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Volumn 284, Issue 3, 2009, Pages 1337-1342

Biomimetic chemistry: Biology as an inspiration

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; AMPHOLYTE; BENZENE; CARBENE; CHOLESTEROL; COCARBOXYLASE; COPPER SULFATE; CYCLODEXTRIN; CYTOCHROME P450; DNA; ENZYME; HISTIDINE; IMIDAZOLE; IRON; KETONE; LANOSTEROL; LIGAND; METALLOPORPHYRIN; PHOSPHORANE DERIVATIVE; PROTON; PYRUVATE DECARBOXYLASE; RNA; SILICON; SOLVENT; STEROID;

EID: 59449084160     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.X800011200     Document Type: Review
Times cited : (85)

References (28)
  • 1
    • 37049121735 scopus 로고
    • Biomimetic chemistry: Centenary lecture
    • Breslow, R. (1972) Biomimetic chemistry: centenary lecture. Chem. Soc. Rev. 1, 553-580
    • (1972) Chem. Soc. Rev , vol.1 , pp. 553-580
    • Breslow, R.1
  • 2
    • 0001136532 scopus 로고
    • Biomimetic chemistry
    • Breslow, R. (1994) Biomimetic chemistry. Pure Appl. Chem. 66, 1573-1582
    • (1994) Pure Appl. Chem , vol.66 , pp. 1573-1582
    • Breslow, R.1
  • 3
    • 2842610709 scopus 로고
    • Biomimetic chemistry and artificial enzymes: Catalysis by design
    • Breslow, R. (1995) Biomimetic chemistry and artificial enzymes: catalysis by design. Acc. Chem. Res. 28, 146-153
    • (1995) Acc. Chem. Res , vol.28 , pp. 146-153
    • Breslow, R.1
  • 4
    • 0005979632 scopus 로고    scopus 로고
    • Biomimetic chemistry: A frontier at the chemistry/biology interface
    • Breslow, R. (1998) Biomimetic chemistry: a frontier at the chemistry/biology interface. Chem. Biol. 5, R27-R28
    • (1998) Chem. Biol , vol.5
    • Breslow, R.1
  • 6
    • 0000260773 scopus 로고
    • Rapid deuterium exchange in thiazolium salts
    • Breslow, R. (1957) Rapid deuterium exchange in thiazolium salts. J. Am. Chem. Soc. 79, 1762
    • (1957) J. Am. Chem. Soc , vol.79 , pp. 1762
    • Breslow, R.1
  • 7
    • 0343567523 scopus 로고
    • Mechanism of thiamine action: Participation of a thiazolium zwitterion
    • Breslow, R. (1957) Mechanism of thiamine action: participation of a thiazolium zwitterion. Chem. Ind. 893- 894
    • (1957) Chem. Ind , pp. 893-894
    • Breslow, R.1
  • 8
    • 3142640259 scopus 로고
    • On the mechanism of thiamine action: IV. Evidence from studies on model systems
    • Breslow, R. (1958) On the mechanism of thiamine action: IV. Evidence from studies on model systems. J. Am. Chem. Soc. 80, 3719-3726
    • (1958) J. Am. Chem. Soc , vol.80 , pp. 3719-3726
    • Breslow, R.1
  • 9
    • 0001070024 scopus 로고
    • Studies on model systems for thiamine action: Synthesis of reactive intermediates and evidence on the function of the pyrimidine ring
    • Breslow, R., and McNelis, E. (1959) Studies on model systems for thiamine action: synthesis of reactive intermediates and evidence on the function of the pyrimidine ring. J. Am. Chem. Soc. 81, 3080-3082
    • (1959) J. Am. Chem. Soc , vol.81 , pp. 3080-3082
    • Breslow, R.1    McNelis, E.2
  • 10
    • 0000712481 scopus 로고    scopus 로고
    • Why natural DNA is based on 2'- deoxyribose, with 3',5'-phosphodiester links
    • Breslow, R., and Sheppard, T. L. (1996) Why natural DNA is based on 2'- deoxyribose, with 3',5'-phosphodiester links. Pure Appl. Chem. 68, 2037-2041
    • (1996) Pure Appl. Chem , vol.68 , pp. 2037-2041
    • Breslow, R.1    Sheppard, T.L.2
  • 11
    • 0029982129 scopus 로고    scopus 로고
    • Selective binding of RNA, but not DNA, by complementary2',5'-linkedDNA
