Category: 112-63-0

Frymark, Justyna; Zabiszak, Michal; Grajewski, Jakub; Hnatejko, Zbigniew; Kolodynska, Dorota; Kaczmarek, Malgorzata T.; Jastrzab, Renata published the artcile< Excess of polyamine as a factor influencing the mode of coordination in the Eu(III)/α-hydroxy acid/spermine system>, Synthetic Route of 112-63-0, the main research area is europium complexation hydroxy acid spermine excess polyamine spectroscopy.

The complexes of europium(III) ions in binary and ternary systems with α-hydroxy acids and biogenic amine – spermine were investigated. Studies have been performed in aqueous solution using the potentiometric method with computer anal. of the data. Anal. of the equilibrium constants of the reactions and spectroscopic data have allowed us to determine the type of coordination and effectiveness of the carboxyl groups in the process of complex formation in the systems studied. Furthermore, the results confirmed the occurrence of non-covalent interactions of protonated spermine with coordinated α-hydroxy acid. The effect of biogenic polyamine concentration was clearly confirmed, and their influence on the stability and coordination mode of ternary complexes was found.

Polyhedron published new progress about Circular dichroism. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Synthetic Route of 112-63-0.

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

Gao, Song; Ren, Fang-Yu; Xie, Wei-Hang; He, Liang-Nian; Li, Hong-Ru published the artcile< Heterogeneous esterification of ricinoleic acid with polyol for the synthesis of polyol ricinoleates as biomass-based lubricant base oil>, Related Products of 112-63-0, the main research area is ricinoleic acid polyol ricinoleats biomass lubricant base oil esterification.

Bio-derived lubricants, especially those derived from vegetable oils, are considered to be promising alternatives to mineral oil-based lubricants due to the features of sustainability and environmental friendliness. In this work, the polyol ricinoleates were prepared by esterification of ricinoleic acid with trimethylolpropane (TMP), neopentyl glycol (NPG) and pentaerythritol (PE) resp. using Lewis acidic stannous oxide as an efficient heterogeneous catalyst, affording the polyol ricinoleates up to 99.7% yield. Remarkably, the solid catalyst was readily recovered and reused at least for five cycles without significant loss of activity. The resulting polyol ricinoleates products were structurally characterized by Fourier transform IR spectroscopy (FT-IR), 1H NMR, 13C NMR, electrospray ionization mass spectra (ESI-MS); and were stable below 300°C through thermogravimetric anal. (TGA). Furthermore, the physicochem. and lubricating properties of as-synthesized polyol esters were also evaluated including viscosity at 40 and 100°C, viscosity index (VI), pour point and flash point, thermal stability and wear scar diameter To our delight, the performance indicators of the target products were comparable or better than the com. lubricants, showing their potential as lubricant base oil. This work represents an alternative access to useful lubricant products via effective and selective conversion of non-edible vegetable oil.

Journal of the American Oil Chemists’ Society published new progress about Base oils. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Related Products of 112-63-0.

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

Majumdar, Krishna C.; Kundu, Anup K. published the artcile< Pyridine hydrobromide perbromide mediated regioselective heterocyclization of ortho-cyclohexenyl phenols>, Computed Properties of 112-63-0, the main research area is pyridine hydrobromide perbromide cyclization cyclohexenylphenol preparation.

A series of 2,6-methano-1-benzoxecin derivatives was prepared in almost quant. yields by regioselective heterocyclization of 2-(2-cyclohexen-1-yl)phenols. The structures of one of the 2,5-methano-1-benzoxecins thus prepared was determined by the synthesis of a mercury compound from the intermediate 2-(2-cyclohexen-1-yl)-4-methoxyphenol. The cyclization of 2-chloro-6-(2-cyclohexen-1-yl)phenol failed and yielded a ring-brominated product instead.

Canadian Journal of Chemistry published new progress about Cyclization, regioselective. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Computed Properties of 112-63-0.

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

Xu, Yang; Yang, Huailei; Shan, Baiyu; Fang, Kuo; Li, Mingyu; Wang, Fang; Bao, Huiwei published the artcile< Simultaneous Determination of Seven Active Components in Desheng Pills by High-performance Liquid Chromatography>, Application In Synthesis of 112-63-0, the main research area is Desheng pill paeoniflorin costunolide high performance liquid chromatog.

