no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
6,6′-Aryl trehalose analogs as potential Mincle ligands
|
Rasheed, Omer K. |
|
|
28 |
14 |
p. |
article |
2 |
Bisphosphonate esters interact with HMG-CoA reductase membrane domain to induce its degradation
|
Toyota, Yosuke |
|
|
28 |
14 |
p. |
article |
3 |
Design, synthesis and evaluation of carbamate-linked uridyl-based inhibitors of human ST6Gal I
|
Montgomery, Andrew P. |
|
|
28 |
14 |
p. |
article |
4 |
Editorial Board
|
|
|
|
28 |
14 |
p. |
article |
5 |
Fibroblast growth factor receptor modulators employing diamines with reduced phospholipidosis-inducing potential
|
Sakai, Hiroki |
|
|
28 |
14 |
p. |
article |
6 |
Graphical Abstract Contents Continued
|
|
|
|
28 |
14 |
p. |
article |
7 |
Graphical abstract TOC
|
|
|
|
28 |
14 |
p. |
article |
8 |
Graphical abstract TOC
|
|
|
|
28 |
14 |
p. |
article |
9 |
N1-Substituted benzimidazole scaffold for farnesoid X receptor (FXR) agonists accompanying prominent selectivity against vitamin D receptor (VDR)
|
Masuda, Arisa |
|
|
28 |
14 |
p. |
article |
10 |
Synthesis and evaluation of new 1-oxa-8-azaspiro[4.5]decane derivatives as candidate radioligands for sigma-1 receptors
|
Tian, Jiale |
|
|
28 |
14 |
p. |
article |
11 |
2β-3,4-Unsaturated sialic acid derivatives: Synthesis optimization, and biological evaluation as Newcastle disease virus hemagglutinin-neuraminidase inhibitors
|
La Rocca, Paolo |
|
|
28 |
14 |
p. |
article |
12 |
Yohimbine as a Starting Point to Access Diverse Natural Product-Like Agents with Re-programmed Activities against Cancer-Relevant GPCR Targets
|
Paciaroni, Nicholas G. |
|
|
28 |
14 |
p. |
article |