Category: 88-68-6

An article Substrate Profiling of the Cobalt Nitrile Hydratase from Rhodococcus rhodochrous ATCC BAA 870 WOS:000513770000238 published article about ENANTIOSELECTIVE BIOTRANSFORMATIONS; INDUSTRIAL-PRODUCTION; J1; HYDROLYSIS; REGIOSELECTIVITY; PURIFICATION; BENZONITRILE; DINITRILES; INSIGHTS; AMIDASE in [Mashweu, Adelaide R.; Chhiba-Govindjee, Varsha P.; Bode, Moira L.; Brady, Dean] Univ Witwatersrand, Sch Chem, Mol Sci Inst, ZA-2050 Johannesburg, South Africa; [Chhiba-Govindjee, Varsha P.] CSIR Chem Prod Cluster, POB 395, ZA-0001 Pretoria, South Africa in 2020, Cited 41. Recommanded Product: 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

The aromatic substrate profile of the cobalt nitrile hydratase from Rhodococcus rhodochrous ATCC BAA 870 was evaluated against a wide range of nitrile containing compounds (>60). To determine the substrate limits of this enzyme, compounds ranging in size from small (90 Da) to large (325 Da) were evaluated. Larger compounds included those with a bi-aryl axis, prepared by the Suzuki coupling reaction, Morita-Baylis-Hillman adducts, heteroatom-linked diarylpyridines prepared by Buchwald-Hartwig cross-coupling reactions and imidazo[1,2-a]pyridines prepared by the Groebke-Blackburn-Bienayme multicomponent reaction. The enzyme active site was moderately accommodating, accepting almost all of the small aromatic nitriles, the diarylpyridines and most of the bi-aryl compounds and Morita-Baylis-Hillman products but not the Groebke-Blackburn-Bienayme products. Nitrile conversion was influenced by steric hindrance around the cyano group, the presence of electron donating groups (e.g., methoxy) on the aromatic ring, and the overall size of the compound.

About 2-Aminobenzamide, If you have any questions, you can contact Mashweu, AR; Chhiba-Govindjee, VP; Bode, ML; Brady, D or concate me.. Recommanded Product: 2-Aminobenzamide

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

Authors Machushynets, NV; Wu, CS; Elsayed, SS; Hankemeier, T; van Wezel, GP in SPRINGER HEIDELBERG published article about COMPLETE GENOME SEQUENCE; NATURAL-PRODUCTS; ANTIBIOTIC PRODUCTION; SECONDARY METABOLISM; MASS-SPECTROMETRY; MOLECULAR NETWORKING; PATHOGENS; PLATFORM; STRESS; LINKS in [Machushynets, Nataliia V.; Wu, Changsheng; Elsayed, Somayah S.; van Wezel, Gilles P.] Leiden Univ, Inst Biol, Mol Biotechnol, Sylviusweg 72, NL-2333 BE Leiden, Netherlands; [Wu, Changsheng] Shandong Univ, Inst Microbial Technol, State Key Lab Microbial Technol, Qingdao 266237, Peoples R China; [Hankemeier, Thomas] Leiden Univ, LACDR, Einsteinweg 55, NL-2333 CC Leiden, Netherlands in 2019, Cited 57. HPLC of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Actinobacteria are a major source of novel bioactive natural products. A challenge in the screening of these microorganisms lies in finding the favorable growth conditions for secondary metabolite production and dereplication of known molecules. Here, we report that Streptomyces sp. MBT27 produces 4-quinazolinone alkaloids in response to elevated levels of glycerol, whereby quinazolinones A (1) and B (2) form a new sub-class of this interesting family of natural products. Global Natural Product Social molecular networking (GNPS) resulted in a quinazolinone-related network that included anthranilic acid (3), anthranilamide (4), 4(3H)-quinazolinone (5), and 2,2-dimethyl-1,2-dihydroquinazolin-4(3H)-one (6). Actinomycins D (7) and X2 (8) were also identified in the extracts of Streptomyces sp. MBT27. The induction of quinazolinone production by glycerol combined with biosynthetic insights provide evidence that glycerol is integrated into the chemical scaffold. The unprecedented 1,4-dioxepane ring, that is spiro-fused into the quinazolinone backbone, is most likely formed by intermolecular etherification of two units of glycerol. Our work underlines the importance of varying the growth conditions for the discovery of novel natural products and for understanding their biosynthesis.

HPLC of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Machushynets, NV; Wu, CS; Elsayed, SS; Hankemeier, T; van Wezel, GP or concate me.

