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Journal of Chromatography. A
|
July 27, 2001
Immobilized penicillin G acylase as reactor and chiral selector in liquid chromatography
G Massolini, E Calleri, E De Lorenzi, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
June 1, 1997
Antimicrobial and genotoxic activities of N-hydroxyalkyl-1, 2-benzisothiazol-3(2H)-one carbamic esters
M L Carmellino, G Pagani, M Terreni, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
September 21, 2001
Synthesis and in vitro activity of D- and L-enantiomers of 5-(trifluoromethyl)uracil nucleoside derivatives
R Salvetti, M Pregnolato, A Verri, et al.
Journal of Medicinal Chemistry
|
July 8, 1999
Molecular modeling and synthesis of inhibitors of herpes simplex virus type 1 uracil-DNA glycosylase
H Sun, C Zhi, G E Wright, et al.
Nucleosides & Nucleotides
|
August 5, 1999
Synthesis and molecular modeling of novel HSV1 uracil-DNA glycosylase inhibitors
M Pregnolato, D Ubiali, A Verri, et al.
Therapeutic Drug Monitoring
|
June 12, 1999
High-performance liquid chromatography method for analyzing the antiretroviral agent efavirenz in human plasma
P Villani, M Pregnolato, S Banfo, et al.
Journal of Medicinal Chemistry
|
January 29, 2000
Synthesis and in vitro anti-mycobacterium activity of N-alkyl-1, 2-dihydro-2-thioxo-3-pyridinecarbothioamides. Preliminary toxicity and pharmacokinetic evaluation
G Pagani, M Pregnolato, D Ubiali, et al.
Bioorganic & Medicinal Chemistry
|
June 27, 2001
5-(Trifluoromethyl)-beta-l-2'-deoxyuridine, the L-enantiomer of trifluorothymidine: stereospecific synthesis and antiherpetic evaluations
R Salvetti, A Marchand, M Pregnolato, et al.
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Search research articles
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Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Journal of Chromatography. A
|
July 27, 2001
Immobilized penicillin G acylase as reactor and chiral selector in liquid chromatography
G Massolini, E Calleri, E De Lorenzi, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
June 1, 1997
Antimicrobial and genotoxic activities of N-hydroxyalkyl-1, 2-benzisothiazol-3(2H)-one carbamic esters
M L Carmellino, G Pagani, M Terreni, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
September 21, 2001
Synthesis and in vitro activity of D- and L-enantiomers of 5-(trifluoromethyl)uracil nucleoside derivatives
R Salvetti, M Pregnolato, A Verri, et al.
Journal of Medicinal Chemistry
|
July 8, 1999
Molecular modeling and synthesis of inhibitors of herpes simplex virus type 1 uracil-DNA glycosylase
H Sun, C Zhi, G E Wright, et al.
Nucleosides & Nucleotides
|
August 5, 1999
Synthesis and molecular modeling of novel HSV1 uracil-DNA glycosylase inhibitors
M Pregnolato, D Ubiali, A Verri, et al.
Therapeutic Drug Monitoring
|
June 12, 1999
High-performance liquid chromatography method for analyzing the antiretroviral agent efavirenz in human plasma
P Villani, M Pregnolato, S Banfo, et al.
Journal of Medicinal Chemistry
|
January 29, 2000
Synthesis and in vitro anti-mycobacterium activity of N-alkyl-1, 2-dihydro-2-thioxo-3-pyridinecarbothioamides. Preliminary toxicity and pharmacokinetic evaluation
G Pagani, M Pregnolato, D Ubiali, et al.
Bioorganic & Medicinal Chemistry
|
June 27, 2001
5-(Trifluoromethyl)-beta-l-2'-deoxyuridine, the L-enantiomer of trifluorothymidine: stereospecific synthesis and antiherpetic evaluations
R Salvetti, A Marchand, M Pregnolato, et al.
Page
of 2