Month: November 2022

Copcu, Burcu; Sayin, Koray; Karakas, Duran published the artcile< Investigations substituent effect on structural, spectral and optical properties of phenylboronic acids>, Related Products of 112-63-0, the main research area is phenylboronic acid substituent effect spectral optical property.

Ortho- and para-substituent arylboronic acid are investigated. Geometric structure and structural properties of these compounds are done. IR and NMR spectrum are calculated for the spectral characterizations. Contour diagram of frontier MOs which are HOMO and LUMO is calculated and mol. electrostatic potential (MEP) map of them are obtained to evaluate the electronic properties and to determine the active site on the mols. Non-linear optical (NLO) properties are investigated. UV-VIS spectrum of studied compounds is calculated and the wavelength of main band is examined Then, some quantum chem. parameters which are total static dipole moment, the average linear polarizability, the anisotropy of the polarizability and first hyperpolarizability are calculated and it was found that B3 is the best NLO material for applications.

Journal of Molecular Structure published new progress about Anisotropy. 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

Vidomanova, Eva; Majercikova, Zuzana; Dibdiakova, Katarina; Pilchova, Ivana; Racay, Peter; Hatok, Jozef published the artcile< The effect of temozolomide on apoptosis-related gene expression changes in glioblastoma cells.>, Synthetic Route of 112-63-0, the main research area is apoptosis; glioblastoma; temozolomide gene expression..

BACKGROUND: Glioblastoma (GB) is the most common and biologically the most aggressive primary brain tumor of the central nervous system (CNS) in adults. Standard treatment for newly diagnosed GB consists of surgical resection, radiotherapy, and chemotherapy with temozolomide (TMZ). Despite numbers of studies, a resistance to chemotherapy is the major obstacle to successful GB treatment. OBJECTIVES: The aim of our study was to detect the sensitivity of glioblastoma T98G cells to TMZ treatment and subsequently to determine the expression changes of apoptosis-associated genes in glioblastoma cells. MATERIAL AND METHODS: The human glioblastoma cell line (T98G) was treated with specified concentrations of TMZ during different time periods. Their viability was measured by colorimetric MTT assay and the activation of the apoptotic pathway was determined by measuring the caspase 3/7 activity. Commercial pre-designed microfluidic array was used to quantify expression of human apoptosis-associated genes. RESULTS: The untreated control of T98G cell line against human brain total RNA standards reported significant changes in several apoptotic genes expression levels. We identified also a deregulation in geneexpression levels between the TMZ treated and untreated T98G cells associated with apoptotic pathways. After 48 hours of exposure of T98G cells to TMZ, we observed a significant deregulation ofseven genes: BBC3, BCL2L1, RIPK1, CASP3, BIRC2, CARD6 and DAPK1. These results can contribute to the importance of apoptosis in glioblastoma cells metabolism and effect of TMZ treatment. CONCLUSIONS: Identification of apoptotic gene panel in T98G cell line could help to improve understanding of brain tumor cells metabolism. Recognizing of the pro-apoptotic and anti-apoptotic genes expression changes could contribute to clarify the sensitivity to TMZ therapy and molecular base in healthy and tumor cells (Tab. 1, Fig. 2, Reference 48).

Bratislavske lekarske listy published new progress about 112-63-0. 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

Ramchandani, Shanaya; Mohan, Chakrabhavi Dhananjaya; Mistry, