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Evaluation of angularly condensed diquinothiazines as potential anticancer agents with the IC 50 values < 3 µM. This anti-proliferative activity was found to be more than for cisplatin

Copper(ii) complexes with 2,2′:6′,2′′-terpyridine, 2,6-di(thiazol-2-yl)pyridine and 2,6-di(pyrazin-2-yl)pyridine substituted with quinolines. Synthesis, structure, antiproliferative activity, and catalytic activity in the oxidation of alkanes and alcohols with peroxides(pyrazin-2-yl)pyridine substituted with quinolines. Synthesis, structure, antiproliferative activity

Influence of anchoring moieties on new benzimidazole-based Schiff base copper(ii) complexes towards estrogen dependent breast cancer cells. The mechanism of action for the effective antiproliferative activity of1has additionally been confirmed by means

Selective Cytotoxic Activity of Prodigiosin@halloysite Nanoformulation (Caco-2) and human colon carcinoma (HCT116) cells proliferative activity. After treatment of Caco-2

SYNERGISTIC ANTI-TUMOR EFFECTS OF ARSENIC TRIOXIDE AND BLUE LED IRRADIATION ON HUMAN OSTEOSARCOMA irradiation at 470 nm in wavelength exhibited superior anti-tumor activity in human osteosarcoma (OS). We

Ультразвуковой контроль эффективности применения комбинации нитей из полидиоксанона и полидезоксирибонуклеотидов у старшей возрастной группы: клинический случай with a decrease in the proliferative activity of the pool of active cells - fibroblasts and, consequently

Burn Wound Healing Activity of Hydroxyethylcellulose Gels with Different Water Extracts Obtained from Various Medicinal Plants in Pseudomonas aeruginosa-Infected Rabbits-positive cells, indicating improved proliferative activity and reduced inflammation. This study confirms

Study of the anti-inflammatory, analgesic, ulcerogenic and anti-ulcerogenic activity of Nisopropenylimidazole zinc complex derivativeThe aim of the study was to investigate the anti-inflammatory, analgesic, ulcerogenic and anti

Design, synthesis and biological evaluation of 2-quinolyl-1,3-tropolone derivatives as new anti-cancer agents synthesized and tested for their anti-proliferative activity against several human cancer cell lines. Two

Design and Synthesis of New Agents for Prostate Cancer Treatment Inspired by Steroidal CYP17 A1 Inhibitors). Some of compounds revealed high anti-proliferative activity in prostate carcinoma LNCaP and PC-3 cells

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