Category: 88-68-6

Formula: C7H8N2O. Ghaleno, MR; Ghaffari-Moghaddam, M; Khajeh, M; Oveisi, AR; Bohlooli, M in [Ghaleno, Mandiyeh Rashki; Ghaffari-Moghaddam, Mansour; Khajeh, Mostafa; Oveisi, Ali Reza] Univ Zabol, Dept Chem, Fac Sci, Zabol, Iran; [Bohlooli, Mousa] Univ Zabol, Dept Biol, Fac Sci, Zabol, Iran published Iron species supported on a mesoporous zirconium metal-organic framework for visible light driven synthesis of quinazolin-4(3H)-ones through one-pot three-step tandem reaction in 2019, Cited 89. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

A bioinspired iron(III)porphyrinic Zr-MOF, PCN-222(Fe), was modified by post-synthetic cluster metalation with iron(III) chloride, as a cheap, earth-abundant, and environmentally friendly metal precursor, towards formation a new multifunctional MOF, namely Fe@PCN-222(Fe). The MOF consists of bimetallic (Zr-oxo-Fe) nodes linked by Fe(III)porphyrin struts. The cluster metalation and pre-activation treatment of PCN-222(Fe) were performed cooperatively using the FeCl3. The respective MOF was characterized through various techniques, such as FT-IR, PXRD, ICP-AES, BET surface area, SEM, UV-Vis DRS, TGA/DSC, PL, and XPS analyses. The solid showed catalytic activity for one-pot tandem synthesis of quinazolin-4(3H)-ones from alcohols and 2-aminobenzamide through a three-consecutive-step reaction (oxidation-cyclization-oxidation) under visible light irradiation using air or oxygen without adding any additive. In addition, its catalytic performance was superior to that of the bare PCN-222(Fe) and the corresponding homogeneous catalysts. The experiments indicate that the solid MOF acts as both a photoredox and Lewis acid catalyst. Hot-filtration and Fe-leaching tests as well as reusability experiments confirm that the nominal MOF acts as an efficient reusable heterogeneous catalyst for at least three runs without significant decrease in its activity. This work demonstrates the potential of using MOFs as supports for single-site metal species towards preparation of multifunctional MOFs for modern organic transformations combining photocatalysis and catalysis. (C) 2018 Elsevier Inc. All rights reserved.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Formula: C7H8N2O. Ghaleno, MR; Ghaffari-Moghaddam, M; Khajeh, M; Oveisi, AR; Bohlooli, M in [Ghaleno, Mandiyeh Rashki; Ghaffari-Moghaddam, Mansour; Khajeh, Mostafa; Oveisi, Ali Reza] Univ Zabol, Dept Chem, Fac Sci, Zabol, Iran; [Bohlooli, Mousa] Univ Zabol, Dept Biol, Fac Sci, Zabol, Iran published Iron species supported on a mesoporous zirconium metal-organic framework for visible light driven synthesis of quinazolin-4(3H)-ones through one-pot three-step tandem reaction in 2019, Cited 89. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

A bioinspired iron(III)porphyrinic Zr-MOF, PCN-222(Fe), was modified by post-synthetic cluster metalation with iron(III) chloride, as a cheap, earth-abundant, and environmentally friendly metal precursor, towards formation a new multifunctional MOF, namely Fe@PCN-222(Fe). The MOF consists of bimetallic (Zr-oxo-Fe) nodes linked by Fe(III)porphyrin struts. The cluster metalation and pre-activation treatment of PCN-222(Fe) were performed cooperatively using the FeCl3. The respective MOF was characterized through various techniques, such as FT-IR, PXRD, ICP-AES, BET surface area, SEM, UV-Vis DRS, TGA/DSC, PL, and XPS analyses. The solid showed catalytic activity for one-pot tandem synthesis of quinazolin-4(3H)-ones from alcohols and 2-aminobenzamide through a three-consecutive-step reaction (oxidation-cyclization-oxidation) under visible light irradiation using air or oxygen without adding any additive. In addition, its catalytic performance was superior to that of the bare PCN-222(Fe) and the corresponding homogeneous catalysts. The experiments indicate that the solid MOF acts as both a photoredox and Lewis acid catalyst. Hot-filtration and Fe-leaching tests as well as reusability experiments confirm that the nominal MOF acts as an efficient reusable heterogeneous catalyst for at least three runs without significant decrease in its activity. This work demonstrates the potential of using MOFs as supports for single-site metal species towards preparation of multifunctional MOFs for modern organic transformations combining photocatalysis and catalysis. (C) 2018 Elsevier Inc. All rights reserved.

Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Ghaleno, MR; Ghaffari-Moghaddam, M; Khajeh, M; Oveisi, AR; Bohlooli, M or concate me.

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

Computed Properties of C7H8N2O. In 2021 BRIT J NUTR published article about WEIGHT CONTROL BEHAVIORS; HIGH-FAT DIET; INSULIN-RESISTANCE; FOOD RESTRICTION; OBESITY; HETEROGENEITY; EXPRESSION; EXPANSION; GLUCOSE; PROTEIN in [Rosas Fernandez, Mariana] Fed Univ Rio Janeiro, Graduate Program Nutr, Rio De Janeiro, RJ, Brazil; [Rosas Fernandez, Mariana; Concha Vilca, Carlos; Batista, Leandro O.; Albuquerque, Kelse T.] Fed Univ Rio Janeiro, Lab Expt Nutr, Rio De Janeiro, RJ, Brazil; [Concha Vilca, Carlos; Albuquerque, Kelse T.] Fed Univ Rio Janeiro, Multicenter Grad Program Physiol Sci, Nutrit Dept, Rio De Janeiro, Brazil; [Figueiredo, Leticia S.; Ribeiro, Rosane A.] Fed Univ Rio Janeiro, Graduate Program Bioact Prod & Biosciences, Rio De Janeiro, Brazil; [Ribeiro, Rosane A.] Univ Estadual Ponta Grossa, Biol & Hlth Sci Sect, Dept Gen Biol, Ponta Grossa, Parana, Brazil; [Tavares do Carmo, Maria das Gracas] Fed Univ Rio Janeiro, Lab Nutrit Biochem, Dept Nutr & Dietet, Rio De Janeiro, Brazil in 2021, Cited 56. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Intermittent food restriction (IFR) is used mainly for weight loss; however, its effects on adipose tissue are not known when alternating with an obesogenic diet. To demonstrate its effects on morphological dynamics of fat deposits, female Wistar rats were distributed into groups: standard control (ST-C), with commercial diet; DIO control (DIO-C), with a diet that induces obesity (DIO) during the first and last 15 d, replaced by a standard diet for thirty intermediate days; standard restricted (ST-R), with standard diet during the first and last 15 d, with six cycles of IFR at 50 % of ST-C; and DIO restricted (DIO-R), in DIO during the first and last 15 d, with six cycles of IFR at 50 % of DIO-C. At 105 d of life, white adipose tissue (WAT) and brown adipose tissue (BAT) deposits were collected, weighed and histology performed. The DIO-R group showed higher total food intake (DIO-R 10 768 center dot 0 (SEM 357 center dot 52) kJ/g v. DIO-C 8868 center dot 6 (SEM 249 center dot 25) kJ/g, P < 0 center dot 0001), energy efficiency during RAI (DIO-R 2 center dot 26 (SEM 0 center dot 05) g/kJ v. DIO-C 0 center dot 70 (SEM 0 center dot 03) g/kJ, P < 0 center dot 0001) and WAT (DIO-R 5 center dot 65 (SEM 0 center dot 30) g/100 g v. DIO-C 4 center dot 56 (SEM 0 center dot 30) g/100 g) than their respective control. Furthermore, IFR groups presented hypertrophy of WAT and BAT, as well as fibrosis in BAT. Thus, IFR can establish prospective resistance to weight loss by favouring changes in adipose tissue morphology, increased energy intake and efficiency. Finally, the DIO diet before and after IFR aggravates the damages caused by the restriction. Welcome to talk about 88-68-6, If you have any questions, you can contact Fernandez, MR; Vilca, CC; Batista, LO; Figueiredo, LS; Ribeiro, RA; do Carmo, MDT; Albuquerque, KT or send Email.. Computed Properties of C7H8N2O

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

In 2019 ADV SYNTH CATAL published article about FRIEDEL-CRAFTS REACTION; GOLD(I)-CATALYZED INTRAMOLECULAR HYDROAMINATION; SEQUENTIAL ALKYNE ACTIVATION; SELECTIVE PDE5 INHIBITOR; NATURAL-PRODUCTS; DIASTEREOSELECTIVE SYNTHESIS; CASCADE CYCLIZATION; INDOLE ALKALOIDS; STEREOSELECTIVE-SYNTHESIS; PRIVILEGED STRUCTURES in [Qiao, Jin; Jia, Xiuwen; Li, Pinyi; Liu, Xiaoyan; Zhao, Jingwei; Zhao, Fei] Chengdu Univ, Sichuan Ind Inst Antibiot, Antibiot Res & Reevaluat Key Lab Sichuan Prov, 168 Hua Guan Rd, Chengdu 610052, Sichuan, Peoples R China; [Zhou, Yu; Wang, Jiang; Liu, Hong] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China; [Zhou, Yu; Wang, Jiang; Liu, Hong] Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China; [Zhou, Yu; Wang, Jiang; Liu, Hong] Univ Chinese Acad Sci, 19 A Yuquan Rd, Beijing 100049, Peoples R China in 2019, Cited 190. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Recommanded Product: 88-68-6

1,3-unsubstituted 2-(1H-indol-2-yl)ethanamines were employed for the first time to react with alkynoic acids (AAs) to achieve gold-catalyzed highly selective cascade reactions to furnish novel indole-fused skeletons. Furthermore, with this powerful gold catalytic system, a library of indole/pyrrole/thiophene/benzene/naphthalene/pyridine-based nitrogen-containing heterocyclic compounds (NCHCs) with scaffold diversity and molecular complexity was constructed rapidly using various amine nucleophiles (ANs) and diverse AAs as the building blocks. This general protocol features excellent selectivity, extraordinarily broad substrate scope, readily available inputs, good to high yields, high bond-forming efficiency, and step economy, thus providing a facile and efficient access to a variety of valuable nitrogen-containing heterocycles.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

COA of Formula: C7H8N2O. In 2020 J CHEM SCI published article about EFFICIENT in [Mondal, Mohabul A.; Mondal, Sudipta; Khan, Abdul A.] Jadavpur Univ, Dept Chem, Kolkata 700032, W Bengal, India in 2020, Cited 11. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

One-pot synthesis of isoindole fused quinazolin 4-ones via intramolecular 1,3 hydride transfer in the presence of acid catalyst has been described. Substrate scope and mechanistic insights were investigated. Substituents on the amide side have a negligible influence on the key step and therefore the method have wide scope for accessing various bicyclic core structure.

COA of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Mondal, MA; Mondal, S; Khan, AA or concate me.

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

In 2021 LETT ORG CHEM published article about GREEN SYNTHESIS; BIOLOGICAL EVALUATION; ASSISTED SYNTHESIS; EFFICIENT; CATALYST; 2,3-DIHYDROQUINAZOLIN-4(1H)-ONES; QUINAZOLINONES; FACILE in [Sina, Kiana Faraji; Yahyazadeh, Asieh; Mahmoodi, Nosrat Ollah] Univ Guilan, Fac Sci, Dept Chem, POB 41335-1914, Rasht, Iran in 2021, Cited 41. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. HPLC of Formula: C7H8N2O

2, 3-Dihydroquinazolinones are of popular compounds with the diversification of biological and pharmacological activities. Among many discovered methods, there are efficient and convenient methods used for the synthesis of 2, 3-dihydroquinazoline-4 (1H)-one and some new bis 2, 3-dihydroquinazoline-4 (1H)-one derivatives which are reported in this study. The mentioned methods include the two-component condensation of one molecule of anthranilamide and one molecule of pyrazole carbaldehyde using montmorillonite-K 10 as a catalyst for the preparation of 2, 3 dihydroquinazoline-4 (1H)-ones. Also, one-pot pseudo-five-component reaction (5MCRs) of two molecules of isatoic anhydride, two molecules of pyrazole carbaldehydes and one molecule of ethan-1, 2-diamine in the presence of the r catalyst (montmorillonite-K10) for the synthesis of bis 2, 3-dihydroquinazoline-4 (1H)-ones. Despite the short times of reactions, high yields of products were obtained, which were validated using FT-IR, (HNMR)-H-1, (CNMR)-C-13, and elemental analysis. Moreover, the compounds were screened for their antimicrobial activities against two-gram-positive bacterial strains: Staphylococcus aureus and Micrococcus Luteus; and against two-gram-negative bacterial strains, as well: Escherichia coli and Pseudomonas aeruginosa, which all were utilized for antibacterial investigations. The results showed moderate or significant antibacterial activities.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Identification of Diketopiperazine-Containing 2-Anilinobenzamides as Potent Sirtuin 2 (SIRT2)-Selective Inhibitors Targeting the Selectivity Pocket, Substrate-Binding Site, and NAD(+)-Binding Site WOS:000473251200008 published article about HISTONE DEACETYLASE SIRT6; GLUCOSE-HOMEOSTASIS; TUMOR-SUPPRESSOR; PROTEIN; CANCER; PROMOTES; PGC-1-ALPHA; ACTIVATION; CHROMAN-4-ONE; ACETYLATION in [Mellini, Paolo; Itoh, Yukihiro; Elboray, Elghareeb E.; Li, Ying; Suzuki, Miki; Takahashi, Yukari; Tojo, Toshifumi; Kurohara, Takashi; Miyake, Yuka; Kitao, Yuki; Kotoku, Masayuki; Iida, Tetsuya; Suzuki, Takayoshi] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Sakyo Ku, 1-5 Shimogamohangi Cho, Kyoto 6060823, Japan; [Elboray, Elghareeb E.] South Valley Univ, Fac Sci, Chem Dept, Qena 83523, Egypt; [Tsumoto, Hiroki; Miura, Yuri] Tokyo Metropolitan Inst Gerontol, Res Team Mech Aging, Itabashi Ku, 35-2 Sakae Cho, Tokyo 1730015, Japan; [Suzuki, Takayoshi] Japan Sci & Technol Agcy JST, CREST, 4-1-8 Honcho Kawaguchi, Saitama 3320012, Japan in 2019, Cited 90. Quality Control of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

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.

Quality Control of 2-Aminobenzamide. Bye, fridends, I hope you can learn more about C7H8N2O, If you have any questions, you can browse other blog as well. See you lster.

