-
1
-
-
0034917716
-
The human ATP-binding cassette (ABC) transporter superfamily
-
M. Dean A. Rzhetsky R. Allikmets The human ATP-binding cassette (ABC) transporter superfamily Genome Res. 11 2001 1156 1166
-
(2001)
Genome Res.
, vol.11
, pp. 1156-1166
-
-
Dean, M.1
Rzhetsky, A.2
Allikmets, R.3
-
2
-
-
0036434614
-
ABCC13, an unusual truncated ABC transporter, is highly expressed in fetal human liver, Biochem
-
H. Yabuuchi S.i. Takayanagi K. Yoshinaga N. Taniguchi H. Aburatani T. Ishikawa ABCC13, an unusual truncated ABC transporter, is highly expressed in fetal human liver, Biochem Biophys. Res. Commun. 299 2002 410 417
-
(2002)
Biophys. Res. Commun.
, vol.299
, pp. 410-417
-
-
Yabuuchi, H.1
Takayanagi, S.I.2
Yoshinaga, K.3
Taniguchi, N.4
Aburatani, H.5
Ishikawa, T.6
-
3
-
-
65549121495
-
Human ATP-binding cassette (ABC) transporter family
-
V. Vasiliou K. Vasiliou D. Nebert Human ATP-binding cassette (ABC) transporter family Hum. Genomics 3 2008 281 290
-
(2008)
Hum. Genomics
, vol.3
, pp. 281-290
-
-
Vasiliou, V.1
Vasiliou, K.2
Nebert, D.3
-
4
-
-
35648963623
-
ABC transporters: How small machines do a big job
-
A.L. Davidson P.C. Maloney ABC transporters: how small machines do a big job Trends Microbiol. 15 2007 448 455
-
(2007)
Trends Microbiol.
, vol.15
, pp. 448-455
-
-
Davidson, A.L.1
Maloney, P.C.2
-
5
-
-
17544368685
-
Multidrug resistance proteins: Role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense
-
E.M. Leslie R.G. Deeley S.P.C. Cole Multidrug resistance proteins: role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense Toxicol. Appl. Pharmacol. 204 2005 216 237
-
(2005)
Toxicol. Appl. Pharmacol.
, vol.204
, pp. 216-237
-
-
Leslie, E.M.1
Deeley, R.G.2
Cole, S.P.C.3
-
7
-
-
43149118341
-
The role of ABC transporters in drug absorption, distribution, metabolism, excretion and toxicity (ADME-Tox)
-
G. Szakács A. Váradi C. Özvegy-Laczka B. Sarkadi The role of ABC transporters in drug absorption, distribution, metabolism, excretion and toxicity (ADME-Tox) Drug Discov. Today 13 2008 379 393
-
(2008)
Drug Discov. Today
, vol.13
, pp. 379-393
-
-
Szakács, G.1
Váradi, A.2
Özvegy-Laczka, C.3
Sarkadi, B.4
-
8
-
-
84922223032
-
The modulation of ABC transporter-mediated multidrug resistance in cancer: A review of the past decade
-
R.J. Kathawala P. Gupta C.R. Ashby Jr. Z.S. Chen The modulation of ABC transporter-mediated multidrug resistance in cancer: a review of the past decade Drug Resist Updat 18 2015 1 17
-
(2015)
Drug Resist Updat
, vol.18
, pp. 1-17
-
-
Kathawala, R.J.1
Gupta, P.2
Ashby, C.R.3
Chen, Z.S.4
-
9
-
-
84878107592
-
Reversal of ATP-binding cassette drug transporter activity to modulate chemoresistance: Why has it failed to provide clinical benefit?
-
M. Yu A. Ocana I.F. Tannock Reversal of ATP-binding cassette drug transporter activity to modulate chemoresistance: why has it failed to provide clinical benefit? Cancer Metastasis Rev. 32 2013 211 227
-
(2013)
Cancer Metastasis Rev.