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

Bera, A; Ali, SA; Manna, SK; Ikbal, M; Misra, S; Saha, A; Samanta, S in [Bera, Anirban; Ali, Sk Asraf; Manna, Susanta Kumar; Samanta, Shubhankar] Bidhannagar Coll, Dept Chem, Kolkata 700064, India; [Bera, Anirban; Saha, Amit] Jadavpur Univ, Dept Chem, Kolkata 700032, India; [Ikbal, Mohammed] Berhampore Girls Coll, Dept Chem, Berhampur 742101, India; [Misra, Sandip] Bidhannagar Coll, Dept Microbiol, Kolkata 700064, India published A solvent- and catalyst-free tandem reaction: synthesis, and photophysical and biological applications of isoindoloquinazolinones in 2020, Cited 54. SDS of cas: 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

An easy green synthetic approach for fused isoindoloquinazolinones has been developed under neat reaction (yields up to 91%) conditions. This new one-pot tandem methodology involves condensation of readily available anthranilamide with 3-(2-formylcycloalkenyl)-acrylic ester under solvent- and catalyst-free conditions. This strategy avoids the use of oxidant, and heavy metal catalysts and also is free from work-up and generation of toxic by-products. A dramatic change of photophysical properties of dihydroisoindoloquinazolinones in basic and aqueous media has also been documented in our study. Moreover, our model synthetic compound shows cytotoxic activity towards metastatic HepG2 and PC3 cancer cell lines.

About 2-Aminobenzamide, If you have any questions, you can contact Bera, A; Ali, SA; Manna, SK; Ikbal, M; Misra, S; Saha, A; Samanta, S or concate me.. SDS of cas: 88-68-6

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

An article Boosting Enantioselectivity of Chiral Organocatalysts with Ultrathin Two-Dimensional Metal-Organic Framework Nanosheets WOS:000495769300028 published article about ASYMMETRIC CATALYSIS; COORDINATION CAGE; BRONSTED ACID; DIHYDROQUINAZOLINONES; SEPARATION; LIGAND; BINOL in [Tan, Chunxia; Dong, Jinqiao; Liu, Yuhao; Liu, Yan; Cui, Yong] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China; [Tan, Chunxia; Dong, Jinqiao; Liu, Yuhao; Liu, Yan; Cui, Yong] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China; [Yang, Kuiwei; Jiang, Jianwen] Natl Univ Singapore, Dept Chem & Biomol Engn, 4 Engn Dr 4, Singapore 117576, Singapore in 2019, Cited 68. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Recommanded Product: 2-Aminobenzamide

The development of methodologies for inducing and tailoring enantioselectivities of catalysts is an important issue in asymmetric catalysis. In this work, we demonstrate for the first time that chiral molecular catalysts can be boosted from completely nonselective to highly enantioselective when installed in nanostructured metal-organic frameworks (MOFs). Exfoliation of layered crystals is one of the most direct synthetic routes to unitrathin nanosheets, but its use in MOFs is limited by the availability of layered MOFs. We illustrate that layered MOFs can be designed using ligand-capped metal clusters and angular organic linkers. This leads to the synthesis of two three-dimensional (3D) layered porous MOFs from Zn-4-p-tert-butylsulfonyl calix[4]arene and chiral angular 1,1′-binaphthol/-biphenol dicarboxylic acids, which can be ultrasonic exfoliated into one- and two-layer nanosheets. The obtained MOF materials are efficient catalysts for asymmetric cascade condensation and cyclization of 2-aminobenzamide and aldehydes to produce 2,3-dihyroquinazolinones. While both binaphthol and biphenol display no enantioselectivity, restriction of their freedom in the MOFs leads to 56-90% and 46-72% ee, respectively, which are increased to 72-94% and 64-82% ee after exposure to external surfaces of the flexible nanosheets. Moreover, the MOF crystals and nanosheets exhibit highly sensitive fluorescent enhancement in the presence of chiral amino alcohols with enantioselectivity factors being, respectively, increased up to 1.4 and 2.3 times of the values of the diols, allowing them to be utilized in chiral sensing. Therefore, the observed enantioselectivities increase in the order organocatalyst < MOF crystals < MOF nanosheets in both catalysis and sensing. This work not only provides a strategy to make 3D layered MOFs and their untrathin nanosheets but also paves the way to utilize nanostructured MOFs to manipulate enantioselectivities of molecular catalysts. Recommanded Product: 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Tan, CX; Yang, KW; Dong, JQ; Liu, YH; Liu, Y; Jiang, JW; Cui, Y or concate me.

