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Bioorganic & Medicinal Chemistry Letters
|
May 23, 2007
Hypoxia-driven elimination of thiopurines from their nitrobenzyl prodrugs
Peter Thomson, Matthew A Naylor, Michael R L Stratford, et al.
Drug Design and Discovery
|
January 1, 1993
Synthesis of the enantiomers of the bioreductively-activated cytotoxin RSU-1069 and its prodrug RB6145 and lack of stereoselectivity in their cytotoxicity and radiosensitization in vitro
M A Naylor, M D Threadgill, H D Showalter, et al.
The Journal of Antibiotics
|
December 1, 1996
Novel C-2 substituted carbapenem derivatives. Part I. Synthesis and biological activity of non-aromatic heterocyclic derivatives
G Burton, N J Clear, A J Eglington, et al.
The Science of the Total Environment
|
May 18, 2020
Geologically controlled sandy beaches: Their geomorphology, morphodynamics and classification
Shari L Gallop, David M Kennedy, Carlos Loureiro, et al.
Biochemical Pharmacology
|
February 29, 2000
The relative importance of NADPH: cytochrome c (P450) reductase for determining the sensitivity of human tumour cells to the indolequinone EO9 and related analogues lacking functionality at the C-2 and C-3 positions
M P Saunders, M Jaffar, A V Patterson, et al.
Journal of Medicinal Chemistry
|
September 1, 1990
Synthesis and evaluation of novel electrophilic nitrofuran carboxamides and carboxylates as radiosensitizers and bioreductively activated cytotoxins
M A Naylor, M A Stephens, S Cole, et al.
Sleep Medicine
|
August 23, 2020
Sleep loss is related to unstable stationary balance in U.S. Army soldiers in an operationally-relevant context
Janna Mantua, Alexxa F Bessey, Bradley M Ritland, et al.
International Journal of Pharmaceutics
|
August 17, 2011
Predicting the human in vivo performance of different oral capsule shell types using a novel in vitro dynamic gastric model
M Vardakou, A Mercuri, T A Naylor, et al.
Anti-Cancer Drug Design
|
December 1, 1993
Heterocyclic mono-N-oxides with potential applications as bioreductive anti-tumour drugs: Part 1. 8-Alkylamino-substituted phenylimidazo [1,2-a] quinoxalines
M A Naylor, M A Stephens, J Nolan, et al.
Anti-Cancer Drug Design
|
April 3, 1998
5-substituted analogues of 3-hydroxymethyl-5-aziridinyl-1-methyl-2-[1H-indole-4,7-dione]prop-2-en- 1-ol (EO9, NSC 382459) and their regioisomers as hypoxia-selective agents: structure-cytotoxicity in vitro
M Jaffar, M A Naylor, N Robertson, et al.
Page
of 21
Search research articles
Search
Showing results (151-160 of 207) with videos related to
Sort By:
Page
of 21
Bioorganic & Medicinal Chemistry Letters
|
May 23, 2007
Hypoxia-driven elimination of thiopurines from their nitrobenzyl prodrugs
Peter Thomson, Matthew A Naylor, Michael R L Stratford, et al.
Drug Design and Discovery
|
January 1, 1993
Synthesis of the enantiomers of the bioreductively-activated cytotoxin RSU-1069 and its prodrug RB6145 and lack of stereoselectivity in their cytotoxicity and radiosensitization in vitro
M A Naylor, M D Threadgill, H D Showalter, et al.
The Journal of Antibiotics
|
December 1, 1996
Novel C-2 substituted carbapenem derivatives. Part I. Synthesis and biological activity of non-aromatic heterocyclic derivatives
G Burton, N J Clear, A J Eglington, et al.
The Science of the Total Environment
|
May 18, 2020
Geologically controlled sandy beaches: Their geomorphology, morphodynamics and classification
Shari L Gallop, David M Kennedy, Carlos Loureiro, et al.
Biochemical Pharmacology
|
February 29, 2000
The relative importance of NADPH: cytochrome c (P450) reductase for determining the sensitivity of human tumour cells to the indolequinone EO9 and related analogues lacking functionality at the C-2 and C-3 positions
M P Saunders, M Jaffar, A V Patterson, et al.
Journal of Medicinal Chemistry
|
September 1, 1990
Synthesis and evaluation of novel electrophilic nitrofuran carboxamides and carboxylates as radiosensitizers and bioreductively activated cytotoxins
M A Naylor, M A Stephens, S Cole, et al.
Sleep Medicine
|
August 23, 2020
Sleep loss is related to unstable stationary balance in U.S. Army soldiers in an operationally-relevant context
Janna Mantua, Alexxa F Bessey, Bradley M Ritland, et al.
International Journal of Pharmaceutics
|
August 17, 2011
Predicting the human in vivo performance of different oral capsule shell types using a novel in vitro dynamic gastric model
M Vardakou, A Mercuri, T A Naylor, et al.
Anti-Cancer Drug Design
|
December 1, 1993
Heterocyclic mono-N-oxides with potential applications as bioreductive anti-tumour drugs: Part 1. 8-Alkylamino-substituted phenylimidazo [1,2-a] quinoxalines
M A Naylor, M A Stephens, J Nolan, et al.
Anti-Cancer Drug Design
|
April 3, 1998
5-substituted analogues of 3-hydroxymethyl-5-aziridinyl-1-methyl-2-[1H-indole-4,7-dione]prop-2-en- 1-ol (EO9, NSC 382459) and their regioisomers as hypoxia-selective agents: structure-cytotoxicity in vitro
M Jaffar, M A Naylor, N Robertson, et al.
Page
of 21