Desheng pills (DSP) consist of six traditional Chinese medicine. This preparation is used fornourishing blood, eliminating stasis, soothing liver and regulating menstruation, and can also be used to treat menoxenia and dysmenorrhea caus ed by qi stagnation and blood stasis. Objective: In this paper, an accurate and sensitive high-performance liquid chromatog.-diode array detector (HPLC-DAD) method was developed and validated for simultaneous determination of seven active components (gallic acid, paeoniflorin, costunolide, dehydrocostuslactone, rutin, leonurine hydrochloride and ferulic acid) in the traditional Chinese formula-Desheng pills. The seven analytes were separated on Agilent ZORBAX SB-C18 column (250mmx 4.6mm, 5μm) maintained at the temperature of 30. Gradient elution was performed with the mobile phase of methanol (A)-0.1% phosphoric acid solution (B) at the flow rate of 1.0mL·min-1. The anal. was carried out at the wavelength of 225 nm, 256 nm, 277 nm and 320 nm with an injection volume of 10μL. The measured seven components showed good linear relationships within their own concentration ranges along with coefficients of determination ≥0.9996. The limits of detection and quantitation of all analytes were in the range of 0.19-13.51μg/mL and 0.59-40.93μg/mL, resp. Average recoveries ranged from 98.82% to 102.01% with RSDs of 1.47%-1.99%. The content of tested components was in the range of 0.053-0.421 mg/g. Conclusion: The proposed method was found to be sensitive, accurate and reproducible, which provided an effective quant. anal. method for quality control of Desheng pills.

Current Pharmaceutical Analysis published new progress about Chinese medicine (Desheng pill). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Application In Synthesis of 112-63-0.

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

Park, Deborah Y.; Tom, Martin C.; Chen, Yanwen; Tewari, Surabhi; Ahluwalia, Manmeet S.; Yu, Jennifer S.; Chao, Samuel T.; Suh, John H.; Peereboom, David M.; Stevens, Glen H. J.; Barnett, Gene H.; Angelov, Lilyana; Mohammadi, Alireza; Hogan, Thomas; Kissel, Courtney; Lapin, Brittany; Schuermeyer, Isabel; Parsons, Michael W.; Naugle, Richard; Murphy, Erin S. published the artcile< Cognitive function after concurrent temozolomide-based chemoradiation therapy in low-grade gliomas>, Name: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is cognitive function low grade glioma temozolomide chemoradiation therapy; Chemoradiation; Cognitive function; Low grade glioma; Neurocognitive testing; Temozolomide.

We sought to evaluate the effects of concurrent temozolomide-based chemoradiation therapy on neurocognitive function in patients with low-grade glioma (LGG). We included adult patients with LGG who were treated postoperatively with radiotherapy (RT) with concurrent and adjuvant temozolomide (TMZ). Patients were evaluated with comprehensive psychometric tests at baseline (prior to RT + TMZ) and at various time intervals following RT + TMZ. Baseline cognitive performance was analyzed by sex, age, education history, history of seizures, IDH mutation status, and 1p/19q codeletion status. Changes in neurocognitive performance were evaluated over time. Thirty-seven LGG patients (mean age 43.6, 59.5% male) had baseline neurocognitive evaluation. Patients with an age > 40 years old at diagnosis and those with an education > 16 years demonstrated superior baseline verbal memory as assessed by HVLT. No other cognitive domains showed differences when stratified by the variables mentioned above. A total of 22 LGG patients had baseline and post RT + TMZ neurocognitive evaluation. Overall, patients showed no statistical difference between group mean test scores prior to and following RT + TMZ on all psychometric measures (with the exception of HVLT Discrimination). Cognitive function remained stable following RT + TMZ in LGG patients evaluated prospectively up to 2 years. The anticipated anal. of RTOG 0424 will provide valuable neurocognitive outcomes specifically for high risk LGG patients treated with RT + TMZ.

Journal of Neuro-Oncology published new progress about Cancer diagnosis. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Name: (9Z,12Z)-Methyl octadeca-9,12-dienoate.

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

Newar, Rajashree; Begum, Wahida; Akhtar, Naved; Antil, Neha; Chauhan, Manav; Kumar, Ajay; Gupta, Poorvi; Malik, Jaideep; Balendra; Manna, Kuntal published the artcile< Mono-Phosphine Metal-Organic Framework-Supported Cobalt Catalyst for Efficient Borylation Reactions>, Product Details of C19H34O2, the main research area is borylation aromatic compound cobalt metal organic framework catalyst; hydroboration alkene styrene cobalt metal organic framework catalyst; crystal structure phenylphosphine cobalt chloride; mol structure phenylphosphine cobalt chloride; aryl alkyl boronic acid ester preparation.

The authors report a metal-organic framework (MOF) supported monoligated phosphine-Co complex, which is an active heterogeneous catalyst for aromatic C-H borylation and alkene hydroboration. The mono(phosphine)-Co catalyst (MOF-P-Co) was prepared by metalation of a porous triarylphosphine-functionalized MOF (MOF-P) with CoCl2 followed by activation with NaEt3BH. The MOF catalyst has a broad substrate scope with excellent functional group tolerance to afford arene- and alkyl-boronate esters in excellent yields and selectivity. MOF-P-Co gave a turnover number (TON) of 30,000 and could be recycled and reused at least 13 times in arene C-H borylation. Importantly, the attempt to prepare the homogeneous control (Ph3P-Co) using PPh3 was unsuccessful due to the facile disproportionation reactions or intermol. ligand exchanges in the solution In contrast, the site isolation of the active mono(phosphine)-Co species within the MOF affords the robust and coordinatively unsaturated metal complexes, allowing to explore their catalytic properties and the reaction mechanism.

European Journal of Inorganic Chemistry published new progress about Alkenes Role: RCT (Reactant), RACT (Reactant or Reagent). 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

Zhao, Peng; Cai, Zehui; Tian, Yange; Li, Junzi; Li, Kangchen; Li, Minyan; Bai, Yunping; Li, Jiansheng published the artcile< Effective-compound combination inhibits the M2-like polarization of macrophages and attenuates the development of pulmonary fibrosis by increasing autophagy through mTOR signaling>, Category: esters-buliding-blocks, the main research area is polarization macrophage pulmonary fibrosis autophagy mTOR signaling; Autophagy; Effective-compound combination; Macrophage; Pulmonary fibrosis; mTOR signal.

The M2 polarization of macrophages substantially contributes to the progression of pulmonary fibrosis (PF). Effective-compound combination (ECC), which is composed of isoliquiritigenin, icariin, nobiletin, peimine, and paeoniflorin, ameliorated bleomycin-induced PF in rats. Hence, we investigated the anti-PF mechanism of ECC with a focus on the suppression of M2 polarization in macrophages in vivo and in vitro. The PF rat model was generated via the intratracheal instillation of bleomycin. Histol. changes, M2 macrophages, and profibrotic mediators were detected. The M2 polarization model was generated by incubating macrophages with IL-4. Quant. PCR and Western blotting were used to measure mRNA and protein levels, resp. ECC attenuated bleomycin-induced PF in rats, which might be associated with reduced macrophage infiltration, M2 polarization, and profibrotic mediator expression. Furthermore, ECC significantly suppressed M2 polarization in IL-4-treated macrophages, which was accompanied by the upregulation of autophagy. An autophagy inhibitor abrogated the inhibitory effect of ECC on M2 polarization. In addition, ECC decreased the levels of p-p70S6K/p-4EBP and p-AKT473/p-GSK3β, which are critical regulators of autophagy. ECC can ameliorate PF, which might be associated with the inhibition of M2 polarization through the promotion of autophagy via mTOR signaling suppression.

International Immunopharmacology published new progress about Animal tissue. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Category: esters-buliding-blocks.

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

Elham, Ghasemian; Sima, Sadrai; Javad, Shokri; Shahram, Sayadi published the artcile< Analytical method validation, pharmacokinetics and bioequivalence study of dimethyl fumarate in healthy Iranian volunteers>, SDS of cas: 112-63-0, the main research area is validation pharmacokinetics bioequivalence dimethyl fumarate.

Pharmacokinetic evaluation of Di-Me Fumarate (DMF) in the Iranian population wasn’t studied. So, the aim of this research is the validation of the anal. method and evaluation of the pharmacokinetic properties and bioequivalence of the generic form of this drug vs. the reference product. 2 Single-dose, test, and reference DMF products were orally administered to 24 healthy volunteers. The washout period was 28 d between the treatments. Monomethyl fumarate as the metabolite of DMF was analyzed by liquid chromatog.-tandem mass spectrometry (LC-MS/MS) and the method was validated. Also, the pharmacokinetic parameters were calculated for bioequivalence evaluation. The anal. method was validated and linear over the range of 31.25-4000 ng/mL (R2 = 0.997). In addition, the method was precise and accurate in the low, medium, and high concentrations The results indicated that the 2 products had similar pharmacokinetics. Further, the 90% CI of the mean ratios of the test vs. the reference products of the log-transformed area under the concentration-time curve over 10 h (0.99 to 1.02) and peak concentration (0.98 to 1.03) were within the acceptable range of 0.8 to 1.25 and the generic product of DMF could be similar to that of the reference product. The applied anal. method is selective, accurate, precise, and repeatable for the anal. of monomethyl fumarate (MMF) in plasma. Also, the bioequivalence study showed no significant difference between the pharmacokinetic parameters of these 2 products. So, the DMF test product can be claimed to be bioequivalent with the reference product.

