Can You Really Do Chemisty Experiments About 2-Aminobenzamide

Welcome to talk about 88-68-6, If you have any questions, you can contact Mellini, P; Itoh, Y; Elboray, EE; Tsumoto, H; Li, Y; Suzuki, M; Takahashi, Y; Tojo, T; Kurohara, T; Miyake, Y; Miura, Y; Kitao, Y; Kotoku, M; Iida, T; Suzuki, T or send Email.. Recommanded Product: 2-Aminobenzamide

Recently I am researching about HISTONE DEACETYLASE SIRT6; GLUCOSE-HOMEOSTASIS; TUMOR-SUPPRESSOR; PROTEIN; CANCER; PROMOTES; PGC-1-ALPHA; ACTIVATION; CHROMAN-4-ONE; ACETYLATION, Saw an article supported by the JST CREST programJapan Science & Technology Agency (JST)Core Research for Evolutional Science and Technology (CREST) [JPMJCR14L2]; JST A-step program [957908]; JSPSMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of Science. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Mellini, P; Itoh, Y; Elboray, EE; Tsumoto, H; Li, Y; Suzuki, M; Takahashi, Y; Tojo, T; Kurohara, T; Miyake, Y; Miura, Y; Kitao, Y; Kotoku, M; Iida, T; Suzuki, T. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide. Recommanded Product: 2-Aminobenzamide

The NAD(+)-dependent deacetylase SIRT2 represents an attractive target for drug development. Here, we designed and synthesized drug-like SIRT2-selective inhibitors based on an analysis of the putative binding modes of recently reported SIRT2-selective inhibitors and evaluated their SIRT2-inhibitory activity. This led us to develop a more drug-like diketopiperazine structure as a hydrogen bond (H-bond) hunter to target the substrate-binding site of SIRT2. Thioamide 53, a conjugate of diketopiperazine and 2-anilinobenzamide which is expected to occupy the selectivity pocket of SIRT2, exhibited potent SIRT2-selective inhibition. Inhibition of SIRT2 by 53 was mediated by the formation of a 53-ADP-ribose conjugate, suggesting that 53 is a mechanism-based inhibitor targeting the selectivity pocket, substrate-binding site, and NAD(+)-binding site. Furthermore, 53 showed potent antiproliferative activity toward breast cancer cells and promoted neurite outgrowth of Neuro-2a cells. These findings should pave the way for the discovery of novel therapeutic agents for cancer and neurological disorders.

Welcome to talk about 88-68-6, If you have any questions, you can contact Mellini, P; Itoh, Y; Elboray, EE; Tsumoto, H; Li, Y; Suzuki, M; Takahashi, Y; Tojo, T; Kurohara, T; Miyake, Y; Miura, Y; Kitao, Y; Kotoku, M; Iida, T; Suzuki, T or send Email.. Recommanded Product: 2-Aminobenzamide

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem