Authors Mittal, RK; Purohit, P in BENTHAM SCIENCE PUBL LTD published article about MOLECULAR-PROPERTIES PREDICTION; CYTOTOXIC EVALUATION; APOPTOSIS PATHWAYS; HIGHLY EFFICIENT; QUINOLINES; ANALOGS; LAVENDAMYCIN; INHIBITORS; ADDUCTS; BENIGN in [Mittal, Ravi K.] Natl Inst Pharmaceut Educ & Res NIPER, Dept Nat Prod, Sect 67, Sas Nagar 160062, Punjab, India; [Purohit, Priyank] HIMT, Dept Pharm, Greater Noida 201308, Uttar Pradesh, India in 2020.0, Cited 42.0. Quality Control of 3-Hydroxybenzaldehyde. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4
Background: The quinoline scaffold has been an attraction due to its pharmacological activities such as anti-HIV, anti-neoplastic, anti-asthmatic, anti-tuberculotic, anti-fungal, and anti-bacterial. Objective: The designed quinoline-3-carboxylate derivatives were synthesized through a two-step reaction and evaluated for antiproliferative activity against MCF-7 and K562 cell lines. Methods: Synthesized compounds were characterized by modern analytical techniques like NMR, 2DNMR, mass. and IR. Moreover, the purity of compounds was analyzed through the HPLC. In the progress of biological results, all synthesized compounds were evaluated for antiproliferative activity against MCF-7 and 1562 cell lines. Results: The synthesized compounds exhibited micromolar inhibition in all over the ranges, however, some of the compounds showed better activity than the standard anticancer drug such, as 4m and 4n with the IC50 value of 0.33 mu M against the MCF-7 cell line, and the compounds 4k and 4m showed potential activity against the K562 cell line with the IC50 value of 0.28 mu M. The anti-cancer activities of compounds were found to be thmugh the up-regulation of intrinsic apoptosis pathways. Conclusion: The biological data of all compounds in both cell lines were utilized for the structural activity relationship of the quinoline-3-carboxylate pharmacophore. The active lead was further validated through rigorous in silico studies for the drug-likeness (QED) and Absorption, Distribution, Metabolism, Excretion, and Toxicity (ADMET) properties. Here in the present research is utilized for the demonstration of an important pharmacophore, which could be utilized for further development to become a lead as an anticancer agent with minimal toxicity.
Quality Control of 3-Hydroxybenzaldehyde. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Mittal, RK; Purohit, P or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles