-
1
-
-
33646160623
-
Inflammation, a key event in cancer development
-
Lu, H., Ouyang, W., Huang, C. Inflammation, a Key Event in Cancer Development. Mol. Cancer Res., 2006;4:221-43.
-
(2006)
Mol. Cancer Res.
, vol.4
, pp. 221-243
-
-
Lu, H.1
Ouyang, W.2
Huang, C.3
-
2
-
-
0034916569
-
Lipid mediator class switching during acute inflammation: Signals in resolution
-
a. Levy, B.D., Clish, C.B., Schmidt, B., Gronert, K., Serhan, C.N. Lipid mediator class switching during acute inflammation: signals in resolution. Nat. Immunol., 2001;2:612-19
-
(2001)
Nat. Immunol.
, vol.2
, pp. 612-619
-
-
Levy, B.D.1
Clish, C.B.2
Schmidt, B.3
Gronert, K.4
Serhan, C.N.5
-
3
-
-
84872711648
-
The effect of extracted bacterial salmonella enteritidis lipopolysaccharide on inducible nitric oxide synthase in human liver hepatocellular carcinoma cell lines in induction and inhibition conditions
-
b. Rastegar, H., Mirzaei, A., Ashtiani, H. R. A., Hedayati, M., Ahmadi, S. The Effect of Extracted Bacterial Salmonella enteritidis Lipopolysaccharide on Inducible Nitric Oxide Synthase in Human Liver Hepatocellular Carcinoma Cell Lines in Induction and Inhibition Conditions. J. pure Appl. Microbiol., 2012;6:39-45.
-
(2012)
J. Pure Appl. Microbiol.
, vol.6
, pp. 39-45
-
-
Rastegar, H.1
Mirzaei, A.2
Ashtiani, H.R.A.3
Hedayati, M.4
Ahmadi, S.5
-
4
-
-
0032506241
-
Inhibition of interferon gamma induced interleukin 12 production: A potential mechanism for the anti-inflammatory activities of tumor necrosis factor
-
Hodge-Dufour, J., Marino, M.W., Horton, M.R. Inhibition of interferon gamma induced interleukin 12 production: A potential mechanism for the anti-inflammatory activities of tumor necrosis factor. Proc. Natl. Acad. Sci.USA, 1998;95:13806-11.
-
(1998)
Proc. Natl. Acad. Sci.USA
, vol.95
, pp. 13806-13811
-
-
Hodge-Dufour, J.1
Marino, M.W.2
Horton, M.R.3
-
5
-
-
0037180812
-
Points of control in inflammation
-
Nathan, C. Points of control in inflammation. Nature, 2002;420:846-52.
-
(2002)
Nature
, vol.420
, pp. 846-852
-
-
Nathan, C.1
-
6
-
-
0024536234
-
Macrophage phagocytosis of aging neutrophils in inflammation
-
Savill, J, Wyllie, A.H., Henson, J.E., Walport, M.J., Henson, RM., Haslett, C. Macrophage phagocytosis of aging neutrophils in inflammation. Programmed cell death in the neutrophil leads to its recognition by macrophages. J Clin. Invest., 1989;83:865-75.
-
(1989)
Programmed Cell Death in the Neutrophil Leads to its Recognition by Macrophages. J Clin. Invest.
, vol.83
, pp. 865-875
-
-
Savill, J.1
Wyllie, A.H.2
Henson, J.E.3
Walport, M.J.4
Henson, R.M.5
Haslett, C.6
-
7
-
-
0034641931
-
Corpse clearance defines the meaning of cell death
-
Savill, J., Fadok, V.A. Corpse clearance defines the meaning of cell death. Nature, 2000;407:784-8.
-
(2000)
Nature
, vol.407
, pp. 784-788
-
-
Savill, J.1
Fadok, V.A.2
-
8
-
-
0036884424
-
A blast from the past: Clearance of apoptotic cells regulates immune responses
-
Savill, J., Dransfield, I., Gregory, C, Haslett, C. A blast from the past: Clearance of apoptotic cells regulates immune responses. Nat. Rev. Immunol., 2002;2:965-75.
-
(2002)
Nat. Rev. Immunol.
