-
1
-
-
84856180178
-
Molecular aspects of tanning
-
Gilchrest BA. Molecular aspects of tanning. J Invest Dermatol 2011;131:E14-17.
-
(2011)
J Invest Dermatol
, vol.131
, pp. E14-E17
-
-
Gilchrest, B.A.1
-
2
-
-
4644237315
-
Melanin pigmentation in mammalian skin and its hormonal regulation
-
Slominski A, Tobin DJ, Shibahara S, Wortsman J. Melanin pigmentation in mammalian skin and its hormonal regulation. Physiol Rev 2004;84:1155-228.
-
(2004)
Physiol Rev
, vol.84
, pp. 1155-1228
-
-
Slominski, A.1
Tobin, D.J.2
Shibahara, S.3
Wortsman, J.4
-
3
-
-
83955164260
-
L-tyrosine and L-dihydroxyphenylalanine as hormone-like regulators of melanocyte functions
-
Slominski A, Zmijewski MA, Pawelek J. L-tyrosine and L-dihydroxyphenylalanine as hormone-like regulators of melanocyte functions. Pigment Cell Melanoma Res 2011;25:14-27.
-
(2011)
Pigment Cell Melanoma Res
, vol.25
, pp. 14-27
-
-
Slominski, A.1
Zmijewski, M.A.2
Pawelek, J.3
-
4
-
-
33847188116
-
Melanocyte biology and skin pigmentation
-
Lin JY, Fisher DE. Melanocyte biology and skin pigmentation. Nature 2007;445:843-50.
-
(2007)
Nature
, vol.445
, pp. 843-850
-
-
Lin, J.Y.1
Fisher, D.E.2
-
5
-
-
79955747797
-
The melanogenesis and mechanisms of skin-lightening agents-existing and new approaches
-
Gillbro JM, Olsson MJ. The melanogenesis and mechanisms of skin-lightening agents-existing and new approaches. Int J Cosmet Sci 2011;33:210-21.
-
(2011)
Int J Cosmet Sci
, vol.33
, pp. 210-221
-
-
Gillbro, J.M.1
Olsson, M.J.2
-
6
-
-
84875549379
-
Molecular mechanisms of UV-induced apoptosis and its effects on skin residential cells: The implication in UV-based phototherapy
-
Lee CH, Wu SB, Hong CH, et al. Molecular mechanisms of UV-induced apoptosis and its effects on skin residential cells: the implication in UV-based phototherapy. Int J Mol Sci 2013;14:6414-35.
-
(2013)
Int J Mol Sci
, vol.14
, pp. 6414-6435
-
-
Lee, C.H.1
Wu, S.B.2
Hong, C.H.3
-
8
-
-
84873708098
-
Mechanistic studies of the inactivation of tyrosinase by resorcinol
-
Stratford MR, Ramsden CA, Riley PA. Mechanistic studies of the inactivation of tyrosinase by resorcinol. Bioorg Med Chem 2013;21:1166-73.
-
(2013)
Bioorg Med Chem
, vol.21
, pp. 1166-1173
-
-
Stratford, M.R.1
Ramsden, C.A.2
Riley, P.A.3
-
9
-
-
84870050261
-
Natural melanogenesis inhibitors acting through the down-regulation of tyrosinase activity
-
Chang TS. Natural melanogenesis inhibitors acting through the down-regulation of tyrosinase activity. Materials 2012;5:1661-85.
-
(2012)
Materials
, vol.5
, pp. 1661-1685
-
-
Chang, T.S.1
-
10
-
-
84862254859
-
Natural and synthetic tyrosinase inhibitors as antibrowning agents: An update
-
Loizzo MR, Tundis R, Menichini F. Natural and synthetic tyrosinase inhibitors as antibrowning agents: an update. Compr Rev Food Sci Food Safety 2012;11:378-98.
-
(2012)
Compr Rev Food Sci Food Safety
, vol.11
, pp. 378-398
-
-
Loizzo, M.R.1
Tundis, R.2
Menichini, F.3
-
11
-
-
84873115218
-
Beneficial effects of marine algal compounds in cosmeceuticals
-
Thomas NV, Kim SK. Beneficial effects of marine algal compounds in cosmeceuticals. Mar Drugs 2013;11:146-64.
-
(2013)
Mar Drugs
, vol.11
, pp. 146-164
-
-
Thomas, N.V.1
Kim, S.K.2
-
12
-
-
67649668609
-
An updated review of tyrosinase inhibitors
-
Chang TS. An updated review of tyrosinase inhibitors. Int J Mol Sci 2009;10:2440-75.
-
(2009)
Int J Mol Sci
, vol.10
, pp. 2440-2475
-
-
Chang, T.S.1
-
13
-
-
23844545621
-
Tyrosinase inhibitors from natural and synthetic sources: Structure, inhibition mechanism and perspective for the future
-
Kim YJ, Uyama H. Tyrosinase inhibitors from natural and synthetic sources: structure, inhibition mechanism and perspective for the future. Cell Mol Life Sci 2005;62:1707-23.
-
(2005)
Cell Mol Life Sci
, vol.62
, pp. 1707-1723
-
-
Kim, Y.J.1
Uyama, H.2
-
14
-
-
0007983538
-
Le bleuissement et le noircissement des champignons
-
Bourquelot E, Bertrand A. Le bleuissement et le noircissement des champignons. Comp Rend Soc Biol 1895;2:582-4.
-
(1895)
Comp Rend Soc Biol
, vol.2
, pp. 582-584
-
-
Bourquelot, E.1
Bertrand, A.2
-
15
-
-
84897972480
-
Tyrosinase: The four oxidation states of the active site and their relevance to enzymatic activation, oxidation and inactivation
-
Ramsden CA, Riley PA. Tyrosinase: the four oxidation states of the active site and their relevance to enzymatic activation, oxidation and inactivation. Bioorg Med Chem 2014;22:2388-95.
-
(2014)
Bioorg Med Chem
, vol.22
, pp. 2388-2395
-
-
Ramsden, C.A.1
Riley, P.A.2
-
16
-
-
84899574027
-
In vitro antioxidant activities, free radical scavenging capacity, and tyrosinase inhibitory of Flavonoid compounds and ferulic acid from Spiranthes sinensis (Pers.) Ames
-
Liang CP, Chang CH, Liang CC, et al. In vitro antioxidant activities, free radical scavenging capacity, and tyrosinase inhibitory of Flavonoid compounds and ferulic acid from Spiranthes sinensis (Pers.) Ames. Molecules 2014;19:4681-94.
-
(2014)
Molecules
, vol.19
, pp. 4681-4694
-
-
Liang, C.P.1
Chang, C.H.2
Liang, C.C.3
-
17
-
-
0034736046
-
Advances in flavonoid research since 1992
-
Harborne JB, Williams CA. Advances in flavonoid research since 1992. Phytochemistry 2000;55:481-504.
-
(2000)
Phytochemistry
, vol.55
, pp. 481-504
-
-
Harborne, J.B.1
Williams, C.A.2
-
18
-
-
0033933718
-
Flavonols from Heterotheca inuloides: Tyrosinase inhibitory activity and structural criteria
-
Kubo I, Kinst-Hori I, Chaudhuri SK, et al. Flavonols from Heterotheca inuloides: tyrosinase inhibitory activity and structural criteria. Bioorg Med Chem 2000;8:1749-55.
-
(2000)
Bioorg Med Chem
, vol.8
, pp. 1749-1755
-
-
Kubo, I.1
Kinst-Hori, I.2
Chaudhuri, S.K.3
-
19
-
-
0028363534
-
Tyrosinase inhibitory flavonoids from Heterotheca inuloides and their structural functions
-
Kubo I, Kinst-Hori I, Ishiguro K, et al. Tyrosinase inhibitory flavonoids from Heterotheca inuloides and their structural functions. Bioorg Med Chem Lett 1994;4:1443-6.
-
(1994)
Bioorg Med Chem Lett
, vol.4
, pp. 1443-1446
-
-
Kubo, I.1
Kinst-Hori, I.2
Ishiguro, K.3
-
20
-
-
0037644565
-
Inhibitory effects of some flavonoids on the activity of mushroom tyrosinase
-
Xie LP, Chen QX, Huang H, et al. Inhibitory effects of some flavonoids on the activity of mushroom tyrosinase. Biochemistry 2003;68:487-91.
-
(2003)
Biochemistry
, vol.68
, pp. 487-491
-
-
Xie, L.P.1
Chen, Q.X.2
Huang, H.3
-
21
-
-
0033569590
-
Inhibition of tyrosinase by green tea components
-
No JK, Soung DY, Kim YJ, et al. Inhibition of tyrosinase by green tea components. Life Sci 1999;65:PL241-6.
-
(1999)
Life Sci
, vol.65
, pp. L241-L246
-
-
No, J.K.1
Soung, D.Y.2
Kim, Y.J.3
-
22
-
-
84883181715
-
Rhamnetin attenuates melanogenesis by suppressing oxidative stress and pro-inflammatory mediators
-
Kim YJ. Rhamnetin attenuates melanogenesis by suppressing oxidative stress and pro-inflammatory mediators. Biol Pharm Bull 2013;36:1341-7.
-
(2013)
Biol Pharm Bull
, vol.36
, pp. 1341-1347
-
-
Kim, Y.J.1
-
23
-
-
84873374660
-
Characterization of tyrosinase inhibitors in the twigs of Cudrania tricuspidata and their structure-activity relationship study
-
Zehng ZP, Tan HY, Chen J, Wang M. Characterization of tyrosinase inhibitors in the twigs of Cudrania tricuspidata and their structure-activity relationship study. Fitoterapia 2013;84:242-7.
-
(2013)
Fitoterapia
, vol.84
, pp. 242-247
-
-
Zehng, Z.P.1
Tan, H.Y.2
Chen, J.3
Wang, M.4
-
25
-
-
0031777027
-
Topical hydroquinone in the treatment of some hyperpigmentary disorders
-
Amer M, Metwalli M. Topical hydroquinone in the treatment of some hyperpigmentary disorders. Int J Dermatol 1998;37:449-50.
-
(1998)
Int J Dermatol
, vol.37
, pp. 449-450
-
-
Amer, M.1
Metwalli, M.2
-
26
-
-
36649036991
-
Skin lightening preparations and the hydroquinone controversy
-
Draelos ZD. Skin lightening preparations and the hydroquinone controversy. Dermatol Ther 2007;20:308-13.
-
(2007)
Dermatol Ther
, vol.20
, pp. 308-313
-
-
Draelos, Z.D.1
-
27
-
-
0020144487
-
Ochronosis following skin bleaching with hydroquinone
-
Findlay GH. Ochronosis following skin bleaching with hydroquinone. J Am Acad Dermatol 1982;6:1092-3.
-
(1982)
J Am Acad Dermatol
, vol.6
, pp. 1092-1093
-
-
Findlay, G.H.1
-
28
-
-
0031689030
-
Human in vivo and in vitro hydroquinone topical bioavailability, metabolism, and disposition
-
Wester RC, Melendres J, Hui X, et al. Human in vivo and in vitro hydroquinone topical bioavailability, metabolism, and disposition. J Toxicol Environ Health A 1998;54:301-17.
-
(1998)
J Toxicol Environ Health A
, vol.54
, pp. 301-317
-
-
Wester, R.C.1
Melendres, J.2
Hui, X.3
-
29
-
-
84982160633
-
Cosmeceuticals for hyperpigmentation: What is available?
-
Sarkar R, Arora P, Garg KV. Cosmeceuticals for hyperpigmentation: what is available? J Cutan Aesthet Surg 2013;6:4-11.
-
(2013)
J Cutan Aesthet Surg
, vol.6
, pp. 4-11
-
-
Sarkar, R.1
Arora, P.2
Garg, K.V.3
-
30
-
-
0034827592
-
A single extraction step in the quantitative analysis of arbutin in bearberry (Arctostaphylos uva-ursi) leaves by high-performance liquid chromatography
-
Parejo I, Viladomat F, Bastida J, Codina C. A single extraction step in the quantitative analysis of arbutin in bearberry (Arctostaphylos uva-ursi) leaves by high-performance liquid chromatography. Phytochem Anal 2001;12:336-9.
-
(2001)
Phytochem Anal
, vol.12
, pp. 336-339
-
-
Parejo, I.1
Viladomat, F.2
Bastida, J.3
Codina, C.4
-
31
-
-
84872010432
-
Biotechnological production of arbutins (α- and β-arbutins), skin-lightening agents, and their derivatives
-
Seo DH, Jung JH, Lee JE, et al. Biotechnological production of arbutins (α- and β-arbutins), skin-lightening agents, and their derivatives. Appl Microbiol Biotechnol 2012;95:1417-25.
-
(2012)
Appl Microbiol Biotechnol
, vol.95
, pp. 1417-1425
-
-
Seo, D.H.1
Jung, J.H.2
Lee, J.E.3
-
32
-
-
0030004467
-
The combination of glycolic acid and hydroquinone or kojic acid for the treatment of melasma and related conditions
-
Garcia A, Fulton JE. The combination of glycolic acid and hydroquinone or kojic acid for the treatment of melasma and related conditions. Dermatol Surg 1996;22:443-7.
-
(1996)
Dermatol Surg
, vol.22
, pp. 443-447
-
-
Garcia, A.1
Fulton, J.E.2
-
33
-
-
0033143896
-
Aloesin and arbutin inhibit tyrosinase activity in a synergistic manner via a different action mechanism
-
Jin YH, Lee SJ, Chung MH, et al. Aloesin and arbutin inhibit tyrosinase activity in a synergistic manner via a different action mechanism. Arch Pharm Res 1999;22:232-6.
-
(1999)
Arch Pharm Res
, vol.22
, pp. 232-236
-
-
Jin, Y.H.1
Lee, S.J.2
Chung, M.H.3
-
34
-
-
22744448200
-
Deoxyarbutin: A novel reversible tyrosinase inhibitor with effective in vivo skin lightening potency
-
Boissy RE, Visscher M, DeLong MA. Deoxyarbutin: a novel reversible tyrosinase inhibitor with effective in vivo skin lightening potency. Exp Dermatol 2005;14:601-8.
-
(2005)
Exp Dermatol
, vol.14
, pp. 601-608
-
-
Boissy, R.E.1
Visscher, M.2
DeLong, M.A.3
-
35
-
-
56549128584
-
Mechanism of tyrosinase inhibition by deoxyArbutin and its second-generation derivatives
-
Chawla S, deLong MA, Visscher MO, et al. Mechanism of tyrosinase inhibition by deoxyArbutin and its second-generation derivatives. Br J Dermatol 2008;159:1267-74.
-
(2008)
Br J Dermatol
, vol.159
, pp. 1267-1274
-
-
Chawla, S.1
DeLong, M.A.2
Visscher, M.O.3
-
36
-
-
71949095673
-
Cosmetic therapy
-
Wolverton SE. ed. 2nd ed. Philadelphia (PA): Saunders
-
Draelos ZD. Cosmetic therapy. In:Wolverton SE. ed. Comprehensive dermatologic drug therapy. 2nd ed. Philadelphia (PA): Saunders; 2007:P761-74.
-
(2007)
Comprehensive Dermatologic Drug Therapy
, pp. 761-774
-
-
Draelos, Z.D.1
-
37
-
-
12944305800
-
The combination of 2% 4-hydroxyanisole (Mequinol) and 0.01% tretinoin is effective in improving the appearance of solar lentigines and related hyperpigmented lesions in two double-blind multicenter clinical studies
-
Fleischer AB, Schwartzel EH, Colby SI, Altman DJ. The combination of 2% 4-hydroxyanisole (Mequinol) and 0.01% tretinoin is effective in improving the appearance of solar lentigines and related hyperpigmented lesions in two double-blind multicenter clinical studies. J Am Acad Dermatol 2000;42:459-67.
-
(2000)
J Am Acad Dermatol
, vol.42
, pp. 459-467
-
-
Fleischer, A.B.1
Schwartzel, E.H.2
Colby, S.I.3
Altman, D.J.4
-
39
-
-
77950854525
-
Trends in utilization of the pharmacological potential of chalcones
-
Batovska DI, Todorova IT. Trends in utilization of the pharmacological potential of chalcones. Curr Clin Pharmacol 2010;5:1-29.
-
(2010)
Curr Clin Pharmacol
, vol.5
, pp. 1-29
-
-
Batovska, D.I.1
Todorova, I.T.2
-
41
-
-
26244463344
-
Isolation and identification of flavonoids in licorice and a study of their inhibitory effects on tyrosinase
-
Fu B, Li H, Wang X, et al. Isolation and identification of flavonoids in licorice and a study of their inhibitory effects on tyrosinase. J Agric Food Chem 2005;53:7408-14.
-
(2005)
J Agric Food Chem
, vol.53
, pp. 7408-7414
-
-
Fu, B.1
Li, H.2
Wang, X.3
-
42
-
-
2142754392
-
Tyrosinase inhibitory prenylated flavonoids from Sophora flavescens
-
Kim SJ, Son KH, Chang HW, et al. Tyrosinase inhibitory prenylated flavonoids from Sophora flavescens. Biol Pharm Bull 2003;26:1348-50.
-
(2003)
Biol Pharm Bull
, vol.26
, pp. 1348-1350
-
-
Kim, S.J.1
Son, K.H.2
Chang, H.W.3
-
43
-
-
38049049927
-
Inhibitory effects of kurarinol, kuraridinol, and trifolirhizin from Sophora flavescens on tyrosinase and melanin synthesis
-
Hyun SK, Lee WH, Jeong M, et al. Inhibitory effects of kurarinol, kuraridinol, and trifolirhizin from Sophora flavescens on tyrosinase and melanin synthesis. Biol Pharm Bull 2008;31:154-8.
-
(2008)
Biol Pharm Bull
, vol.31
, pp. 154-158
-
-
Hyun, S.K.1
Lee, W.H.2
Jeong, M.3
-
44
-
-
59949085461
-
Inhibitory effect of 2,4,2′,4′-tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone on tyrosinase activity and melanin biosynthesis
-
Zhang X, Hu X, Hou A, Wang H. Inhibitory effect of 2,4,2′,4′-tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone on tyrosinase activity and melanin biosynthesis. Biol Pharm Bull 2009;32:86-90.
-
(2009)
Biol Pharm Bull
, vol.32
, pp. 86-90
-
-
Zhang, X.1
Hu, X.2
Hou, A.3
Wang, H.4
-
45
-
-
3042522850
-
Chalcones as potent tyrosinase inhibitors: The effect of hydroxyl positions and numbers
-
Nerya O, Musa R, Khatib S, et al. Chalcones as potent tyrosinase inhibitors: the effect of hydroxyl positions and numbers. Phytochemistry 2004;65:1389-95.
-
(2004)
Phytochemistry
, vol.65
, pp. 1389-1395
-
-
Nerya, O.1
Musa, R.2
Khatib, S.3
-
46
-
-
10444280081
-
Chalcones as potent tyrosinase inhibitors: The importance of a 2,4-substituted resorcinol moiety
-
Khatib S, Nerya O, Musa R, et al. Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety. Bioorg Med Chem 2005;13:433-41.
-
(2005)
Bioorg Med Chem
, vol.13
, pp. 433-441
-
-
Khatib, S.1
Nerya, O.2
Musa, R.3
-
47
-
-
33846933805
-
Synthesis and evaluation of 2′,4′,6′-trihydroxychalcones as a new class of tyrosinase inhibitors
-
Jun N, Hong G, Jun K. Synthesis and evaluation of 2′,4′,6′-trihydroxychalcones as a new class of tyrosinase inhibitors. Bioorg Med Chem 2007;15:2396-402.
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 2396-2402
-
-
Jun, N.1
Hong, G.2
Jun, K.3
-
48
-
-
84870172291
-
Tyrosinase inhibitors from the Wood of Atrocarpus heterophyllus
-
Nguyen NT, Nguyen MH, Nguyen HX, et al. Tyrosinase inhibitors from the Wood of Atrocarpus heterophyllus. J Nat Prod 2012;75:1951-5.
-
(2012)
J Nat Prod
, vol.75
, pp. 1951-1955
-
-
Nguyen, N.T.1
Nguyen, M.H.2
Nguyen, H.X.3
-
49
-
-
33645851331
-
N-Benzylbenzamides: A new class of potent tyrosinase inhibitors
-
Cho SJ, Roh JS, Sun WS, et al. N-Benzylbenzamides: a new class of potent tyrosinase inhibitors. Bioorg Med Chem Lett 2006;16:2682-4.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 2682-2684
-
-
Cho, S.J.1
Roh, J.S.2
Sun, W.S.3
-
50
-
-
84862813681
-
Adamantyl N-benzylbenzamide: New series of depigmentation agents with tyrosinase inhibitory activity
-
Baek HS, Hong YD, Lee CS, et al. Adamantyl N-benzylbenzamide: new series of depigmentation agents with tyrosinase inhibitory activity. Bioorg Med Chem Lett 2012;22:2110-13.
-
(2012)
Bioorg Med Chem Lett
, vol.22
, pp. 2110-2113
-
-
Baek, H.S.1
Hong, Y.D.2
Lee, C.S.3
-
51
-
-
84862823921
-
Synthesis and structure-activity relationships and effects of phenylpropanoid amides of octopamine and dopamine on tyrosinase inhibition and antioxidation
-
Wu Z, Zheng L, Li Y, et al. Synthesis and structure-activity relationships and effects of phenylpropanoid amides of octopamine and dopamine on tyrosinase inhibition and antioxidation. Food Chem 2012;134:1128-31.
-
(2012)
Food Chem
, vol.134
, pp. 1128-1131
-
-
Wu, Z.1
Zheng, L.2
Li, Y.3
-
52
-
-
79551477736
-
Benzyl benzoates: New phlorizin analogs as mushroom tyrosinase inhibitors
-
Fang Y, Chen Y, Feng G, Ma L. Benzyl benzoates: new phlorizin analogs as mushroom tyrosinase inhibitors. Bioorg Med Chem 2011;19:1167-71.
-
(2011)
Bioorg Med Chem
, vol.19
, pp. 1167-1171
-
-
Fang, Y.1
Chen, Y.2
Feng, G.3
Ma, L.4
-
53
-
-
84866239644
-
Synthesis, biological evaluation, and molecular docking of N-{3-[3-(9-methyl-9H-carbazol-3-yl)-acryloyl]-phenyl}-benzamide/amide derivatives as xanthine oxidase and tyrosinase inhibitors
-
Bandgar BP, Adsul LK, Chavan HV, et al. Synthesis, biological evaluation, and molecular docking of N-{3-[3-(9-methyl-9H-carbazol-3-yl)-acryloyl]-phenyl}-benzamide/amide derivatives as xanthine oxidase and tyrosinase inhibitors. Bioorg Med Chem 2012;20:5649-57.
-
(2012)
Bioorg Med Chem
, vol.20
, pp. 5649-5657
-
-
Bandgar, B.P.1
Adsul, L.K.2
Chavan, H.V.3
-
54
-
-
38749149509
-
Stilbenes with tyrosinase inhibitory activity
-
Likhitwitayawuid K. Stilbenes with tyrosinase inhibitory activity. Curr Sci India 2008;94:44-53.
-
(2008)
Curr Sci India
, vol.94
, pp. 44-53
-
-
Likhitwitayawuid, K.1
-
55
-
-
6944250259
-
Role of resveratrol in prevention and therapy of cancer: Preclinical and clinical studies
-
Aggarwal BB, Bhardwaj A, Aggarwal RS, et al. Role of resveratrol in prevention and therapy of cancer: preclinical and clinical studies. Anticancer Res 2004;24:2783-840.
-
(2004)
Anticancer Res
, vol.24
, pp. 2783-2840
-
-
Aggarwal, B.B.1
Bhardwaj, A.2
Aggarwal, R.S.3
-
56
-
-
0032562101
-
Oxyresveratrol as the potent inhibitor on dopa oxidase activity of mushroom tyrosinase
-
Shin NH, Ryu SY, Choi EJ, et al. Oxyresveratrol as the potent inhibitor on dopa oxidase activity of mushroom tyrosinase. Biochem Biophys Res Commun 1998;243:801-3.
-
(1998)
Biochem Biophys Res Commun
, vol.243
, pp. 801-803
-
-
Shin, N.H.1
Ryu, S.Y.2
Choi, E.J.3
-
57
-
-
0031806944
-
The inhibitory components from Artocarpus incisus on melanin biosynthesis
-
Shimizu K, Kondo R, Sakai K, et al. The inhibitory components from Artocarpus incisus on melanin biosynthesis. Planta Med 1998;64:408-12.
-
(1998)
Planta Med
, vol.64
, pp. 408-412
-
-
Shimizu, K.1
Kondo, R.2
Sakai, K.3
-
58
-
-
0035195770
-
A new dimeric stilbene with tyrosinase inhibitory activity from Artocarpus gomezianus
-
Likhitwitayawuid K, Sritularak B. A new dimeric stilbene with tyrosinase inhibitory activity from Artocarpus gomezianus. J Nat Prod 2001;64:1457-9.
-
(2001)
J Nat Prod
, vol.64
, pp. 1457-1459
-
-
Likhitwitayawuid, K.1
Sritularak, B.2
-
59
-
-
2442541170
-
Inhibitory effects of resveratrol derivatives from Dipterocarpaceae plants on tyrosinase activity
-
Ohguchi K, Tanaka T, Ito T, et al. Inhibitory effects of resveratrol derivatives from Dipterocarpaceae plants on tyrosinase activity. Biosci Biotechnol Biochem 2003;67:1587-9.
-
(2003)
Biosci Biotechnol Biochem
, vol.67
, pp. 1587-1589
-
-
Ohguchi, K.1
Tanaka, T.2
Ito, T.3
-
60
-
-
33748766664
-
Chemical transformations of oxyresveratrol (trans-2,4,3′,5′-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent
-
Likhitwitayawuid K, Sornsute A, Sritularak B, Ploypradith P. Chemical transformations of oxyresveratrol (trans-2,4,3′,5′-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent. Bioorg Med Chem Lett 2006;16:5650-3.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 5650-5653
-
-
Likhitwitayawuid, K.1
Sornsute, A.2
Sritularak, B.3
Ploypradith, P.4
-
61
-
-
0038782508
-
Effects of hydroxystilbene derivatives on tyrosinase activity
-
Ohguchi K, Tanaka K, Kido T, et al. Effects of hydroxystilbene derivatives on tyrosinase activity. Biochem Biophys Res Commun 2003;307:861-3.
-
(2003)
Biochem Biophys Res Commun
, vol.307
, pp. 861-863
-
-
Ohguchi, K.1
Tanaka, K.2
Kido, T.3
-
62
-
-
0036549924
-
(4-Methoxy-benzylidene)-(3-methoxy-phenyl)-amine, a nitrogen analog of stilbene as a potent inhibitor of melanin production
-
Choi SY, Kim S, Kim H, et al. (4-Methoxy-benzylidene)-(3-methoxy-phenyl)-amine, a nitrogen analog of stilbene as a potent inhibitor of melanin production. Chem Pharm Bull 2002;50:450-2.
-
(2002)
Chem Pharm Bull
, vol.50
, pp. 450-452
-
-
Choi, S.Y.1
Kim, S.2
Kim, H.3
-
63
-
-
33846070701
-
Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase
-
Song S, Lee H, Jin Y, et al. Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase. Bioorg Med Chem Lett 2007;17:461-4.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 461-464
-
-
Song, S.1
Lee, H.2
Jin, Y.3
-
64
-
-
84873534737
-
A Novel Synthesized Tyrosinase Inhibitor: (E)-2-((2,4-Dihydroxyphenyl)diazenyl)phenyl 4-methylbenzenesulfonate as an azo-Resveratrol Analog
-
Bae SJ, Ha YM, Kim JA, et al. A Novel Synthesized Tyrosinase Inhibitor: (E)-2-((2,4-Dihydroxyphenyl)diazenyl)phenyl 4-methylbenzenesulfonate as an azo-Resveratrol Analog. Biosci Biotechnol Biochem 2013;77:65-72.
-
(2013)
Biosci Biotechnol Biochem
, vol.77
, pp. 65-72
-
-
Bae, S.J.1
Ha, Y.M.2
Kim, J.A.3
-
65
-
-
84870058327
-
Design, synthesis, and evaluation of (E)-N-substituted benzylidene-aniline derivatives as tyrosinase inhibitors
-
Bae SJ, Ha YM, Park YJ, et al. Design, synthesis, and evaluation of (E)-N-substituted benzylidene-aniline derivatives as tyrosinase inhibitors. Eur J Med Chem 2012;57:383-90.
-
(2012)
Eur J Med Chem
, vol.57
, pp. 383-390
-
-
Bae, S.J.1
Ha, Y.M.2
Park, Y.J.3
-
66
-
-
84870242089
-
Synthesis of novel azo-resveratrol, azo-oxyresveratrol and their derivatives as potent tyrosinase inhibitors
-
Song YM, Ha YM, Kim JA, et al. Synthesis of novel azo-resveratrol, azo-oxyresveratrol and their derivatives as potent tyrosinase inhibitors. Bioorg Med Chem Lett 2012;22:7451-5.
-
(2012)
Bioorg Med Chem Lett
, vol.22
, pp. 7451-7455
-
-
Song, Y.M.1
Ha, Y.M.2
Kim, J.A.3
-
67
-
-
84879472132
-
Stab F, 4-n-butylresorcinol, a highly effective tyrosinase inhibitor of the topical treatment of hyperpigmentation
-
Kolbe L, Mann T, Gerwat W, et al. Stab F, 4-n-butylresorcinol, a highly effective tyrosinase inhibitor of the topical treatment of hyperpigmentation. JEADV 2013;27:19-23.
-
(2013)
JEADV
, vol.27
, pp. 19-23
-
-
Kolbe, L.1
Mann, T.2
Gerwat, W.3
-
69
-
-
33751426673
-
From miso, sake and shoyu to cosmetics: A century of science for kojic acid
-
Bentley R. From miso, sake and shoyu to cosmetics: a century of science for kojic acid. Nat Prod Rep 2006;23:1046-62.
-
(2006)
Nat Prod Rep
, vol.23
, pp. 1046-1062
-
-
Bentley, R.1
-
70
-
-
0000389791
-
Effect of kojic acid on the oxidation of N-acetyldopamine by mushroom tyrosinase
-
Kahn V, Ben-Shalom N, Zakin V. Effect of kojic acid on the oxidation of N-acetyldopamine by mushroom tyrosinase. J Agric Food Chem 1997;45:4460-5.
-
(1997)
J Agric Food Chem
, vol.45
, pp. 4460-4465
-
-
Kahn, V.1
Ben-Shalom, N.2
Zakin, V.3
-
71
-
-
84871836075
-
Depigmenting effect of kojic acid esters in hyperpigmented B16F1 melanoma cells
-
Lajis AF, Hamid M, Ariff AB. Depigmenting effect of kojic acid esters in hyperpigmented B16F1 melanoma cells. J Biomed Biotech 2012;2012:952452.
-
(2012)
J Biomed Biotech
, vol.2012
-
-
Lajis, A.F.1
Hamid, M.2
Ariff, A.B.3
-
72
-
-
0006519411
-
Synthesis and radical polymerization of styrene derivative bearing Kojic acid moieties
-
Tomita I, Mitsuhashi K, Endo T. Synthesis and radical polymerization of styrene derivative bearing Kojic acid moieties. J Polym Sci A1 1996;34:271-6.
-
(1996)
J Polym Sci A1
, vol.34
, pp. 271-276
-
-
Tomita, I.1
Mitsuhashi, K.2
Endo, T.3
-
73
-
-
0028246253
-
Synthesis and iron (III) binding properties of 3-hydroxypyrid-4-ones derived from Kojic acid
-
Molenda JJ, Basinger MA, Hanusa TP, Jones MM. Synthesis and iron (III) binding properties of 3-hydroxypyrid-4-ones derived from Kojic acid. J Inorg Biochem 1994;55:131-46.
-
(1994)
J Inorg Biochem
, vol.55
, pp. 131-146
-
-
Molenda, J.J.1
Basinger, M.A.2
Hanusa, T.P.3
Jones, M.M.4
-
74
-
-
2342586185
-
Solid-phase synthesis of kojic acid-tripeptides and their tyrosinase inhibitory activity, storage stability, and toxicity
-
Kim H, Choi J, Cho JK, et al. Solid-phase synthesis of kojic acid-tripeptides and their tyrosinase inhibitory activity, storage stability, and toxicity. Bioorg Med Chem Lett 2004;14:2843-6.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 2843-2846
-
-
Kim, H.1
Choi, J.2
Cho, J.K.3
-
75
-
-
84873369425
-
Synthesis and tyrosinase inhibitory properties of some novel derivatives of kojic acid
-
Saghaie L, Pourfarzam M, Fassihi A, Sartippour B. Synthesis and tyrosinase inhibitory properties of some novel derivatives of kojic acid. Res Pharm Sci. 2013;8:233-42.
-
(2013)
Res Pharm Sci.
, vol.8
, pp. 233-242
-
-
Saghaie, L.1
Pourfarzam, M.2
Fassihi, A.3
Sartippour, B.4
-
76
-
-
50449108769
-
Synthesis of new antimelanogenic compounds containing two molecules of kojic acid
-
Rho HS, Baek HS, Ahn SM, et al. Synthesis of new antimelanogenic compounds containing two molecules of kojic acid. Bull Kor Chem Soc 2008;29:1569-71.
-
(2008)
Bull Kor Chem Soc
, vol.29
, pp. 1569-1571
-
-
Rho, H.S.1
Baek, H.S.2
Ahn, S.M.3
-
77
-
-
69949111761
-
Kojic acid-amino acid coujugates as tyrosinase inhibitors
-
Noh JM, Kwak SY, Seo HS, et al. Kojic acid-amino acid coujugates as tyrosinase inhibitors. Bioorg Med Chem Lett 2009;19:5586-9.
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 5586-5589
-
-
Noh, J.M.1
Kwak, S.Y.2
Seo, H.S.3
-
78
-
-
84880001515
-
Design and synthesis of hydroxypyridinone-L-phenylalanine conjugates as potential tyrosinase inhibitors
-
Li DF, Hu PP, Liu MS, et al. Design and synthesis of hydroxypyridinone-L-phenylalanine conjugates as potential tyrosinase inhibitors. J Agric Food Chem 2013;61:6597-603.
-
(2013)
J Agric Food Chem
, vol.61
, pp. 6597-6603
-
-
Li, D.F.1
Hu, P.P.2
Liu, M.S.3
-
79
-
-
0036783677
-
Modulation of melanogenesis by aloesin: A competitive inhibitor of tyrosinase
-
Jones K, Hughes J, Hong M, et al. Modulation of melanogenesis by aloesin: a competitive inhibitor of tyrosinase. Pigment Cell Res 2002;15:335-40.
-
(2002)
Pigment Cell Res
, vol.15
, pp. 335-340
-
-
Jones, K.1
Hughes, J.2
Hong, M.3
-
80
-
-
0036414688
-
Aloesin inhibits hyperpigmentation induced by UV radiation
-
Choi S, Lee SK, Kim JE, et al. Aloesin inhibits hyperpigmentation induced by UV radiation. Clin Exp Dermatol 2002;27:513-15.
-
(2002)
Clin Exp Dermatol
, vol.27
, pp. 513-515
-
-
Choi, S.1
Lee, S.K.2
Kim, J.E.3
-
82
-
-
0042423512
-
Mushroom tyrosinase inhibitory activity of esculetin isolated from seeds of Euphorbia lathyris L
-
Masamoto Y, Ando H, Murata Y, et al. Mushroom tyrosinase inhibitory activity of esculetin isolated from seeds of Euphorbia lathyris L. Biosci Biotechnol Biochem 2003;67:631-4.
-
(2003)
Biosci Biotechnol Biochem
, vol.67
, pp. 631-634
-
-
Masamoto, Y.1
Ando, H.2
Murata, Y.3
-
83
-
-
16644381707
-
Tyrosinase-inhibitory furanocoumarin from Angelica dahurica
-
Piao XL, Baek SH, Park MK, Park JH. Tyrosinase-inhibitory furanocoumarin from Angelica dahurica. Biol Pharm Bull 2004;27:1144-6.
-
(2004)
Biol Pharm Bull
, vol.27
, pp. 1144-1146
-
-
Piao, X.L.1
Baek, S.H.2
Park, M.K.3
Park, J.H.4
-
84
-
-
17444421649
-
Tyrosinase inhibitors from Rhododendron collettianum and their structure-activity relationship (SAR) studies
-
Ahmad VU, Ullah F, Hussain J, et al. Tyrosinase inhibitors from Rhododendron collettianum and their structure-activity relationship (SAR) studies. Chem Pharm Bull 2004;52:1458-61.
-
(2004)
Chem Pharm Bull
, vol.52
, pp. 1458-1461
-
-
Ahmad, V.U.1
Ullah, F.2
Hussain, J.3
-
85
-
-
34047271603
-
p-Coumaric acid, a common dietary phenol, inhibits platelet activity in vitro and in vivo
-
Luceri C, Giannini L, Lodovici M, et al. p-Coumaric acid, a common dietary phenol, inhibits platelet activity in vitro and in vivo. Br J Nutr 2007;97:458-63.
-
(2007)
Br J Nutr
, vol.97
, pp. 458-463
-
-
Luceri, C.1
Giannini, L.2
Lodovici, M.3
-
86
-
-
84866361670
-
Synthesis of small molecule-peptide conjugates as potential whitening agents
-
Lee HS, Shin KH, Ryu GS, et al. Synthesis of small molecule-peptide conjugates as potential whitening agents. Bull Korean Chem Soc 2012;33:3004-8.
-
(2012)
Bull Korean Chem Soc
, vol.33
, pp. 3004-3008
-
-
Lee, H.S.1
Shin, K.H.2
Ryu, G.S.3
-
87
-
-
0014939358
-
Physicochemical and kinetic properties of mushroom tyrosinase
-
Duckworth HW, Coleman JE. Physicochemical and kinetic properties of mushroom tyrosinase. J Biol Chem 1970;245:1613-25.
-
(1970)
J Biol Chem
, vol.245
, pp. 1613-1625
-
-
Duckworth, H.W.1
Coleman, J.E.2
-
88
-
-
84937572308
-
Kinetic of mushroom tyrosinase inhibition by benzaldehyde derivarives
-
Maghsoudi S, Adibi H, Hanzeh M, et al. Kinetic of mushroom tyrosinase inhibition by benzaldehyde derivarives. J Rep Pharm Sci 2013;2:156-64.
-
(2013)
J Rep Pharm Sci
, vol.2
, pp. 156-164
-
-
Maghsoudi, S.1
Adibi, H.2
Hanzeh, M.3
-
89
-
-
0141993651
-
Tyrosinase inhibition kinetics of anisic acid
-
Kubo I, Chen QX, Nihei K, et al. Tyrosinase inhibition kinetics of anisic acid. Z Naturforsch C 2003;58:713-18.
-
(2003)
Z Naturforsch C
, vol.58
, pp. 713-718
-
-
Kubo, I.1
Chen, Q.X.2
Nihei, K.3
-
90
-
-
25444509223
-
Effects of mushroom tyrosinase on anisaldehyde
-
Ha TJ, Tamura S, Kubo I. Effects of mushroom tyrosinase on anisaldehyde. J Agric Food Chem 2005;53:7024-8.
-
(2005)
J Agric Food Chem
, vol.53
, pp. 7024-7028
-
-
Ha, T.J.1
Tamura, S.2
Kubo, I.3
-
91
-
-
17444389708
-
Inhibitory effects of cinnamic acid and its derivatives on the diphenolase activity of mushroom (Agaricus bisporus) tyrosinase
-
Shi Y, Chen QX, Wang Q, et al. Inhibitory effects of cinnamic acid and its derivatives on the diphenolase activity of mushroom (Agaricus bisporus) tyrosinase. Food Chem 2005;92:707-12.
-
(2005)
Food Chem
, vol.92
, pp. 707-712
-
-
Shi, Y.1
Chen, Q.X.2
Wang, Q.3
-
92
-
-
0037070326
-
Tyrosinase inhibitors of Pulsatilla cernua root-derived materials
-
Lee HS. Tyrosinase inhibitors of Pulsatilla cernua root-derived materials. J Agric Food Chem 2002;50:1400-3.
-
(2002)
J Agric Food Chem
, vol.50
, pp. 1400-1403
-
-
Lee, H.S.1
-
94
-
-
0001397165
-
Tyrosinase inhibitors from cumin
-
Kubo I, Kinst-Hori I. Tyrosinase inhibitors from cumin. J Agric Food Chem 1998;46:5338-41.
