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Chembiochem : a European Journal of Chemical Biology
|
June 13, 2012
Universal caging group for the in-cell detection of glutathione transferase applied to 19F NMR and bioluminogenic probes
Mika Ito, Aya Shibata, Jie Zhang, et al.
The Journal of Organic Chemistry
|
July 22, 2022
Design and Synthesis of Cyclopropane Congeners of Resolvin E3, an Endogenous Pro-Resolving Lipid Mediator, as Its Stable Equivalents
Shota Arai, Koichi Fujiwara, Masahiro Kojima, et al.
The Journal of Organic Chemistry
|
September 18, 2020
Synthesis of Resolvin E3, a Proresolving Lipid Mediator, and Its Deoxy Derivatives: Identification of 18-Deoxy-resolvin E3 as a Potent Anti-Inflammatory Agent
Hayato Fukuda, Hiroyuki Ikeda, Ryuta Muromoto, et al.
Journal of Medicinal Chemistry
|
September 15, 2006
Synthesis of adenophostin A analogues conjugating an aromatic group at the 5'-position as potent IP3 receptor ligands
Tetsuya Mochizuki, Yoshihiko Kondo, Hiroshi Abe, et al.
Pharmacology Research & Perspectives
|
June 10, 2017
Structure-specific effects of lipidated oxytocin analogs on intracellular calcium levels, parental behavior, and oxytocin concentrations in the plasma and cerebrospinal fluid in mice
Stanislav M Cherepanov, Shigeru Yokoyama, Akira Mizuno, et al.
Psychopharmacology
|
November 2, 2017
Resolvin E1/E2 ameliorate lipopolysaccharide-induced depression-like behaviors via ChemR23
Satoshi Deyama, Kento Shimoda, Hiroe Suzuki, et al.
Journal of Medicinal Chemistry
|
July 1, 2015
Discovery of Novel Indazole Derivatives as Highly Potent and Selective Human β3-Adrenergic Receptor Agonists with the Possibility of Having No Cardiovascular Side Effects
Yasuhiro Wada, Hiromitsu Shirahashi, Taisuke Iwanami, et al.
Journal of Medicinal Chemistry
|
March 17, 2006
A systematic study of C-glucoside trisphosphates as myo-inositol trisphosphate receptor ligands. Synthesis of beta-C-glucoside trisphosphates based on the conformational restriction strategy
Masaru Terauchi, Hiroshi Abe, Stephen C Tovey, et al.
Chemical Communications (Cambridge, England)
|
August 30, 2017
A covalent G-site inhibitor for glutathione S-transferase Pi (GSTP<sub>1-1</sub>)
Yuko Shishido, Fumiaki Tomoike, Yasuaki Kimura, et al.
ACS Medicinal Chemistry Letters
|
January 21, 2017
Discovery of Novel Seven-Membered Prostacyclin Analogues as Potent and Selective Prostaglandin FP and EP3 Dual Agonists
Isamu Sugimoto, Tohru Kambe, Tomotaka Okino, et al.
Page
of 19
Search research articles
Search
Showing results (141-150 of 182) with videos related to
Sort By:
Page
of 19
Chembiochem : a European Journal of Chemical Biology
|
June 13, 2012
Universal caging group for the in-cell detection of glutathione transferase applied to 19F NMR and bioluminogenic probes
Mika Ito, Aya Shibata, Jie Zhang, et al.
The Journal of Organic Chemistry
|
July 22, 2022
Design and Synthesis of Cyclopropane Congeners of Resolvin E3, an Endogenous Pro-Resolving Lipid Mediator, as Its Stable Equivalents
Shota Arai, Koichi Fujiwara, Masahiro Kojima, et al.
The Journal of Organic Chemistry
|
September 18, 2020
Synthesis of Resolvin E3, a Proresolving Lipid Mediator, and Its Deoxy Derivatives: Identification of 18-Deoxy-resolvin E3 as a Potent Anti-Inflammatory Agent
Hayato Fukuda, Hiroyuki Ikeda, Ryuta Muromoto, et al.
Journal of Medicinal Chemistry
|
September 15, 2006
Synthesis of adenophostin A analogues conjugating an aromatic group at the 5'-position as potent IP3 receptor ligands
Tetsuya Mochizuki, Yoshihiko Kondo, Hiroshi Abe, et al.
Pharmacology Research & Perspectives
|
June 10, 2017
Structure-specific effects of lipidated oxytocin analogs on intracellular calcium levels, parental behavior, and oxytocin concentrations in the plasma and cerebrospinal fluid in mice
Stanislav M Cherepanov, Shigeru Yokoyama, Akira Mizuno, et al.
Psychopharmacology
|
November 2, 2017
Resolvin E1/E2 ameliorate lipopolysaccharide-induced depression-like behaviors via ChemR23
Satoshi Deyama, Kento Shimoda, Hiroe Suzuki, et al.
Journal of Medicinal Chemistry
|
July 1, 2015
Discovery of Novel Indazole Derivatives as Highly Potent and Selective Human β3-Adrenergic Receptor Agonists with the Possibility of Having No Cardiovascular Side Effects
Yasuhiro Wada, Hiromitsu Shirahashi, Taisuke Iwanami, et al.
Journal of Medicinal Chemistry
|
March 17, 2006
A systematic study of C-glucoside trisphosphates as myo-inositol trisphosphate receptor ligands. Synthesis of beta-C-glucoside trisphosphates based on the conformational restriction strategy
Masaru Terauchi, Hiroshi Abe, Stephen C Tovey, et al.
Chemical Communications (Cambridge, England)
|
August 30, 2017
A covalent G-site inhibitor for glutathione S-transferase Pi (GSTP<sub>1-1</sub>)
Yuko Shishido, Fumiaki Tomoike, Yasuaki Kimura, et al.
ACS Medicinal Chemistry Letters
|
January 21, 2017
Discovery of Novel Seven-Membered Prostacyclin Analogues as Potent and Selective Prostaglandin FP and EP3 Dual Agonists
Isamu Sugimoto, Tohru Kambe, Tomotaka Okino, et al.
Page
of 19