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Volumn 2013, Issue , 2013, Pages

Synthesis of novel compounds as new potent tyrosinase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

1 [2 [4 [[[1 [[(4 METHYL 2 SULFANYLPHENYL)SULFANYL]CARBONYL] 2 [4 (TRIFLUOROMETHOXY)PHENYL] 1 ETHENYL]AMINO]CARBONYL]PHENYL] 1 DIAZENYL] 2 NAPHTHYL ACETATE; 1 [2 [4 [[[2 (4 FLUOROPHENYL) 1 [[(4 METHYL 2 SULFANYLPHENYL)SULFANYL] CARBONYL] 1 ETHENYL]AMINO]CARBONYL]PHENYL] 1 DIAZENYL] 2 NAPHTHYL ACETATE; 2 [2 [4 [[[1 [[(4 METHYL 2 SULFANYLPHENYL) SULFANYL]CARBONYL] 2 [4 (TRIFLUOROMETHOXY)PHENYL] 1 ETHENYL]AMINO]CARBONYL]PHENYL] 1 DIAZENYL] 1 NAPHTHYL ACETATE; 2 [2 [4 [[[2 (4 FLUOROPHENYL) 1 [[(4 METHYL 2 SULFANYLPHENYL) SULFANYL CARBONYL] 1 ETHENYL] AMINO]CARBONYL]PHENYL] 1 DIAZENYL] 1 NAPHTHYL ACETATE; 4 METHYL 2 SULFANYLPHENYL 2 [[4 [2 [4 (DIMETHYLAMINO)PHENYL] 1 DIAZENYL]BENZOYL]AMINO] 3 (4 FLUOROPHENYL) 2 PROPENETHIOATE; 4 METHYL 2 SULFANYLPHENYL 2 [[4 [2 [4 (DIMETHYLAMINO)PHENYL] 1 DIAZENYL]BENZOYL]AMINO] 3 [4 (TRIFLUOROMETHOXY)PHENYL] 2 PROPENETHIOATE; AZO COMPOUND; KOJIC ACID; MELANIN; MONOPHENOL MONOOXYGENASE; OXYGENASE INHIBITOR; TYROSINASE INHIBITOR; UNCLASSIFIED DRUG; ENZYME INHIBITOR;

EID: 84887418491     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2013/207181     Document Type: Article
Times cited : (11)

References (20)
  • 1
    • 0037070326 scopus 로고    scopus 로고
    • Tyrosinase inhibitors of Pulsatilla cernua root-derived materials
    • DOI 10.1021/jf011230f
    • Lee H.-S., Tyrosinase inhibitors of Pulsatilla cernua root-derived materials. Journal of Agricultural and Food Chemistry 2002 50 6 1400 1403 2-s2.0-0037070326 10.1021/jf011230f (Pubitemid 34233199)
    • (2002) Journal of Agricultural and Food Chemistry , vol.50 , Issue.6 , pp. 1400-1403
    • Lee, H.-S.1
  • 2
    • 0042423512 scopus 로고    scopus 로고
    • Mushroom tyrosinase inhibitory activity of esculetin isolated from seeds of Euphorbia lathyris L
    • Masamoto Y., Ando H., Murata Y., Shimoishi Y., Tada M., Takahata K., Mushroom tyrosinase inhibitory activity of esculetin isolated from seeds of Euphorbia lathyris L. Bioscience, Biotechnology and Biochemistry 2003 67 3 631 634 2-s2.0-0042423512 (Pubitemid 39251963)
    • (2003) Bioscience, Biotechnology and Biochemistry , vol.67 , Issue.3 , pp. 631-634
    • Masamoto, Y.1    Ando, H.2    Murata, Y.3    Shimoishi, Y.4    Tada, M.5    Takahata, K.6
  • 3
    • 84866239644 scopus 로고    scopus 로고
    • 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 P. B., Adsul L. K., Chavan H. V., Shringare S. N., Korbad B. L., Jalde S. S., Lonikar S. V., Nile S. H., Shirfule A. L., 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. Bioorganic and Medicinal Chemistry 2012 20 18 5649 5657
    • (2012) Bioorganic and Medicinal Chemistry , vol.20 , Issue.18 , pp. 5649-5657
    • Bandgar, P.B.1    Adsul, L.K.2    Chavan, H.V.3    Shringare, S.N.4    Korbad, B.L.5    Jalde, S.S.6    Lonikar, S.V.7    Nile, S.H.8    Shirfule, A.L.9
