-
1
-
-
33744487399
-
Preparation, antimicrobial activity and toxicity of 2-amino-4- arylthiazole derivatives
-
P.M. Bonilla, A.P. Cardena, E.Q. Marmol, J.L.A. Tellez, and G.J.M. Rejon Preparation, antimicrobial activity and toxicity of 2-amino-4-arylthiazole derivatives Heteroatom Chem. 17 2006 254 260
-
(2006)
Heteroatom Chem.
, vol.17
, pp. 254-260
-
-
Bonilla, P.M.1
Cardena, A.P.2
Marmol, E.Q.3
Tellez, J.L.A.4
Rejon, G.J.M.5
-
2
-
-
77951948974
-
Synthesis and antibacterial evaluation of some novel 2-arylamino-4- phenyl-thiazolyl derivatives
-
K.A. Parmar, B.G. Suthar, and S. Parajapati Synthesis and antibacterial evaluation of some novel 2-arylamino-4-phenyl-thiazolyl derivatives Bull. Korean Chem. Soc. 31 2010 793 797
-
(2010)
Bull. Korean Chem. Soc.
, vol.31
, pp. 793-797
-
-
Parmar, K.A.1
Suthar, B.G.2
Parajapati, S.3
-
3
-
-
77956928074
-
Synthesis and biological evaluation of some substituted aminothiazole derivatives
-
A.K. Prajapati, and V.P. Modi Synthesis and biological evaluation of some substituted aminothiazole derivatives J. Chil. Chem. Soc. 55 2010 240 243
-
(2010)
J. Chil. Chem. Soc.
, vol.55
, pp. 240-243
-
-
Prajapati, A.K.1
Modi, V.P.2
-
4
-
-
77956032489
-
Synthesis and anti-microbial activity of (Z)-4-(4-substituted-thiazol-2- yl)-1-(2-oxoindolin-3-ylidene) semicarbazide and its derivatives
-
S.M. Basavarajaiah, and B.H.M. Mruthyunjayaswamy Synthesis and anti-microbial activity of (Z)-4-(4-substituted-thiazol-2-yl)-1-(2-oxoindolin-3- ylidene) semicarbazide and its derivatives Indian J. Chem. 49B 2010 1117 1126
-
(2010)
Indian J. Chem.
, vol.49 B
, pp. 1117-1126
-
-
Basavarajaiah, S.M.1
Mruthyunjayaswamy, B.H.M.2
-
5
-
-
84863409444
-
Synthesis, characterization and antimicrobial activity of new pyrrole derivatives
-
A. Idhayadhulla, R.S. Kumar, and A.J.A. Nasser Synthesis, characterization and antimicrobial activity of new pyrrole derivatives J. Mex. Chem. Soc. 55 2011 218 223
-
(2011)
J. Mex. Chem. Soc.
, vol.55
, pp. 218-223
-
-
Idhayadhulla, A.1
Kumar, R.S.2
Nasser, A.J.A.3
-
6
-
-
0028943543
-
Novel thiazole based heterocycles as inhibitors of LFA-l/ICAM-1 mediated cell adhesion
-
P.J. Sanfilippo, M.C. Jetter, R. Cordova, R.A. Noe, E. Chourmouzis, C.Y. Lau, and E. Wangt Novel thiazole based heterocycles as inhibitors of LFA-l/ICAM-1 mediated cell adhesion J. Med. Chem. 38 1995 1057 1059
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1057-1059
-
-
Sanfilippo, P.J.1
Jetter, M.C.2
Cordova, R.3
Noe, R.A.4
Chourmouzis, E.5
Lau, C.Y.6
Wangt, E.7
-
7
-
-
84887025556
-
Synthesis of novel thiazole derivatives as analgesic agents
-
G. Saravanan, V. Alagarsamy, C.R. Prakash, P.D. Kumar, and T.P. Selvam Synthesis of novel thiazole derivatives as analgesic agents Asian J. Res. Pharm. Sci. 1 2011 134 138
-
(2011)
Asian J. Res. Pharm. Sci.
, vol.1
, pp. 134-138
-
-
Saravanan, G.1
Alagarsamy, V.2
Prakash, C.R.3
Kumar, P.D.4
Selvam, T.P.5
-
8
-
-
77349097539
-
Triazole incorporated thiazoles as a new class of anticonvulsants: Design, synthesis and in vivo screening
-
N. Siddiqui, and W. Ahsan Triazole incorporated thiazoles as a new class of anticonvulsants: design, synthesis and in vivo screening Eur. J. Med. Chem. 45 2010 1536 1543
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 1536-1543
-
-
Siddiqui, N.1
Ahsan, W.2
-
9
-
-
79952701822
-
Synthesis, anticonvulsant and toxicity screening of thiazolyl-thiadiazole derivatives
-
N. Siddiqui, and W. Ahsan Synthesis, anticonvulsant and toxicity screening of thiazolyl-thiadiazole derivatives Med. Chem. Res. 20 2011 261 268
-
(2011)
Med. Chem. Res.
, vol.20
, pp. 261-268
-
-
Siddiqui, N.1
Ahsan, W.2
-
10
-
-
3242877443
-
Synthesis and biological evaluation of new 4,5-disubstituted-thiazolyl amides, derivatives of 4-hydroxy-piperidine or of 4-N-methyl piperazine
-
A. Geronikaki, D.H. Litina, C. Chatziopoulos, and G. Soloupis Synthesis and biological evaluation of new 4,5-disubstituted thiazolyl amides, derivatives of 4-hydroxypiperidine or of 4-N-methyl piperazine Molecules 8 2003 472 479 (Pubitemid 38999145)
-
(2003)
Molecules
, vol.8
, Issue.6
, pp. 472-479
-
-
Geronikaki, A.1
Hadjipavlou-Litina, D.2
Chatziopoulos, C.3
Soloupis, G.4
-
11
-
-
77954348948
-
Synthesis and hypolipidemic activity of novel 2-(4-(2-substituted aminothiazole-4-yl) phenoxy) acetic acid derivatives
-
S.N. Mokale, P.T. Sanap, and D.B. Shinde Synthesis and hypolipidemic activity of novel 2-(4-(2-substituted aminothiazole-4-yl) phenoxy) acetic acid derivatives Eur. J. Med. Chem. 45 2010 3096 3100
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 3096-3100
-
-
Mokale, S.N.1
Sanap, P.T.2
Shinde, D.B.3
-
12
-
-
0141923187
-
Synthesis and biological evaluation of benzo[d]isothiazole, benzothiazole and thiazole Schiff bases
-
DOI 10.1016/S0968-0896(03)00493-0
-
P. Vicini, A. Geronikaki, M. Incerti, B. Busonera, G. Poni, C.A. Cabras, and P.L. Colla Synthesis and biological evaluation of benzo[d]isothiazole, benzothiazole and thiazole Schiff bases Bioorg. Med. Chem. 11 2003 4785 4789 (Pubitemid 37230135)
-
(2003)
Bioorganic and Medicinal Chemistry
, vol.11
, Issue.22
, pp. 4785-4789
-
-
Vicini, P.1
Geronikaki, A.2
Incerti, M.3
Busonera, B.4
Poni, G.5
Cabras, C.A.6
La Colla, P.7
-
13
-
-
46249124820
-
Syntheses and reactions of methyl [3-(4-phenyl-thiazol-2-yl)-thioureido] alkanoates and related compounds
