Category: 112-63-0

Jiang, Haiwei; Yan, Rongwei; Cai, Chang; Chen, Xingfan; Zhao, Fenghua; Fan, Liangliang; Xu, Chunbao Charles; Yang, Weiran published the artcile< Hydrothermal liquefaction of Cd-enriched Amaranthus hypochondriacus L. in ethanol-water co-solvent: Focus on low-N bio-oil and heavy metal/metal-like distribution>, Electric Literature of 112-63-0, the main research area is hydrothermal liquefaction cadmium amaranthus hypochondriacus; ethanol water nitrogen bio oil heavy metal.

The high nitrogen content in bio-oil from protein-rich biomass will cause the possible pollution problems by NOX emissions during combustion. In this study, Cd-enriched Amaranthus hypochondriacus L. (AHL) was treated by hydrothermal liquefaction (HTL) in ethanol-water co-solvent aiming to reduce the nitrogen content of the bio-oil. Besides, aqueous phase recycling (APR) was applied to achieve a higher bio-oil yield. HTL in ethanol-water co-solvent with APR three times resulted in the maximum bio-oil yield (47.26%) and greatly reduced the nitrogenous compounds content of bio-oil. During the APR process, the increase of total nitrogen (TN) content in the aqueous phase indicated that organic-N in the organic phase transformed into NH+4 to the aqueous phase. Acetic acid (13.87-22.37 mg/mL) was dominated in the aqueous phase, leading to a low pH value (6.27-5.29), which could serve as the possible catalyst for the HTL process during APR that can be the reason for the higher bio-oil yield. After the HTL process, Cr, Cu, Cd and Pb remained mostly in bio-char while As was present largely in the aqueous phase. Thus, this study demonstrated that the APR for HTL process in ethanol-water co-solvent can be a hopeful method to dispose the high-protein biomass for improved bio-oil yield and quality.

Fuel published new progress about Alcohols Role: TEM (Technical or Engineered Material Use), USES (Uses). 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

Garcia-Padilla, Carlos; Lozano-Velasco, Estefania; Munoz-Gallardo, Maria del Mar; Castillo-Casas, Juan Manuel; Cano-Carrillo, Sheila; Martinez-Amaro, Francisco Jose; Garcia-Lopez, Virginio; Aranega, Amelia; Franco, Diego; Garcia-Martinez, Virginio; Lopez-Sanchez, Carmen published the artcile< LncRNA H19 Impairs Chemo and Radiotherapy in Tumorigenesis>, Application In Synthesis of 112-63-0, the main research area is review tumorigenesis LncRNA H19 impair chemotherapy radiotherapy; chemo-resistance; lncRNA H19; radio-resistance; tumorigenesis.

A review. Various treatments based on drug administration and radiotherapy have been devoted to preventing, palliating, and defeating cancer, showing high efficiency against the progression of this disease. Recently, in this process, malignant cells have been found which are capable of triggering specific mol. mechanisms against current treatments, with neg. consequences in the prognosis of the disease. It is therefore fundamental to understand the underlying mechanisms, including the genes-and their signaling pathway regulators-involved in the process, in order to fight tumor cells. Long non-coding RNAs, H19 in particular, have been revealed as powerful protective factors in various types of cancer. However, they have also evidenced their oncogenic role in multiple carcinomas, enhancing tumor cell proliferation, migration, and invasion. In this review, we analyze the role of lncRNA H19 impairing chemo and radiotherapy in tumorigenesis, including breast cancer, lung adenocarcinoma, glioma, and colorectal carcinoma.

International Journal of Molecular Sciences published new progress about Antitumor agents. 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

Liu, Jinwei; Li, Xining; Wang, Juntong; Gu, Le; Lv, Guangfu; Lin, Zhe; Zhen, Xiaowen; Li, Yong published the artcile< Study on chemical constituents and antioxidant activity of the flat-European hybrid hazelnut (C. heterophylla Fisch. x C. avellana L.) oil>, Name: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is Corylus oil antioxidant filbertone fatty acid sterol.

