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Volumn 18, Issue 11, 2013, Pages 14320-14339

Tuning a 96-well microtiter plate fluorescence-based assay to identify AGE inhibitors in crude plant extracts

Author keywords

Advanced glycation end products; Automation; Fluorescence; Natural products; Pentosidine; Plant extract screening; Vesperlysines

Indexed keywords

ADVANCED GLYCATION END PRODUCT; ARGININE; DRUG DERIVATIVE; LYSINE; PENTOSIDINE; PLANT EXTRACT;

EID: 84888587511     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules181114320     Document Type: Article
Times cited : (96)

References (68)
  • 1
    • 0000916315 scopus 로고
    • Action des acides aminés sur les sucres; Formation des mélanoïdes par voie méthodique
    • Maillard, L.C. Action des acides aminés sur les sucres; formation des mélanoïdes par voie méthodique. C. R. Acad. Sci. 1912, 154, 66-67.
    • (1912) C. R. Acad. Sci. , vol.154 , pp. 66-67
    • Maillard . L, C.1
  • 2
    • 0030024095 scopus 로고    scopus 로고
    • Long-term assessment of glucose control by haemoglobin-AGE measurement
    • Wolffenbuttel, B.H.; Giordano, D.; Founds, H.W.; Bucala, R. Long-term assessment of glucose control by haemoglobin-AGE measurement. Lancet 1996, 347, 513-515.
    • (1996) Lancet , vol.347 , pp. 513-515
    • Wolffenbuttel, B.H.1    Giordano, D.2    Founds, H.W.3    Bucala, R.4
  • 3
    • 33745190013 scopus 로고    scopus 로고
    • Inhibitors of the Maillard reaction and AGE breakers as therapeutics for multiple diseases
    • Reddy, V.P.; Beyaz, A. Inhibitors of the Maillard reaction and AGE breakers as therapeutics for multiple diseases. Drug Discov. Today 2006, 11, 646-654.
    • (2006) Drug Discov. Today , vol.11 , pp. 646-654
    • Reddy, V.P.1    Beyaz, A.2
  • 4
    • 33749128745 scopus 로고    scopus 로고
    • Advanced glycation endproducts (AGEs): Pharmacological inhibition in diabetes
    • Peyroux, J.; Sternberg, M. Advanced glycation endproducts (AGEs): Pharmacological inhibition in diabetes. Pathol. Biol. 2006, 54, 405-419.
    • (2006) Pathol. Biol. , vol.54 , pp. 405-419
    • Peyroux, J.1    Sternberg, M.2
  • 5
    • 84888631047 scopus 로고    scopus 로고
    • WHO, Diabetes. Available online (accessed 20 June 2012)
    • WHO, Diabetes. Available online: http://www.who.int/topics/diabetes- mellitus/en/ (accessed 20 June 2012).
  • 6
    • 0035856980 scopus 로고    scopus 로고
    • Biochemistry and molecular cell biology of diabetic complications
    • Brownlee, M. Biochemistry and molecular cell biology of diabetic complications. Nature 2001, 414, 813-820.
    • (2001) Nature , vol.414 , pp. 813-820
    • Brownlee, M.1
  • 7
    • 0035135246 scopus 로고    scopus 로고
    • Advanced glycation end-products: A review
    • Singh, R.; Barden, A.; Mori, T.; Beilin, L. Advanced glycation end-products: A review. Diabetologia 2001, 44, 129-146.
    • (2001) Diabetologia , vol.44 , pp. 129-146
    • Singh, R.1    Barden, A.2    Mori, T.3    Beilin, L.4
  • 10
    • 23744476305 scopus 로고    scopus 로고
    • The maillard reaction in eye diseases
    • Stitt, A.W. The maillard reaction in eye diseases. Ann. N.Y. Acad. Sci. 2005, 1043, 582-97.
    • (2005) Ann. N.Y. Acad. Sci. , vol.1043 , pp. 582-597
    • Stitt . A, W.1
  • 11
    • 84855185039 scopus 로고    scopus 로고
    • Standards of medical care in diabetes-2012
    • DiabetesCare. Standards of medical care in diabetes-2012. Diabetes Care 2012, 35 (Suppl. 1), S11-S63.
    • (2012) Diabetes Care , vol.35 , Issue.SUPPL. 1
    • Diabetescare1
  • 12
    • 79959853014 scopus 로고    scopus 로고
    • Relationship between antioxidant and antiglycation ability of saponins, polyphenols, and polysaccharides in Chinese herbal medicines used to treat diabetes
    • Chen, Y.F.; Roan, H.Y.; Lii, C.K.; Huang, Y.C.; Wang, T.S. Relationship between antioxidant and antiglycation ability of saponins, polyphenols, and polysaccharides in Chinese herbal medicines used to treat diabetes. J. Med. Plants Res. 2011, 5, 2322-2331.
    • (2011) J. Med. Plants Res. , vol.5 , pp. 2322-2331
    • Chen, Y.F.1    Roan, H.Y.2    Lii, C.K.3    Huang, Y.C.4    Wang, T.S.5
  • 14
    • 84862833280 scopus 로고    scopus 로고
    • Naturally occurring inhibitors against the formation of advanced glycation end-products
    • Peng, X.; Ma, J.; Chen, F.; Wang, M. Naturally occurring inhibitors against the formation of advanced glycation end-products. Food Funct. 2011, 2, 289-301.
    • (2011) Food Funct. , vol.2 , pp. 289-301
    • Peng, X.1    Ma, J.2    Chen, F.3    Wang, M.4
  • 15
    • 44449179863 scopus 로고    scopus 로고
    • Possible involvement of advanced glycation end-products (AGEs) in the pathogenesis of Alzheimer's disease
    • Takeuchi, M.; Yamagishi, S.-I. Possible involvement of advanced glycation end-products (AGEs) in the pathogenesis of Alzheimer's disease. Curr. Pharm. Des. 2008, 14, 973-978.
    • (2008) Curr. Pharm. Des. , vol.14 , pp. 973-978
    • Takeuchi, M.1    Yamagishi, S.-I.2
  • 16
    • 2342648312 scopus 로고    scopus 로고
    • The AGE of the matrix: Chemistry, consequence and cure
    • DeGroot, J. The AGE of the matrix: Chemistry, consequence and cure. Curr. Opin. Pharmacol. 2004, 4, 301-305.
    • (2004) Curr. Opin. Pharmacol. , vol.4 , pp. 301-305
    • Degroot, J.1
  • 17
    • 44949216859 scopus 로고    scopus 로고
    • Advanced glycation end-products (AGEs): Involvement in aging and in neurodegenerative diseases
    • Grillo, M.A.; Colombatto, S. Advanced glycation end-products (AGEs): Involvement in aging and in neurodegenerative diseases. Amino Acids 2008, 35, 29-36.
    • (2008) Amino Acids , vol.35 , pp. 29-36
    • Grillo, M.A.1    Colombatto, S.2
  • 18
    • 0033551042 scopus 로고    scopus 로고
    • Amadorins: Novel post-Amadori inhibitors of advanced glycation reactions
    • Khalifah, R.G.; Baynes, J.W.; Hudson, B.G. Amadorins: Novel post-Amadori inhibitors of advanced glycation reactions. Biochem. Biophys. Res. Commun. 1999, 257, 251-258.
    • (1999) Biochem. Biophys. Res. Commun. , vol.257 , pp. 251-258
    • Khalifah, R.G.1    Baynes, J.W.2    Hudson, B.G.3
  • 19
    • 0142026785 scopus 로고    scopus 로고
    • Intervention against the Maillard reaction in vivo
    • Monnier, V.M. Intervention against the Maillard reaction in vivo. Arch. Biochem. Biophys. 2003, 419, 1-15.
    • (2003) Arch. Biochem. Biophys. , vol.419 , pp. 1-15
    • Monnier . V, M.1
  • 21
    • 84858308226 scopus 로고    scopus 로고
    • Natural products as sources of new drugs over the 30 Years from 1981 to 2010
    • Newman, D.J.; Cragg, G.M. Natural products as sources of new drugs over the 30 Years from 1981 to 2010. J. Nat. Prod. 2012, 75, 311-335.
    • (2012) J. Nat. Prod. , vol.75 , pp. 311-335
    • Newman, D.J.1    Cragg, G.M.2
  • 22
    • 2342424434 scopus 로고    scopus 로고
    • Metformin: Its botanical background
    • Bailey, C.J.; Day, C. Metformin: Its botanical background. Pract. Diabetes Int. 2004, 21, 115-117.
    • (2004) Pract. Diabetes Int. , vol.21 , pp. 115-117
    • Bailey, C.J.1    Day, C.2
  • 23
    • 33750563272 scopus 로고    scopus 로고
    • Towards the control and inhibition of glycation- The role of the guanidine reaction center with aldehydic and diketonic dicarbonyls
    • Saraiva, M.A.; Borges, C.M.; Florêncio, M.H. Towards the control and inhibition of glycation- the role of the guanidine reaction center with aldehydic and diketonic dicarbonyls. A mass spectrometry study. J. Mass Spectrom. 2006, 41, 1346-1368.
    • (2006) A Mass Spectrometry Study. J. Mass Spectrom. , vol.41 , pp. 1346-1368
    • Saraiva, M.A.1    Borges, C.M.2    Florêncio, M.H.3
  • 24
    • 0030446569 scopus 로고    scopus 로고
    • Inhibition of protein glycation and advanced glycation end products by ascorbic acid and other vitamins and nutrients
    • Vinson, J.A.; Howard, T.B. Inhibition of protein glycation and advanced glycation end products by ascorbic acid and other vitamins and nutrients. J. Nutr. Biochem. 1996, 7, 659-663.
    • (1996) J. Nutr. Biochem. , vol.7 , pp. 659-663
    • Vinson, J.A.1    Howard, T.B.2
  • 25
    • 79957811092 scopus 로고    scopus 로고
    • Inhibition of advanced glycation endproduct formation by foodstuffs
    • Wu, C.-H.; Huang, S.-M.; Lin, J.-A.; Yen, G.-C. Inhibition of advanced glycation endproduct formation by foodstuffs. Food Funct. 2011, 2, 224-234.
    • (2011) Food Funct. , vol.2 , pp. 224-234
    • Wu, C.-H.1    Huang, S.-M.2    Lin, J.-A.3    Yen, G.-C.4
  • 29
    • 69949184453 scopus 로고    scopus 로고
    • Astragalosides isolated from the root of Astragalus Radix inhibit the formation of advanced glycation end products
    • Motomura, K.; Fujiwara, Y.; Kiyota, N.; Tsurushima, K.; Takeya, M.; Nohara, T.; Nagai, R.; Ikeda, T. Astragalosides isolated from the root of Astragalus Radix inhibit the formation of advanced glycation end products. J. Agric. Food Chem. 2009, 57, 7666-7672.
    • (2009) J. Agric. Food Chem. , vol.57 , pp. 7666-7672
    • Motomura, K.1    Fujiwara, Y.2    Kiyota, N.3    Tsurushima, K.4    Takeya, M.5    Nohara, T.6    Nagai, R.7    Ikeda, T.8
  • 30
    • 48649103658 scopus 로고    scopus 로고
    • A procedure for the rapid screening of Maillard reaction inhibitors
    • Fatima, S.; Jairajpuri, D.S.; Saleemuddin, M. A procedure for the rapid screening of Maillard reaction inhibitors. J. Biochem. Biophys. Meth. 2008, 70, 958-965.