, vol.32
, pp. 211-227
-
-
Yu, M.1
Ocana, A.2
Tannock, I.F.3
-
10
-
-
84876817977
-
P-glycoprotein inhibition as a therapeutic approach for overcoming multidrug resistance in cancer: Current status and future perspectives
-
Z. Binkhathlan A. Lavasanifar P-glycoprotein inhibition as a therapeutic approach for overcoming multidrug resistance in cancer: current status and future perspectives Curr. Cancer Drug Targets 13 2013 326 346
-
(2013)
Curr. Cancer Drug Targets
, vol.13
, pp. 326-346
-
-
Binkhathlan, Z.1
Lavasanifar, A.2
-
11
-
-
0036364467
-
Multidrug resistance in cancer: Role of ATP-dependent transporters
-
M.M. Gottesman T. Fojo S.E. Bates Multidrug resistance in cancer: role of ATP-dependent transporters Nat. Rev. Cancer 2 2002 48 58
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 48-58
-
-
Gottesman, M.M.1
Fojo, T.2
Bates, S.E.3
-
13
-
-
0027095653
-
Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line
-
S. Cole G. Bhardwaj J. Gerlach J. Mackie C. Grant K. Almquist A. Stewart E. Kurz A. Duncan R. Deeley Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line Science 258 1992 1650 1654
-
(1992)
Science
, vol.258
, pp. 1650-1654
-
-
Cole, S.1
Bhardwaj, G.2
Gerlach, J.3
Mackie, J.4
Grant, C.5
Almquist, K.6
Stewart, A.7
Kurz, E.8
Duncan, A.9
Deeley, R.10
-
15
-
-
0028844581
-
Expression of multidrug resistance-associated protein in NIH/3T3 cells confers multidrug resistance associated with increased drug efflux and altered intracellular drug distribution
-
L.M. Breuninger S. Paul K. Gaughan T. Miki A. Chan S.A. Aaronson G.D. Kruh Expression of multidrug resistance-associated protein in NIH/3T3 cells confers multidrug resistance associated with increased drug efflux and altered intracellular drug distribution Cancer Res. 55 1995 5342 5347
-
(1995)
Cancer Res.
, vol.55
, pp. 5342-5347
-
-
Breuninger, L.M.1
Paul, S.2
Gaughan, K.3
Miki, T.4
Chan, A.5
Aaronson, S.A.6
Kruh, G.D.7
-
16
-
-
33644673861
-
Cyclooxygenase-independent down-regulation of multidrug resistance-associated protein-1 expression by celecoxib in human lung cancer cells
-
H.-K. Kang E. Lee H. Pyo S.-J. Lim Cyclooxygenase-independent down-regulation of multidrug resistance-associated protein-1 expression by celecoxib in human lung cancer cells Mol. Cancer Ther. 4 2005 1358 1363
-
(2005)
Mol. Cancer Ther.
, vol.4
, pp. 1358-1363
-
-
Kang, H.-K.1
Lee, E.2
Pyo, H.3
Lim, S.-J.4
-
17
-
-
33645747683
-
Association of high-level MRP1 expression with poor clinical outcome in a large prospective study of primary neuroblastoma
-
M. Haber J. Smith S.B. Bordow C. Flemming S.L. Cohn W.B. London G.M. Marshall M.D. Norris Association of high-level MRP1 expression with poor clinical outcome in a large prospective study of primary neuroblastoma J. Clin. Oncol. 24 2006 1546 1553
-
(2006)
J. Clin. Oncol.
, vol.24
, pp. 1546-1553
-
-
Haber, M.1
Smith, J.2
Bordow, S.B.3
Flemming, C.4
Cohn, S.L.5
London, W.B.6
Marshall, G.M.7
Norris, M.D.8
-
18
-
-
58149506377
-
Role of multidrug resistance-associated protein 1 in the pathogenesis of allergic airway inflammation, Am
-
M. Yoshioka H. Sagara F. Takahashi N. Harada K. Nishio A. Mori H. Ushio K. Shimizu T. Okada M. Ota Y.M. Ito O. Nagashima R. Atsuta T. Suzuki T. Fukuda Y. Fukuchi K. Takahashi Role of multidrug resistance-associated protein 1 in the pathogenesis of allergic airway inflammation, Am J. Physiol. Lung Cell Mol. Physiol. 296 2009 L30 L36
-
(2009)
J. Physiol. Lung Cell Mol. Physiol.
, vol.296
, pp. L30-L36
-
-
Yoshioka, M.1
Sagara, H.2
Takahashi, F.3
Harada, N.4
Nishio, K.5
Mori, A.6
Ushio, H.7
Shimizu, K.8
Okada, T.9
Ota, M.10
Ito, Y.M.11
Nagashima, O.12
Atsuta, R.13
Suzuki, T.14
Fukuda, T.15
Fukuchi, Y.16
Takahashi, K.17
-
19
-
-
33847366629
-
Inhibition of MRP1/ABCC1, MRP2/ABCC2, and MRP3/ABCC3 by Nucleoside, nucleotide, and non-nucleoside reverse transcriptase inhibitors
-
J. Weiss D. Theile N. Ketabi-Kiyanvash H. Lindenmaier W.E. Haefeli Inhibition of MRP1/ABCC1, MRP2/ABCC2, and MRP3/ABCC3 by Nucleoside, nucleotide, and non-nucleoside reverse transcriptase inhibitors Drug Metab. Disposition 35 2007 340 344
-
(2007)
Drug Metab. Disposition
, vol.35
, pp. 340-344
-
-
Weiss, J.1
Theile, D.2
Ketabi-Kiyanvash, N.3
Lindenmaier, H.4
Haefeli, W.E.5
-
20
-
-
84892608351
-
MRP1 overexpression determines poor prognosis in prospectively treated patients with localized high-risk soft tissue sarcoma of limbs and trunk Wall: An ISG/GEIS study
-
J. Martin-Broto A.M. Gutierrez R.F. Ramos J.A. Lopez-Guerrero S. Ferrari S. Stacchiotti P. Picci S. Calabuig P. Collini M. Gambarotti S. Bague A.P. Dei Tos E. Palassini P. Luna J. Cruz R. Cubedo J. Martinez-Trufero A. Poveda P.G. Casali A. Fernandez-Serra A. Lopez-Pousa A. Gronchi MRP1 overexpression determines poor prognosis in prospectively treated patients with localized high-risk soft tissue sarcoma of limbs and trunk Wall: an ISG/GEIS study Mol. Cancer Ther. 13 2014 249 259
-
(2014)
Mol. Cancer Ther.
, vol.13
, pp. 249-259
-
-
Martin-Broto, J.1
Gutierrez, A.M.2
Ramos, R.F.3
Lopez-Guerrero, J.A.4
Ferrari, S.5
Stacchiotti, S.6
Picci, P.7
Calabuig, S.8
Collini, P.9
Gambarotti, M.10
Bague, S.11
Dei Tos, A.P.12
Palassini, E.13
Luna, P.14
Cruz, J.15
Cubedo, R.16
Martinez-Trufero, J.17
Poveda, A.18
Casali, P.G.19
Fernandez-Serra, A.20
Lopez-Pousa, A.21
Gronchi, A.22
more..
-
21
-
-
84888581611
-
Targeting multidrug resistance protein 1 (MRP1, ABCC1): Past, present, and future
-
S.P.C. Cole Targeting multidrug resistance protein 1 (MRP1, ABCC1): past, present, and future Annu. Rev. Pharmacool. Toxicol. 54 2014 95 117
-
(2014)
Annu. Rev. Pharmacool. Toxicol.
, vol.54
, pp. 95-117
-
-
Cole, S.P.C.1
-
23
-
-
0037311322
-
Effect of flavonoids on MRP1-mediated transport in Panc-1 cells
-
H. Nguyen S. Zhang M.E. Morris Effect of flavonoids on MRP1-mediated transport in Panc-1 cells J. Pharm. Sci. 92 2003 250 257
-
(2003)
J. Pharm. Sci.
, vol.92
, pp. 250-257
-
-
Nguyen, H.1
Zhang, S.2
Morris, M.E.3
-
24
-
-
53349117254
-
Substrates and inhibitors of human multidrug resistance associated proteins and the implications in drug development
-
S.-F. Zhou L.-L. Wang Y.M. Di C.C. Xue W. Duan C.G. Li Y. Li Substrates and inhibitors of human multidrug resistance associated proteins and the implications in drug development Curr. Med. Chem. 15 2008 1981 2039
-
(2008)
Curr. Med. Chem.
, vol.15
, pp. 1981-2039
-
-
Zhou, S.-F.1
Wang, L.-L.2
Di, Y.M.3
Xue, C.C.4
Duan, W.5
Li, C.G.6
Li, Y.7
-
25
-
-
69249094554
-
Small-Molecule multidrug Resistance-Associated protein 1 inhibitor reversan increases the therapeutic Index of chemotherapy in mouse models of neuroblastoma
-
C.A. Burkhart F. Watt J. Murray M. Pajic A. Prokvolit C. Xue C. Flemming J. Smith A. Purmal N. Isachenko P.G. Komarov K.V. Gurova A.C. Sartorelli G.M. Marshall M.D. Norris A.V. Gudkov M. Haber Small-Molecule multidrug Resistance-Associated protein 1 inhibitor reversan increases the therapeutic Index of chemotherapy in mouse models of neuroblastoma Cancer Res. 69 2009 6573 6580
-
(2009)
Cancer Res.
, vol.69
, pp. 6573-6580
-
-
Burkhart, C.A.1
Watt, F.2
Murray, J.3
Pajic, M.4
Prokvolit, A.5
Xue, C.6
Flemming, C.7
Smith, J.8
Purmal, A.9
Isachenko, N.10
Komarov, P.G.11
Gurova, K.V.12
Sartorelli, A.C.13
Marshall, G.M.14
Norris, M.D.15
Gudkov, A.V.16
Haber, M.17
-
26
-
-
50349094786
-
Pharmacophore mapping of a series of pyrrolopyrimidines, indolopyrimidines and their congeners as multidrug-resistance-associated protein (MRP1) modulators
-
N. Tawari S. Bag M. Degani Pharmacophore mapping of a series of pyrrolopyrimidines, indolopyrimidines and their congeners as multidrug-resistance-associated protein (MRP1) modulators J. Mol. Model. 14 2008 911 921
-
(2008)
J. Mol. Model.
, vol.14
, pp. 911-921
-
-
Tawari, N.1
Bag, S.2
Degani, M.3
-
27
-
-
84969313699
-
Virtual screening of ABCC1 transporter nucleotidebinding domains as a therapeutic target in multidrug resistant cancer
-
R. Kanin S. Sergio Mares P. Jeffrey Virtual screening of ABCC1 transporter nucleotidebinding domains as a therapeutic target in multidrug resistant cancer Bioinformation 8 2012
-
(2012)
Bioinformation
, vol.8
-
-
Kanin, R.1
Sergio Mares, S.2
Jeffrey, P.3
-
28
-
-
69949099322
-
Modulation of multidrug resistance protein 1 (MRP1/ABCC1)-Mediated multidrug resistance by bivalent apigenin homodimers and their derivatives
-
I.L.K. Wong K.-F. Chan K.H. Tsang C.Y. Lam Y. Zhao T.H. Chan L.M.C. Chow Modulation of multidrug resistance protein 1 (MRP1/ABCC1)-Mediated multidrug resistance by bivalent apigenin homodimers and their derivatives J. Med. Chem. 52 2009 5311 5322
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5311-5322
-
-
Wong, I.L.K.1
Chan, K.-F.2
Tsang, K.H.3
Lam, C.Y.4
Zhao, Y.5
Chan, T.H.6
Chow, L.M.C.7
-
29
-
-
79957819263
-
Solid phase synthesis of tariquidar-related modulators of ABC transporters preferring breast cancer resistance protein (ABCG2)
-
C. Ochoa-Puentes P. Höcherl M. Kühnle S. Bauer K. Bürger G. Bernhardt A. Buschauer B. König Solid phase synthesis of tariquidar-related modulators of ABC transporters preferring breast cancer resistance protein (ABCG2) Bioorg. Med. Chem. Lett. 21 2011 3654 3657
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 3654-3657
-
-
Ochoa-Puentes, C.1
Höcherl, P.2
Kühnle, M.3
Bauer, S.4
Bürger, K.5
Bernhardt, G.6
Buschauer, A.7
König, B.8
-
30
-
-
34250626127
-
Tariquidar analogues: Synthesis by CuI-catalysed N/O-Aryl coupling and inhibitory activity against the ABCB1 transporter
-
M. Egger X. Li C. Müller G. Bernhardt A. Buschauer B. König Tariquidar analogues: synthesis by CuI-catalysed N/O-Aryl coupling and inhibitory activity against the ABCB1 transporter Eur. J. Org. Chem. 2007 2007 2643 2649
-
(2007)
Eur. J. Org. Chem.
, vol.2007
, pp. 2643-2649
-
-
Egger, M.1
Li, X.2
Müller, C.3
Bernhardt, G.4
Buschauer, A.5
König, B.6
-
31
-
-
64349122714
-
Potent and selective inhibitors of breast Cancer resistance protein (ABCG2) derived from the p-glycoprotein (ABCB1) modulator tariquidar
-
M. Kühnle M. Egger C. Müller A. Mahringer G. Bernhardt G. Fricker B. König A. Buschauer Potent and selective inhibitors of breast Cancer resistance protein (ABCG2) derived from the p-glycoprotein (ABCB1) modulator tariquidar J. Med. Chem. 52 2009 1190 1197
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1190-1197
-
-
Kühnle, M.1
Egger, M.2
Müller, C.3
Mahringer, A.4
Bernhardt, G.5
Fricker, G.6
König, B.7
Buschauer, A.8
-
34
-
-
84866743102
-
Synthesis and biological evaluation of novel piperazine derivatives of flavone as potent anti-inflammatory and antimicrobial agent
-
G.D. Hatnapure A.P. Keche A.H. Rodge S.S. Birajdar R.H. Tale V.M. Kamble Synthesis and biological evaluation of novel piperazine derivatives of flavone as potent anti-inflammatory and antimicrobial agent Bioorg. Med. Chem. Lett. 22 2012 6385 6390
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 6385-6390
-
-
Hatnapure, G.D.1
Keche, A.P.2
Rodge, A.H.3
Birajdar, S.S.4
Tale, R.H.5
Kamble, V.M.6
-
35
-
-
0029007262
-
Structure determination and synthesis of fluoro nissl Green: An RNA-binding fluorochrome
-
C.A. Merlic S. Motamed B. Quinn Structure determination and synthesis of fluoro nissl Green: an RNA-binding fluorochrome J. Org. Chem. 60 1995 3365 3369
-
(1995)
J. Org. Chem.
, vol.60
, pp. 3365-3369
-
-
Merlic, C.A.1
Motamed, S.2
Quinn, B.3
-
36
-
-
34247182705
-
Phase evolution and magnetic properties of PrxFe82g'xg'yTiyCo10B4C4 (x Combining double low line 9-10.5; Y Combining double low line 0, 2) nanocomposites
-
A.H. Li C.H. Chiu H.W. Chang W.C. Chang W. Li Phase evolution and magnetic properties of PrxFe82g'xg'yTiyCo10B4C4 (x Combining double low line 9-10.5; y Combining double low line 0, 2) nanocomposites J. Alloys Compd. 437 2007 197 202
-
(2007)
J. Alloys Compd.
, vol.437
, pp. 197-202
-
-
Li, A.H.1
Chiu, C.H.2
Chang, H.W.3
Chang, W.C.4
Li, W.5
-
37
-
-
84856382939
-
Substituted chromones as highly potent nontoxic inhibitors, specific for the breast Cancer resistance protein
-
G. Valdameri E. Genoux-Bastide B. Peres C. Gauthier J. Guitton R. Terreux S.M.B. Winnischofer M.E.M. Rocha A. Boumendjel A. Di Pietro Substituted chromones as highly potent nontoxic inhibitors, specific for the breast Cancer resistance protein J. Med. Chem. 55 2012 966 970
-
(2012)
J. Med. Chem.
, vol.55
, pp. 966-970
-
-
Valdameri, G.1
Genoux-Bastide, E.2
Peres, B.3
Gauthier, C.4
Guitton, J.5
Terreux, R.6
Winnischofer, S.M.B.7
Rocha, M.E.M.8
Boumendjel, A.9
Di Pietro, A.10
-
38
-
-
84879560505
-
8-Benzamidochromen-4-one-2-carboxylic acids: Potent and selective agonists for the Orphan g protein-coupled receptor GPR35
-
M. Funke D. Thimm A.C. Schiedel C.E. Müller 8-Benzamidochromen-4-one-2-carboxylic acids: potent and selective agonists for the Orphan g protein-coupled receptor GPR35 J. Med. Chem. 56 2013 5182 5197
-
(2013)
J. Med. Chem.
, vol.56
, pp. 5182-5197
-
-
Funke, M.1
Thimm, D.2
Schiedel, A.C.3
Müller, C.E.4
-
40
-
-
84954148195
-
-
University of Regensburg
-
S. Bauer Quinoline Carboxamides as Modulators of Breast Cancer Resistance Protein (ABCG2): Investigations on Potency, Selectivity, Mechanism of Action, Cytotoxicity, Stability and Drug-like properties., in 2014 University of Regensburg
-
(2014)
Quinoline Carboxamides as Modulators of Breast Cancer Resistance Protein (ABCG2): Investigations on Potency, Selectivity, Mechanism of Action, Cytotoxicity, Stability and Drug-like properties., in
-
-
Bauer, S.1
-
42
-
-
0022272171
-
Mechanism of toxicity of nitro compounds used in the chemotherapy of trichomoniasis
-
S.N. Moreno R. Docampo Mechanism of toxicity of nitro compounds used in the chemotherapy of trichomoniasis Environ. Health Perspect. 64 1985 199 208
-
(1985)
Environ. Health Perspect.
, vol.64
, pp. 199-208
-
-
Moreno, S.N.1
Docampo, R.2
-
44
-
-
20344390019
-
Design, synthesis, and biological testing of thiosalicylamides as a novel class of calcium channel blockers
-
A.S. Mehanna J.Y. Kim Design, synthesis, and biological testing of thiosalicylamides as a novel class of calcium channel blockers Biorg. Med. Chem. 13 2005 4323 4331
-
(2005)
Biorg. Med. Chem.
, vol.13
, pp. 4323-4331
-
-
Mehanna, A.S.1
Kim, J.Y.2
-
45
-
-
33747660228
-
Synthesis and biological evaluation of benzopyran analogues bearing class III antiarrhythmic pharmacophores
-
M. Koufaki C. Kiziridi P. Papazafiri A. Vassilopoulos A. Varro Z. Nagy A. Farkas A. Makriyannis Synthesis and biological evaluation of benzopyran analogues bearing class III antiarrhythmic pharmacophores Biorg. Med. Chem. 14 2006 6666 6678
-
(2006)
Biorg. Med. Chem.
, vol.14
, pp. 6666-6678
-
-
Koufaki, M.1
Kiziridi, C.2
Papazafiri, P.3
Vassilopoulos, A.4
Varro, A.5
Nagy, Z.6
Farkas, A.7
Makriyannis, A.8
-
46
-
-
33748759801
-
Small-molecule activation of procaspase-3 to caspase-3 as a personalized anticancer strategy
-
K.S. Putt G.W. Chen J.M. Pearson J.S. Sandhorst M.S. Hoagland J.T. Kwon S.K. Hwang H. Jin M.I. Churchwell M.H. Cho D.R. Doerge W.G. Helferich P.J. Hergenrother Small-molecule activation of procaspase-3 to caspase-3 as a personalized anticancer strategy Nat. Chem. Biol. 2 2006 543 550
-
(2006)
Nat. Chem. Biol.
, vol.2
, pp. 543-550
-
-
Putt, K.S.1
Chen, G.W.2
Pearson, J.M.3
Sandhorst, J.S.4
Hoagland, M.S.5
Kwon, J.T.6
Hwang, S.K.7
Jin, H.8
Churchwell, M.I.9
Cho, M.H.10
Doerge, D.R.11
Helferich, W.G.12
Hergenrother, P.J.13
-
47
-
-
70349640055
-
Discovery of novel protease activated receptors 1 antagonists with potent antithrombotic activity in vivo
-
M. Perez M. Lamothe C. Maraval E. Mirabel C. Loubat B. Planty C. Horn J. Michaux S. Marrot R. Letienne C. Pignier A. Bocquet F. Nadal-Wollbold D. Cussac L. de Vries B. Le Grand Discovery of novel protease activated receptors 1 antagonists with potent antithrombotic activity in vivo J. Med. Chem. 52 2009 5826 5836
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5826-5836
-
-
Perez, M.1
Lamothe, M.2
Maraval, C.3
Mirabel, E.4
Loubat, C.5
Planty, B.6
Horn, C.7
Michaux, J.8
Marrot, S.9
Letienne, R.10
Pignier, C.11
Bocquet, A.12
Nadal-Wollbold, F.13
Cussac, D.14
De Vries, L.15
Le Grand, B.16
-
48
-
-
1242307864
-
Biologically active compounds through catalysis: Efficient synthesis of N-(heteroarylcarbonyl)-N '-(arylalkyl)piperazines
-
K. Kumar D. Michalik I.G. Castro A. Tillack A. Zapf M. Arlt T. Heinrich H. Bottcher M. Beller Biologically active compounds through catalysis: efficient synthesis of N-(heteroarylcarbonyl)-N '-(arylalkyl)piperazines Chem-Eur J. 10 2004 746 757
-
(2004)
Chem-Eur J.
, vol.10
, pp. 746-757
-
-
Kumar, K.1
Michalik, D.2
Castro, I.G.3
Tillack, A.4
Zapf, A.5
Arlt, M.6
Heinrich, T.7
Bottcher, H.8
Beller, M.9
-
49
-
-
70349433777
-
Procaspase-3 activation as an Anti-Cancer strategy: Structure-activity relationship of procaspase-activating compound 1 (PAC-1) and its cellular co-localization with Caspase-3
-
Q.P. Peterson D.C. Hsu D.R. Goode C.J. Novotny R.K. Totten P.J. Hergenrother Procaspase-3 activation as an Anti-Cancer strategy: structure-activity relationship of procaspase-activating compound 1 (PAC-1) and its cellular co-localization with Caspase-3 J. Med. Chem. 52 2009 5721 5731
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5721-5731
-
-
Peterson, Q.P.1
Hsu, D.C.2
Goode, D.R.3
Novotny, C.J.4
Totten, R.K.5
Hergenrother, P.J.6
-
50
-
-
84954151262
-
-
Bernd; Stegmeier, Karlheinz; Pill, Johannes, carboxylic acid derivatives and drugs containing them, in, Boehringer Mannh. G.m.b.H., Fed. Rep. Ger.
-
E.C.W. Witte, Hans Peter; Hagenbruch, Bernd; Stegmeier, Karlheinz; Pill, Johannes, carboxylic acid derivatives and drugs containing them, in, Boehringer Mannh. G.m.b.H., Fed. Rep. Ger.., 1983, pp. 97.
-
(1983)
Hans Peter; Hagenbruch
, pp. 97
-
-
Witte, E.C.W.1
-
51
-
-
84872156428
-
Design, synthesis and biological evaluation of novel piperazine derivatives as CCR5 antagonists
-
T. Liu Z. Weng X. Dong L. Chen L. Ma S. Cen N. Zhou Y. Hu Design, synthesis and biological evaluation of novel piperazine derivatives as CCR5 antagonists PLoS One 8 2013 e53636
-
(2013)
PLoS One
, vol.8
, pp. e53636
-
-
Liu, T.1
Weng, Z.2
Dong, X.3
Chen, L.4
Ma, L.5
Cen, S.6
Zhou, N.7
Hu, Y.8
-
52
-
-
27744484135
-
Synthesis and biological evaluation as AChE inhibitors of new indanones and thiaindanones related to donepezil
-
Z. Omran T. Cailly E. Lescot J.S.D. Santos J.H. Agondanou V. Lisowski F. Fabis A.M. Godard S. Stiebing G. Le Flem M. Boulouard F. Dauphin P. Dallemagne S. Rault Synthesis and biological evaluation as AChE inhibitors of new indanones and thiaindanones related to donepezil Eur. J. Med. Chem. 40 2005 1222 1245
-
(2005)
Eur. J. Med. Chem.
, vol.40
, pp. 1222-1245
-
-
Omran, Z.1
Cailly, T.2
Lescot, E.3
Santos, J.S.D.4
Agondanou, J.H.5
Lisowski, V.6
Fabis, F.7
Godard, A.M.8
Stiebing, S.9
Le Flem, G.10
Boulouard, M.11
Dauphin, F.12
Dallemagne, P.13
Rault, S.14
-
53
-
-
84859866823
-
Design, synthesis, and biological activity of novel 1,4-disubstituted piperidine/piperazine derivatives as CCR5 antagonist-based HIV-1 entry inhibitors
-
M.X. Dong L. Lu H.T. Li X.H. Wang H. Lu S.B. Jiang Q.Y. Dai Design, synthesis, and biological activity of novel 1,4-disubstituted piperidine/piperazine derivatives as CCR5 antagonist-based HIV-1 entry inhibitors Bioorg. Med. Chem. Lett. 22 2012 3284 3286
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 3284-3286
-
-
Dong, M.X.1
Lu, L.2
Li, H.T.3
Wang, X.H.4
Lu, H.5
Jiang, S.B.6
Dai, Q.Y.7
-
54
-
-
84863268463
-
Structure-based optimization of the piperazino-containing 1,3-disubstituted ureas affording sub-nanomolar inhibitors of soluble epoxide hydrolase
-
S.X. Huang B. Cao C. Morisseau Y. Tin B.D. Hammock Y.Q. Long Structure-based optimization of the piperazino-containing 1,3-disubstituted ureas affording sub-nanomolar inhibitors of soluble epoxide hydrolase Medchemcomm 3 2012 379 384
-
(2012)
Medchemcomm
, vol.3
, pp. 379-384
-
-
Huang, S.X.1
Cao, B.2
Morisseau, C.3
Tin, Y.4
Hammock, B.D.5
Long, Y.Q.6
-
56
-
-
79952364637
-
Synthesis and biological evaluation of 2,4-diaminoquinazoline derivatives as novel heat shock protein 90 inhibitors
-
D.A. Thorat M.R. Doddareddy S.H. Seo T.-J. Hong Y.S. Cho J.-S. Hahn A.N. Pae Synthesis and biological evaluation of 2,4-diaminoquinazoline derivatives as novel heat shock protein 90 inhibitors Bioorg. Med. Chem. Lett. 21 2011 1593 1597
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 1593-1597
-
-
Thorat, D.A.1
Doddareddy, M.R.2
Seo, S.H.3
Hong, T.-J.4
Cho, Y.S.5
Hahn, J.-S.6
Pae, A.N.7
-
57
-
-
84862587418
-
Gas-Phase chemistry of benzyl cations in dissociation of n-benzylammonium and n-benzyliminium ions studied by mass spectrometry
-
Y. Chai L. Wang H. Sun C. Guo Y. Pan Gas-Phase chemistry of benzyl cations in dissociation of n-benzylammonium and n-benzyliminium ions studied by mass spectrometry J. Am. Soc. Mass. Spectrom. 23 2012 823 833
-
(2012)
J. Am. Soc. Mass. Spectrom.
, vol.23
, pp. 823-833
-
-
Chai, Y.1
Wang, L.2
Sun, H.3
Guo, C.4
Pan, Y.5
-
58
-
-
33748272311
-
A mild and efficient procedure for the preparation of chromone-2-carboxylates
-
J.H. Yu Y.S. Yang R.Y. Ji A mild and efficient procedure for the preparation of chromone-2-carboxylates Chin. Chem. Lett. 17 2006 1005 1008
-
(2006)
Chin. Chem. Lett.
, vol.17
, pp. 1005-1008
-
-
Yu, J.H.1
Yang, Y.S.2
Ji, R.Y.3
-
60
-
-
84856914519
-
New Tacrine-4-oxo-4 h -chromene hybrids as Multifunctional agents for the treatment of Alzheimer's disease, with cholinergic, antioxidant, and β-amyloid-reducing properties
-
M.I. Fernández-Bachiller C. Pérez L. Monjas J. Rademann M.I. Rodríguez-Franco New Tacrine-4-oxo-4 h -chromene hybrids as Multifunctional agents for the treatment of Alzheimer's disease, with cholinergic, antioxidant, and β-amyloid-reducing properties J. Med. Chem. 55 2012 1303 1317
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1303-1317
-
-
Fernández-Bachiller, M.I.1
Pérez, C.2
Monjas, L.3
Rademann, J.4
Rodríguez-Franco, M.I.5
-
61
-
-
84954146944
-
Preparation of chromone derivatives as osteogenesis promoters and process for the preparation of the same
-
Masahiro; Mori, Akira Japan
-
T.K. Yasuma, Masahiro; Mori, Akira, Preparation of chromone derivatives as osteogenesis promoters and process for the preparation of the same, in, Takeda chemical Industries, Ltd., Japan, 2001, pp. 64.
-
(2001)
Takeda Chemical Industries, Ltd.
, pp. 64
-
-
Yasuma, T.K.1
-
62
-
-
0029011403
-
Synthesis and activity against multidrug resistance in Chinese hamster Ovary cells of new acridone-4-carboxamides
-
N. Dodic B. Dumaitre A. Daugan P. Pianetti Synthesis and activity against multidrug resistance in chinese hamster Ovary cells of new acridone-4-carboxamides J. Med. Chem. 38 1995 2418 2426
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2418-2426
-
-
Dodic, N.1
Dumaitre, B.2
Daugan, A.3
Pianetti, P.4
-
63
-
-
0033593855
-
Reversal of P-glycoprotein mediated multidrug resistance by novel anthranilamide derivatives
-
M. Roe A. Folkes P. Ashworth J. Brumwell L. Chima S. Hunjan I. Pretswell W. Dangerfield H. Ryder P. Charlton Reversal of P-glycoprotein mediated multidrug resistance by novel anthranilamide derivatives Bioorg. Med. Chem. Lett. 9 1999 595 600
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 595-600
-
-
Roe, M.1
Folkes, A.2
Ashworth, P.3
Brumwell, J.4
Chima, L.5
Hunjan, S.6
Pretswell, I.7
Dangerfield, W.8
Ryder, H.9
Charlton, P.10
-
65
-
-
0033610801
-
Functional multidrug resistance protein (MRP1) lacking the n-terminal transmembrane domain
-
É. Bakos R. Evers G. Szakács G.E. Tusnády E. Welker K. Szabó M. de Haas L. van Deemter P. Borst A. Váradi B. Sarkadi Functional multidrug resistance protein (MRP1) lacking the n-terminal transmembrane domain J. Biol. Chem. 273 1998 32167 32175
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 32167-32175
-
-
Bakos, É.1
Evers, R.2
Szakács, G.3
Tusnády, G.E.4
Welker, E.5
Szabó, K.6
De Haas, M.7
Van Deemter, L.8
Borst, P.9
Váradi, A.10
Sarkadi, B.11
-
66
-
-
0026543285
-
Standardized kinetic microassay to quantify differential chemosensitivity on the basis of proliferative activity
-
G. Bernhardt H. Reile H. Birnböck T. Spruß H. Schönenberger Standardized kinetic microassay to quantify differential chemosensitivity on the basis of proliferative activity J. Cancer Res. Clin. Oncol. 118 1992 35 43
-
(1992)
J. Cancer Res. Clin. Oncol.
, vol.118
, pp. 35-43
-
-
Bernhardt, G.1
Reile, H.2
Birnböck, H.3
Spruß, T.4
Schönenberger, H.5
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