  • 5
    • 77953130632 scopus 로고    scopus 로고
    • New potent inhibitors of tyrosinase: Novel clues to binding of 1,3,4-thiadiazole-2(3 H)-thiones, 1,3,4-oxadiazole-2(3 H)-thiones, 4-amino-1,2,4-triazole-5(4 H)-thiones, and substituted hydrazides to the dicopper active site
    • 2-s2.0-77953130632 10.1016/j.bmc.2010.04.021
    • Ghani U., Ullah N., New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3 H)-thiones, 1,3,4-oxadiazole-2(3 H)-thiones, 4-amino-1,2,4-triazole-5(4 H)-thiones, and substituted hydrazides to the dicopper active site. Bioorganic and Medicinal Chemistry 2010 18 11 4042 4048 2-s2.0-77953130632 10.1016/j.bmc.2010.04.021
    • (2010) Bioorganic and Medicinal Chemistry , vol.18 , Issue.11 , pp. 4042-4048
    • Ghani, U.1    Ullah, N.2
  • 6
    • 0041430876 scopus 로고    scopus 로고
    • Heterocyclo-substituted sulfa drugs: Part XII. Mercapto-S-azo- benzothiazol dyes and their metal complexes
    • DOI 10.1080/10426500307893
    • Awad I. M. A., Osman A. H., Aly A. A. M., Heterocyclo-substituted sulfa drugs: part XII. Mercapto-S-azo-benzothiazol dyes and their metal complexes. Phosphorus, Sulfur and Silicon and the Related Elements 2003 178 6 1339 1352 2-s2.0-0041430876 10.1080/10426500307893 (Pubitemid 37028482)
    • (2003) Phosphorus, Sulfur and Silicon and the Related Elements , vol.178 , Issue.6 , pp. 1339-1352
    • Awad, I.M.A.1    Osman, A.H.2    Aly, A.A.M.3
  • 7
    • 42749085981 scopus 로고    scopus 로고
    • Enhancement of solubility via esterification: Synthesis and characterization of octakis (ester)-substituted phthalocyanines
    • 2-s2.0-42749085981 10.1016/j.dyepig.2008.02.001
    • Akkurt B., Hamuryudan E., Enhancement of solubility via esterification: synthesis and characterization of octakis (ester)-substituted phthalocyanines. Dyes and Pigments 2008 79 2 153 158 2-s2.0-42749085981 10.1016/j.dyepig.2008.02. 001
    • (2008) Dyes and Pigments , vol.79 , Issue.2 , pp. 153-158
    • Akkurt, B.1    Hamuryudan, E.2
  • 8
    • 80053630396 scopus 로고    scopus 로고
    • Synthesis and spectroelectrochemistry of new phthalocyanines with ester functionalities
    • 2-s2.0-80053630396 10.1016/j.dyepig.2011.07.015
    • Sevim A. M., Arkan S., Koca A., Gül A., Synthesis and spectroelectrochemistry of new phthalocyanines with ester functionalities. Dyes and Pigments 2012 92 3 1114 1121 2-s2.0-80053630396 10.1016/j.dyepig.2011.07.015
    • (2012) Dyes and Pigments , vol.92 , Issue.3 , pp. 1114-1121
    • Sevim, A.M.1    Arkan, S.2    Koca, A.3    Gül, A.4
  • 9
    • 58349096501 scopus 로고    scopus 로고
    • New azo ligands containing azomethine groups in the pyridazine-based chain: Aynthesis and characterization
    • 2-s2.0-58349096501 10.1016/j.dyepig.2008.07.019
    • Khanmohammadi H., Darvishpour M., New azo ligands containing azomethine groups in the pyridazine-based chain: aynthesis and characterization. Dyes and Pigments 2009 81 3 167 173 2-s2.0-58349096501 10.1016/j.dyepig.2008.07.019
