New learning discoveries about 50-84-0

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An article Acylation of 25-hydroxyprotopanaxatriol with aromatic acids increases cytotoxicity WOS:000484878400054 published article about PANAX-GINSENG; IN-VITRO; ANTITUMOR EVALUATION; ANTICANCER ACTIVITY; PROSTATE-CANCER; GINSENOSIDES; DERIVATIVES; PROLIFERATION; SEMISYNTHESIS; APOPTOSIS in [Lv, Liyan; Piao, Huri] Yanbian Univ, Key Lab Nat Resources Changbai Mt & Funct Mol, Minist Educ, Coll Pharm, Yanji 133002, Peoples R China; [Lv, Liyan; Lu, Jincai] Shenyang Pharmaceut Univ, Dept Med Plant, Shenyang 110016, Liaoning, Peoples R China; [Zhang, Hongyu; Wang, Xude; Su, Guangyue; Zhao, Yuqing] Shenyang Pharmaceut Univ, Sch Funct Food & Wine, Shenyang, Liaoning, Peoples R China; [Zhao, Yuqing] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Liaoning, Peoples R China in 2019, Cited 36. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0. Application In Synthesis of 2,4-Dichlorobenzoic acid

20(R)-25-hydroxyprotopanaxadiol (25-OH-PPD) is a natural compound showing a variety of anti-tumor effects. In an attempt to search for a new anti-cancer compound with higher antitumor activities, we designed and synthesized a series of 25-OH-PPD derivatives. Cytotoxicity assay of these derivatives towards MCF-7, A549, U87, HO-8901, Hela cancer cell lines and normal IOSE144 cell lines were tested by MTF assay. Results showed that compared with compound 25-OH-PPD, Compounds 4, 5, 6, 10, 11 showed strong anticancer activity, and all compounds showed low toxicity or no toxicity for normal cells. In particular, compound 6 exhibited the best anti-tumor activity in all cancer cell lines (MCF-7, A549, U87, HO-8901, and Hela) with IC50 values of 5.04 mu M, 1.36 mu M, 3.24 mu M, 3.47 mu M, 4.57 mu M, respectively. Among the five cell lines, all the compounds showed strong inhibition on A549 cells. Further studies showed that Compound 6 significantly inhibited the proliferation of A549 cells by inducing apoptosis. Our results indicate that Compound 6 is a potential anticancer inhibitor and provides a theoretical basis for further research.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics