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Showing results (81-90 of 106) with videos related to

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Journal of Medicinal Chemistry|October 13, 1995
2-Substituted penems with amino acid-related side chains: synthesis and antibacterial activity of a new series of beta-lactam antibioticsM Altamura, E Perrotta, P Sbraci, et al.
Molecular Pharmacology|June 1, 1995
5-Iodo-2'-deoxy-L-uridine and (E)-5-(2-bromovinyl)-2'-deoxy-L-uridine: selective phosphorylation by herpes simplex virus type 1 thymidine kinase, antiherpetic activity, and cytotoxicity studiesS Spadari, G Ciarrocchi, F Focher, et al.
The Journal of Antibiotics|September 1, 1982
Biological activity of (5R,6S,8R)-6-alpha-hydroxyethyl-2-acetoxymethyl-2-penem-3-carboxylateA Sanfilippo, C Della Bruna, D Jabes, et al.
Biopolymers|October 1, 1995
Synthesis and biological evaluation of novel NK-1 tachykinin receptor antagonists: the use of cycloalkyl amino acids as a templateA Sisto, F Bonelli, F Centini, et al.
Nature: New Biology|November 17, 1971
Structure of daunomycin; x-ray analysis of N-Br-acetyl-daunomycin solvateR Angiuli, E Foresti, L Riva di Sanseverino, et al.
The Journal of Antibiotics|July 1, 1983
Synthesis and biological properties of sodium (5R, 6S, 8R)-6 alpha-hydroxyethyl-2-carbamoyloxymethyl-2-penem-3-carboxylate (FCE 22101) and its orally absorbed esters FCE 22553 and FCE 22891G Franceschi, M Foglio, M Alpegiani, et al.
Journal of Medicinal Chemistry|October 30, 1992
L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growthS Spadari, G Maga, F Focher, et al.
Journal of Molecular Recognition : JMR|November 1, 1989
Association of anthracyclines and synthetic hexanucleotides. Structural factors influencing sequence specificityV Rizzo, C Battistini, A Vigevani, et al.
Cancer Research|August 1, 1987
Chemical and biological characterization of 4'-iodo-4'-deoxydoxorubicinB Barbieri, F C Giuliani, T Bordoni, et al.
Anticancer Research|September 1, 1986
DNA polymerases and DNA topoisomerases as targets for the development of anticancer drugsS Spadari, G Pedrali-Noy, F Focher, et al.
Pageof 11

Showing results (81-90 of 106) with videos related to

Sort By:
Pageof 11
Journal of Medicinal Chemistry|October 13, 1995
2-Substituted penems with amino acid-related side chains: synthesis and antibacterial activity of a new series of beta-lactam antibioticsM Altamura, E Perrotta, P Sbraci, et al.
Molecular Pharmacology|June 1, 1995
5-Iodo-2'-deoxy-L-uridine and (E)-5-(2-bromovinyl)-2'-deoxy-L-uridine: selective phosphorylation by herpes simplex virus type 1 thymidine kinase, antiherpetic activity, and cytotoxicity studiesS Spadari, G Ciarrocchi, F Focher, et al.
The Journal of Antibiotics|September 1, 1982
Biological activity of (5R,6S,8R)-6-alpha-hydroxyethyl-2-acetoxymethyl-2-penem-3-carboxylateA Sanfilippo, C Della Bruna, D Jabes, et al.
Biopolymers|October 1, 1995
Synthesis and biological evaluation of novel NK-1 tachykinin receptor antagonists: the use of cycloalkyl amino acids as a templateA Sisto, F Bonelli, F Centini, et al.
Nature: New Biology|November 17, 1971
Structure of daunomycin; x-ray analysis of N-Br-acetyl-daunomycin solvateR Angiuli, E Foresti, L Riva di Sanseverino, et al.
The Journal of Antibiotics|July 1, 1983
Synthesis and biological properties of sodium (5R, 6S, 8R)-6 alpha-hydroxyethyl-2-carbamoyloxymethyl-2-penem-3-carboxylate (FCE 22101) and its orally absorbed esters FCE 22553 and FCE 22891G Franceschi, M Foglio, M Alpegiani, et al.
Journal of Medicinal Chemistry|October 30, 1992
L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growthS Spadari, G Maga, F Focher, et al.
Journal of Molecular Recognition : JMR|November 1, 1989
Association of anthracyclines and synthetic hexanucleotides. Structural factors influencing sequence specificityV Rizzo, C Battistini, A Vigevani, et al.
Cancer Research|August 1, 1987
Chemical and biological characterization of 4'-iodo-4'-deoxydoxorubicinB Barbieri, F C Giuliani, T Bordoni, et al.
Anticancer Research|September 1, 1986
DNA polymerases and DNA topoisomerases as targets for the development of anticancer drugsS Spadari, G Pedrali-Noy, F Focher, et al.
Pageof 11