, vol.2
, pp. 965-975
-
-
Savill, J.1
Dransfield, I.2
Gregory, C.3
Haslett, C.4
-
9
-
-
0032519925
-
Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF
-
Fadok, V. A., Bratton, D.L., Konowal, A., Freed, P.W., Westcott, J. Y., Henson, P.M. Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF. J. Clin. Invest., 1998;101:890-8.
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 890-898
-
-
Fadok, V.A.1
Bratton, D.L.2
Konowal, A.3
Freed, P.W.4
Westcott, J.Y.5
Henson, P.M.6
-
10
-
-
0033485401
-
Transcriptional and translational regulation of inflammatory mediator production by endogenous TGF-beta in macrophages that have ingested apoptotic cells
-
McDonald, P.P., Fadok, V.A., Bratton, D., Henson, P.M. Transcriptional and translational regulation of inflammatory mediator production by endogenous TGF-beta in macrophages that have ingested apoptotic cells. J. Immunol., 1999;163:6164-72.
-
(1999)
J. Immunol.
, vol.163
, pp. 6164-6172
-
-
McDonald, P.P.1
Fadok, V.A.2
Bratton, D.3
Henson, P.M.4
-
11
-
-
0036143018
-
Phosphatidylserine-dependent ingestion of apoptotic cells promotes TGF-betal secretion and the resolution of inflammation
-
Huynh, M. L. N., Fadok, V.A., Henson, P.M. Phosphatidylserine-dependent ingestion of apoptotic cells promotes TGF-betal secretion and the resolution of inflammation. J. Clin. Invest., 2002;109:41-50.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 41-50
-
-
Huynh, M.L.N.1
Fadok, V.A.2
Henson, P.M.3
-
12
-
-
5444256371
-
Inflammation as a tumor promoter in cancer induction
-
Philip, M., Rowley, D.A., Schreiber, H. Inflammation as a tumor promoter in cancer induction, Semin. Cancer Biol., 2004;14:433-9.
-
(2004)
Semin. Cancer Biol.
, vol.14
, pp. 433-439
-
-
Philip, M.1
Rowley, D.A.2
Schreiber, H.3
-
13
-
-
0037180757
-
Inflammation and cancer
-
Coussens, L.M., Werb, Z. Inflammation and cancer. Nature, 2002;420:860-7.
-
(2002)
Nature
, vol.420
, pp. 860-867
-
-
Coussens, L.M.1
Werb, Z.2
-
14
-
-
1642385412
-
Inflammation and cancer II. Role of chronic inflammation and cytokine gene polymorphisms in the pathogenesis of gastrointestinal malignancy
-
Macarthur, M., Hold, G.L., El-Omar, E.M. Inflammation and Cancer II. Role of chronic inflammation and cytokine gene polymorphisms in the pathogenesis of gastrointestinal malignancy. J. Am. Physiol Gast Liver Physiol., 2004;286: G515-G20.
-
(2004)
J. Am. Physiol Gast Liver Physiol.
, vol.286
-
-
Macarthur, M.1
Hold, G.L.2
El-Omar, E.M.3
-
15
-
-
84874604885
-
-
New York, NY, USA: Marcel Dekker
-
Martin, Y.C., Austel, K.E. (eds.): Paths to Better and Safer Drugs, Modern Drug Research, New York, NY, USA: Marcel Dekker, 1989; pp. 243-73.
-
(1989)
Paths to Better and Safer Drugs, Modern Drug Research
, pp. 243-273
-
-
Martin, Y.C.1
Austel, K.E.2
-
16
-
-
33746505684
-
-
rd. edn., Stuttgart, Germany: Deutscher Apotheker Verlag
-
rd. edn., Stuttgart, Germany: Deutscher Apotheker Verlag, 2000; p. 51.
-
(2000)
Arzneistoffe
, pp. 51
-
-
Roth, H.J.1
Fenner, H.2
-
17
-
-
3242746917
-
Advances in the discovery of novel antibacterial agents during the year 2002
-
Harris, CR., Thorarensen, A. Advances in the discovery of novel antibacterial agents during the year 2002. Curr. Med. Chem., 2004;11:2213-43.
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 2213-2243
-
-
Harris, C.R.1
Thorarensen, A.2
-
18
-
-
19944429772
-
A diarylquinoline drug active on the ATP synthase of mycobacterium tuberculosis
-
Andries, K., Verhasselt, P., Guillemont, J., Gohlmann, H.W., Neefs, J.M., Winkler, H., Van Gestel, J., Timmerman, P., Zhu, M., Lee, E. A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis. Science, 2005;307:223-6.