-
W. Fathalla Syntheses and reactions of methyl [3-(4-phenyl-thiazol-2-yl)- thioureido] alkanoates and related compounds ARKIVOC 12 2008 245 255
-
(2008)
ARKIVOC
, vol.12
, pp. 245-255
-
-
Fathalla, W.1
-
15
-
-
77649238025
-
1 receptor antagonists
-
1 receptor antagonists Bioorg. Med. Chem. 18 2010 2195 2203
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 2195-2203
-
-
Scheiff, A.B.1
Yerande, S.G.2
El-Tayeb, A.3
Li, W.4
Inamdar, G.S.5
Vasu, K.K.6
Sudarsanam, V.7
Müller, C.E.8
-
16
-
-
0033526107
-
4-Phenylthiazole derivatives inhibit IL-6 secretion in osteoblastic cells and suppress bone weight loss in ovariectomized mice
-
DOI 10.1016/S0960-894X(99)00122-5, PII S0960894X99001225
-
K. Yamaguchi, M. Yada, T. Tsuji, Y. Hatanaka, K.I. Goda, and T. Kobori 4-phenylthiazole derivatives inhibit IL-6 secretion in osteoblastic cells and suppress the bone weight loss in the ovariectomized mice Bioorg. Med. Chem. Lett. 9 1999 957 960 (Pubitemid 29179888)
-
(1999)
Bioorganic and Medicinal Chemistry Letters
, vol.9
, Issue.7
, pp. 957-960
-
-
Yamaguchi, K.1
Yada, M.2
Tsuji, T.3
Hatanaka, Y.4
Goda, K.-I.5
Kobori, T.6
-
17
-
-
2442652804
-
Design of new cognition enhancers: From computer prediction to synthesis and biological evaluation
-
DOI 10.1021/jm031086k
-
A.A. Geronikaki, J.C. Dearden, D. Filimonov, I. Galaeva, T.L. Garibova, T. Gloriozova, V. Krajneva, A. Lagunin, F.Z. Macaev, G. Molodavkin, V.V. Poroikov, S.I. Pogrebnoi, F. Shepeli, T.A. Voronina, M. Tsitlakidou, and L. Vlad Design of new cognition enhancers: from computer prediction to synthesis and biological evaluation J. Med. Chem. 47 2004 2870 2876 (Pubitemid 38656740)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.11
, pp. 2870-2876
-
-
Geronikaki, A.A.1
Dearden, J.C.2
Filimonov, D.3
Galaeva, I.4
Garibova, T.L.5
Gloriozova, T.6
Krajneva, V.7
Lagunin, A.8
Macaev, F.Z.9
Molodavkin, G.10
Poroikov, V.V.11
Pogrebnoi, S.I.12
Shepeli, F.13
Voronina, T.A.14
Tsitlakidou, M.15
Vlad, L.16
-
18
-
-
14544299554
-
Substituted thiazolamide coupled to a redox delivery system: A new γ-secretase inhibitor with enhanced pharmacokinetic profile
-
DOI 10.1039/b415090b
-
Y. Laras, G. Quelever, C. Garino, N. Pietrancosta, M. Sheha, F. Bihel, M.S. Wolfec, and J.L. Kraus Substituted thiazolamide coupled to a redox delivery system: a new γ-secretase inhibitor with enhanced pharmacokinetic profile Org. Biomol. Chem. 3 2005 612 618 (Pubitemid 40296614)
-
(2005)
Organic and Biomolecular Chemistry
, vol.3
, Issue.4
, pp. 612-618
-
-
Laras, Y.1
Quelever, G.2
Garino, C.3
Pietrancosta, N.4
Sheha, M.5
Bihel, F.6
Wolfe, M.S.7
Kraus, J.-L.8
-
19
-
-
79960016629
-
Substituted 2-aminothiazoles are exceptional inhibitors of neuronal degeneration in tau-driven models of Alzheimer's disease
-
I. Lagoja, C. Pannecouque, G. Griffioen, S. Wera, V.M. Rojasdelaparra, and A.V. Aerschot Substituted 2-aminothiazoles are exceptional inhibitors of neuronal degeneration in tau-driven models of Alzheimer's disease Eur. J. Pharm. Sci. 43 2011 386 392
-
(2011)
Eur. J. Pharm. Sci.
, vol.43
, pp. 386-392
-
-
Lagoja, I.1
Pannecouque, C.2
Griffioen, G.3
Wera, S.4
Rojasdelaparra, V.M.5
Aerschot, A.V.6
-
20
-
-
0015609611
-
A clinical review of bleomycin - A new antineoplastic agent
-
R.H. Blum, S.K. Carter, and K. agre A clinical review of bleomycin-a new antineoplastic agent Cancer 31 1973 903 914
-
(1973)
Cancer
, vol.31
, pp. 903-914
-
-
Blum, R.H.1
Carter, S.K.2
Agre, K.3
-
21
-
-
77950631247
-
Voreloxin, a first-in-class anticancer quinolone derivative in relapsed/refractory solid tumors: A report on two dosing schedules
-
R.H. Advani, H.I. Hurwitz, M.S. Gordon, S.W. Ebbinghaus, D.S. Mendelson, H.A. Wakelee, U. Hoch, J.A. Silverman, N.A. Havrilla, C.J. Berman, J.A. Fox, R.S. Allen, and D.C. Adelman Voreloxin, a first-in-class anticancer quinolone derivative in relapsed/refractory solid tumors: a report on two dosing schedules Clin. Cancer Res. 16 2010 2167 2175
-
(2010)
Clin. Cancer Res.
, vol.16
, pp. 2167-2175
-
-
Advani, R.H.1
Hurwitz, H.I.2
Gordon, M.S.3
Ebbinghaus, S.W.4
Mendelson, D.S.5
Wakelee, H.A.6
Hoch, U.7
Silverman, J.A.8
Havrilla, N.A.9
Berman, C.J.10
Fox, J.A.11
Allen, R.S.12
Adelman, D.C.13
-
22
-
-
3042701597
-
Epothilones: Mechanism of action and biologic activity
-
DOI 10.1200/JCO.2004.12.001
-
S. Goodin, M. Kane, and E. Rubin Epothilones: mechanism of action and biologic activity J. Clin. Oncol. 22 2004 2015 2025 (Pubitemid 41095195)
-
(2004)
Journal of Clinical Oncology
, vol.22
, Issue.10
, pp. 2015-2025
-
-
Goodin, S.1
Kane, M.P.2
Rubin, E.H.3
-
23
-
-
0034857182
-
The epothilones, eleutherobins, and related types of molecules
-
DOI 10.2174/1381612013397410
-
S. Stachel, K. Biswas, and S. Danishefsky The epothilones, eleutherobins and related types of molecules Curr. Pharm. Des. 7 2001 1277 1290 (Pubitemid 32798809)
-
(2001)
Current Pharmaceutical Design
, vol.7
, Issue.13
, pp. 1277-1290
-
-
Stachel, S.J.1
Biswas, K.2
Danishefsky, S.J.3
-
24
-
-
37448999906
-
Dasatinib: A tyrosine kinase inhibitor for the treatment of chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia
-
M. Steinberg Dasatinib: a tyrosine kinase inhibitor for the treatment of chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia Clin. Ther. 29 2007 2289 2308
-
(2007)
Clin. Ther.
, vol.29
, pp. 2289-2308
-
-
Steinberg, M.1
-
26
-
-
78651277432
-
Dasatinib, a multikinase inhibitor: Therapy, safety, and appropriate management of adverse events
-
S. Shayani Dasatinib, a multikinase inhibitor: therapy, safety, and appropriate management of adverse events Ther. Drug Monit. 32 2010 680 687
-
(2010)
Ther. Drug Monit.
, vol.32
, pp. 680-687
-
-
Shayani, S.1
-
27
-
-
70449704101
-
Synthesis and anticancer activity of N-bis(trifluoromethyl)alkyl- N′-thiazolyl and N-bis(trifluoromethyl)alkyl-N′-benzothiazolyl ureas
-
E.L. Luzina, and A.V. Popov Synthesis and anticancer activity of N-bis(trifluoromethyl)alkyl-N′-thiazolyl and N-bis(trifluoromethyl)alkyl- N′-benzothiazolyl ureas Eur. J. Med. Chem. 44 2009 4944 4953
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 4944-4953
-
-
Luzina, E.L.1
Popov, A.V.2
-
28
-
-
2342576239
-
Synthesis and biological activity of N-aryl-2-aminothiazoles: Potent pan inhibitors of cyclin-dependent kinases
-
DOI 10.1016/j.bmcl.2004.02.105, PII S0960894X04004342
-
R.N. Misra, H.Y. Xiao, D.K. Williams, K.S. Kim, S. Lu, K.A. Keller, J.G. Mulheron, R. Batorsky, J.S. Tokarski, J.S. Sack, S.D. Kimball, F.Y. Lee, and K.R. Webster Synthesis and biological activity of N-aryl-2-aminothiazoles: potent pan inhibitors of cyclin-dependent kinases Bioorg. Med. Chem. Lett. 14 2004 2973 2977 (Pubitemid 38578421)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.11
, pp. 2973-2977
-
-
Misra, R.N.1
Xiao, H.-Y.2
Williams, D.K.3
Kim, K.S.4
Lu, S.5
Keller, K.A.6
Mulheron, J.G.7
Batorsky, R.8
Tokarski, J.S.9
Sack, J.S.10
Kimball, S.D.11
Lee, F.Y.12
Webster, K.R.13
-
29
-
-
84995646145
-
Thiazole containing nitrogen mustards: Synthesis, structural evaluation, cytotoxicity and DNA binding studies
-
N.M. Raghavendra, S. Renuka, S.D. Gupta, and P. Divya Thiazole containing nitrogen mustards: synthesis, structural evaluation, cytotoxicity and DNA binding studies Lett. Drug Des. Discov. 8 2011 838 842
-
(2011)
Lett. Drug Des. Discov.
, vol.8
, pp. 838-842
-
-
Raghavendra, N.M.1
Renuka, S.2
Gupta, S.D.3
Divya, P.4
-
30
-
-
84887014773
-
2-Aminothiazole derivative as a new class of TrkA kinase inhibitor
-
J. Kim, Y. Moon, and S.W. Ham 2-Aminothiazole derivative as a new class of TrkA kinase inhibitor Bull. Korean Chem. Soc. 32 2011 2893 2894
-
(2011)
Bull. Korean Chem. Soc.
, vol.32
, pp. 2893-2894
-
-
Kim, J.1
Moon, Y.2
Ham, S.W.3
-
31
-
-
69949090680
-
2-Arylamino-4-amino-5-aroylthiazoles. "one-pot" synthesis and biological evaluation of a new class of inhibitors of tubulin polymerization
-
R. Romagnoli, P.G. Baraldi, M.D. Carrion, O.C. Lopez, C.L. Cara, G. Basso, G. Viola, M. Khedr, J. Balzarini, S. Mahboobi, A. Sellmer, A. Brancale, and E. Hamel 2-Arylamino-4-amino-5-aroylthiazoles. "One-pot" synthesis and biological evaluation of a new class of inhibitors of tubulin polymerization J. Med. Chem. 52 2009 5551 5555
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5551-5555
-
-
Romagnoli, R.1
Baraldi, P.G.2
Carrion, M.D.3
Lopez, O.C.4
Cara, C.L.5
Basso, G.6
Viola, G.7
Khedr, M.8
Balzarini, J.9
Mahboobi, S.10
Sellmer, A.11
Brancale, A.12
Hamel, E.13
-
32
-
-
0037140727
-
Synthesis of 5-deazathiogirollines: Analogs of a natural antitumor agent
-
DOI 10.1016/S0040-4020(02)00383-6, PII S0040402002003836
-
B. Schiavi, A. Ahond, A. Al-Mourabit, C. Poupat, A. Chiaroni, C. Gaspard, and P. Potier Synthesis of 5-deazathiogirollines: analogs of a natural antitumor agent Tetrahedron 58 2002 4201 4215 (Pubitemid 34518687)
-
(2002)
Tetrahedron
, vol.58
, Issue.21
, pp. 4201-4215
-
-
Schiavi, B.1
Ahond, A.2
Al-Mourabit, A.3
Poupat, C.4
Chiaroni, A.5
Gaspard, C.6
Potier, P.7
-
33
-
-
77955552154
-
Therapeutic effects of cantharidin analogues without bridging ether oxygen on human hepatocellular carcinoma cells
-
C.B. Yeh, C.J. Su, J.M. Hwang, and M.C. Chou Therapeutic effects of cantharidin analogues without bridging ether oxygen on human hepatocellular carcinoma cells Eur. J. Med. Chem. 45 2010 3981 3985
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 3981-3985
-
-
Yeh, C.B.1
Su, C.J.2
Hwang, J.M.3
Chou, M.C.4
-
34
-
-
84866731059
-
Substituted thiazoles VII. Synthesis and antitumor activity of certain 2-(substituted amino)-4-phenyl-1,3-thiazole analogs
-
G.S. Hassan, S.M. El-Messery, F.A.M. Al-Omary, and H.I. El-Subbagh Substituted thiazoles VII. Synthesis and antitumor activity of certain 2-(substituted amino)-4-phenyl-1,3-thiazole analogs Bioorg. Med. Chem. Lett. 22 2012 6318 6323
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 6318-6323
-
-
Hassan, G.S.1
El-Messery, S.M.2
Al-Omary, F.A.M.3
El-Subbagh, H.I.4
-
35
-
-
70449560887
-
Synthesis and anticancer activities of some thiazole derivatives
-
I. Kayagil, and S. Demirayak Synthesis and anticancer activities of some thiazole derivatives Phosphorus Sulfur Silicon Relat. Elem. 184 2009 2197 2207
-
(2009)
Phosphorus Sulfur Silicon Relat. Elem.
, vol.184
, pp. 2197-2207
-
-
Kayagil, I.1
Demirayak, S.2
-
36
-
-
0014749951
-
Potential antineoplastics: 1-thiocarbamoyl-3-methyl-4-arylhydrazono-2- pyrazolin-5-one, 2-amino-4-phenyl-5-arylazothiazoles, and N-phenyl-N′-2 (4-phenyl-5-arylazothiazolyl) thiocarbamides
-
H.G. Garg, and R.A. Sharma Potential antineoplastics: 1-thiocarbamoyl-3-methyl-4-arylhydrazono-2-pyrazolin-5-one, 2-amino-4-phenyl-5- arylazothiazoles, and N-phenyl-N′-2 (4-phenyl-5-arylazothiazolyl) thiocarbamides J. Pharm. Sci. 59 1970 348 353
-
(1970)
J. Pharm. Sci.
, vol.59
, pp. 348-353
-
-
Garg, H.G.1
Sharma, R.A.2
-
37
-
-
33846861750
-
Synthesis and antitumor activity evaluation of some schiff bases derived from 2-aminothiazole derivatives
-
DOI 10.1002/hc.20256
-
X. Zhou, L. Shao, Z. Jin, J.B. Liu, H. Dai, and J.X. Fang Synthesis and antitumor activity evaluation of some Schiff bases derived from 2-aminothiazole derivatives Heteroatom Chem. 18 2007 55 59 (Pubitemid 46225945)
-
(2007)
Heteroatom Chemistry
, vol.18
, Issue.1
, pp. 55-59
-
-
Zhou, X.1
Shao, L.2
Jin, Z.3
Liu, J.-B.4
Dai, H.5
Fang, J.-X.6
-
38
-
-
0032925404
-
2,4-Disubstituted thiazoles, Part III: Synthesis and antitumor activity of ethyl 2-substituted-aminothiazole-4-carboxylate analogs
-
DOI 10.1002/(SICI)1521-4184(19994)332:4<137::AID-ARDP137>3.0.CO;2-0
-
H.I. El-Subbagh, A.H. Abadia, and J. Lehmann 2,4-Disubstituted thiazoles, part III 1: synthesis and antitumor activity of ethyl 2-substituted aminothiazole-4-carboxylate analogs Arch. Pharm. 332 1999 137 142 (Pubitemid 29190037)
-
(1999)
Archiv der Pharmazie
, vol.332
, Issue.4
, pp. 137-142
-
-
El-Subbagh, H.I.1
Abadi, A.H.2
Lehmann, J.3
-
39
-
-
84887025749
-
Design, synthesis of new peptide derivatives and evaluated DNA binding activity, anticancer and antimicrobial activity
-
A.A. El-Henawy Design, synthesis of new peptide derivatives and evaluated DNA binding activity, anticancer and antimicrobial activity J. Am. Sci. 6 11 2010 240 249
-
(2010)
J. Am. Sci.
, vol.6
, Issue.11
, pp. 240-249
-
-
El-Henawy, A.A.1
-
40
-
-
79960194931
-
Synthesis and biological activities of 2-amino-thiazole-5-carboxylic acid phenylamide derivatives
-
W. Liu, J. Zhou, F. Qi, K. Bensdorf, Z. Li, H. Zhang, H. Qian, W. Huang, X. Cai, P. Cao, A. Wellner, and R. Gust Synthesis and biological activities of 2-amino-thiazole-5-carboxylic acid phenylamide derivatives Arch. Pharm. 344 2011 451 458
-
(2011)
Arch. Pharm.
, vol.344
, pp. 451-458
-
-
Liu, W.1
Zhou, J.2
Qi, F.3
Bensdorf, K.4
Li, Z.5
Zhang, H.6
Qian, H.7
Huang, W.8
Cai, X.9
Cao, P.10
Wellner, A.11
Gust, R.12
-
41
-
-
0036578986
-
Synthesis and antiproliferative activity in vitro of new 3-substituted aminopyrazolo[3,4-b]pyridines
-
K. Poreba, A. Opolski, and J. Wietrzyk Synthesis and antiproliferative activity in vitro of new 3-substituted aminopyrazolo[3,4-b]pyridines Acta Pol. Pharm. 59 2002 215 222
-
(2002)
Acta Pol. Pharm.
, vol.59
, pp. 215-222
-
-
Poreba, K.1
Opolski, A.2
Wietrzyk, J.3
-
42
-
-
0142105991
-
Synthesis and antiproliferative activity in vitro of new 3-substituted aminoisoxazolo[5,4-b]pyridines
-
K. Poreba, J. Wietrzyk, and A. Opolski Synthesis and antiproliferative activity in vitro of new 3-substituted aminoisoxazolo[5,4-b]pyridines Acta Pol. Pharm. 60 2003 293 301 (Pubitemid 37279471)
-
(2003)
Acta Poloniae Pharmaceutica - Drug Research
, vol.60
, Issue.4
, pp. 293-301
-
-
Poreba, K.1
Wietrzyk, J.2
Opolski, A.3
-
43
-
-
84887026312
-
A remarkably high-speed solution-phase combinatorial synthesis of 2-substituted amino-4-arylthiazoles in polar solvents in the absence of a catalyst under ambient conditions and study of their antimicrobial activities
-
S.N. Dighe, P.K. Chaskar, K.S. Jain, M.S. Phoujdar, and K.V. Srinivasan A remarkably high-speed solution-phase combinatorial synthesis of 2-substituted amino-4-arylthiazoles in polar solvents in the absence of a catalyst under ambient conditions and study of their antimicrobial activities ISRN Org. Chem. 2011 2011 1 6
-
(2011)
ISRN Org. Chem.
, vol.2011
, pp. 1-6
-
-
Dighe, S.N.1
Chaskar, P.K.2
Jain, K.S.3
Phoujdar, M.S.4
Srinivasan, K.V.5
-
44
-
-
84855758520
-
Novel 1,3,4-heterodiazole analogues: Synthesis and in vitro antitumor activity
-
A.T. Taher, H.H. Georgey, and H.I. El-Subbagh Novel 1,3,4-heterodiazole analogues: synthesis and in vitro antitumor activity Eur. J. Med. Chem. 47 2012 445 451
-
(2012)
Eur. J. Med. Chem.
, vol.47
, pp. 445-451
-
-
Taher, A.T.1
Georgey, H.H.2
El-Subbagh, H.I.3
-
45
-
-
42749094088
-
Reactions of 4-(2-aminothiazole-4-yl)-3-methyl-5-oxo-1-phenyl-2- pyrazoline; Synthesis of thiazolo[3,2-a]pyrimidine and imidazo[2,1-b]thiazole derivatives
-
M.S.K. Youssef, R.A. Ahmed, M.S. Abbady, S.A. Abdel-Mohsen, and A.A. Omar Reactions of 4-(2-aminothiazole-4-yl)-3-methyl-5-oxo-1-phenyl-2-pyrazoline; synthesis of thiazolo[3,2-a]pyrimidine and imidazo[2,1-b]thiazole derivatives Monatsh. Chem. 139 2008 553 559
-
(2008)
Monatsh. Chem.
, vol.139
, pp. 553-559
-
-
Youssef, M.S.K.1
Ahmed, R.A.2
Abbady, M.S.3
Abdel-Mohsen, S.A.4
Omar, A.A.5
-
46
-
-
43149083065
-
Synthesis, ultra-short acting hypnotic activity, and metabolic profile of ethyl 8-oxo-5,6,7,8-tetrahydro-thiazolo[3,2-a][1,3]diazepin-3-carboxylate (HIE-124)
-
A.A. Kadi, H.A. El-Kashef, A.A.M. Abdel-Aziz, G.S. Hassan, J. Tettey, M.H. Grant, J. Lehmann, and H.I. El-Subbagh Synthesis, ultra-short acting hypnotic activity, and metabolic profile of ethyl 8-oxo-5,6,7,8-tetrahydro- thiazolo[3,2-a][1,3]diazepin-3-carboxylate (HIE-124) Arch. Pharm. 341 2008 81 89
-
(2008)
Arch. Pharm.
, vol.341
, pp. 81-89
-
-
Kadi, A.A.1
El-Kashef, H.A.2
Abdel-Aziz, A.A.M.3
Hassan, G.S.4
Tettey, J.5
Grant, M.H.6
Lehmann, J.7
El-Subbagh, H.I.8
-
47
-
-
77949484716
-
Synthesis of 3-((2,4-dichlorophenoxy)methyl)-1,2,4-triazolo(thiadiazoles and thiadiazines) as anti-inflammatory and molluscicidal agents
-
M.F. El Shehry, A.A. Abu-Hashem, and E.M. El-Telbani Synthesis of 3-((2,4-dichlorophenoxy)methyl)-1,2,4-triazolo(thiadiazoles and thiadiazines) as anti-inflammatory and molluscicidal agents Eur. J. Med. Chem. 45 2010 1906 1911
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 1906-1911
-
-
El Shehry, M.F.1
Abu-Hashem, A.A.2
El-Telbani, E.M.3
-
48
-
-
84859534357
-
Synthesis of some novel fused imidazo[2,1-b]1,3-thiazole and imidazo[2,1-b]thiazolo[5,4-d]isoxazole derivatives
-
H.R. Jaberi, and H. Noorizadeh Synthesis of some novel fused imidazo[2,1-b]1,3-thiazole and imidazo[2,1-b]thiazolo[5,4-d]isoxazole derivatives E-J. Chem. 9 2012 1518 1525
-
(2012)
E-J. Chem.
, vol.9
, pp. 1518-1525
-
-
Jaberi, H.R.1
Noorizadeh, H.2
-
49
-
-
0003589718
-
Reaction of propiolactone with heterocyclic amines
-
C.D. Hurd, and S. Hayao Reaction of propiolactone with heterocyclic amines J. Am. Chem. Soc. 77 1955 117 121
-
(1955)
J. Am. Chem. Soc.
, vol.77
, pp. 117-121
-
-
Hurd, C.D.1
Hayao, S.2
-
50
-
-
84884164910
-
Synthesis and biological evaluation of substituted thiazolamines, imidazo[2,1-b]thiazol-6-(5H)-ones, thiazolo[3,2-a]pyrimidin-5-ones and thiazolyl thioureas
-
N. Swathi, T. Kumar, K. Haribabu, and C. Subrahmanyam Synthesis and biological evaluation of substituted thiazolamines, imidazo[2,1-b]thiazol-6-(5H) -ones, thiazolo[3,2-a]pyrimidin-5-ones and thiazolyl thioureas Indian J. Heterocycl. Chem. 21 2012 263 268
-
(2012)
Indian J. Heterocycl. Chem.
, vol.21
, pp. 263-268
-
-
Swathi, N.1
Kumar, T.2
Haribabu, K.3
Subrahmanyam, C.4
-
51
-
-
33845351607
-
Antihelminthic activity of some newly synthesized 5(6)-(un)substituted- 1H-benzimidazol-2-ylthioacetylpiperazine derivatives
-
DOI 10.1016/j.ejmech.2006.07.005, PII S0223523406002662
-
A.T. Mavrova, K.K. Anichina, D.I. Vuchev, J.A. Tsenov, P.S. Denkova, M.S. Kondeva, and M.K. Micheva Antihelminthic activity of some newly synthesized 5(6)-(un)substituted-1H-benzimidazol-2-ylthioacetylpiperazine derivatives Eur. J. Med. Chem. 41 2006 1412 1420 (Pubitemid 44883392)
-
(2006)
European Journal of Medicinal Chemistry
, vol.41
, Issue.12
, pp. 1412-1420
-
-
Mavrova, A.Ts.1
Anichina, K.K.2
Vuchev, D.I.3
Tsenov, J.A.4
Denkova, P.S.5
Kondeva, M.S.6
Micheva, M.K.7
-
52
-
-
84887019356
-
-
NCI web site
-
NCI web site, www.dtp.nci.nih.gov.
-
-
-
-
53
-
-
0026676380
-
The National Cancer Institute: Cancer drug discovery and development program
-
M.R. Grever, S.A. Schepartz, and B.A. Chabner The national cancer institute cancer drug discovery and development program Semin.Oncol. 19 1992 622 638 (Pubitemid 23004840)
-
(1992)
Seminars in Oncology
, vol.19
, Issue.6
, pp. 622-638
-
-
Grever, M.R.1
Schepartz, S.A.2
Chabner, B.A.3
-
54
-
-
0025775062
-
Feasibility of a high flux anticancer drug screen utilizing a derive panel of human tumor cell lines in culture
-
A. Monks, D. Scudiero, P. Skehan, R. Shoemaker, K. Paull, D. Vistica, C. Hose, J. Langley, P. Cronise, and A.V. Wolff Feasibility of a high flux anticancer drug screen utilizing a derive panel of human tumor cell lines in culture J. Natl. Cancer Inst. 83 1991 757 766
-
(1991)
J. Natl. Cancer Inst.
, vol.83
, pp. 757-766
-
-
Monks, A.1
Scudiero, D.2
Skehan, P.3
Shoemaker, R.4
Paull, K.5
Vistica, D.6
Hose, C.7
Langley, J.8
Cronise, P.9
Wolff, A.V.10
-
55
-
-
0028906786
-
Some practical consideration and applications of the national cancer institute in vitro anticancer drug discovery screen
-
M.R. Boyd, and K.D. Paull Some practical consideration and applications of the national cancer institute in vitro anticancer drug discovery screen Drug Dev. Res. 34 1995 91 109
-
(1995)
Drug Dev. Res.
, vol.34
, pp. 91-109
-
-
Boyd, M.R.1
Paull, K.D.2
-
56
-
-
84887026000
-
-
http://dtp.nci.nih.gov/docs/compare/compare.html.
