Researchers
Nikolić, Katarina
Type
- 214 Conference Paper
- 182 Article
- 3 Text book
- 2 Book parts
- 2 Other
- 1 Reviews
Date issued
- 372 2000 - 2027
- 32 1000 - 1999
Results 161-180 of 404
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Synthesis, In Silico, and In Vitro Evaluation of Anti-Leishmanial Activity of Oxadiazoles and Indolizine Containing Compounds Flagged against Anti-Targets![]() | Stevanović, Strahinja; Senćanski, Milan
Baltas, Michel; García-Sosa, Alfonso;
| Article | 21M21 |
| 2019 | Rational design of multi-target compounds with potential anticancer activity![]() | Dobričić, Vladimir D. | Conference Paper | Mp. category will be shown later |
| 2019 | Pentafluorosulfanyl (SF5) moiety as promising substituent in synthesis and design of novel D2 and D3 receptors ligands | Milica Elek; Annika Frank; Đoković, Nemanja B. | Conference Paper | Mp. category will be shown later |
| 2019 | 3D-QSAR studies and design of selective PI3K-α kinase inhibitors as potential antineoplastics | M. Jovanovic | Conference Paper | Mp. category will be shown later |
| 2019 | Development and Screening of Novel Chemical Probes Targeting Histone Methyltransferase | Si, Yang; Bon, Corentin; Ružić, Dušan | Conference Paper | Mp. category will be shown later |
| 2019 | Ultra-performance liquid chromatography tandem mass spectrometry for the rapid, simultaneous analysis of ziprasidone and its impurities | Carapić, Marija; Nikolić, Katarina | Article | 22M22 |
| 2019 | Preclinical data on (2-imidazolin-4-yl) phosphonates | Nikolić, Katarina M.
L. F. Callado; E. Hernández; J. M. García-Fuster; J. A. García-Sevilla; J. Brea; M. I. Loza; L. Naesens; C. Escolano;
| Conference Paper | Mp. category will be shown later |
| 2019 | Development and Screening of Novel Chemical Probes Targeting Histone Methyltransferases | Yang Si; Corentin Bon; Ružić, Dušan B. | Conference Paper | Mp. category will be shown later |
| 2019 | Structure and ligand based drug design strategies in the development of novel serotonin 5-HTt2a receptor antagonists | Radan, Milica | Conference Paper | Mp. category will be shown later |
| 2018 | Rational drug design of histone deacetylase 6 inhibitors | Dusan Ruzic; Nikolić, Katarina M. | Conference Paper | Mp. category will be shown later |
| 2018 | Primena metoda multivarijantnih analiza glavnih komponenti i hijerarhijskog grupisanja u ispitivanju razdvajanja jedinjenja ziprasidona tečnom hromatografijom | Čarapić M.; Nikolić, Katarina M. | Conference Paper | Mp. category will be shown later |
| 2018 | Primena PAMPA tehnike i QSPR analize u proceni gastrointestinalne apsorpcije i dizajniranju novih biološki aktivnih jedinjenja | Dobričić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2018 | DESIGN OF NOVEL β-HYDROXY-β- - ARYLALKANOIC ACIDS WITH IMPROVED - GASTROINTESTINAL ABSORPTION BASED ON - QSRR STUDIES![]() | Jelena Savić | Conference Paper | Mp. category will be shown later |
| 2018 | A theoretical study on ionization of sartans in aqueous media and on interactions with surfactant micelles | Popović-Nikolić, Marija | Article | 22M22 |
| 2018 | Rational design of selective histone deacetylase inhibitors | D. Ruzić; Đoković, Nemanja B. | Conference Paper | Mp. category will be shown later |
| 2018 | 3D-QSAR study of pyrazolo[3,4-d]pyrimidines and 1,3,4-thiadiazoles as BCR-ABL1 inhibitors | Đoković, Nemanja B. | Conference Paper | Mp. category will be shown later |
| 2018 | Comparative electrochemical studies of kinetic and thermodynamic parameters of Quinoxaline and Brimonidine redox process | Rupar, Jelena | Article | 21aM21a |
| 2018 | 3D molecular pharmacophore determination of PI3K-α kinase inhibitors | Gagić, Žarko | Conference Paper | Mp. category will be shown later |
| 2018 | Molecular modeling and analysis of the 3D pharmacophore structure of the selective PI3K-α inhibitors as antitumor agents | Jovanović, Milan | Article | 52M52 |
| 2018 | Kompjuterski dizajn agonista i antognista 5‐HT2A receptora | Radan, Milica | Conference Paper | Mp. category will be shown later |
