-
1
-
-
30344436995
-
Novel 5-(2-hydroxyphenyl)-3-substituted-2, 3-dihydro-1,3,4-oxadiazole-2-thione derivatives: promising anticancer agents
-
Aboraia A., Rahman H.M.A., Mahfuz N., Mohmoud A., Gendy E.L. Novel 5-(2-hydroxyphenyl)-3-substituted-2, 3-dihydro-1,3,4-oxadiazole-2-thione derivatives: promising anticancer agents. Bioorg. Med. Chem. 2006, 14:1236-1246.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 1236-1246
-
-
Aboraia, A.1
Rahman, H.M.A.2
Mahfuz, N.3
Mohmoud, A.4
Gendy, E.L.5
-
2
-
-
0038734404
-
Genotoxicity of two anticancer drugs, gemcitabine and topotecan, in mouse bone marrow in vivo
-
Aydemir N., Bilaloglu R. Genotoxicity of two anticancer drugs, gemcitabine and topotecan, in mouse bone marrow in vivo. Mutat. Res. 2003, 537:43-51.
-
(2003)
Mutat. Res.
, vol.537
, pp. 43-51
-
-
Aydemir, N.1
Bilaloglu, R.2
-
3
-
-
79957948101
-
-
Textbook of Organic Chemistry, 5th ed., S Chand and Company Ltd., New Delhi
-
Bahl, A.A., 2004. Textbook of Organic Chemistry, 5th ed., S Chand and Company Ltd., New Delhi, p. 364.
-
(2004)
, pp. 364
-
-
Bahl, A.A.1
-
4
-
-
39049103420
-
Design, synthesis and evaluation of antiinflammatory, analgesic and ulcerogenicity studies of novel S-substituted phenacyl-1,3,4-oxadiazole-2-thiol and Schiff bases of diclofenac acid as nonulcerogenic derivatives
-
Bhandari S., Bothara K., Raut M., Patil A., Sarkate A., Mokale V. Design, synthesis and evaluation of antiinflammatory, analgesic and ulcerogenicity studies of novel S-substituted phenacyl-1,3,4-oxadiazole-2-thiol and Schiff bases of diclofenac acid as nonulcerogenic derivatives. Bioorg. Med. Chem. 2008, 16:1822-1831.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 1822-1831
-
-
Bhandari, S.1
Bothara, K.2
Raut, M.3
Patil, A.4
Sarkate, A.5
Mokale, V.6
-
5
-
-
0034675333
-
The Endogenous Oxindoles 5-Hydroxyoxindole and Isatin are Antiproliferative and Proapoptotic
-
Cane A., Tournaire M.C., Barritault D., Crumeyrolle-Arias M. The Endogenous Oxindoles 5-Hydroxyoxindole and Isatin are Antiproliferative and Proapoptotic. Biochem. Biophys. Res. Commun. 2000, 276:379-384.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.276
, pp. 379-384
-
-
Cane, A.1
Tournaire, M.C.2
Barritault, D.3
Crumeyrolle-Arias, M.4
-
6
-
-
33745211022
-
In vitro and in vivo evaluation of isatin-beta-thiosemicarbazone and marboran against vaccinia and cowpox virus infections
-
Debra C.Q., Kathy A.K., Kern E.R. In vitro and in vivo evaluation of isatin-beta-thiosemicarbazone and marboran against vaccinia and cowpox virus infections. Antiviral Res. 2006, 71:24-30.
-
(2006)
Antiviral Res.
, vol.71
, pp. 24-30
-
-
Debra, C.Q.1
Kathy, A.K.2
Kern, E.R.3
-
7
-
-
0038798651
-
Synthesis and primary cytotoxicity evaluation of 3-[[(3-phenyl-4(3H)-quinazolinone-2-yl)mercaptoacetyl]hydrazono]-1H-2-indolinones
-
Gursoy A., Karal N. Synthesis and primary cytotoxicity evaluation of 3-[[(3-phenyl-4(3H)-quinazolinone-2-yl)mercaptoacetyl]hydrazono]-1H-2-indolinones. Eur. J. Med. Chem. 2003, 38:633-643.
-
(2003)
Eur. J. Med. Chem.
, vol.38
, pp. 633-643
-
-
Gursoy, A.1
Karal, N.2
-
8
-
-
38149093408
-
Cytotoxic 3, 5-bis(benzylidene)piperidin-4-ones and N-acyl analogs displaying selective toxicity for malignant cells
-
Hari H.P., Umashankar D., Wilson J.Q., Masami K., Hiroshi S., Jonathan R.D. Cytotoxic 3, 5-bis(benzylidene)piperidin-4-ones and N-acyl analogs displaying selective toxicity for malignant cells. Eur. J. Med. Chem. 2008, 43:1-7.
-
(2008)
Eur. J. Med. Chem.
, vol.43
, pp. 1-7
-
-
Hari, H.P.1
Umashankar, D.2
Wilson, J.Q.3
Masami, K.4
Hiroshi, S.5
Jonathan, R.D.6
-
9
-
-
0141555348
-
-
Organic synthesis collective, 2nd ed. John Wiley and Sons, New York
-
Henry, G., Blatt, A.H., 1964. Organic synthesis collective, vol. I, 2nd ed. John Wiley and Sons, New York, pp. 327-334.
-
(1964)
, vol.1
, pp. 327-334
-
-
Henry, G.1
Blatt, A.H.2
-
10
-
-
34447274051
-
Synthesis and structure-antituberculosis activity relationship of 1H-indole-2, 3-dione derivatives
-
Karal N., Gursoy A., Kandemirli F., Shvets N., Kaynak F.B., Ozbey S., Kovalishyne V., Dimoglo A. Synthesis and structure-antituberculosis activity relationship of 1H-indole-2, 3-dione derivatives. Bioorg. Med. Chem. 2007, 15:5888-5904.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 5888-5904
-
-
Karal, N.1
Gursoy, A.2
Kandemirli, F.3
Shvets, N.4
Kaynak, F.B.5
Ozbey, S.6
Kovalishyne, V.7
Dimoglo, A.8
-
11
-
-
26844573597
-
Synthesis and antimicrobial study of novel heterocyclic compounds from hydroxybenzophenones
-
Khanum S.A., Shashikanth S., Umesh S., Kavitha R. Synthesis and antimicrobial study of novel heterocyclic compounds from hydroxybenzophenones. Eur. J. Med. Chem. 2005, 40:1156-1162.
-
(2005)
Eur. J. Med. Chem.
, vol.40
, pp. 1156-1162
-
-
Khanum, S.A.1
Shashikanth, S.2
Umesh, S.3
Kavitha, R.4
-
12
-
-
34250200740
-
Synthesis of some novel heterocyclic compounds derived from diflunisal hydrazide as potential anti-infective and anti-inflammatory agents
-
Kucukguzel S.G., Kucukguzel I.K., Tatar E., Rollas S., Sahin F., Gulluce M., Clercq E.D., Kabasakal L. Synthesis of some novel heterocyclic compounds derived from diflunisal hydrazide as potential anti-infective and anti-inflammatory agents. Eur. J. Med. Chem. 2007, 42:893-901.
-
(2007)
Eur. J. Med. Chem.
, vol.42
, pp. 893-901
-
-
Kucukguzel, S.G.1
Kucukguzel, I.K.2
Tatar, E.3
Rollas, S.4
Sahin, F.5
Gulluce, M.6
Clercq, E.D.7
Kabasakal, L.8
-
13
-
-
8944260413
-
N-Heteroaryl-2-phenyl-3-(benzyloxy)piperidines: a novel class of potent orally active human NK1 antagonists
-
Ladduwahetty T., Baker R., Cascieri M.A., Chamber J.M., Haworth K., Keown L.E., MacIntyre E., Metzger J.M., Owen S., Ryeroft W., Sadowski S., Seward E., Shepheard S.L., Swain C.L., Tattersall F.D., Watt A.P., Willianmson D.W., Hargreaves R.J. N-Heteroaryl-2-phenyl-3-(benzyloxy)piperidines: a novel class of potent orally active human NK1 antagonists. J. Med. Chem. 1996, 39:2907-2913.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2907-2913
-
-
Ladduwahetty, T.1
Baker, R.2
Cascieri, M.A.3
Chamber, J.M.4
Haworth, K.5
Keown, L.E.6
MacIntyre, E.7
Metzger, J.M.8
Owen, S.9
Ryeroft, W.10
Sadowski, S.11
Seward, E.12
Shepheard, S.L.13
Swain, C.L.14
Tattersall, F.D.15
Watt, A.P.16
Willianmson, D.W.17
Hargreaves, R.J.18
-
14
-
-
0035821595
-
Potent and selective nonpeptide inhibitors of caspases 3 and 7
-
Lee D., Long S.A., Murray J.H., Adams J.L., Nuttall M.E., Nadeau D.P., Kikly K., Winkler J.D., Sung C.M., Ryan M.D., Levy M.A., Keller P.M., DeWolf W.E. Potent and selective nonpeptide inhibitors of caspases 3 and 7. J. Med. Chem. 2001, 44:2015-2020.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2015-2020
-
-
Lee, D.1
Long, S.A.2
Murray, J.H.3
Adams, J.L.4
Nuttall, M.E.5
Nadeau, D.P.6
Kikly, K.7
Winkler, J.D.8
Sung, C.M.9
Ryan, M.D.10
Levy, M.A.11
Keller, P.M.12
DeWolf, W.E.13
-
15
-
-
0037428819
-
Antitumour 2-(4-aminophenyl)benzothiazoles generate DNA adducts in sensitive tumour cells in vitro and in vivo
-
Leong C.O., Gaskell M., Martin E.A., Heydon R.T., Farmer P.B., Bibby M.C., Cooper P.A., Double J.A., Bradshaw T.D., Stevens M.F. Antitumour 2-(4-aminophenyl)benzothiazoles generate DNA adducts in sensitive tumour cells in vitro and in vivo. Br. J. Cancer 2003, 88:470-477.
-
(2003)
Br. J. Cancer
, vol.88
, pp. 470-477
-
-
Leong, C.O.1
Gaskell, M.2
Martin, E.A.3
Heydon, R.T.4
Farmer, P.B.5
Bibby, M.C.6
Cooper, P.A.7
Double, J.A.8
Bradshaw, T.D.9
Stevens, M.F.10
-
16
-
-
18144398613
-
Antimycobacterial activity of new 3-substituted 5-(pyridin-4-yl)-3H-1,3,4-oxadiazol-2-one and 2-thione derivatives. Preliminary molecular modeling investigations
-
Mamolo M.G., Zampieri D., Voi L., Fermeglia M., Ferrone M., Pricl S., Scialinoc G., Banfi E. Antimycobacterial activity of new 3-substituted 5-(pyridin-4-yl)-3H-1,3,4-oxadiazol-2-one and 2-thione derivatives. Preliminary molecular modeling investigations. Bioorg. Med. Chem. 2005, 13:3797-3808.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 3797-3808
-
-
Mamolo, M.G.1
Zampieri, D.2
Voi, L.3
Fermeglia, M.4
Ferrone, M.5
Pricl, S.6
Scialinoc, G.7
Banfi, E.8
-
17
-
-
0025775062
-
Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines
-
Monks A., Scudiero D., Skehan P., Shoemaker R., Paull K., Vistica D., Hose C., Langley J., Cronise P. Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. J. Natl. Cancer Inst. 1991, 83:757-766.
-
(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
-
18
-
-
0028352765
-
Anti-inflammatory activity of substituted 1,3,4-oxadiazoles
-
Nargund L.V.G., Reddy G.R.N., Hariprasad V. Anti-inflammatory activity of substituted 1,3,4-oxadiazoles. J. Pharm. Sci. 1994, 83:246-248.
