Tag: M.W=100-150

An article Synthesis, Crystal Structure, and Agricultural Antimicrobial Evaluation of Novel Quinazoline Thioether Derivatives Incorporating the 1,2,4-Triazolo[4,3-a]pyridine Moiety WOS:000492802400006 published article about BIOLOGICAL EVALUATION; INSECTICIDAL ACTIVITY; FUNGICIDAL ACTIVITIES; DESIGN; ANTIFUNGAL; SERIES; ORYZAE; BASE in [Fan, Zhijiang; Shi, Jun; Luo, Na; Ding, Muhan; Bao, Xiaoping] Guizhou Univ, Ctr Res & Dev Fine Chem, State Key Lab Breeding Base Green Pesticide & Agr, Key Lab Green Pesticide & Agr Bioengn,Minist Educ, Guiyang 550025, Guizhou, Peoples R China in 2019, Cited 46. Category: thiomorpholine. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

A total of 22 quinazoline thioether derivatives incorporating a 1,2,4-triazolo[4,3-a]pyridine moiety were designed, synthesized, and evaluated as antimicrobial agents in agriculture. Among these compounds, the chemical structure of compound 61 was further confirmed via single-crystal X-ray diffraction analysis. The bioassay results revealed that some of the compounds possessed noticeable in vitro antibacterial activities against the tested phytopathogenic bacteria. For example, compounds 6b and 6g had EC50 values as low as 10.0 and 24.7 mu g/mL against Xanthomonas axonopodis pv. citri (Xac), respectively, which were significantly better than that of the commercial agrobactericide bismerthiazol (56.9 mu g/mL). Particularly, compound 6b was also found to be capable of suppressing the pathogenic bacterium Xanthomonas oryzae pv. oryzae (Xoo) approximately 12-fold more potent than control bismerthiazol, in terms of their EC 50 values (7.2 versus 89.8 mu g/mL). Importantly, the most active compound 6b turned out to be one with the highest hydrophilicity and the lowest molecular weight within the series. In vivo bioassays further showed the application prospect of 6b as a promising plant bactericide for controlling Xoo. Additionally, in vitro antifungal activities of these compounds were also evaluated at the concentration of 50 mu g/mL. Overall, the present study demonstrated the potential of 1,2,4-triazolo[4,3-a]pyridine-bearing quinazoline thioether derivatives as efficient agricultural antibacterial agents for crop protection.

About 2-Aminobenzamide, If you have any questions, you can contact Fan, ZJ; Shi, J; Luo, N; Ding, MH; Bao, XP or concate me.. Category: thiomorpholine

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An article Triazolopyridazine derivatives: Synthesis, cytotoxic evaluation, c-Met kinase activity and molecular docking WOS:000489699400094 published article about NATIONAL-CANCER-INSTITUTE; HEPATOCYTE GROWTH-FACTOR; DRUG DISCOVERY; INHIBITORS; DESIGN; OPTIMIZATION in [Ahmed, Eman M.; Khalil, Nadia A.; Taher, Azza T.] Cairo Univ, Fac Pharm, Pharmaceut Organ Chem Dept, Cairo, Egypt; [Taher, Azza T.] October 6 Univ, Pharmaceut Organ Chem Dept, Fac Pharm, Giza, Egypt; [Refaey, Rana H.; Nissan, Yassin M.] October Univ Modern Sci & Arts MSA, Pharmaceut Chem Dept, Fac Pharm, Giza, Egypt; [Nissan, Yassin M.] Cairo Univ, Pharmaceut Chem Dept, Fac Pharm, Kasr Elini St, Cairo 11562, Egypt in 2019, Cited 34. Application In Synthesis of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Novel series of some triazolo [4,3-b]pyridazine derivatives were designed and synthesized. All the newly synthesized compounds were evaluated for their cytotoxic activity at 10(-5) M concentration towards 60 cancer cell lines according to USA NCI protocol. Most of the synthesized compounds showed good activity against SR (leukemia) cell panel. The most active compounds, 2f and 4a were subjected for further evaluation at a five dose level screening and their efficacy for c-Met kinase inhibition was determined in vitro. Binding mode of these derivatives was explored via molecular docking.

Application In Synthesis of 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Ahmed, EM; Khalil, NA; Taher, AT; Refaey, RH; Nissan, YM or send Email.

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Thiomorpholine – Wikipedia,
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I found the field of Biotechnology & Applied Microbiology; Science & Technology – Other Topics very interesting. Saw the article Ni-modified magnetic nanoparticles for affinity purification of His-tagged proteins from the complex matrix of the silkworm fat body published in 2020. Computed Properties of C7H8N2O, Reprint Addresses Park, EY (corresponding author), Shizuoka Univ, Grad Sch Sci & Technol, Dept Biosci, 836 Ohya, Shizuoka 4228529, Japan.; Park, EY (corresponding author), Shizuoka Univ, Res Inst Green Sci & Technol, Green Chem Res Div, Lab Biotechnol, 836 Ohya, Shizuoka 4228529, Japan.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

Purification of recombinant proteins is often a challenging matter because high purity and high recovery are desired. If the expressed recombinant protein is also in a complex matrix, such as from the silkworm expression system, purification becomes more challenging. Even if purification from the silkworm expression system is troublesome, it benefits from a high capacity for the production of recombinant proteins. In this study, magnetic nanoparticles (MNPs) were investigated as a suitable tool for the purification of proteins from the complex matrix of the silkworm fat body. The MNPs were modified with nickel so that they have an affinity for His-tagged proteins, as the MNP purification protocol itself does not need special equipment except for a magnet. Among the three different kinds of investigated MNPs, MNPs with sizes of 100 nm to 200 nm and approximately 20 nm-thick nickel shells were the most suitable for our purpose. With them, the total protein amount was reduced by up to at least approximately 77.7%, with a protein recovery of around 50.8% from the silkworm fat body. The minimum binding capacity was estimated to be 83.3 mu g protein/mg MNP. Therefore, these MNPs are a promising tool as a purification pretreatment of complex sample matrices.

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.. Computed Properties of C7H8N2O

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

COA of Formula: C7H8N2O. Recently I am researching about IN-VITRO; CANCER; QUINOXALINONES; EPIGENETICS; EXPRESSION; PHYSIOLOGY; ROLES, Saw an article supported by the National Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21176018]. Published in ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER in ISSY-LES-MOULINEAUX ,Authors: Cheng, CH; Yun, F; He, J; Ullah, S; Yuan, QP. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

A series of novel 2-aminobenzamide derivatives decorated with thioquinazolinone were designed and synthesized as histone deacetylase (HDAC) inhibitors. These derivatives were evaluated for their anti-proliferative activities against several human cancer cell lines including A375, Hela, A549, HCT116 and SMMC7721. It’s significantly indicated that some inhibitors exhibited potent antiproliferative activities towards all the studied cancer cell lines. Compounds 7a, 4i, 4o, and 4p exhibited higher antiproliferative activities towards three cancer cell lines: A375, A549 and SMMC7721 compared to CS055, MS275, and C1994. Compound 4p showed more than 4000-fold the isoform selectivity for HDACI and more than 250-fold selectivity for HDAC2 compared with HDAC6. The molecular docking analysis reasonably explained the HDAC inhibitory activity and isoform selectivity. In addition, compounds 7a, 4i, 4o, and 4p showed potent inhibitory activities in migration assay and colony formation analysis, and also promoted cell apoptosis. Moreover, compounds 7a, 4i, and 4o inhibited the growth of SMMC7721 cells at S phase of the cell cycle. The immunofluorometric analysis indicated that compounds 7a, 4i, 4o, and 4p could increase the acetylation status of H3K9. Furthermore, in vivo anticancer efficacy of compound 4p was assessed in the A549 xenograft models, and 4p demonstrated potent antitumor activity (TGI = 62.5%). This study provided an effective strategy for further development of tumor-targeting therapy. (C) 2019 Elsevier Masson SAS. All rights reserved.

