-
1
-
-
33845362839
-
Design, synthesis, and preliminary evaluation of doxazolidine carbamates as prodrugs activated by carboxylesterases
-
DOI 10.1021/jm060597e
-
Burkhart DJ, Barthel BL, Post GC, Kalet BT, Nafe JW, Shoemaker RK, Koch TH. Design, synthesis, and preliminary evaluation of doxazolidine carbamates as prodrugs activated by carboxylesterases. J Med Chem 2006;49:7002-7012. (Pubitemid 44885988)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.24
, pp. 7002-7012
-
-
Burkhart, D.J.1
Barthel, B.L.2
Post, G.C.3
Kalet, B.T.4
Nafie, J.W.5
Shoemaker, R.K.6
Koch, T.H.7
-
2
-
-
0035924183
-
Diaminoindanes as microsomal triglyceride transfer protein inhibitors
-
DOI 10.1021/jm010294e
-
Ksander GM, de Jesus R, Yuan A, Fink C, Moskal M, Carlson E, Kukkola P, Bilci N, Wallace E, Neubert A, Feldman D, Mogelesky T, Poirier K, Jeune M, Steele R, Wasvery J, Stephan Z, Cahill E, Webb R, Navarrete A, Lee W, Gibson J, Alexander N, Sharif H, Hospattankar A. Diaminoindanes as microsomal triglyceride transfer protein inhibitors. J Med Chem 2001;44:4677-4687. (Pubitemid 33144477)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.26
, pp. 4677-4687
-
-
Ksander, G.M.1
DeJesus, R.2
Yuan, A.3
Fink, C.4
Moskal, M.5
Carlson, E.6
Kukkola, P.7
Bilci, N.8
Wallace, E.9
Neubert, A.10
Feldman, D.11
Mogelesky, T.12
Poirier, K.13
Jeune, M.14
Steele, R.15
Wasvery, J.16
Stephan, Z.17
Cahill, E.18
Webb, R.19
Navarrete, A.20
Lee, W.21
Gibson, J.22
Alexander, N.23
Sharif, H.24
Hospattankar, A.25
more..
-
3
-
-
34147100699
-
Stabilization of G-quadruplex DNA and down-regulation of oncogene c-myc by quindoline derivatives
-
DOI 10.1021/jm0610088
-
Ou TM, Lu YJ, Zhang C, Huang ZS, Wang XD, Tan JH, Chen Y, Ma DL, Wong KY, Tang JCO, Chan ASC, Gu LQ. Stabilization of G-quadruplex DNA and down-regulation of oncogene c-myc by quindoline derivatives. J Med Chem 2007;50:1465-1474. (Pubitemid 46566333)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.7
, pp. 1465-1474
-
-
Ou, T.-M.1
Lu, Y.-J.2
Zhang, C.3
Huang, Z.-S.4
Wang, X.-D.5
Tan, J.-H.6
Chen, Y.7
Ma, D.-L.8
Wong, K.-Y.9
Tang, J.C.-O.10
Chan, A.S.-C.11
Gu, L.-Q.12
-
4
-
-
4644276576
-
New cytotoxic cyclic peptides and dianthramide from Dianthus superbus
-
Hsieh PW, Chang FR, Wu CC, Wu KY, Li CM, Chen SL, Wu YC. New cytotoxic cyclic peptides and dianthramide from Dianthus superbus. J Nat Prod 2004;67:1522-1527.
-
(2004)
J Nat Prod
, vol.67
, pp. 1522-1527
-
-
Hsieh, P.W.1
Chang, F.R.2
Wu, C.C.3
Wu, K.Y.4
Li, C.M.5
Chen, S.L.6
Wu, Y.C.7
-
5
-
-
0028142387
-
A specifc inhibitor of the epidermal growth factor receptor tyrosine kinase
-
Fry DW, Kraker AJ, McMichael A, Ambroso LA, Nelson JM, Leopold WR, Connors RW, Bridges AJ. A specifc inhibitor of the epidermal growth factor receptor tyrosine kinase. Science 1994;265:1093-1995.
-
(1994)
Science
, vol.265
, pp. 1093-1995
-
-
Fry, D.W.1
Kraker, A.J.2
McMichael, A.3
Ambroso, L.A.4
Nelson, J.M.5
Leopold, W.R.6
Connors, R.W.7
Bridges, A.J.8
-
6
-
-
0028106163
-
Epidermal growth factor receptor tyrosine kinase. Investigation of catalytic mechanism, structure based searching and discovery of a potent inhibitor
-
Ward WHJ, Cook PN, Slater AM, Davies DH, Holdgate GA, Green LR. Epidermal growth factor receptor tyrosine kinase. Investigation of catalytic mechanism, structure based searching and discovery of a potent inhibitor. Biochem Pharmacol 1994;48:659-666.
-
(1994)
Biochem Pharmacol
, vol.48
, pp. 659-666
-
-
Whj, W.1
Cook, P.N.2
Slater, A.M.3
Davies, D.H.4
Holdgate, G.A.5
Green, L.R.6
-
7
-
-
0035899182
-
6-Substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity
-
DOI 10.1021/jm0005555
-
Tsou HR, Mamuya N, Johnson BD, Reich MF, Gruber BC, Ye F, Nilakantan R, Shen R, Discafani C, DeBlanc R, Davis R, Koehn FE, Greenberger LM, Wang YF, Wissner A. 6-Substituted-4-(3-bromophenylamino) quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity. J Med Chem 2001;44:2719-2734. (Pubitemid 32879714)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.17
, pp. 2719-2734
-
-
Tsou, H.R.1
Mamuya, N.2
Johnson, B.D.3
Reich, M.F.4
Gruber, B.C.5
Ye, F.6
Nilakantan, R.7
Shen, R.8
Discafani, C.9
DeBlanc, R.10
Davis, R.11
Koehn, F.E.12
Greenberger, L.M.13
Wang, Y.-F.14
Wissner, A.15
-
8
-
-
0030039555
-
Tyrosine kinase inhibitors 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth receptor
-
Bridges AJ, Zhou H, Cody DR, Rewcastle GW, McMichael A, Showalter HDH, Fry DW, Kraker AJ, Denny W. Tyrosine kinase inhibitors 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7- dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth receptor. J Med Chem 1996;39:267-276.
-
(1996)
J Med Chem
, vol.39
, pp. 267-276
-
-
Bridges, A.J.1
Zhou, H.2
Cody, D.R.3
Rewcastle, G.W.4
McMichael, A.5
Hdh, S.6
Fry, D.W.7
Kraker, A.J.8
Denny, W.9
-
9
-
-
33745123646
-
The combi-targeting concept: Synthesis of stable nitrosoureas designed to inhibit the epidermal growth factor receptor (EGFR)
-
DOI 10.1021/jm0600390
-
Domarkas J, Dudouit F, Williams C, Qiyu Q, Banerjee R, Brahimi F, Jean-Claude BJ. Te combi-targeting concept: synthesis of stable nitrosoureas designed to inhibit the epidermal growth factor rceptor (EGFR). J Med Chem 2006;49:3544-3552. (Pubitemid 43902460)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.12
, pp. 3544-3552
-
-
Domarkas, J.1
Dudouit, F.2
Williams, C.3
Qiyu, Q.4
Banerjee, R.5
Brahimi, F.6
Jean-Claude, B.J.7
-
10
-
-
0142124197
-
Receptor-Guided Alignment-Based Comparative 3D-QSAR Studies of Benzylidene Malonitrile Tyrphostins as EGFR and HER-2 Kinase Inhibitors
-
DOI 10.1021/jm030065n
-
Kamath S, Buolamwini JK. Receptor-guided alignment-based comparative 3D-QSAR studies of benzylidene malonitrile tyrphostins as EGFR and HER-2 kinase inhibitors. J Med Chem 2003;46:4657-4668. (Pubitemid 37271615)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.22
, pp. 4657-4668
-
-
Kamath, S.1
Buolamwini, J.K.2
-
11
-
-
0036785528
-
Inhibition of epidermal growth factor receptor.mediated signaling by "combi-triazene" BJ2000, a new probe for combi-targeting postulates
-
Brahimi F, Matheson SL, Dudouit F, McNamee JP, Tari AM, Jean-Claude BJ. Inhibition of epidermal growth factor receptor.mediated signaling by "combi-triazene" BJ2000, a new probe for combi-targeting postulates. J Pharmacol Exp Ter 2002;303:238-246.
-
(2002)
J Pharmacol Exp ter
, vol.303
, pp. 238-246
-
-
Brahimi, F.1
Matheson, S.L.2
Dudouit, F.3
McNamee, J.P.4
Tari, A.M.5
Jean-Claude, B.J.6
-
12
-
-
0035119740
-
Design of a chimeric 3-methyl-1,2,3-triazene with mixed receptor tyrosine kinase and DNA damaging properties: A novel tumor targeting strategy
-
Matheson SL, McNamee J, Jean-Claude BJ. Design of a chimeric 3-methyl-1,2,3-triazene with mixed receptor tyrosine kinase and DNA damaging properties: a novel tumor targeting strategy. J Pharmacol Exp Ter 2001;296:832-840. (Pubitemid 32187355)
-
(2001)
Journal of Pharmacology and Experimental Therapeutics
, vol.296
, Issue.3
, pp. 832-840
-
-
Matheson, S.L.1
McNamee, J.2
Jean-Claude, B.J.3
-
13
-
-
0027930576
-
Expression of epidermal growth factor receptor and proliferating cell nuclear antigen predicts response of esophageal squamous cell carcinoma to chemoradiotherapy
-
DOI 10.1002/1097-0142(19940915)74:6<1693::AID-CNCR2820740609>3.0. CO;2-#
-
Hickey K, Grehan D, Reid IM, O'Briain S, Walsh TN, Hennessy TPJ. Expression of epidermal growth-factor receptor and proliferating cell nuclear antigen predicts response of neophageal squamous-cell carcinoma to chemoradiotherapy. Cancer 1994;74:1693-1698. (Pubitemid 24301821)
-
(1994)
Cancer
, vol.74
, Issue.6
, pp. 1693-1698
-
-
Hickey, K.1
Grehan, D.2
Reid, I.M.3
O'Briain, S.4
Walsh, T.N.5
Hennessy, T.P.J.6
-
15
-
-
0028670125
-
Te biology of ErbB-2 neu her-2 and its role in cancer
-
Hynes NE, Stern DF. Te biology of ErbB-2 neu her-2 and its role in cancer. Biochim Biophys Acta 1994;1198:165-184.
-
(1994)
Biochim Biophys Acta
, vol.1198
, pp. 165-184
-
-
Hynes, N.E.1
Stern, D.F.2
-
16
-
-
0026028343
-
Prevalence of aberrant expression of the epidermal growth-factor receptor in human cancers
-
Gullick WJ. Prevalence of aberrant expression of the epidermal growth-factor receptor in human cancers. Br Med Bull 1991;47:87-98.
-
(1991)
Br Med Bull
, vol.47
, pp. 87-98
-
-
Gullick, W.J.1
-
17
-
-
0028800035
-
Frequent expression of a mutant epidermal growth-factor receptor in multiple human tumors
-
Moscatello DK, Holgado-Mudruga M, Godwin AK, Ramirez G, Gunn G, Zoltick PW, Biegel JA, Hayes RL, Wong AJ. Frequent expression of a mutant epidermal growth-factor receptor in multiple human tumors. Cancer Res 1995;55:5536-5539.
-
(1995)
Cancer Res
, vol.55
, pp. 5536-5539
-
-
Moscatello, D.K.1
Holgado-Mudruga, M.2
Godwin, A.K.3
Ramirez, G.4
Gunn, G.5
Zoltick, P.W.6
Biegel, J.A.7
Hayes, R.L.8
Wong, A.J.9
-
18
-
-
0030832167
-
Cell surface localization and density of the tumor-associated variant of the epidermal growth factor receptor, EGFRvIII
-
Wikstrand C J, McLendon RE, Friedman A, Bigner DD. Cell surface localization and density of the tumor-associated variant of the epidermal growth factor receptor, EGFRvIII. Cancer Res 1997;57:4130-4140. (Pubitemid 27427708)
-
(1997)
Cancer Research
, vol.57
, Issue.18
, pp. 4130-4140
-
-
Wikstrand, C.J.1
McLendon, R.E.2
Friedman, A.H.3
Bigner, D.D.4
-
19
-
-
0032830412
-
The rationale and strategy used to develop a series of highly potent, irreversible, inhibitors of the epidermal growth factor receptor family of tyrosine kinases
-
Bridges AJ. Te rationale and strategy used to develop a series of highly potent, irreversible, inhibitors of the epidermal growth factor receptor family of tyrosine kinases. Curr Med Chem 1999;6:825-843. (Pubitemid 29422197)
-
(1999)
Current Medicinal Chemistry
, vol.6
, Issue.9
, pp. 825-843
-
-
Bridges, A.J.1
-
20
-
-
0033014592
-
Small molecule inhibitors of receptor tyrosine kinases
-
DOI 10.1358/dof.1999.024.05.858622
-
Boschelli DH. Small molecule inhibitors of receptor tyrosine kinases. Drugs Future 1999;24:515-537. (Pubitemid 29304797)
-
(1999)
Drugs of the Future
, vol.24
, Issue.5
, pp. 515-537
-
-
Boschelli, D.H.1
-
21
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function
-
Morris GM, Goodsell DS, Halliday RS, Huey R, Hart WE, Belew RK, Olson AJ. Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function. J Comput Chem 1998;19:1639-1662. (Pubitemid 128590223)
-
(1998)
Journal of Computational Chemistry
, vol.19
, Issue.14
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
Olson, A.J.7
-
22
-
-
0029705324
-
Automated docking of flexible ligands: Applications of AutoDock
-
Goodsell DS, Morris GM, Olson AJ, Automated docking of fexible ligands: applications of AutoDock. J. Mol. Recognit. 1996;9,1-5. (Pubitemid 126565462)
-
(1996)
Journal of Molecular Recognition
, vol.9
, Issue.1
, pp. 1-5
-
-
Goodsell, D.S.1
Morris, G.M.2
Olson, A.J.3
-
23
-
-
33947716119
-
Software news and update a semiempirical free energy force field with charge-based desolvation
-
DOI 10.1002/jcc.20634
-
Huey R, Morris GM, Olson AJ, Goodsell DS. A semiempirical free energy force feld with charge-based desolvation. J Comput Chem 2007;28:1145-1152. (Pubitemid 46506716)
-
(2007)
Journal of Computational Chemistry
, vol.28
, Issue.6
, pp. 1145-1152
-
-
Huey, R.1
Morris, G.M.2
Olson, A.J.3
Goodsell, D.S.4
-
24
-
-
58149166932
-
A cation-pi interaction in the binding site of the glycine receptor is mediated by a phenylalanine residue
-
Pless SA, Millen KS, Hanek AP, Lynch JW, Lester HA, Lummis SCR, Dougherty DA. A cation-pi interaction in the binding site of the glycine receptor is mediated by a phenylalanine residue. J Neurosci 2008;28:10937-10942.
-
(2008)
J Neurosci
, vol.28
, pp. 10937-10942
-
-
Pless, S.A.1
Millen, K.S.2
Hanek, A.P.3
Lynch, J.W.4
Lester, H.A.5
Scr, L.6
Dougherty, D.A.7
-
25
-
-
51149094684
-
Synthesis antiproliferative activity, and structure-activity relationships of 3-aryl-1H-quinolin-4-ones
-
Xiao ZP, Li HQ, Shi L, Lv PC, Song ZC, Zhua HL. Synthesis, antiproliferative activity, and structure-activity relationships of 3-aryl-1H-quinolin-4-ones. Chem Med Chem 2008;3:1077-1082.
-
(2008)
Chem Med Chem
, vol.3
, pp. 1077-1082
-
-
Xiao, Z.P.1
Li, H.Q.2
Shi, L.3
Lv, P.C.4
Song, Z.C.5
Zhua, H.L.6
-
26
-
-
0035899182
-
6-Substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity
-
DOI 10.1021/jm0005555
-
Tsou HR, Mamuya N, Johnson BD, Reich MF, Gruber BC, Ye F, Nilakantan R, Shen R, Discafani C, DeBlanc R, Davis R, Koehn FE, Greenberger LM, Wang YF, Wissner A. 6-Substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity. J Med Chem 2001;44:2719-2734. (Pubitemid 32879714)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.17
, pp. 2719-2734
-
-
Tsou, H.R.1
Mamuya, N.2
Johnson, B.D.3
Reich, M.F.4
Gruber, B.C.5
Ye, F.6
Nilakantan, R.7
Shen, R.8
Discafani, C.9
DeBlanc, R.10
Davis, R.11
Koehn, F.E.12
Greenberger, L.M.13
Wang, Y.-F.14
Wissner, A.15
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