Hazelnut oil, extracted from hazelnuts, can be used as a functional food with many nutritional benefits. To completely assess its chem. constituents in hazelnut oil, one main cultivar of a flat-European hybrid hazelnut (C. heterophylla Fisch. x C. avellana L.) cv. ‘Dawei’ was taken as the material, and a new optimized silyl-etherification derivatization was established by being followed with Gas chromatog.-mass spectrometry (GC-MS). Meanwhile, an ESR (ESR) method was used to elucidate the scavenging capacity of free radicals. In result, the filbertone (exclusive marker), 16 fatty acids (8 saturated and 8 unsaturated), 4 sterols and 5 other components were identified at once. Furthermore, hybrid hazelnut oil, filbertone and two sterols that contained in hazelnut oil were used to test the scavenge free radical activities. The results showed that the hybrid hazelnut oil expressed meaningful IC50 values (DPPH: 66.39, hydroxyl: 66.64, alkyl: 118.82 and O2-: 75.38μg/mL). In conclusion, this study selected an effective derivatization method for the chem. constituents detection, and provided detailed data, which laid an exptl. foundation for quality control of a hybrid hazelnut oil. In addition, the free radical scavenging activity was observed, which provided a basis for the development of antioxidant products in hybrid hazelnut oil.

Journal of Biobased Materials and Bioenergy published new progress about Antioxidants. 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

Tatum, James L.; Kalen, Joseph D.; Jacobs, Paula M.; Riffle, Lisa A.; James, Amy; Thang, Lai; Sanders, Chelsea; Hollingshead, Melinda G.; Basuli, Falguni; Shi, Jianfeng; Doroshow, James H. published the artcile< 3′-[18F]fluoro-3′-deoxythymidine ([18F]FLT) Positron Emission Tomography as an In Vivo Biomarker of inhibition of CDK 4/6-Rb pathway by Palbociclib in a patient derived bladder tumor>, Application of C19H34O2, the main research area is CDK4/6; FLT PET; Imaging biomarkers; Palbociclib; Response biomarker.

Abstract: Background: Several new generation CDK4/6 inhibitors have been developed and approved for breast cancer therapy in combination with endocrine therapeutics. Application of these inhibitors either alone or in combination in other solid tumors has been proposed, but no imaging biomarkers of response have been reported in non-breast cancer animal models. The purpose of this study was to evaluate 3′-[18F]fluoro-3′-deoxythymidine ([18F]FLT) Positron Emission Tomog. (PET) as in vivo biomarker of response to palbociclib in a non-breast cancer model. Methods: Twenty-four NSG mice bearing patient derived xenografts (PDX) of a well-characterized bladder tumor were randomized into 4 treatment groups: vehicle (n = 6); palbociclib (n = 6); temozolomide (n = 6); and palbociclib plus temozolomide (n = 6) and treated with two cycles of therapy or vehicle. Tumor uptake of [18F]FLT was determined by micro-PET/CT at baseline, 3 days, and 9 days post initiation of therapy. Following the second cycle of therapy, the mice were maintained until their tumors reached a size requiring humane termination. Results: [18F]FLT uptake decreased significantly in the palbociclib and combination arms (p = 0.0423 and 0.0106 resp. at day 3 and 0.0012 and 0.0031 at day 9) with stable tumor volume In the temozolomide arm [18F]FLT uptake increased with day 9 uptake significantly different than baseline (p = 0.0418) and progressive tumor growth was observed during the treatment phase. All groups exhibited progressive disease after day 22, 10 days following cessation of therapy. Conclusion: Significant decreases in [18F]FLT uptake as early as three days post initiation of therapy with palbociclib, alone or in combination with temozolomide, in this bladder cancer model correlates with an absence of tumor growth during therapy that persists until day 18 for the palbociclib group and day 22 for the combination group (6 days and 10 days) following cessation of therapy. These results support early modulation of [18F]FLT as an in vivo biomarker predictive of palbociclib therapy response in a non-breast cancer model.

