| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Butenolides from a marine-derived fungus Aspergillus terreus with antitumor activities against pancreatic ductal adenocarcinoma cells
|
Qi, Changxing
|
|
2018
|
26 |
22 |
p. 5903-5910
|
article
|
| 2 |
Design and optimization of 2,3-dihydrobenzo[b][1,4]dioxine propanoic acids as novel GPR40 agonists with improved pharmacokinetic and safety profiles
|
Guo, Bin
|
|
2018
|
26 |
22 |
p. 5780-5791
|
article
|
| 3 |
Design and synthesis of boron containing monosaccharides by the hydroboration of d-glucal for use in boron neutron capture therapy (BNCT)
|
Itoh, Taiki
|
|
2018
|
26 |
22 |
p. 5922-5933
|
article
|
| 4 |
Design, synthesis, and ex vivo evaluation of a selective inhibitor for retinaldehyde dehydrogenase enzymes
|
Harper, Angelica R.
|
|
2018
|
26 |
22 |
p. 5766-5779
|
article
|
| 5 |
Discovery of a non-toxic [1,2,4]triazolo[1,5-a]pyrimidin-7-one (WS-10) that modulates ABCB1-mediated multidrug resistance (MDR)
|
Chang, Liming
|
|
2018
|
26 |
22 |
p. 5974-5985
|
article
|
| 6 |
Editorial Board
|
|
|
2018
|
26 |
22 |
p. ii
|
article
|
| 7 |
Erratum to “Discovery of a Non-toxic [1,2,4] Triazolo[1,5-A] Pyrimidin-7-One (WS-10) that Modulates ABCB1-Mediated Multidrug Resistance (MDR)” [Bioorganic & Medicinal Chemistry 26/18 (2018) 5006–5017]
|
Chang, Liming
|
|
2018
|
26 |
22 |
p. 5973
|
article
|
| 8 |
Graphical abstract TOC
|
|
|
2018
|
26 |
22 |
p. IBC
|
article
|
| 9 |
Graphical abstract TOC
|
|
|
2018
|
26 |
22 |
p. I-IV
|
article
|
| 10 |
Graphical abstract TOC
|
|
|
2018
|
26 |
22 |
p. OBC
|
article
|
| 11 |
Isolation, leishmanicidal evaluation and molecular docking simulations of piperidine alkaloids from Senna spectabilis
|
Lacerda, Rosimeire Borges Moreira
|
|
2018
|
26 |
22 |
p. 5816-5823
|
article
|
| 12 |
Lobaric acid and pseudodepsidones inhibit NF-κB signaling pathway by activation of PPAR-γ
|
Carpentier, Claudia
|
|
2018
|
26 |
22 |
p. 5845-5851
|
article
|
| 13 |
Matrix metalloproteinase-12 inhibitors: synthesis, structure-activity relationships and intestinal absorption of novel sugar-based biphenylsulfonamide carboxylates
|
Cuffaro, Doretta
|
|
2018
|
26 |
22 |
p. 5804-5815
|
article
|
| 14 |
Modifying aroylhydrazone prochelators for hydrolytic stability and improved cytoprotection against oxidative stress
|
Wang, Qin
|
|
2018
|
26 |
22 |
p. 5962-5972
|
article
|
| 15 |
Novel fluorescent triazinobenzimidazole derivatives as probes for labelling human A1 and A2B adenosine receptor subtypes
|
Barresi, Elisabetta
|
|
2018
|
26 |
22 |
p. 5885-5895
|
article
|
| 16 |
PPARγ-sparing thiazolidinediones as insulin sensitizers. Design, synthesis and selection of compounds for clinical development
|
Tanis, Steven P.
|
|
2018
|
26 |
22 |
p. 5870-5884
|
article
|
| 17 |
Probing the ligand preferences of the three types of bacterial pantothenate kinase
|
Guan, Jinming
|
|
2018
|
26 |
22 |
p. 5896-5902
|
article
|
| 18 |
Resveratrol-maltol hybrids as multi-target-directed agents for Alzheimer’s disease
|
Cheng, Gang
|
|
2018
|
26 |
22 |
p. 5759-5765
|
article
|
| 19 |
Screening, synthesis, crystal structure, and molecular basis of 6-amino-4-phenyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitriles as novel AKR1C3 inhibitors
|
Zheng, Xuehua
|
|
2018
|
26 |
22 |
p. 5934-5943
|
article
|
| 20 |
Syntheses of prodrug-type 2′-O-methyldithiomethyl oligonucleotides modified at natural four nucleoside residues and their conversions into natural 2′-hydroxy oligonucleotides under reducing condition
|
Hayashi, Junsuke
|
|
2018
|
26 |
22 |
p. 5838-5844
|
article
|
| 21 |
Synthesis and biological evaluation of novel N-substituted nipecotic acid derivatives with a trans-alkene spacer as potent GABA uptake inhibitors
|
Tóth, Krisztián
|
|
2018
|
26 |
22 |
p. 5944-5961
|
article
|
| 22 |
Synthesis and in vitro antitumor activity of novel alkenyl derivatives of pyridoxine, bioisosteric analogs of feruloyl methane
|
Pavelyev, Roman S.
|
|
2018
|
26 |
22 |
p. 5824-5837
|
article
|
| 23 |
Synthesis and in vitro evaluation of diverse heterocyclic diphenolic compounds as inhibitors of DYRK1A
|
Zhou, Qingqing
|
|
2018
|
26 |
22 |
p. 5852-5869
|
article
|
| 24 |
Synthesis, DNA and protein interactions and human topoisomerase inhibition of novel Spiroacridine derivatives
|
Gouveia, Rawny Galdino
|
|
2018
|
26 |
22 |
p. 5911-5921
|
article
|
| 25 |
Synthetic construction of sugar-amino acid hybrid polymers involving globotriaose or lactose and evaluation of their biological activities against Shiga toxins produced by Escherichia coli O157:H7
|
Matsuoka, Koji
|
|
2018
|
26 |
22 |
p. 5792-5803
|
article
|
Journal description