| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Anthranilic acid derivatives as nuclear receptor modulators—Development of novel PPAR selective and dual PPAR/FXR ligands
|
Merk, Daniel
|
|
2015
|
23 |
3 |
p. 499-514
16 p.
|
artikel
|
| 2 |
4-Dechloro-14-deoxy-oxacyclododecindione and 14-deoxy-oxacylododecindione, two inhibitors of inducible connective tissue growth factor expression from the imperfect fungus Exserohilum rostratum
|
Richter, Julia
|
|
2015
|
23 |
3 |
p. 556-563
8 p.
|
artikel
|
| 3 |
Design and synthesis of a novel series of histamine H3 receptor antagonists through a scaffold hopping strategy
|
Gao, Zhongli
|
|
2015
|
23 |
3 |
p. 429-438
10 p.
|
artikel
|
| 4 |
Design and synthesis of novel 2-pyrazoline-1-ethanone derivatives as selective MAO inhibitors
|
Tong, Xu
|
|
2015
|
23 |
3 |
p. 515-525
11 p.
|
artikel
|
| 5 |
Design, synthesis, and biological evaluation of aminothiazole derivatives against the fungal pathogens Histoplasma capsulatum and Cryptococcus neoformans
|
Khalil, Ahmed
|
|
2015
|
23 |
3 |
p. 532-547
16 p.
|
artikel
|
| 6 |
Design, synthesis, and evaluation of hybrid vitamin D3 side chain analogues as hedgehog pathway inhibitors
|
Banerjee, Upasana
|
|
2015
|
23 |
3 |
p. 548-555
8 p.
|
artikel
|
| 7 |
Discovery and SAR study of c-Met kinase inhibitors bearing an 3-amino-benzo[d]isoxazole or 3-aminoindazole scaffold
|
Jiang, Xiaolong
|
|
2015
|
23 |
3 |
p. 564-578
15 p.
|
artikel
|
| 8 |
Discovery of triazolone derivatives as novel, potent stearoyl-CoA desaturase-1 (SCD1) inhibitors
|
Sun, Shaoyi
|
|
2015
|
23 |
3 |
p. 455-465
11 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2015
|
23 |
3 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Evaluation of two novel antioxidants with differential effects on curcumin-induced apoptosis in C2 skeletal myoblasts; involvement of JNKs
|
Peleli, Maria
|
|
2015
|
23 |
3 |
p. 390-400
11 p.
|
artikel
|
| 11 |
Exploring the gyrase ATPase domain for tailoring newer anti-tubercular drugs: Hit to lead optimization of a novel class of thiazole inhibitors
|
Jeankumar, Variam Ullas
|
|
2015
|
23 |
3 |
p. 588-601
14 p.
|
artikel
|
| 12 |
Ferrocenes as potential chemotherapeutic drugs: Synthesis, cytotoxic activity, reactive oxygen species production and micronucleus assay
|
Pérez, Wanda I.
|
|
2015
|
23 |
3 |
p. 471-479
9 p.
|
artikel
|
| 13 |
Fine tuning of 4,6-bisphenyl-2-(3-alkoxyanilino)pyrimidine focusing on the activity-sensitive aminoalkoxy moiety for a therapeutically useful inhibitor of receptor for advanced glycation end products (RAGE)
|
Han, Young Taek
|
|
2015
|
23 |
3 |
p. 579-587
9 p.
|
artikel
|
| 14 |
Flavonoids as noncompetitive inhibitors of Dengue virus NS2B-NS3 protease: Inhibition kinetics and docking studies
|
de Sousa, Lorena Ramos Freitas
|
|
2015
|
23 |
3 |
p. 466-470
5 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2015
|
23 |
3 |
p. 365-372
8 p.
|
artikel
|
| 16 |
Identification of the dioxygenase-generated intermediate formed during biosynthesis of the dihydropyrrole moiety common to anthramycin and sibiromycin
|
Saha, Shalini
|
|
2015
|
23 |
3 |
p. 449-454
6 p.
|
artikel
|
| 17 |
IND-2, a pyrimido[1″,2″:1,5]pyrazolo[3,4-b]quinoline derivative, circumvents multi-drug resistance and causes apoptosis in colon cancer cells
|
Karthikeyan, Chandrabose
|
|
2015
|
23 |
3 |
p. 602-611
10 p.
|
artikel
|
| 18 |
Investigation of fatty acid conjugates of 3,5-bisarylmethylene-4-piperidone derivatives as antitumor agents and human topoisomerase-IIα inhibitors
|
Potter, Elizabeth
|
|
2015
|
23 |
3 |
p. 411-421
11 p.
|
artikel
|
| 19 |
Natural antitubulin agents: Importance of 3,4,5-trimethoxyphenyl fragment
|
Negi, Arvind S.
|
|
2015
|
23 |
3 |
p. 373-389
17 p.
|
artikel
|
| 20 |
Non-transpeptidase binding arylthioether β-lactams active against Mycobacterium tuberculosis and Moraxella catarrhalis
|
Beck, Tim N.
|
|
2015
|
23 |
3 |
p. 632-647
16 p.
|
artikel
|
| 21 |
Novel agonists of benzodiazepine receptors: Design, synthesis, binding assay and pharmacological evaluation of 1,2,4-triazolo[1,5-a]pyrimidinone and 3-amino-1,2,4-triazole derivatives
|
Faizi, Mehrdad
|
|
2015
|
23 |
3 |
p. 480-487
8 p.
|
artikel
|
| 22 |
Selective binding to monoamine oxidase A: In vitro and in vivo evaluation of 18F-labeled β-carboline derivatives
|
Schieferstein, Hanno
|
|
2015
|
23 |
3 |
p. 612-623
12 p.
|
artikel
|
| 23 |
Sulfonamide inhibition studies of the η-class carbonic anhydrase from the malaria pathogen Plasmodium falciparum
|
Vullo, Daniela
|
|
2015
|
23 |
3 |
p. 526-531
6 p.
|
artikel
|
| 24 |
Synthesis and biological activities of some new isonicotinic acid 2-(2-hydroxy-8-substituted-tricyclo[7.3.1.02.7]tridec-13-ylidene)-hydrazides
|
Matei, Lilia
|
|
2015
|
23 |
3 |
p. 401-410
10 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of DAPY–DPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase
|
Wu, Hai-Qiu
|
|
2015
|
23 |
3 |
p. 624-631
8 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of isoindoloisoquinolinone, pyroloisoquinolinone and benzoquinazolinone derivatives as poly(ADP-ribose) polymerase-1 inhibitors
|
Suyavaran, Arumugam
|
|
2015
|
23 |
3 |
p. 488-498
11 p.
|
artikel
|
| 27 |
Synthesis and evaluation of multi-functional NO-donor/insulin-secretagogue derivatives for the treatment of type II diabetes and its cardiovascular complications
|
Digiacomo, Maria
|
|
2015
|
23 |
3 |
p. 422-428
7 p.
|
artikel
|
| 28 |
Transformation of naltrexone into mesembrane and investigation of the binding properties of its intermediate derivatives to opioid receptors
|
Konoura, Kazuya
|
|
2015
|
23 |
3 |
p. 439-448
10 p.
|
artikel
|
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