Journal of Translational Medicine published new progress about 112-63-0. 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

Lin, Songwen; Wang, Chunyang; Ji, Ming; Wu, Deyu; Lv, Yuanhao; Sheng, Li; Han, Fangbin; Dong, Yi; Zhang, Kehui; Yang, Yakun; Li, Yan; Chen, Xiaoguang; Xu, Heng published the artcile< Discovery of new thienopyrimidine derivatives as potent and orally efficacious phosphoinositide 3-kinase inhibitors>, Category: esters-buliding-blocks, the main research area is thienopyrimidine synthesis antitumor SAR pharmacokinetics phosphoinositide kinase PI3K; Acetylation; Anti-tumor activities; Phosphoinositide 3-kinase inhibitors; Thienopyrimidine.

A series of new thienopyrimidine derivatives has been discovered as potent PI3K inhibitors. The systematic SAR studies for these analogs are described. Among them, I and II exhibit nanomolar enzymic potencies and sub-micromolar cellular anti-proliferative activities. I displays favorable pharmacokinetic profiles, while II easily undergoes deacetylation to yield a major metabolite I. Furthermore, I and II potently inhibit tumor growth in a dose-dependent manner in the NCI-H460 xenograft model with an acceptable safety profile.

Bioorganic & Medicinal Chemistry published new progress about Acetylation. 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

Go, Wooseok; Kim, Jongwoo; Pyo, Jinho; Wolfenstine, Jeffrey B.; Kim, Youngsik published the artcile< Investigation on the Structure and Properties of Na3.1Zr1.55Si2.3P0.7O11 as a Solid Electrolyte and Its Application in a Seawater Battery>, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is sodium superionic conductor solid electrolyte seawater battery; NASICON; ceramic; ionic conductivity; seawater battery; solid electrolyte.

The ionic conductivity, bend strength, and electrochem. performance in a seawater battery (SWB) of an Na3.1Zr1.55Si2.3P0.7O11 (vA-NASICON) solid electrolyte were compared to those of Na3Zr2Si2PO12 (H-NASICON). vA-NASICON exhibited three times higher total ionic conductivity (8.6 x 10-4 S/cm) than H-NASICON (2.9 x 10-4 S/cm). This is due to the higher bulk ionic conductivity and lower grain boundary resistance of vA-NASICON. The higher bulk conductivity of vA-NASICON is a result of its higher Na content, leading to a larger concentration of charge carriers and/or the formation of a higher conductive rhombohedral phase. The lower grain boundary resistance of vA-NASICON is a result of its larger grain size and reduced ZrO2 content. The bend strength of vA-NASICON (95 MPa) was 30% higher than that of the H-NASICON ceramic. The higher bend strength of vA-NASICON was attributed to its reduced ZrO2 secondary phase (1.1 vol %) compared to that of H-NASICON (2.6 vol %). When the vA-NASICON ceramic was tested in the SWB as a solid electrolyte, an 8.27% improved voltage efficiency and 81% higher power output were demonstrated, compared to those of H-NASICON, as a result of its higher total ionic conductivity and mech. strength. At the same time, the vA-NASICON membrane revealed comparable cycle life (1000 h) to that of H-NASICON. These results suggest that vA-NASICON can be a better alternative than H-NASICON for use in the SWB.

ACS Applied Materials & Interfaces published new progress about Ball milling. 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

Wen, Jie; Zhang, Xiaopeng; Pan, Mingwang; Yuan, Jinfeng; Jia, Zhanyu; Zhu, Lei published the artcile< A robust, tough and multifunctional polyurethane/tannic acid hydrogel fabricated by physical-chemical dual crosslinking>, Application of C19H34O2, the main research area is polyurethane tannic acid hydrogel fabricated robust tough property; double crosslinking; mechanical properties; multifunction; polyurethane hydrogel; tannic acid.

