| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adenosine analogs as inhibitors of tyrosyl-tRNA synthetase: Design, synthesis and antibacterial evaluation
|
Wei, Wei
|
|
2015
|
23 |
20 |
p. 6602-6611
10 p.
|
artikel
|
| 2 |
A novel family of diarylpyrimidines (DAPYs) featuring a diatomic linker: Design, synthesis and anti-HIV activities
|
Gu , Shuang-Xi
|
|
2015
|
23 |
20 |
p. 6587-6593
7 p.
|
artikel
|
| 3 |
Cardiovascular activity of the chiral xanthone derivatives
|
Szkaradek , Natalia
|
|
2015
|
23 |
20 |
p. 6714-6724
11 p.
|
artikel
|
| 4 |
Design, synthesis, and biological evaluation of amide imidazole derivatives as novel metabolic enzyme CYP26A1 inhibitors
|
Sun, Bin
|
|
2015
|
23 |
20 |
p. 6763-6773
11 p.
|
artikel
|
| 5 |
Design, synthesis and pharmacological evaluation of pyrimidobenzothiazole-3-carboxylate derivatives as selective L-type calcium channel blockers
|
Chikhale, Rupesh
|
|
2015
|
23 |
20 |
p. 6689-6713
25 p.
|
artikel
|
| 6 |
Design, synthesis and structure–activity relationship studies of novel phenoxyacetamide-based free fatty acid receptor 1 agonists for the treatment of type 2 diabetes
|
Li, Zheng
|
|
2015
|
23 |
20 |
p. 6666-6672
7 p.
|
artikel
|
| 7 |
Discovery and SAR study of 2-(1-propylpiperidin-4-yl)-3H-imidazo[4,5-c]pyridine-7-carboxamide: A potent inhibitor of poly(ADP-ribose) polymerase-1 (PARP-1) for the treatment of cancer
|
Zhu , Qihua
|
|
2015
|
23 |
20 |
p. 6551-6559
9 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2015
|
23 |
20 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Effect of alkyl group on transnitrosation of N-nitrosothiazolidine thiocarboxamides
|
Inami, Keiko
|
|
2015
|
23 |
20 |
p. 6733-6739
7 p.
|
artikel
|
| 10 |
Elaboration of a fragment library hit produces potent and selective aspartate semialdehyde dehydrogenase inhibitors
|
Thangavelu, Bharani
|
|
2015
|
23 |
20 |
p. 6622-6631
10 p.
|
artikel
|
| 11 |
Enzymatic synthesis and RNA interference of nucleosides incorporating stable isotopes into a base moiety
|
Hatano, Akihiko
|
|
2015
|
23 |
20 |
p. 6683-6688
6 p.
|
artikel
|
| 12 |
From carbohydrates to drug-like fragments: Rational development of novel α-amylase inhibitors
|
Al-Asri, Jamil
|
|
2015
|
23 |
20 |
p. 6725-6732
8 p.
|
artikel
|
| 13 |
Graphical contents list
|
|
|
2015
|
23 |
20 |
p. 6535-6541
7 p.
|
artikel
|
| 14 |
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19
|
Shirotani, Naoki
|
|
2015
|
23 |
20 |
p. 6594-6601
8 p.
|
artikel
|
| 15 |
Molecular modeling studies and synthesis of novel quinoxaline derivatives with potential anticancer activity as inhibitors of c-Met kinase
|
Abbas, Hebat-Allah S.
|
|
2015
|
23 |
20 |
p. 6560-6572
13 p.
|
artikel
|
| 16 |
Mucin–drugs interaction: The case of theophylline, prednisolone and cephalexin
|
Pontremoli, Carlotta
|
|
2015
|
23 |
20 |
p. 6581-6586
6 p.
|
artikel
|
| 17 |
Nitrogenated honokiol derivatives allosterically modulate GABAA receptors and act as strong partial agonists
|
Bernaskova, Marketa
|
|
2015
|
23 |
20 |
p. 6757-6762
6 p.
|
artikel
|
| 18 |
Rhododendrol glycosides as stereospecific tyrosinase inhibitors
|
Iwadate, Takehiro
|
|
2015
|
23 |
20 |
p. 6650-6658
9 p.
|
artikel
|
| 19 |
Solid- and solution-phase synthesis and application of R6G dual-labeled oligonucleotide probes
|
Skoblov, Aleksander Yu.
|
|
2015
|
23 |
20 |
p. 6749-6756
8 p.
|
artikel
|
| 20 |
Soluble epoxide hydrolase inhibitory activity of anthraquinone components from Aloe
|
Sun, Ya Nan
|
|
2015
|
23 |
20 |
p. 6659-6665
7 p.
|
artikel
|
| 21 |
Synthesis and antiviral activity of maleopimaric and quinopimaric acids’ derivatives
|
Tretyakova, Elena V.
|
|
2015
|
23 |
20 |
p. 6543-6550
8 p.
|
artikel
|
| 22 |
Synthesis, in vitro biological activities and in silico study of dihydropyrimidines derivatives
|
Barakat, Assem
|
|
2015
|
23 |
20 |
p. 6740-6748
9 p.
|
artikel
|
| 23 |
Synthesis of alkylsulfonyl and substituted benzenesulfonyl curcumin mimics as dual antagonist of L-type Ca2+ channel and endothelin A/B2 receptor
|
Park , Chong-Bin
|
|
2015
|
23 |
20 |
p. 6673-6682
10 p.
|
artikel
|
| 24 |
Synthesis of chiral ND-322, ND-364 and ND-364 derivatives as selective inhibitors of human gelatinase
|
Yan, Yugang
|
|
2015
|
23 |
20 |
p. 6632-6640
9 p.
|
artikel
|
| 25 |
Synthesis of methyl (132 R/S)-alkyl-pyropheophorbide a and a non-epimerized chlorophyll a mimic
|
Ogasawara, Shin
|
|
2015
|
23 |
20 |
p. 6612-6621
10 p.
|
artikel
|
| 26 |
Synthesis of novel acridine bis-sulfonamides with effective inhibitory activity against the carbonic anhydrase isoforms I, II, IX and XII
|
Esirden, İbrahim
|
|
2015
|
23 |
20 |
p. 6573-6580
8 p.
|
artikel
|
| 27 |
1,3,7-Triethyl-substituted xanthines—possess nanomolar affinity for the adenosine A1 receptor
|
Van der Walt, Mietha M.
|
|
2015
|
23 |
20 |
p. 6641-6649
9 p.
|
artikel
|
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