TY - JOUR
T1 - Evaluation of series of isobenzofuranone dimers as PKCα ligands
T2 - Implication for the distance between the two ligand binding sites
AU - Baba, Yoshiyasu
AU - Mayumi, Satoshi
AU - Hirai, Go
AU - Kawasaki, Hidekazu
AU - Ogoshi, Yosuke
AU - Yanagisawa, Takeshi
AU - Hashimoto, Yuichi
AU - Sodeoka, Mikiko
N1 - Funding Information:
This work was supported in part by grants from Uehara Memorial Foundation, and Hoh-ansha Foundation, Kanagawa Academy of Science and Technology Research Grants, a Grant-in-Aid for Creative Scientific Research (No 13NP0401) and a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science, and a Grant-in-Aid for the COE project, Giant Molecules and Complex Systems, from The Ministry of Education, Culture, Sports, Science, and Technology.
PY - 2004/6/7
Y1 - 2004/6/7
N2 - Protein kinase C (PKC) is a family of enzymes, which play important roles in intracellular signal transduction. To examine the distance between the two ligand binding sites (C1A and C1B) of PKC, we designed and synthesized two series of isobenzofuranone dimers. Peak binding activities were observed for the C3-acyl chain dimers having a C10-C12 linker and for the C7 dimers having a C14-C16.
AB - Protein kinase C (PKC) is a family of enzymes, which play important roles in intracellular signal transduction. To examine the distance between the two ligand binding sites (C1A and C1B) of PKC, we designed and synthesized two series of isobenzofuranone dimers. Peak binding activities were observed for the C3-acyl chain dimers having a C10-C12 linker and for the C7 dimers having a C14-C16.
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U2 - 10.1016/j.bmcl.2004.02.098
DO - 10.1016/j.bmcl.2004.02.098
M3 - Article
C2 - 15125970
AN - SCOPUS:2342643572
SN - 0960-894X
VL - 14
SP - 2969
EP - 2972
JO - Bioorganic and Medicinal Chemistry Letters
JF - Bioorganic and Medicinal Chemistry Letters
IS - 11
ER -