Commonly synthetic polyethylene glycol polyurethane (PEG-PU) hydrogels possess poor mech. properties, such as robustness and toughness, which limits their load-bearing application. Hence, it remains a challenge to prepare PEG-PU hydrogels with excellent mech. properties. Herein, a novel double-crosslinked (DC) PEG-PU hydrogel was fabricated by combining chem. with phys. crosslinking, where trimethylolpropane (TMP) was used as the first chem. crosslinker and polyphenol compound tannic acid (TA) was introduced into the single crosslinked PU network by simple immersion process. The second phys. crosslinking was formed by numerous hydrogen bonds between urethane groups of PU and phenol hydroxyl groups in TA, which can endow PEG-PU hydrogel with good mech. properties, self-recovery and a self-healing capability. The research results indicated that as little as a 30 mg·mL-1 TA solution enhanced the tensile strength and fracture energy of PEG-PU hydrogel from 0.27 to 2.2 MPa, 2.0 to 9.6 KJ·m-2, resp. Moreover, the DC PEG-PU hydrogel possessed good adhesiveness to diverse substrates because of TA abundant catechol groups. This work shows a simple and versatile method to prepare a multifunctional DC single network PEG-PU hydrogel with excellent mech. properties, and is expected to facilitate developments in the biomedical field.

Polymers (Basel, Switzerland) published new progress about Adhesives. 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

Patra, Atanu; Gelat, Fabien; Pannecoucke, Xavier; Poisson, Thomas; Besset, Tatiana; Biju, Akkattu T. published the artcile< Synthesis of 4-Difluoromethylquinolines by NHC-Catalyzed Umpolung of Imines>, Computed Properties of 112-63-0, the main research area is aldimine preparation heterocyclic carbene catalyzed umpolung intramol cyclization; fluoromethylquinoline preparation; benzaldehyde condensation fluoropropenylaniline.

The N-heterocyclic carbene (NHC)-catalyzed umpolung of aldimines for the synthesis of 4-difluoromethylquinoline derivatives is reported. In the presence of NHCs, the intramol. cyclization of aldimines bearing a moderately electron-poor double bond due to the presence of the -CF3 group likely proceeds via the intermediacy of the aza-Breslow intermediate. The key to the success of this aza-Stetter type transformation is the NHC generated from the bicyclic triazolium salt using DBU as the base.

Organic Letters published new progress about Aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 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

Watanabe, Yutaka; Hirofuji, Hajimu; Ozaki, Shoichiro published the artcile< Synthesis of a phosphatidylinositol 3,4,5-trisphosphate>, Related Products of 112-63-0, the main research area is phosphatidylinositol trisphosphate; distearylglycerol phosphite regioselective phosphorylation inositol.

A phosphatidylinositol 3,4,5-trisphosphate I (R = R1) was synthesized from myo-inositol via regioselective phosphorylation of inositol I (R = H) with dibenzyl 1,2-distearyl-sn-glycerol phosphite.

Tetrahedron Letters published new progress about Phosphorylation. 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

Cotrina, Ellen Y.; Pinto, Marta; Bosch, Lluis; Vila, Marta; Blasi, Daniel; Quintana, Jordi; Centeno, Nuria B.; Arsequell, Gemma; Planas, Antoni; Valencia, Gregorio published the artcile< Modulation of the Fibrillogenesis Inhibition Properties of Two Transthyretin Ligands by Halogenation>, Product Details of C19H34O2, the main research area is fibrillogenesis transthyretin ligand halogenation.

The amyloidogenic protein transthyretin (TTR) is thought to aggregate into amyloid fibrils by tetramer dissociation which can be inhibited by a number of small mol. compounds Our anal. of a series of crystallog. protein-inhibitor complexes has shown no clear correlation between the observed mol. interactions and the in vitro activity of the inhibitors. From this anal., it emerged that halogen bonding (XB) could be mediating some key interactions. Anal. of the halogenated derivatives of two well-known TTR inhibitors has shown that while flufenamic acid affinity for TTR was unchanged by halogenation, diflunisal gradually improves binding up to 1 order of magnitude after iodination through interactions that can be interpreted as a suboptimal XB (carbonyl Thr106: I…O distance 3.96-4.05 Å; C-I…O angle 152-156°) or as rather optimized van der Waals contacts or as a mixture of both. These results illustrate the potential of halogenation strategies in designing and optimizing TTR fibrillogenesis inhibitors.

Journal of Medicinal Chemistry published new progress about Drug design. 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