Some scientific research about 837-52-5

From this literature《Synthesis and biological evaluation of certain new cyclohexane-1-carboxamides as apoptosis inducers》,we know some information about this compound(837-52-5)HPLC of Formula: 837-52-5, but this is not all information, there are many literatures related to this compound(837-52-5).

HPLC of Formula: 837-52-5. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 7-Chloro-4-(piperazin-1-yl)quinoline, is researched, Molecular C13H14ClN3, CAS is 837-52-5, about Synthesis and biological evaluation of certain new cyclohexane-1-carboxamides as apoptosis inducers. Author is Abd-Allah, Walaa Hamada; Elshafie, Mohamed Fathy.

Series of 1-(N-phenyl-2-(heteroalicyclic-1-yl)acetamido)cyclohexane-1-carboxamide derivatives (5a-m) and 1-(phenyl(heteroalicyclic-1-ylmethyl)amino)cyclohexane-1-carboxamide (6a-f) were designed and synthesized with biol. interest through coupling of 1-(2-chloro-N-phenylacetamido)cyclohexane-1-carboxamide (4) and (phenylamino)cycloakanecarboxamide (2) with different amines. The structures of the target compounds were elucidated via IR, 1H and 13C NMR, MS, and microanal. Compounds 5a-m and 6a-f were evaluated for their in vitro antitumor activity against four different cancer cell lines, MCF-7, HepG2, A549, and Caco-2. Compound 5i exhibited a promising activity against breast cancer cell line (IC50 value = 3.25 μM) compared with doxorubicin (IC50 value = 6.77 μM). Results from apoptosis and cell cycle anal. for compound 5i revealed good antitumor activity against MCF-7 cancer cell line and potent inhibition.

From this literature《Synthesis and biological evaluation of certain new cyclohexane-1-carboxamides as apoptosis inducers》,we know some information about this compound(837-52-5)HPLC of Formula: 837-52-5, but this is not all information, there are many literatures related to this compound(837-52-5).

Reference:
Bromide – Wikipedia,
bromide – Wiktionary