-
1
-
-
4544341583
-
Novel analogues of sydnone: Synthesis, characterization and antibacterial evaluation
-
A.M. Mohammed, M.G. Magdy, N.N. Magde, and A.H.B. Waleed, Novel analogues of sydnone: Synthesis, characterization and antibacterial evaluation, Arch. Pharm. 337 (2004), pp. 427-433.
-
(2004)
Arch. Pharm
, vol.337
, pp. 427-433
-
-
Mohammed, A.M.1
Magdy, M.G.2
Magde, N.N.3
Waleed, A.H.B.4
-
2
-
-
34548565604
-
Synthesis and antimicrobial evaluation of new chalcones containing piperazine or 2,5-dichlorothiophene moiety
-
V. Tomar, G. Bhattacharjee, K. Kumar, and A. Kumar, Synthesis and antimicrobial evaluation of new chalcones containing piperazine or 2,5-dichlorothiophene moiety, Bioorg. Med. Chem. Lett. 17 (2007), pp. 5321-5324.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 5321-5324
-
-
Tomar, V.1
Bhattacharjee, G.2
Kumar, K.3
Kumar, A.4
-
3
-
-
0022453198
-
Semisynthesis of A 23187 (Calcimycin) analogs IV. Cation carrier properties in mitochondria of analogs with modified benzoxazole rings
-
M. Prudhomme, J. Guyot, and G. Jeminet, Semisynthesis of A 23187 (Calcimycin) analogs IV. Cation carrier properties in mitochondria of analogs with modified benzoxazole rings, J. Antibiot. 39 (1986), pp. 934-937.
-
(1986)
J. Antibiot
, vol.39
, pp. 934-937
-
-
Prudhomme, M.1
Guyot, J.2
Jeminet, G.3
-
4
-
-
4444231537
-
A novel calcimycin antibiotic from Gram-positive actinomycete frankia microsymbiont
-
H.K. Sarma, B.K. Sharma, and S.C. Tiwari, A novel calcimycin antibiotic from Gram-positive actinomycete frankia microsymbiont, Curr. Sci. 85 (2003), pp. 1401-1403.
-
(2003)
Curr. Sci
, vol.85
, pp. 1401-1403
-
-
Sarma, H.K.1
Sharma, B.K.2
Tiwari, S.C.3
-
5
-
-
0034790758
-
Isolation and biological activity of frankamide
-
J.P. Haansu, K.D. Klika, V.V. Ochaveranko, K. Pihlaja, K.K. Haatela, and P.M. Vourela, Isolation and biological activity of frankamide, J. Ind. Microbiol. Biotechnol. 27 (2001), pp. 62-66.
-
(2001)
J. Ind. Microbiol. Biotechnol
, vol.27
, pp. 62-66
-
-
Haansu, J.P.1
Klika, K.D.2
Ochaveranko, V.V.3
Pihlaja, K.4
Haatela, K.K.5
Vourela, P.M.6
-
6
-
-
0036613953
-
Synthesis and antimicrobial activity of some 2-(p-substituted-phenyl)benzoxazol-5-yl- arylcarboxyamides
-
O.T. Arpaci, E.A. Sener, I. Yalcin, and N. Altanlar, Synthesis and antimicrobial activity of some 2-(p-substituted-phenyl)benzoxazol-5-yl- arylcarboxyamides, Arch. Pharm. 335 (2002), pp. 283-288.
-
(2002)
Arch. Pharm
, vol.335
, pp. 283-288
-
-
Arpaci, O.T.1
Sener, E.A.2
Yalcin, I.3
Altanlar, N.4
-
7
-
-
4544350748
-
Synthesis and antimicrobial activity of new 2-[p-substituted-benzyl]-5-[substituted-carbonylamino]benzoxazoles
-
I. Yildiz-Oren, B. Tekiner, I. Yalçin, O. Temiz-Arpaci, E. Aki-Şener, and N. Altanlar, Synthesis and antimicrobial activity of new 2-[p-substituted-benzyl]-5-[substituted-carbonylamino]benzoxazoles, Arch. Pharm. 337 (2004), pp. 402-410.
-
(2004)
Arch. Pharm
, vol.337
, pp. 402-410
-
-
Yildiz-Oren, I.1
Tekiner, B.2
Yalçin, I.3
Temiz-Arpaci, O.4
Aki-Şener, E.5
Altanlar, N.6
-
8
-
-
35148825557
-
Synthesis and in vitro antimicrobial activity of new 2-[p-substituted-benzyl]-5-[substituted-carbonylamino]benzoxazoles
-
B. Tekiner-Gulbas, O. Temiz-Arpaci, I. Yildiz, and N. Altanlar, Synthesis and in vitro antimicrobial activity of new 2-[p-substituted-benzyl]-5-[substituted-carbonylamino]benzoxazoles, Eur. J. Med. Chem. 42 (2007), pp. 1293-1299.
-
(2007)
Eur. J. Med. Chem
, vol.42
, pp. 1293-1299
-
-
Tekiner-Gulbas, B.1
Temiz-Arpaci, O.2
Yildiz, I.3
Altanlar, N.4
-
9
-
-
17844374872
-
Synthesis and antimicrobial activity of some 5-[(2-morpholin-4-yl)acetamido] and/or 5-[2-(4-substitutedpiperazin-1-yl) acetamido]-2-(p-substituted-phenyl)benzoxazoles
-
O. Temiz-Arpaci, A. Ozdemir, I. Yalçin, I. Yildiz, E. Aki-Sener, and N. Altanlar, Synthesis and antimicrobial activity of some 5-[(2-morpholin-4-yl)acetamido] and/or 5-[2-(4-substitutedpiperazin-1-yl) acetamido]-2-(p-substituted-phenyl)benzoxazoles, Arch. Pharm. 338 (2005), pp. 105-111.
-
(2005)
Arch. Pharm
, vol.338
, pp. 105-111
-
-
Temiz-Arpaci, O.1
Ozdemir, A.2
Yalçin, I.3
Yildiz, I.4
Aki-Sener, E.5
Altanlar, N.6
-
10
-
-
0037131751
-
Heterocyclic benzazole derivatives with antimycobacterial in vitro activity
-
J. Koci, V. Klimesova, K. Waisser, J. Kaustova, H.M. Dahse, and U. Mollmann, Heterocyclic benzazole derivatives with antimycobacterial in vitro activity, Bioorg. Med. Chem. Lett. 12 (2002), pp. 3275-3278.
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, pp. 3275-3278
-
-
Koci, J.1
Klimesova, V.2
Waisser, K.3
Kaustova, J.4
Dahse, H.M.5
Mollmann, U.6
-
11
-
-
85195091662
-
-
M. Ueki, K. Ueno, S. Miyadoh, K. Abe, K. Shibata, and M. Tanuguchi, UK-1, A novel cytotoxic metabolite from streptomyces sp. 517-02. I. Taxonomy, fermentation, isolation, physicochemical and biological properties, J. Antibiot. 46 (1993), pp. 1089-1094.
-
M. Ueki, K. Ueno, S. Miyadoh, K. Abe, K. Shibata, and M. Tanuguchi, UK-1, A novel cytotoxic metabolite from streptomyces sp. 517-02. I. Taxonomy, fermentation, isolation, physicochemical and biological properties, J. Antibiot. 46 (1993), pp. 1089-1094.
-
-
-
-
12
-
-
0029780539
-
Antitumor benzothiazoles. 3. Synthesis of 2-(4-aminophenyl)benzothiazoles and evaluation of their activities against breast cancer cell lines in vitro and in vivo
-
D.F. Shi, T.D. Bradshaw, S. Wrigley, C.J. McCall, P. Lelieveld, I. Fichtner, and M.F.G. Stevens, Antitumor benzothiazoles. 3. Synthesis of 2-(4-aminophenyl)benzothiazoles and evaluation of their activities against breast cancer cell lines in vitro and in vivo, J. Med. Chem. 39 (1996), pp. 3375-3384.
-
(1996)
J. Med. Chem
, vol.39
, pp. 3375-3384
-
-
Shi, D.F.1
Bradshaw, T.D.2
Wrigley, S.3
McCall, C.J.4
Lelieveld, P.5
Fichtner, I.6
Stevens, M.F.G.7
-
13
-
-
0031012286
-
The total synthesis of UK-1
-
M.R. DeLuca and S. Kerwin, The total synthesis of UK-1, Tetrahedron Lett. 38 (1997), pp. 199-202.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 199-202
-
-
DeLuca, M.R.1
Kerwin, S.2
-
14
-
-
0032875978
-
The novel bis(benzoxazole) cytotoxic natural product UK-1 is a magnesium ion dependent DNA binding agent and inhibitor of human Topoisomerase II
-
M.B. Reynolds, M.R. DeLuca, and S. Kerwin, The novel bis(benzoxazole) cytotoxic natural product UK-1 is a magnesium ion dependent DNA binding agent and inhibitor of human Topoisomerase II, Bioorg. Chem. 27 (1999), pp. 326-337.
-
(1999)
Bioorg. Chem
, vol.27
, pp. 326-337
-
-
Reynolds, M.B.1
DeLuca, M.R.2
Kerwin, S.3
-
15
-
-
0002100506
-
Novel coumarin derivatives with expected biological activity
-
Z.M. Nofal, M.I. El-Zahar, and S.S. Abd El-Karim, Novel coumarin derivatives with expected biological activity, Molecules 5 (2000), pp. 99-113.
-
(2000)
Molecules
, vol.5
, pp. 99-113
-
-
Nofal, Z.M.1
El-Zahar, M.I.2
Abd El-Karim, S.S.3
-
16
-
-
0026489556
-
Synthesis and evaluation of 2-pyridinone derivatives as HIV-1 specific reverse transcriptase inhibitors. 2. Analogues of 3-aminopyridin-2(1H)-one
-
W.S. Saari, J.S. Wai, T.E. Fisher, C.M. Thomas, J.M. Hoffman, C.S. Roomey, A.M. Smith, J.H. Jones, D.L. Bamberger, M.E. Goldman, O'brien J.A., Nunberg J.H., Quintero J.C., Schleif Q.A., Emini E.A., and Anderson P.S., Synthesis and evaluation of 2-pyridinone derivatives as HIV-1 specific reverse transcriptase inhibitors. 2. Analogues of 3-aminopyridin-2(1H)-one, J. Med. Chem. 35 (1992), pp. 3792-3802.
-
(1992)
J. Med. Chem
, vol.35
, pp. 3792-3802
-
-
Saari, W.S.1
Wai, J.S.2
Fisher, T.E.3
Thomas, C.M.4
Hoffman, J.M.5
Roomey, C.S.6
Smith, A.M.7
Jones, J.H.8
Bamberger, D.L.9
Goldman, M.E.10
O'brien, J.A.11
Nunberg, J.H.12
Quintero, J.C.13
Schleif, Q.A.14
Emini, E.A.15
Anderson, P.S.16
-
17
-
-
0027213264
-
A nonnucleoside reverse transcriptase inhibitor active on human immuno deficiency virus type 1 isolates resistant to related inhibitors
-
M.E. Goldman, J.A. O'brien, T.L. Ruffing, W.A. Schleif, V.V. Sardana, V.W. Byrnes, J.H. Condra, J.M. Hoffman, and E.A. Emini, A nonnucleoside reverse transcriptase inhibitor active on human immuno deficiency virus type 1 isolates resistant to related inhibitors, Antimicrob. Agents Chemother. 37 (1993), pp. 947-949.
-
(1993)
Antimicrob. Agents Chemother
, vol.37
, pp. 947-949
-
-
Goldman, M.E.1
O'brien, J.A.2
Ruffing, T.L.3
Schleif, W.A.4
Sardana, V.V.5
Byrnes, V.W.6
Condra, J.H.7
Hoffman, J.M.8
Emini, E.A.9
-
18
-
-
0027229213
-
Synthesis and evaluation of 2-pyridinone derivatives as HIV-1 specific reverse transcriptase inhibitors. 4. 3-2-(benzoxazol-2-yl) ethyl-5-ethyl-6-methylpyridin-2-(1H)-one and analogues
-
J.M. Hoffman, A.M. Smith, C.S. Rooney, T.E. Fisher, J.S. Wai, C.M. Thomas, D.L. Bambmerger, J.L. Barnes, T.M. Williams, J.H. Jones, Olson B.D., O'brien J.A., Goldmah M.E., Nunberg J.H., Quintero J.C., Schleif W.A., Emini E.A., and Anderson P.S., Synthesis and evaluation of 2-pyridinone derivatives as HIV-1 specific reverse transcriptase inhibitors. 4. 3-2-(benzoxazol-2-yl) ethyl-5-ethyl-6-methylpyridin-2-(1H)-one and analogues, J. Med. Chem. 36 (1993), pp. 953-966.
-
(1993)
J. Med. Chem
, vol.36
, pp. 953-966
-
-
Hoffman, J.M.1
Smith, A.M.2
Rooney, C.S.3
Fisher, T.E.4
Wai, J.S.5
Thomas, C.M.6
Bambmerger, D.L.7
Barnes, J.L.8
Williams, T.M.9
Jones, J.H.10
Olson, B.D.11
O'brien, J.A.12
Goldmah, M.E.13
Nunberg, J.H.14
Quintero, J.C.15
Schleif, W.A.16
Emini, E.A.17
Anderson, P.S.18
-
19
-
-
85195035676
-
-
R.T. Davey, R.L. Dewar, G.F. Reed, M.B. Vasudevachari, M.A. Polis, J.A. Kovacs, J. Falloon, R.E. Walker, H. Masur, S.E. Haneiwich, O'Neil D.G., Decker M.R., Metcalf J.A., Deloria M.A., Laskin O.L., Salzman N., and Lone H.C., Plasma viremia as a sensitive indicator of the antiretroviral activity of L-697,661, Proc. Nat. Acad. Sci. USA. 90 (1993), pp. 5608-5612.
-
R.T. Davey, R.L. Dewar, G.F. Reed, M.B. Vasudevachari, M.A. Polis, J.A. Kovacs, J. Falloon, R.E. Walker, H. Masur, S.E. Haneiwich, O'Neil D.G., Decker M.R., Metcalf J.A., Deloria M.A., Laskin O.L., Salzman N., and Lone H.C., Plasma viremia as a sensitive indicator of the antiretroviral activity of L-697,661, Proc. Nat. Acad. Sci. USA. 90 (1993), pp. 5608-5612.
-
-
-
-
20
-
-
0028898824
-
Combination therapy with zidovudine prevents selection of human immunodeficiency virus type 1 variants expressing high-level resistance to L-697,661, a nonnucleoside reverse transcriptase inhibitor
-
S. Staszewski, F.E. Massari, A. Kober, R. Göhler, S. Durr, K.W. Anderson, C.L. Schneider, J.A. Waterburry, K.K. Bakshi, and V.I. Taylor, Combination therapy with zidovudine prevents selection of human immunodeficiency virus type 1 variants expressing high-level resistance to L-697,661, a nonnucleoside reverse transcriptase inhibitor, J. Infect. Dis. 171 (1995), pp. 1159-1165.
-
(1995)
J. Infect. Dis
, vol.171
, pp. 1159-1165
-
-
Staszewski, S.1
Massari, F.E.2
Kober, A.3
Göhler, R.4
Durr, S.5
Anderson, K.W.6
Schneider, C.L.7
Waterburry, J.A.8
Bakshi, K.K.9
Taylor, V.I.10
-
21
-
-
0028304576
-
Effect of template secondary structure on the inhibition of HIV-1 reverse transcriptase by a pyridinone non-nucleoside inhibitor
-
D.B. Olsen, S.S. Carroll, J.C. Culberson, J.A. Shafer, and L.C. Kuo, Effect of template secondary structure on the inhibition of HIV-1 reverse transcriptase by a pyridinone non-nucleoside inhibitor, Nucl. Acids Res. 22 (1994), pp. 1437-1443.
-
(1994)
Nucl. Acids Res
, vol.22
, pp. 1437-1443
-
-
Olsen, D.B.1
Carroll, S.S.2
Culberson, J.C.3
Shafer, J.A.4
Kuo, L.C.5
-
22
-
-
0347506087
-
Synthesis of 2-(bromodifloromethyl)benzoxazole and 5-(bromodifloromethyl)-1,2,4-oxadiazoles
-
W.R. Dolbier, C.R. Burkholder, and M. Medebielle, Synthesis of 2-(bromodifloromethyl)benzoxazole and 5-(bromodifloromethyl)-1,2,4-oxadiazoles, J. Fluorine Chem. 95 (1999), pp. 127-130.
-
(1999)
J. Fluorine Chem
, vol.95
, pp. 127-130
-
-
Dolbier, W.R.1
Burkholder, C.R.2
Medebielle, M.3
-
23
-
-
0029934807
-
Structure-activity relationships of benzimidazoles and related heterocycles as topoisomerase I poison
-
J.S. Kim, Q. Sun, B. Gatto, C. Yu, A. Liu, L.F. Liu, and E.J. La Voie, Structure-activity relationships of benzimidazoles and related heterocycles as topoisomerase I poison, Bioorg. Med. Chem. 4 (1996), pp. 621-630.
-
(1996)
Bioorg. Med. Chem
, vol.4
, pp. 621-630
-
-
Kim, J.S.1
Sun, Q.2
Gatto, B.3
Yu, C.4
Liu, A.5
Liu, L.F.6
La Voie, E.J.7
-
24
-
-
0026658420
-
Total synthesis of the ionophore antibiotic CP-61, 405 (routiennocin)
-
D. Diez-Martin, N.R. Kotecha, S.V. Ley, S. Mantegani, J.C. Menendez, H.M. Organ, and A.D. White, Total synthesis of the ionophore antibiotic CP-61, 405 (routiennocin), Tetrahedron 48 (1992), pp. 7899-7938.
-
(1992)
Tetrahedron
, vol.48
, pp. 7899-7938
-
-
Diez-Martin, D.1
Kotecha, N.R.2
Ley, S.V.3
Mantegani, S.4
Menendez, J.C.5
Organ, H.M.6
White, A.D.7
-
26
-
-
0040914011
-
A method for the correlation of biological activity and chemical structure
-
C. Hansch and T. Fujita, A method for the correlation of biological activity and chemical structure, J. Am. Chem. Soc. 86 (1964), pp. 1616-1626.
-
(1964)
J. Am. Chem. Soc
, vol.86
, pp. 1616-1626
-
-
Hansch, C.1
Fujita, T.2
-
27
-
-
34249036722
-
QSAR of Genotoxic Active Benzazoles
-
B. Tekiner-Gulbas, O. Temiz-Arpaci, E. Oksuzoglu, H. Eroglu, I. Yildiz, N. Diril, E. Aki-Sener, and I. Yalcin, QSAR of Genotoxic Active Benzazoles, SAR QSAR Environ. Res. 18 (2007), pp. 251-263.
-
(2007)
SAR QSAR Environ. Res
, vol.18
, pp. 251-263
-
-
Tekiner-Gulbas, B.1
Temiz-Arpaci, O.2
Oksuzoglu, E.3
Eroglu, H.4
Yildiz, I.5
Diril, N.6
Aki-Sener, E.7
Yalcin, I.8
-
28
-
-
39349091825
-
Some Benzoxazoles and Benzimidazoles as DNA Topoisomerase I and II Inhibitors
-
E. Oksuzoglu, B. Tekiner-Gulbas, S. Alper, O. Temiz-Arpaci, T. Ertan, I. Yildiz, N. Diril, E. Sener-Aki, and I. Yalcin, Some Benzoxazoles and Benzimidazoles as DNA Topoisomerase I and II Inhibitors, J. Enzym. Inhib. Med. Chem. 23 (2008), pp. 37-42.
-
(2008)
J. Enzym. Inhib. Med. Chem
, vol.23
, pp. 37-42
-
-
Oksuzoglu, E.1
Tekiner-Gulbas, B.2
Alper, S.3
Temiz-Arpaci, O.4
Ertan, T.5
Yildiz, I.6
Diril, N.7
Sener-Aki, E.8
Yalcin, I.9
-
29
-
-
38049160718
-
A study on the genotoxic activities of some new benzoxazoles
-
E. Oksuzoglu, O. Temiz-Arpaci, B. Tekiner-Gulbas, H. Eroglu, G. Sen, S. Alper, I. Yildiz, N. Diril, E. Aki-Sener, and I. Yalcin, A study on the genotoxic activities of some new benzoxazoles, Med. Chem. Res. 16 (2007), pp. 1-14.
-
(2007)
Med. Chem. Res
, vol.16
, pp. 1-14
-
-
Oksuzoglu, E.1
Temiz-Arpaci, O.2
Tekiner-Gulbas, B.3
Eroglu, H.4
Sen, G.5
Alper, S.6
Yildiz, I.7
Diril, N.8
Aki-Sener, E.9
Yalcin, I.10
-
30
-
-
33646696219
-
-
Clinical and Laboratory Standards Institute CLSI, formerly NCCLS, Approved Standard, Clinical and Laboratory Standarts Institute, 940 West Valley Road, Wayne, Pennsylvania, USA
-
Clinical and Laboratory Standards Institute (CLSI) (formerly NCCLS): Performance Standards for Antimicrobial Disk Susceptibility Tests; Approved Standard, M2-A9. Clinical and Laboratory Standarts Institute, 940 West Valley Road, Wayne, Pennsylvania, USA, 2006.
-
(2006)
Performance Standards for Antimicrobial Disk Susceptibility Tests
-
-
-
32
-
-
0003443227
-
-
Clinical and Laboratory Standards Institute CLSI, formerly NCCLS, Approved Standard, M27-A. Clinical and Laboratory Standarts Institute, 940 West Valley Road, Wayne, Pennsylvania, USA
-
Clinical and Laboratory Standards Institute (CLSI) (formerly NCCLS): Reference Method for Broth Dilution Antifungal Susceptibility Testing Yeast; Approved Standard, M27-A. Clinical and Laboratory Standarts Institute, 940 West Valley Road, Wayne, Pennsylvania, USA, 2006.
-
(2006)
Reference Method for Broth Dilution Antifungal Susceptibility Testing Yeast
-
-
-
33
-
-
0003955925
-
-
American Chemical Society, Washington, DC
-
C. Hansch, A. Leo, and D. Hoekman, Exploring QSAR: Hydrophobic, Electronic, and Steric Constants, American Chemical Society, Washington, DC, 1995.
-
(1995)
Exploring QSAR: Hydrophobic, Electronic, and Steric Constants
-
-
Hansch, C.1
Leo, A.2
Hoekman, D.3
-
34
-
-
85195096564
-
-
Accelrys Inc, Cerius2
-
2, 2004.
-
(2004)
-
-
-
35
-
-
40249094605
-
QSAR and pharmacophore analysis on amides against drug-resistant S. aureus
-
I. Yildiz, T. Ertan, K. Bolelli, O. Temiz-Arpaci, I. Yalcin, and E. Aki, QSAR and pharmacophore analysis on amides against drug-resistant S. aureus, SAR QSAR Environ. Res. 19 (2008), pp. 101-113.
-
(2008)
SAR QSAR Environ. Res
, vol.19
, pp. 101-113
-
-
Yildiz, I.1
Ertan, T.2
Bolelli, K.3
Temiz-Arpaci, O.4
Yalcin, I.5
Aki, E.6
-
36
-
-
84987083710
-
Validation of QSAR
-
S. Wold, Validation of QSAR, Quant. Struct.-Act. Relat. 10 (1991), pp. 191-193.
-
(1991)
Quant. Struct.-Act. Relat
, vol.10
, pp. 191-193
-
-
Wold, S.1
-
37
-
-
0003431470
-
-
Wadsworth & Brooks/Cole, Pacific Grove, CA
-
J.O. Rawlings, Applied Regression Analysis, Wadsworth & Brooks/Cole, Pacific Grove, CA, 1988, pp. 186-189.
-
(1988)
Applied Regression Analysis
, pp. 186-189
-
-
Rawlings, J.O.1
-
38
-
-
0030017445
-
The future of antifungal theraphy
-
J.R. Graybill, The future of antifungal theraphy, Clin. Infect. Dis. 22 (1996), pp. 166-178.
-
(1996)
Clin. Infect. Dis
, vol.22
, pp. 166-178
-
-
Graybill, J.R.1
-
39
-
-
34249034157
-
-
R. Mannhold, P. Krogsgaard-Larsen, and H. Timmerman, eds, Wiley-VCH, Weinheim
-
H. Kubinyi, in QSAR Hansch Analysis and Related Approaches, R. Mannhold, P. Krogsgaard-Larsen, and H. Timmerman, eds., Wiley-VCH, Weinheim, 1993, p. 63.
-
(1993)
QSAR Hansch Analysis and Related Approaches
, pp. 63
-
-
Kubinyi, H.1
|