-
-
-
-
57
-
-
0024312538
-
Display and analysis of patterns of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm
-
K.D. Paull, R.H. Shoemaker, L. Hodes, A. Monks, D.A. Scudiero, L. Rubinstein, J. Plowman, and M.R. Boyd Display and analysis of patterns of differential activity of drugs against human tumor cell lines: development of mean graph and COMPARE algorithm J. Natl. Cancer Inst. 81 1989 1088 1092 (Pubitemid 19175145)
-
(1989)
Journal of the National Cancer Institute
, vol.81
, Issue.14
, pp. 1088-1092
-
-
Paull, K.D.1
Shoemaker, R.H.2
Hodes, L.3
Monks, A.4
Scudiero, D.A.5
Rubinstein, L.6
Plowman, J.7
Boyd, M.R.8
-
58
-
-
0036136167
-
COMPARE: A web accessible tool for investigating mechanisms of cell growth inhibition
-
DOI 10.1016/S1093-3263(01)00126-7, PII S1093326301001267
-
D.W. Zaharevitz, S.L. Holbeck, C. Bowerman, and P.A. Svetlik COMPARE: a web accessible tool for investigating mechanisms of cell growth inhibition J. Mol. Graphics Modell. 20 2002 297 303 (Pubitemid 34017547)
-
(2002)
Journal of Molecular Graphics and Modelling
, vol.20
, Issue.4
, pp. 297-303
-
-
Zaharevitz, D.W.1
Holbeck, S.L.2
Bowerman, C.3
Svetlik, P.A.4
-
60
-
-
33846569938
-
Targeting mammalian target of rapamycin (mTOR) for health and diseases
-
DOI 10.1016/j.drudis.2006.12.008, PII S1359644606004910
-
C.K. Tsang, H. Qi, L.F. Liu, and X.F.S. Zheng Targeting mammalian target of rapamycin (mTOR) for health and diseases Drug Discov. Today 12 2007 112 124 (Pubitemid 46176669)
-
(2007)
Drug Discovery Today
, vol.12
, Issue.3-4
, pp. 112-124
-
-
Tsang, C.K.1
Qi, H.2
Liu, L.F.3
Zheng, X.F.S.4
-
61
-
-
0037623419
-
Molecular actions of sirolimus: Sirolimus and mTOR
-
R.A. Kirken, and Y.L. Wang Molecular actions of sirolimus: sirolimus and mTOR Transplant. Proc. 35 2003 227 230
-
(2003)
Transplant. Proc.
, vol.35
, pp. 227-230
-
-
Kirken, R.A.1
Wang, Y.L.2
-
62
-
-
0022885694
-
A phase I trial of spirohydantoin mustard (NSC 172112) in patients with advanced cancer
-
T.D. Brown, D.S. Ettinger, and R.C. Donehower A phase I trial of spirohydantoin mustard (NSC 172112) in patients with advanced cancer J. Clin. Oncol. 4 1986 1270 1276 (Pubitemid 16043879)
-
(1986)
Journal of Clinical Oncology
, vol.4
, Issue.8
, pp. 1270-1276
-
-
Brown, T.D.1
Ettinger, D.S.2
Donehower, R.C.3
-
63
-
-
0023526090
-
Prolonged infusion of hemaxamethylene bisacetamide: A phase I and pharmacological study
-
E.K. Rowinsky, D.S. Ettinger, W.P. McGuire, D.A. Noe, L.B. Grochow, and R.C. Donehower Prolonged infusion of hexamethylene bisacetamide: a phase I and pharmacological study Cancer Res. 47 1987 5788 5795 (Pubitemid 18046782)
-
(1987)
Cancer Research
, vol.47
, Issue.21
, pp. 5788-5795
-
-
Rowinsky, E.K.1
Ettinger, D.S.2
McGuire, W.P.3
Noe, D.A.4
Grochow, L.B.5
Donehower, R.C.6
-
64
-
-
0026099077
-
Flavone acetic acid - An interesting novel therapeutic agent or just another disappointment?
-
M.C. Bibby Flavone acetic acid - an interesting novel therapeutic agent or just another disappointment? Br. J. Cancer 63 1991 3 5
-
(1991)
Br. J. Cancer
, vol.63
, pp. 3-5
-
-
Bibby, M.C.1
-
65
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
DOI 10.1016/S0169-409X(96)00423-1, PII S0169409X96004231
-
C.A. Lipinski, F. Lombardo, and B.W. Dominy Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Deliv. Rev. 23 1997 3 25 (Pubitemid 27046991)
-
(1997)
Advanced Drug Delivery Reviews
, vol.23
, Issue.1-3
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
66
-
-
84887019718
-
-
Schrödinger, LLC New York, NY
-
Canvas, Version 1.2 2009 Schrödinger, LLC New York, NY
-
(2009)
Canvas, Version 1.2
-
-
-
67
-
-
84887019650
-
-
http://www.organic-chemistry.org/prog/peo.
-
-
-
-
68
-
-
0033981358
-
Computational methods for the prediction of 'drug-likeness'
-
D.E. Clark, and S.D. Pickett Computational methods for the prediction of 'drug-likeness' Drug Discov. Today 5 2000 49 58
-
(2000)
Drug Discov. Today
, vol.5
, pp. 49-58
-
-
Clark, D.E.1
Pickett, S.D.2
-
69
-
-
33846518797
-
In silico target fishing: Predicting biological targets from chemical structure
-
DOI 10.1016/j.ddtec.2006.12.008, PII S1740674906000813
-
J.L. Jenkins, A. Bender, and J.W. Davies In silico target fishing: predicting biological targets from chemical structure Drug Discov. Today Technol. 3 2006 413 421 (Pubitemid 46158395)
-
(2006)
Drug Discovery Today: Technologies
, vol.3
, Issue.4
, pp. 413-421
-
-
Jenkins, J.L.1
Bender, A.2
Davies, J.W.3
-
70
-
-
77954264038
-
PharmMapper server: A web server for potential drug target identification via pharmacophore mapping approach
-
X. Liu, S. Ouyang, B. Yu, K. Huang, Y. Liu, J. Gong, S. Zheng, Z. Li, H. Li, and H. Jiang PharmMapper server: a web server for potential drug target identification via pharmacophore mapping approach Nucleic Acids Res. 38 2010 609 614
-
(2010)
Nucleic Acids Res.
, vol.38
, pp. 609-614
-
-
Liu, X.1
Ouyang, S.2
Yu, B.3
Huang, K.4
Liu, Y.5
Gong, J.6
Zheng, S.7
Li, Z.8
Li, H.9
Jiang, H.10
-
71
-
-
4444281995
-
3 substitutions
-
DOI 10.1016/j.bmcl.2004.07.031, PII S0960894X04009230
-
3 substitutions Bioorg. Med. Chem. Lett. 14 2004 4897 4902 (Pubitemid 39165590)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.19
, pp. 4897-4902
-
-
Barrett, D.G.1
Catalano, J.G.2
Deaton, D.N.3
Hassell, A.M.4
Long, S.T.5
Miller, A.B.6
Miller, L.R.7
Shewchuk, L.M.8
Wells-Knecht, K.J.9
Willard Jr., D.H.10
Wright, L.L.11
-
72
-
-
78649727076
-
New molecular targets in bone metastases
-
D. Santinia, S. Galluzzoa, A. Zoccolia, F. Pantanoa, M.E. Frattoa, B. Vincenzia, L. Lombardib, C. Gucciardinoa, N. Silvestrisc, E. Rivad, S. Rizzoe, A. Russoe, E. Maiellob, G. Coluccic, and G. Toninia New molecular targets in bone metastases Cancer Treat. Rev. 36 2010 6 10
-
(2010)
Cancer Treat. Rev.
, vol.36
, pp. 6-10
-
-
Santinia, D.1
Galluzzoa, S.2
Zoccolia, A.3
Pantanoa, F.4
Frattoa, M.E.5
Vincenzia, B.6
Lombardib, L.7
Gucciardinoa, C.8
Silvestrisc, N.9
Rivad, E.10
Rizzoe, S.11
Russoe, A.12
Maiellob, E.13
Coluccic, G.14
Toninia, G.15
-
73
-
-
0000263910
-
Design of potent and selective human cathepsin K inhibitors that span the active site
-
DOI 10.1073/pnas.94.26.14249
-
S.K. Thompson, S.M. Halbert, M.J. Bossard, T.A. Tomaszek, M.A. Levy, B. Zhao, W.W. Smith, S.S. Abdel-Meguid, C.A. Janson, K.J. D'Alessio, M.S. Mcqueney, B.Y. Amegadzie, C.R. Hanning, R.L. Dejarlais, J. Briand, S.K. Sarkar, M.J. Huddleston, C.F. Ijames, S.A. Carr, K.T. Garnes, A. Shu, J.R. Heys, J. Bradbeer, D. Zembryki, L.L. Rykaczewski, I.E. James, M.W. Lark, F.H. Drake, M. Gowen, J.G. Gleason, and D.F. Vener Design of potent and selective human cathepsin K inhibitors that span the active site Proc. Natl. Acad. Sci. U. S. A. 94 1997 14249 14254 (Pubitemid 28041359)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.26
, pp. 14249-14254
-
-
Thompson, S.K.1
Halbert, S.M.2
Bossard, M.J.3
Tomaszek, T.A.4
Levy, M.A.5
Zhao, B.6
Smith, W.W.7
Abdel-Meguid, S.S.8
Janson, C.A.9
D'Alessio, K.J.10
Mcqueney, M.S.11
Amegadzie, B.Y.12
Hanning, C.R.13
Desjarlais, R.L.14
Briand, J.15
Sarkar, S.K.16
Huddleston, M.J.17
Ijames, C.F.18
Carr, S.A.19
Garnes, K.T.20
Shu, A.21
Heys, J.R.22
Bradbeer, J.23
Zembryki, D.24
Lee-Rykaczewski, L.25
James, I.E.26
Lark, M.W.27
Drake, F.H.28
Gowen, M.29
Gleason, J.G.30
Veber, D.F.31
more..
-
74
-
-
34548202165
-
Vitamin D signalling pathways in cancer: Potential for anticancer therapeutics
-
DOI 10.1038/nrc2196, PII NRC2196
-
K.K. Deeb, D.L. Trump, and C.S. Johnson Vitamin D signalling pathways in cancer: potential for anticancer therapeutics Nat. Rev. Cancer 7 2007 684 700 (Pubitemid 47327412)
-
(2007)
Nature Reviews Cancer
, vol.7
, Issue.9
, pp. 684-700
-
-
Deeb, K.K.1
Trump, D.L.2
Johnson, C.S.3
-
75
-
-
84857735521
-
Current status of vitamin D signaling and its therapeutic applications
-
C. Carlberg, and F. Molnár Current status of vitamin D signaling and its therapeutic applications Curr. Top. Med. Chem. 12 2012 528 547
-
(2012)
Curr. Top. Med. Chem.
, vol.12
, pp. 528-547
-
-
Carlberg, C.1
Molnár, F.2
-
76
-
-
0028853821
-
Folate-based thymidylate synthase inhibitors as anticancer drugs
-
A.L. Jackman, and A.H. Calvert Folate-based thymidylate synthase inhibitors as anticancer drugs Ann. Oncol. 6 1995 871 881
-
(1995)
Ann. Oncol.
, vol.6
, pp. 871-881
-
-
Jackman, A.L.1
Calvert, A.H.2
-
77
-
-
17144429703
-
Novel 2-amino-4-oxo-5-arylthio-substituted-pyrrolo[2,3-d]pyrimidines as nonclassical antifolate inhibitors of thymidylate synthase
-
DOI 10.1016/j.bmcl.2005.03.029
-
A. Gangjee, H.D. Jaina, and R.L. Kisliuk Novel 2-amino-4-oxo-5-arylthio- substituted pyrrolo[2,3-d]pyrimidines as nonclassical antifolate inhibitors of thymidylate synthase Bioorg. Med. Chem. Lett. 15 2005 2225 2230 (Pubitemid 40523077)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.9
, pp. 2225-2230
-
-
Gangjee, A.1
Jain, H.D.2
Kisliuk, R.L.3
-
78
-
-
33750530573
-
Synthesis and evaluation of a classical 2,4-diamino-5-substituted-furo[2, 3-d]pyrimidine and a 2-amino-4-oxo-6-substituted-pyrrolo[2,3-d]pyrimidine as antifolates
-
DOI 10.1016/j.bmc.2006.08.029, PII S0968089606006870
-
A. Gangjee, J. Yang, J.J. McGuireb, and R.L. Kisliukc Synthesis and evaluation of a classical 2,4-diamino-5-substituted furo[2,3-d]pyrimidine and a 2-amino-4-oxo-6-substituted pyrrolo[2,3-d]pyrimidine as antifolates Bioorg. Med. Chem. 14 2006 8590 8598 (Pubitemid 44667525)
-
(2006)
Bioorganic and Medicinal Chemistry
, vol.14
, Issue.24
, pp. 8590-8598
-
-
Gangjee, A.1
Yang, J.2
McGuire, J.J.3
Kisliuk, R.L.4
-
79
-
-
68549132502
-
4 hydrolase inhibitors using metabolomics biased fragment crystallography
-
4 hydrolase inhibitors using metabolomics biased fragment crystallography J. Med. Chem. 52 2009 4694 4715
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4694-4715
-
-
Davies, D.R.1
Mamat, B.2
Magnusson, O.T.3
Christensen, J.4
Haraldsson, M.H.5
Mishra, R.6
Pease, B.7
Hansen, E.8
Singh, J.9
Zembower, D.10
Kim, H.11
Kiselyov, A.S.12
Burgin, A.B.13
Gurney, M.E.14
Stewart, L.J.15
-
80
-
-
77950923265
-
4 hydrolase inhibitors based on piperidine and piperazine scaffolds
-
4 hydrolase inhibitors based on piperidine and piperazine scaffolds Bioorg. Med. Chem. Lett. 20 2010 2851 2854
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 2851-2854
-
-
Sandanayaka, V.1
Mamat, B.2
Bhagat, N.3
Bedell, L.4
Halldorsdottir, G.5
Sigthorsdottir, H.6
Andrésson, P.7
Kiselyov, A.8
Gurney, M.9
Singh, J.10
-
81
-
-
0037032835
-
The protein kinase complement of the human genome
-
DOI 10.1126/science.1075762
-
G. Manning, D.B. Whyte, R. Martinez, T. Hunter, and S. Sudarsanam The protein kinase complement of the human genome Science 298 2002 1912 1934 (Pubitemid 35425239)
-
(2002)
Science
, vol.298
, Issue.5600
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
82
-
-
62449319246
-
Characterization of a novel mitogen-activated protein kinase kinase 1/2 inhibitor with a unique mechanism of action for cancer therapy
-
S. Daouti, H. Wang, W. Li, B. Higgins, K. Kolinsky, K. Packman, A. Specian Jr., N. Kong, N. Huby, Y. Wen, Q. Xiang, F.J.P. dlaski, Y. He, N. Fotouhi, D. Heimbrook, and H. Niu Characterization of a novel mitogen-activated protein kinase kinase 1/2 inhibitor with a unique mechanism of action for cancer therapy Cancer Res. 69 2009 1924 1932
-
(2009)
Cancer Res.
, vol.69
, pp. 1924-1932
-
-
Daouti, S.1
Wang, H.2
Li, W.3
Higgins, B.4
Kolinsky, K.5
Packman, K.6
Specian, Jr.A.7
Kong, N.8
Huby, N.9
Wen, Y.10
Xiang, Q.11
Dlaski, F.J.P.12
He, Y.13
Fotouhi, N.14
Heimbrook, D.15
Niu, H.16
-
83
-
-
84861494447
-
Discovery of novel allosteric mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors possessing bidentate Ser212 interactions
-
R.A. Heald, P. Jackson, P. Savy, M. Jones, E. Gancia, B. Burton, R. Newman, J. Boggs, E. Chan, J. Chan, E. Choo, M. Merchant, P. Rudewicz, M. Ultsch, C. Wiesmann, Q. Yue, M. Belvin, and S. Price Discovery of novel allosteric mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors possessing bidentate Ser212 interactions J. Med. Chem. 55 2012 4594 4604
-
(2012)
J. Med. Chem.
, vol.55
, pp. 4594-4604
-
-
Heald, R.A.1
Jackson, P.2
Savy, P.3
Jones, M.4
Gancia, E.5
Burton, B.6
Newman, R.7
Boggs, J.8
Chan, E.9
Chan, J.10
Choo, E.11
Merchant, M.12
Rudewicz, P.13
Ultsch, M.14
Wiesmann, C.15
Yue, Q.16
Belvin, M.17
Price, S.18
-
84
-
-
13544256790
-
Src protein-tyrosine kinase structure and regulation
-
DOI 10.1016/j.bbrc.2004.09.171
-
R. Roskoski Jr. Src protein-tyrosine kinase structure and regulation Biochem. Biophys. Res. Commun. 324 2004 1155 1164 (Pubitemid 40292143)
-
(2004)
Biochemical and Biophysical Research Communications
, vol.324
, Issue.4
, pp. 1155-1164
-
-
Roskoski Jr., R.1
-
85
-
-
0033575680
-
Structure-based design and synthesis of a novel class of Src SH2 inhibitors
-
DOI 10.1016/S0960-894X(99)00388-1, PII S0960894X99003881
-
J.L. Buchanan, R.S. Bohacek, G.P. Luke, M. Hatada, X. Lu, D.C. Dalgamo, S.S. Narula, R. Yuan, and D.A. Holt Structure-based design and synthesis of a novel class of SRC SH2 inhibitor Bioorg. Med. Chem. Lett. 9 1999 2353 2358 (Pubitemid 29391521)
-
(1999)
Bioorganic and Medicinal Chemistry Letters
, vol.9
, Issue.16
, pp. 2353-2358
-
-
Buchanan, J.L.1
Bohacek, R.S.2
Luke, G.P.3
Hatada, M.4
Lu, X.5
Dalgarno, D.C.6
Narula, S.S.7
Yuan, R.8
Holt, D.A.9
-
86
-
-
20544455834
-
3D-QSAR studies on c-Src kinase inhibitors and docking analyses of a potent dual kinase inhibitor of c-Src and c-Abl kinases
-
DOI 10.1016/j.bmc.2005.04.065, PII S0968089605003779
-
R. Thaimattam, P.R. Daga, R. Banerjeea, and J. Iqbal 3D-QSAR studies on c-Src kinase inhibitors and docking analyses of a potent dual kinase inhibitor of c-Src and c-Abl kinases Bioorg. Med. Chem. 13 2005 4704 4712 (Pubitemid 40848348)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.15
, pp. 4704-4712
-
-
Thaimattam, R.1
Daga, P.R.2
Banerjee, R.3
Iqbal, J.4
-
87
-
-
79954415847
-
Synthesis and pharmacological evaluation of thieno[2,3-b]pyridine derivatives as novel c-Src inhibitors
-
I. Pevet, C. Brulé, A. Tizot, A. Gohier, F. Cruzalegui, J.A. Boutin, and S. Goldstein Synthesis and pharmacological evaluation of thieno[2,3-b]pyridine derivatives as novel c-Src inhibitors Bioorg. Med. Chem. 19 2011 2517 2528
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 2517-2528
-
-
Pevet, I.1
Brulé, C.2
Tizot, A.3
Gohier, A.4
Cruzalegui, F.5
Boutin, J.A.6
Goldstein, S.7
-
88
-
-
77956543862
-
First-line single agent treatment with gefitinib in patients with advanced non-small-cell lung cancer
-
Y.M. Yin, Y.T. Geng, Y.F. Shao, X.L. Hu, W. Li, Y.Q. Shu, and Z.X. Wang First-line single agent treatment with gefitinib in patients with advanced non-small-cell lung cancer J. Exp. Clin. Cancer Res. 29 2010 126 132
-
(2010)
J. Exp. Clin. Cancer Res.
, vol.29
, pp. 126-132
-
-
Yin, Y.M.1
Geng, Y.T.2
Shao, Y.F.3
Hu, X.L.4
Li, W.5
Shu, Y.Q.6
Wang, Z.X.7
-
89
-
-
79851511500
-
Gefitinib as first-line treatment for patients with advanced non-small-cell lung cancer with activating epidermal growth factor receptor mutation: Review of the evidence
-
C. Gridelli, F.D. Marinisb, M.D. Maioc, D. Cortinovisd, F. Cappuzzoe, and T. Mokf Gefitinib as first-line treatment for patients with advanced non-small-cell lung cancer with activating epidermal growth factor receptor mutation: review of the evidence Lung Cancer 71 2011 249 257
-
(2011)
Lung Cancer
, vol.71
, pp. 249-257
-
-
Gridelli, C.1
Marinisb, F.D.2
Maioc, M.D.3
Cortinovisd, D.4
Cappuzzoe, F.5
Mokf, T.6
-
91
-
-
67849110009
-
SePreSA: A server for the prediction of populations susceptible to serious adverse drug reactions implementing the methodology of a chemical-protein interactome
-
L. Yang, H. Luo, J. Chen, Q. Xing, and L. He SePreSA: a server for the prediction of populations susceptible to serious adverse drug reactions implementing the methodology of a chemical-protein interactome Nucleic Acids Res. 37 2009 406 412
-
(2009)
Nucleic Acids Res.
, vol.37
, pp. 406-412
-
-
Yang, L.1
Luo, H.2
Chen, J.3
Xing, Q.4
He, L.5
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