CKD712, (S)-1-(α-naphthylmethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, inhibits the lipopolysaccharide-stimulated secretion of HMGB1 by inhibiting PI3K and classical protein kinase C-Reference-Cited by-同舟云学术

CKD712, (S)-1-(α-naphthylmethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, inhibits the lipopolysaccharide-stimulated secretion of HMGB1 by inhibiting PI3K and classical protein kinase C

Published:2011-09 Issue:9 Volume:11 Page:1160-1165
ISSN:1567-5769
Container-title:International Immunopharmacology
language:en
Short-container-title:International Immunopharmacology

Author:

Oh Young Joo,Youn Ju Ho,Min Hyun Jin,Kim Dal-Hyun,Lee Sung-Sook,Choi In-Hong,Shin Jeon-Soo

Funder

Korean Health 21 R&D Project (A080694) of the Ministry of Health & Welfare

Brain Korea 21 Project for Medical Sciences, Republic of Korea

Publisher

Elsevier BV

Subject

Pharmacology,Immunology,Immunology and Allergy

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5. The receptor for advanced glycation end products (RAGE) is a cellular binding site for amphoterin. Mediation of neurite outgrowth and co-expression of rage and amphoterin in the developing nervous system;Hori;J Biol Chem,1995

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