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D W Hobbs

Showing results (1-10 of 6) with videos related to

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Journal of Receptor and Signal Transduction Research|January 16, 2002
Library design concepts and implementation strategiesD W Hobbs, T Guo
Combinatorial Chemistry & High Throughput Screening|August 24, 2004
The different strategies for designing GPCR and kinase targeted librariesJ F Lowrie, R K Delisle, D W Hobbs, et al.
Journal of Medicinal Chemistry|August 1, 1986
Synthesis and anti-herpes-virus activity of acyclic 2'-deoxyguanosine analogues related to 9-[(1,3-dihydroxy-2-propoxy)methyl]guanineJ C Martin, D P McGee, G A Jeffrey, et al.
Journal of Medicinal Chemistry|October 16, 1992
Orally active, nonpeptide oxytocin antagonistsB E Evans, J L Leighton, K E Rittle, et al.
Journal of Medicinal Chemistry|June 17, 1998
Development of orally active oxytocin antagonists: studies on 1-(1-[4-[1-(2-methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl]piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and related pyridinesI M Bell, J M Erb, R M Freidinger, et al.
Bioorganic & Medicinal Chemistry Letters|May 13, 2008
Rational design of novel, potent piperazinone and imidazolidinone BACE1 inhibitorsJ N Cumming, T X Le, S Babu, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Receptor and Signal Transduction Research|January 16, 2002
Library design concepts and implementation strategiesD W Hobbs, T Guo
Combinatorial Chemistry & High Throughput Screening|August 24, 2004
The different strategies for designing GPCR and kinase targeted librariesJ F Lowrie, R K Delisle, D W Hobbs, et al.
Journal of Medicinal Chemistry|August 1, 1986
Synthesis and anti-herpes-virus activity of acyclic 2'-deoxyguanosine analogues related to 9-[(1,3-dihydroxy-2-propoxy)methyl]guanineJ C Martin, D P McGee, G A Jeffrey, et al.
Journal of Medicinal Chemistry|October 16, 1992
Orally active, nonpeptide oxytocin antagonistsB E Evans, J L Leighton, K E Rittle, et al.
Journal of Medicinal Chemistry|June 17, 1998
Development of orally active oxytocin antagonists: studies on 1-(1-[4-[1-(2-methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl]piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and related pyridinesI M Bell, J M Erb, R M Freidinger, et al.
Bioorganic & Medicinal Chemistry Letters|May 13, 2008
Rational design of novel, potent piperazinone and imidazolidinone BACE1 inhibitorsJ N Cumming, T X Le, S Babu, et al.
Pageof 1