    • (2009) Dyes and Pigments , vol.81 , Issue.3 , pp. 167-173
    • Khanmohammadi, H.1    Darvishpour, M.2
  • 10
    • 78751494663 scopus 로고    scopus 로고
    • Synthesis of a new series of 2-(2-hydroxynaphthylazo)aryltellurium compounds
    • 2-s2.0-78751494663 10.1080/10426507.2010.485154
    • Al-Rubaie A. Z., Al-Fregi A. A., Al-Jadaan S. A. S., Synthesis of a new series of 2-(2-hydroxynaphthylazo)aryltellurium compounds. Phosphorus, Sulfur and Silicon and the Related Elements 2011 186 1 115 124 2-s2.0-78751494663 10.1080/10426507.2010.485154
    • (2011) Phosphorus, Sulfur and Silicon and the Related Elements , vol.186 , Issue.1 , pp. 115-124
    • Al-Rubaie, A.Z.1    Al-Fregi, A.A.2    Al-Jadaan, S.A.S.3
  • 11
    • 22644443877 scopus 로고    scopus 로고
    • Thienylpyrrole azo dyes: Synthesis, solvatochromic and electrochemical properties
    • DOI 10.1016/j.tet.2005.06.039, PII S0040402005010343
    • Raposo M. M. M., Sousa A. M. R. C., Fonseca A. M. C., Kirsch G., Thienylpyrrole azo dyes: synthesis, solvatochromic and electrochemical properties. Tetrahedron 2005 61 34 8249 8256 2-s2.0-22644443877 10.1016/j.tet.2005.06.039 (Pubitemid 41024853)
    • (2005) Tetrahedron , vol.61 , Issue.34 , pp. 8249-8256
    • Raposo, M.M.M.1    Sousa, A.M.R.C.2    Fonseca, A.M.C.3    Kirsch, G.4
  • 12
    • 30944453877 scopus 로고    scopus 로고
    • Synthesis of 4-amino-1H-benzo[4,5]imidazo[1,2-A]pyrimidin-2-one and its disperse azo dyes. Part 1: Phenylazo derivatives
    • DOI 10.1016/j.dyepig.2005.06.006, PII S0143720805002160
    • Karci F., Demirçali A., Şener I., Tilki T., Synthesis of 4-amino-1 H -benzo[4,5]imidazo[1,2- H ]pyrimidin-2-one and its disperse azo dyes. Part 1: phenylazo derivatives. Dyes and Pigments 2006 71 2 90 96 2-s2.0-30944453877 10.1016/j.dyepig.2005.06.006 (Pubitemid 43115455)
    • (2006) Dyes and Pigments , vol.71 , Issue.2 , pp. 90-96
    • Karci, F.1    Demircali, A.2    Sener, I.3    Tilki, T.4
  • 13
    • 34748840870 scopus 로고    scopus 로고
    • Synthesis of some new azo dyes derived from 4-hydroxy coumarin and spectrometric determination of their acidic dissociation constants
    • DOI 10.1016/j.molliq.2007.03.005, PII S0167732207000876
    • Yazdanbakhsh M. R., Ghanadzadeh A., Moradi E., Synthesis of some new azo dyes derived from 4-hydroxy coumarin and spectrometric determination of their acidic dissociation constants. Journal of Molecular Liquids 2007 136 1-2 165 168 2-s2.0-34748840870 10.1016/j.molliq.2007.03.005 (Pubitemid 47488536)
    • (2007) Journal of Molecular Liquids , vol.136 , Issue.1-2 , pp. 165-168
    • Yazdanbakhsh, M.R.1    Ghanadzadeh, A.2    Moradi, E.3
  • 14
    • 3843067618 scopus 로고    scopus 로고
    • Resistance to purine and pyrimidine nucleoside and nucleobase analogs by the human MDR1 transfected murine leukemia cell line L1210/VMDRC.06
    • DOI 10.1016/j.bcp.2004.06.004, PII S0006295204004150
