Category: 88-68-6

Chernyshov, VV; Gatilov, YV; Yarovaya, OI; Koskin, IP; Yarovoy, SS; Brylev, KA; Salakhutdinov, NF in [Chernyshov, Vladimir V.; Gatilov, Yuri, V; Yarovaya, Olga, I; Koskin, Igor P.; Salakhutdinov, Nariman F.] NN Vorozhtsov Novosibirsk Inst Organ Chem SB RAS, 9 Acad Lavrentiev Ave, Novosibirsk 630090, Russia; [Chernyshov, Vladimir V.; Gatilov, Yuri, V; Yarovaya, Olga, I; Brylev, Konstantin A.] Novosibirsk State Univ, Pirogova St 2, Novosibirsk 630090, Russia; [Yarovoy, Spartak S.; Brylev, Konstantin A.] Nikolaey Inst Inorgan Chem SB RAS, 3 Acad Lavrentiev Ave, Novosibirsk 630090, Russia published The first example of the stereoselective synthesis and crystal structure of a spirobicycloquinazolinone based on (-)-fenchone and anthranilamide in 2019, Cited 41. Category: thiomorpholine. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

The possibility of a single-stage solvent-free stereoselective synthesis of a spirocyclic compound from the natural bicyclic monoterpenoid (-)-fenchone and anthranilamide has been shown for the first time. The molecular and crystal structure of (1R,2S,4S)-1,3,3-trimethyl-10H-spiro[bicyclo[2.2.1]heptane-2,2′-quinazolin]-4′(3’H)-one, C17H22N2O, was established by X-ray diffraction though the chirality was assumed via the known reactant connectivity and H-1 and C-13 NMR spectroscopy. It has shown that in the molecule, for steric reasons, there is an elongation of the Me2C-C(N)N bond to 1.603 (5) A degrees. The formation of dimers via N-H center dot center dot center dot O C hydrogen bonds with an interaction energy of 93.30 kJ mol(-1) and through cavities (33.7% of the unit-cell volume) was established in the packing of the molecules. There are no pi-stacking interactions in the structure.

Category: thiomorpholine. About 2-Aminobenzamide, If you have any questions, you can contact Chernyshov, VV; Gatilov, YV; Yarovaya, OI; Koskin, IP; Yarovoy, SS; Brylev, KA; Salakhutdinov, NF or concate me.

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

I found the field of Chemistry very interesting. Saw the article Photocatalyst-free visible-light-promoted quinazolinone synthesis at room temperature utilizing aldehydes generated in situ via C=C bond cleavage published in 2021. Category: thiomorpholine, Reprint Addresses Xie, ZB; Le, ZG (corresponding author), East China Univ Technol, Jiangxi Prov Key Lab Synthet Chem, Nanchang 330013, Jiangxi, Peoples R China.; Xie, ZB; Le, ZG (corresponding author), East China Univ Technol, Sch Chem Biol & Mat Sci, Nanchang 330013, Jiangxi, Peoples R China.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

This is the first report on a facile tandem route for synthesizing quinazolinones at room temperature from various aminobenzamides and in situ-generated aldehydes. The latter was formed via C=C bond cleavage, and the overall reaction proceeded using molecular oxygen as a clean oxidant in the absence of a photocatalyst. Visible light, which was indispensable for the entire course of the reaction, played multiple roles. It initially cleaved styrene to an aldehyde, then facilitated its cyclization with an o-substituted aniline, and finally promoted the dehydrogenation of the cyclized intermediate. The previous step provided the feedstock for the next step in the reaction, thereby preventing volatilization, oxidation, and polymerization of the aldehyde. Thus, the overall process is simple, environmentally benign, and economically feasible.

Category: thiomorpholine. About 2-Aminobenzamide, If you have any questions, you can contact Xie, ZB; Lan, J; Yan, LY; Chen, XH; Li, Q; Meng, J; Le, ZG or concate me.

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

Recently I am researching about HUMAN CYTOCHROME-P450 ENZYMES; IN-VITRO; CANCER-RISK; ESTROGEN METABOLISM; DRUG; HYDROXYLATION; POLYMORPHISM; DERIVATIVES; VALIDATION; INITIATION, Saw an article supported by the UKIERI; HEIF-UK; CYP-Design Ltd.; UGC-UKIERI; UGCUniversity Grants Commission, India [201516-MANF-2015-17-MAH-60712]; DST-FISTDepartment of Science & Technology (India) [SR/FST/CSI-242/2012]. Published in ELSEVIER SCIENCE BV in AMSTERDAM ,Authors: Sonawane, VR; Siddique, MUM; Gatchie, L; Williams, IS; Bharate, SB; Jayaprakash, V; Sinha, BN; Chaudhuri, B. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide. COA of Formula: C7H8N2O

Microsomal cytochrome P450 (CYP) enzymes, isolated from recombinant bacterial/insect/yeast cells, are extensively used for drug metabolism studies. However, they may not always portray how a developmental drug would behave in human cells with intact intracellular transport mechanisms. This study emphasizes the usefulness of human HEK293 kidney cells, grown in ‘suspension’ for expression of CYPs, in finding potent CYP1A1/CYP1B1 inhibitors, as possible anticancer agents. With live cell-based assays, quinazolinones 9i/9b were found to be selective CYP1A1/CYP1B1 inhibitors with IC50 values of 30/21 nM, and > 150-fold selectivity over CYP2/3 enzymes, whereas they were far less active using commercially-available CYP1A1/CYP1B1 microsomal enzymes (IC50, > 10/1.3-1.7 mu M). Compound 9i prevented CYP1A1-mediated benzo [a]pyrene-toxicity in normal fibroblasts whereas 9b completely reversed cisplatin resistance in PC-3/prostate, COR-L23/1ung, MIAPaCa-2/pancreatic and LS174T/colon cancer cells, underlining the human-cell-assays’ potential. Our results indicate that the most potent CYP1A1/CYP1B1 inhibitors would not have been identified if one had relied merely on microsomal enzymes.

COA of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Sonawane, VR; Siddique, MUM; Gatchie, L; Williams, IS; Bharate, SB; Jayaprakash, V; Sinha, BN; Chaudhuri, B or concate me.

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

An article Anthranilamide (aam)-substituted arylboranes in direct carbon-carbon bond-forming reactions WOS:000459737100006 published article about CROSS-COUPLING REACTION; BORONIC ACIDS; FORMAL HYDROBORATION; CATALYZED BORYLATION; ITERATIVE SYNTHESIS; GENERAL-SOLUTION; COPPER; ALKYNES; ARYL; STRATEGY in [Kamio, Shintaro; Kageyuki, Ikuo; Osaka, Itaru; Yoshida, Hiroto] Hiroshima Univ, Grad Sch Engn, Dept Appl Chem, Higashihiroshima 7398527, Japan in 2019, Cited 34. HPLC of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Anthranilamide (aam)-substituted arylboranes, which were reported to serve as masked boranes in the Suzuki-Miyaura coupling, have been found to be directly cross-coupled just by use of an aqueous medium. The excellent stability of 2-pyridyl-B(aam) toward protodeborylation allowed their smooth cross-coupling.

About 2-Aminobenzamide, If you have any questions, you can contact Kamio, S; Kageyuki, I; Osaka, I; Yoshida, H or concate me.. HPLC of Formula: C7H8N2O

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

HPLC of Formula: C7H8N2O. Authors Yang, L; Hou, HQ; Li, L; Wang, J; Zhou, SY; Wu, M; Ke, F in ROYAL SOC CHEMISTRY published article about in [Yang, Li; Li, Lan; Ke, Fang] Yibin Univ, Coll Chem & Chem Engn, Yibin, Sichuan, Peoples R China; [Hou, Huiqing; Wang, Jin; Zhou, Sunying; Wu, Mei; Ke, Fang] Fujian Med Univ, Fuzhou, Fujian, Peoples R China in 2021, Cited 64. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

An efficient and practical electrochemically catalyzed transition metal-free process for the synthesis of substituted quinazolinones from simple and readily available o-aminobenzonitriles and aldehydes in water has been accomplished. I-2/base and water play an unprecedented and vital role in the reaction. By electrochemically catalysed hydrolysis of o-aminobenzonitriles, the synthesis of quinazolinones with benzaldehyde was first proposed. The synthetic utility of this method was demonstrated by gram-scale operation, as well as the preparation of bioactive N-(2,5-dichlorophenyl)-6-(2,2,2-trifluoroethoxy) pteridin-4-amine, which enables straightforward, practical and environmentally benign quinazolinone formation.

About 2-Aminobenzamide, If you have any questions, you can contact Yang, L; Hou, HQ; Li, L; Wang, J; Zhou, SY; Wu, M; Ke, F or concate me.. HPLC of Formula: C7H8N2O

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

Krapf, MK; Gallus, J; Spindler, A; Wiese, M in [Krapf, Michael K.; Gallus, Jennifer; Spindler, Anna; Wiese, Michael] Univ Bonn, Inst Pharmaceut, Immenburg 4, D-53121 Bonn, Germany published Synthesis and biological evaluation of quinazoline derivatives – A SAR study of novel inhibitors of ABCG2 in 2019, Cited 51. Product Details of 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Multidrug resistance (MDR) is a major obstacle for effective chemotherapeutic treatment of cancer frequently leading to failure of the therapy. MDR is often associated with the overexpression of ABC transport proteins like ABCB1 or ABCG2 which efflux harmful substances out of cells at the cost of ATP hydrolysis. One way to overcome MDR is to apply potent inhibitors of ABC transporters to restore the sensitivity of the cells toward cytostatic agents. This study focusses on the synthesis and evaluation of novel 2,4-disubstituted quinazoline derivatives regarding the structure-activity-relationship (SAR), their ability to reverse MDR and their mode of interaction with ABCG2. Hence, the inhibitory potency and selectivity toward ABCG2 was determined. Moreover, the intrinsic cytotoxicity and the reversal of MDR were investigated. Interaction type studies with the substrate Hoechst 33342 and conformational analyses of ABCG2 with 5D3 monoclonal antibody were performed for a better understanding of the underlying mechanisms. In our study we could further enhance the inhibitory effect against ABCG2 (compound 31, IC50: 55 nM) and identify the structural features that are crucial for inhibitory potency, the impact on transport activity and binding to the protein. (C) 2018 Elsevier Masson SAS. All rights reserved,

Product Details of 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Krapf, MK; Gallus, J; Spindler, A; Wiese, M or concate me.

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

Name: 2-Aminobenzamide. Recently I am researching about DIORGANYL DISELENIDES SYNTHESIS; C-H ACTIVATION; ELECTROPHILIC CYCLIZATION; IRON(III) CHLORIDE; BETA-PHENYLETHYLAMINES; CATALYZED ANNULATION; TANDEM CYCLIZATION; BOND FORMATION; DERIVATIVES; 2-ALKYNYLBENZALDEHYDES, Saw an article supported by the JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [17550099]; MEXT: MonbukagakushoMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT). Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Sonawane, AD; Sonawane, RA; Win, KMN; Ninomiya, M; Koketsu, M. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

An efficient, metal free and environment friendly synthesis of isoquinoline-fused benzimidazole has been developed via in situ air oxidation. Also, syntheses of isoquinoline-fused quinazolinone heteroacenes were successfully achieved. The synthesized isoquinoline-fused benzimidazole and isoquinoline-fused quinazolinone derivatives showed lambda(max), F-max and phi(f) values in the ranges 356-394 nm, 403-444 nm and 0.063-0.471, respectively, in CHCl3.

