-
1
-
-
84905171834
-
Synthesis and evaluation of some new benzimidazole derivatives as potential antimicrobial agents
-
B. Soni, M.S. Ranawat, A. Bhandari, P. Sharma, D. Choudhary, R. Sharma, and R.P. Prakash Synthesis and evaluation of some new benzimidazole derivatives as potential antimicrobial agents Pharm. Glob. 9 2012 5 10
-
(2012)
Pharm. Glob.
, vol.9
, pp. 5-10
-
-
Soni, B.1
Ranawat, M.S.2
Bhandari, A.3
Sharma, P.4
Choudhary, D.5
Sharma, R.6
Prakash, R.P.7
-
2
-
-
84870156616
-
Aqueous synthesis of 1-H-2-substituted benzimidazoles via transition-metal-free intramolecular amination of aryl iodides
-
C. Chen, C. Chen, B. Li, J. Tao, and J. Peng Aqueous synthesis of 1-H-2-substituted benzimidazoles via transition-metal-free intramolecular amination of aryl iodides Molecules 17 2012 12506 12520
-
(2012)
Molecules
, vol.17
, pp. 12506-12520
-
-
Chen, C.1
Chen, C.2
Li, B.3
Tao, J.4
Peng, J.5
-
4
-
-
0018604552
-
Domperidone or metoclopramide in preventing chemotherapeutically induced nausea and vomiting
-
I.L. Swann, E.N. Thompson, and K. Qureshi Domperidone or metoclopramide in preventing chemotherapeutically induced nausea and vomiting Br. Med. J. 2 1979 1188
-
(1979)
Br. Med. J.
, vol.2
, pp. 1188
-
-
Swann, I.L.1
Thompson, E.N.2
Qureshi, K.3
-
5
-
-
59749085010
-
A small-molecule screen identifies the antipsychotic drug Pimozide as an inhibitor of Listeria monocytogenes infection
-
L.A. Lieberman, and D.E. Higgins A small-molecule screen identifies the antipsychotic drug Pimozide as an inhibitor of Listeria monocytogenes infection Antimicrobial Agents Chemother. 53 2009 756 764
-
(2009)
Antimicrobial Agents Chemother.
, vol.53
, pp. 756-764
-
-
Lieberman, L.A.1
Higgins, D.E.2
-
6
-
-
50949127251
-
Synthesis, reactivity and biological activity of benzimidazoles
-
M. Alamgir, D. Black, and N. Kumar Synthesis, reactivity and biological activity of benzimidazoles Top. Heterocycl. Chem. 9 2007 88 94
-
(2007)
Top. Heterocycl. Chem.
, vol.9
, pp. 88-94
-
-
Alamgir, M.1
Black, D.2
Kumar, N.3
-
7
-
-
33745617661
-
Synthesis and X-ray crystal structure of pyrrolo[1,2-a]benzimidazoles
-
A. M Awadallah, K. Seppelt, and H. Shorafa Synthesis and X-ray crystal structure of pyrrolo[1,2-a]benzimidazoles Tetrahedron 62 2006 7744 7746
-
(2006)
Tetrahedron
, vol.62
, pp. 7744-7746
-
-
Awadallah A, M.1
Seppelt, K.2
Shorafa, H.3
-
8
-
-
0342514570
-
Synthesis and antimycobacterial activity of some coupling products from 4-aminobenzoic acid hydrazones
-
Ş.G. Küçükgüzel, S. Rollas, İ. Küçükgüzel, and M. Kiraz Synthesis and antimycobacterial activity of some coupling products from 4-aminobenzoic acid hydrazones Eur. J. Med. Chem. 34 1999 1093 1100
-
(1999)
Eur. J. Med. Chem.
