-
1
-
-
81755188279
-
The chemical biology of naphthoquinones and its environmental implications
-
Kumagai Y, Shinkai Y, Miura T, et al. The chemical biology of naphthoquinones and its environmental implications. Annu Rev Pharmacol Toxicol 2012;52:221-47
-
(2012)
Annu Rev Pharmacol Toxicol
, Issue.52
, pp. 221-247
-
-
Kumagai, Y.1
Shinkai, Y.2
Miura, T.3
-
2
-
-
27744440806
-
The molecular mechanism involved in the cytotoxicity of alkannin derivatives
-
Wu HQ, Huang Z, Bu XZ, et al. The molecular mechanism involved in the cytotoxicity of alkannin derivatives. Eur J Med Chem 2005;40:1341-5
-
(2005)
Eur J Med Chem
, vol.40
, pp. 1341-1345
-
-
Wu, H.Q.1
Huang, Z.2
Bu, X.Z.3
-
3
-
-
0029922170
-
Homogeneous oxidation of aromatics in nucleus with peracetic acid catalyzed by iron and manganese phthalocyanin complexes
-
Barkanova SV, Derkacheva VM, Dolotova OA, et al. Homogeneous oxidation of aromatics in nucleus with peracetic acid catalyzed by iron and manganese phthalocyanin complexes. Tetrahedron Lett 1996;37:1637-40
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 1637-1640
-
-
Barkanova, S.V.1
Derkacheva, V.M.2
Dolotova, O.A.3
-
4
-
-
0007577005
-
Convenient synthesis of 1,4-naphthoquinones from polymethoxynaphthalenes oxidative demethylation with silver-catalyzed ammoniumperoxodisulfate
-
Tanoue Y, Sakata K, Hashimoto M, et al. Convenient synthesis of 1,4-naphthoquinones from polymethoxynaphthalenes. Oxidative demethylation with silver-catalyzed ammoniumperoxodisulfate. Bull Chem Soc Jpn 1994;67:2593-5
-
(1994)
Bull Chem Soc Jpn
, vol.67
, pp. 2593-2595
-
-
Tanoue, Y.1
Sakata, K.2
Hashimoto, M.3
-
5
-
-
0034686878
-
A versatile synthesis of the 1,4-dihydroxynaphthoquinone nucleus
-
Menegazzo I, Sandona G, Moro S, et al. A versatile synthesis of the 1,4-dihydroxynaphthoquinone nucleus. Tetrahedron Lett 2000;41:6631-4
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 6631-6634
-
-
Menegazzo, I.1
Sandona, G.2
Moro, S.3
-
6
-
-
84882745712
-
-
WO005534 Institute, Inc., assignee. Proteasome inhibitors for selectively inducing apoptosis in cancer cells
-
Lawrence H, Ge Y, Sebti SM, et al. Inventors. H Lee Moffitt Cancer and Research Institute, Inc., assignee. Proteasome inhibitors for selectively inducing apoptosis in cancer cells. WO005534; 2010
-
(2010)
Inventors H Lee Moffitt Cancer and Research
-
-
Lawrence, H.1
Ge, Y.2
Sebti, S.M.3
-
7
-
-
0142054051
-
Bortezomib (PS-341): A novel, first-in-class proteasome inhibitor for the treatment of multiple myeloma and other cancers
-
Richardson PG, Hideshima T, Anderson KC. Bortezomib (PS-341): A novel, first-in-class proteasome inhibitor for the treatment of multiple myeloma and other cancers. Cancer Control 2003;10:361-9
-
(2003)
Cancer Control
, vol.10
, pp. 361-369
-
-
Richardson, P.G.1
Hideshima, T.2
Anderson, K.C.3
-
8
-
-
21044456766
-
Over-expression, purification and characterization of recombinant human arylamine N-Acetyltransferase 1
-
Wang H, Vath GM, Kawamura A, et al. Over-expression, purification and characterization of recombinant human arylamine N-Acetyltransferase 1. Protein J 2005;24:65-77
-
(2005)
Protein J
, vol.24
, pp. 65-77
-
-
Wang, H.1
Vath, G.M.2
Kawamura, A.3
-
9
-
-
40649109723
-
Mouse N-Acetyltransferase type 2, the homologue of human N-Acetyltransferase type 1
-
Kawamura A, Westwood I, Wakefield L, et al. Mouse N-Acetyltransferase type 2, the homologue of human N-Acetyltransferase type 1. Biochem Pharmacol 2008;75:1550-60
-
(2008)
Biochem Pharmacol
, vol.75
, pp. 1550-1560
-
-
Kawamura, A.1
Westwood, I.2
Wakefield, L.3
-
10
-
-
84882760086
-
-
WO005142
-
Russel AJ, Sim E, Davies SG, et al. Inventors. Chemistry Research Laboratory, 12 Mansfield Road, Oxford OX1 3TA, assignee. 1,4-quinones and their sulfur analogues useful as ligands of N-Acetyltransferase. WO005142; 2011
-
(2011)
Inventors Chemistry Research Laboratory 12 Mansfield Road, Oxford OX1 3TA, Assignee 1,4-Quinones And Their Sulfur Analogues Useful As Ligands Of N-Acetyltransferase
-
-
Russel, A.J.1
Sim, E.2
Davies, S.G.3
-
11
-
-
0034688873
-
Cdc25A and the splicing variant Cdc25B2, but not Cdc25B1-B3 or C, are over-expressed in aggressive human non-Hodgkin's lymphomas
-
Hernandez L, Bea S, et al. Cdc25A and the splicing variant Cdc25B2, but not Cdc25B1-B3 or C, are over-expressed in aggressive human non-Hodgkin's lymphomas. Int J Cancer 2000;89:148-52
-
(2000)
Int J Cancer
, vol.89
, pp. 148-152
-
-
Hernandez, L.1
Bea, S.2
-
12
-
-
84882799255
-
Inventors
-
Nishiyama S, Imoto M, Shinbashi A, et al. Inventors. Keio University, Japan, assignee. Preparation of naphthoquinone derivatives, and Cdc25 phosphatase inhibitors and antitumor agents containing them. JP220037; 2005
-
(2005)
Keio University, Japan, assignee. Preparation of naphthoquinone derivatives, and Cdc25 phosphatase inhibitors and antitumor agents containing them. JP220037
-
-
Nishiyama, S.1
Imoto, M.2
Shinbashi, A.3
-
13
-
-
33750215412
-
Fluorinated Cpd5, a pure arylating K-vitamin derivative, inhibits human hepatoma cell growth by inhibiting Cdc25 and activating MAPK
-
Kar S, Wang M, Ham SW, et al. Fluorinated Cpd5, a pure arylating K-vitamin derivative, inhibits human hepatoma cell growth by inhibiting Cdc25 and activating MAPK. Biochem Pharmacol 2006;72:1217-27
-
(2006)
Biochem Pharmacol
, vol.72
, pp. 1217-1227
-
-
Kar, S.1
Wang, M.2
Ham, S.W.3
-
14
-
-
84882809368
-
Inventors
-
Nishiyama S, Imoto M, Shinbashi A, et al. Inventors. Keio University, Japan, assignee. Preparation of naphthoquinones, their use as tyrosine inhibitors, cell proliferation inhibitors and antibacterial agents and their medical compositions. JP316001; 2006
-
(2006)
Keio University, Japan, assignee. Preparation of naphthoquinones, their use as tyrosine inhibitors, cell proliferation inhibitors and antibacterial agents and their medical compositions. JP316001
-
-
Nishiyama, S.1
Imoto, M.2
Shinbashi, A.3
-
15
-
-
0025815451
-
Identification of p53 as a sequence-specific DNA binding protein
-
Kern SE, Kinzler KW, Bruskin K, et al. Identification of p53 as a sequence-specific DNA binding protein. Science 1991;252:1708-11
-
(1991)
Science
, vol.252
, pp. 1708-1711
-
-
Kern, S.E.1
Kinzler, K.W.2
Bruskin, K.3
-
16
-
-
77952956786
-
P53 Inhibits tumor cell invasion via the degradation of snail protein in hepatocellular carcinoma
-
Lim S, Kim H, Jung G. p53 Inhibits tumor cell invasion via the degradation of snail protein in hepatocellular carcinoma. FEBS Lett 2010;584:2231-6
-
(2010)
FEBS Lett
, Issue.584
, pp. 2231-2236
-
-
Lim, S.1
Kim, H.2
Jung, G.3
-
17
-
-
84882757976
-
Inventors
-
Pusan National University, Industry University Cooperation Foundation, the Industry and Academic Cooperation in Chungnam National University S. Korea, assignee WO059004
-
Park BJ, Ha NC, Lee SH, et al. Inventors. Pusan National University, Industry University Cooperation Foundation, the Industry and Academic Cooperation in Chungnam National University S. Korea, assignee. Preparation of naphthoquinone derivatives as inhibitors of p53 snail binding. WO059004; 2010
-
(2010)
Preparation of Naphthoquinone Derivatives As Inhibitors Of P53 Snail Binding
-
-
Park, B.J.1
Ha, N.C.2
Lee, S.H.3
-
19
-
-
4143061295
-
Synthesis of novel rhinacanthins and related anticancer naphthoquinone esters
-
Kongkathip N, Luangkamin S, Kongkathip B, et al. Synthesis of novel rhinacanthins and related anticancer naphthoquinone esters. J Med Chem 2004;47:4427-38
-
(2004)
J Med Chem
, vol.47
, pp. 4427-4438
-
-
Kongkathip, N.1
Luangkamin, S.2
Kongkathip, B.3
-
21
-
-
84882789244
-
Inventors Emory University, USA, assignee WO042500
-
Min J, Du Y, Thepchatin P, et al. Inventors. Emory University, USA, assignee. Heat shock protein 90 inhibitors, methods of preparing same and methods for their use. WO042500; 2010
-
(2010)
Heat Shock Protein 90 Inhibitors, Methods Of Preparing Same And Methods For Their Use
-
-
Min, J.1
Du, Y.2
Thepchatin, P.3
-
23
-
-
24944508703
-
Normal and Leukaemic stem cells
-
Bonnet D. Normal and Leukaemic stem cells. Br J Haematol 2005;130:469-79
-
(2005)
Br J Haematol
, vol.130
, pp. 469-479
-
-
Bonnet, D.1
-
26
-
-
84882808069
-
-
Inventors Pellficure Pharmaceuticals Inc. USA. Assignee WO018948
-
Borgstrom P; Inventors. Pellficure Pharmaceuticals, Inc. USA. Assignee. Novel treatment of prostrate carcinoma. WO018948; 2012
-
(2012)
Novel Treatment Of Prostrate Carcinoma
-
-
Borgstrom, P.1
-
27
-
-
44449135067
-
A 12 week open label, phase I/IIa study using Apatone- for the treatment of prostate cancer patients who have failed standard therapy
-
Tareen B, Summers JL, Jamison J, et al. A 12 week open label, phase I/IIa study using Apatone- for the treatment of prostate cancer patients who have failed standard therapy. Int J Med Sci 2008;5:62-7
-
(2008)
Int J Med Sci
, vol.5
, pp. 62-67
-
-
Tareen, B.1
Summers, J.L.2
Jamison, J.3
-
29
-
-
34548166601
-
Electron transfer reaction mechanism of cisplatin with DNA at the molecular level
-
Lu QB, Kalantari S, Wang CR. Electron transfer reaction mechanism of cisplatin with DNA at the molecular level. Mol Pharm 2007;4:624-8
-
(2007)
Mol Pharm
, vol.4
, pp. 624-628
-
-
Lu, Q.B.1
Kalantari, S.2
Wang, C.R.3
-
30
-
-
34250155229
-
Molecular mechanism of combination treatments of low dose cisplatin with radiotherapy and photodynamic therapy
-
Lu QB. Molecular mechanism of combination treatments of low dose cisplatin with radiotherapy and photodynamic therapy. J Med Chem 2007;50:2601-4
-
(2007)
J Med Chem
, vol.50
, pp. 2601-2604
-
-
Lu, Q.B.1
-
34
-
-
0016755143
-
A lapachol derivative active against mouse lymphocytic leukemia P-388
-
Linardi MDF, de Oliveira MM, Sampaio MRP. A lapachol derivative active against mouse lymphocytic leukemia P-388. J Med Chem 1975;18:1159-61
-
(1975)
J Med Chem
, vol.18
, pp. 1159-1161
-
-
Linardi, M.D.F.1
De Oliveira, M.M.2
Sampaio, M.R.P.3
-
36
-
-
0024470179
-
Studies on inhibitors of skin tumor promotion VI. Inhibitory effects of quinones on Epstein-Barr virus activation
-
Konoshima T, Kozuka M, Koyama J, et al. Studies on inhibitors of skin tumor promotion VI. Inhibitory effects of quinones on Epstein-Barr virus activation. J Nat Prod 1989;52:987-95
-
(1989)
J Nat Prod
, vol.52
, pp. 987-995
-
-
Konoshima, T.1
Kozuka, M.2
Koyama, J.3
-
37
-
-
0027974482
-
Production of antitumor-promoting furano-naphthoquinones in Tabebuia avellanedae cell cultures
-
Ueda S, Umemura T, Dohguchi K, et al. Production of antitumor-promoting furano-naphthoquinones in Tabebuia avellanedae cell cultures. Phytochemistry 1994;36:323-5
-
(1994)
Phytochemistry
, vol.36
, pp. 323-325
-
-
Ueda, S.1
Umemura, T.2
Dohguchi, K.3
-
38
-
-
0031744501
-
Antitumor-promoting naphthoquinones from Catapa ovate
-
Fujiwara A, Mori T, Iida A, et al. Antitumor-promoting naphthoquinones from Catapa ovate. J Nat Prod 1998;61:629-32
-
(1998)
J Nat Prod
, vol.61
, pp. 629-632
-
-
Fujiwara, A.1
Mori, T.2
Iida, A.3
-
39
-
-
0031586753
-
Antitumor promoting effects of naphthoquinone derivatives on short term Epstein-Barr early antigen activation assay and in mouse skin carcinogenesis
-
Kapadia GJ, Balasubramanian V, Tokuda H, et al. Antitumor promoting effects of naphthoquinone derivatives on short term Epstein-Barr early antigen activation assay and in mouse skin carcinogenesis. Cancer Lett 1997;113:47-53
-
(1997)
Cancer Lett
, vol.113
, pp. 47-53
-
-
Kapadia, G.J.1
Balasubramanian, V.2
Tokuda, H.3
-
40
-
-
0035965937
-
Cancer chemopreventive activity of naphthoquinones and their analogs from Avicennia plants
-
Itoigawa M, Ito C, Tan HTW, et al. Cancer chemopreventive activity of naphthoquinones and their analogs from Avicennia plants. Cancer Lett 2011;174:135-9
-
(2011)
Cancer Lett
, Issue.174
, pp. 135-139
-
-
Itoigawa, M.1
Ito, C.2
Tan, H.T.W.3
-
41
-
-
0037249112
-
Inhibitory effects of lapachol derivatives on Epstein-Barr virus activation
-
Sacau EP, Estvez-Braun A, Ravelo AG, et al. Inhibitory effects of lapachol derivatives on Epstein-Barr virus activation. Bioorg Med Chem 2003;11:483-8
-
(2003)
Bioorg Med Chem
, vol.11
, pp. 483-488
-
-
Sacau, E.P.1
Estvez-Braun, A.2
Ravelo, A.G.3
-
42
-
-
0037378176
-
Synthesis And Cytotoxicity Of 611- Dihydropyrido- And 611-dihydrobenzo [2,3-b]phenazine-6,11-dione derivatives
-
Kim YS, Park SY, Lee HJ, et al. Synthesis and cytotoxicity of 6,11- dihydropyrido- and 6,11-dihydrobenzo [2,3-b]phenazine-6,11-dione derivatives. Bioorg Med Chem 2003;11:1709-14
-
(2003)
Bioorg Med Chem
, Issue.11
, pp. 1709-1714
-
-
Kim, Y.S.1
Park, S.Y.2
Lee, H.J.3
-
43
-
-
0022530901
-
Streptonigrin-1. Structure-Activity relationships among simple bicyclic analogues. Rate dependence of DNA degradation on quinone reduction potential
-
Shaikh IA, Johnson F, Grollman AP. Streptonigrin-1. Structure-Activity relationships among simple bicyclic analogues. Rate dependence of DNA degradation on quinone reduction potential. J Med Chem 1986;29:1329-40
-
(1986)
J Med Chem
, vol.29
, pp. 1329-1340
-
-
Shaikh, I.A.1
Johnson, F.2
Grollman, A.P.3
-
44
-
-
0016830817
-
Potential bioreductive alkylating agents 5 Antineoplastic activity of quinone-5,8- diones, naphthazarins and naphthoquinones
-
Lin AJ, Lillis BJ, Sartorelli AC. Potential bioreductive alkylating agents. 5. Antineoplastic activity of quinone-5,8- diones, naphthazarins and naphthoquinones. J Med Chem 1975;18:917-21
-
(1975)
J Med Chem
, Issue.18
, pp. 917-921
-
-
Lin, A.J.1
Lillis, B.J.2
Sartorelli, A.C.3
-
45
-
-
0025133171
-
Induction of mammalian DNA topoisomerase II dependent DNA cleavage by antitumor antibiotic Streptonigrin
-
Yamashita Y, Kawada S, Fujii N, et al. Induction of mammalian DNA topoisomerase II dependent DNA cleavage by antitumor antibiotic Streptonigrin. Cancer Res 1990;50:5841-4
-
(1990)
Cancer Res
, vol.50
, pp. 5841-5844
-
-
Yamashita, Y.1
Kawada, S.2
Fujii, N.3
-
46
-
-
0029969531
-
Role of NAD(P)H quinone oxidoreductase (DTdiaphorase) in cytotoxicity and induction of DNA damage by Streptonigrin
-
Beall HD, Siegel D, Liu Y, et al. Role of NAD(P)H: Quinone oxidoreductase (DTdiaphorase) in cytotoxicity and induction of DNA damage by Streptonigrin. Biochem Biopharmacol 1996;51:645-52
-
(1996)
Biochem Biopharmacol
, vol.51
, pp. 645-652
-
-
Beall, H.D.1
Siegel, D.2
Liu, Y.3
-
47
-
-
0024584484
-
Effects of sodium ascorbate (vitamin C) and 2-methyl-1,4-naphthoquinone (vitamin K3) treatment on human tumor cell growth in vitro
-
Noto V, Taper HS, Jiang YH, et al. Effects of sodium ascorbate (vitamin C) and 2-methyl-1,4-naphthoquinone (vitamin K3) treatment on human tumor cell growth in vitro. Cancer 1989;63:901-6
-
(1989)
Cancer
, vol.63
, pp. 901-906
-
-
Noto, V.1
Taper, H.S.2
Jiang, Y.H.3
-
48
-
-
0025997412
-
Menadione-induced DNA damage in a human tumor cell line
-
Ngo EO, Sun TP, Chang JY. Menadione-induced DNA damage in a human tumor cell line. Biochem Pharmacol 1991;42:1961-8
-
(1991)
Biochem Pharmacol
, vol.42
, pp. 1961-1968
-
-
Ngo, E.O.1
Sun, T.P.2
Chang, J.Y.3
-
49
-
-
0027337571
-
Vitamin K3 inhibits growth of human hepatoma HepG2 cells by decreasing activities of both p34CDC2 kinase and phosphatase
-
Juan CC, Wu FYH. Vitamin K3 inhibits growth of human hepatoma HepG2 cells by decreasing activities of both p34CDC2 kinase and phosphatase. Biochem Biophys Res Commun 1993;190:907-13
-
(1993)
Biochem Biophys Res Commun
, vol.190
, pp. 907-913
-
-
Juan, C.C.1
Wu, F.Y.H.2
-
50
-
-
0023718438
-
Stimulation of endogenous endonuclease activity in hepatocytes exposed to oxidative stress
-
McKonkey DJ, Hartzell P, Nicotera P. Stimulation of endogenous endonuclease activity in hepatocytes exposed to oxidative stress. Toxicol Lett 1998;42:123-30
-
(1998)
Toxicol Lett
, vol.42
, pp. 123-130
-
-
McKonkey, D.J.1
Hartzell, P.2
Nicotera, P.3
-
51
-
-
0027485461
-
Bcl-2 functions in an antioxidant pathway to prevent apoptosis
-
Hockenbery DM, Oltvai ZN, Yin XM. Bcl-2 functions in an antioxidant pathway to prevent apoptosis. Cell 1993;75:241-51
-
(1993)
Cell
, vol.75
, pp. 241-251
-
-
Hockenbery, D.M.1
Oltvai, Z.N.2
Yin, X.M.3
-
52
-
-
0027516607
-
Comparison of antitumor activity of vitamin K1-,K2 and K-3 on human tumor cells by two (MTT and SRB) cell viability assays
-
Wu FYH, Liao WC, Chang HM. Comparison of antitumor activity of vitamin K1-, K2 and K-3 on human tumor cells by two (MTT and SRB) cell viability assays. Life Sci 1993;52:1797-804
-
(1993)
Life Sci
, Issue.52
, pp. 1797-1804
-
-
Wu, F.Y.H.1
Liao, W.C.2
Chang, H.M.3
-
53
-
-
0037037395
-
Synthesis and anticancer evaluation of Vitamin K3 analogues
-
Chen C, Liu YZ, Shia KS, et al. Synthesis and anticancer evaluation of Vitamin K3 analogues. Bioorg Med Chem Lett 2002;12:2729-32
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 2729-2732
-
-
Chen, C.1
Liu, Y.Z.2
Shia, K.S.3
-
54
-
-
84882773201
-
-
Inventors. Wuhan Botanical garden, Chinese Academy of Sciences Method for separating naphthoquinones from Arnebia euchroma. CN102228499
-