International Journal of Pharmacy and Pharmaceutical Sciences published new progress about Drug bioequivalence. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, SDS of cas: 112-63-0.

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

Li, Xiaoning; Li, Yehui; Wang, Xiang; Peng, Qingrui; Hui, Wei; Hu, ·Aiyun; Wang, Haijun published the artcile< Zr-DBS with Sulfonic Group: A Green and Highly Efficient Catalyst for Alcoholysis of Furfuryl Alcohol to Ethyl Levulinate>, Electric Literature of 112-63-0, the main research area is zirconium dodecylbenzenesulfonate alcoholysis catalyst furfuryl alc ethyl levulinate; green chem synergetic effect.

The alcoholysis of furfuryl alc. (FA) produce Et levulinate (EL) plays a crucial role in the field of biomass conversion. In this work, a novel Zr-base catalyst with sulfonic groups in its structure was prepared by the co-precipitation of sodium dodecyl benzene sulfonate and ZrOCl2 (Zr-DBS) under non-toxic conditions. It was found that Zr-DBS has an excellent catalytic performance for this reaction and an EL yield of 95.27% could be achieved. Besides, Zr-DBS could be easily separated from the reaction system and reused at least four times without a significantly decrease in activity. Meanwhile, Zr-DBS was characterized by Fourier transform IR spectroscopy (FT-IR), powder X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), N2 adsorption-desorption, inductively coupled plasma optical emission spectroscopy (ICP-OES) and temperature-programmed desorption of ammonia (NH3-TPD). The main reason for the high catalytic activity of the Zr-DBS was that the synergetic effects of Lewis and Bronsted acid sites and appropriate textural properties.

Catalysis Letters published new progress about Acidity. 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

Krall, Jacob; Jensen, Claus Hatt; Bavo, Francesco; Falk-Petersen, Christina Birkedal; Haugaard, Anne Staehr; Vogensen, Stine Byskov; Tian, Yongsong; Nittegaard-Nielsen, Mia; Sigurdardottir, Sara Bjork; Kehler, Jan; Kongstad, Kenneth Thermann; Gloriam, David E.; Clausen, Rasmus Praetorius; Harpsoee, Kasper; Wellendorph, Petrine; Froelund, Bente published the artcile< Molecular Hybridization of Potent and Selective γ-Hydroxybutyric Acid (GHB) Ligands: Design, Synthesis, Binding Studies, and Molecular Modeling of Novel 3-Hydroxycyclopent-1-enecarboxylic Acid (HOCPCA) and trans-γ-Hydroxycrotonic Acid (T-HCA) Analogs>, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is hydroxybutyric acid ligand preparation binding affinity structure activity relationship; mol modeling hydroxybutyric acid ligand; hydroxycyclopentenecarboxylic acid analog preparation GHB ligand high affinity; hydroxycrotonic acid analog preparation GHB ligand high affinity.

γ-Hydroxybutyric acid (GHB) is a neuroactive substance with specific high-affinity binding sites. To facilitate target identification and ligand optimization, we herein report a comprehensive structure-affinity relationship study for novel ligands targeting these binding sites. A mol. hybridization strategy was used based on the conformationally restricted 3-hydroxycyclopent-1-enecarboxylic acid (HOCPCA) and the linear GHB analog trans-4-hydroxycrotonic acid (T-HCA). In general, all structural modifications performed on HOCPCA led to reduced affinity. In contrast, introduction of diarom. substituents into the 4-position of T-HCA led to high-affinity analogs (medium nanomolar Ki) for the GHB high-affinity binding sites as the most high-affinity analogs reported to date. The SAR data formed the basis for a three-dimensional pharmacophore model for GHB ligands, which identified mol. features important for high-affinity binding, with high predictive validity. These findings will be valuable in the further processes of both target characterization and ligand identification for the high-affinity GHB binding sites.

Journal of Medicinal Chemistry published new progress about Molecular modeling. 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