-
(1998)
J Agric Food Chem
, vol.46
, pp. 5338-5341
-
-
Kubo, I.1
Kinst-Hori, I.2
-
95
-
-
0028176278
-
Inhibitor binding to the binuclear active site of tyrosinase: Temperature, pH and solvent deuterium isotope effects
-
Conrad JS, Dawso SR, Hubbard ER, et al. Inhibitor binding to the binuclear active site of tyrosinase: temperature, pH and solvent deuterium isotope effects. Biochemistry 1994;33:5739-44.
-
(1994)
Biochemistry
, vol.33
, pp. 5739-5744
-
-
Conrad, J.S.1
Dawso, S.R.2
Hubbard, E.R.3
-
97
-
-
33846530804
-
Identification and kinetic study of tyrosinase inhibitors found in sake lees
-
Jeon HJ, Noda M, Maruyama M, et al. Identification and kinetic study of tyrosinase inhibitors found in sake lees. J Agric Food Chem 2006;54:9827-33.
-
(2006)
J Agric Food Chem
, vol.54
, pp. 9827-9833
-
-
Jeon, H.J.1
Noda, M.2
Maruyama, M.3
-
98
-
-
39149123777
-
Tyrosinase inhibitors and sesquiterpene diglycosides from Guioa villosa
-
Magid AA, Voutguenne-Nazabadioko L, Bontemps G, et al. Tyrosinase inhibitors and sesquiterpene diglycosides from Guioa villosa. Planta Med 2008;74:55-60.
-
(2008)
Planta Med
, vol.74
, pp. 55-60
-
-
Magid, A.A.1
Voutguenne-Nazabadioko, L.2
Bontemps, G.3
-
99
-
-
38949129695
-
Identification of geranic acid, a tyrosinase inhibitor in lemongrass (Cymbopogon citratus)
-
Masuda T, Odaka Y, Ogawa N, et al. Identification of geranic acid, a tyrosinase inhibitor in lemongrass (Cymbopogon citratus). J Agric Food Chem 2008;56:597-601.
-
(2008)
J Agric Food Chem
, vol.56
, pp. 597-601
-
-
Masuda, T.1
Odaka, Y.2
Ogawa, N.3
-
101
-
-
30344474608
-
Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure-activity relationship
-
Khan MT, Khan SB, Ather A. Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure-activity relationship. Bioorg Med Chem 2006;14:938-43.
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 938-943
-
-
Khan, M.T.1
Khan, S.B.2
Ather, A.3
-
102
-
-
36549027860
-
Tyrosinase inhibitory pentacyclic triterpenes and analgesic and spasmolytic activities of methanol extracts of Rhododendron collettianum
-
Ullah F, Hussain H, Hussain J, et al. Tyrosinase inhibitory pentacyclic triterpenes and analgesic and spasmolytic activities of methanol extracts of Rhododendron collettianum. Phytother Res 2007;21:1076-81.
-
(2007)
Phytother Res
, vol.21
, pp. 1076-1081
-
-
Ullah, F.1
Hussain, H.2
Hussain, J.3
-
103
-
-
42949111608
-
Anthraquinones from Polygonum cuspidatum as tyrosinase inhibitors for dermal use
-
Leu YL, Hwang TL, Hu JW, Fang JY. Anthraquinones from Polygonum cuspidatum as tyrosinase inhibitors for dermal use. Phytother Res 2008;22:552-6.
-
(2008)
Phytother Res
, vol.22
, pp. 552-556
-
-
Leu, Y.L.1
Hwang, T.L.2
Hu, J.W.3
Fang, J.Y.4
-
104
-
-
34248356669
-
Tyrosinase inhibitory and antileishmanial constituents from the rhizomes of Paris polyphylla
-
Devkota KP, Khan MT, Ranjit R, et al. Tyrosinase inhibitory and antileishmanial constituents from the rhizomes of Paris polyphylla. Nat Prod Res 2007;21:321-7.
-
(2007)
Nat Prod Res
, vol.21
, pp. 321-327
-
-
Devkota, K.P.1
Khan, M.T.2
Ranjit, R.3
-
105
-
-
32844456498
-
Tyrosinase inhibitory lignans from the methanol extract of the roots of Vitex negundo Linn, and their structure-activity relationship
-
Azhar-Ul-Haq, Malik A, Khan MT, et al. Tyrosinase inhibitory lignans from the methanol extract of the roots of Vitex negundo Linn, and their structure-activity relationship. Phytomedicine 2006;13:255-60.
-
(2006)
Phytomedicine
, vol.13
, pp. 255-260
-
-
Azhar-Ul-Haq1
Malik, A.2
Khan, M.T.3
-
106
-
-
77955332765
-
(-)-N-Formylanonaine from Michelia alba as a human tyrosinase inhibitor and antioxidant
-
Wang HM, Chen CY, Chen CY, et al. (-)-N-Formylanonaine from Michelia alba as a human tyrosinase inhibitor and antioxidant. Bioorg Med Chem 2010;18:5241-7.
-
(2010)
Bioorg Med Chem
, vol.18
, pp. 5241-5247
-
-
Wang, H.M.1
Chen, C.Y.2
Chen, C.Y.3
-
107
-
-
84862003254
-
New lignan glucosides with tyrosinase inhibitory activities from exocarp of Castanea henryi
-
Wu B, Zhang X, Wu X. New lignan glucosides with tyrosinase inhibitory activities from exocarp of Castanea henryi. Carbohydr Res. 2012;355:45-9.
-
(2012)
Carbohydr Res.
, vol.355
, pp. 45-49
-
-
Wu, B.1
Zhang, X.2
Wu, X.3
-
108
-
-
84874093371
-
Melanogenesis-inhibitory activity of aromatic glycosides from the stem bark of Acer buergerianum
-
Akihisa T, Orido M, Akazawa H, et al. Melanogenesis-inhibitory activity of aromatic glycosides from the stem bark of Acer buergerianum. Chem Biodivers 2013;10:167-75.
-
(2013)
Chem Biodivers
, vol.10
, pp. 167-175
-
-
Akihisa, T.1
Orido, M.2
Akazawa, H.3
-
109
-
-
84861490028
-
Antioxidant, antimicrobial and tyrosinase inhibitory activities of xanthones isolated from Artocarpus obtusus F.M. Jarrett
-
Hashim NM, Rahmani M, Ee GC, et al. Antioxidant, antimicrobial and tyrosinase inhibitory activities of xanthones isolated from Artocarpus obtusus F.M. Jarrett. Molecules 2012;17:6071-82.
-
(2012)
Molecules
, vol.17
, pp. 6071-6082
-
-
Hashim, N.M.1
Rahmani, M.2
Ee, G.C.3
-
110
-
-
44649198318
-
Analogues of N-hydroxy-N′-phenylthiourea and N-hydroxy-N′-phenylurea as inhibitors of tyrosinase and melanin formation
-
Criton M, Le Mellay-Hamon V. Analogues of N-hydroxy-N′-phenylthiourea and N-hydroxy-N′-phenylurea as inhibitors of tyrosinase and melanin formation. Bioorg Med Chem Lett 2008;18:3607-10.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 3607-3610
-
-
Criton, M.1
Le Mellay-Hamon, V.2
-
111
-
-
0034997903
-
Synthesis of N-substituted N-nitrosohydroxylamines as inhibitors of mushroom tyrosinase
-
Shiino M, Watanabe Y, Umezawa K. Synthesis of N-substituted N-nitrosohydroxylamines as inhibitors of mushroom tyrosinase. Bioorg Med Chem 2001;9:1233-40.
-
(2001)
Bioorg Med Chem
, vol.9
, pp. 1233-1240
-
-
Shiino, M.1
Watanabe, Y.2
Umezawa, K.3
-
112
-
-
21044437985
-
Synthesis of methyl ether analogues of sildenafil (Viagra) possessing tyrosinase inhibitory potential
-
Khan KM, Maharvi GM, Perveen S, et al. Synthesis of methyl ether analogues of sildenafil (Viagra) possessing tyrosinase inhibitory potential. Chem Biodivers 2005;2:470-6.
-
(2005)
Chem Biodivers
, vol.2
, pp. 470-476
-
-
Khan, K.M.1
Maharvi, G.M.2
Perveen, S.3
-
113
-
-
17444374605
-
Structure-activity relationships of tyrosinase inhibitory combinatorial library of 2,5-disubstituted-1,3,4-oxadiazole analogues
-
Khan MT, Choudhary MI, Khan KM, et al. Structure-activity relationships of tyrosinase inhibitory combinatorial library of 2,5-disubstituted-1,3,4-oxadiazole analogues. Bioorg Med Chem 2005;13:3385-95.
-
(2005)
Bioorg Med Chem
, vol.13
, pp. 3385-3395
-
-
Khan, M.T.1
Choudhary, M.I.2
Khan, K.M.3
-
114
-
-
33746031797
-
Oxazolones: New tyrosinase inhibitors; synthesis and their structure-activity relationships
-
Khan KM, Mughal UR, Khan MT, et al. Oxazolones: new tyrosinase inhibitors; synthesis and their structure-activity relationships. Bioorg Med Chem 2006;14:6027-33.
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 6027-6033
-
-
Khan, K.M.1
Mughal, U.R.2
Khan, M.T.3
-
115
-
-
28844498529
-
Tetraketones: A new class of tyrosinase inhibitors
-
Khan KM, Maharvi GM, Khan MT, et al. Tetraketones: a new class of tyrosinase inhibitors. Bioorg Med Chem 2006;14:344-51.
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 344-351
-
-
Khan, K.M.1
Maharvi, G.M.2
Khan, M.T.3
-
116
-
-
19444376688
-
4,4′-Dihydroxybiphenyl as a new potent tyrosinase inhibitor
-
Kim YJ, No JK, Lee JH, Chung HY. 4,4′-Dihydroxybiphenyl as a new potent tyrosinase inhibitor. Biol Pharm Bull 2005;28:323-7.
-
(2005)
Biol Pharm Bull
, vol.28
, pp. 323-327
-
-
Kim, Y.J.1
No, J.K.2
Lee, J.H.3
Chung, H.Y.4
-
117
-
-
24944433492
-
Potent inhibitory effects of N-aryl S-alkylthiocarbamate derivatives on the dopa oxidase activity of mushroom tyrosinase
-
Lee KH, Koketsu M, Choi SY, et al. Potent inhibitory effects of N-aryl S-alkylthiocarbamate derivatives on the dopa oxidase activity of mushroom tyrosinase. Chem Pharm Bull 2005;53:747-9.
-
(2005)
Chem Pharm Bull
, vol.53
, pp. 747-749
-
-
Lee, K.H.1
Koketsu, M.2
Choi, S.Y.3
-
118
-
-
77954214886
-
Synthesis and biological activity of oxadiazole and triazolothiadiazole derivatives as tyrosinase inhibitors
-
Lam KW, Syahida A, Ul-Haq Z, et al. Synthesis and biological activity of oxadiazole and triazolothiadiazole derivatives as tyrosinase inhibitors. Bioorg Med Chem Lett 2010;20:3755-9.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 3755-3759
-
-
Lam, K.W.1
Syahida, A.2
Ul-Haq, Z.3
-
119
-
-
84855853000
-
Design, synthesis and biological evaluation of 2-(substituted phenyl)thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors
-
Ha YM, Park YJ, Lee JY, et al. Design, synthesis and biological evaluation of 2-(substituted phenyl)thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors. Biochimie 2012;94:533-40.
-
(2012)
Biochimie
, vol.94
, pp. 533-540
-
-
Ha, Y.M.1
Park, Y.J.2
Lee, J.Y.3
-
120
-
-
84863116655
-
Synthesis and antityrosinase mechanism of benzaldehyde thiosemicarbazones: Novel tyrosinase inhibitors
-
Chen LH, Hu YH, Song W, et al. Synthesis and antityrosinase mechanism of benzaldehyde thiosemicarbazones: novel tyrosinase inhibitors. J Agric Food Chem 2012;60:1542-7.
-
(2012)
J Agric Food Chem
, vol.60
, pp. 1542-1547
-
-
Chen, L.H.1
Hu, Y.H.2
Song, W.3
-
121
-
-
77958064836
-
Structural characteristics of thiosemicarbazones as inhibitors of melanogenesis
-
Lee KC, Thanigaimalai P, Sharma VK, et al. Structural characteristics of thiosemicarbazones as inhibitors of melanogenesis. Bioorg Med Chem Lett 2010;20:6794-6.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 6794-6796
-
-
Lee, K.C.1
Thanigaimalai, P.2
Sharma, V.K.3
-
122
-
-
80052928807
-
Refinement of arylthiosemicarbazone pharmacophore in inhibition of mushroom tyrosinase
-
Yi W, Dubois C, Yahiaoui S, et al. Refinement of arylthiosemicarbazone pharmacophore in inhibition of mushroom tyrosinase. Eur J Med Chem 2011;46:4330-5.
-
(2011)
Eur J Med Chem
, vol.46
, pp. 4330-4335
-
-
Yi, W.1
Dubois, C.2
Yahiaoui, S.3
-
123
-
-
77951707743
-
Rational design and synthesis of 4-O-substituted phenylmethylenethiosemicarbazones as novel tyrosinase inhibitors
-
Yi W, Cao R, Chen Z, et al. Rational design and synthesis of 4-O-substituted phenylmethylenethiosemicarbazones as novel tyrosinase inhibitors. Chem Pharm Bull 2010;58:752-4.
-
(2010)
Chem Pharm Bull
, vol.58
, pp. 752-754
-
-
Yi, W.1
Cao, R.2
Chen, Z.3
-
124
-
-
73549117206
-
Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors
-
Yi W, Cao R, Peng W, et al. Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors. Eur J Med Chem 2010;45:639-46.
-
(2010)
Eur J Med Chem
, vol.45
, pp. 639-646
-
-
Yi, W.1
Cao, R.2
Peng, W.3
-
125
-
-
77956907512
-
Synthesis and biological evaluation of a novel series of bis-salicylaldehydes as mushroom tyrosinase inhibitors
-
Delogu G, Podda G, Corda M, et al. Synthesis and biological evaluation of a novel series of bis-salicylaldehydes as mushroom tyrosinase inhibitors. Bioorg Med Chem Lett 2010;20:6138-40.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 6138-6140
-
-
Delogu, G.1
Podda, G.2
Corda, M.3
-
126
-
-
79959275179
-
Synthesis and antityrosinase activities of alkyl 3,4-dihydroxybenzoates
-
Pan ZZ, Li HL, Yu XJ, et al. Synthesis and antityrosinase activities of alkyl 3,4-dihydroxybenzoates. J Agric Food Chem 2011;59:6645-9.
-
(2011)
J Agric Food Chem
, vol.59
, pp. 6645-6649
-
-
Pan, Z.Z.1
Li, H.L.2
Yu, X.J.3
-
127
-
-
81255205266
-
Evaluation of new chalcone derivatives as polyphenol oxidase inhibitors
-
Sonmez F, Sevmezler S, Atahan A, et al. Evaluation of new chalcone derivatives as polyphenol oxidase inhibitors. Bioorg Med Chem Lett 2011;21:7479-82.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 7479-7482
-
-
Sonmez, F.1
Sevmezler, S.2
Atahan, A.3
-
128
-
-
79956100956
-
New halogenated phenylcoumarins as tyrosinase inhibitors
-
Matos MJ, Santana L, Uriarte E, et al. New halogenated phenylcoumarins as tyrosinase inhibitors. Bioorg Med Chem Lett 2011;21:3342-5.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 3342-3345
-
-
Matos, M.J.1
Santana, L.2
Uriarte, E.3
-
129
-
-
84855265970
-
Antioxidation and tyrosinase inhibition of polyphenolic curcumin analogs
-
Du ZY, Jiang YF, Tang ZK, et al. Antioxidation and tyrosinase inhibition of polyphenolic curcumin analogs. Biosci Biotechnol Biochem 2011;75:2351-8.
-
(2011)
Biosci Biotechnol Biochem
, vol.75
, pp. 2351-2358
-
-
Du, Z.Y.1
Jiang, Y.F.2
Tang, Z.K.3
-
130
-
-
84856220890
-
Curcumin-like diarylpentanoid analogues as melanogenesis inhibitors
-
Hosoya T, Nakata A, Yamasaki F, et al. Curcumin-like diarylpentanoid analogues as melanogenesis inhibitors. J Nat Med 2012;66:166-76.
