| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acyl-2-aminobenzimidazoles: A novel class of neuroprotective agents targeting mGluR5
|
He, Xinhua
|
|
2015
|
23 |
9 |
p. 2211-2220
10 p.
|
artikel
|
| 2 |
α-Adrenoceptor antagonistic and hypotensive properties of novel arylpiperazine derivatives of pyrrolidin-2-one
|
Zaręba, Paula
|
|
2015
|
23 |
9 |
p. 2104-2111
8 p.
|
artikel
|
| 3 |
A unique hinge binder of extremely selective aminopyridine-based Mps1 (TTK) kinase inhibitors with cellular activity
|
Kusakabe, Ken-ichi
|
|
2015
|
23 |
9 |
p. 2247-2260
14 p.
|
artikel
|
| 4 |
Cell-based biological evaluations of 5-(3-bromo-4-phenethoxybenzylidene)thiazolidine-2,4-dione as promising wound healing agent
|
Piao, Yu Lan
|
|
2015
|
23 |
9 |
p. 2098-2103
6 p.
|
artikel
|
| 5 |
Design and synthesis of novel anti-tuberculosis agents from the celecoxib pharmacophore
|
Salunke, Santosh B.
|
|
2015
|
23 |
9 |
p. 1935-1943
9 p.
|
artikel
|
| 6 |
Design and synthesis of novel quinoline–aminopiperidine hybrid analogues as Mycobacterium tuberculosis DNA gyraseB inhibitors
|
Medapi, Brahmam
|
|
2015
|
23 |
9 |
p. 2062-2078
17 p.
|
artikel
|
| 7 |
Design and synthesis of piperazine derivatives as a novel class of γ-secretase modulators that selectively lower Aβ42 production
|
Takai, Takafumi
|
|
2015
|
23 |
9 |
p. 1923-1934
12 p.
|
artikel
|
| 8 |
Design, synthesis and biological evaluation of a highly-potent and cancer cell selective folate–taxoid conjugate
|
Seitz, Joshua D.
|
|
2015
|
23 |
9 |
p. 2187-2194
8 p.
|
artikel
|
| 9 |
Design, synthesis and biological evaluation of novel homocamptothecin analogues as potent antitumor agents
|
Wang, Lei
|
|
2015
|
23 |
9 |
p. 1950-1962
13 p.
|
artikel
|
| 10 |
Design, synthesis and biological evaluation of N-phenylthieno[2,3-d]pyrimidin-4-amines as inhibitors of FGFR1
|
Gryshchenko, A.A.
|
|
2015
|
23 |
9 |
p. 2287-2293
7 p.
|
artikel
|
| 11 |
Design, synthesis and biological evaluation of tasiamide B derivatives as BACE1 inhibitors
|
Liu, Jian
|
|
2015
|
23 |
9 |
p. 1963-1974
12 p.
|
artikel
|
| 12 |
Design, synthesis and in vitro cell-based evaluation of the anti-cancer activities of hispolon analogs
|
Balaji, Neduri V.
|
|
2015
|
23 |
9 |
p. 2148-2158
11 p.
|
artikel
|
| 13 |
Design, synthesis and preliminary bioactivity studies of 2-thioxo-4-thiazolidinone derivatives as Bcl-2 inhibitors
|
Wan, Yichao
|
|
2015
|
23 |
9 |
p. 1994-2003
10 p.
|
artikel
|
| 14 |
Development of a clickable activity-based protein profiling (ABPP) probe for agmatine deiminases
|
Marchenko, Mikhail
|
|
2015
|
23 |
9 |
p. 2159-2167
9 p.
|
artikel
|
| 15 |
Discovery of a potent, orally available dual CysLT1 and CysLT2 antagonist with dicarboxylic acid
|
Itadani, Satoshi
|
|
2015
|
23 |
9 |
p. 2079-2097
19 p.
|
artikel
|
| 16 |
Discovery of novel pyrazolopyrimidinone analogs as potent inhibitors of phosphodiesterase type-5
|
Sawant, Sanghapal D.
|
|
2015
|
23 |
9 |
p. 2121-2128
8 p.
|
artikel
|
| 17 |
Editorial board
|
|
|
2015
|
23 |
9 |
p. IFC-
1 p.
|
artikel
|
| 18 |
Effect of arginine methylation on the RNA recognition and cellular uptake of Tat-derived peptides
|
Li, Jhe-Hao
|
|
2015
|
23 |
9 |
p. 2281-2286
6 p.
|
artikel
|
| 19 |
Graphical contents list
|
|
|
2015
|
23 |
9 |
p. 1883-1893
11 p.
|
artikel
|
| 20 |
Identification of novel class of falcipain-2 inhibitors as potential antimalarial agents
|
Chakka, Sai Kumar
|
|
2015
|
23 |
9 |
p. 2221-2240
20 p.
|
artikel
|
| 21 |
Investigation into novel thiophene- and furan-based 4-amino-7-chloroquinolines afforded antimalarials that cure mice
|
Opsenica, Igor M.
|
|
2015
|
23 |
9 |
p. 2176-2186
11 p.
