Category: 112-63-0

Schwenninger, R.; Ongania, K. H. published the artcile< Synthesis of benzanellated carbacephams. II>, Product Details of C19H34O2, the main research area is carbacepham benzo; benzocarbacepham.

The treatment of 2-(oxo-1-azetidinyl)benzyltriphenylphosphonium salts with base leads to carbacephems I [R = H, OMe, OCH2Ph; R1 = H, OPh] which can be reduced to the title compounds The reaction of I with acids does not result in 3-oxocephams by cleavage of the enol ether function. Instead, the 3-alkoxyquinolines have been obtained.

Monatshefte fuer Chemie published new progress about β-Lactams Role: SPN (Synthetic Preparation), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Product Details of C19H34O2.

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

DeSimone, R. W.; Blum, C. A. published the artcile< Substituted 3-(2-benzoxazyl)-benzimidazol-2-(1H)-ones: A new class of GABAA brain receptor ligands>, Reference of 112-63-0, the main research area is benzoxazolylbenzimidazolone preparation GABA receptor ligand; structure activity benzoxazolylbenzimidazolone GABA receptor binding; benzodiazepine receptor ligand preparation structure activity.

A novel class of potent benzodiazepine receptor (BZR) ligands I (R = H, Me; X = CH, N; Y = O, S; Z = CH, N; R1, R2 = H, F, MeO; R3, R4, R5 = H, F) and II (n = 1, 2), has been designed and synthesized aided by mol. modeling of known benzodiazepine ligands such as CGS-8216 and the use of known pharmacophore models. The structure-activity relationship was studied.

Bioorganic & Medicinal Chemistry Letters published new progress about GABAA receptors Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Reference of 112-63-0.

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

Enders, Dieter; Henseler, Alexander; Lowins, Sebastian published the artcile< N-Heterocyclic carbene catalyzed nucleophilic acylation of trifluoromethyl ketimines>, Formula: C19H34O2, the main research area is fluoromethyl ketimine furaldehyde nucleophilic acylation heterocyclic carbene catalyst; amino fluoromethyl ketone preparation.

An efficient N-heterocyclic carbene (NHC)-catalyzed nucleophilic acylation of trifluoromethyl ketimines was developed. The combination of N-aryl trifluoromethyl ketimines with furan-2-aldehydes led chemoselectively to the corresponding 伪-amino 伪-trifluoromethyl ketones in moderate to very good yields (32-87%) providing ready access to this pharmaceutically important class of compounds

Synthesis published new progress about Acylation (nucleophilic). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Formula: C19H34O2.

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

Gaff, Jessica; Octaviana, Fitri; Pillay, Prinisha; Mbenda, Huguette Gaelle Ngassa; Ariyanto, Ibnu A.; Gan, June Anne; Cherry, Catherine L.; Kamerman, Peter; Laws, Simon M.; Price, Patricia published the artcile< TNF-block genotypes influence susceptibility to HIV-associated sensory neuropathy in Indonesians and South Africans>, Quality Control of 112-63-0, the main research area is TNF DDX39B sensory neuropathy HIV infection population; 8.1 ancestral haplotype; DDX39B and BAT1; HIV; TNF-block; sensory neuropathy.

HIV-associated sensory neuropathy (HIV-SN) is a disabling complication of HIV disease and antiretroviral therapies (ART). Since stavudine was removed from recommended treatment schedules, the prevalence of HIV-SN has declined and associated risk factors have changed. With stavudine, rs1799964*C (TNF-1031) associated with HIV-SN in Caucasians and Indonesians but not in South Africans. Here, we investigate associations between HIV-SN and rs1799964*C and 12 other polymorphisms spanning TNF and seven neighboring genes (the TNF-block) in Indonesians (n = 202; 34/168 cases) and South Africans (n = 75; 29/75 cases) treated without stavudine. Haplotypes were derived using fastPHASE and haplotype networks built with PopART. There were no associations with rs1799964*C in either population. However, rs9281523*C in intron 10 of BAT1 (alternatively DDX39B) independently associated with HIV-SN in Indonesians after correcting for lower CD4 T-cell counts and >500 copies of HIV RNA/mL (model p = 0.0011, Pseudo R2 = 0.09). rs4947324*T (between NFKBIL1 and LTA) independently associated with reduced risk of HIV-SN and shared haplotype 1 (containing no minor alleles) associated with increased risk of HIV-SN after correcting for greater body weight, a history of tuberculosis and nadir CD4 T-cell counts (model: p = 0.0003, Pseudo R2 = 0.22). These results confirm TNF-block genotypes influence susceptibility of HIV-SN. However, critical genotypes differ between ethnicities and with stavudine use.

International Journal of Molecular Sciences published new progress about Allele frequency. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Quality Control of 112-63-0.

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

Saidjalolov, Saidbakhrom; Braud, Emmanuelle; Edoo, Zainab; Iannazzo, Laura; Rusconi, Filippo; Riomet, Margaux; Sallustrau, Antoine; Taran, Frederic; Arthur, Michel; Fonvielle, Matthieu; Etheve-Quelquejeu, Melanie published the artcile< Click and Release Chemistry for Activity-Based Purification of 尾-Lactam Targets>, Electric Literature of 112-63-0, the main research area is click release chem beta lactam target screening; Activity-based probe; Antibiotic; Click and release; Iminosydnone; Peptidoglycan.

尾-Lactams, the cornerstone of antibiotherapy, inhibit multiple and partially redundant targets referred to as transpeptidases or penicillin-binding proteins. These enzymes catalyze the essential crosslinking step of the polymerization of cell wall peptidoglycan. The understanding of the mechanisms of action of 尾-lactams and of resistance to these drugs requires the development of reliable methods to characterize their targets. Here, we describe an activity-based purification method of 尾-lactam targets based on click and release chem. We synthesized alkyne-carbapenems with suitable properties with respect to the kinetics of acylation of a model target, the Ldtfm L,D-transpeptidase, the stability of the resulting acylenzyme, and the reactivity of the alkyne for the cycloaddition of an azido probe containing a biotin moiety for affinity purification and a bioorthogonal cleavable linker. The probe provided access to the fluorescent target in a single click and release step.

Chemistry – A European Journal published new progress about Antibiotic resistance. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Electric Literature of 112-63-0.

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

Zhou, Lipeng; Gao, Dongting; Yang, Jingru; Yang, Xiaomei; Su, Yunlai; Lu, Tianliang published the artcile< Conversion of recalcitrant cellulose to alkyl levulinates and levulinic acid via oxidation pretreatment combined with alcoholysis over Al2(SO4)3>, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is cellulose oxidation aluminum sulfate catalyst alcoholysis alkyl levulinate.

Conversion of cellulose to chems. is an economic and environmental route for biomass utilization. In this work, efficient conversion of cellulose to alkyl levulinates and levulinic acid was realized by oxidation pretreatment combined with alcoholysis over Al2(SO4)3 catalyst. Proper pre-oxidation conditions including oxidation temperature and time are important. By pre-oxidation, part of hydroxymethyl groups on cellulose was converted to carboxyl groups which provide the Bronsted acid sites near the glycosidic bonds to improve the depolymerization of cellulose to monosaccharide. Al2(SO4)3路18H2O can play both Bronsted and Lewis acid roles in methanol and catalyze the conversion of monosaccharide to alkyl levulinates and levulinic acid. After pre-oxidation at optimized conditions, cellulose can be converted into Me levulinate and levulinic acid over Al2(SO4)3 in methanol efficiently, and total yield of Me levulinate and levulinic acid can reach 66.8% at 180掳C for 3 h. Furthermore, the simple and cheap Al2(SO4)3 catalyst is recyclable which is important for the practical application.

Cellulose (Dordrecht, Netherlands) published new progress about Alcoholysis. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate.

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

Smagowicz, J.; Wierzchowski, K. L. published the artcile< The phosphorescence of hindered aminopyrimidines>, Reference of 112-63-0, the main research area is phosphorescence aminopyridimidine; pyrimidine alkyl amino phosphorescence; alkylpyrimidine phosphorescence.

The quantum yields, lifetimes, and polarizations of phosphorescence of 4- and 5-aminopyrimidines and their hindered alkyl derivatives were measured in solvents of different polarity at 90掳K. The model presented for interpretation of these data allows determining the matrix elements of spin-orbit coupling between the emitting singlet and triplet states. These elements are 0.2-0.8 cm-1 in aminopyrimidines and increase as the amino group becomes more twisted relative to the ring. Spin-orbit coupling of higher 1(n,蟺*) states with emitting triplets is 鈭?0 times stronger than that of the lowest 1(l,a蟺*).

Journal of Luminescence published new progress about Amino group. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Reference of 112-63-0.

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

Mai, Yang; Ouyang, Yaqi; Yu, Mian; Qin, Yujia; Girardi, Michael; Saltzman, W. Mark; Cocco, Emiliano; Zhao, Chao; Yu, Liu; Jia, Yizhen; Xiao, Lingyun; Dou, Liu; Deng, Wenbin; Liu, Yang; Xie, Julin; Deng, Yang published the artcile< Topical formulation based on disease-specific nanoparticles for single-dose cure of psoriasis>, Application of C19H34O2, the main research area is psoriasis topical formulation disease specific nanoparticle; Disease-specific treatment; Formulation optimization; Local drug delivery; Psoriasis; Single-dose cure; Surface-modified nanoparticles.

First-line treatments for mild to moderate psoriasis are typically topical formulations containing corticosteroids, however, the therapeutic efficacy of these formulations is compromised by limited penetration and skin retention. Even more challenging, off-target corticosteroids are known to adversely affect healthy skin, including induction of epidermal and dermal atrophy. Here, we report a nanoparticle-based topical formulation that cures psoriasis in a single dose, but leaves healthy skin intact. Specifically, we developed tris(hydroxymethyl)aminomethane-modified bioadhesive nanoparticles (Tris-BNPs) that exploit the high permeability characteristic of psoriasis to penetrate only psoriatic skin but not the healthy skin. Furthermore, as Tris-BNPs diffuse and penetrate into the epidermis, the Tris mols. slowly diffuse away, exposing the aldehyde groups of BNPs, which can bind to amine groups present within lesional skin, leading to long local retention of BNPs in lesions of psoriatic skin. The accumulated BNPs within lesions release corticosteroids over a 鈭?3 day period to maintain local drug concentration above the therapeutic level. In addition to deeper penetration and longer retention compared with com. psoriasis treatments, the topical applied Tris-BNPs were not affected by sweating, humidity, or active wiping due to their preferential accumulation between the stratum corneum and the basal cells of the epidermis. Overall, Tris-BNP as a topical formulation hold promise to overcome the limitations of current psoriasis treatment.

Journal of Controlled Release published new progress about Adhesion, physical. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Application of C19H34O2.

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

Ruff, Yves; Martinez, Roberto; Pelle, Xavier; Nimsgern, Pierre; Fille, Pascale; Ratnikov, Maxim; Berst, Frederic published the artcile< An Amphiphilic Polymer-Supported Strategy Enables Chemical Transformations under Anhydrous Conditions for DNA-Encoded Library Synthesis>, Application of C19H34O2, the main research area is amphiphilic polymer chem transformation anhydrous DNA library; DNA-encoded libraries; decarboxylative coupling; drug discovery; encoded library technologies; solid-supported synthesis.

The use of DNA-encoded libraries has emerged as a powerful hit generation technol. Combining the power of combinatorial chem. to enumerate large compound collections with the efficiency of affinity selection in pools, the methodol. makes it possible to interrogate vast chem. space against biol. targets of pharmaceutical relevance. Thus, the chem. transformations employed for the synthesis of encoded libraries play a crucial role in the identification of diverse and drug-like starting points. Currently established transformations have mostly been limited to water-compatible reactions to accommodate the growing oligonucleotide tag. Herein, we describe the development of a practical catch-and-release methodol. utilizing a cationic, amphiphilic PEG-based polymer to perform chem. transformations on immobilized DNA conjugates under anhydrous conditions. We demonstrate the usefulness of our APTAC (amphiphilic polymer-facilitated transformations under anhydrous conditions) approach by performing several challenging transformations on DNA-conjugated small mols. in pure organic solvents: the addition of a carbanion equivalent to a DNA-conjugated ketone in THF, the synthesis of saturated heterocycles using the tin (Sn) amine protocol (SnAP) in dichloromethane, and the dual-catalytic (Ir/Ni) metallaphotoredox decarboxylative cross-coupling of carboxylic acids to DNA-conjugated aryl halides in DMSO. In addition, we demonstrate the feasibility of the latter in multititer-plate format.

ACS Combinatorial Science published new progress about Immobilization, molecular. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Application of C19H34O2.

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

Xu, Xiaoshan; Luo, Liuhong; Song, Chang; Li, Jianjun; Chen, Huanhuan; Zhu, Qiuying; Lan, Guanghua; Liang, Shujia; Shen, Zhiyong; Cao, Zhiqiang; Feng, Yi; Liao, Lingjie; Xing, Hui; Shao, Yiming; Ruan, Yuhua published the artcile< Survey of pretreatment HIV drug resistance and the genetic transmission networks among HIV-positive individuals in southwestern China, 2014-2020>, Safety of (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is human immunodeficiency virus drug resistance genetic transmission China; Antiretroviral therapy (ART); Drug resistance mutations (DRMs); Genetic transmission networks; HIV; Pretreatment drug resistance (PDR).

Pretreatment drug resistance (PDR) can limit the effectiveness of HIV antiretroviral therapy (ART). The aim of this study was to assess the prevalence of PDR among HIV-pos. individuals that initiated antiretroviral therapy in 2014-2020 in southwestern China. Consecutive cross-sectional surveys were conducted in Qinzhou, Guangxi. We obtained blood samples from individuals who were newly diagnosed with HIV in 2014-2020. PDR and genetic networks analyses were performed by HIV-1 pol sequences using the Stanford HIV-database algorithm and HIV-TRACE, resp. Univariate and multivariate logistic regression models were used to explore the potential factors associated with PDR. In total, 3236 eligible HIV-pos. individuals were included. The overall prevalence of PDR was 6.0% (194/3236). The PDR frequency to NNRTI (3.3%) was much higher than that of NRTI (1.7%, p < 0.001) and PI (1.2%, p < 0.001). A multivariate logistic regression anal. revealed that PDR was significantly higher among individuals aged 18-29 (adjusted odds ratio (aOR): 1.79, 95% CI 1.28-2.50) or 30-49 (aOR: 2.82, 95% CI 1.73-4.82), and harboring CRF08_BC (aOR: 3.23, 95% CI 1.58-6.59). A total of 1429 (43.8%) sequences were linked forming transmission clusters ranging in size from 2 to 119 individuals. Twenty-two individuals in 10 clusters had the same drug resistant mutations (DRMs), mostly to NNRTIs (50%, 5/10). The overall prevalence of PDR was medium, numerous cases of the same DRMs among genetically linked individuals in networks further illustrated the importance of surveillance studies for mitigating PDR. BMC Infectious Diseases published new progress about Antiviral agents. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Safety of (9Z,12Z)-Methyl octadeca-9,12-dienoate.

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