Yuan X, Yuan P; Inventors. Wuhan Botanical garden, Chinese Academy of Sciences, Peop. Rep. China. Method for separating naphthoquinones from Arnebia euchroma. CN102228499; 2011
-
(2011)
Peop. Rep. China
-
-
Yuan, X.1
Yuan, P.2
-
55
-
-
27744440806
-
The molecular mechanism involved in the cytotoxicity of alkannin derivatives
-
Wu HQ, Huang ZS, Bu XZ, et al. The molecular mechanism involved in the cytotoxicity of alkannin derivatives. Eur J Med Chem 2005;40:1341-5
-
(2005)
Eur J Med Chem
, vol.40
, pp. 1341-1345
-
-
Wu, H.Q.1
Huang, Z.S.2
Bu, X.Z.3
-
56
-
-
84882740789
-
Inventors
-
Zhejiang University, Peop. Rep. China, assignee CN101654406
-
Wang Y, Su Y, Xie J, et al. Inventors. Zhejiang University, Peop. Rep. China, assignee. Naphthoquinone cycloalkoxy substituted alkannin derivatives useful in the treatment of cancer. CN101654406; 2010
-
(2010)
Naphthoquinone Cycloalkoxy Substituted Alkannin Derivatives Useful In The Treatment Of Cancer
-
-
Wang, Y.1
Su, Y.2
Xie, J.3
-
58
-
-
84882797530
-
-
Inventors KR007967 University, S. Korea. Assignee. 6-(1-Oxopropyl)-5,8- dimethoxy- 1,4-naphthoquinone compound for inhibiting induction of angiogenesis caused by hypoxia induced in malignant tumor and pharmaceutical composition containing the same
-
Kim SH, Lee HJ; Inventors. Industry Academic Cooperation Foundation of Kyunghee University, S. Korea. Assignee. 6-(1-Oxopropyl)-5,8-dimethoxy- 1,4-naphthoquinone compound for inhibiting induction of angiogenesis caused by hypoxia induced in malignant tumor and pharmaceutical composition containing the same. KR007967; 2006
-
(2006)
Industry Academic Cooperation Foundation of Kyunghee
-
-
Kim, S.H.1
Lee, H.J.2
-
59
-
-
84882765472
-
-
Inventors. Kyunghee University, S Kore KR000241
-
Kim SH, Lee HJ, Lee EO, et al. Inventors. Kyunghee University, S Korea. Assignee. 6-[1,4-{bis(2-chloroethyl) amino}aminophenyl]butanoyloxy]pentyl- 5,8-dimethoxy-1,4-naphthoquinone having anticancer activity, a method for preparing same compound and pharmaceutical compositions containing it. KR000241; 2006
-
(2006)
Assignee 6-[1,4-{bis(2-Chloroethyl) Amino}Aminophenyl]Butanoyloxy]Pentyl- 5,8-Dimethoxy-1,4-Naphthoquinone Having Anticancer Activity, A Method For Preparing Same Compound And Pharmaceutical Compositions Containing It
-
-
Kim, S.H.1
Lee, H.J.2
Lee, E.O.3
-
62
-
-
84882748305
-
-
Inventors CN102060834
-
Wu L, Yang C, Ma S, et al. Inventors. Faming Zhuunli Shenquing, Peop. Rep. China. Assignee. 14-(4-Flourophenyl)- 14H-dibenzo[a,i]xanth-8,13-dione and its synthesis method and medical application as antitumor agent. CN102060834; 2011
-
(2011)
Faming Zhuunli Shenquing, Peop. Rep. China. Assignee 14-(4-Flourophenyl)- 14H-Dibenzo[A,I]Xanth-8,13-Dione And Its Synthesis Method And Medical Application As Antitumor Agent
-
-
Wu, L.1
Yang, C.2
Ma, S.3
-
63
-
-
84882743522
-
-
Inventors Guanzhou Institute of Biomedicine and Health, Chinese academy of Sciences, Peop. Rep China. Faming Zhuanli Shenqing, assignee CN101838248
-
Ding K, Pei D, Zhou J, et al. Inventors. Guanzhou Institute of Biomedicine and Health, Chinese academy of Sciences, Peop. Rep. China. Faming Zhuanli Shenqing, assignee. Preparation of 1,4-naphthoquinone compounds as antitumor agents. CN101838248; 2010
-
(2010)
Preparation of 1,4-Naphthoquinone Compounds As Antitumor Agents
-
-
Ding, K.1
Pei, D.2
Zhou, J.3
-
65
-
-
84882774549
-
-
Inventors Fluoforma Fr.; Universite Bordeaux 1 France. Assignee WO125196
-
Depierre G, Dessolin J, Laguerre M, et al. Inventors. Fluoforma, Fr.; Universite Bordeaux 1, France. Assignee. Amino acid N-[(1,4-naphthoquinon-3-yl) amide derivatives, their preparation, pharmaceutical compositions containing them and their use for prevention or treatment of diseases associated with abnormal cellular proliferation such as neoplasm. WO125196; 2007
-
(2007)
Amino Acid N-[ (1,4-Naphthoquinon-3-Yl) Amide Derivatives, Their Preparation, Pharmaceutical Compositions Containing Them And Their Use For Prevention Or Treatment Of Diseases Associated With Abnormal Cellular Proliferation Such As Neoplasm
-
-
Depierre, G.1
Dessolin, J.2
Laguerre, M.3
-
66
-
-
84882736535
-
-
Inventors Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Peop. Rep. China. Assignee CN1690044
-
Duan W, Zhang J, Ding J, et al. Inventors. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Peop. Rep. China. Assignee. Preparation of 1,4-naphthoquinone derivatives as anticancer agents. CN1690044; 2005
-
(2005)
Preparation of 1,4-Naphthoquinone Derivatives As Anticancer Agents
-
-
Duan, W.1
Zhang, J.2
Ding, J.3
-
68
-
-
1242294362
-
Design, synthesis and evaluation of novel 1,4-naphthoquinone derivatives as antifungal and anticancer agents
-
Tandon VK, Chhor RB, Singh RV, et al. Design, synthesis and evaluation of novel 1,4-naphthoquinone derivatives as antifungal and anticancer agents. Bioorg Med Chem Lett 2004;14:1079-83
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 1079-1083
-
-
Tandon, V.K.1
Chhor, R.B.2
Singh, R.V.3
-
69
-
-
2342516894
-
Synthesis and evaluation of novel 1,4-naphthoquinone derivatives as antiviral, antifungal and anticancer agents
-
Tandon VK, Singh RV, Yadav DP. Synthesis and evaluation of novel 1,4-naphthoquinone derivatives as antiviral, antifungal and anticancer agents. Bioorg Med Chem Lett 2004;14:2901-4
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 2901-2904
-
-
Tandon, V.K.1
Singh, R.V.2
Yadav, D.P.3
-
70
-
-
33644761814
-
Synthesis and cytotoxicity of new heterocyclic terpenylnaphthoquinones
-
Corral JMMD, Castro MA, Gordaliza M, et al. Synthesis and cytotoxicity of new heterocyclic terpenylnaphthoquinones. Bioorg Med Chem 2006;14:2816-27
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 2816-2827
-
-
Corral, J.M.M.D.1
Castro, M.A.2
Gordaliza, M.3
-
71
-
-
60549110668
-
3-disubstituted-1,4- naphthoquinones, 12H-benzo[b] phenothiazine-6,11- diones and related compounds: Synthesis and biological evaluation as potential antiproliferative and antifungal agents
-
Tandon VK, Maurya HK, Tripathi A, et al. 2,3-disubstituted-1,4- naphthoquinones, 12H-benzo[b] phenothiazine-6,11-diones and related compounds: Synthesis and biological evaluation as potential antiproliferative and antifungal agents. Eur J Med Chem 2009;44:1086-92
-
(2009)
Eur J Med Chem
, vol.2
, Issue.44
, pp. 1086-1092
-
-
Tandon, V.K.1
Maurya, H.K.2
Tripathi, A.3
-
72
-
-
13944260443
-
Synthesis and cytotoxic evaluation of novel spirohydantoin derivatives of the dihydrothien [2,3-b]naphtho-4,9-dione system
-
Gomez-Monterrey I, Santelli G, Campiglia P, et al. Synthesis and cytotoxic evaluation of novel spirohydantoin derivatives of the dihydrothien[2,3-b]naphtho-4,9-dione system. J Med Chem 2005;48:1152-7
-
(2005)
J Med Chem
, Issue.48
, pp. 1152-1157
-
-
Gomez-Monterrey, I.1
Santelli, G.2
Campiglia, P.3
-
75
-
-
0026666922
-
Comparative cellular pharmacology of daunorubicin and idarubicin in human multidrug-resistant leukemia cells
-
Berman E, McBride M. Comparative cellular pharmacology of daunorubicin and idarubicin in human multidrug-resistant leukemia cells. Blood 1992;79:3267-73
-
(1992)
Blood
, vol.79
, pp. 3267-3273
-
-
Berman, E.1
McBride, M.2
-
76
-
-
0032620102
-
Apoptosis by anthracyclines at therapeutic concentrations in MDR1-human leukemic cells
-
Chiodini B, Bassan R, Barbui T. Apoptosis by anthracyclines at therapeutic concentrations in MDR1-human leukemic cells. Adv Exp Med Biol 1999;457:313-24
-
(1999)
Adv Exp Med Biol
, vol.457
, pp. 313-324
-
-
Chiodini, B.1
Bassan, R.2
Barbui, T.3
-
77
-
-
0033968882
-
In vitro effect of multidrug resistance modifiers on idarubicinol efflux in blasts of acute myeloid leukemia
-
Schroder JK, Kasimir-Bauer S, Seeber S, et al. In vitro effect of multidrug resistance modifiers on idarubicinol efflux in blasts of acute myeloid leukemia. J Cancer Res Clin Oncol 2000;126:111-16
-
(2000)
J Cancer Res Clin Oncol
, vol.126
, pp. 111-116
-
-
Schroder, J.K.1
Kasimir-Bauer, S.2
Seeber, S.3
-
78
-
-
0033000043
-
Idarubicin overcomes P-glycoprotein-related multidrug resistance: Comparison with doxorubicin and daunorbicin in human multiple myeloma cell lines
-
Roovers DJ, Vliet MV, Bloem AC, et al. Idarubicin overcomes P-glycoprotein-related multidrug resistance: Comparison with doxorubicin and daunorbicin in human multiple myeloma cell lines. Leuk Res 1999;23:539-48
-
(1999)
Leuk Res
, vol.23
, pp. 539-548
-
-
Roovers, D.J.1
Vliet, M.V.2
Bloem, A.C.3
-
79
-
-
8044231335
-
Induction of apoptosis in multi-drug resistance (MDR) human glioblastoma cells by SN-38, a metabolite of the camptothecin derivative CPT-11
-
Nakatsu S, Kondo S, Kondo Y, et al. Induction of apoptosis in multi-drug resistance (MDR) human glioblastoma cells by SN-38, a metabolite of the camptothecin derivative CPT-11. Cancer Chemother Pharmacol 1997;39:417-23
-
(1997)
Cancer Chemother Pharmacol
, vol.39
, pp. 417-423
-
-
Nakatsu, S.1
Kondo, S.2
Kondo, Y.3
-
80
-
-
0031962772
-
CPT-11 sensitivity in relation to the expression of P170-glycoprotein and multidrug resistance-Associated protein
-
Jansen WJ, Hulscher TM, Ark-Otte J, et al. CPT-11 sensitivity in relation to the expression of P170-glycoprotein and multidrug resistance-Associated protein. Br J Cancer 1998;77:359-65
-
(1998)
Br J Cancer
, vol.77
, pp. 359-365
-
-
Jansen, W.J.1
Hulscher, T.M.2
Ark-Otte, J.3
-
81
-
-
0031814730
-
Inhibitory effects of a novel marine terpenoid on sensitive and multidrug resistant KB cell lines
-
Pec MK, Hellan M, Moser-Thier K, et al. Inhibitory effects of a novel marine terpenoid on sensitive and multidrug resistant KB cell lines. Anticancer Res 1998;18:3027-32
-
(1998)
Anticancer Res
, vol.18
, pp. 3027-3032
-
-
Pec, M.K.1
Hellan, M.2
Moser-Thier, K.3
-
82
-
-
0038206850
-
Cytotoxicity, apoptosis induction and downregulation of MDR-1 expression by the anti-topoisomerase II agent, salvicine, in multidrug-resistant tumor cells
-
Miao ZH, Tang T, Zhang YX, et al. Cytotoxicity, apoptosis induction and downregulation of MDR-1 expression by the anti-topoisomerase II agent, salvicine, in multidrug-resistant tumor cells. Int J Cancer 2003;106:108-15
-
(2003)
Int J Cancer
, vol.106
, pp. 108-115
-
-
Miao, Z.H.1
Tang, T.2
Zhang, Y.X.3
|