|
artikel
|
| 22 |
Novel arylazopyrazole inhibitors of cyclin-dependent kinases
|
Jorda, Radek
|
|
2015
|
23 |
9 |
p. 1975-1981
7 p.
|
artikel
|
| 23 |
Novel 2-(2-phenalkyl)-1H-benzo[d]imidazoles as antitubercular agents. Synthesis, biological evaluation and structure–activity relationship
|
Gobis, Katarzyna
|
|
2015
|
23 |
9 |
p. 2112-2120
9 p.
|
artikel
|
| 24 |
Nucleobase modified neamines with a lysine as a linker, their inhibition specificity for TAR-Tat derived from HIV-1
|
Inoue, Ryo
|
|
2015
|
23 |
9 |
p. 2139-2147
9 p.
|
artikel
|
| 25 |
SiO2 nanoparticles as platform for delivery of 3′-triazole analogues of AZT-triphosphate into cells
|
Vasilyeva, Svetlana V.
|
|
2015
|
23 |
9 |
p. 2168-2175
8 p.
|
artikel
|
| 26 |
Structure–activity relationships of a novel pyranopyridine series of Gram-negative bacterial efflux pump inhibitors
|
Nguyen, Son T.
|
|
2015
|
23 |
9 |
p. 2024-2034
11 p.
|
artikel
|
| 27 |
Structure–activity relationships of benzhydrol derivatives based on 1′-acetoxychavicol acetate (ACA) and their inhibitory activities on multiple myeloma cell growth via inactivation of the NF-κB pathway
|
Misawa, Takashi
|
|
2015
|
23 |
9 |
p. 2241-2246
6 p.
|
artikel
|
| 28 |
Structure–activity relationships of substituted 1H-indole-2-carboxamides as CB1 receptor allosteric modulators
|
Nguyen, Thuy
|
|
2015
|
23 |
9 |
p. 2195-2203
9 p.
|
artikel
|
| 29 |
Synthesis and ABCG2 inhibitory evaluation of 5-N-acetylardeemin derivatives
|
Hayashi, Daigo
|
|
2015
|
23 |
9 |
p. 2010-2023
14 p.
|
artikel
|
| 30 |
Synthesis and antimycobacterial properties of ring-substituted 6-hydroxynaphthalene-2-carboxanilides
|
Kos, Jiri
|
|
2015
|
23 |
9 |
p. 2035-2043
9 p.
|
artikel
|
| 31 |
Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
|
Zakharenko, Alexandra
|
|
2015
|
23 |
9 |
p. 2044-2052
9 p.
|
artikel
|
| 32 |
Synthesis and evaluation of 123 / 131I-Iochlonicotinamide as a novel SPECT probe for malignant melanoma
|
Chang, Chih-Chao
|
|
2015
|
23 |
9 |
p. 2261-2269
9 p.
|
artikel
|
| 33 |
Synthesis and fungicidal activity of N-thiazol-4-yl-salicylamides, a new family of anti-oomycete compounds
|
Sulzer-Mosse, Sarah
|
|
2015
|
23 |
9 |
p. 2129-2138
10 p.
|
artikel
|
| 34 |
Synthesis and structure–activity relationships of boswellic acid derivatives as potent VEGFR-2 inhibitors
|
Shen, Sida
|
|
2015
|
23 |
9 |
p. 1982-1993
12 p.
|
artikel
|
| 35 |
Synthesis, crystal structures, and urease inhibition of an acetohydroxamate-coordinated oxovanadium(V) complex derived from N′-(3-bromo-2-hydroxybenzylidene)-4-methoxybenzohydrazide
|
Qu, Dan
|
|
2015
|
23 |
9 |
p. 1944-1949
6 p.
|
artikel
|
| 36 |
Synthesis of nitro(benzo)thiazole acetamides and in vitro antiprotozoal effect against amitochondriate parasites Giardia intestinalis and Trichomonas vaginalis
|
Navarrete-Vázquez, Gabriel
|
|
2015
|
23 |
9 |
p. 2204-2210
7 p.
|
artikel
|
| 37 |
Synthesis of N-methylarylnitrones derived from alkyloxybenzaldehydes and antineoplastic effect on human cancer cell lines
|
Costa, Débora S.S.
|
|
2015
|
23 |
9 |
p. 2053-2061
9 p.
|
artikel
|
| 38 |
Synthesis of novel 24-amino-25,26,27-trinorlanost-8-enes: Cytotoxic and apoptotic potential in U937 cells
|
O’Keeffe, Roisin
|
|
2015
|
23 |
9 |
p. 2270-2280
11 p.
|
artikel
|
| 39 |
Synthetic approaches to the 2013 new drugs
|
Ding, Hong X.
|
|
2015
|
23 |
9 |
p. 1895-1922
28 p.
|
artikel
|
| 40 |
The CERT antagonist HPA-12: First practical synthesis and individual binding evaluation of the four stereoisomers
|
Santos, Cécile
|
|
2015
|
23 |
9 |
p. 2004-2009
6 p.
|
artikel
|
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