    • Sheppard, T. L., and Breslow, R. C. (1996) Selective binding of RNA, but not DNA, by complementary2',5'-linkedDNA. J.Am. Chem. Soc. 118, 9810-9811
    • (1996) J.Am. Chem. Soc , vol.118 , pp. 9810-9811
    • Sheppard, T.L.1    Breslow, R.C.2
  • 13
    • 0016395141 scopus 로고
    • Remote functionalization of steroids by a radical relay mechanism
    • Breslow, R., Corcoran, R. J., and Snider, B. B. (1974) Remote functionalization of steroids by a radical relay mechanism. J. Am. Chem. Soc. 96, 6791-6792
    • (1974) J. Am. Chem. Soc , vol.96 , pp. 6791-6792
    • Breslow, R.1    Corcoran, R.J.2    Snider, B.B.3
  • 14
    • 0030826460 scopus 로고    scopus 로고
    • An artificial cytochrome P450 that hydroxylates unactivated carbons with regio-and stereoselectivity and useful catalytic turnovers
    • Breslow, R., Huang, Y., Zhang, X., and Yang, J. (1997) An artificial cytochrome P450 that hydroxylates unactivated carbons with regio-and stereoselectivity and useful catalytic turnovers. Proc. Natl. Acad. Sci. U. S. A. 94, 11156-11158
    • (1997) Proc. Natl. Acad. Sci. U. S. A , vol.94 , pp. 11156-11158
    • Breslow, R.1    Huang, Y.2    Zhang, X.3    Yang, J.4
  • 15
    • 84890969654 scopus 로고    scopus 로고
    • Breslow, R, ed, Wiley-VCH, Weinheim, Germany
    • Breslow, R. (ed) (2005) Artificial Enzymes, Wiley-VCH, Weinheim, Germany
    • (2005) Artificial Enzymes
  • 16
    • 84890969654 scopus 로고    scopus 로고
    • Artificial enzymes
    • Breslow, R, ed pp, Wiley-VCH, Weinheim, Germany
    • Breslow, R. (2005) Artificial enzymes. In: Artificial Enzymes (Breslow, R., ed) pp. 1-35, Wiley-VCH, Weinheim, Germany
    • (2005) Artificial Enzymes , pp. 1-35
    • Breslow, R.1
  • 18
    • 0030010889 scopus 로고    scopus 로고
    • Further studies on the buffer-catalyzed cleavage and isomerization of uridyluridine: Medium and ionic strength effects on catalysis by morpholine, imidazole, and acetate buffers help clarify the mechanisms involved and their relationship to the mechanism used by the enzyme ribonuclease and by a ribonuclease mimic
    • Breslow, R., Dong, S. D., Webb, Y., and Xu, R. (1996) Further studies on the buffer-catalyzed cleavage and isomerization of uridyluridine: medium and ionic strength effects on catalysis by morpholine, imidazole, and acetate buffers help clarify the mechanisms involved and their relationship to the mechanism used by the enzyme ribonuclease and by a ribonuclease mimic. J. Am. Chem. Soc. 118, 6588-6600
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 6588-6600
    • Breslow, R.1    Dong, S.D.2    Webb, Y.3    Xu, R.4
  • 19
    • 0001577045 scopus 로고
    • Geometry ofenolization using a bifunctional cyclodextrin-based catalyst
    • Breslow, R., and Graff, A. (1993) Geometry ofenolization using a bifunctional cyclodextrin-based catalyst. J. Am. Chem. Soc. 115, 10988-10989
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 10988-10989
    • Breslow, R.1    Graff, A.2
  • 20
    • 0142072616 scopus 로고    scopus 로고
    • Hydrophobically directed selective reduction of ketones
    • Biscoe, M., and Breslow, R. (2003) Hydrophobically directed selective reduction of ketones. J. Am. Chem. Soc. 125, 12718-12719
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 12718-12719
    • Biscoe, M.1    Breslow, R.2
  • 21
    • 0025141786 scopus 로고
    • Surface tension measurements showthat chaotropic salting-in denaturants are not just water-structure breakers
    • Breslow, R., and Guo, T. (1990) Surface tension measurements showthat chaotropic salting-in denaturants are not just water-structure breakers. Proc. Natl. Acad. Sci. U. S. A. 87,167-169
    • (1990) Proc. Natl. Acad. Sci. U. S. A , vol.87 , pp. 167-169
    • Breslow, R.1    Guo, T.2
  • 22
    • 0037051612 scopus 로고    scopus 로고
    • Antihydrophobic cosolvent effects for alkylation reactions in water solution, particularly oxygen versus carbon alkylations of phenoxide ions
    • Breslow, R., Groves, K., and Mayer, M. U. (2002) Antihydrophobic cosolvent effects for alkylation reactions in water solution, particularly oxygen versus carbon alkylations of phenoxide ions. J. Am. Chem. Soc. 124, 3622-3635
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 3622-3635
    • Breslow, R.1    Groves, K.2    Mayer, M.U.3
  • 23
    • 84890998264 scopus 로고    scopus 로고
    • Vitamin B6 enzyme models
    • Breslow, R, ed pp, Wiley-VCH, Weinheim, Germany
    • Liu, L., and Breslow, R. (2005) Vitamin B6 enzyme models. In: Artificial Enzymes (Breslow, R., ed) pp. 37-62, Wiley-VCH, Weinheim, Germany
    • (2005) Artificial Enzymes , pp. 37-62
    • Liu, L.1    Breslow, R.2
  • 24
    • 84890994442 scopus 로고    scopus 로고
    • Evolution ofsynthetic polymers with enzymelike catalytic activities
    • Breslow, R, ed, pp, Wiley-VCH, Weinheim, Germany
    • Klotz, I. M., and Suh, J. (2005) Evolution ofsynthetic polymers with enzymelike catalytic activities. In: Artificial Enzymes (Breslow, R., ed.) pp. 63-88, Wiley-VCH, Weinheim, Germany
    • (2005) Artificial Enzymes , pp. 63-88
    • Klotz, I.M.1    Suh, J.2
  • 25
    • 0037202195 scopus 로고    scopus 로고
    • Liu, L.,Rozenman, M.,andBreslow,R. (2002) Hydrophobic effects on rates and substrate selectivities in polymeric transaminase mimics. J. Am. Chem. Soc. 124, 12660-12661
    • Liu, L.,Rozenman, M.,andBreslow,R. (2002) Hydrophobic effects on rates and substrate selectivities in polymeric transaminase mimics. J. Am. Chem. Soc. 124, 12660-12661
  • 26
    • 3042811413 scopus 로고    scopus 로고
    • Transamination reactions with multiple turnovers catalyzed by hydrophobic pyridoxamine cofactors in the presence of polyethylenimine polymers
    • Liu, L., Zhou, W., Chruma, J. J., and Breslow, R. (2004) Transamination reactions with multiple turnovers catalyzed by hydrophobic pyridoxamine cofactors in the presence of polyethylenimine polymers. J. Am. Chem. Soc. 126, 8136-8137
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 8136-8137
    • Liu, L.1    Zhou, W.2    Chruma, J.J.3    Breslow, R.4
  • 27
    • 48849087244 scopus 로고    scopus 로고
    • Enantioselective synthesis and enantiomeric amplification ofamino acids under prebiotic conditions
    • Levine, M., Kenesky, C. S., Mazori, D., and Breslow, R. (2008) Enantioselective synthesis and enantiomeric amplification ofamino acids under prebiotic conditions. Org. Lett. 10, 2433-2436
    • (2008) Org. Lett , vol.10 , pp. 2433-2436
    • Levine, M.1    Kenesky, C.S.2    Mazori, D.3    Breslow, R.4
  • 28
    • 33846122993 scopus 로고    scopus 로고
    • Dimethylsulphoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug
    • Marks, P. A., and Breslow, R. (2007) Dimethylsulphoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug. Nat. Biotechnol. 25, 84-90
    • (2007) Nat. Biotechnol , vol.25 , pp. 84-90
    • Marks, P.A.1    Breslow, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.