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Proceedings of the National Academy of Sciences of the United States of America
|
June 2, 2016
Transposon mutagenesis identifies genes and cellular processes driving epithelial-mesenchymal transition in hepatocellular carcinoma
Takahiro Kodama, Justin Y Newberg, Michiko Kodama, et al.
Chemistry & Biology
|
May 1, 2012
Highly selective inhibitors of monoacylglycerol lipase bearing a reactive group that is bioisosteric with endocannabinoid substrates
Jae Won Chang, Micah J Niphakis, Kenneth M Lum, et al.
Journal of Medicinal Chemistry
|
April 28, 2007
Discovery of 3-piperidinyl-1-cyclopentanecarboxamide as a novel scaffold for highly potent CC chemokine receptor 2 antagonists
Lihu Yang, Gabor Butora, Richard X Jiao, et al.
Journal of Medicinal Chemistry
|
February 4, 1994
Selective protection and relative importance of the carboxylic acid groups of zaragozic acid A for squalene synthase inhibition
T Biftu, J J Acton, G D Berger, et al.
Neuropharmacology
|
September 2, 2015
Stimulation of in vivo dopamine transmission and intravenous self-administration in rats and mice by JWH-018, a Spice cannabinoid
M A De Luca, Z Bimpisidis, M Melis, et al.
Eneuro
|
February 12, 2020
Corticotropin-Releasing Factor Receptor-1 Neurons in the Lateral Amygdala Display Selective Sensitivity to Acute and Chronic Ethanol Exposure
Abigail E Agoglia, ManHua Zhu, Rose Ying, et al.
ACS Applied Bio Materials
|
January 8, 2022
Using Aldehyde Synergism To Direct the Design of Degradable Pro-Antimicrobial Networks
Dahlia N Amato, Douglas V Amato, Yetunde Adewunmi, et al.
Journal of Medicinal Chemistry
|
September 18, 1992
Development, synthesis, and biological evaluation of (-)-trans-(2S,5S)-2-[3-[(2-oxopropyl)sulfonyl]-4-n-propoxy-5-(3- hydroxypropoxy)-phenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran, a potent orally active platelet-activating factor (PAF) antagonist and its water-soluble prodrug phosphate ester
N N Girotra, T Biftu, M M Ponpipom, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 15, 2012
Discovery of vinylcycloalkyl-substituted benzimidazole TRPM8 antagonists effective in the treatment of cold allodynia
Raul R Calvo, Sanath K Meegalla, Daniel J Parks, et al.
Journal of Medicinal Chemistry
|
November 11, 1994
Structure-activity relationships of C1 and C6 side chains of zaragozic acid A derivatives
M M Ponpipom, N N Girotra, R L Bugianesi, et al.
Page
of 43
Search research articles
Search
Showing results (351-360 of 424) with videos related to
Sort By:
Page
of 43
Proceedings of the National Academy of Sciences of the United States of America
|
June 2, 2016
Transposon mutagenesis identifies genes and cellular processes driving epithelial-mesenchymal transition in hepatocellular carcinoma
Takahiro Kodama, Justin Y Newberg, Michiko Kodama, et al.
Chemistry & Biology
|
May 1, 2012
Highly selective inhibitors of monoacylglycerol lipase bearing a reactive group that is bioisosteric with endocannabinoid substrates
Jae Won Chang, Micah J Niphakis, Kenneth M Lum, et al.
Journal of Medicinal Chemistry
|
April 28, 2007
Discovery of 3-piperidinyl-1-cyclopentanecarboxamide as a novel scaffold for highly potent CC chemokine receptor 2 antagonists
Lihu Yang, Gabor Butora, Richard X Jiao, et al.
Journal of Medicinal Chemistry
|
February 4, 1994
Selective protection and relative importance of the carboxylic acid groups of zaragozic acid A for squalene synthase inhibition
T Biftu, J J Acton, G D Berger, et al.
Neuropharmacology
|
September 2, 2015
Stimulation of in vivo dopamine transmission and intravenous self-administration in rats and mice by JWH-018, a Spice cannabinoid
M A De Luca, Z Bimpisidis, M Melis, et al.
Eneuro
|
February 12, 2020
Corticotropin-Releasing Factor Receptor-1 Neurons in the Lateral Amygdala Display Selective Sensitivity to Acute and Chronic Ethanol Exposure
Abigail E Agoglia, ManHua Zhu, Rose Ying, et al.
ACS Applied Bio Materials
|
January 8, 2022
Using Aldehyde Synergism To Direct the Design of Degradable Pro-Antimicrobial Networks
Dahlia N Amato, Douglas V Amato, Yetunde Adewunmi, et al.
Journal of Medicinal Chemistry
|
September 18, 1992
Development, synthesis, and biological evaluation of (-)-trans-(2S,5S)-2-[3-[(2-oxopropyl)sulfonyl]-4-n-propoxy-5-(3- hydroxypropoxy)-phenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran, a potent orally active platelet-activating factor (PAF) antagonist and its water-soluble prodrug phosphate ester
N N Girotra, T Biftu, M M Ponpipom, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 15, 2012
Discovery of vinylcycloalkyl-substituted benzimidazole TRPM8 antagonists effective in the treatment of cold allodynia
Raul R Calvo, Sanath K Meegalla, Daniel J Parks, et al.
Journal of Medicinal Chemistry
|
November 11, 1994
Structure-activity relationships of C1 and C6 side chains of zaragozic acid A derivatives
M M Ponpipom, N N Girotra, R L Bugianesi, et al.
Page
of 43