COA of Formula: C7H8N2O. 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.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Recently I am researching about ENERGY; IMPROVE; SMART, Saw an article supported by the Young Scholar Fellowship Program by the Ministry of Science and Technology (MOST) in Taiwan [MOST 108-2636-E-027-003]; Research Center of Energy Conservation for New Generation of Residential, Commercial, and Industrial Sectors from The Featured Areas Research Center Program within the framework of Higher Education Sprout Project by the Ministry of Education (MOE) in Tai. Computed Properties of C7H8N2O. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Hsiao, YJ; Lin, LY. The CAS is 64-10-8. Through research, I have a further understanding and discovery of 1-Phenylurea

Flexible fiber-type solid-state supercapacitors (FSCs) are demanded for energy storage of wearable soft electronics. A flexible carbon fiber (CF) with high electrical conductivity and good energy storage ability can act as the current collector and the active material simultaneously. Improving the energy storage ability of the CF without depositing active materials is highly promising to avoid active materials from peeling off, especially under bending conditions. In this study, the CF is treated with acid mixtures containing different HNO3 to H2SO4 ratios. The roughened surface and the production of graphene quantum dots and functional groups are achieved for the acid-treated CF, especially for the CF treated with the acid mixtures. The largely enhanced specific capacitance (C-L) is first obtained for the optimized CF electrode (641.08 mF/cm at 5 mV/s) treated with the acid mixture containing the HNO3 to H2SO4 ratio of 1 to 3. The FSC also shows a maximum energy density of 16.57 mu W h/cm at the power density of 62.50 mu W/cm, as well as a C-L retention of 77% and Coulombic efficiency of 100% in 5000 times of a charge/discharge cycling process. Excellent flexibility is also attained for the FSC with no shape distortion of cyclic voltammetry curves measured under the bending angle of 180 degrees and with 1000 times of repeated bending. This work proposes a simple acid treatment to largely enhance the energy storage ability of pure CF electrodes. The bifunctional substance with current collecting and energy storing abilities is expected to be well developed in the future for applying on numerous efficient flexible energy storage devices.

Computed Properties of C7H8N2O. Welcome to talk about 64-10-8, If you have any questions, you can contact Hsiao, YJ; Lin, LY or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

SDS of cas: 64-10-8. In 2020.0 MOLECULES published article about GAS-CHROMATOGRAPHY; FRUITS; PROCYMIDONE; CUCUMBERS; PROVINCE; CARBARYL; STORAGE; FOODS; CHINA in [Ramadan, Mohamed F. A.] Agr Res Ctr, Pesticide Anal Res Dept, Cent Agr Pesticide Lab, Dokki 12618, Egypt; [Ramadan, Mohamed F. A.; Abdel-Hamid, Mohamed M. A.; Altorgoman, Montasser M. F.] Abha Food Safety Lab, Abha 61421, Saudi Arabia; [Abdel-Hamid, Mohamed M. A.] Alexandria Univ, Fac Sci, Dept Chem, Alexandria 21524, Egypt; [Altorgoman, Montasser M. F.] Alexandria Univ, Fac Sci, Dept Biochem, Alexandria 51521, Egypt; [AlGaramah, Hamed A.; Awwad, Nasser S.] King Khalid Univ, RCAMS, POB 9004, Abha 61413, Saudi Arabia; [Alawi, Mohammed A.] Inspect & License Dept Asir Municipal, Abha 61421, Saudi Arabia; [Shati, Ali A.] King Khalid Univ, Fac Sci, Biol Dept, Abha 9004, Saudi Arabia; [Shweeta, Hoda A.] Umm Al Qura Univ, Coll Pharm, POB 715, Mecca 21955, Saudi Arabia in 2020.0, Cited 46.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

