| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Advances in inhibition of protein-protein interactions targeting hypoxia-inducible factor-1 for cancer therapy
|
Li, Jia
|
|
2019
|
27 |
7 |
p. 1145-1158
|
artikel
|
| 2 |
Alkyl derivatives of 1,3,5-triazine as histamine H4 receptor ligands
|
Łażewska, Dorota
|
|
2019
|
27 |
7 |
p. 1254-1262
|
artikel
|
| 3 |
Antibacterial activity of indolyl-quinolinium derivatives and study their mode of action
|
Cai, Senyuan
|
|
2019
|
27 |
7 |
p. 1274-1282
|
artikel
|
| 4 |
Cellular delivery and enhanced anticancer activity of berberine complexed with a cationic derivative of γ–cyclodextrin
|
Popiołek, Iwona
|
|
2019
|
27 |
7 |
p. 1414-1420
|
artikel
|
| 5 |
Design and development of novel N-(pyrimidin-2-yl)-1,3,4-oxadiazole hybrids to treat cognitive dysfunctions
|
Tripathi, Prabhash Nath
|
|
2019
|
27 |
7 |
p. 1327-1340
|
artikel
|
| 6 |
Design and molecular modeling of novel P38α MAPK inhibitors targeting breast cancer, synthesized from oxygen heterocyclic natural compounds
|
Abdelhafez, Omaima M.
|
|
2019
|
27 |
7 |
p. 1308-1319
|
artikel
|
| 7 |
Design and synthesis of potent myostatin inhibitory cyclic peptides
|
Rentier, Cédric
|
|
2019
|
27 |
7 |
p. 1437-1443
|
artikel
|
| 8 |
Design and synthesis of various quinizarin derivatives as potential anticancer agents in acute T lymphoblastic leukemia
|
Hu, Xiufang
|
|
2019
|
27 |
7 |
p. 1362-1369
|
artikel
|
| 9 |
Design and total synthesis of (-)-codonopsinine, (-)-codonopsine and codonopsinine analogues by O-(2-oxopyrrolidin-5-yl)trichloroacetimidate as amidoalkylating agent with improved antimicrobial activity via solid lipid nanoparticle formulations
|
El-Nezhawy, Ahmed O.H.
|
|
2019
|
27 |
7 |
p. 1263-1273
|
artikel
|
| 10 |
Design, synthesis and biological evaluation of imidazo[1,5-a]pyrazin-8(7H)-one derivatives as BRD9 inhibitors
|
Zheng, Peiyuan
|
|
2019
|
27 |
7 |
p. 1391-1404
|
artikel
|
| 11 |
Design, synthesis and biological evaluation of pyridone–aminal derivatives as MNK1/2 inhibitors
|
Yuan, Xinrui
|
|
2019
|
27 |
7 |
p. 1211-1225
|
artikel
|
| 12 |
Detection of esterase activity by chromogenic and fluorogenic probe based on an O-nitrobenzoxadiazole (O-NBD) unit
|
Okada, Kana
|
|
2019
|
27 |
7 |
p. 1444-1448
|
artikel
|
| 13 |
3,5-Dialkoxypyridine analogues of bedaquiline are potent antituberculosis agents with minimal inhibition of the hERG channel
|
Sutherland, Hamish S.
|
|
2019
|
27 |
7 |
p. 1292-1307
|
artikel
|
| 14 |
Discovery of (S)-6-methoxy-chroman-3-carboxylic acid (4-pyridin-4-yl-phenyl)-amide as potent and isoform selective ROCK2 inhibitors
|
Pan, Jinpeng
|
|
2019
|
27 |
7 |
p. 1382-1390
|
artikel
|
| 15 |
Editorial Board
|
|
|
2019
|
27 |
7 |
p. ii
|
artikel
|
| 16 |
Enantioselective resolution of side-chain modified gem-difluorinated alcohols catalysed by Candida antarctica lipase B and monitored by capillary electrophoresis
|
Pomeisl, Karel
|
|
2019
|
27 |
7 |
p. 1246-1253
|
artikel
|
| 17 |
Expansion of a novel lead targeting M. tuberculosis DHFR as antitubercular agents
|
Sharma, Kalicharan
|
|
2019
|
27 |
7 |
p. 1421-1429
|
artikel
|
| 18 |
Further insights of selenium-containing analogues of WC-9 against Trypanosoma cruzi
|
Chao, María N.
|
|
2019
|
27 |
7 |
p. 1350-1361
|
artikel
|
| 19 |
Graphical abstract TOC
|
|
|
2019
|
27 |
7 |
p. OBC
|
artikel
|
| 20 |
Graphical abstract TOC
|
|
|
2019
|
27 |
7 |
p. I-VI
|
artikel
|
| 21 |
Graphical abstract TOC
|
|
|
2019
|
27 |
7 |
p. IBC
|
artikel
|
| 22 |
Investigation of B,C-ring truncated deguelin derivatives as heat shock protein 90 (HSP90) inhibitors for use as anti-breast cancer agents
|
Kim, Ho Shin
|
|
2019
|
27 |
7 |
p. 1370-1381
|
artikel
|
| 23 |
Ketamine esters and amides as short-acting anaesthetics: Structure-activity relationships for the side-chain
|
Dimitrov, Ivaylo V.
|
|
2019
|
27 |
7 |
p. 1226-1231
|
artikel
|
| 24 |
Novel multi-target directed ligands based on annelated xanthine scaffold with aromatic substituents acting on adenosine receptor and monoamine oxidase B. Synthesis, in vitro and in silico studies
|
Załuski, Michał
|
|
2019
|
27 |
7 |
p. 1195-1210
|
artikel
|
| 25 |
Screening oxime libraries by means of mass spectrometry (MS) binding assays: Identification of new highly potent inhibitors to optimized inhibitors γ-aminobutyric acid transporter 1
|
Kern, Felix
|
|
2019
|
27 |
7 |
p. 1232-1245
|
artikel
|
| 26 |
Semisynthesis of epoxy-pimarane diterpenoids from kirenol and their FXa inhibition activities
|
Wang, Jianbin
|
|
2019
|
27 |
7 |
p. 1320-1326
|
artikel
|
| 27 |
Specificity of extended O-aryloxycarbonyl hydroxamates as inhibitors of a class C β-lactamase
|
Malico, Alexandra A.
|
|
2019
|
27 |
7 |
p. 1430-1436
|
artikel
|
| 28 |
Structure-activity relationships for unit C pyridyl analogues of the tuberculosis drug bedaquiline
|
Blaser, Adrian
|
|
2019
|
27 |
7 |
p. 1283-1291
|
artikel
|
| 29 |
Synthesis and biological evaluation of paclitaxel and vorinostat co-prodrugs for overcoming drug resistance in cancer therapy in vitro
|
Liu, Shuangxi
|
|
2019
|
27 |
7 |
p. 1405-1413
|
artikel
|
| 30 |
Synthesis and characterization of small interfering RNAs with haloalkyl groups at their 3′-dangling ends
|
Chandela, Akash
|
|
2019
|
27 |
7 |
p. 1341-1349
|
artikel
|
| 31 |
Thieno[2,3-d]pyrimidine as a promising scaffold in medicinal chemistry: Recent advances
|
Ali, Eslam M.H.
|
|
2019
|
27 |
7 |
p. 1159-1194
|
artikel
|
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