About 2-Aminobenzamide, If you have any questions, you can contact Sonawane, AD; Sonawane, RA; Win, KMN; Ninomiya, M; Koketsu, M or concate me.. Name: 2-Aminobenzamide

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

An article 1,2,4-Triazolo[1,5-a]pyrimidines: Efficient one-step synthesis and functionalization as influenza polymerase PA-PB1 interaction disruptors WOS:000661282500009 published article about SUBUNIT INTERACTIONS; SMALL-MOLECULE; INHIBITORS; VIRUSES; COMPLEX in [Pismataro, Maria Chiara; Felicetti, Tommaso; Nizi, Maria Giulia; Barreca, Maria Letizia; Cecchetti, Violetta; Tabarrini, Oriana; Massari, Serena] Univ Perugia, Dept Pharmaceut Sci, Via Del Liceo 1, I-06123 Perugia, Italy; [Bertagnin, Chiara; Bonomini, Anna; Loregian, Arianna] Univ Padua, Dept Mol Med, Via Gabelli 63, I-35121 Padua, Italy; [Jochmans, Dirk; De Jonghe, Steven; Neyts, Johan] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Rega Inst Med Res, Lab Virol & Chemotherapy, Herestr 49,Box 1043, B-3000 Leuven, Belgium in 2021, Cited 46. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Application In Synthesis of 2-Aminobenzamide

In the search for new anti-influenza virus (IV) compounds, we have identified the 1,2,4-triazolo[1,5-a] pyrimidine (TZP) as a very suitable scaffold to obtain compounds able to disrupt IV RNA-dependent RNA polymerase (RdRP) PA-PB1 subunits heterodimerization. In this work, in order to acquire further SAR insights for this class of compounds and identify more potent derivatives, we designed and synthesized additional series of analogues to investigate the role of the substituents around the TZP core. To this aim, we developed four facile and efficient one-step procedures for the synthesis of 5-phenyl-, 6- phenyl- and 7-phenyl-2-amino-[1,2,4]triazolo[1,5-a]pyrimidines, and 2-amino-5-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ol. Two analogues having the ethyl carboxylate moiety at the C-2 position of the TZP were also prepared in good yields. Then, the scaffolds herein synthesized and two previous scaffolds were functionalized and evaluated for their anti-IAV activity, leading to the identification of compound 22 that showed both anti-PA-PB1 (IC50 = 19.5 mM) and anti-IAV activity (EC50 = 16 mM) at non-toxic concentrations, thus resulting among the most active TZP derivatives reported to date by us. A selection of the synthesized compounds, along with a set of in-house available analogues, was also tested against SARS-CoV-2. The most promising compound 49 from this series displayed an EC50 value of 34.47 mM, high-lighting the potential of the TPZ scaffold in the search for anti-CoV agents. (C) 2021 Elsevier Masson SAS. All rights reserved.

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Pismataro, MC; Felicetti, T; Bertagnin, C; Nizi, MG; Bonomini, A; Barreca, ML; Cecchetti, V; Jochmans, D; De Jonghe, S; Neyts, J; Loregian, A; Tabarrini, O; Massari, S or concate me.

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

An article Effect of Fe(iii)-based MOFs on the catalytic efficiency of the tandem cyclooxidative reaction between 2-aminobenzamide and alcohols WOS:000564479900023 published article about METAL-ORGANIC FRAMEWORKS; HETEROGENEOUS CATALYST; OXIDATIVE SYNTHESIS; AEROBIC OXIDATION; QUINAZOLINONES; HYDROGENATION; CYTOTOXICITY; SYSTEMS in [Minh-Huy Dinh Dang; Trang Thi Minh Nguyen; Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Thang Bach Phan; Tan Le Hoang Doan] Ctr Innovat Mat & Architectures INOMAR, Ho Chi Minh City, Vietnam; [Minh-Huy Dinh Dang; Trang Thi Minh Nguyen; Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Thang Bach Phan; Phuong Hoang Tran; Tan Le Hoang Doan] Vietnam Natl Univ Ho Chi Minh City, Ho Chi Minh City, Vietnam; [Phuong Hoang Tran] Univ Sci, Fac Chem, Dept Organ Chem, Ho Chi Minh City, Vietnam in 2020, Cited 63. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Application In Synthesis of 2-Aminobenzamide

The catalytic properties of metal-organic frameworks (MOFs) containing triangular Fe(iii) clusters in the promotion of organic syntheses and photocatalysis applications have been receiving substantial attention for decades. These clusters are appealing due to the strong Lewis acidity afforded by coordinatively unsaturated sites upon the removal of solvent from the framework. In this paper, triangular Fe(iii) cluster-based MOFs were shown to be highly efficient heterogeneous catalysts for the solvent-free one-pot condensation of 2-aminobenzamide and alcohols to form quinazolin-4-ones under microwave irradiation. The Fe-MOF catalysts ranging from microporous to mesoporous structures with a variety of geometrical pore structures were investigated. Because of the open accessible spaces for reactants and high density of active sites, MOF-907, built from trimer Fe clusters and a mixture of two linkers, was more effective than other Fe(iii)-MOFs. The catalyst can be used for a broad substrate scope and recycled several times without a significant drop-off in its activity.

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Dang, MHD; Nguyen, TTM; Nguyen, LHT; Nguyen, TTT; Phan, TB; Tran, PH; Doan, TLH or concate me.

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

Zima, V; Albinana, CB; Rojikova, K; Pokorna, J; Pachl, P; Rezacova, P; Hudlicky, J; Navratil, V; Majer, P; Konvalinka, J; Kozisek, M; Machara, A in [Zima, Vaclav; Albinana, Carlos Berenguer; Hudlicky, Jason; Machara, Ales] Charles Univ Prague, Fac Sci, Dept Organ Chem, Hlavova 8, Prague 12800 2, Czech Republic; [Zima, Vaclav; Albinana, Carlos Berenguer; Rojikova, Katerina; Pokorna, Jana; Pachl, Petr; Rezacova, Pavlina; Hudlicky, Jason; Navratil, Vaclav; Majer, Pavel; Konvalinka, Jan; Kozisek, Milan; Machara, Ales] Gilead Sci, Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo 2, Prague 16610 6, Czech Republic; [Zima, Vaclav; Albinana, Carlos Berenguer; Rojikova, Katerina; Pokorna, Jana; Pachl, Petr; Rezacova, Pavlina; Hudlicky, Jason; Navratil, Vaclav; Majer, Pavel; Konvalinka, Jan; Kozisek, Milan; Machara, Ales] IOCB Res Ctr, Flemingovo 2, Prague 16610 6, Czech Republic; [Rojikova, Katerina] Charles Univ Prague, Fac Med 1, Katerinska 1660-32, Prague 12108, Czech Republic; [Rezacova, Pavlina] Acad Sci Czech Republ, Inst Mol Genet, Videnska 1083, Prague 14000 4, Czech Republic; [Konvalinka, Jan] Charles Univ Prague, Fac Sci, Dept Biochem, Hlavova 8, Prague 12800 2, Czech Republic published Investigation of flexibility of neuraminidase 150-loop using tamiflu derivatives in influenza A viruses H1N1 and H5N1 in 2019, Cited 62. Safety of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

This study focuses on design, synthesis and in vitro evaluation of inhibitory potency of two series of sialylmimetic that target an exosite (150-cavity) adjacent to the active site of influenza neuraminidases from A/California/07/2009 (H1N1) pandemic strain and A/chicken/Nakorn-Patom/Thailand/CU-K2-2004 (H5N1). The structure-activity analysis as well as 3-D structure of the complex of parental compound with the pandemic neuraminidase p09N1 revealed high flexibility of the 150-cavity towards various modification of the neuraminidase inhibitors. Furthermore, our comparison of two methods for inhibition constant determination performed at slightly different pH values suggest that the experimental conditions of the measurement could dramatically influence the outcome of the analysis in the compound-dependent manner. Therefore, previously reported Ki values determined at non-physiological pH should be carefully scrutinized.

About 2-Aminobenzamide, If you have any questions, you can contact Zima, V; Albinana, CB; Rojikova, K; Pokorna, J; Pachl, P; Rezacova, P; Hudlicky, J; Navratil, V; Majer, P; Konvalinka, J; Kozisek, M; Machara, A or concate me.. Safety of 2-Aminobenzamide

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