-
(1994)
J. Pharm. Sci.
, vol.83
, pp. 246-248
-
-
Nargund, L.V.G.1
Reddy, G.R.N.2
Hariprasad, V.3
-
19
-
-
33750727334
-
Resistance to cisplatin and adriamycin is associated with the inhibition of glutathione efflux in MCF-7-derived cells
-
Osbild S., Brault L., Battaglia E., Bagrel D. Resistance to cisplatin and adriamycin is associated with the inhibition of glutathione efflux in MCF-7-derived cells. Anticancer Res. 2006, 26:3595-3600.
-
(2006)
Anticancer Res.
, vol.26
, pp. 3595-3600
-
-
Osbild, S.1
Brault, L.2
Battaglia, E.3
Bagrel, D.4
-
20
-
-
0033395476
-
Synthesis, antibacterial, antifungal and anti-HIV evaluation of Schiff and Mannich bases of isatin derivatives with 3-amino-2-methylmercapto quinazolin-4(3H)-one
-
Pandeya S.N., Sriram D., Nath G., Clercq E.D. Synthesis, antibacterial, antifungal and anti-HIV evaluation of Schiff and Mannich bases of isatin derivatives with 3-amino-2-methylmercapto quinazolin-4(3H)-one. Pharm. Acta Helv. 1999, 74:11-17.
-
(1999)
Pharm. Acta Helv.
, vol.74
, pp. 11-17
-
-
Pandeya, S.N.1
Sriram, D.2
Nath, G.3
Clercq, E.D.4
-
21
-
-
0032849363
-
Synthesis and antimicrobial activity of Schiff and Mannich bases of isatin and its derivatives with pyrimidine
-
Pandeya S.N., Sriram D., Nath G., Clercq E.D. Synthesis and antimicrobial activity of Schiff and Mannich bases of isatin and its derivatives with pyrimidine. Il Farmaco 1999, 54:624-628.
-
(1999)
Il Farmaco
, vol.54
, pp. 624-628
-
-
Pandeya, S.N.1
Sriram, D.2
Nath, G.3
Clercq, E.D.4
-
22
-
-
0025341331
-
New colorimetric cytotoxicity assay for anticancer-drug screening
-
Skehan P., Storeng R., Scudiero D., Monks A., McMohan J., Vistica D., Warren J.T., Bokesch H., Kenney S., Boyd M.R. New colorimetric cytotoxicity assay for anticancer-drug screening. J. Natl. Cancer Inst. 1990, 82:1107-1112.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1107-1112
-
-
Skehan, P.1
Storeng, R.2
Scudiero, D.3
Monks, A.4
McMohan, J.5
Vistica, D.6
Warren, J.T.7
Bokesch, H.8
Kenney, S.9
Boyd, M.R.10
-
23
-
-
0035159356
-
Synthesis and pharmacological activities of hydrazones, Schiff and Mannich bases of isatin derivatives
-
Sridhar S.K., Ramesh A. Synthesis and pharmacological activities of hydrazones, Schiff and Mannich bases of isatin derivatives. Biol. Pharm. Bull. 2001, 24(10):1149-1152.
-
(2001)
Biol. Pharm. Bull.
, vol.24
, Issue.10
, pp. 1149-1152
-
-
Sridhar, S.K.1
Ramesh, A.2
-
24
-
-
1542593260
-
Synthesis of substituted 2-phenylbenzothiazoles and 5(6)-nitro-1,3-disubsituted-benzimidazoline-2-thiones as CNS active agents
-
Varma R.S., Chauhan S. Synthesis of substituted 2-phenylbenzothiazoles and 5(6)-nitro-1,3-disubsituted-benzimidazoline-2-thiones as CNS active agents. Ind. J. Chem. 1988, 27B:438-442.
-
(1988)
Ind. J. Chem.
, vol.27
, pp. 438-442
-
-
Varma, R.S.1
Chauhan, S.2
-
25
-
-
1942488330
-
Anticonvulsant activity of Schiff bases of isatin derivatives
-
Verma M., Pandeya S.N., Singh K., Stable J.P. Anticonvulsant activity of Schiff bases of isatin derivatives. Acta Pharm. 2004, 54:49-56.
-
(2004)
Acta Pharm.
, vol.54
, pp. 49-56
-
-
Verma, M.1
Pandeya, S.N.2
Singh, K.3
Stable, J.P.4
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