Target Validation Information | |||||
---|---|---|---|---|---|
Target ID | T97035 | ||||
Target Name | Tyrosine oxidase | ||||
Target Type | Successful |
||||
Drug Potency against Target | 3-hydroxyphenethyl 3,4,5-trihydroxybenzoate | Drug Info | IC50 = 15210 nM | [528984] | |
4',4-Dihydroxychalcone | Drug Info | Ki = 2900 nM | [530713] | ||
Broussonin C | Drug Info | Ki = 290 nM | [529832] | ||
1-hydroxy-3-(4-(trifluoromethyl)phenyl)urea | Drug Info | IC50 = 4300 nM | [529488] | ||
ASKENDOSIDE B | Drug Info | IC50 = 13950 nM | [527850] | ||
2,4,3',5'-tetrahydroxybibenzyl | Drug Info | Ki = 5600 nM | [528382] | ||
OXYRESVERATROL | Drug Info | IC50 = 12700 nM | [528382] | ||
1-Cyclopentylidenethiosemicarbazide | Drug Info | IC50 = 170 nM | [529513] | ||
Kazinol C | Drug Info | Ki = 11200 nM | [529832] | ||
1-hydroxy-3-phenylurea | Drug Info | IC50 = 290 nM | [529488] | ||
4'-(p-Toluenesulfonamide)-4-hydroxychalcone | Drug Info | Ki = 12600 nM | [530713] | ||
4'-(4-Nitrobenzensulfonamide)-4-hydroxychalcone | Drug Info | Ki = 11400 nM | [530713] | ||
1-Ethylidenethiosemicarbazide | Drug Info | IC50 = 230 nM | [529513] | ||
1-(4-bromophenyl)-3-hydroxyurea | Drug Info | IC50 = 2700 nM | [529488] | ||
1-(4-Methylpent-3-en-2-ylidene)thiosemicarbazide | Drug Info | IC50 = 11500 nM | [529513] | ||
1-(Butan-2-ylidene)thiosemicarbazide | Drug Info | IC50 = 280 nM | [529513] | ||
PHENYLTHIOUREA | Drug Info | IC50 = 1800 nM | [529488] | ||
1-(But-2-enylidene)thiosemicarbazide | Drug Info | IC50 = 1000 nM | [529513] | ||
5-(pyridin-4-yl)-1,3,4-oxadiazole-2(3H)-thione | Drug Info | Ki = 14200 nM | [530900] | ||
5-benzhydryl-1,3,4-thiadiazole-2(3H)-thione | Drug Info | Ki = 5200 nM | [530900] | ||
4-(6-hydroxynaphthalen-2-yl)benzene-1,3-diol | Drug Info | IC50 = 34 nM | [528496] | ||
7-(3,5-dihydroxyphenyl)naphthalene-1,3-diol | Drug Info | IC50 = 490 nM | [528496] | ||
1-(2,5-Dimethyl-1H-pyrrol-1-yl)thiourea | Drug Info | IC50 = 850 nM | [529513] | ||
2,2'-bi(1,3,4-thiadiazole)-5,5'(4H,4'H)-dithione | Drug Info | Ki = 2900 nM | [530900] | ||
1-Cyclohexylidenethiosemicarbazide | Drug Info | IC50 = 950 nM | [529513] | ||
1-(1-(pyrazin-2-yl)ethylidene)thiosemicarbazide | Drug Info | IC50 = 880 nM | [529360] | ||
1-Propylidenethiosemicarbazide | Drug Info | IC50 = 200 nM | [529513] | ||
4'-Amino-4-hydroxychalcone | Drug Info | Ki = 3900 nM | [530713] | ||
1-(Propan-2-ylidene)thiosemicarbazide | Drug Info | IC50 = 86 nM | [529513] | ||
1-(1-(4-fluorophenyl)ethylidene)thiosemicarbazide | Drug Info | IC50 = 170 nM | [529360] | ||
5-phenyl-1,3,4-thiadiazole-2(3H)-thione | Drug Info | Ki = 1310 nM | [530900] | ||
5-(3-hydroxyphenyl)-1,3,4-oxadiazole-2(3H)-thione | Drug Info | Ki = 18500 nM | [530900] | ||
3hydroxy-1-methyl-1-phenylurea | Drug Info | IC50 = 16000 nM | [529488] | ||
2-(ethylthiomethyl)-5-hydroxy-4H-pyran-4-one | Drug Info | IC50 = 2600 nM | [531202] | ||
2-(cyclohexylthiomethyl)-5-hydroxy-4H-pyran-4-one | Drug Info | IC50 = 87 nM | [531202] | ||
6-(3-Hydroxy-phenyl)-naphthalen-2-ol | Drug Info | IC50 = 6400 nM | [528496] | ||
2-(heptylthiomethyl)-5-hydroxy-4H-pyran-4-one | Drug Info | IC50 = 2650 nM | [531202] | ||
2-(hexylthiomethyl)-5-hydroxy-4H-pyran-4-one | Drug Info | IC50 = 190 nM | [531202] | ||
5-benzhydryl-1,3,4-oxadiazole-2(3H)-thione | Drug Info | Ki = 6760 nM | [530900] | ||
1-(1-p-tolylethylidene)thiosemicarbazide | Drug Info | IC50 = 270 nM | [529360] | ||
1-(1-(thiophen-2-yl)ethylidene)thiosemicarbazide | Drug Info | IC50 = 140 nM | [529360] | ||
5-phenyl-1,3,4-oxadiazole-2(3H)-thione | Drug Info | Ki = 6470 nM | [530900] | ||
1-(3-Phenylallylidene)thiosemicarbazide | Drug Info | IC50 = 2700 nM | [529513] | ||
1-(1,4-diacetylphenyl)dithiosemicarbazide | Drug Info | IC50 = 150 nM | [529360] | ||
4'-(4-Aminobenzensulfonamide)-4-hydroxychalcone | Drug Info | Ki = 16700 nM | [530713] | ||
5-(pyridin-4-yl)-1,3,4-thiadiazole-2(3H)-thione | Drug Info | Ki = 2470 nM | [530900] | ||
5,5'-methylenebis(1,3,4-oxadiazole-2(3H)-thione) | Drug Info | Ki = 4420 nM | [530900] | ||
5-cyclohexyl-1,3,4-oxadiazole-2(3H)-thione | Drug Info | Ki = 4940 nM | [530900] | ||
5-hydroxy-2-(pentylthiomethyl)-4H-pyran-4-one | Drug Info | IC50 = 97 nM | [531202] | ||
HINOKITIOL | Drug Info | Ki = 60 nM | [531217] | ||
ETHISTERONE | Drug Info | IC50 = 2610 nM | [528526] | ||
1-(3-phenoxypropyl)-4-(piperidin-1-yl)piperidine | Drug Info | IC50 = 19520 nM | [528953] | ||
N-butylresorcinol | Drug Info | IC50 = 150 nM | [529942] | ||
4-adamantyl resorcinol | Drug Info | IC50 = 900 nM | [529942] | ||
N-(2,4-dihydroxybenzyl)-3,4,5-trihydroxybenzamide | Drug Info | IC50 = 17000 nM | [528063] | ||
KAZINOL S | Drug Info | Ki = 15600 nM | [529832] | ||
1-(1-phenylethylidene)thiosemicarbazide | Drug Info | IC50 = 340 nM | [529360] | ||
1-(1-(pyridin-3-yl)ethylidene)thiosemicarbazide | Drug Info | IC50 = 820 nM | [529360] | ||
SRI-224 | Drug Info | IC50 = 110 nM | [530419] | ||
3,4-dihydroxybenzaldehyde-O-ethyloxime | Drug Info | IC50 = 300 nM | [530419] | ||
TROPOLONE | Drug Info | IC50 = 400 nM | [530419] | ||
1-(1-(4-bromophenyl)ethylidene)thiosemicarbazide | Drug Info | IC50 = 520 nM | [529360] | ||
5-(6-hydroxy-2-naphthyl)-1,2,3-benzenetriol | Drug Info | IC50 = 2950 nM | [531026] | ||
1-(3-Methylbutylidene)thiosemicarbazide | Drug Info | IC50 = 620 nM | [529513] | ||
SODIUM ZINC DIHYDROLIPOYLHISTIDINATE | Drug Info | IC50 = 1300 nM | [528613] | ||
1-(4-(benzyloxy)phenyl)-3-hydroxyurea | Drug Info | IC50 = 6300 nM | [529488] | ||
1-hydroxy-3-(4-nitrophenyl)urea | Drug Info | IC50 = 2600 nM | [529488] | ||
4'-(Benzensulfonamide)-4-hydroxychalcone | Drug Info | Ki = 13300 nM | [530713] | ||
4'-(4-Fluorobenzensulfonamide)-4-hydroxychalcone | Drug Info | Ki = 14900 nM | [530713] | ||
5,5'-methylenebis(1,3,4-thiadiazole-2(3H)-thione) | Drug Info | Ki = 490 nM | [530900] | ||
5-(6-hydroxynaphthalen-2-yl)benzene-1,3-diol | Drug Info | IC50 = 16520 nM | [528496] | ||
4-hexyl resorcinol | Drug Info | IC50 = 980 nM | [529847] | ||
KOJIC ACID | Drug Info | IC50 = 12000 nM | [531245] | ||
2-hydroxy-3-isopropyl-2,4,6-cycloheptatrien-1-one | Drug Info | Ki = 3300 nM | [531217] | ||
N-(2,4-dihydroxybenzyl)-3,4-dihydroxybenzamide | Drug Info | IC50 = 11000 nM | [528063] | ||
N-(2,4-dihydroxybenzyl)-3,5-dihydroxybenzamide | Drug Info | Ki = 1300 nM | [528063] | ||
5-(4-hydroxyphenyl)-1,3,4-oxadiazole-2(3H)-thione | Drug Info | Ki = 1770 nM | [530900] | ||
1'-(4-Methyl-benzyl)-[1,4']bipiperidinyl | Drug Info | IC50 = 1720 nM | [528953] | ||
1-(3-Oxocyclohexylidene)thiosemicarbazide | Drug Info | IC50 = 15100 nM | [529513] | ||
2-hydroxy-5-isopropyl-2,4,6-cycloheptatrien-1-one | Drug Info | Ki = 20 nM | [531217] | ||
5-benzyl-1,3,4-oxadiazole-2(3H)-thione | Drug Info | Ki = 3670 nM | [530900] | ||
2-(butylthiomethyl)-5-hydroxy-4H-pyran-4-one | Drug Info | IC50 = 1480 nM | [531202] | ||
2,2',4,4'-tetrahydroxychalcone | Drug Info | IC50 = 5000 nM | [528649] | ||
2,2',4,4'-tetrahydroxy-6'-methoxychalcone | Drug Info | IC50 = 3100 nM | [528649] | ||
7,3',4'-trihydroxyisoflavone | Drug Info | IC50 = 5230 nM | [530587] | ||
7,8,4'-trihydroxyisoflavone | Drug Info | IC50 = 11210 nM | [530587] | ||
4-hydroxyphenethyl 3,4,5-trihydroxybenzoate | Drug Info | IC50 = 4930 nM | [528984] | ||
2-hydroxyphenethyl 3,4,5-trihydroxybenzoate | Drug Info | IC50 = 14500 nM | [528984] | ||
4,4'-(ethane-1,2-diyl)dibenzene-1,3-diol | Drug Info | IC50 = 370 nM | [529682] | ||
5-hydroxy-2-(propylthiomethyl)-4H-pyran-4-one | Drug Info | IC50 = 1930 nM | [531202] | ||
Kazinol F | Drug Info | Ki = 770 nM | [529832] | ||
References | |||||
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Ref 528382 | Bioorg Med Chem Lett. 2006 Nov 1;16(21):5650-3. Epub 2006 Aug 17.Chemical transformations of oxyresveratrol (trans-2,4,3',5'-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent. | ||||
Ref 528382 | Bioorg Med Chem Lett. 2006 Nov 1;16(21):5650-3. Epub 2006 Aug 17.Chemical transformations of oxyresveratrol (trans-2,4,3',5'-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
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Ref 529488 | Bioorg Med Chem Lett. 2008 Jun 15;18(12):3607-10. Epub 2008 May 4.Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. | ||||
Ref 530713 | Eur J Med Chem. 2010 May;45(5):2010-7. Epub 2010 Jan 28.Evaluation of anti-pigmentary effect of synthetic sulfonylamino chalcone. | ||||
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Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 529488 | Bioorg Med Chem Lett. 2008 Jun 15;18(12):3607-10. Epub 2008 May 4.Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 529488 | Bioorg Med Chem Lett. 2008 Jun 15;18(12):3607-10. Epub 2008 May 4.Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 528496 | Bioorg Med Chem Lett. 2007 Jan 15;17(2):461-4. Epub 2006 Oct 12.Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase. | ||||
Ref 528496 | Bioorg Med Chem Lett. 2007 Jan 15;17(2):461-4. Epub 2006 Oct 12.Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 530713 | Eur J Med Chem. 2010 May;45(5):2010-7. Epub 2010 Jan 28.Evaluation of anti-pigmentary effect of synthetic sulfonylamino chalcone. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 529488 | Bioorg Med Chem Lett. 2008 Jun 15;18(12):3607-10. Epub 2008 May 4.Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. | ||||
Ref 531202 | Bioorg Med Chem Lett. 2010 Nov 15;20(22):6569-71. Epub 2010 Sep 21.Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties. | ||||
Ref 531202 | Bioorg Med Chem Lett. 2010 Nov 15;20(22):6569-71. Epub 2010 Sep 21.Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties. | ||||
Ref 528496 | Bioorg Med Chem Lett. 2007 Jan 15;17(2):461-4. Epub 2006 Oct 12.Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase. | ||||
Ref 531202 | Bioorg Med Chem Lett. 2010 Nov 15;20(22):6569-71. Epub 2010 Sep 21.Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties. | ||||
Ref 531202 | Bioorg Med Chem Lett. 2010 Nov 15;20(22):6569-71. Epub 2010 Sep 21.Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 530713 | Eur J Med Chem. 2010 May;45(5):2010-7. Epub 2010 Jan 28.Evaluation of anti-pigmentary effect of synthetic sulfonylamino chalcone. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 531202 | Bioorg Med Chem Lett. 2010 Nov 15;20(22):6569-71. Epub 2010 Sep 21.Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties. | ||||
