31 articles for SH Jung
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Improvement of therapeutic index of phosphodiesterase type IV inhibitors as anti-Asthmatics.
Lead Gene
Discovery of enantioselectivity of urea inhibitors of soluble epoxide hydrolase.
Chungnam National University
Phenolic Compounds from the Leaves and Twigs of Osteomeles schwerinae That Inhibit Rat Lens Aldose Reductase and Vessel Dilation in Zebrafish Larvae.
Institute of Oriental Medicine
Discovery of novel pyrimidine and malonamide derivatives as TGR5 agonists.
Chung-Ang University
Exploration of benzamidochromenone derivatives with conformational restrictor as interleukin-5 inhibitors.
Chungnam National University
The discovery of inhibitors of Fas-mediated cell death pathway using the combined computational method.
Chungnam National University
Design and synthesis of novel chromenone derivatives as interleukin-5 inhibitors.
Chungnam National University
Identification of novel chromenone derivatives as interleukin-5 inhibitors.
Chungnam National University
Novel interleukin-5 inhibitors based on hydroxyethylaminomethyl-4H-chromen-4-one scaffold.
Chungnam National University
Design and synthesis of novel hydroxyalkylaminomethylchromones for their IL-5 inhibitory activity.
Chungnam National University
The scope of thallium nitrate oxidative cyclization of chalcones; synthesis and evaluation of isoflavone and aurone analogs for their inhibitory activity against interleukin-5.
Chungnam National University
Synthesis, biological evaluation and structural determination of beta-aminoacyl-containing cyclic hydrazine derivatives as dipeptidyl peptidase IV (DPP-IV) inhibitors.
Korea Research Institute of Chemical Technology
Synthesis and DP-IV inhibition of cyano-pyrazoline derivatives as potent anti-diabetic agents.
Korea Research Institute of Chemical Technology
Structural requirement of phenylthiourea analogs for their inhibitory activity of melanogenesis and tyrosinase.
Chungnam National University
Evaluation of 3,4-dihydroquinazoline-2(1H)-thiones as inhibitors of alpha-MSH-induced melanin production in melanoma B16 cells.
Chungnam National University
Synthesis of (aryloxyacetylamino)-isonicotinic/nicotinic acid analogues as potent hypoxia-inducible factor (HIF)-1alpha inhibitors.
Molecular Cancer Research Center
Discovery of 2,6-Naphthyridine Analogues as Selective FGFR4 Inhibitors for Hepatocellular Carcinoma.
Sungkyunkwan University
Synthesis and structure-activity relationship of novel indene N-oxide derivatives as potent peroxisome proliferator activated receptor gamma (PPARgamma) agonists.
Korea Research Institute of Chemical Technology
Asymmetric synthesis of chiral piperazinylpropylisoxazoline ligands for dopamine receptors.
Sungshin Women'S University
Indenone derivatives: a novel template for peroxisome proliferator-activated receptor gamma (PPARgamma) agonists.
Korea Research Institute of Chemical Technology
Synthesis and PTP1B inhibition of 1,2-naphthoquinone derivatives as potent anti-diabetic agents.
Korea Research Institute of Chemical Technology
Discovery of benzimidazole analogs as a novel interleukin-5 inhibitors.
Chungnam National University
Refinement of the pharmacophore of 3,4-dihydroquinazoline-2(1H)-thiones for their anti-melanogenesis activity.
Chungnam National University
Identification of novel 2-benzyl-1-indanone analogs as interleukin-5 inhibitors.
Chungnam National University
Discovery of novel 3-(hydroxyalkoxy)-2-alkylchromen-4-one analogs as interleukin-5 inhibitors.
Chungnam National University
Novel analogs of N-acylhydroxyethylaminomethyl-4H-chromen-4-one scaffold as IL-5 inhibitors.
Chungnam National University
Compounds for inhibiting TNIK and medical uses thereof
Korea Research Institute of Chemical Technology
Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer
University of Pittsburgh