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D Mol

Showing results (41-50 of 47) with videos related to

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Journal of Medicinal Chemistry|September 25, 2009
2-{3-[4-(Alkylsulfinyl)phenyl]-1-benzofuran-5-yl}-5-methyl-1,3,4-oxadiazole derivatives as novel inhibitors of glycogen synthase kinase-3beta with good brain permeabilityMorihisa Saitoh, Jun Kunitomo, Eiji Kimura, et al.
Bioorganic & Medicinal Chemistry Letters|September 28, 2011
Design, synthesis, and structure-activity relationships of spirolactones bearing 2-ureidobenzothiophene as acetyl-CoA carboxylases inhibitorsTohru Yamashita, Makoto Kamata, Satoshi Endo, et al.
Science (New York, N.Y.)|October 9, 2010
Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonistsBeili Wu, Ellen Y T Chien, Clifford D Mol, et al.
The Journal of Biological Chemistry|January 29, 2013
Conserved structural chemistry for incision activity in structurally non-homologous apurinic/apyrimidinic endonuclease APE1 and endonuclease IV DNA repair enzymesSusan E Tsutakawa, David S Shin, Clifford D Mol, et al.
Nature Communications|July 15, 2026
A unified catalytic mechanism in bifunctional DNA glycosylases with an evolutionarily conserved aspartate-lysine dyadAleem Syed, Leonardo F Serafim, Andrew S Arvai, et al.
Bioorganic & Medicinal Chemistry|January 3, 2012
A new class of non-thiazolidinedione, non-carboxylic-acid-based highly selective peroxisome proliferator-activated receptor (PPAR) γ agonists: design and synthesis of benzylpyrazole acylsulfonamidesKentaro Rikimaru, Takeshi Wakabayashi, Hidenori Abe, et al.
Bioorganic & Medicinal Chemistry|April 17, 2012
Structure-activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ AgonistsKentaro Rikimaru, Takeshi Wakabayashi, Hidenori Abe, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Journal of Medicinal Chemistry|September 25, 2009
2-{3-[4-(Alkylsulfinyl)phenyl]-1-benzofuran-5-yl}-5-methyl-1,3,4-oxadiazole derivatives as novel inhibitors of glycogen synthase kinase-3beta with good brain permeabilityMorihisa Saitoh, Jun Kunitomo, Eiji Kimura, et al.
Bioorganic & Medicinal Chemistry Letters|September 28, 2011
Design, synthesis, and structure-activity relationships of spirolactones bearing 2-ureidobenzothiophene as acetyl-CoA carboxylases inhibitorsTohru Yamashita, Makoto Kamata, Satoshi Endo, et al.
Science (New York, N.Y.)|October 9, 2010
Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonistsBeili Wu, Ellen Y T Chien, Clifford D Mol, et al.
The Journal of Biological Chemistry|January 29, 2013
Conserved structural chemistry for incision activity in structurally non-homologous apurinic/apyrimidinic endonuclease APE1 and endonuclease IV DNA repair enzymesSusan E Tsutakawa, David S Shin, Clifford D Mol, et al.
Nature Communications|July 15, 2026
A unified catalytic mechanism in bifunctional DNA glycosylases with an evolutionarily conserved aspartate-lysine dyadAleem Syed, Leonardo F Serafim, Andrew S Arvai, et al.
Bioorganic & Medicinal Chemistry|January 3, 2012
A new class of non-thiazolidinedione, non-carboxylic-acid-based highly selective peroxisome proliferator-activated receptor (PPAR) γ agonists: design and synthesis of benzylpyrazole acylsulfonamidesKentaro Rikimaru, Takeshi Wakabayashi, Hidenori Abe, et al.
Bioorganic & Medicinal Chemistry|April 17, 2012
Structure-activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ AgonistsKentaro Rikimaru, Takeshi Wakabayashi, Hidenori Abe, et al.
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