Ref 531217 | Bioorg Med Chem. 2010 Nov 15;18(22):8112-8. Epub 2010 Oct 12.Structural insights into the hot spot amino acid residues of mushroom tyrosinase for the bindings of thujaplicins. | ||||
Ref 528526 | Bioorg Med Chem. 2007 Feb 1;15(3):1483-503. Epub 2006 Nov 2.TOMOCOMD-CARDD descriptors-based virtual screening of tyrosinase inhibitors: evaluation of different classification model combinations using bond-based linear indices. | ||||
Ref 528953 | Eur J Med Chem. 2007 Nov-Dec;42(11-12):1370-81. Epub 2007 Feb 23.Dragon method for finding novel tyrosinase inhibitors: Biosilico identification and experimental in vitro assays. | ||||
Ref 529942 | Bioorg Med Chem Lett. 2009 Mar 1;19(5):1532-3. Epub 2009 Jan 1.Studies on depigmenting activities of dihydroxyl benzamide derivatives containing adamantane moiety. | ||||
Ref 529942 | Bioorg Med Chem Lett. 2009 Mar 1;19(5):1532-3. Epub 2009 Jan 1.Studies on depigmenting activities of dihydroxyl benzamide derivatives containing adamantane moiety. | ||||
Ref 528063 | Bioorg Med Chem Lett. 2006 May 15;16(10):2682-4. Epub 2006 Mar 2.N-Benzylbenzamides: a new class of potent tyrosinase inhibitors. | ||||
Ref 529832 | Bioorg Med Chem. 2009 Jan 1;17(1):35-41. Epub 2008 Nov 18.Tyrosinase inhibitory effects of 1,3-diphenylpropanes from Broussonetia kazinoki. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 530419 | Bioorg Med Chem Lett. 2009 Nov 1;19(21):6157-60. Epub 2009 Sep 10.Discovery of 4-functionalized phenyl-O-beta-D-glycosides as a new class of mushroom tyrosinase inhibitors. | ||||
Ref 530419 | Bioorg Med Chem Lett. 2009 Nov 1;19(21):6157-60. Epub 2009 Sep 10.Discovery of 4-functionalized phenyl-O-beta-D-glycosides as a new class of mushroom tyrosinase inhibitors. | ||||
Ref 530419 | Bioorg Med Chem Lett. 2009 Nov 1;19(21):6157-60. Epub 2009 Sep 10.Discovery of 4-functionalized phenyl-O-beta-D-glycosides as a new class of mushroom tyrosinase inhibitors. | ||||
Ref 529360 | Bioorg Med Chem. 2008 Feb 1;16(3):1096-102.1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. | ||||
Ref 531026 | Bioorg Med Chem Lett. 2010 Aug 15;20(16):4882-4. Epub 2010 Jun 19.A newly synthesized, potent tyrosinase inhibitor: 5-(6-hydroxy-2-naphthyl)-1,2,3-benzenetriol. | ||||
Ref 529513 | Eur J Med Chem. 2009 Apr;44(4):1773-8. Epub 2008 Apr 27.A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. | ||||
Ref 528613 | Bioorg Med Chem. 2007 Mar 1;15(5):1967-75. Epub 2006 Dec 31.Modulating effects of a novel skin-lightening agent, alpha-lipoic acid derivative, on melanin production by the formation of DOPA conjugate products. | ||||
Ref 529488 | Bioorg Med Chem Lett. 2008 Jun 15;18(12):3607-10. Epub 2008 May 4.Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. | ||||
Ref 529488 | Bioorg Med Chem Lett. 2008 Jun 15;18(12):3607-10. Epub 2008 May 4.Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. | ||||
Ref 530713 | Eur J Med Chem. 2010 May;45(5):2010-7. Epub 2010 Jan 28.Evaluation of anti-pigmentary effect of synthetic sulfonylamino chalcone. | ||||
Ref 530713 | Eur J Med Chem. 2010 May;45(5):2010-7. Epub 2010 Jan 28.Evaluation of anti-pigmentary effect of synthetic sulfonylamino chalcone. | ||||
Ref 530900 | Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. Epub 2010 Apr 13.New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site. | ||||
Ref 528496 | Bioorg Med Chem Lett. 2007 Jan 15;17(2):461-4. Epub 2006 Oct 12.Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase. | ||||
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