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

Category: thiomorpholine. In 2020 FRONT CHEM published article about DEPENDENT RNA-POLYMERASE; SOLUBILITY MEASUREMENT; BVDV INFECTION; PESTIVIRUS; AGENTS; REPLICATION; DISCOVERY; ACCURACY; DISEASE; TARGETS in [Fernandez, Gabriela A.; Fidalgo, Daniela M.; Adler, Natalia S.; Battini, Leandro; Bollini, Mariela] Ctr Invest Bionanociencias CIBION, Lab Quim Med, Consejo Nacl Invest Cient Tecn CONICET, Buenos Aires, DF, Argentina; [Castro, Eliana F.] Ctr Invest Ciencias Vet & Agro, Inst Virol & Innovac Tecnol, Inst Nacl Tecnol Agropecuaria, Consejo Nacl Invest Cient & Tecn CONICET, Buenos Aires, DF, Argentina; [Castro, Eliana F.; Espana de Marco, Maria J.] Univ Buenos Aires, Fac Farm & Bioquim, Dept Microbiol Inmunol Biotecnol & Genet, Buenos Aires, DF, Argentina; [Rosas, Rocio A.; Fabiani, Matias; Cavallaro, Lucia V.] Univ Buenos Aires, Inst Invest Bacteriol & Virol Mol IBaViM, Dept Microbiol Inmunol Biotecnol & Genet, Catedra Virol,Fac Farm & Bioquim, Buenos Aires, DF, Argentina; [Rosas, Rocio A.; Fabiani, Matias] Consejo Nacl Invest Cient & Tecn CONICET, Buenos Aires, DF, Argentina; [Bruno, Ana M.] Univ Buenos Aires, Fac Farm & Bioquim, Dept Quim Organ, Buenos Aires, DF, Argentina in 2020, Cited 54. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Bovine viral diarrhea virus (BVDV) belongs to the Pestivirus genus (Flaviviridae). In spite of the availability of vaccines, the virus is still causing substantial financial losses to the livestock industry. In this context, the use of antiviral agents could be an alternative strategy to control and reduce viral infections. The viral RNA-dependent RNA polymerase (RdRp) is essential for the replication of the viral genome and constitutes an attractive target for the identification of antiviral compounds. In a previous work, we have identified potential molecules that dock into an allosteric binding pocket of BVDV RdRp via a structure-based virtual screening approach. One of them, N-(2-morpholinoethyl)-2-phenylquinazolin-4-amine [1, 50% effective concentration (EC50) = 9.7 +/- 0.5 mu M], was selected to perform different chemical modifications. Among 24 derivatives synthesized, eight of them showed considerable antiviral activity. Molecular modeling of the most active compounds showed that they bind to a pocket located in the fingers and thumb domains in BVDV RdRp, which is different from that identified for other non-nucleoside inhibitors (NNIs) such as thiosemicarbazone (TSC). We selected compound 2-[4-(2-phenylquinazolin-4-yl)piperazin-1-yl]ethanol (1.9; EC50 = 1.7 +/- 0.4 mu M) for further analysis. Compound 1.9 was found to inhibit the in vitro replication of TSC-resistant BVDV variants, which carry the N264D mutation in the RdRp. In addition, 1.9 presented adequate solubility in different media and a high-stability profile in murine and bovine plasma.

Category: thiomorpholine. Welcome to talk about 88-68-6, If you have any questions, you can contact Fernandez, GA; Castro, EF; Rosas, RA; Fidalgo, DM; Adler, NS; Battini, L; de Marco, MEJ; Fabiani, M; Bruno, AM; Bollini, M; Cavallaro, LV or send Email.

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

An article Solvent-Free, Mechanochemically Scalable Synthesis of 2,3-Dihydroquinazolin-4(1H)-one Using Bronsted Acid Catalyst WOS:000480370500099 published article about QUINAZOLINONE; MECHANOSYNTHESIS; CHEMISTRY; GREEN; COMPLEXES; HYDROXIDE; EFFICIENT; PROTOCOL; BENIGN; UREAS in [Yashwantrao, Gauravi; Jejurkar, Valmik P.; Kshatriya, Rajpratap; Saha, Satyajit] Inst Chem Technol, Dept Dyestuff Technol, Mumbai 400019, Maharashtra, India in 2019, Cited 76. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Product Details of 88-68-6

Although the synthesis of novel N-heterocyclic molecules is extremely demanding as well as challenging, the involvement of toxic solvents often triggers environmental safety concerns, resulting in process-engineering challenges. Herein, we have demonstrated a rapid, environmentally benign and energy efficient scalable method for the synthesis of 2,3-dihydroquinazolin-4(1H)-one by grinding in a mortar pestle as well as mechanochemically via ball milling using p-TSA catalyst. The ability to accomplish the reaction in the absence of solvent via grinding or milling with p-TSA catalyst, with an immediate reduction in the cost and operational procedures, features the significant advantages of this protocol. The scalability and significance of the operational parameters during mechanochemical milling in the tubular ball mill were also demonstrated. Excellent yield in short duration, large substrate scope, product scalability, and easy recoverability are the prime features of this mechanochemical solvent-free protocol for the synthesis of 2,3-dihydroquinazolin-4(1H)-one. The study also demonstrated the significant role of ball diameter to improve the efficiency of the milling operation in this mechanochemical synthesis.