-
(2012)
J Nat Med
, vol.66
, pp. 166-176
-
-
Hosoya, T.1
Nakata, A.2
Yamasaki, F.3
-
131
-
-
79952282871
-
Synthesis and evaluation of bibenzyl glycosides as potent tyrosinase inhibitors
-
Tajima R, Oozeki H, Muraoka S, et al. Synthesis and evaluation of bibenzyl glycosides as potent tyrosinase inhibitors. Eur J Med Chem 2011;46:1374-81.
-
(2011)
Eur J Med Chem
, vol.46
, pp. 1374-1381
-
-
Tajima, R.1
Oozeki, H.2
Muraoka, S.3
-
132
-
-
79957528363
-
Analogs of 5-(substituted benzylidene)hydantoin as inhibitors of tyrosinase and melanin formation
-
Ha YM, Kim JA, Park YJ, et al. Analogs of 5-(substituted benzylidene)hydantoin as inhibitors of tyrosinase and melanin formation. Biochim Biophys Acta 2011;1810:612-19.
-
(2011)
Biochim Biophys Acta
, vol.1810
, pp. 612-619
-
-
Ha, Y.M.1
Kim, J.A.2
Park, Y.J.3
-
133
-
-
79953290155
-
Evaluation of dihydropyrimidin-(2H)-one analogues and rhodanine derivatives as tyrosinase inhibitors
-
Liu J, Wu F, Chen L, et al. Evaluation of dihydropyrimidin-(2H)-one analogues and rhodanine derivatives as tyrosinase inhibitors. Bioorg Med Chem Lett 2011;21:2376-9.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 2376-2379
-
-
Liu, J.1
Wu, F.2
Chen, L.3
-
134
-
-
67651172776
-
Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities
-
Yan Q, Cao R, Yi W, et al. Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities. Eur J Med Chem 2009;44:4235-43.
-
(2009)
Eur J Med Chem
, vol.44
, pp. 4235-4243
-
-
Yan, Q.1
Cao, R.2
Yi, W.3
-
135
-
-
84863384399
-
Characterization of a novel tyrosinase inhibitor, (2RS,4R)-2-(2,4-dihydroxylphenyl) thiazolidine-4-carboxylic acid (MHY384)
-
Han YK, Park YJ, Ha YM, et al. Characterization of a novel tyrosinase inhibitor, (2RS,4R)-2-(2,4-dihydroxylphenyl) thiazolidine-4-carboxylic acid (MHY384). Biochim Biophys Acta 2012;1820:542-9.
-
(2012)
Biochim Biophys Acta
, vol.1820
, pp. 542-549
-
-
Han, Y.K.1
Park, Y.J.2
Ha, Y.M.3
-
136
-
-
84879415446
-
De novo tyrosinase inhibitor: 4-(6,7-dihydro-5H-indeno[5,6-d]thiazol-2-yl)benzene-1,3-diol(MHY1556)
-
Park JW, Ha YM, Moon KM, Kim SR. De novo tyrosinase inhibitor: 4-(6,7-dihydro-5H-indeno[5,6-d]thiazol-2-yl)benzene-1,3-diol(MHY1556). Bioorg Med Chem Lett 2013;23:4172-6.
-
(2013)
Bioorg Med Chem Lett
, vol.23
, pp. 4172-4176
-
-
Park, J.W.1
Ha, Y.M.2
Moon, K.M.3
Kim, S.R.4
-
138
-
-
77956343202
-
Design and synthesis of biphenyl derivatives as mushroom tyrosinase inhibitors
-
Bao K, Dai Y, Zhu ZB, et al. Design and synthesis of biphenyl derivatives as mushroom tyrosinase inhibitors. Bioorg Med Chem 2010;18:6708-14.
-
(2010)
Bioorg Med Chem
, vol.18
, pp. 6708-6714
-
-
Bao, K.1
Dai, Y.2
Zhu, Z.B.3
-
139
-
-
84875214535
-
Synthesis of novel azo compounds containing 5(4H)-oxazolone ring as potent tyrosinase inhibitors
-
Hamidian H, Tagizadeh R, Fozooni S, et al. Synthesis of novel azo compounds containing 5(4H)-oxazolone ring as potent tyrosinase inhibitors. Bioorg Med Chem 2013;21:2088-92.
-
(2013)
Bioorg Med Chem
, vol.21
, pp. 2088-2092
-
-
Hamidian, H.1
Tagizadeh, R.2
Fozooni, S.3
-
140
-
-
84875229179
-
Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors
-
Zhou Z, Zhuo J, Yan S, Ma L. Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors. Bioorg Med Chem 2013;21:2156-62.
-
(2013)
Bioorg Med Chem
, vol.21
, pp. 2156-2162
-
-
Zhou, Z.1
Zhuo, J.2
Yan, S.3
Ma, L.4
-
141
-
-
77954214886
-
Synthesis and biological activity of oxadiazole and triazolothiadiazole derivatives as tyrosinase inhibitor
-
Lam KW, Syahida A, Ul-Haq Z, et al. Synthesis and biological activity of oxadiazole and triazolothiadiazole derivatives as tyrosinase inhibitor. Bioorg Med Chem Lett 2010;20:3755-9.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 3755-3759
-
-
Lam, K.W.1
Syahida, A.2
Ul-Haq, Z.3
-
142
-
-
84867855807
-
Discovery of small molecules that inhibit melanogenesis via regulation of tyrosinase expression
-
Song J, Lee HE, Kim YJ, et al. Discovery of small molecules that inhibit melanogenesis via regulation of tyrosinase expression. Bioorg Med Chem Lett 2012;22:6943-6.
-
(2012)
Bioorg Med Chem Lett
, vol.22
, pp. 6943-6946
-
-
Song, J.1
Lee, H.E.2
Kim, Y.J.3
-
143
-
-
33748347520
-
Melanogenesis inhibitory and free radical scavenging activities of diarylheptanoids and other phenolic compounds from the bark of Acer nikoense
-
Akazawa H, Akihisa T, Taguchi Y, et al. Melanogenesis inhibitory and free radical scavenging activities of diarylheptanoids and other phenolic compounds from the bark of Acer nikoense. Biol Pharm Bull 2006;29:1970-2.
-
(2006)
Biol Pharm Bull
, vol.29
, pp. 1970-1972
-
-
Akazawa, H.1
Akihisa, T.2
Taguchi, Y.3
-
144
-
-
84908012884
-
Tyrosinase-catalyzed oxidation of rhododendrol produces 2-methylchromane-6,7-dione, the putative ultimate toxic metabolite: Implications for melanocyte toxicity
-
Ito S, Ojika M, Yamashita T, Wakamatsu K. Tyrosinase-catalyzed oxidation of rhododendrol produces 2-methylchromane-6,7-dione, the putative ultimate toxic metabolite: implications for melanocyte toxicity. Pigment Cell Melanoma Res 2014;27:744-53.
-
(2014)
Pigment Cell Melanoma Res
, vol.27
, pp. 744-753
-
-
Ito, S.1
Ojika, M.2
Yamashita, T.3
Wakamatsu, K.4
-
145
-
-
0021345926
-
N-acetyl-p-benzoquinone imine: A cytochrome P-450-mediated oxidation product of acetaminophen
-
Dahlin DC, Miwa GT, Lu AY, Nelson SD. N-acetyl-p-benzoquinone imine: a cytochrome P-450-mediated oxidation product of acetaminophen. Proc Natl Acad Sci USA 1984;81:1327-31.
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 1327-1331
-
-
Dahlin, D.C.1
Miwa, G.T.2
Lu, A.Y.3
Nelson, S.D.4
-
146
-
-
84911412519
-
Human tyrosinase is able to oxidize both enantiomers of rhododendrol
-
Ito S, Gerwat W, Kolbe L, et al. Human tyrosinase is able to oxidize both enantiomers of rhododendrol. Pigment Cell Melanoma Res 2014;27:1149-53.
-
(2014)
Pigment Cell Melanoma Res
, vol.27
, pp. 1149-1153
-
-
Ito, S.1
Gerwat, W.2
Kolbe, L.3
|