| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
AMPK inhibitor BML-275 induces neuroprotection through decreasing cyt c and AIF expression after transient brain ischemia
|
Hu, Yue
|
|
|
52 |
C |
p.
|
artikel
|
| 2 |
Analogs of TIQ-A as inhibitors of human mono-ADP-ribosylating PARPs
|
Maksimainen, Mirko M.
|
|
|
52 |
C |
p.
|
artikel
|
| 3 |
An assessment of the mutational load caused by various reactions used in DNA encoded libraries
|
Sauter, Basilius
|
|
|
52 |
C |
p.
|
artikel
|
| 4 |
Design, Synthesis, and Antiviral activity of 1,2,3,4-Tetrahydropyrimidine derivatives acting as novel entry inhibitors to target at “Phe43 cavity” of HIV-1 gp120
|
Senapathi, Jagadeesh
|
|
|
52 |
C |
p.
|
artikel
|
| 5 |
Design, synthesis and biological evaluation of a novel spiro oxazolidinedione as potent p300/CBP HAT inhibitor for the treatment of ovarian cancer
|
Ding, Hong
|
|
|
52 |
C |
p.
|
artikel
|
| 6 |
Development of novel radioiodinated exendin-4 derivatives targeting GLP-1 receptor for detection of β-cell mass
|
Ogawa, Yu
|
|
|
52 |
C |
p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
|
52 |
C |
p.
|
artikel
|
| 8 |
From natural products to HDAC inhibitors: An overview of drug discovery and design strategy
|
Qiu, Xiang
|
|
|
52 |
C |
p.
|
artikel
|
| 9 |
Graphical Abstract Contents Continued
|
|
|
|
52 |
C |
p.
|
artikel
|
| 10 |
Graphical abstract TOC
|
|
|
|
52 |
C |
p.
|
artikel
|
| 11 |
Graphical abstract TOC
|
|
|
|
52 |
C |
p.
|
artikel
|
| 12 |
Identification of novel influenza polymerase PB2 inhibitors using virtual screening approach and molecular dynamics simulation analysis of active compounds
|
Xu, Lei
|
|
|
52 |
C |
p.
|
artikel
|
| 13 |
IsoChichibabin desmosine-13C3,15N1 synthesis and quantitative LC-MS/MS analysis of desmosine and isodesmosine in human skin
|
Hirose, Mika
|
|
|
52 |
C |
p.
|
artikel
|
| 14 |
LipE guided discovery of isopropylphenyl pyridazines as pantothenate kinase modulators
|
Sharma, Lalit Kumar
|
|
|
52 |
C |
p.
|
artikel
|
| 15 |
Macrocyclic BACE1 inhibitors with hydrophobic cross-linked structures: Optimization of ring size and ring structure
|
Otani, Takuya
|
|
|
52 |
C |
p.
|
artikel
|
| 16 |
Microbial transformation of pentacyclic triterpenes for anti-inflammatory agents on the HMGB1 stimulated RAW 264.7 cells by Streptomyces olivaceus CICC 23628
|
Zhu, Yuyuan
|
|
|
52 |
C |
p.
|
artikel
|
| 17 |
Optimized protocols for assessing libraries of poorly soluble sortase A inhibitors for antibacterial activity against medically-relevant bacteria, toxicity and enzyme inhibition
|
Alharthi, Sitah
|
|
|
52 |
C |
p.
|
artikel
|
| 18 |
Peptidomimetic analogues of an Arg-Trp-x-x-Trp motif responsible for interaction of translocase MraY with bacteriophage ϕX174 lysis protein E
|
Kerr, Rachel V.
|
|
|
52 |
C |
p.
|
artikel
|
| 19 |
Structure-activity relationship around PI-2620 highlights the importance of the nitrogen atom position in the tricyclic core
|
Kroth, Heiko
|
|
|
52 |
C |
p.
|
artikel
|
| 20 |
Structure-based drug design of novel and highly potent pyruvate dehydrogenase kinase inhibitors
|
Bessho, Yuki
|
|
|
52 |
C |
p.
|
artikel
|
| 21 |
Structure-based screening combined with computational and biochemical analyses identified the inhibitor targeting the binding of DNA Ligase 1 to UHRF1
|
Kori, Satomi
|
|
|
52 |
C |
p.
|
artikel
|
| 22 |
Studies on the Importance of the 7α-, and 12α- hydroxyl groups of N-Aryl-3α,7α,12α-trihydroxy-5β-cholan-24-amides on their Antigermination Activity Against a Hypervirulent Strain of Clostridioides (Clostridium) difficile
|
Sharma, Shiv K.
|
|
|
52 |
C |
p.
|
artikel
|
| 23 |
Synthesis and structure-activity relationship studies of 2,4-thiazolidinediones and analogous heterocycles as inhibitors of dihydrodipicolinate synthase
|
Christoff, Rebecca M.
|
|
|
52 |
C |
p.
|
artikel
|
| 24 |
Synthetic development of sugar amino acid oligomers towards novel podophyllotoxin analogues
|
Bouchard, Megan
|
|
|
52 |
C |
p.
|
artikel
|
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