    • (2008) J. Biochem. Biophys. Meth. , vol.70 , pp. 958-965
    • Fatima, S.1    Jairajpuri, D.S.2    Saleemuddin, M.3
  • 31
    • 0031555853 scopus 로고    scopus 로고
    • Acid-stable fluorescent advanced glycation end products: Vesperlysines A, B, and C are formed as crosslinked products in the Maillard reaction between lysine or proteins with glucose
    • Nakamura, K.; Nakazawa, Y.; Ienaga, K. Acid-stable fluorescent advanced glycation end products: Vesperlysines A, B, and C are formed as crosslinked products in the Maillard reaction between lysine or proteins with glucose. Biochem. Biophys. Res. Commun. 1997, 232, 227-230.
    • (1997) Biochem. Biophys. Res. Commun. , vol.232 , pp. 227-230
    • Nakamura, K.1    Nakazawa, Y.2    Ienaga, K.3
  • 32
    • 0024852380 scopus 로고
    • Structure elucidation of a senescence cross-link from human extracellular matrix. Implication of pentoses in the aging process
    • Sell, D.R.; Monnier, V.M. Structure elucidation of a senescence cross-link from human extracellular matrix. Implication of pentoses in the aging process. J. Biol. Chem. 1989, 264, 21597-21602.
    • (1989) J. Biol. Chem. , vol.264 , pp. 21597-21602
    • Sell, D.R.1    Monnier, V.M.2
  • 33
    • 80054683350 scopus 로고    scopus 로고
    • Formation and determination of a-dicarbonyls and an AGE cross-link, pyrropyridine in glycated proteins and in vivo
    • Watanabe, H.; Iwaki, S.; Aida, K.; Hayase, F. Formation and determination of a-dicarbonyls and an AGE cross-link, pyrropyridine in glycated proteins and in vivo. Int. Congr. Ser. 2002, 1245, 153-156.
    • (2002) Int. Congr. Ser. , vol.1245 , pp. 153-156
    • Watanabe, H.1    Iwaki, S.2    Aida, K.3    Hayase, F.4
  • 34
    • 78349302760 scopus 로고    scopus 로고
    • Advanced glycation end-products and bone fractures
    • Vashishth, D. Advanced glycation end-products and bone fractures. BoneKEy Osteovision 2009, 6, 268-278.
    • (2009) BoneKEy Osteovision , vol.6 , pp. 268-278
    • Vashishth, D.1
  • 35
    • 0001112738 scopus 로고
    • Aging of proteins: Isolation and identification of a fluorescent chromophore from the reaction of polypeptides with glucose
    • Pongor, S.; Ulrich, P.C.; Bencsath, F.A.; Cerami, A. Aging of proteins: Isolation and identification of a fluorescent chromophore from the reaction of polypeptides with glucose. Proc. Natl. Acad. Sci. USA 1984, 81, 2684-2688.
    • (1984) Proc. Natl. Acad. Sci. USA , vol.81 , pp. 2684-2688
    • Pongor, S.1    Ulrich, P.C.2    Bencsath, F.A.3    Cerami, A.4
  • 36
    • 0031214523 scopus 로고    scopus 로고
    • Protein modification by methylglyoxal: Chemical nature and synthetic mechanism of a major fluorescent adduct
    • Shipanova, I.N.; Glomb, M.A.; Nagaraj, R.H. Protein modification by methylglyoxal: Chemical nature and synthetic mechanism of a major fluorescent adduct. Arch. Biochem. Biophys. 1997, 344, 29-36.
    • (1997) Arch. Biochem. Biophys. , vol.344 , pp. 29-36
    • Shipanova, I.N.1    Glomb, M.A.2    Nagaraj, R.H.3
  • 37
    • 77957831206 scopus 로고    scopus 로고
    • Automating a 96-well microtiter plate assay for identification of AGEs inhibitors or inducers: Application to the screening of a small natural compounds library
    • Derbré, S.; Gatto, J.; Pelleray, A.; Coulon, L.; Séraphin, D.; Richomme, P. Automating a 96-well microtiter plate assay for identification of AGEs inhibitors or inducers: Application to the screening of a small natural compounds library. Anal. Bioanal. Chem. 2010, 398, 1747-1758.
    • (2010) Anal. Bioanal. Chem. , vol.398 , pp. 1747-1758
    • Derbré, S.1    Gatto, J.2    Pelleray, A.3    Coulon, L.4    Séraphin, D.5    Richomme, P.6
  • 38
    • 84857846434 scopus 로고    scopus 로고
    • Two fluorescent wavelengths, 440(ex)/520(em) nm and 370(ex)/440(em) nm, reflect advanced glycation and oxidation end products in Human skin without diabetes
    • Beisswenger, P.J.; Howell, S.; Mackenzie, T.; Corstjens, H.; Muizzuddin, N.; Matsui, M.S. Two fluorescent wavelengths, 440(ex)/520(em) nm and 370(ex)/440(em) nm, reflect advanced glycation and oxidation end products in Human skin without diabetes. Diabetes Technol. Ther. 2012, 14, 285-292.
    • (2012) Diabetes Technol. Ther. , vol.14 , pp. 285-292
    • Beisswenger, P.J.1    Howell, S.2    Mackenzie, T.3    Corstjens, H.4    Muizzuddin, N.5    Matsui, M.S.6
  • 39
    • 84888633556 scopus 로고    scopus 로고
    • The nomenclature used in the manuscript does not refer to the structure of AGEs but rather to their fluorescent properties
    • The nomenclature used in the manuscript does not refer to the structure of AGEs but rather to their fluorescent properties.
  • 40
    • 84888624009 scopus 로고    scopus 로고
    • 370 nm and 440 nm were most commonly used as excitation and emission wavelengths
    • 370 nm and 440 nm were most commonly used as excitation and emission wavelengths.
  • 41
    • 79960173276 scopus 로고    scopus 로고
    • Advanced glycation end products inhibitors from Alpinia zerumbet rhizomes
    • Chompoo, J.; Upadhyay, A.; Kishimoto, W.; Makise, T.; Tawata, S. Advanced glycation end products inhibitors from Alpinia zerumbet rhizomes. Food Chemistry 2011, 129, 709-715.
    • (2011) Food Chemistry , vol.129 , pp. 709-715
    • Chompoo, J.1    Upadhyay, A.2    Kishimoto, W.3    Makise, T.4    Tawata, S.5
  • 42
    • 79951517881 scopus 로고    scopus 로고
    • Rapid isolation of geraniin from Nephelium lappaceum rind waste and its anti-hyperglycemic activity
    • Palanisamy, U.D.; Ling, L.T.; Manaharan, T.; Appleton, D. Rapid isolation of geraniin from Nephelium lappaceum rind waste and its anti-hyperglycemic activity. Food Chem. 2011, 127, 21-27.
    • (2011) Food Chem. , vol.127 , pp. 21-27
    • Palanisamy, U.D.1    Ling, L.T.2    Manaharan, T.3    Appleton, D.4
  • 43
    • 34447512444 scopus 로고    scopus 로고
    • Inhibitors of aldose reductase and advanced glycation end-products formation from the leaves of stelechocarpus cauliflorus R.E. Fr
    • Wirasathien, L.; Pengsuparp, T.; Suttisri, R.; Ueda, H.; Moriyasu, M.; Kawanishi, K. Inhibitors of aldose reductase and advanced glycation end-products formation from the leaves of Stelechocarpus cauliflorus R.E. Fr. Phytomedicine 2007, 14, 546-550.
    • (2007) Phytomedicine , vol.14 , pp. 546-550
    • Wirasathien, L.1    Pengsuparp, T.2    Suttisri, R.3    Ueda, H.4    Moriyasu, M.5    Kawanishi, K.6
  • 44
    • 79955525480 scopus 로고    scopus 로고
    • Antidiabetic complications and anti-alzheimer activities of sophoflavescenol, a prenylated flavonol from Sophora flavescens, and its structure activity relationship
    • Jung, H.A.; Jin, S.E.; Park, J.-S.; Choi, J.S. Antidiabetic complications and anti-alzheimer activities of sophoflavescenol, a prenylated flavonol from Sophora flavescens, and its structure activity relationship. Phytother. Res. 2011, 25, 709-715.
    • (2011) Phytother. Res. , vol.25 , pp. 709-715
    • Jung, H.A.1    Jin, S.E.2    Park, J.-S.3    Choi, J.S.4
  • 45
    • 35348943839 scopus 로고    scopus 로고
    • Inhibitory effects of ethyl acetate extract of Teucrium polium on in vitro protein glycoxidation
    • Ardestani, A.; Yazdanparast, R. Inhibitory effects of ethyl acetate extract of Teucrium polium on in vitro protein glycoxidation. Food Chem. Toxicol. 2007, 45, 2402-2411.
    • (2007) Food Chem. Toxicol. , vol.45 , pp. 2402-2411
    • Ardestani, A.1    Yazdanparast, R.2
  • 46
    • 0033003760 scopus 로고    scopus 로고
    • A simple statistical parameter for use in evaluation and validation of high throughput screening assays
    • Zhang, J.-H.; Chung, T.D. Y.; Oldenburg, K.R. A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J. Biomol. Screen. 1999, 4, 67-73.
    • (1999) J. Biomol. Screen. , vol.4 , pp. 67-73
    • Zhang, J.-H.1    Chung, T.D.Y.2    Oldenburg, K.R.3
  • 47
    • 44849083214 scopus 로고    scopus 로고
    • Novel analytic criteria and effective plate designs for quality control in genome-scale RNAi screens
    • Zhang, X.D. Novel analytic criteria and effective plate designs for quality control in genome-scale RNAi screens. J. Biomol. Screen. 2008, 13, 363-377.
    • (2008) J. Biomol. Screen. , vol.13 , pp. 363-377
    • Zhang . X, D.1
  • 48
    • 33947167826 scopus 로고    scopus 로고
    • A pair of new statistical parameters for quality control in RNA interference high-throughput screening assays
    • Zhang, X.D. A pair of new statistical parameters for quality control in RNA interference high-throughput screening assays. Genomics 2007, 89, 552-561.
    • (2007) Genomics , vol.89 , pp. 552-561
    • Zhang . X, D.1
  • 49
    • 0032997958 scopus 로고    scopus 로고
    • Skin collagen glycation, glycoxidation, and crosslinking are lower in subjects with long-term intensive versus conventional therapy of type 1 diabetes-Relevance of glycated collagen products versus HbA(1c) as markers of diabetic complications
    • Monnier, V.M.; Bautista, O.; Kenny, D.; Sell, D.R.; Fogarty, J.; Dahms, W.; Cleary, P.A.; Lachin, J.; Genuth, S. Skin collagen glycation, glycoxidation, and crosslinking are lower in subjects with long-term intensive versus conventional therapy of type 1 diabetes-Relevance of glycated collagen products versus HbA(1c) as markers of diabetic complications. Diabetes 1999, 48, 870-880.
    • (1999) Diabetes , vol.48 , pp. 870-880
    • Monnier, V.M.1    Bautista, O.2    Kenny, D.3    Sell, D.R.4    Fogarty, J.5    Dahms, W.6    Cleary, P.A.7    Lachin, J.8    Genuth, S.9
  • 52
    • 84863688909 scopus 로고    scopus 로고
    • In vivo localization at the cellular level of stilbene fluorescence induced by Plasmopara viticola in grapevine leaves
    • Bellow, S.; Latouche, G.; Brown, S.C.; Poutaraud, A.; Cerovic, Z.G. In vivo localization at the cellular level of stilbene fluorescence induced by Plasmopara viticola in grapevine leaves. J. Exp. Bot. 2012, 63, 3697-3707.
    • (2012) J. Exp. Bot. , vol.63 , pp. 3697-3707
    • Bellow, S.1    Latouche, G.2    Brown, S.C.3    Poutaraud, A.4    Cerovic, Z.G.5
  • 53
    • 68149168863 scopus 로고    scopus 로고
    • Solvent effect on the UV/Vis absorption and fluorescence spectroscopic properties of berberine
    • Diaz, M.S.; Freile, M.L.; Gutierrez, M.I. Solvent effect on the UV/Vis absorption and fluorescence spectroscopic properties of berberine. Photochem. Photobiol. Sci. 2009, 8, 970-974.
    • (2009) Photochem. Photobiol. Sci. , vol.8 , pp. 970-974
    • Diaz, M.S.1    Freile, M.L.2    Gutierrez, M.I.3
  • 55
    • 29744431899 scopus 로고    scopus 로고
    • Time-resolved spectral studies of blue-green fluorescence of artichoke (Cynara cardunculus L var ccolymus) leaves: Identification of chlorogenic acid as one of the major fluorophores and age-mediated changes
    • Morales, F.; Cartelat, A.; Alvarez-Fernandez, A.; Moya, I.; Cerovic, Z.G. Time-resolved spectral studies of blue-green fluorescence of artichoke (Cynara cardunculus L. var. ccolymus) leaves: Identification of chlorogenic acid as one of the major fluorophores and age-mediated changes. J. Agric. Food Chem. 2005, 53, 9668-9678.
    • (2005) J. Agric. Food Chem. , vol.53 , pp. 9668-9678
    • Morales, F.1    Cartelat, A.2    Alvarez-Fernandez, A.3    Moya, I.4    Cerovic, Z.G.5
  • 56
    • 0033948838 scopus 로고    scopus 로고
    • The fluorescent oxidation products of dihydroxyphenylalanine and its esters
    • Smith, G.J.; Haskell, T.G. The fluorescent oxidation products of dihydroxyphenylalanine and its esters. J. Photochem. Photobiol. B 2000, 55, 103-108.
    • (2000) J. Photochem. Photobiol. B , vol.55 , pp. 103-108
    • Smith, G.J.1    Haskell, T.G.2
  • 57
    • 0035877337 scopus 로고    scopus 로고
    • High-performance liquid chromatographic assay with fluorescence detection for the determination of cephaeline and emetine in human plasma and urine
    • Asano, T.; Sadakane, C.; Ishihara, K.; Yanagisawa, T.; Kimura, M.; Kamei, H. High-performance liquid chromatographic assay with fluorescence detection for the determination of cephaeline and emetine in human plasma and urine. J. Chromatogr. B: Biomed. Sci. Appl. 2001, 757, 197-206.
    • (2001) J. Chromatogr. B: Biomed. Sci. Appl. , vol.757 , pp. 197-206
    • Asano, T.1    Sadakane, C.2    Ishihara, K.3    Yanagisawa, T.4    Kimura, M.5    Kamei, H.6
  • 58
    • 0001401638 scopus 로고
    • PH effects on fluorescence of umbelliferone
    • Fink, D.W.; Koehler, W.R. pH effects on fluorescence of umbelliferone. Anal. Chem. 1970, 42, 990-993.
    • (1970) Anal. Chem. , vol.42 , pp. 990-993
    • Fink, D.W.1    Koehler, W.R.2
  • 60
    • 84857430527 scopus 로고    scopus 로고
    • Chelation: A fundamental mechanism of action of AGE inhibitors, AGE breakers, and other inhibitors of diabetes complications
    • Nagai, R.; Murray, D.B.; Metz, T.O.; Baynes, J.W. Chelation: A fundamental mechanism of action of AGE inhibitors, AGE breakers, and other inhibitors of diabetes complications. Diabetes 2012, 61, 549-559.
    • (2012) Diabetes , vol.61 , pp. 549-559
    • Nagai, R.1    Murray, D.B.2    Metz, T.O.3    Baynes, J.W.4
  • 61
    • 84888585267 scopus 로고    scopus 로고
    • version 12.5; Systat Software GmbH: Erkrath, Germany
    • Sigmaplot Software, version 12.5; Systat Software GmbH: Erkrath, Germany, 2011.
    • (2011) Sigmaplot Software
  • 62
    • 0346761466 scopus 로고
    • The electronic states of the azines. VII. 1,2,4-triazine, studied by photon absorption, near-threshold electron energy loss spectroscopy and ab initio multi-reference configuration interaction calculations
    • Palmer, M.H.; Walker, I.C.; Guest, M.F.; Siggel, M.R. F. The electronic states of the azines. VII. 1,2,4-triazine, studied by photon absorption, near-threshold electron energy loss spectroscopy and ab initio multi-reference configuration interaction calculations. Chem. Phys. 1995, 201, 381-391.
    • (1995) Chem. Phys. , vol.201 , pp. 381-391
    • Palmer, M.H.1    Walker, I.C.2    Guest, M.F.3    Siggel, M.R.F.4
  • 63
    • 0026658334 scopus 로고
    • Chiral formamidines-The total asymmetric-synthesis of (-)-8- azaestrone and related (-)-8-aza-12-oxo-17-desoxoestrone
    • Meyers, A.I.; Elworthy, T.R. Chiral formamidines-The total asymmetric-synthesis of (-)-8- azaestrone and related (-)-8-aza-12-oxo-17- desoxoestrone. J. Org. Chem. 1992, 57, 4732-4740.
    • (1992) J. Org. Chem. , vol.57 , pp. 4732-4740
    • Meyers, A.I.1    Elworthy, T.R.2
  • 66
    • 43449123023 scopus 로고    scopus 로고
    • Phenolic content and antioxidative capacity of green and white tea extracts depending on extraction conditions and the solvent used
    • Rusak, G.; Komes, D.; Likic, S.; Horzic, D.; Kovac, M. Phenolic content and antioxidative capacity of green and white tea extracts depending on extraction conditions and the solvent used. Food Chem. 2008, 110, 852-858.
    • (2008) Food Chem. , vol.110 , pp. 852-858
    • Rusak, G.1    Komes, D.2    Likic, S.3    Horzic, D.4    Kovac, M.5
  • 67
    • 4243522573 scopus 로고    scopus 로고
    • 2nd ed.; Editions Tec & Doc: Paris, France
    • Wichtl, M.; Anton, R. Plantes Thérapeutiques, 2nd ed.; Editions Tec & Doc: Paris, France, 2003; p. 689.
    • (2003) Plantes Thérapeutiques , pp. 689
    • Wichtl, M.1    Anton, R.2
  • 68
    • 84857239177 scopus 로고    scopus 로고
    • Preparative isolation, fast centrifugal partition chromatography purification and biological activity of cajaflavanone from Derris ferruginea Stems
    • Morel, S.; Landreau, A.; Nguyen, V.H.; Derbré, S.; Grellier, P.; Le Pape, P.; Pagniez, F.; Litaudon, M.; Richomme, P. Preparative isolation, fast centrifugal partition chromatography purification and biological activity of cajaflavanone from Derris ferruginea Stems. Phytochem. Anal. 2012, 23, 152-158.
    • (2012) Phytochem. Anal. , vol.23 , pp. 152-158
    • Morel, S.1    Landreau, A.2    Nguyen, V.H.3    Derbré, S.4    Grellier, P.5    Le Pape, P.6    Pagniez, F.7    Litaudon, M.8    Richomme, P.9


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