. , 2006, Trends in molecular medicine.
[41] M. Tachibana,et al. Cochlear melanocytes and MITF signaling. , 2001, The journal of investigative dermatology. Symposium proceedings.
[42] H. Matsuda,et al. Pseudoguaiane-type sesquiterpenes and inhibitors on nitric oxide production from Dichrocephala integrifolia , 2006 .
[43] D. Y. Lee,et al. Molecular structure and stereochemistry of silybin A, silybin B, isosilybin A, and isosilybin B, Isolated from Silybum marianum (milk thistle). , 2003, Journal of natural products.
[44] V. Hearing,et al. Mammalian tyrosinase--the critical regulatory control point in melanocyte pigmentation. , 1987, The International journal of biochemistry.
[45] Se-Jae Kim,et al. Involvement of Extracellular Signal-Regulated Kinase in Nobiletin-Induced Melanogenesis in Murine B16/F10 Melanoma Cells , 2007, Bioscience, biotechnology, and biochemistry.
[46] Hyunsu Bae,et al. Survey and mechanism of skin depigmenting and lightening agents , 2006, Phytotherapy research : PTR.
[47] H. Matsuda,et al. Nigellamines A3, A4, A5, and C, new dolabellane-type diterpene alkaloids, with lipid metabolism-promoting activities from the Egyptian medicinal food black cumin. , 2004, Chemical & pharmaceutical bulletin.
[48] H. Matsuda,et al. Novel dolabellane-type diterpene alkaloids with lipid metabolism promoting activities from the seeds of Nigella sativa. , 2004, Organic letters.
[49] A. Motoyama,et al. A novel melanin inhibitor: hydroperoxy traxastane-type triterpene from flowers of Arnica montana. , 2007, Biological & pharmaceutical bulletin.
[50] H. Tatematsu,et al. Stereostructures of Two Biflavanones from Stellera chamaejasme L. , 1986 .
[51] M. Saito,et al. Inhibitory Effect of Quercetin Isolated from Rose Hip (Rosa canina L.) against Melanogenesis by Mouse Melanoma Cells , 2009, Bioscience, biotechnology, and biochemistry.
[52] Geoffrey D. Brown,et al. Coniferaldehyde derivatives from tissue culture of Artemisia annua and Tanacetum parthenium , 1999 .
[53] G. Prota. Progress in the chemistry of melanins and related metabolites , 1988, Medicinal research reviews.
[54] T. Ohmoto,et al. Studies on the constituents of Ailanthus integrifolia. , 1994, Chemical & pharmaceutical bulletin.
[55] T. Satake,et al. Chemical and chemotaxonomical studies on filices. LI. Chemical studies on the constituents of Costa Rican ferns. 3. , 1981 .
[56] M. Choi,et al. Whitening activity of luteolin related to the inhibition of cAMP pathway in α-MSH-stimulated B16 melanoma cells , 2008, Archives of pharmacal research.
[57] W. Hartung,et al. Tissue culture of the desert plant Anastatica hiërochuntica , 1995, Plant Cell Reports.
[58] Masayuki Yoshikawa,et al. Melanogenesis inhibitors from the rhizomes of Alpinia officinarum in B16 melanoma cells. , 2009, Bioorganic & medicinal chemistry.
[59] I. Kubo,et al. Effects of quercetin on mushroom tyrosinase and B16-F10 melanoma cells. , 2007, Molecules.
[60] K. Wakamatsu,et al. Eumelanin biosynthesis is regulated by coordinate expression of tyrosinase and tyrosinase-related protein-1 genes. , 1993, Experimental cell research.
[61] 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.
[62] Shiming Li,et al. Revised structure for a neolignan from Brucea javanica , 1998 .