This study’s aim was to determine the pesticide residues in 10 different vegetable commodities from the Asir region, Saudi Arabia. We evaluated 211 vegetable samples, collected from supermarkets between March 2018 and September 2018, for a total of 80 different pesticides using ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) and gas chromatography-tandem mass spectrometry (GC-MS/MS) after extraction with a multi-residue method (the QuEChERS method). The results were assessed according to the maximum residue limit (MRL) provided by European regulations for each pesticide in each commodity. All lettuce, cauliflower, and carrot samples were found to be free from pesticide residues. A total of 145 samples (68.7%) contained detectable pesticide residues at or lower than MRLs, and 44 samples (20.9%) contained detectable pesticide residues above MRLs. MRL values were exceeded most often in chili pepper (14 samples) and cucumber (10 samples). Methomyl, imidacloprid, metalaxyl, and cyproconazole were the most frequently detected pesticides. Based on the results of this study, we recommend that a government-supported program for the monitoring of pesticide residues in vegetables be established to promote consumers’ health and achieve sustainable farming systems.

Welcome to talk about 64-10-8, If you have any questions, you can contact Ramadan, MFA; Abdel-Hamid, MMA; Altorgoman, MMF; AlGaramah, HA; Alawi, MA; Shati, AA; Shweeta, HA; Awwad, NS or send Email.. SDS of cas: 64-10-8

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Product Details of 88-68-6. I found the field of Chemistry very interesting. Saw the article Phosphomolybdic Acid (PMA)-catalyzed One-pot Synthesis of 2,3-Dihydroquinazolines published in 2019, Reprint Addresses Huang, GL; Liu, B (corresponding author), Yunnan Normal Univ, Sch Chem & Chem Engn, Kunming 650500, Yunnan, Peoples R China.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide.

We have developed a new method for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones in good to excellent yields via phosphomolybdic acid (PMA)-catalyzed cyclocondensation of 2-aminobenzamides with aldehydes or ketones in N,N-dimethylformamide (DMF) at room temperature. The present method proves to be efficient in terms of short reaction time, high yield, simple workup and easy purification.

Product Details of 88-68-6. Welcome to talk about 88-68-6, If you have any questions, you can contact Chen, CH; Xuejiao, A; Li, X; Huang, GL; Liu, B or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Microwave assisted synthesis and photophysical properties of blue emissive 2-amino-3-carboxamide-1,1 ‘-biaryls and 4-(arylamino)-[1,1 ‘-biphenyl]-3-carboxamides via Suzuki and Chan-Evans-Lam coupling WOS:000509632600011 published article about ACETOGENIC ISOQUINOLINE ALKALOIDS; 1ST TOTAL-SYNTHESIS; ONE-POT SYNTHESIS; ARYL HALIDES; SOLVENT-FREE; CATALYST; QUINAZOLINONES; FRAGMENTATION; DERIVATIVES; EFFICIENT in [Novanna, Motakatla; Kannadasan, Sathananthan] Vellore Inst Technol, Sch Adv Sci, Dept Chem, Vellore 632014, Tamil Nadu, India; [Shanmugam, Ponnusamy] CSIR, CLRI, Organ & Bioorgan Chem Div, Chennai 600020, Tamil Nadu, India in 2020, Cited 50. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Product Details of 88-68-6

An efficient microwave assisted synthesis of 2-amino-3-carboxamide-1,1′-biaryls derivatives 4a-p and terphenyl derivative 5a from 2-amino-5-iodobenzamide 2a, 2-amino-3,5-diiodobenzamide 2b and (het)aryl boronic acids via Suzuki coupling has been achieved. Synthetic utility of the product 4-amino-4′-cyano-[1,1′-biphenyl]-3-carboxamide 4j has been demonstrated for the synthesis of 4-(aryl amino)-[1,1′-biphenyl]-3-carboxamide derivatiyes 10a-c via Chan-Evans-Lam coupling reaction. Furthermore, 4-(4′-oxo-3′, 4′-dihydro-1’H-spirof[fluorene-9,2′-quinazolin]-6′-yl)benzonitrile 12a was obtained from biaryl derivative 4j and fluorenone 11a and 6(4-methoxyphenyl)2-(ferrocenyl) quinazolin-4(3H)-one 12b from biaryl derivative 4k and ferrocenealdehyde lib using phosphotungstic acid as green catalyst and solvent free microwave irradiation condition. Remarkably, all the synthesized 2-amino-3-carboxamide-1,1′-biaryls and 4-(aryl amino)-[1,1′-biphenyl]-3-carboxamide derivatives 4a-p showed luminescence in the blue region with large Stokes shift. Significantly, 2-amino-3-carboxamide-1,1′-biaryls 4d and 4j showed high fluorescence quantum yields (Phi(f)) 0.54 and 0.84, respectively.