-
(2005)
Science
, vol.307
, pp. 223-226
-
-
Andries, K.1
Verhasselt, P.2
Guillemont, J.3
Gohlmann, H.W.4
Neefs, J.M.5
Winkler, H.6
Van Gestel, J.7
Timmerman, P.8
Zhu, M.9
Lee, E.10
-
19
-
-
2142662107
-
Ring-substituted quinolines as potential anti-tuberculosis agents
-
Vangapandu, S., Jain, M., Jain, R., Kaur, S., Singh, P.P. Ring-substituted quinolines as potential anti-tuberculosis agents. Bioorg. Med. Chem., 2004;12:2501-8.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 2501-2508
-
-
Vangapandu, S.1
Jain, M.2
Jain, R.3
Kaur, S.4
Singh, P.P.5
-
20
-
-
44449127718
-
Anti-mycobacterial activity of quinolones. Triazoloquinolones a new class of potent anti-mycobacterial agents
-
Carta, A., Piras, S., Palomba, M, Jabes, D., Molicotti, P., Zanetti, S. Anti-mycobacterial activity of quinolones. Triazoloquinolones a new class of potent anti-mycobacterial agents. Anti Infective Agents Med. Chem., 2008;7:134-47.
-
(2008)
Anti Infective Agents Med. Chem.
, vol.7
, pp. 134-147
-
-
Carta, A.1
Piras, S.2
Palomba, M.3
Jabes, D.4
Molicotti, P.5
Zanetti, S.6
-
21
-
-
14444274329
-
Novel nonpeptide CCK-B antagonists: Design and development of quinazolinone derivatives as potent, selective, and orally active CCKB antagonists
-
Padia, J.K., Field, M., Hilton, J;, Meecham, K., Pablo, J., Pinnock, R., Roth, B.D., Singh, L., Suman-Chauhan, N., Trivedi, B.K. Novel nonpeptide CCK-B antagonists: Design and development of quinazolinone derivatives as Potent, Selective, and orally active CCKB Antagonists. J. Med. Chem., 1998;41:1042-9.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1042-1049
-
-
Padia, J.K.1
Field, M.2
Hilton, J.3
Meecham, K.4
Pablo, J.5
Pinnock, R.6
Roth, B.D.7
Singh, L.8
Suman-Chauhan, N.9
Trivedi, B.K.10
-
22
-
-
0035821397
-
Antitumor agents. Part 204: Synthesis and biological evaluation of substituted 2-aryl quinazolinones
-
Xia, Y., Yang, Z.Y., Hour, M.J., Kuo, S.C., Xia, P., Bastow, K.F., Nakanishi, Y, Nampoothiri, P., Hackl, T., Hamel, E. Antitumor agents. Part 204: Synthesis and biological evaluation of substituted 2-aryl quinazolinones. Bioorg. Med. Chem. Lett., 2001;11:1193-6.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1193-1196
-
-
Xia, Y.1
Yang, Z.Y.2
Hour, M.J.3
Kuo, S.C.4
Xia, P.5
Bastow, K.F.6
Nakanishi, Y.7
Nampoothiri, P.8
Hackl, T.9
Hamel, E.10
-
23
-
-
0021999825
-
Studies on 4(1H)-quinazolinones. 5. Synthesis and antiinflammatory activity of 4(1H)-quinazolinone derivatives
-
Kenichi, O., Yoshihisa, Y, Toyonari, O., Toru, I., Yoshio, I. Studies on 4(1H)-quinazolinones. 5. Synthesis and antiinflammatory activity of 4(1H)-quinazolinone derivatives. J. Med. Chem., 1985;28:568-76.
-
(1985)
J. Med. Chem.
, vol.28
, pp. 568-576
-
-
Kenichi, O.1
Yoshihisa, Y.2
Toyonari, O.3
Toru, I.4
Yoshio, I.5
-
24
-
-
0001770701
-
-
Thygarajan B.S., (ed.): New York, NY, USA, Wiley Interscience
-
Buchanan, J.G., Sable, H.Z. Selective Organic Transformations, Thygarajan B.S., (ed.): New York, NY, USA, Wiley Interscience, 1972; Volume 2, pp. 1-95.
-
(1972)
Selective Organic Transformations
, vol.2
, pp. 1-95
-
-
Buchanan, J.G.1
Sable, H.Z.2
-
25
-
-
33750473750
-
Synthesis of new 4(3H)-quinazolinone derivatives using 5(4H)-oxazolones
-
Hamidian, H., Tikdari, A.M., Khabazzadeh, H. Synthesis of new 4(3H)-quinazolinone derivatives using 5(4H)-oxazolones. Molecules, 2006;11:377-82.
-
(2006)
Molecules
, vol.11
, pp. 377-382
-
-
Hamidian, H.1
Tikdari, A.M.2
Khabazzadeh, H.3
-
26
-
-
33646269147
-
Quinoline-based fused heterocyclic systems are found as potential anticancer
-
Birendra, N.G., Jiban, C. S. K., Jogendra, N.B. Quinoline-based fused heterocyclic systems are found as potential anticancer. J. Heterocycl. Chem., 1984;21:1225-9.
-
(1984)
J. Heterocycl. Chem.
, vol.21
, pp. 1225-1229
-
-
Birendra, N.G.1
Jiban, C.S.K.2
Jogendra, N.B.3
-
27
-
-
0019124833
-
Synthesis of some new 5-methyl-2-benzoxazolinone derivatives and investigation on their analgesic-antiinflammatory activities
-
Kothari, P.J., Mehlhoff, M.A., Singh, S.P., Parmar, S.S., Stenberg, V.I. Synthesis of some new 5-methyl-2-benzoxazolinone derivatives and investigation on their analgesic-antiinflammatory Activities. J. Heterocycl. Chem., 1980;17:1369-72.
-
(1980)
J. Heterocycl. Chem.
, vol.17
, pp. 1369-1372
-
-
Kothari, P.J.1
Mehlhoff, M.A.2
Singh, S.P.3
Parmar, S.S.4
Stenberg, V.I.5
-
28
-
-
0019835828
-
Studies on potential pesticides 13 synthesis and evaluation of s(3-substituted-phenoxymethyl-4-aryl/cyclohexyl-4h-1,2,4-triazol-5-yl) -2-mercaptomethyl benzimidazoles for antibacterial and insecticidal activities
-
Sengupta, A.K., Misra, H.K. Studies on potential pesticides 13 Synthesis and evaluation of s(3-substituted-phenoxymethyl-4-aryl/cyclohexyl-4h-1,2,4- triazol-5-yl)-2-mercaptomethyl benzimidazoles for antibacterial and insecticidal activities. J. Indian Chem. Soc., 1981;8:508.
-
(1981)
J. Indian Chem. Soc.
, vol.8
, pp. 508
-
-
Sengupta, A.K.1
Misra, H.K.2
-
29
-
-
0020393630
-
Synthesis of aryloxy/aryl acetyl thiosemicarbazides, substituted 1,3,4-oxadiazoles, 1,3,4-thiadiazoles, 1,2,4-triazoles and related compounds as potential fungicides
-
a. Sarmah, S.C., Bahel, S.C. Synthesis of aryloxy/aryl acetyl thiosemicarbazides, substituted 1,3,4-oxadiazoles, 1,3,4-thiadiazoles, 1,2,4-triazoles and related compounds as potential Fungicides. J. Indian Chem. Soc., 1982;59:877-80.
-
(1982)
J. Indian Chem. Soc.
, vol.59
, pp. 877-880
-
-
Sarmah, S.C.1
Bahel, S.C.2
-
30
-
-
44049107913
-
Synthesis and antifungal activity of 4-amino-5-aryl-1,2,4-triazoles
-
b. Kumar, U., Bansal, M., Gupta, S. K., Saharyar, M. Synthesis and Antifungal Activity of 4-amino-5-aryl-1,2,4-triazoles. J. Pure Appl. Microbiol., 2007;1:341-344.
-
(2007)
J. Pure Appl. Microbiol.
, vol.1
, pp. 341-344
-
-
Kumar, U.1
Bansal, M.2
Gupta, S.K.3
Saharyar, M.4
-
31
-
-
0023929951
-
Structure-activity profile of a series of novel triazoloquinazoline adenosine antagonists
-
Francis, J.E., Cash, W.D., Psychoyos, S., Ghai, G., Wenk, P., Friedmann, R.C., Atkins, C., Warren, V, Furness, P., Hyun, T.L. Structure-activity profile of a series of novel triazoloquinazoline adenosine antagonists. J. Med. Chem., 1988;31:1014-20.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 1014-1020
-
-
Francis, J.E.1
Cash, W.D.2
Psychoyos, S.3
Ghai, G.4
Wenk, P.5
Friedmann, R.C.6
Atkins, C.7
Warren, V.8
Furness, P.9
Hyun, T.L.10
-
32
-
-
0031824990
-
Derivatives of the triazoloquinazoline adenosine antagonist (CGS15943) having high potency at the human A2B and A3 receptor subtypes
-
Kim, Y.-C., De Zwart, M., Chang, L., Mora, S., Kuenzel, J., Melman, N., Jzerman, A.P., Jacobson, K.A. Derivatives of the triazoloquinazoline adenosine antagonist (CGS15943) having high potency at the human A2B and A3 receptor subtypes. J. Med. Chem., 1998;41:2835-45.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2835-2845
-
-
Kim, Y.-C.1
De Zwart, M.2
Chang, L.3
Mora, S.4
Kuenzel, J.5
Melman, N.6
Jzerman, A.P.7
Jacobson, K.A.8
-
33
-
-
0035222579
-
Selective adenosine A2A receptor antagonists
-
Ongini, E., Monoppoli, A., Cacciari, B., Baraldi, P.G. Selective adenosine A2A receptor Antagonists. Il Farmaco, 2001;56:87-90.
-
(2001)
Il Farmaco
, vol.56
, pp. 87-90
-
-
Ongini, E.1
Monoppoli, A.2
Cacciari, B.3
Baraldi, P.G.4
-
34
-
-
0025979697
-
Synthesis and benzodiazepine binding activity of a series of novel [1,2,4]triazolo[1,5-c]quinazolin-5(6H)-ones
-
Francis, J.E., Cash, W.D., Barbaz, B.S., Bernard, P.S., Lovell, R.A., Mazzenga, G.G, Friedmann, R.G, Hyun, J.L., Braunwalder, A.F., Loo, P.S. Synthesis and benzodiazepine binding activity of a series of novel [1,2,4]triazolo[1,5-c]quinazolin-5(6H)-ones. J. Med. Chem., 1991;34:281-90.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 281-290
-
-
Francis, J.E.1
Cash, W.D.2
Barbaz, B.S.3
Bernard, P.S.4
Lovell, R.A.5
Mazzenga, G.G.6
Friedmann, R.G.7
Hyun, J.L.8
Braunwalder, A.F.9
Loo, P.S.10
-
35
-
-
15044350987
-
Synthesis and pharmacological investigation of novel 1-substituted-4- phenyl-1,2,4-triazolo [4,3-a]quinazolin-5(4H)-ones as a new class of H1-antihistaminic agents
-
Alagarsamy, V., Giridhar, R., Yadav, M.R. Synthesis and pharmacological investigation of novel 1-substituted-4-phenyl-1,2,4-triazolo [4,3-a]quinazolin-5(4H)-ones as a new class of H1-antihistaminic agents. Bioorg. Med. Chem. Lett., 2005;15:1877-80.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 1877-1880
-
-
Alagarsamy, V.1
Giridhar, R.2
Yadav, M.R.3
-
36
-
-
34247554190
-
Synthesis and pharmacological investigation of novel 4-benzyl-1- substituted-4H-[1,2,4]triazolo [4,3-a]quinazolin-5-ones as new class of H1-antihistaminic agents
-
Alagarsamy, V., Solomon, V.R., Murugan, M. Synthesis and pharmacological investigation of novel 4-benzyl-1-substituted-4H-[1,2,4]triazolo [4,3-a]quinazolin-5-ones as new class of H1-antihistaminic agents. Bioorg. Med. Chem., 2007;15:4009-15.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 4009-4015
-
-
Alagarsamy, V.1
Solomon, V.R.2
Murugan, M.3
-
37
-
-
79957805936
-
A new series of 2-alkoxy(aralkoxy)[1,2,4]triazolo[1,5 a]quinazolin-5-ones as adenosine receptor antagonists
-
Al-Salahi, R., Geffken, D., Koellner, M. A new series of 2-Alkoxy(aralkoxy)[1,2,4]triazolo[1,5 a]quinazolin-5-ones as Adenosine Receptor Antagonists. Chem. Pharm. Bull., 2011;59:730-3.
-
(2011)
Chem. Pharm. Bull.
, vol.59
, pp. 730-733
-
-
Al-Salahi, R.1
Geffken, D.2
Koellner, M.3
-
38
-
-
79957467954
-
Synthesis of novel 2-alkoxy(aralkoxy)-4H-[1,2,4]triazolo[1,5-a] quinazolin-5-ones starting with dialkyl-N-cyanoimidocarbonates
-
Al-Salahi, R., Geffken, D. Synthesis of novel 2-alkoxy(aralkoxy)-4H-[1,2, 4]triazolo[1,5-a]quinazolin-5-ones starting with dialkyl-N-cyanoimidocarbonates. J. Heterocycl Chem., 2011;48:656-62.
-
(2011)
J. Heterocycl Chem.
, vol.48
, pp. 656-662
-
-
Al-Salahi, R.1
Geffken, D.2
-
39
-
-
84877578248
-
Antimicrobial activity of a newly synthesized 2-methylsulfanyl-[1,2,4] triazolo[1,5-a]quinazolin-5-one and its derivatives
-
Al-Salahi, R., Marzouk, M., Awad, G., Al-Omer M., Ezzeldin, E. Antimicrobial activity of a newly synthesized 2-methylsulfanyl-[1,2,4] triazolo[1,5-a]quinazolin-5-one and its derivatives. J. Pharm. Pharmacol., 2013;65:790-7.
-
(2013)
J. Pharm. Pharmacol.
, vol.65
, pp. 790-797
-
-
Al-Salahi, R.1
Marzouk, M.2
Awad, G.3
Al-Omer, M.4
Ezzeldin, E.5
-
40
-
-
78149460389
-
Synthesis and reactivity of [1,2,4]triazolo-annelated quinazolines
-
Al-Salahi R., Geffken, D. Synthesis and reactivity of [1,2,4]triazolo-annelated quinazolines, Molecules, 2010;15:7016-34.
-
(2010)
Molecules
, vol.15
, pp. 7016-7034
-
-
Al-Salahi, R.1
Geffken, D.2
-
41
-
-
22844437902
-
Anti-microbial activity of some substituted triazolo-quinazolines
-
Jantova, S., Ovadekova, R., Letasiova, S., Spirkova, K., Stankovsky, S. Anti-microbial activity of some substituted triazolo-quinazolines. Folia Microbiol., 2005;50:90-4.
-
(2005)
Folia Microbiol.
, vol.50
, pp. 90-94
-
-
Jantova, S.1
Ovadekova, R.2
Letasiova, S.3
Spirkova, K.4
Stankovsky, S.5
-
42
-
-
77950520478
-
Non-classical antifolates. Part 2: Synthesis, biological evaluation, and molecular modeling study of some new 2,6-substituted-quinazolin-4-ones
-
Al-Omary, M.F., Abouzeid, L. A., Nagi, M.N., Habib, E.E., Abdel-Aziz, A. El-Azab, A.S., Abdel-Hamide, S.G., Al-Omar, M.A., Al-Obaid, A.M., El-Subbagh, H.I. Non-classical antifolates. Part 2: Synthesis, Biological evaluation, And molecular modeling study of some new 2,6-substituted-quinazolin-4-ones. Bioorg. Med. Chem., 2010;18:2849-63.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 2849-2863
-
-
Al-Omary, M.F.1
Abouzeid, L.A.2
Nagi, M.N.3
Habib, E.E.4
Abdel-Aziz, A.5
El-Azab, A.S.6
Abdel-Hamide, S.G.7
Al-Omar, M.A.8
Al-Obaid, A.M.9
El-Subbagh, H.I.10
-
43
-
-
0024595042
-
Reexamination and further development of a precise and rapid dye method for measuring cell growth/cell kill
-
Hansen, M.B., Nielsen, S.E., Berg, K. Reexamination and further development of a precise and rapid dye method for measuring cell growth/cell kill. J. Immunol. Meth., 1989;119:203-10.
-
(1989)
J. Immunol. Meth.
, vol.119
, pp. 203-210
-
-
Hansen, M.B.1
Nielsen, S.E.2
Berg, K.3
-
44
-
-
0037294150
-
Mechanism-based in vitro screening of potential cancer chemo-preventive agents
-
Gerhaeuser, C, Elke Heiss, K.K., Neumann, I., Gamal-Eldeen, A., Knauft, J., Liu, G.-Y., Sitthimonchai, S., Fran, N., Mechanism-based in vitro screening of potential cancer chemo-preventive agents. Mutat. Res., 2003;523(4):163-72.
-
(2003)
Mutat. Res.
, vol.523
, Issue.4
, pp. 163-172
-
-
Gerhaeuser, C.1
Elke Heiss, K.K.2
Neumann, I.3
Gamal-Eldeen, A.4
Knauft, J.5
Liu, G.-Y.6
Sitthimonchai, S.7
Fran, N.8
-
45
-
-
0022186670
-
Measurement of protein using bicinchoninic acid
-
Smith, P.K., Krohn, R.I., Hermanson, G.T., Mallia, A.K., Gartner, F.H., Provenzano, M.D., Fujimoto, E.K., Goeke, N.M., Olson, B.J., Klenk, D.C. Measurement of protein using bicinchoninic acid. Anal. Biochem., 1985;150:76-85.
-
(1985)
Anal. Biochem.
, vol.150
, pp. 76-85
-
-
Smith, P.K.1
Krohn, R.I.2
Hermanson, G.T.3
Mallia, A.K.4
Gartner, F.H.5
Provenzano, M.D.6
Fujimoto, E.K.7
Goeke, N.M.8
Olson, B.J.9
Klenk, D.C.10
-
46
-
-
79961211503
-
Synthesis of 2-methylsulfanyl-4H-[1,2,4]triazolo[1,5-a]quinazolin 5-one and derivatives
-
Al-Salahi, R., Geffken, D. Synthesis of 2-methylsulfanyl-4H-[1,2,4] triazolo[1,5-a]quinazolin 5-one and derivatives. Synth. Comm., 2011;41:3512-23.
-
(2011)
Synth. Comm.
, vol.41
, pp. 3512-3523
-
-
Al-Salahi, R.1
Geffken, D.2
-
47
-
-
0000147542
-
Recent advances in chemoprevention of cancer
-
Hong, W.K., Sporn, M.B. Recent advances in chemoprevention of cancer. Science, 1997;278:1073-7.
-
(1997)
Science
, vol.278
, pp. 1073-1077
-
-
Hong, W.K.1
Sporn, M.B.2
-
48
-
-
0035150912
-
The molecular biology of cancer
-
Bertram, J.S. The molecular biology of cancer. Mol. Asp. Med., 2000;21:167-223.
-
(2000)
Mol. Asp. Med.
, vol.21
, pp. 167-223
-
-
Bertram, J.S.1
-
49
-
-
33646028804
-
Molecular targets of dietary agents for prevention and therapy of cancer
-
Aggarwal, B.B., Shishodia, S. Molecular targets of dietary agents for prevention and therapy of cancer. Biochem. Pharmacol., 2006;71:1397-421.
-
(2006)
Biochem. Pharmacol.
, vol.71
, pp. 1397-1421
-
-
Aggarwal, B.B.1
Shishodia, S.2
-
50
-
-
1542376883
-
Enzyme-catalyzed activation of anticancer prodrugs
-
Rooseboom, M., Commandeur, J. N. M., Vermeulen, N. P. E. Enzyme-catalyzed activation of anticancer prodrugs. Pharmacol. Rev., 2004;56:53-102.
-
(2004)
Pharmacol. Rev.
, vol.56
, pp. 53-102
-
-
Rooseboom, M.1
Commandeur, J.N.M.2
Vermeulen, N.P.E.3
-
51
-
-
0000511766
-
Thiazolo[3,2-a] benzimidazoles
-
Alper, A.E., Taurine, A. Thiazolo[3,2-a] benzimidazoles. Can. J. Chem., 1967;45:2903-12.
-
(1967)
Can. J. Chem.
, vol.45
, pp. 2903-2912
-
-
Alper, A.E.1
Taurine, A.2
-
52
-
-
0034653356
-
Epoxide hydrolase-polymorphism and role in toxicology
-
365-370
-
Omiecinski, C.J., Hassett, C, Hosagrahara, V. Epoxide hydrolase-polymorphism and role in Toxicology, Toxicol. Lett., 2000;112-113, 365-70.
-
(2000)
Toxicol. Lett.
, pp. 112-113
-
-
Omiecinski, C.J.1
Hassett, C.2
Hosagrahara, V.3
|