Month: October 2022

Chen, Wei; Li, Yuxin; Zhou, Yunyun; Ma, Yi; Li, Zhengming published the artcile< Design, synthesis and SAR study of novel sulfonylurea derivatives containing arylpyrimidine moieties as potential anti-phytopathogenic fungal agents>, HPLC of Formula: 6961-82-6, the main research area is sulfonyl urea pyrimidinyl preparation plant pathogen antifungal activity.

Herein, three series of novel sulfonylureas (SUs) containing aromatic-substituted pyrimidines I (Ar = 4-methylphenyl, 2-furyl, 2-thienyl; R1 = H, Cl, Br, I; R2 = NO2, COOMe, Cl; R3 = H, NO2) were designed and synthesized according to pharmacophore-combination and bioisosterism strategy. The in vitro fungicidal activities against ten phytopathogenic fungi indicated that most of the title compounds I exhibited broad-spectrum and excellent fungicidal activities. Based on the preliminary fungicidal activities, a CoMFA model was constructed and the 3D-QSAR anal. indicated that either a bulky group around the 5-position of the pyrimidine ring or electropos. group around the 2-position of the benzene ring would be favor to fungicidal activities. In order to study interaction mechanism, compound I (Ar = 2-furyl; R1 = Br; R2 = Cl; R3 = H) was automatically docked into yeast acetohydroxyacid synthase (AHAS) and it further indicated that bearing bulky groups-aryl at the pyrimidine ring was critical to enhance antifungal activities. It revealed that the antifungal activity of derivatives I probably results from the inhibition of fungal AHAS. Thus, the present results strongly showed that SUs should be considered as lead compounds or model mols. to develop novel anti-phytopathogenic fungal agents.

Chinese Chemical Letters published new progress about Agrochemical fungicides. 6961-82-6 belongs to class amides-buliding-blocks, and the molecular formula is C6H6ClNO2S, HPLC of Formula: 6961-82-6.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Rohokale, Rajendra S.; Kalshetti, Rupali G.; Ramana, Chepuri V. published the artcile< Iridium(III)-Catalyzed Alkynylation of 2-(Hetero)arylquinazolin-4-one Scaffolds via C-H Bond Activation>, Application of C9H12N2O3, the main research area is alkynylarylquinazolinone derivative preparation; arylquinazolinone ethynylbenziodoxolone alkynylation iridium catalyst.

The directed C-H alkynylation of 2-(hetero)arylquinazolin-4-ones has been explored with the ethynylbenziodoxolone reagent TIPS-EBX employing an Ir(III) catalyst. Complementary conditions for either monoalkynylation or dialkynylation have been developed. Also demonstrated is the broad scope of this reaction and the compatibility of various functional groups such as -F, -Cl, -Br, -CF3, -OMe, -NO2, and alkyl, etc.

Journal of Organic Chemistry published new progress about Alkynylation. 5004-88-6 belongs to class amides-buliding-blocks, and the molecular formula is C9H12N2O3, Application of C9H12N2O3.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Singh, Awadhesh Kumar; Singh, Ritu published the artcile< Pharmacotherapy in obesity: a systematic review and meta-analysis of randomized controlled trials of anti-obesity drugs>, Application In Synthesis of 96829-58-2, the main research area is meta analysis obesity orlistat phentermine lorcaserin topiramate naltrexone pharmacotherapy; Obesity; anti-obesity drugs; liraglutide 3.0 mg; lorcaserin; naltrexone plus bupropion; orlistat; phentermine plus topiramate.

Meta-anal. of obesity poses a significant increase in morbidity and mortality and thus five anti-obesity drugs have been approved currently by US FDA. Several phase 3 trials have shown a significant improvement in cardio-metabolic profile including significant weight reduction with these agents compared to placebo. We systematically searched the database of PubMed, Embase, The Cochrane Library and The ClinicalTrials.gov up to 30 Sept. 2019 and retrieved all the randomized controlled trials (RCTs) that were conducted with these five drugs for ≥1 yr and explicitly reported their efficacy vs. placebo. Subsequently, we have conducted the meta-anal. to primarily study the effect of these anti-obesity drugs on weight reduction We addnl. reviewed the effect of these drugs on other cardio-metabolic parameters including key adverse events. This meta-anal. finds a significant reduction in body weight with orlistat (N = 10,435; Δ -3.07 Kg, 95% CI, -3.76 to -2.37), phentermine plus topiramate (N = 2985; Δ -9.77 Kg; 95% CI, -11.73 to -7.81), lorcaserin (N = 16,856; Δ -3.08 Kg; 95% CI, -3.49 to -2.66), naltrexone plus bupropion (N = 3239; Δ -4.39 Kg; 95% CI, -5.05 to -3.72) and liraglutide (N = 4978; Δ -5.25 Kg; 95% CI, -6.17 to -4.32), compared to placebo (all p < 0.00001). Expert Review of Clinical Pharmacology published new progress about Antiobesity agents. 96829-58-2 belongs to class amides-buliding-blocks, and the molecular formula is C29H53NO5, Application In Synthesis of 96829-58-2.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Baruah, Prayasee; Das, Abhinandan; Paul, Debojit; Chakrabarty, Suman; Aguan, Kripamoy; Mitra, Sivaprasad published the artcile< Sulfonylurea Class of Antidiabetic Drugs Inhibit Acetylcholinesterase Activity: Unexplored Auxiliary Pharmacological Benefit toward Alzheimer's Disease>, SDS of cas: 94-20-2, the main research area is antidiabetic sulfonylurea drugrepurposing AChE inhibitor Alzheimer’s.

Contemporary literature documents extensive research on common causative mechanisms, pathogenic pathways and dual effective remedies for Alzheimer’s disease (AD) and Type 2 diabetes mellitus (T2DM). Tolbutamide (TBM), chlorpropamide (CPM), and glyburide (GLY) are three sulfonylurea antidiabetic drugs of different generations. All these drugs were found to exhibit moderate to strong inhibitory efficiency on the neurotransmitter degrading enzyme acetylcholinesterase (AChE) with GLY (IC50 = 0.74 ± 0.02μM) being the most potent, followed by CPM (IC50 = 5.72 ± 0.24μM) and TBM (IC50 = 28.9 ± 1.60μM). Notably, the inhibition efficiency of GLY is even comparable with the FDA approved AD drug, donepezil (DON). The larger size of GLY spans almost the full gorge of AChE ranging from catalytic active site (CAS) to the peripheral active site (PAS) with relatively strong binding affinity (6.0 x 105 M-1) and acts as a competitive inhibitor for AChE. On the other hand, while they show relatively weak binding ((2-6) x 104 M-1), both CPM and TBM act as noncompetitive binders. While these two drugs can bind to PAS, MD simulation results predict an alternative noncompetitive inhibition mechanism for CPM. These results open the possibility of repurposing the antidiabetic drugs, particularly GLY, in the treatment of AD. The consequential side effect of excess acetylcholine production, due to the administration of these drugs to AD-unaffected patients, can be rectified by using colloidal gold and silver nanofluids as potential AChE activity boosters.

ACS Pharmacology & Translational Science published new progress about Alzheimer disease. 94-20-2 belongs to class amides-buliding-blocks, and the molecular formula is C10H13ClN2O3S, SDS of cas: 94-20-2.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Kwiatkowski, Jacek; Liu, Boping; Pang, Shermaine; Binte Ahmad, Nur Huda; Wang, Gang; Poulsen, Anders; Yang, Haiyan; Poh, Yong Rui; Tee, Doris Hui Ying; Ong, Esther; Retna, Priya; Dinie, Nurul; Kwek, Perlyn; Wee, John Liang Kuan; Manoharan, Vithya; Low, Choon Bing; Seah, Peck Gee; Pendharkar, Vishal; Sangthongpitag, Kanda; Joy, Joma; Baburajendran, Nithya; Jansson, Anna Elisabet; Nacro, Kassoum; Hill, Jeffrey; Keller, Thomas H.; Hung, Alvin W. published the artcile< Stepwise Evolution of Fragment Hits against MAPK Interacting Kinases 1 and 2>, Name: 2-Amino-4-bromobenzamide, the main research area is pyridine benzamide preparation mitogen protein kinase pharmacokinetic SAR docking.

Dysregulation of translation initiation factor 4E (eIF4E) activity occurs in various cancers. Mitogen-activated protein kinase (MAPK) interacting kinases 1 and 2 (MNK1 and MNK2) play a fundamental role in activation of eIF4E. Structure-activity relationship-driven expansion of a fragment hit led to discovery of dual MNK1 and MNK2 inhibitors based on a novel pyridine-benzamide scaffold. The compounds possess promising in vitro and in vivo pharmacokinetic profiles and show potent on target inhibition of eIF4E phosphorylation in cells.

Journal of Medicinal Chemistry published new progress about Antitumor agents. 112253-70-0 belongs to class amides-buliding-blocks, and the molecular formula is C7H7BrN2O, Name: 2-Amino-4-bromobenzamide.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Kannan, S.; Gamare, J. S.; Chetty, K. V.; Drew, M. G. B. published the artcile< Coordination and extraction studies of an unexplored bi-functional ligand, carbamoyl methyl pyrazole (CMPz) with uranium(VI), lanthanum(III) and cerium(III) nitrates>, Synthetic Route of 5326-82-9, the main research area is rare earth pyrazoleacetamide preparation structure; crystal structure uranium cerium pyrazoleacetamide nitrato; extraction uranium plutonium octylpyrazoleacetamide ligand; pyrazoleacetamide preparation uranium cerium lanthanum complexation; thermal decomposition uranyl pyrazoleacetamide complex.

The bi-functional carbamoyl Me pyrazole ligands, C5H7N2CH2CONBu2 (L1), C5H7N2CH2CONiBu2 (L2), C3H3N2CH2CONBu2 (L3), C3H3N2CH2CONiBu2 (L4) and C5H7N2CH2CON(C8H17)2 (L5) were synthesized and characterized by spectroscopic and elemental anal. methods. The selected coordination chem. of L1 to L4 with [UO2(NO3)2·6H2O], [La(NO3)3·6H2O] and [Ce(NO3)3·6H2O] was evaluated. Structures for [UO2(NO3)2 C5H7N2CH2CONBu2] (6) [UO2(NO3)2 C5H7N2CH2CONiBu2] (7) and [Ce(NO3)3{C3H3N2CH2CONiBu2}2] (11) were determined by single crystal x-ray diffraction methods. Preliminary extraction studies of the ligand L5 with U(VI) and Pu(IV) in tracer level showed an appreciable extraction for U(VI) and Pu(IV) up to 10 M HNO3 but not for Am(III). Thermal studies of 6 and 7 in air revealed that the ligands can be destroyed completely on incineration.

Polyhedron published new progress about Crystal structure. 5326-82-9 belongs to class amides-buliding-blocks, and the molecular formula is C10H20ClNO, Synthetic Route of 5326-82-9.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Qiao, Jin-Bao; Zhang, Ya-Qian; Yao, Qi-Wei; Zhao, Zhen-Zhen; Peng, Xuejing; Shu, Xing-Zhong published the artcile< Enantioselective Reductive Divinylation of Unactivated Alkenes by Nickel-Catalyzed Cyclization-Coupling Reaction>, Computed Properties of 1524-40-9, the main research area is methylene five membered heterocycle carbocycle chemoselective regioselective enantioselective preparation; bromo diene vinyl electrophile divinylation cyclization coupling nickel catalyst.

An enantioselective cross-electrophile divinylation reaction of nonaromatic substrates, 2-bromo-1,6-dienes was reported. The approach thus offered a route to new chiral cyclic architectures, which were key structural motifs found in various biol. active compounds The reaction proceeded under mild conditions, and use of chiral t-Bu-pmrox and 3,5-difluoro-pyrox ligands resulted in formation of divinylated products with high chemo-, regio-, and enantioselectivity. The method was applicable for incorporation of chiral hetero- and carbocycles into complex mols.