, vol.34
, pp. 1093-1100
-
-
Küçükgüzel, Ş.G.1
Rollas, S.2
Küçükgüzel, I.3
Kiraz, M.4
-
9
-
-
0343542649
-
Synthesis, characterization and antimicrobial evaluation of ethyl 2-arylhydrazono-3-oxobutyrates
-
Ş.G. Küçükgüzel, S. Rollas, H. Erdeniz, and M. Kiraz Synthesis, characterization and antimicrobial evaluation of ethyl 2-arylhydrazono-3-oxobutyrates Eur. J. Med. Chem. 34 1999 153 160
-
(1999)
Eur. J. Med. Chem.
, vol.34
, pp. 153-160
-
-
Küçükgüzel, Ş.G.1
Rollas, S.2
Erdeniz, H.3
Kiraz, M.4
-
11
-
-
0033770231
-
Synthesis and antimicrobial activity of new 6-phenylimidazo[2,1-b] thiazole derivatives
-
N. Ulusoy, G. Çapan, G. Ötük, and M. Kiraz Synthesis and antimicrobial activity of new 6-phenylimidazo[2,1-b]thiazole derivatives Boll. Chim. Farm. 139 2000 167 172
-
(2000)
Boll. Chim. Farm.
, vol.139
, pp. 167-172
-
-
Ulusoy, N.1
Çapan, G.2
Ötük, G.3
Kiraz, M.4
-
12
-
-
84861849790
-
Synthesis and antibacterial, antifungal activities of some 2r,4c-diaryl-3-azabicyclo[3.3.1]nonan-9-one-4-aminobenzoyl hydrazones
-
J. John, F. Xaiver, K. Krishnasamy, and C. Sankar Synthesis and antibacterial, antifungal activities of some 2r,4c-diaryl-3-azabicyclo[3.3.1] nonan-9-one-4-aminobenzoyl hydrazones Med. Chem. Res. 21 2012 345 350
-
(2012)
Med. Chem. Res.
, vol.21
, pp. 345-350
-
-
John, J.1
Xaiver, F.2
Krishnasamy, K.3
Sankar, C.4
-
13
-
-
0034099495
-
Anticonvulsant properties of various acetylhydrazones, oxamoylhydrazones and semicarbazones derived from aromatic and unsaturated carbonyl compounds
-
J.R. Dimmock, S.C. Vashishtha, and J.P. Stables Anticonvulsant properties of various acetylhydrazones, oxamoylhydrazones and semicarbazones derived from aromatic and unsaturated carbonyl compounds Eur. J. Med. Chem. 35 2000 241 248
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 241-248
-
-
Dimmock, J.R.1
Vashishtha, S.C.2
Stables, J.P.3
-
14
-
-
0032033125
-
Synthesis and evaluation of analgesic, antiinflammatory and antiplatelet properties of new 2-pyridylarylhydrazone derivatives
-
A.R. Todeschini, A.L. Miranda, C.M. Silva, and S.C. Parrini Synthesis and evaluation of analgesic, antiinflammatory and antiplatelet properties of new 2-pyridylarylhydrazone derivatives Eur. J. Med. Chem. 33 1998 189 199
-
(1998)
Eur. J. Med. Chem.
, vol.33
, pp. 189-199
-
-
Todeschini, A.R.1
Miranda, A.L.2
Silva, C.M.3
Parrini, S.C.4
-
15
-
-
0034064517
-
Synthesis and analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole
-
P.C. Lima, L.M. Lima, K.C. Silva, P.H. Leda, A.L.P. Miranda, C.A.M. Fraga, and E.J. Barreiro Synthesis and analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole Eur. J. Med. Chem. 35 2000 187 203
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 187-203
-
-
Lima, P.C.1
Lima, L.M.2
Silva, K.C.3
Leda, P.H.4
Miranda, A.L.P.5
Fraga, C.A.M.6
Barreiro, E.J.7
-
16
-
-
17444420766
-
Synthesis and vasodilatory activity of new N-acylhydrazone derivatives, designed as LASSBio-294 analogues
-
A.G. Silva, G. Zapata-Suto, A.E. Kummerle, C.A.M. Fraga, E.J. Barreiro, and R.T. Sudo Synthesis and vasodilatory activity of new N-acylhydrazone derivatives, designed as LASSBio-294 analogues Bioorg. Med. Chem. 13 2005 3431 3437
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 3431-3437
-
-
Silva, A.G.1
Zapata-Suto, G.2
Kummerle, A.E.3
Fraga, C.A.M.4
Barreiro, E.J.5
Sudo, R.T.6
-
17
-
-
34247546722
-
Synthesis and characterization of Benzoyl Vanillin hydrazone and its complexes with biological activities, synthesis and reactivity in inorganic
-
L. Zhang, and N. Tang Synthesis and characterization of Benzoyl Vanillin hydrazone and its complexes with biological activities, synthesis and reactivity in inorganic Metal-organic Nano-metal Chem. 37 2007 185 188
-
(2007)
Metal-organic Nano-metal Chem.
, vol.37
, pp. 185-188
-
-
Zhang, L.1
Tang, N.2
-
18
-
-
51849098130
-
Synthesis, characterization and antileucemic activity of 7-Hydroxy-8-acetylcoumarin benzoylhydrazone
-
A. Kotali, I.S. Lafazanis, A. Papageorgiou, E. Chrysogelou, T. Lialiaris, and Z. Sinakos Synthesis, characterization and antileucemic activity of 7-Hydroxy-8-acetylcoumarin benzoylhydrazone Molbank 2008 M574
-
(2008)
Molbank
, pp. 574
-
-
Kotali, A.1
Lafazanis, I.S.2
Papageorgiou, A.3
Chrysogelou, E.4
Lialiaris, T.5
Sinakos, Z.6
-
19
-
-
11144324314
-
Advanced glycation endproducts - Role in pathology of diabetic complications
-
N. Ahmed Advanced glycation endproducts - role in pathology of diabetic complications Diabetes Res. Clin. Pract. 67 2005 3 21
-
(2005)
Diabetes Res. Clin. Pract.
, vol.67
, pp. 3-21
-
-
Ahmed, N.1
-
20
-
-
0028453652
-
Glycation and diabetic complications
-
M. Brownlee Glycation and diabetic complications Diabetes 43 1994 836 841
-
(1994)
Diabetes
, vol.43
, pp. 836-841
-
-
Brownlee, M.1
-
21
-
-
0035128915
-
Differences in the modulating potential of advanced glycation end product (AGE) peptides versus AGE proteins
-
W. Deuther-Conrad, S. Franke, M. Sommer, T. Henle, and G. Stein Differences in the modulating potential of advanced glycation end product (AGE) peptides versus AGE proteins Kidney Int. Suppl. 78 2001 63 66
-
(2001)
Kidney Int. Suppl.
, vol.78
, pp. 63-66
-
-
Deuther-Conrad, W.1
Franke, S.2
Sommer, M.3
Henle, T.4
Stein, G.5
-
22
-
-
18944375783
-
Glucose, advanced glycation end products, and diabetes complications: What is new and what works
-
M. Peppa, J. Uribarri, and H. Vlassara Glucose, advanced glycation end products, and diabetes complications: what is new and what works Clin. Diabetes 21 2003 186 187
-
(2003)
Clin. Diabetes
, vol.21
, pp. 186-187
-
-
Peppa, M.1
Uribarri, J.2
Vlassara, H.3
-
23
-
-
0142026785
-
Intervention against the Maillard reaction in vivo
-
V.M. Monnier Intervention against the Maillard reaction in vivo Arch. Biochem. Biophys. 419 2003 1 15
-
(2003)
Arch. Biochem. Biophys.
