Bu çalışmada dört farklı pirazol/kinolin türevinin different (Exp 54, Exp 56, Exp 57 ve Exp 65) olası sitotoksik etkilerini HeLa An /1 hücrelerinde değerlendirdik. xCELLigence RTCA-DP sistemi (xCELLigence Gerçek Zamanlı Hücre Analiz Sistemi- İkili Plaka) bu maddelerin olası sitotoksik özelliklerinin değerlendirilmesi amacıyla kullanıldı. Bu sistem, hücre çoğalması ve ölümünün sürekli ve işaretleme olmaksızın takip edilmesine imkan tanımaktadır. Bulgularımız yalnızca Exp 65 in HeLa An /1 hücrelerine karşı güçlü sitotoksik aktiviteye sahip olduğunu göstermiştir. Bu bileşiğin IC₅₀ değeri 8.729 ± 1.361µM dır. xCELLigence RTCA-DP sistemi verileriyle uyumlu bir şekilde HeLa An/1 hücrelerinde faz- kontrast mikroskobi bulguları Exp 65...
Two new pyrazole derivatives, namely compound 1 and compound 2, have been synthesized, and their bio...
A series of N-substituted pyrazole derivatives have been synthesized and tested for their anticancer...
AbstractWe designed new pyrazole derivatives as inhibitors of the cell cycle kinases and developed a...
Dünya genelinde birçok araştırmacı, kanser hücrelerine karşı seçici, daha az yan etkili ve daha iyi ...
The research aim was to test cytotoxic effects in vitro of seven novel pyrazolothiazolopyrimidine de...
The research aim was to test cytotoxic effects in vitro of seven novel pyrazolothiazolopyrimidine de...
The 2-pyrazoline derivatives have a wide range of biological effects, such as anti-viral, anti-bacte...
Abstract: Background: In previous papers we demonstrated that the activity of short heteroretinoids...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
A new series of pyrazoline derivatives 1b–12b was designed, synthesized and evaluated for antiprolif...
A new series of pyrazoline derivatives 1b–12b was designed, synthesized and evaluated for antiprolif...
Cancer is a major public health concern worldwide. Adverse effects of cancer treatments still compro...
The major challenge in modern drug discovery has been the design and development of new anticancer d...
Pyrazole moiety is one of the main scaffold for many anticancer drug candidates.Many pyrazole deriva...
Two new pyrazole derivatives, namely compound 1 and compound 2, have been synthesized, and their bio...
A series of N-substituted pyrazole derivatives have been synthesized and tested for their anticancer...
AbstractWe designed new pyrazole derivatives as inhibitors of the cell cycle kinases and developed a...
Dünya genelinde birçok araştırmacı, kanser hücrelerine karşı seçici, daha az yan etkili ve daha iyi ...
The research aim was to test cytotoxic effects in vitro of seven novel pyrazolothiazolopyrimidine de...
The research aim was to test cytotoxic effects in vitro of seven novel pyrazolothiazolopyrimidine de...
The 2-pyrazoline derivatives have a wide range of biological effects, such as anti-viral, anti-bacte...
Abstract: Background: In previous papers we demonstrated that the activity of short heteroretinoids...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
A new series of pyrazoline derivatives 1b–12b was designed, synthesized and evaluated for antiprolif...
A new series of pyrazoline derivatives 1b–12b was designed, synthesized and evaluated for antiprolif...
Cancer is a major public health concern worldwide. Adverse effects of cancer treatments still compro...
The major challenge in modern drug discovery has been the design and development of new anticancer d...
Pyrazole moiety is one of the main scaffold for many anticancer drug candidates.Many pyrazole deriva...
Two new pyrazole derivatives, namely compound 1 and compound 2, have been synthesized, and their bio...
A series of N-substituted pyrazole derivatives have been synthesized and tested for their anticancer...
AbstractWe designed new pyrazole derivatives as inhibitors of the cell cycle kinases and developed a...