Recently I am researching about MYOFIBROBLAST DIFFERENTIATION; MURINE MODEL; FIBROSIS; PATHWAY; TISSUE; CYTOSKELETON; CONTRACTION; DERIVATIVES; MECHANISMS; BLEOMYCIN, Saw an article supported by the NIH NIAMS award [R01AR066049]; NIH NIGMS award [R01GM115459-01A1]; University of Michigan Mi-TRAC award – Michigan Economic Development Corporation; NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASESUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USANIH National Institute of Arthritis & Musculoskeletal & Skin Diseases (NIAMS) [R01AR066049, T32AR007080] Funding Source: NIH RePORTER; NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCESUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USANIH National Institute of General Medical Sciences (NIGMS) [R01GM115459] Funding Source: NIH RePORTER. Safety of 2,4-Dichlorobenzoic acid. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Kahl, DJ; Hutchings, KM; Lisabeth, EM; Haak, AJ; Leipprandt, JR; Dexheimer, T; Khanna, D; Tsou, PS; Campbell, PL; Fox, DA; Wen, B; Sun, DX; Bailie, M; Neubig, RR; Larsen, SD. The CAS is 50-84-0. Through research, I have a further understanding and discovery of 2,4-Dichlorobenzoic acid
Through a phenotypic high-throughput screen using a serum response element luciferase promoter, we identified a novel 5-aryl-1,3,4-oxadiazol-2-ylthiopropionic acid lead inhibitor of Rho/myocardin-related transcription factor (MRTF)/serum response factor (SRF)-mediated gene transcription with good potency (IC50 = 180 nM). We were able to rapidly improve the cellular potency by 5 orders of magnitude guided by sharply defined and synergistic SAR. The remarkable potency and depth of the SAR, as well as the relatively low molecular weight of the series, suggests, but does not prove, that binding to the unknown molecular target may be occurring through a covalent mechanism. The series nevertheless has no observable cytotoxicity up to 100 mu M. Ensuing pharmacokinetic optimization resulted in the development of two potent and orally bioavailable anti-fibrotic agents that were capable of dose-dependently reducing connective tissue growth factor gene expression in vitro as well as significantly reducing the development of bleomycin-induced dermal fibrosis in mice in vivo.
Safety of 2,4-Dichlorobenzoic acid. Bye, fridends, I hope you can learn more about C7H4Cl2O2, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics