-
1
-
-
2642566088
-
Anthracyclines: molecular advances and pharmacologic developments in antitumor activity and cardiotoxicity
-
Minotti G., Menna P., Salvatorelli E., Cairo G., and Gianni L. Anthracyclines: molecular advances and pharmacologic developments in antitumor activity and cardiotoxicity. Pharmacol. Rev. 56 2 (2004) 185-229
-
(2004)
Pharmacol. Rev.
, vol.56
, Issue.2
, pp. 185-229
-
-
Minotti, G.1
Menna, P.2
Salvatorelli, E.3
Cairo, G.4
Gianni, L.5
-
2
-
-
0026714331
-
The anthracyclines: will we ever find a better doxorubicin?
-
Weiss R.B. The anthracyclines: will we ever find a better doxorubicin?. Semin. Oncol. 19 6 (1992) 670-686
-
(1992)
Semin. Oncol.
, vol.19
, Issue.6
, pp. 670-686
-
-
Weiss, R.B.1
-
3
-
-
0034665414
-
Human carbonyl reductase overexpression in the heart advances the development of doxorubicin-induced cardiotoxicity in transgenic mice
-
Forrest G.L., Gonzalez B., Tseng W., Li X., and Mann J. Human carbonyl reductase overexpression in the heart advances the development of doxorubicin-induced cardiotoxicity in transgenic mice. Cancer Res. 60 18 (2000) 5158-5164
-
(2000)
Cancer Res.
, vol.60
, Issue.18
, pp. 5158-5164
-
-
Forrest, G.L.1
Gonzalez, B.2
Tseng, W.3
Li, X.4
Mann, J.5
-
4
-
-
0242321133
-
Protection from doxorubicin-induced cardiac toxicity in mice with a null allele of carbonyl reductase 1
-
Olson L.E., Bedja D., Alvey S.J., Cardounel A.J., Gabrielson K.L., and Reeves R.H. Protection from doxorubicin-induced cardiac toxicity in mice with a null allele of carbonyl reductase 1. Cancer Res. 63 20 (2003) 6602-6606
-
(2003)
Cancer Res.
, vol.63
, Issue.20
, pp. 6602-6606
-
-
Olson, L.E.1
Bedja, D.2
Alvey, S.J.3
Cardounel, A.J.4
Gabrielson, K.L.5
Reeves, R.H.6
-
5
-
-
0026576715
-
Anthracyclines and their C-13 alcohol metabolites: growth inhibition and DNA damage following incubation with human tumor cells in culture
-
Kuffel M.J., Reid J.M., and Ames M.M. Anthracyclines and their C-13 alcohol metabolites: growth inhibition and DNA damage following incubation with human tumor cells in culture. Cancer Chemother. Pharmacol. 30 1 (1992) 51-57
-
(1992)
Cancer Chemother. Pharmacol.
, vol.30
, Issue.1
, pp. 51-57
-
-
Kuffel, M.J.1
Reid, J.M.2
Ames, M.M.3
-
6
-
-
0033988708
-
Development of daunorubicin resistance in tumour cells by induction of carbonyl reduction
-
Ax W., Soldan M., Koch L., and Maser E. Development of daunorubicin resistance in tumour cells by induction of carbonyl reduction. Biochem. Pharmacol. 59 3 (2000) 293-300
-
(2000)
Biochem. Pharmacol.
, vol.59
, Issue.3
, pp. 293-300
-
-
Ax, W.1
Soldan, M.2
Koch, L.3
Maser, E.4
-
7
-
-
0030070454
-
Induction of daunorubicin carbonyl reducing enzymes by daunorubicin in sensitive and resistant pancreas carcinoma cells
-
Soldan M., Netter K.J., and Maser E. Induction of daunorubicin carbonyl reducing enzymes by daunorubicin in sensitive and resistant pancreas carcinoma cells. Biochem. Pharmacol. 51 2 (1996) 117-123
-
(1996)
Biochem. Pharmacol.
, vol.51
, Issue.2
, pp. 117-123
-
-
Soldan, M.1
Netter, K.J.2
Maser, E.3
-
8
-
-
0028843727
-
Protection against daunorubicin cytotoxicity by expression of a cloned human carbonyl reductase cDNA in K562 leukemia cells
-
Gonzalez B., Akman S., Doroshow J., Rivera H., Kaplan W.D., and Forrest G.L. Protection against daunorubicin cytotoxicity by expression of a cloned human carbonyl reductase cDNA in K562 leukemia cells. Cancer Res. 55 20 (1995) 4646-4650
-
(1995)
Cancer Res.
, vol.55
, Issue.20
, pp. 4646-4650
-
-
Gonzalez, B.1
Akman, S.2
Doroshow, J.3
Rivera, H.4
Kaplan, W.D.5
Forrest, G.L.6
-
9
-
-
34547679864
-
Increased resistance of tumor cells to daunorubicin after transfection of cDNAs coding for anthracycline inactivating enzymes
-
Plebuch M., Soldan M., Hungerer C., Koch L., and Maser E. Increased resistance of tumor cells to daunorubicin after transfection of cDNAs coding for anthracycline inactivating enzymes. Cancer Lett. 255 1 (2007) 49-56
-
(2007)
Cancer Lett.
, vol.255
, Issue.1
, pp. 49-56
-
-
Plebuch, M.1
Soldan, M.2
Hungerer, C.3
Koch, L.4
Maser, E.5
-
10
-
-
0036137430
-
Human heart cytosolic reductases and anthracycline cardiotoxicity
-
Mordente A., Meucci E., Martorana G.E., Giardina B., and Minotti G. Human heart cytosolic reductases and anthracycline cardiotoxicity. IUBMB Life 52 1/2 (2001) 83-88
-
(2001)
IUBMB Life
, vol.52
, Issue.1-2
, pp. 83-88
-
-
Mordente, A.1
Meucci, E.2
Martorana, G.E.3
Giardina, B.4
Minotti, G.5
-
11
-
-
46049101685
-
-
X. Zhang, R.D. Olson, G.M. Walsh, 13-Deoxyanthracycline derivates and processes for preparing them, 1999, Patent WO9908687.
-
X. Zhang, R.D. Olson, G.M. Walsh, 13-Deoxyanthracycline derivates and processes for preparing them, 1999, Patent WO9908687.
-
-
-
-
12
-
-
0036746965
-
Inhibition of aldose reductase enhances HeLa cell sensitivity to chemotherapeutic drugs and involves activation of extracellular signal-regulated kinases
-
Lee E.K., Regenold W.T., and Shapiro P. Inhibition of aldose reductase enhances HeLa cell sensitivity to chemotherapeutic drugs and involves activation of extracellular signal-regulated kinases. Anticancer Drugs 13 8 (2002) 859-868
-
(2002)
Anticancer Drugs
, vol.13
, Issue.8
, pp. 859-868
-
-
Lee, E.K.1
Regenold, W.T.2
Shapiro, P.3
-
13
-
-
33846945701
-
Carbonyl reductases: the complex relationships of mammalian carbonyl- and quinone-reducing enzymes and their role in physiology
-
Oppermann U. Carbonyl reductases: the complex relationships of mammalian carbonyl- and quinone-reducing enzymes and their role in physiology. Annu. Rev. Pharmacol. Toxicol. 47 (2007) 293-322
-
(2007)
Annu. Rev. Pharmacol. Toxicol.
, vol.47
, pp. 293-322
-
-
Oppermann, U.1
-
14
-
-
33645963469
-
Multiplicity of mammalian reductases for xenobiotic carbonyl compounds
-
Matsunaga T., Shintani S., and Hara A. Multiplicity of mammalian reductases for xenobiotic carbonyl compounds. Drug Metab. Pharmacokinet. 21 1 (2006) 1-18
-
(2006)
Drug Metab. Pharmacokinet.
, vol.21
, Issue.1
, pp. 1-18
-
-
Matsunaga, T.1
Shintani, S.2
Hara, A.3
-
16
-
-
0028998039
-
Reduction of drug ketones by dihydrodiol dehydrogenases, carbonyl reductase and aldehyde reductase of human liver
-
Ohara H., Miyabe Y., Deyashiki Y., Matsuura K., and Hara A. Reduction of drug ketones by dihydrodiol dehydrogenases, carbonyl reductase and aldehyde reductase of human liver. Biochem. Pharmacol. 50 2 (1995) 221-227
-
(1995)
Biochem. Pharmacol.