    • Zeng H., Lin Z. P., Sartorelli A. C., Resistance to purine and pyrimidine nucleoside and nucleobase analogs by the human MDR1 transfected murine leukemia cell line L1210/VMDRC.06. Biochemical Pharmacology 2004 68 5 911 921 2-s2.0-3843067618 10.1016/j.bcp.2004.06.004 (Pubitemid 39044518)
    • (2004) Biochemical Pharmacology , vol.68 , Issue.5 , pp. 911-921
    • Zeng, H.1    Lin, Z.P.2    Sartorelli, A.C.3
  • 15
    • 3142698398 scopus 로고    scopus 로고
    • Synthesis and QSAR studies of pyrimido[4,5-d]pyrimidine-2,5-dione derivatives as potential antimicrobial agents
    • DOI 10.1016/j.bmcl.2004.06.014, PII S0960894X04007681
    • Sharma P., Rane N., Gurram V. K., Synthesis and QSAR studies of pyrimido[4,5- d ]pyrimidine-2,5-dione derivatives as potential antimicrobial agents. Bioorganic and Medicinal Chemistry Letters 2004 14 16 4185 4190 2-s2.0-3142698398 10.1016/j.bmcl.2004.06.014 (Pubitemid 38916932)
    • (2004) Bioorganic and Medicinal Chemistry Letters , vol.14 , Issue.16 , pp. 4185-4190
    • Sharma, P.1    Rane, N.2    Gurram, V.K.3
  • 16
    • 3042545685 scopus 로고    scopus 로고
    • 1 receptor antagonists
    • DOI 10.1016/j.bmcl.2004.05.056, PII S0960894X04007073
    • Huang C. Q., Wilcoxen K. M., Grigoriadis D. E., McCarthy J. R., Chen C., Design and synthesis of 3-(2-pyridyl)pyrazolo[1,5- a ]pyrimidines as potent CRF1 receptor antagonists. Bioorganic and Medicinal Chemistry Letters 2004 14 15 3943 3947 2-s2.0-3042545685 10.1016/j.bmcl.2004.05.056 (Pubitemid 38844401)
    • (2004) Bioorganic and Medicinal Chemistry Letters , vol.14 , Issue.15 , pp. 3943-3947
    • Huang, C.Q.1    Wilcoxen, K.M.2    Grigoriadis, D.E.3    McCarthy, J.R.4    Chen, C.5
  • 17
    • 84864701263 scopus 로고    scopus 로고
    • Antimicrobial activities of a series of diphenyl(arylamino)(1-phenyl-3- (pyridin-2-Yl)-1H-pyrazol-4-Yl)methylphosphonates phosphorus
    • Abdel-Megeed M. F., Badr B. E., Azaam M. M., El-Hiti G. A., Antimicrobial activities of a series of diphenyl(arylamino)(1-phenyl-3-(pyridin-2-Yl)-1H- pyrazol-4-Yl)methylphosphonates phosphorus. Phosphorus, Sulfur, and Silicon and the Related Elements 2012 187 10 1202 1207
    • (2012) Phosphorus, Sulfur, and Silicon and the Related Elements , vol.187 , Issue.10 , pp. 1202-1207
    • Abdel-Megeed, M.F.1    Badr, B.E.2    Azaam, M.M.3    El-Hiti, G.A.4
  • 20
    • 72449211223 scopus 로고    scopus 로고
    • The cytotoxicity of γ -secretase inhibitor i to breast cancer cells is mediated by proteasome inhibition, not by γ -secretase inhibition
    • 2-s2.0-72449211223 10.1186/bcr2347
    • Han J., Ma I., Hendzel M. J., Allalunis-Turner J., The cytotoxicity of γ -secretase inhibitor I to breast cancer cells is mediated by proteasome inhibition, not by γ -secretase inhibition. Breast Cancer Research 2009 11 4, article R57 2-s2.0-72449211223 10.1186/bcr2347
    • (2009) Breast Cancer Research , vol.11 , Issue.4
    • Han, J.1    Ma, I.2    Hendzel, M.J.3    Allalunis-Turner, J.4


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