, vol.419
, pp. 1-15
-
-
Monnier, V.M.1
-
24
-
-
33746920337
-
Advanced glycation end products: Sparking the development of diabetic vascular injury
-
A. Goldin, J.A. Beckman, A.M. Schmidt, and M.A. Creager Advanced glycation end products: sparking the development of diabetic vascular injury Circulation 114 2006 597 605
-
(2006)
Circulation
, vol.114
, pp. 597-605
-
-
Goldin, A.1
Beckman, J.A.2
Schmidt, A.M.3
Creager, M.A.4
-
25
-
-
78349297565
-
Oxidative stress and diabetic complications
-
Ferdinando Giacco, and Michael Brownlee Oxidative stress and diabetic complications Circ. Res. 107 2010 1058 1070
-
(2010)
Circ. Res.
, vol.107
, pp. 1058-1070
-
-
Giacco, F.1
Brownlee, M.2
-
26
-
-
84863768768
-
Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers
-
K.M. Khan, M. Taha, F. Naz, S. Ali, S. Perveen, and M.I. Choudhary Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers Med. Chem. 8 2012 705 710
-
(2012)
Med. Chem.
, vol.8
, pp. 705-710
-
-
Khan, K.M.1
Taha, M.2
Naz, F.3
Ali, S.4
Perveen, S.5
Choudhary, M.I.6
-
27
-
-
84863657274
-
2,4,6-Trichlorophenylhydrazine schiff bases as DPPH radical and super oxide anion scavengers
-
K.M. Khan, Z. Shah, V.U. Ahmad, M. Khan, M. Taha, S. Ali, S. Perveen, M.I. Choudhary, and W. Voelter 2,4,6-Trichlorophenylhydrazine schiff bases as DPPH radical and super oxide anion scavengers Med. Chem. 8 2012 452 461
-
(2012)
Med. Chem.
, vol.8
, pp. 452-461
-
-
Khan, K.M.1
Shah, Z.2
Ahmad, V.U.3
Khan, M.4
Taha, M.5
Ali, S.6
Perveen, S.7
Choudhary, M.I.8
Voelter, W.9
-
28
-
-
84883413388
-
Oxindole derivatives: Synthesis and antiglycation activity
-
K.M. Khan, M. Khan, N. Ambreen, M. Taha, F. Rahim, S. Rasheed, S. Saied, H. Shafi, S. Perveen, and M.I. Choudhary Oxindole derivatives: synthesis and antiglycation activity Med. Chem. 9 2013 681 688
-
(2013)
Med. Chem.
, vol.9
, pp. 681-688
-
-
Khan, K.M.1
Khan, M.2
Ambreen, N.3
Taha, M.4
Rahim, F.5
Rasheed, S.6
Saied, S.7
Shafi, H.8
Perveen, S.9
Choudhary, M.I.10
-
29
-
-
84879727205
-
Acylhydrazide schiff bases: Synthesis and antiglycation activity
-
K.M. Khan, M. Taha, F. Rahim, M.I. Fakhri, W. Jamil, M. Khan, S. Rasheed, A. Karim, S. Perveen, and M.I. Choudhary Acylhydrazide schiff bases: synthesis and antiglycation activity J. Pak. Chem. Soc. 35 2013 929 937
-
(2013)
J. Pak. Chem. Soc.
, vol.35
, pp. 929-937
-
-
Khan, K.M.1
Taha, M.2
Rahim, F.3
Fakhri, M.I.4
Jamil, W.5
Khan, M.6
Rasheed, S.7
Karim, A.8
Perveen, S.9
Choudhary, M.I.10
-
30
-
-
84877977297
-
Synthesis of benzophenonehydrazone schiff bases and their in vitro antiglycating activities
-
K.M. Khan, F. Rahim, N. Ambreen, M. Taha, M. Khan, H. Jahan, A. Najeebullah Shaikh, S. Iqbal, S. Perveen, and M.I. Choudhary Synthesis of benzophenonehydrazone schiff bases and their in vitro antiglycating activities Med. Chem. 9 2013 588 595
-
(2013)
Med. Chem.