Journal of the American Chemical Society published new progress about Alkadienes Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 1524-40-9 belongs to class amides-buliding-blocks, and the molecular formula is C6H6FNO2S, Computed Properties of 1524-40-9.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Liu, Wei; Wu, Ge; Gao, Wenxia; Ding, Jinchang; Huang, Xiaobo; Liu, Miaochang; Wu, Huayue published the artcile< Palladium-catalyzed oxidative C=C bond cleavage with molecular oxygen: one-pot synthesis of quinazolinones from 2-amino benzamides and alkenes>, Recommanded Product: 2-Amino-4-bromobenzamide, the main research area is aminobenzamide alkene palladium catalyst one pot tandem reaction; arylquinazolinone preparation green chem.

Palladium-catalyzed oxidative cleavage/cyclization was disclosed for the concise synthesis of various quinazolinone derivatives from readily available 2-aminobenzamides and terminal alkenes with excellent functional group tolerance. The synthetic features regarding the use of oxygen as a green oxidant and its utility were illustrated in the synthesis of sildenafil.

Organic Chemistry Frontiers published new progress about Anilines Role: RCT (Reactant), RACT (Reactant or Reagent). 112253-70-0 belongs to class amides-buliding-blocks, and the molecular formula is C7H7BrN2O, Recommanded Product: 2-Amino-4-bromobenzamide.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Grib, Ismahene; Berredjem, Malika; Rachedi, Khadidja Otmane; Djouad, Seif-Eddine; Bouacida, Sofiane; Bahadi, Rania; Ouk, Tan-Sothea; Kadri, Mekki; Ben Hadda, Taibi; Belhani, Billel published the artcile< Novel N-sulfonylphthalimides: Efficient synthesis, X-ray characterization, spectral investigations, POM analyses, DFT computations and antibacterial activity>, Safety of Morpholine-4-sulfonamide, the main research area is sulfonylphthalimide preparation antibacterial DFT; phthalic anhydride sulfonamide condensation ultrasonication.

Some novel N-sulfonylphthalimides I [R = NPh2, N-piperidinyl, morpholino, etc.] were synthesized in good yields by condensation of anhydride phthalic with various sulfonamides in one step. These compounds were screened for their antibacterial activity against E. coli, S. aureus, Morganella morganii and Klebsiella pneumoniae. So it will benificial to test these mols. against other biotargets different of bacterial strains such as viruses, fungus and parasites. The mol. structure of I [R = 3,4-dihydro-1H-isoquinolin-2-yl] was obtained by X-ray diffraction on mono crystal. The crystal packing could be described as alternating layers in zigzag parallel to (100) plane along the c axis, which were connected together with C-H···O hydrogen bonds.

Journal of Molecular Structure published new progress about Amines Role: PAC (Pharmacological Activity), PRP (Properties), RCT (Reactant), SPN (Synthetic Preparation), THU (Therapeutic Use), BIOL (Biological Study), RACT (Reactant or Reagent), PREP (Preparation), USES (Uses) (sulfonyl-). 25999-04-6 belongs to class amides-buliding-blocks, and the molecular formula is C4H10N2O3S, Safety of Morpholine-4-sulfonamide.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Li, Sifan; Wang, Yu; Wu, Zibo; Shi, Weiliang; Lei, Yibo; Davies, Paul W.; Shu, Wei published the artcile< A Radical-Initiated Fragmentary Rearrangement Cascade of Ene-Ynamides to [1,2]-Annulated Indoles via Site-Selective Cyclization>, Synthetic Route of 1524-40-9, the main research area is annulated indole regioselective preparation; ene ynamide fragmentary rearrangement cascade radical initiated.

Herein, a radical triggered fragmentary cyclization cascade reaction of ene-ynamides was presented, providing a rapid access into [1,2]-annulated indoles I [R = H, Me, SMe, etc.; R1 = Ph, 4-MeC6H4, 3-pyridyl, etc.; R2 = H, Me, n-Bu; n = 1,2,3] by an intermol. radical addition, intramol. cyclization, desulfonylative aryl migration, and site-selective C(sp2)-N cyclization sequence. DFT calculations support oxidation of N-centered radical species to cations prior to the C-N bond formation, followed by an unusual aza-Nazarov cyclization.

Organic Letters published new progress about Alkenes Role: RCT (Reactant), RACT (Reactant or Reagent). 1524-40-9 belongs to class amides-buliding-blocks, and the molecular formula is C6H6FNO2S, Synthetic Route of 1524-40-9.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics