-
1
-
-
79953171465
-
Design, synthesis and in vitro antimicrobial evaluation of novel imidazo[1,2-a]pyridine and imidazo[2,1-b] [1,3]benzothiazole motifs
-
Al-Tel, T.H., Al-Qawasmeh, R.A., Zaarour, R., 2011. Design, synthesis and in vitro antimicrobial evaluation of novel Imidazo[1,2-a]pyridine and imidazo[2,1-b] [1,3]benzothiazole motifs. Eur. J. Med. Chem. 46, 1874-1881.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 1874-1881
-
-
Al-Tel, T.H.1
Al-Qawasmeh, R.A.2
Zaarour, R.3
-
2
-
-
70350336880
-
Role of human CYP1A1 and NAT2 in 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine-induced mutagenicity and DNA adducts
-
Bendaly, J., Metry, K.J., Doll, M.A., Jiang, G., States, J.C., Smith, N.B., Neale, J.R., Holloman, J.L, Pierce, W.M., Hein, D.W., 2009. Role of human CYP1A1 and NAT2 in 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-induced mutagenicity and DNA adducts. Xenobiotica 39, 399-406.
-
(2009)
Xenobiotica
, vol.39
, pp. 399-406
-
-
Bendaly, J.1
Metry, K.J.2
Doll, M.A.3
Jiang, G.4
States, J.C.5
Smith, N.B.6
Neale, J.R.7
Holloman, J.L.8
Pierce, W.M.9
Hein, D.W.10
-
3
-
-
33644986999
-
Synthesis and SAR studies of very potent imidazopyridine antiprotozoal agents
-
Biftu, T., Feng, D., Fisher, M., Liang, G.B., Qian, X., Scribner, A., Dennis, R., Lee, S., Liberator, P.A., Brown, C, Gurnett, A., Leavitt, P.S., Thompson, D., Mathew, J., Misura, A., Samaras, S., Tamas, T., Sina, J.F., McNulty, K.A., McKnight, CG., Schmatz, D.M., Wyvratt, M., 2006. Synthesis and SAR studies of very potent imidazopyridine antiprotozoal agents. Bioorg. Med. Chem. Lett. 16, 2479-2483.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 2479-2483
-
-
Biftu, T.1
Feng, D.2
Fisher, M.3
Liang, G.B.4
Qian, X.5
Scribner, A.6
Dennis, R.7
Lee, S.8
Liberator, P.A.9
Brown, C.10
Gurnett, A.11
Leavitt, P.S.12
Thompson, D.13
Mathew, J.14
Misura, A.15
Samaras, S.16
Tamas, T.17
Sina, J.F.18
McNulty, K.A.19
McKnight, C.G.20
Schmatz, D.M.21
Wyvratt, M.22
more..
-
4
-
-
33845922215
-
Heterocyclic amines: Chemistry and health
-
DOI 10.1002/mnfr.200600086
-
Cheng, K.W., Chen, F., Wang, M., 2006. Heterocyclic amines: chemistry and health. Mol. Nutr. Food Res. 50, 1150-1170. (Pubitemid 46043100)
-
(2006)
Molecular Nutrition and Food Research
, vol.50
, Issue.12
, pp. 1150-1170
-
-
Cheng, K.-W.1
Chen, F.2
Wang, M.3
-
5
-
-
84873692024
-
Antimutagenic and antioxidant activity of novel 4-substituted phenyl-2,2'-bichalcophenes and aza-analogues
-
El-Sayed, WM., Hussin, W.A., 2013. Antimutagenic and antioxidant activity of novel 4-substituted phenyl-2,2'-bichalcophenes and aza-analogues. Drug Des. Devel. Ther. 7, 73-81.
-
(2013)
Drug Des. Devel. Ther.
, vol.7
, pp. 73-81
-
-
El-Sayed, W.M.1
Hussin, W.A.2
-
6
-
-
33846249245
-
The anti-mutagenicity of 2-substitiuted selenazolidine-4-(R)-carboxylic acids
-
El-Sayed, W.M., Hussin, W.A., Franklin, M.R., 2007. The anti-mutagenicity of 2-substitiuted selenazolidine-4-(R)-carboxylic acids. Mutat. Res. 627, 136-145.
-
(2007)
Mutat. Res.
, vol.627
, pp. 136-145
-
-
El-Sayed, W.M.1
Hussin, W.A.2
Franklin, M.R.3
-
7
-
-
79959451461
-
Synthesis, antibacterial and potential anti-HIV activity of some novel imidazole analogs
-
Ganguly, S., Vithlani, V.V., Kesharwani, A.K., Kuhu, R., Baskar, L., Mitramazumder, P., Sharon, A., Dev, A., 2011. Synthesis, antibacterial and potential anti-HIV activity of some novel imidazole analogs. Acta. Pharm. 61, 187-201.
-
(2011)
Acta. Pharm.
, vol.61
, pp. 187-201
-
-
Ganguly, S.1
Vithlani, V.V.2
Kesharwani, A.K.3
Kuhu, R.4
Baskar, L.5
Mitramazumder, P.6
Sharon, A.7
Dev, A.8
-
9
-
-
80053465790
-
Mutagenicity and anti-mutagenicity of acanthopanax divaricatus var
-
Hong, CE., Cho, M.C, Jang, H.A., Lyu, S.Y., 2011. Mutagenicity and anti-mutagenicity of Acanthopanax divaricatus var. albeofructus. J. Toxicol. Sci. 36, 661-668.
-
(2011)
Albeofructus. J. Toxicol. Sci.
, vol.36
, pp. 661-668
-
-
Hong, C.E.1
Cho, M.C.2
Jang, H.A.3
Lyu, S.Y.4
-
10
-
-
0026726554
-
Suicide inhibitors of cytochrome P450 1A1 and P450 2B1
-
Hopkins, N.E., Foroozesh, M.K., Alworth, WL, 1992. Suicide inhibitors of cytochrome P450 1A1 and P450 2B1. Biochem. Pharmacol. 44, 787-796.
-
(1992)
Biochem. Pharmacol.
, vol.44
, pp. 787-796
-
-
Hopkins, N.E.1
Foroozesh, M.K.2
Alworth, W.L.3
-
11
-
-
38549177533
-
Synthesis and antiprotozoal activity of novel bis-benzamidino imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines
-
DOI 10.1016/j.bmc.2007.10.042, PII S0968089607009108
-
Ismail, MA, Arafa, R.K., Wenzler, T., Brun, R., Tanious, FA, Wilson, W.D., Boykin, D.W., 2008. Synthesis and antiprotozoal activity of novel bis-benzamidino imidazo [1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a] pyridines. Bioorg. Med. Chem 16, 683-691. (Pubitemid 351163070)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.2
, pp. 683-691
-
-
Ismail, M.A.1
Arafa, R.K.2
Wenzler, T.3
Brun, R.4
Tanious, F.A.5
Wilson, W.D.6
Boykin, D.W.7
-
12
-
-
3042552194
-
Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro- imidazo[1, 2-a]pyridines as antiprotozoal agents
-
DOI 10.1021/jm0400092
-
Ismail, M.A., Brun, R., Wenzler, T., Tanious, F.A., Wilson, W.D., Boykin, D.W., 2004. Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro- imidazo[1,2-a] pyridines as antiprotozoal agents. J. Med. Chem. 47, 3658-3664. (Pubitemid 38822026)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.14
, pp. 3658-3664
-
-
Ismail, M.A.1
Brun, R.2
Wenzler, T.3
Tanious, F.A.4
Wilson, W.D.5
Boykin, D.W.6
-
13
-
-
27844511986
-
Light-dependent mutagenesis by benzo[a]pyrene is mediated via oxidative DNA damage
-
DOI 10.1002/em.20141
-
Kim, S.R., Kokubo, K., Matsui, K., Yamada, N., Kanke, Y., Fukuoka, M., Yamada, M., Nohmi, T, 2005. Light-dependent mutagenesis by benzo[a]pyrene is mediated via oxidative DNA damage. Environ. Mol. Mutagen. 46, 141-149. (Pubitemid 41642305)
-
(2005)
Environmental and Molecular Mutagenesis
, vol.46
, Issue.3
, pp. 141-149
-
-
Kim, S.-R.1
Kokubo, K.2
Matsui, K.3
Yamada, N.4
Kanke, Y.5
Fukuoka, M.6
Yamada, M.7
Nohmi, T.8
-
14
-
-
9944252325
-
Antioxidant and antimutagenic activity of N-(2-carboxyethyl)chitosan
-
DOI 10.1016/j.taap.2004.05.009, PII S0041008X04002790
-
Kogan, G., Skorik, YA, Zitnanová, I., Krizková, L, Duracková, Z., Gomes, CA, Yatluk, Y.G., Krajcovic, J., 2004. Antioxidant and antimutagenic activity of N-(2-carboxyethyl) chitosan. Toxicol. Appl. Pharmacol. 201, 303-310. (Pubitemid 39593628)
-
(2004)
Toxicology and Applied Pharmacology
, vol.201
, Issue.3
, pp. 303-310
-
-
Kogan, G.1
Skorik, Y.A.2
Zitnanova, I.3
Krizkova, L.4
Durackova, Z.5
Gomes, C.A.R.6
Yatluk, Y.G.7
Krajcovic, J.8
-
15
-
-
0035102180
-
Metabolism of 2-amino-3,8-dimethylimidazo[4,5-f]-quinoxaline in human hepatocytes: 2-amino-3-methylimidazo[4,5-f]quinoxaline-8-carboxylic acid is a major detoxication pathway catalyzed by cytochrome P450 1A2
-
DOI 10.1021/tx000176e
-
Langouët, S., Welti, D.H., Kerriguy, N., Fay, LB., Huynh-Ba, T., Markovic, J., Guengerich, F.P., Guillouzo, A., Turesky, R.J., 2001. Metabolism of 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline in human hepatocytes: 2-amino-3-methylimidazo[4,5-f]quinoxaline-8-carboxylic acid is a major detoxification pathway catalyzed by cytochrome P450 1A2. Chem. Res. Toxicol. 14, 211-221. (Pubitemid 32173323)
-
(2001)
Chemical Research in Toxicology
, vol.14
, Issue.2
, pp. 211-221
-
-
Langouet, S.1
Welti, D.H.2
Kerriguy, N.3
Fay, L.B.4
Huynh-Ba, T.5
Markovic, J.6
Guengerich, F.P.7
Guillouzo, A.8
Turesky, R.J.9
-
16
-
-
84868484417
-
HS-173, a novel phospha-tidylinositol 3-kinase (PI3K) inhibitor, has anti-tumor activity through promoting apoptosis and inhibiting angiogenesis
-
Lee, H., Jung, K.H., Jeong, Y, Hong, S., Hong, S.S., 2013. HS-173, a novel phospha-tidylinositol 3-kinase (PI3K) inhibitor, has anti-tumor activity through promoting apoptosis and inhibiting angiogenesis. Cancer Lett. 328, 152-159.
-
(2013)
Cancer Lett.
, vol.328
, pp. 152-159
-
-
Lee, H.1
Jung, K.H.2
Jeong, Y.3
Hong, S.4
Hong, S.S.5
-
17
-
-
84857140273
-
A novel imidazopyridine analogue as a phosphatidylinositol 3-kinase inhibitor against human breast cancer
-
Lee, H., Li, G.Y, Jeong, Y, Jung, K.H., Lee, J.H., Ham, K., Hong, S., Hong, S.S., 2012. A novel imidazopyridine analogue as a phosphatidylinositol 3-kinase inhibitor against human breast cancer. Cancer Lett. 318, 68-75.
-
(2012)
Cancer Lett.
, vol.318
, pp. 68-75
-
-
Lee, H.1
Li, G.Y.2
Jeong, Y.3
Jung, K.H.4
Lee, J.H.5
Ham, K.6
Hong, S.7
Hong, S.S.8
-
18
-
-
85030414915
-
A novel imidazopyridine derivative, HS-106, induces apoptosis of breast cancer cells and represses angiogenesis by targeting the PI3K/mTOR pathway
-
Li, G.Y., Jung, K.H., Lee, H., Son, M.K., Seo, J.H., Hong, S.W., Jeong, Y., Hong, S., Hong, S.S., 2012. A novel imidazopyridine derivative, HS-106, induces apoptosis of breast cancer cells and represses angiogenesis by targeting the PI3K/mTOR pathway. Cancer Lett. 12, 601-605.
-
(2012)
Cancer Lett.
, vol.12
, pp. 601-605
-
-
Li, G.Y.1
Jung, K.H.2
Lee, H.3
Son, M.K.4
Seo, J.H.5
Hong, S.W.6
Jeong, Y.7
Hong, S.8
Hong, S.S.9
-
19
-
-
79959864191
-
Water-mediated binding of agents that target the DNA minor groove
-
Liu, Y., Kumar, A., Depauw, S., Nhili, R., David-Cordonnier, M.H., Lee, M.P., Ismail, M.A., Farahat, A.A., Say, M., Chackal-Catoen, S., Batista-Parra, A., Neidle, S., Boykin, D.W., Wilson, W.D., 2011. Water-mediated binding of agents that target the DNA minor groove. J. Am. Chem. Soc. 133, 10171-10183.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 10171-10183
-
-
Liu, Y.1
Kumar, A.2
Depauw, S.3
Nhili, R.4
David-Cordonnier, M.H.5
Lee, M.P.6
Ismail, M.A.7
Farahat, A.A.8
Say, M.9
Chackal-Catoen, S.10
Batista-Parra, A.11
Neidle, S.12
Boykin, D.W.13
Wilson, W.D.14
-
20
-
-
84967546681
-
Metabolic activation and detoxification of polycyclic aromatic hydrocarbons
-
Luch, A.A. (Ed.) Imperial College Press, London
-
Luch, A., Baird, W.M., 2005. Metabolic activation and detoxification of polycyclic aromatic hydrocarbons. In: Luch, A.A. (Ed.), The Carcinogenic Effects of Polycyclic Aromatic Hydrocarbons. Imperial College Press, London, pp. 19-96.
-
(2005)
The Carcinogenic Effects of Polycyclic Aromatic Hydrocarbons
, pp. 19-96
-
-
Luch, A.1
Baird, W.M.2
-
21
-
-
0020533372
-
Revised methods for the Salmonella mutagenicity test
-
Maron, D.M., Ames, B.N., 1983. Revised methods for the Salmonella mutagenicity test. Mutat. Res. 113, 173-215. (Pubitemid 13120319)
-
(1983)
Mutation Research
, vol.113
, Issue.3-4
, pp. 173-215
-
-
Maron, D.M.1
Ames, B.N.2
-
23
-
-
41149177030
-
BYK191023 (2-[2-(4-methoxy-pyridin-2-yl)-ethyl]-3H-imidazo[4,5-b] pyridine) is an NADPH- and time-dependent irreversible inhibitor of inducible nitric-oxide synthase
-
DOI 10.1124/mol.107.041319
-
Tiso, M., Strub, A., Hesslinger, C., Kenney, C.T., Boer, R., Stuehr, D.J., 2008. BYK191023 (2-[2-(4-methoxy-pyridin-2-yl)-ethyl]-3h-imidazo[4,5-b] pyridine) is an NADPH-and time-dependent irreversible inhibitor of inducible nitric-oxide synthase. Mol. Pharmacol. 73, 1244-1253. (Pubitemid 351439206)
-
(2008)
Molecular Pharmacology
, vol.73
, Issue.4
, pp. 1244-1253
-
-
Tiso, M.1
Strub, A.2
Hesslinger, C.3
Kenney, C.T.4
Boer, R.5
Stuehr, D.J.6
-
24
-
-
0032465960
-
Identification of rodent carcinogens and noncarcinogens using genetic toxicity tests: Premises, promises, and performance
-
DOI 10.1006/rtph.1998.1234
-
Zeiger, E., 1998. Identification of rodent carcinogens and noncarcinogens using genetic toxicity tests: Premises, promises, and performance. Regul. Toxicol. Pharmacol. 28, 85-95. (Pubitemid 29076774)
-
(1998)
Regulatory Toxicology and Pharmacology
, vol.28
, Issue.2
, pp. 85-95
-
-
Zeiger, E.1
-
25
-
-
61449180086
-
Activation of aminoimidazole carcinogens by nitrosation: Mutagenicity and nucleotide adducts
-
Zenser, T.V., Lakshmi, V.M., Schut, H.A., Zhou, H.J., Josephy, P.D., 2009. Activation of aminoimidazole carcinogens by nitrosation: mutagenicity and nucleotide adducts. Mutat. Res. 673, 109-115.
-
(2009)
Mutat. Res.
, vol.673
, pp. 109-115
-
-
Zenser, T.V.1
Lakshmi, V.M.2
Schut, H.A.3
Zhou, H.J.4
Josephy, P.D.5
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