Welcome to talk about 88-68-6, If you have any questions, you can contact Yashwantrao, G; Jejurkar, VP; Kshatriya, R; Saha, S or send Email.. Product Details of 88-68-6

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

Safety of 2-Aminobenzamide. Moslin, R; Zhang, YL; Wrobleski, ST; Lin, SQ; Mertzman, M; Spergel, S; Tokarski, JS; Strnad, J; Gillooly, K; McIntyre, KW; Zupa-Fernandez, A; Cheng, LH; Sun, HD; Chaudhry, C; Huang, C; D’Arienzo, C; Heimrich, E; Yang, XX; Muckelbauer, JK; Chang, C; Tredup, J; Mulligan, D; Xie, DL; Aranibar, N; Chiney, M; Burke, JR; Lombardo, L; Carter, PH; Weinstein, DS in [Moslin, Ryan; Zhang, Yanlei; Wrobleski, Stephen T.; Lin, Shuqun; Mertzman, Michael; Spergel, Steven; Lombardo, Louis; Carter, Percy H.; Weinstein, David S.] Bristol Myers Squibb Res & Dev, Immunosci Discovery Chem, POB 4000, Princeton, NJ 08543 USA; [Strnad, Joann; Gillooly, Kathleen; McIntyre, Kim W.; Zupa-Fernandez, Adriana; Cheng, Lihong; Heimrich, Elizabeth; Yang, Xiaoxia; Burke, James R.] Bristol Myers Squibb Res & Dev, Immunosci Discovery Biol, POB 4000, Princeton, NJ 08543 USA; [Tokarski, John S.; Muckelbauer, Jodi K.; Chang, ChiehYing; Tredup, Jeffrey; Mulligan, Dawn; Xie, Dianlin] Bristol Myers Squibb Res & Dev, Mol Struct & Design, Mol Discovery Technol, POB 4000, Princeton, NJ 08543 USA; [Sun, Huadong; Huang, Christine; D’Arienzo, Celia; Aranibar, Nelly; Chiney, Manoj] Bristol Myers Squibb Res & Dev, Lead Discovery & Optimizat, POB 4000, Princeton, NJ 08543 USA; [Chaudhry, Charu] Bristol Myers Squibb Res & Dev, Metab & Pharmacokinet Dept, Pharmaceut Candidate Optimizat, POB 4000, Princeton, NJ 08543 USA; [Weinstein, David S.] Vividion Therapeut Inc, Chem, 5820 Nancy Ridge Dr, San Diego, CA 92121 USA published Identification of N-Methyl Nicotinamide and N-Methyl Pyridazine-3-Carboxamide Pseudokinase Domain Ligands as Highly Selective Allosteric Inhibitors of Tyrosine Kinase 2 (TYK2) in 2019, Cited 53. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

As a member of the Janus OAK) family of nonreceptor tyrosine kinases, TYK2 plays an important role in mediating the signaling of pro-inflammatory cytokines including IL-12, IL-23, and type 1 interferons. The nicotinamide 4, identified by a SPA-based high-throughput screen targeting the TYK2 pseudokinase domain, potently inhibits IL-23 and IFN alpha signaling in cellular assays. The described work details the optimization of this poorly selective hit (4) to potent and selective molecules such as 47 and 48. The discoveries described herein were critical to the eventual identification of the clinical TYK2 JH2 inhibitor (see following report in this issue). Compound 48 provided robust inhibition in a mouse IL-12-induced IFN gamma pharmacodynamic model as well as efficacy in an IL-23 and IL-12-dependent mouse colitis model. These results demonstrate the ability of TYK2 JH2 domain binders to provide a highly selective alternative to conventional TYK2 orthosteric inhibitors.

Welcome to talk about 88-68-6, If you have any questions, you can contact Moslin, R; Zhang, YL; Wrobleski, ST; Lin, SQ; Mertzman, M; Spergel, S; Tokarski, JS; Strnad, J; Gillooly, K; McIntyre, KW; Zupa-Fernandez, A; Cheng, LH; Sun, HD; Chaudhry, C; Huang, C; D’Arienzo, C; Heimrich, E; Yang, XX; Muckelbauer, JK; Chang, C; Tredup, J; Mulligan, D; Xie, DL; Aranibar, N; Chiney, M; Burke, JR; Lombardo, L; Carter, PH; Weinstein, DS or send Email.. Safety of 2-Aminobenzamide

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