, vol.50
, Issue.2
, pp. 221-227
-
-
Ohara, H.1
Miyabe, Y.2
Deyashiki, Y.3
Matsuura, K.4
Hara, A.5
-
17
-
-
0019495032
-
Purification and properties of an NADPH-dependent carbonyl reductase from human brain. Relationship to prostaglandin 9-ketoreductase and xenobiotic ketone reductase
-
Wermuth B. Purification and properties of an NADPH-dependent carbonyl reductase from human brain. Relationship to prostaglandin 9-ketoreductase and xenobiotic ketone reductase. J. Biol. Chem. 256 3 (1981) 1206-1213
-
(1981)
J. Biol. Chem.
, vol.256
, Issue.3
, pp. 1206-1213
-
-
Wermuth, B.1
-
18
-
-
0026059372
-
Genomic sequence and expression of a cloned human carbonyl reductase gene with daunorubicin reductase activity
-
Forrest G.L., Akman S., Doroshow J., Rivera H., and Kaplan W.D. Genomic sequence and expression of a cloned human carbonyl reductase gene with daunorubicin reductase activity. Mol. Pharmacol. 40 4 (1991) 502-507
-
(1991)
Mol. Pharmacol.
, vol.40
, Issue.4
, pp. 502-507
-
-
Forrest, G.L.1
Akman, S.2
Doroshow, J.3
Rivera, H.4
Kaplan, W.D.5
-
19
-
-
0032959371
-
Diabetes complications and their potential prevention: aldose reductase inhibition and other approaches
-
Costantino L., Rastelli G., Vianello P., Cignarella G., and Barlocco D. Diabetes complications and their potential prevention: aldose reductase inhibition and other approaches. Med. Res. Rev. 19 1 (1999) 3-23
-
(1999)
Med. Res. Rev.
, vol.19
, Issue.1
, pp. 3-23
-
-
Costantino, L.1
Rastelli, G.2
Vianello, P.3
Cignarella, G.4
Barlocco, D.5
-
20
-
-
0035544952
-
Aldose reductase inhibitors
-
Oka M., and Kato N. Aldose reductase inhibitors. J. Enzyme Inhib. 16 6 (2001) 465-473
-
(2001)
J. Enzyme Inhib.
, vol.16
, Issue.6
, pp. 465-473
-
-
Oka, M.1
Kato, N.2
-
21
-
-
26444477394
-
A novel series of non-carboxylic acid, non-hydantoin inhibitors of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran-2-sulfonyl)-2H-pyridazin-3-one and congeners
-
Mylari B.L., Armento S.J., Beebe D.A., Conn E.L., Coutcher J.B., Dina M.S., O'Gorman M.T., Linhares M.C., Martin W.H., Oates P.J., Tess D.A., Withbroe G.J., and Zembrowski W.J. A novel series of non-carboxylic acid, non-hydantoin inhibitors of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran-2-sulfonyl)-2H-pyridazin-3-one and congeners. J. Med. Chem. 48 20 (2005) 6326-6339
-
(2005)
J. Med. Chem.
, vol.48
, Issue.20
, pp. 6326-6339
-
-
Mylari, B.L.1
Armento, S.J.2
Beebe, D.A.3
Conn, E.L.4
Coutcher, J.B.5
Dina, M.S.6
O'Gorman, M.T.7
Linhares, M.C.8
Martin, W.H.9
Oates, P.J.10
Tess, D.A.11
Withbroe, G.J.12
Zembrowski, W.J.13
-
22
-
-
33750869527
-
A selective aldose reductase inhibitor of a new structural class prevents or reverses early retinal abnormalities in experimental diabetic retinopathy
-
Sun W., Oates P.J., Coutcher J.B., Gerhardinger C., and Lorenzi M. A selective aldose reductase inhibitor of a new structural class prevents or reverses early retinal abnormalities in experimental diabetic retinopathy. Diabetes 55 10 (2006) 2757-2762
-
(2006)
Diabetes
, vol.55
, Issue.10
, pp. 2757-2762
-
-
Sun, W.1
Oates, P.J.2
Coutcher, J.B.3
Gerhardinger, C.4
Lorenzi, M.5
-
23
-
-
3042595713
-
Human carbonyl reduction pathways and a strategy for their study in vitro
-
Rosemond M.J., and Walsh J.S. Human carbonyl reduction pathways and a strategy for their study in vitro. Drug Metab. Rev. 36 2 (2004) 335-361
-
(2004)
Drug Metab. Rev.
, vol.36
, Issue.2
, pp. 335-361
-
-
Rosemond, M.J.1
Walsh, J.S.2
-
24
-
-
0016738950
-
Flavonoids as inhibitors of lens aldose reductase
-
Varma S.D., Mikuni I., and Kinoshita J.H. Flavonoids as inhibitors of lens aldose reductase. Science 188 4194 (1975) 1215-1216
-
(1975)
Science
, vol.188
, Issue.4194
, pp. 1215-1216
-
-
Varma, S.D.1
Mikuni, I.2
Kinoshita, J.H.3
-
25
-
-
21744448078
-
An unbiased cell morphology-based screen for new, biologically active small molecules
-
Tanaka M., Bateman R., Rauh D., Vaisberg E., Ramachandani S., Zhang C., Hansen K.C., Burlingame A.L., Trautman J.K., Shokat K.M., and Adams C.L. An unbiased cell morphology-based screen for new, biologically active small molecules. PLoS Biol. 3 5 (2005) e128
-
(2005)
PLoS Biol.
, vol.3
, Issue.5
-
-
Tanaka, M.1
Bateman, R.2
Rauh, D.3
Vaisberg, E.4
Ramachandani, S.5
Zhang, C.6
Hansen, K.C.7
Burlingame, A.L.8
Trautman, J.K.9
Shokat, K.M.10
Adams, C.L.11
-
26
-
-
0041694227
-
Anthracycline secondary alcohol metabolite formation in human or rabbit heart: biochemical aspects and pharmacologic implications
-
Mordente A., Minotti G., Martorana G.E., Silvestrini A., Giardina B., and Meucci E. Anthracycline secondary alcohol metabolite formation in human or rabbit heart: biochemical aspects and pharmacologic implications. Biochem. Pharmacol. 66 6 (2003) 989-998
-
(2003)
Biochem. Pharmacol.
, vol.66
, Issue.6
, pp. 989-998
-
-
Mordente, A.1
Minotti, G.2
Martorana, G.E.3
Silvestrini, A.4
Giardina, B.5
Meucci, E.6
-
27
-
-
0028788099
-
Modulation of the in vitro cardiotoxicity of doxorubicin by flavonoids
-
Husken B.C., de Jong J., Beekman B., Onderwater R.C., van der Vijgh W.J., and Bast A. Modulation of the in vitro cardiotoxicity of doxorubicin by flavonoids. Cancer Chemother. Pharmacol. 37 1/2 (1995) 55-62
-
(1995)
Cancer Chemother. Pharmacol.
, vol.37
, Issue.1-2
, pp. 55-62
-
-
Husken, B.C.1
de Jong, J.2
Beekman, B.3
Onderwater, R.C.4
van der Vijgh, W.J.5
Bast, A.6
-
28
-
-
0004136246
-
-
Cold Spring harbor Laboratory Press, Cold Spring Harbor, New York
-
Sambrook J., Fritch E., and Maniatis T. Molecular Cloning: A Laboratory Manual (1989), Cold Spring harbor Laboratory Press, Cold Spring Harbor, New York
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritch, E.2
Maniatis, T.3
-
29
-
-
0028953840
-
Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds
-
Mumberg D., Muller R., and Funk M. Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds. Gene 156 1 (1995) 119-122
-
(1995)
Gene
, vol.156
, Issue.1
, pp. 119-122
-
-
Mumberg, D.1
Muller, R.2
Funk, M.3
-
30
-
-
0025675856
-
High efficiency transformation of Escherichia coli with plasmids
-
Inoue H., Nojima H., and Okayama H. High efficiency transformation of Escherichia coli with plasmids. Gene 96 1 (1990) 23-28
-
(1990)
Gene
, vol.96
, Issue.1
, pp. 23-28
-
-
Inoue, H.1
Nojima, H.2
Okayama, H.3
-
31
-
-
0028954118
-
Studies on the transformation of intact yeast cells by the LiAc/SS-DNA/PEG procedure
-
Gietz R.D., Schiestl R.H., Willems A.R., and Woods R.A. Studies on the transformation of intact yeast cells by the LiAc/SS-DNA/PEG procedure. Yeast 11 4 (1995) 355-360
-
(1995)
Yeast
, vol.11
, Issue.4
, pp. 355-360
-
-
Gietz, R.D.1
Schiestl, R.H.2
Willems, A.R.3
Woods, R.A.4
-
33
-
-
33846805635
-
Characterization of a potent and selective small-molecule inhibitor of the PIM1 kinase
-
Holder S., Zemskova M., Zhang C., Tabrizizad M., Bremer R., Neidigh J.W., and Lilly M.B. Characterization of a potent and selective small-molecule inhibitor of the PIM1 kinase. Mol. Cancer Ther. 6 1 (2007) 163-172
-
(2007)
Mol. Cancer Ther.
, vol.6
, Issue.1
, pp. 163-172
-
-
Holder, S.1
Zemskova, M.2
Zhang, C.3
Tabrizizad, M.4
Bremer, R.5
Neidigh, J.W.6
Lilly, M.B.7
-
34
-
-
1442276491
-
Crystal structure of human prostaglandin F synthase (AKR1C3)
-
Komoto J., Yamada T., Watanabe K., and Takusagawa F. Crystal structure of human prostaglandin F synthase (AKR1C3). Biochemistry 43 8 (2004) 2188-2198
-
(2004)
Biochemistry
, vol.43
, Issue.8
, pp. 2188-2198
-
-
Komoto, J.1
Yamada, T.2
Watanabe, K.3
Takusagawa, F.4
-
35
-
-
29644437917
-
Reduction of 13-deoxydoxorubicin and daunorubicinol anthraquinones by human carbonyl reductase
-
Slupe A., Williams B., Larson C., Lee L.M., Primbs T., Bruesch A.J., Bjorklund C., Warner D.L., Peloquin J., Shadle S.E., Gambliel H.A., Cusack B.J., Olson R.D., and Charlier Jr. H.A. Reduction of 13-deoxydoxorubicin and daunorubicinol anthraquinones by human carbonyl reductase. Cardiovasc. Toxicol. 5 4 (2005) 365-376
-
(2005)
Cardiovasc. Toxicol.
, vol.5
, Issue.4
, pp. 365-376
-
-
Slupe, A.1
Williams, B.2
Larson, C.3
Lee, L.M.4
Primbs, T.5
Bruesch, A.J.6
Bjorklund, C.7
Warner, D.L.8
Peloquin, J.9
Shadle, S.E.10
Gambliel, H.A.11
Cusack, B.J.12
Olson, R.D.13
Charlier Jr., H.A.14
-
36
-
-
0023182118
-
Kinetics of carbonyl reductase from human brain
-
Bohren K.M., von Wartburg J.P., and Wermuth B. Kinetics of carbonyl reductase from human brain. Biochem. J. 244 1 (1987) 165-171
-
(1987)
Biochem. J.
, vol.244
, Issue.1
, pp. 165-171
-
-
Bohren, K.M.1
von Wartburg, J.P.2
Wermuth, B.3
-
37
-
-
34249009348
-
A functional genetic polymorphism on human carbonyl reductase 1 (CBR1 V88I) impacts on catalytic activity and NADPH binding affinity
-
Gonzalez-Covarrubias V., Ghosh D., Lakhman S.S., Pendyala L., and Blanco J.G. A functional genetic polymorphism on human carbonyl reductase 1 (CBR1 V88I) impacts on catalytic activity and NADPH binding affinity. Drug Metab. Dispos. 35 6 (2007) 973-980
-
(2007)
Drug Metab. Dispos.
, vol.35
, Issue.6
, pp. 973-980
-
-
Gonzalez-Covarrubias, V.1
Ghosh, D.2
Lakhman, S.S.3
Pendyala, L.4
Blanco, J.G.5
-
38
-
-
0033557429
-
Identification of the reactive cysteine residue (Cys227) in human carbonyl reductase
-
Tinguely J.N., and Wermuth B. Identification of the reactive cysteine residue (Cys227) in human carbonyl reductase. Eur. J. Biochem. 260 1 (1999) 9-14
-
(1999)
Eur. J. Biochem.
, vol.260
, Issue.1
, pp. 9-14
-
-
Tinguely, J.N.1
Wermuth, B.2
-
39
-
-
0027967454
-
Expression, crystallization and preliminary crystallographic analysis of human carbonyl reductase
-
Bohren K.M., Wermuth B., Harrison D., Ringe D., Petsko G.A., and Gabbay K.H. Expression, crystallization and preliminary crystallographic analysis of human carbonyl reductase. J. Mol. Biol. 244 5 (1994) 659-664
-
(1994)
J. Mol. Biol.
, vol.244
, Issue.5
, pp. 659-664
-
-
Bohren, K.M.1
Wermuth, B.2
Harrison, D.3
Ringe, D.4
Petsko, G.A.5
Gabbay, K.H.6
|