Product Details of 88-68-6. Welcome to talk about 88-68-6, If you have any questions, you can contact Novanna, M; Kannadasan, S; Shanmugam, P or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Efficacy and Safety Over 2 Years of Exenatide Plus Dapagliflozin in the DURATION-8 Study: A Multicenter, Double-Blind, Phase 3, Randomized Controlled Trial WOS:000571872200053 published article about TYPE-2 DIABETES-MELLITUS; ADD-ON THERAPY; SGLT2 INHIBITORS; TOLERABILITY; METFORMIN in [Jabbour, Serge A.] Thomas Jefferson Univ, Philadelphia, PA 19107 USA; [Frias, Juan P.] Natl Res Inst, Los Angeles, CA USA; [Ahmed, Azazuddin] Apex Med Res, Chicago, IL USA; [Hardy, Elise] AstraZeneca, Gaithersburg, MD USA; [Choi, Jasmine] Statum Res, Irvine, CA USA; [Sjostrom, C. David] AstraZeneca, Gothenburg, Sweden; [Guja, Cristian] Carol Davila Univ Med & Pharm, Bucharest, Romania in 2020.0, Cited 17.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8. Name: 1-Phenylurea

OBJECTIVE In patients with type 2 diabetes uncontrolled with metformin, exenatide once weekly (QW) plus dapagliflozin produced greater reductions in glycemic parameters (glycated hemoglobin [HbA(1c)], fasting plasma glucose [FPG], and 2-h postprandial glucose [2-h PPG]), weight, and systolic blood pressure (SBP) than exenatide QW or dapagliflozin alone after 28 weeks of treatment in DURATION-8. Following a 24-week extension period, improvements were sustained at 52 weeks. In this study, we investigated efficacy and safety at 104 weeks after randomization. RESEARCH DESIGN AND METHODS DURATION-8 was a 104-week, multicenter, double-blind, randomized, active-controlled, phase 3 trial. In total, 695 adults (aged >= 18 years) with type 2 diabetes and inadequate glycemic control (HbA(1c)8.0-12.0% [64-108 mmol/mol]) despite stable metformin monotherapy (>= 1,500 mg/day) were randomly assigned (1:1:1) to receive exenatide 2 mg QW plus once-daily dapagliflozin 10 mg, exenatide QW plus placebo, or dapagliflozin plus placebo. All 104-week evaluations were exploratory. RESULTS At week 104, 431 (62.0%) patients completed treatment. The adjusted least squares mean change (SE) from baseline to week 104 in HbA(1c)was greater with exenatide QW plus dapagliflozin (-1.70% [0.11]) versus exenatide QW plus placebo (-1.29% [0.12];P= 0.007) and dapagliflozin plus placebo (-1.06% [0.12];P< 0.001). Clinically relevant changes in FPG, 2-h PPG, weight, and SBP were also observed with exenatide QW plus dapagliflozin. There were no unexpected safety findings, and exenatide QW plus dapagliflozin was well tolerated, with no episodes of major hypoglycemia. CONCLUSIONS In this exploratory analysis, among those individuals who completed the trial without rescue therapy, there was clinically relevant efficacy over 2 years with exenatide QW plus dapagliflozin, with no unexpected safety findings. Name: 1-Phenylurea. Welcome to talk about 64-10-8, If you have any questions, you can contact Jabbour, SA; Frias, JP; Ahmed, A; Hardy, E; Choi, J; Sjostrom, CD; Guja, C or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

In 2020 MOLECULES 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. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Category: thiomorpholine

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.

Category: thiomorpholine. Welcome to talk about 88-68-6, If you have any questions, you can contact Mashweu, AR; Chhiba-Govindjee, VP; Bode, ML; Brady, D or send Email.

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