Tag: M.W=250-300

Ghalib, Raza Murad; Hashim, Rokiah; Sulaiman, Othman; Mehdi, Sayed Hasan; Anis, Zurida; Rahman, Syed Ziaur; Ahamed, B. M. Khadeer; Abdul Majid, Amin Malik Shah published the artcile< Phytochemical analysis, cytotoxic activity and constituents-activity relationships of the leaves of Cinnamomum iners (Reinw. ex Blume-Lauraceae)>, SDS of cas: 112-63-0, the main research area is Cinnamomum antitumor leaf tumor.

The leaves of Cinnamomum iners (Reinw. ex Blume-Lauraceae) have been refluxed successively with chloroform and alc. to get chloroform extract and alc. extract Both the extracts have been assayed for cytotoxicity against human colorectal tumor cells. The chloroform extract exhibited significant cytotoxicity with IC50 31 μg mL-1 (p < 0.01). However, ethanol extract was found to be much less cytotoxic with IC50 > 200 μg mL-1. The chloroform extract has been further proceeded for chem. anal. by GC-TOFMS and 178 components were identified including acids, amines, amides, aldehydes, alcs., esters, benzene derivatives, bicyclic compounds, terpenes, hydrocarbons, naphthalene derivatives, furan derivatives, azulenes, etc. Nine components representing 51.73% of the total chloroform extract were detected as major components. Caryophyllene (14.41%) and Eicosanoic acid Et ester (12.17%) are the most prominent components of the chloroform extract Components of the chloroform extract β-Caryophyllene (14.41%) as most abundant compound supports potent cytotoxicity as shown by chloroform extract

Natural Product Research published new progress about Antitumor agents. 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

Rehman, Fawad Ur; Liu, Yang; Yang, Qingshan; Yang, Haoying; Liu, Runhan; Zhang, Dongya; Muhammad, Pir; Liu, Yanjie; Hanif, Sumaira; Ismail, Muhammad; Zheng, Meng; Shi, Bingyang published the artcile< Heme Oxygenase-1 targeting exosomes for temozolomide resistant glioblastoma synergistic therapy>, Safety of (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is glioblastoma synergistic therapy heme oxygenase exosome; Exosome; Glioblastoma; HMOX1; Temozolomide resistance; siRNA.

Glioblastoma (GBM) is a highly fatal and recurrent brain cancer without a complete prevailing remedy. Although the synthetic nanotechnol.-based approaches exhibit excellent therapeutic potential, the associated cytotoxic effects and organ clearance failure rest major obstacles from bench to clinics. Here, we explored allogeneic bone marrow mesenchymal stem cells isolated exosomes (BMSCExo) decorated with heme oxygenase-1 (HMOX1) specific short peptide (HSSP) as temozolomide (TMZ) and small interfering RNA (siRNA) nanocarrier for TMZ resistant glioblastoma therapy. The BMSCExo had excellent TMZ and siRNA loading ability and could traverse the blood-brain barrier (BBB) by leveraging its intrinsic brain accumulation property. Notably, with HSSP decoration, the TMZ or siRNA encapsulated BMSCExo exhibited excellent TMZ resistant GBM targeting ability both in vitro and in vivo due to the overexpression of HMOX1 in TMZ resistant GBM cells. Further, the HSSP decorated BMSCExo delivered the STAT3 targeted siRNA to the TMZ resistant glioma and restore the TMZ sensitivity, consequently achieved the synergistically drug resistant GBM treatment with TMZ. Our results showed this biomimetic nanoplatform can serve as a flexible, robust and inert system for GBM treatment, especially emphasizing the drug resistant challenge.

Journal of Controlled Release published new progress about Antibiotic resistance. 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

Ma, Zhiwei; Liu, Xiaofeng; Liu, Juntao; Tao, Jingchao published the artcile< Highly enantioselective Michael addition catalyzed by new primary amine-squaramide organocatalysts>, Electric Literature of 112-63-0, the main research area is enantioselective Michael addition primary amine squaramide organocatalyst.

The asym. Michael addition reaction of α,α-disubstituted aldehydes to maleimides catalyzed by new bifunctional primary amine-squaramides has been developed. This organocatalytic asym. reaction provides easy access to functionalized succinimides with a broad substrate scope. Both enantiomers of desired succinimide derivatives were obtained in good to excellent yields (up to 98%) with excellent enantioselectivities (up to > 99% ee).

Youji Huaxue published new progress about Michael reaction. 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

Chen, Qiling; Hao, Nan; Zhao, Lili; Yang, Xiangke; Yuan, Yuxin; Zhao, Yuzhu; Wang, Fu; Qiu, Zuobing; He, Ling; Shi, Kan; Liu, Shuwen published the artcile< Comparative functional analysis of malate metabolism genes in Oenococcus oeni and Lactiplantibacillus plantarum at low pH and their roles in acid stress response>, SDS of cas: 112-63-0, the main research area is Oenococcus Lactiplantibacillus pH acid stress response malate metabolism gene; Lactiplantibacillus plantarum; Malate metabolism; Malic enzyme; Malolactic enzyme; Oenococcus oeni.

Oenococcus oeni and Lactiplantibacillus plantarum are major wine-associated lactic acid bacteria that pos. influence wine by carrying out malolactic fermentation O. oeni is the most widely used com. starter in winemaking because of its fast and efficient malate metabolism capacity under harsh wine conditions. To date, very little is known about the specific mol. mechanism underlying the differences in malate metabolism between O. oeni and L. plantarum under harsh wine conditions. Therefore, in this study, the functions of genes encoding malic enzyme (ME) and malolactic enzyme (MLE) under acid stress in O. oeni and L. plantarum, previously described to have the ability to direct malate metabolism, were comparatively verified through genetic manipulation in L. plantarum. Results showed that the MLE was the only enzyme responsible for direct malate metabolism under acid stress in O. oeni and L. plantarum. In addition, the MLEs in O. oeni and L. plantarum were pos. related to acid tolerance by metabolizing malate and increasing the medium pH. Furthermore, the MLE in O. oeni exhibited significantly higher malate metabolism activity than that in L. plantarum under acid stress.

Food Research International published new progress about Cell viability. 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

Reinerte, Sanita; Avotina, Liga; Zarins, Arturs; Cabulis, Ugis; Viksna, Arturs published the artcile< TG/DTA-FTIR as a method for analysis of tall oil based rigid polyurethane foam decomposition gaseous products in a low oxygen environment>, HPLC of Formula: 112-63-0, the main research area is tall oil rigid polyurethane foam decomposition gaseous oxygen.

This study is an investigation of the suitability of the thermogravimetry and DTA method coupled with Fourier Transform IR spectrometry (TG/DTA-FTIR) for a thermal degradation gaseous product anal. of a rigid polyurethane-polyisocyanurate (PU-PIR) foam synthesized from high functionality tall oil fatty acids (TOFA) based polyols. The FTIR spectra of the TG-generated gaseous thermal degradation products of three PU-PIR formulations with varied high functionality TO based polyol content (45, 75 and 95 pbw) and a different tier of isocyanate (NCO) indexes (110, 150, 200, 300 and 400) for each formulation were compared to the spectra of a formulation developed using conventional raw materials. The chem. bands of known chem. compounds and unknown compounds containing specific groups for the foams were evaluated; the focus was on the maximum release rate for specific chem. compounds (CO2; -NCO; H2O; C=O) to determine the temperature zone values of the main thermal degradation phases. The experiments were carried out at a low oxygen environment, providing valuable data on the trends for the excretion of specific gaseous substances from the rigid PU-PUR foam that could be released in a real fire, where organic building materials that possess a porous matrix might be present and the nature of the combustion process is predominantly heterogeneous oxidation

Polymer Degradation and Stability published new progress about Combustion. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, HPLC of Formula: 112-63-0.

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

Bates, Gareth W.; Triyanti; Light, Mark E.; Albrecht, Markus; Gale, Philip A. published the artcile< 2,7-Functionalized Indoles as Receptors for Anions>, Product Details of C19H34O2, the main research area is indole carboxamide amido ureido thioureido preparation structure anion complexation; stability constant phosphate carboxylate chloride amido ureido thioureido indolecarboxamide; titration NMR anion complexation indolecarboxamide amido ureido thioureido derivative; hydrogen bond phosphate carboxylate indolecarboxamide amido ureido thioureido derivative; crystal structure indolecarboxamide amido ureido thioureido derivative; mol structure indolecarboxamide amido ureido thioureido derivative.

A series of 7-amido- and 7-ureido- and 7-thioureido-1H-indole-2-carboxamide derivatives were prepared by reduction and acylation of the corresponding 7-nitro-1H-indolecarboxamides; the compounds exhibit binding properties towards dihydrophosphate, acetate, benzoate and chloride ions. Amidation of 7-nitro-1H-indole-2-carboxylic acid by amines RNH2 gave N-R-7-nitro-1H-indole-2-carboxamides (8a,b; R = Bu, Ph), which were reduced to the corresponding N-R-7-amino-1H-indole-2-carboxamides (9a,b). Reaction of 9a,b with BuCOCl, PhCOCl, PhCH2COCl, BuNCO, PhNCO and PhNCS gave N-R-7-R1NH-1H-indole-2-carboxamides (1 R = Bu, R1 = BuCO; 2 R = Ph, R1 = PhCO; 3 R = Ph, R1 = PhCH2CO; 4 R = Bu, R1 = BuNHCO; 5 R = Ph, R1 = PhNHCO, 6 R = Ph, R1 = PhNHCS). Stability constants were measured in aqueous solution for complexation of 1-6 with H2PO4-, MeCO2-, PhCO2- and Cl- anions. Anion complexation studies show a marked difference in the mode of interaction of carboxylates with indole-ureas vs. indole-amides.

Journal of Organic Chemistry published new progress about Acylation. 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

Chen, Zhaoyan; Tian, Fangyuan; Chen, Xi published the artcile< Cost-Effectiveness Analysis of a Three-Drug Regimen Containing Bevacizumab for the Treatment of Recurrent Pediatric Medulloblastoma in China: Based on a COG Randomized Phase II Screening Trial.>, Application of C19H34O2, the main research area is bevacizumab; cost-effectiveness; irinotecan; recurrent pediatric medulloblastoma; temozolomide.

Background: Medulloblastoma is the most common malignant brain tumor of childhood, accounting for 6 to 7 percent of all childhood CNS tumors. The purpose of this study was to evaluate the economic efficacy of a bevacizumab combined with temozolomide + irinotecan regimen for the treatment of recurrent pediatric medulloblastoma in China. Methods: The data analyzed were from a randomized phase II screening trial that showed an improved survival benefit in child patients with recurrent medulloblastoma treated with a T+I+B combination regimen. A Markov model is constructed to estimate the incremental cost-effectiveness ratio (ICER) from the perspective of Chinese society. The uncertainty in the model is solved by one-way certainty and probabilistic sensitivity analysis. Results: Our base case analysis showed that the total costs of treatment increased from $8,786.403 to $27,603.420 with the combination bevacizumab vs. the two-agent chemotherapy regimen. Treatment with T+I+B combination therapy was associated with an increase in effectiveness of 0.280 QALYs from 0.867 to 1.147 QALYs T+I regimen. The incremental cost-effectiveness ratio was $67,203.632/QALY, which exceeded our pre-specified willingness-to-pay threshold ($38,136.26/QALY). Cost changes associated with grade 3-4 AE management, tests used, or hospitalization costs had little effect on the ICER values predicted by sensitivity analysis. Conclusions: Taken together, the results of this study suggest that the combination of bevacizumab with temozolomide and irinotecan is not a cost-effective option from the perspective of Chinese payers as a first-line treatment option for children with recurrent medulloblastoma in China.

Frontiers in public health 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

Flores-Romero, Hector; Hohorst, Lisa; John, Malina; Albert, Marie-Christine; King, Louise E.; Beckmann, Laura; Szabo, Tamas; Hertlein, Vanessa; Luo, Xu; Villunger, Andreas; Frenzel, Lukas P.; Kashkar, Hamid; Garcia-Saez, Ana J. published the artcile< BCL-2-family protein tBID can act as a BAX-like effector of apoptosis>, Application of C15H22N2O2, the main research area is tBID BAX BCL2 BCL2A1 TRAIL immunity Shigella necrosulfonamide apoptosis; BCL-2 proteins; apoptosis; mitochondrial permeabilization; pore formation.

During apoptosis, the BCL-2-family protein tBID promotes mitochondrial permeabilization by activating BAX and BAK and by blocking anti-apoptotic BCL-2 members. Here, we report that tBID can also mediate mitochondrial permeabilization by itself, resulting in release of cytochrome c and mitochondrial DNA, caspase activation and apoptosis even in absence of BAX and BAK. This previously unrecognized activity of tBID depends on helix 6, homologous to the pore-forming regions of BAX and BAK, and can be blocked by pro-survival BCL-2 proteins. Importantly, tBID-mediated mitochondrial permeabilization independent of BAX and BAK is physiol. relevant for SMAC release in the immune response against Shigella infection. Furthermore, it can be exploited to kill leukemia cells with acquired venetoclax resistance due to lack of active BAX and BAK. Our findings define tBID as an effector of mitochondrial permeabilization in apoptosis and provide a new paradigm for BCL-2 proteins, with implications for anti-bacterial immunity and cancer therapy.

EMBO Journal published new progress about Ablation (genetic ablation). 347174-05-4 belongs to class esters-buliding-blocks, and the molecular formula is C15H22N2O2, Application of C15H22N2O2.

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

Jonsson, Erlendur; Ellison, James H. J.; Wang, Evelyna; Kunz, Vera; Liu, Tao; Temprano, Israel; Grey, Clare P. published the artcile< On the solvation of redox mediators and implications for their reactivity in Li-air batteries>, Reference of 112-63-0, the main research area is triethylphosphine oxide tetraglyme solvation lithium air battery.

Lithium-air batteries are a promising energy storage technol. for transport applications, given their exceptionally high energy d. However, their development is significantly hampered by high overpotentials, which lead to poor efficiency and short lifetimes. Redox mediators provide a solution to this problem by shuttling electrons from the electrode to the active species at just above the redox potential of the mediator. Thus, knowing the redox potential and having the ability to tune it are critical to electrochem. performance. We focus on LiI as a model mediator-given its addnl. role in controlling LiOH vs Li2O2 chem.-and use cyclic voltammetry (CV), NMR, UV/Vis spectrometry, and mol. dynamics (MD) simulations to monitor the effects of electrolyte composition on solvation. Li+ and I- solvation in common Li-air solvents, the electrochem. implications, and the applicability of each technique to probe the nature of the solvation shell and its effect on the electrochem. properties are explored. Starting with a simple thermodn. model, we then used UV/Vis spectrometry to probe I- solvation, 1H NMR spectroscopy to study water solvation and 31P of the probe mol. triethylphosphine oxide (TEPO) to explore Li+ solvation; we find that no single descriptor can provide an accurate description of the solvation environment. Instead, we use all these methods in combination with the MD results to help rationalize the CV data. We find that the I- solvation improves significantly in tetraglyme (G4), with increasing salt and water concentration, but minimal effects on changing salt/water concentrations are seen in DMSO. In contrast, increasing salt concentration increases the Li+ activity in DMSO but not in G4. Furthermore, a simple model considering the equilibrium between the different species was used to explain the 1H NMR data.

Journal of the Electrochemical Society published new progress about Battery anodes. 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

Serafim, Rodolfo Bortolozo; Cardoso, Cibele; Arfelli, Vanessa Cristina; Valente, Valeria; Archangelo, Leticia Frohlich published the artcile< PIMREG expression level predicts glioblastoma patient survival and affects temozolomide resistance and DNA damage response>, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is GLI1 PIMERG DNA damage glioblastoma; ATM; ATR; DNA damage response; GBM; Gliomas; Temozolomide resistance.

PIMREG expression strongly correlates with cellular proliferation in both malignant and normal cells. Throughout embryo development, PIMREG expression is prominent in the central nervous system. Recent studies have described elevated PIMREG expression in different types of tumors, which correlates with patient survival and tumor aggressiveness. Given the emerging significance of PIMREG in carcinogenesis and its putative role in the context of the nervous system, we investigated the expression and function of PIMREG in gliomas, the most common primary brain tumors. We performed an extensive anal. of PIMREG expression in tumors samples from glioma patients. We then assessed the effects of PIMREG silencing and overexpression on the sensitivity of glioblastoma cell lines treated with genotoxic agents commonly used for treating patients and assessed for treatment response, proliferation and migration. Our anal. shows that glioblastoma exhibits the highest levels of PIMREG expression among all cancers analyzed and that elevated PIMREG expression is a biomarker for glioma progression and patient outcome. Moreover, PIMREG is induced by genotoxic agents, and its silencing renders glioblastoma cells sensitive to temozolomide treatment and affects ATR- and ATM-dependent signaling. Our data demonstrate that PIMREG is involved in DNA damage response and temozolomide resistance of glioblastoma cells and further supports a role for PIMREG in tumorigenesis.

Biochimica et Biophysica Acta, Molecular Basis of Disease published new progress about Apoptosis. 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