, vol.9
, pp. 588-595
-
-
Khan, K.M.1
Rahim, F.2
Ambreen, N.3
Taha, M.4
Khan, M.5
Jahan, H.6
Najeebullah Shaikh, A.7
Iqbal, S.8
Perveen, S.9
Choudhary, M.I.10
-
31
-
-
80755125969
-
Synthesis of 2,4,6-Trichlorophenyl hydrazones and their inhibitory potential against glycation of protein
-
K.M. Khan, Z. Shah, V.U. Ahmad, M. Khan, M. Taha, F. Rahim, H. Jahun, S. Perveen, and M.I. Choudhary Synthesis of 2,4,6-Trichlorophenyl hydrazones and their inhibitory potential against glycation of protein Med. Chem. 7 2011 572 580
-
(2011)
Med. Chem.
, vol.7
, pp. 572-580
-
-
Khan, K.M.1
Shah, Z.2
Ahmad, V.U.3
Khan, M.4
Taha, M.5
Rahim, F.6
Jahun, H.7
Perveen, S.8
Choudhary, M.I.9
-
32
-
-
71749117357
-
Synthesis of Bis-Schiff bases of isatins and their antiglycation activity
-
K.M. Khan, M. Khan, M. Ali, M. Taha, S. Rasheed, S. Perveen, and M.I. Choudhary Synthesis of Bis-Schiff bases of isatins and their antiglycation activity Bioorg. Med. Chem. 17 2009 7795 7801
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 7795-7801
-
-
Khan, K.M.1
Khan, M.2
Ali, M.3
Taha, M.4
Rasheed, S.5
Perveen, S.6
Choudhary, M.I.7
-
33
-
-
77954310776
-
Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazone moiety
-
Y. Özkay, Y. Tanah, H. Karaka, and İ. Iskdaǧ Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazone moiety Eur. J. Med. Chem. 45 2010 3293 3298
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 3293-3298
-
-
Özkay, Y.1
Tanah, Y.2
Karaka, H.3
Iskdaǧ, I.4
-
34
-
-
84867700668
-
Synthesis of biologically active catecholic compounds via ortho-selective oxygenation of phenolic compounds using hypervalent iodine (V) reagents
-
R. Bernini, G. Fabrizi, L. Pouysegu, D. Deffieux, and S. Quideau Synthesis of biologically active catecholic compounds via ortho-selective oxygenation of phenolic compounds using hypervalent iodine (V) reagents Curr. Org. Synth. 9 2012 650 669
-
(2012)
Curr. Org. Synth.
, vol.9
, pp. 650-669
-
-
Bernini, R.1
Fabrizi, G.2
Pouysegu, L.3
Deffieux, D.4
Quideau, S.5
-
35
-
-
84860306951
-
Convenient synthesis of 1-aryl-dihydroxyisochromans exhibiting antioxidant activity
-
R. Bernini, F. Crisante, G. Fabrizi, and P. Gentili Convenient synthesis of 1-aryl-dihydroxyisochromans exhibiting antioxidant activity Curr. Org. Chem. 16 2012 1051 1057
-
(2012)
Curr. Org. Chem.
, vol.16
, pp. 1051-1057
-
-
Bernini, R.1
Crisante, F.2
Fabrizi, G.3
Gentili, P.4
-
36
-
-
84892722585
-
Synthesis and DPPH radical scavenging activity of novel compounds obtained from tyrosol and cinnamic acid derivatives
-
M. Barontini, R. Bernini, R. Carastro, P. Gentili, and A. Romani Synthesis and DPPH radical scavenging activity of novel compounds obtained from tyrosol and cinnamic acid derivatives New. J. Chem. 38 2014 809 816
-
(2014)
New. J. Chem.
, vol.38
, pp. 809-816
-
-
Barontini, M.1
Bernini, R.2
Carastro, R.3
Gentili, P.4
Romani, A.5
-
37
-
-
78651397186
-
Plant polyphenols: Chemical properties, biological activities, and synthesis
-
S. Quideau, D. Deffieux, C. Douat-Casassus, and L. Pouységu Plant polyphenols: chemical properties, biological activities, and synthesis Angew. Chem. Int. Ed. 50 2011 586 621
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 586-621
-
-
Quideau, S.1
Deffieux, D.2
Douat-Casassus, C.3
Pouységu, L.4
-
38
-
-
84890856883
-
Antioxidant properties of phenolic Schiff bases: Structure-activity relationship and mechanism of action
-
E.H. Anouar, S. Raweh, I. Bayach, M. Taha, M.S. Baharudin, F.D. Meo, M.H. Hasan, A. Adam, N.H. Ismail, and J.F. Weber Antioxidant properties of phenolic Schiff bases: structure-activity relationship and mechanism of action J. Comput. Aided Mol. Des. 27 2013 951 964
-
(2013)
J. Comput. Aided Mol. Des.
, vol.27
, pp. 951-964
-
-
Anouar, E.H.1
Raweh, S.2
Bayach, I.3
Taha, M.4
Baharudin, M.S.5
Meo, F.D.6
Hasan, M.H.7
Adam, A.8
Ismail, N.H.9
Weber, J.F.10
-
39
-
-
77955418560
-
Selective and efficient oxidative modifications of flavonoids with 2-iodoxybenzoic acid (IBX)
-
M. Barontini, R. Bernini, F. Crisante, and G. Fabrizi Selective and efficient oxidative modifications of flavonoids with 2-iodoxybenzoic acid (IBX) Tetrahedron 66 2010 6047 6053
-
(2010)
Tetrahedron
, vol.66
, pp. 6047-6053
-
-
Barontini, M.1
Bernini, R.2
Crisante, F.3
Fabrizi, G.4
-
40
-
-
84877584824
-
Synthesis of 2-methoxybenzoylhydrazone and evaluation of their antileishmanial activity
-
M. Taha, M.S. Baharudin, N.H. Ismail, K.M. Khan, F. Jaafar, M. Samreen, S. Siddiqui, and M.I. Choudhary Synthesis of 2-methoxybenzoylhydrazone and evaluation of their antileishmanial activity Bioorg. Med. Chem. Lett. 23 2013 3463 3466
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 3463-3466
-
-
Taha, M.1
Baharudin, M.S.2
Ismail, N.H.3
Khan, K.M.4
Jaafar, F.5
Samreen, M.6
Siddiqui, S.7
Choudhary, M.I.8
-
41
-
-
66149137584
-
Leishmanicidal potential of N-substituted morpholine derivatives: Synthesis and structure-activity relationships
-
K.M. Khan, M. Khan, Z. Khan, M. Taha, G.M. Maharvi, Z.S. Saify, S. Parveen, and M.I. Choudhary Leishmanicidal potential of N-substituted morpholine derivatives: synthesis and structure-activity relationships Nat. Prod. Res. 23 2009 479 484
-
(2009)
Nat. Prod. Res.
, vol.23
, pp. 479-484
-
-
Khan, K.M.1
Khan, M.2
Khan, Z.3
Taha, M.4
Maharvi, G.M.5
Saify, Z.S.6
Parveen, S.7
Choudhary, M.I.8
-
42
-
-
80755176746
-
Synthesis and in vitro leishmanicidal activity of disulfide derivatives
-
K.M. Khan, M. Taha, F. Naz, M. Khan, F. Rahim, Samreen S. Perveen, and M.I. Choudhary Synthesis and in vitro leishmanicidal activity of disulfide derivatives Med. Chem. 7 2011 704 710
-
(2011)
Med. Chem.
, vol.7
, pp. 704-710
-
-
Khan, K.M.1
Taha, M.2
Naz, F.3
Khan, M.4
Rahim, F.5
Perveen, S.S.6
Choudhary, M.I.7
|