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

Recently I am researching about BIOLOGICAL EVALUATION; AMPK; ADIPOGENESIS/LIPOGENESIS; DERIVATIVES; INHIBITORS; DESIGN; MICE, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21672265, 81930098, 81872732, 81703336]; Special Fund for Science and Technology Development in Guangdong Province [2016A020217004]; Science and Technology Program of Guangzhou [201704020104]; Natural Science Foundation of Guangdong ProvinceNational Natural Science Foundation of Guangdong Province [2017A030308003]; 111 ProjectMinistry of Education, China – 111 Project [B16047]; Ministry of Education of ChinaMinistry of Education, China [IRT-17R111]; Fundamental Research Funds for the Central UniversitiesFundamental Research Funds for the Central Universities [31610915]; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01Y093]; Guangdong Provincial Key Laboratory of Construction Foundation [2017B030314030]. Computed Properties of C7H8N2O. Published in ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER in ISSY-LES-MOULINEAUX ,Authors: Rao, Y; Xu, Z; Hu, YT; Li, C; Xu, YH; Song, QQ; Yu, H; Song, BB; Chen, SB; Li, QJ; Huang, SL; Tan, JH; Ou, TM; Wang, HG; Zhong, GP; Ye, JM; Huang, ZS. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

Discovery of novel anti-obesity agents is a challenging and promising research area. Based on our previous works, we synthesized 40 novel beta-indoloquinazoline analogues by altering the skeleton and introducing preferential side chains, evaluated their lipid-lowering activity and summarized the structure-activity relationships. In combination with an evaluation of the lipid-lowering efficacies, AMP-dependent activated protein kinase (AMPK) activating ability and liver microsomal stability, compound 23 (named as IQZ23) was selected for further studies. IQZ23 exerted a high efficacy in decreasing the triglyceride level (EC50 = 0.033 mu M) in 3T3-L1 adipocytes. Mechanistic studies revealed the lipid-lowering activity of IQZ23 was dependent on the AMPK pathway by modulating ATP synthase activity. This activation was accompanied by mitochondrial biogenesis and oxidation capacity increased, and insulin sensitivity enhanced in pertinent cell models by various interventions. Correspondingly, IQZ23 (20 mg/kg, i.p.) treatment significantly reversed high fat and cholesterol diet (HFC)- induced body weight increases and accompanying clinical symptoms of obesity in mice but without indicative toxicity. These results indicate that IQZ23 could be a useful candidate for the treatment of obesity and related metabolic disorders. (c) 2020 Elsevier Masson SAS. All rights reserved.

Computed Properties of C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Rao, Y; Xu, Z; Hu, YT; Li, C; Xu, YH; Song, QQ; Yu, H; Song, BB; Chen, SB; Li, QJ; Huang, SL; Tan, JH; Ou, TM; Wang, HG; Zhong, GP; Ye, JM; Huang, ZS or concate me.

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

An article A colorimetric chemosensor for selective detection of copper ions WOS:000569984400001 published article about EFFECTIVE CORE POTENTIALS; FLUORESCENT CHEMOSENSOR; MOLECULAR CALCULATIONS; AQUEOUS-SOLUTION; QUANTUM DOTS; CU2+; SENSOR; ZN2+; RECOGNITION; FLUORIDE in [Kim, Ahran; Chae, Ju Byeong; Rha, Chang Joo; Kim, Cheal] Seoul Natl Univ Sci & Technol SNUT, Dept Fine Chem, Seoul 139733, South Korea in 2020, Cited 55. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. SDS of cas: 88-68-6

A water-applicable hexamethylbenzene (HMB) chemosensor, (E)-2-((2-hydroxy-3-methoxybenzylidene)amino)benzamide, displayed a selective colour change from colourless to yellow in the existence of copper ions. The detection limit was computed as 1.57 mu mol/L, which is substantially lower than the World Health Organisation guideline (31.5 mu mol/L) for copper ions. Probe HMB could also sense and quantify copper ions in real water samples. The coordination mode of HMB to copper ions was demonstrated through Job plot, electrospray ionisation mass spectroscopy and proton nuclear magnetic resonance titration, and was also supported by theoretical studies.

SDS of cas: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Kim, A; Chae, JB; Rha, CJ; Kim, C or concate me.

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

An article Metal-free C-H methylation and acetylation of heteroarenes with PEG-400 WOS:000540914400013 published article about PALLADIUM-CATALYZED ALKYLATION; THERMAL OXIDATIVE-DEGRADATION; POLYETHYLENE-GLYCOL; STEREOSELECTIVE-SYNTHESIS; SELECTIVE ALKYLATION; ALPHA-METHYLATION; C(SP(3))-H BONDS; METHANOL; ARYLACRYLAMIDES; HETEROCYCLES in [Kudale, Vishal Suresh; Wang, Jeh-Jeng] Kaohsiung Med Univ, Dept Med & Appl Chem, 100,Shiquan 1st Rd, Kaohsiung 807, Taiwan; [Wang, Jeh-Jeng] Kaohsiung Med Univ Hosp, Dept Med Res, 100 Tzyou 1st Rd, Kaohsiung 807, Taiwan in 2020, Cited 59. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. HPLC of Formula: C7H8N2O

The generation of a methyl carbon source from renewable and cheap sources is challenging. Herein, we describe a novel and an efficient route for methylation and acetylation of aza-heteroarenes using PEG-400 under O-2 and TsOH center dot H2O for the first time by tuning the reaction conditions using a different set of starting materials. The key features of the current protocol are oxidative C-O and C-C bond scission under metal-free conditions with good functional group tolerance, and a broad substrate scope. The potential applicability of the designed methodology was demonstrated for the synthesis of central nervous system (CNS) depressant and anticonvulsant drug molecules by a one-pot strategy.

HPLC of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Kudale, VS; Wang, JJ 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. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Recommanded Product: 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.

Recommanded Product: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Kamio, S; Kageyuki, I; Osaka, I; Yoshida, H or concate me.

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

Name: 2-Aminobenzamide. Aalinejad, M; Pesyan, NN; Heidari, N; Batmani, H; Asl, AD in [Aalinejad, Michael; Pesyan, Nader Noroozi; Batmani, Hana; Asl, Aria Danandeh] Urmia Univ, Dept Organ Chem, Fac Chem, Orumiyeh 57159, Iran; [Heidari, Nosrat] Urmia Univ, Dept Phys Chem, Fac Chem, Orumiyeh 57159, Iran published Supramolecular Fe3O4@PEG/-diaza crown ether@Ni: a novel magnetically reusable nano catalyst for the clean synthesis of 2-aryl-2,3-dihydroquinazolin-4(1H)-ones in 2019, Cited 46. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Ni@diaza crown ether complex supported on magnetic nanoparticle was provided by grafting technique. The catalytic activity of Fe3O4@diaza crown ether@Ni was explored through one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones and it was used as an efficient and recoverably constant nanocatalyst. FT-IR, SEM, TEM, XRD, BET, ICP, EDS, and TGA techniques were employed to specify the nanocatalyst. This heterogeneous catalyst demonstrated acceptable recyclability and could be used again several times with no considerable loss of its catalytic activity.

About 2-Aminobenzamide, If you have any questions, you can contact Aalinejad, M; Pesyan, NN; Heidari, N; Batmani, H; Asl, AD or concate me.. SDS of cas: 88-68-6

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

Quality Control of 2-Aminobenzamide. I found the field of Biochemistry & Molecular Biology very interesting. Saw the article Reactive OFF-ON type alkylating agents for higher-ordered structures of nucleic acids published in 2019, Reprint Addresses Nagatsugi, F (corresponding author), Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, 2-1-1 Katahira, Sendai, Miyagi 9808577, Japan.; Nagatsugi, F (corresponding author), Tohoku Univ, Grad Sch Sci, Dept Chem, Aoba Ku, Sendai, Miyagi 9808578, Japan.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide.

Higher-ordered structure motifs of nucleic acids, such as the G-quadruplex (G-4), mismatched and bulge structures, are significant research targets because these structures are involved in genetic control and diseases. Selective alkylation of these higher-order structures is challenging due to the chemical instability of the alkylating agent and side-reactions with the single- or double-strand DNA and RNA. We now report the reactive OFF-ON type alkylating agents, vinyl-quinazolinone (VQ) precursors with a sulfoxide, thiophenyl or thiomethyl group for the OFF-ON control of the vinyl reactivity. The stable VQ precursors conjugated with aminoacridine, which bind to the G-4 DNA, selectively reacted with a T base on the G-4 DNA in contrast to the single- and double-strand DNA. Additionally, the VQ precursor reacted with the T or U base in the AP-site, G-4 RNA and T-T mismatch structures. These VQ precursors would be a new candidate for the T or U specific alkylation in the higher-ordered structures of nucleic acids.

Quality Control of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Onizuka, K; Hazemi, ME; Sato, N; Tsuji, G; Ishikawa, S; Ozawa, M; Tanno, K; Yamada, K; Nagatsugi, F or concate me.

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