| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cell surface clicked navigation system to direct specific bone targeting
|
Kim, Young
|
|
2018
|
26 |
3 |
p. 758-764
|
artikel
|
| 2 |
Antiobesity and emetic effects of a short-length peptide YY analog and its PEGylated and alkylated derivatives
|
Niida, Ayumu
|
|
2018
|
26 |
3 |
p. 566-572
|
artikel
|
| 3 |
A review on the hybrids of hydroxycinnamic acid as multi-target-directed ligands against Alzheimer’s disease
|
Zhang, Xiao
|
|
2018
|
26 |
3 |
p. 543-550
|
artikel
|
| 4 |
Benzimidazole design, synthesis, and docking to build selective carbonic anhydrase VA inhibitors
|
Čapkauskaitė, Edita
|
|
2018
|
26 |
3 |
p. 675-687
|
artikel
|
| 5 |
Design, synthesis and evaluate of novel dual FGFR1 and HDAC inhibitors bearing an indazole scaffold
|
Liu, Jian
|
|
2018
|
26 |
3 |
p. 747-757
|
artikel
|
| 6 |
Design, synthesis, and evaluation of polyamine-memantine hybrids as NMDA channel blockers
|
Kumamoto, Takuya
|
|
2018
|
26 |
3 |
p. 603-608
|
artikel
|
| 7 |
Design, synthesis and evaluation of γ-turn mimetics as LSD1-selective inhibitors
|
Ota, Yosuke
|
|
2018
|
26 |
3 |
p. 775-785
|
artikel
|
| 8 |
Development of dual casein kinase 1δ/1ε (CK1δ/ε) inhibitors for treatment of breast cancer
|
Monastyrskyi, Andrii
|
|
2018
|
26 |
3 |
p. 590-602
|
artikel
|
| 9 |
Discovery of EBI-1051: A novel and orally efficacious MEK inhibitor with benzofuran scaffold
|
Lu, Biao
|
|
2018
|
26 |
3 |
p. 581-589
|
artikel
|
| 10 |
Discovery of new thienopyrimidine derivatives as potent and orally efficacious phosphoinositide 3-kinase inhibitors
|
Lin, Songwen
|
|
2018
|
26 |
3 |
p. 637-646
|
artikel
|
| 11 |
Editorial Board
|
|
|
2018
|
26 |
3 |
p. ii
|
artikel
|
| 12 |
Fusarithioamide B, a new benzamide derivative from the endophytic fungus Fusarium chlamydosporium with potent cytotoxic and antimicrobial activities
|
Ibrahim, Sabrin R.M.
|
|
2018
|
26 |
3 |
p. 786-790
|
artikel
|
| 13 |
Graphical abstract TOC
|
|
|
2018
|
26 |
3 |
p. OBC
|
artikel
|
| 14 |
Graphical abstract TOC
|
|
|
2018
|
26 |
3 |
p. IBC
|
artikel
|
| 15 |
Graphical abstract TOC continued
|
|
|
2018
|
26 |
3 |
p. II-VI
|
artikel
|
| 16 |
Identification of highly potent and orally available free fatty acid receptor 1 agonists bearing isoxazole scaffold
|
Li, Zheng
|
|
2018
|
26 |
3 |
p. 703-711
|
artikel
|
| 17 |
Identification of novel quinazolinedione derivatives as RORγt inverse agonist
|
Fukase, Yoshiyuki
|
|
2018
|
26 |
3 |
p. 721-736
|
artikel
|
| 18 |
Induction of apoptosis by pyrazolo[3,4-d]pyridazine derivative in lung cancer cells via disruption of Bcl-2/Bax expression balance
|
Mohamed, Mervat S.
|
|
2018
|
26 |
3 |
p. 623-629
|
artikel
|
| 19 |
Inhibition of protein tyrosine phosphatase 1B (PTP1B) and α-glucosidase by xanthones from Cratoxylum cochinchinense, and their kinetic characterization
|
Li, Zuo Peng
|
|
2018
|
26 |
3 |
p. 737-746
|
artikel
|
| 20 |
New photodynamic molecular beacons (PMB) as potential cancer-targeted agents in PDT
|
Stallivieri, Aurélie
|
|
2018
|
26 |
3 |
p. 688-702
|
artikel
|
| 21 |
Novel fluconazole derivatives with promising antifungal activity
|
Thamban Chandrika, Nishad
|
|
2018
|
26 |
3 |
p. 573-580
|
artikel
|
| 22 |
One-step synthesis of carbohydrate esters as antibacterial and antifungal agents
|
AlFindee, Madher N.
|
|
2018
|
26 |
3 |
p. 765-774
|
artikel
|
| 23 |
Structural optimization of N1-aryl-benzimidazoles for the discovery of new non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains
|
Monforte, Anna Maria
|
|
2018
|
26 |
3 |
p. 661-674
|
artikel
|
| 24 |
Structure-activity relationships of cryptopleurine analogs with E-ring modifications as anti-hepatitis C virus agents
|
Wang, Ying
|
|
2018
|
26 |
3 |
p. 630-636
|
artikel
|
| 25 |
Structure-based design, synthesis, and biological evaluation of imidazo[1,2-b]pyridazine-based p38 MAP kinase inhibitors
|
Kaieda, Akira
|
|
2018
|
26 |
3 |
p. 647-660
|
artikel
|
| 26 |
Synthesis and biological evaluation of cyclopeptide GG-8-6 and its analogues as anti-hepatocellular carcinoma agents
|
Chen, Jie-Tao
|
|
2018
|
26 |
3 |
p. 609-622
|
artikel
|
| 27 |
Synthesis and biological evaluation of 6-substituted-5-fluorouridine ProTides
|
Slusarczyk, Magdalena
|
|
2018
|
26 |
3 |
p. 551-565
|
artikel
|
| 28 |
Theoretical research in structure characteristics of different inhibitors and differences of binding modes with CBP bromodomain
|
Wang, Xue-Song
|
|
2018
|
26 |
3 |
p. 712-720
|
artikel
|
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