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Idrugs : the Investigational Drugs Journal
|
May 10, 2008
Biapenem American Cyanamid Co
S L Dax
Journal of Combinatorial Chemistry
|
September 11, 2001
Solid-phase Mannich condensation of amines, aldehydes, and alkynes: investigation of diverse aldehyde inputs
M A Youngman, S L Dax
Current Medicinal Chemistry
|
April 29, 1999
Multi-component methodologies in solid-phase organic synthesis
S L Dax, J J McNally, M A Youngman
Bioorganic & Medicinal Chemistry Letters
|
August 11, 2000
N-acylated alpha-(3-pyridylmethyl)-beta-aminotetralin antagoinists of the human neuropeptide Y Y5 receptor
J J McNally, M A Youngman, T W Lovenberg, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 4, 2000
N-(sulfonamido)alkyl[tetrahydro-1H-benzo[e]indol-2-yl]amines: potent antagonists of human neuropeptide Y Y5 receptor
J J McNally, M A Youngman, T W Lovenberg, et al.
British Journal of Anaesthesia
|
July 4, 2014
GAL-021, a new intravenous BKCa-channel blocker, is well tolerated and stimulates ventilation in healthy volunteers
J F McLeod, J M Leempoels, S X Peng, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 31, 2001
Aminopyrazoles with high affinity for the human neuropeptide Y5 receptor
C P Kordik, C Luo, B C Zanoni, et al.
Journal of Medicinal Chemistry
|
May 15, 1992
Dual-action penems and carbapenems
A J Corraz, S L Dax, N K Dunlap, et al.
Journal of Medicinal Chemistry
|
February 12, 2000
alpha-Substituted N-(sulfonamido)alkyl-beta-aminotetralins: potent and selective neuropeptide Y Y5 receptor antagonists
M A Youngman, J J McNally, T W Lovenberg, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 13, 2006
The novel, orally active, delta opioid RWJ-394674 is biotransformed to the potent mu opioid RWJ-413216
E E Codd, J R Carson, R W Colburn, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Idrugs : the Investigational Drugs Journal
|
May 10, 2008
Biapenem American Cyanamid Co
S L Dax
Journal of Combinatorial Chemistry
|
September 11, 2001
Solid-phase Mannich condensation of amines, aldehydes, and alkynes: investigation of diverse aldehyde inputs
M A Youngman, S L Dax
Current Medicinal Chemistry
|
April 29, 1999
Multi-component methodologies in solid-phase organic synthesis
S L Dax, J J McNally, M A Youngman
Bioorganic & Medicinal Chemistry Letters
|
August 11, 2000
N-acylated alpha-(3-pyridylmethyl)-beta-aminotetralin antagoinists of the human neuropeptide Y Y5 receptor
J J McNally, M A Youngman, T W Lovenberg, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 4, 2000
N-(sulfonamido)alkyl[tetrahydro-1H-benzo[e]indol-2-yl]amines: potent antagonists of human neuropeptide Y Y5 receptor
J J McNally, M A Youngman, T W Lovenberg, et al.
British Journal of Anaesthesia
|
July 4, 2014
GAL-021, a new intravenous BKCa-channel blocker, is well tolerated and stimulates ventilation in healthy volunteers
J F McLeod, J M Leempoels, S X Peng, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 31, 2001
Aminopyrazoles with high affinity for the human neuropeptide Y5 receptor
C P Kordik, C Luo, B C Zanoni, et al.
Journal of Medicinal Chemistry
|
May 15, 1992
Dual-action penems and carbapenems
A J Corraz, S L Dax, N K Dunlap, et al.
Journal of Medicinal Chemistry
|
February 12, 2000
alpha-Substituted N-(sulfonamido)alkyl-beta-aminotetralins: potent and selective neuropeptide Y Y5 receptor antagonists
M A Youngman, J J McNally, T W Lovenberg, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 13, 2006
The novel, orally active, delta opioid RWJ-394674 is biotransformed to the potent mu opioid RWJ-413216
E E Codd, J R Carson, R W Colburn, et al.
Page
of 1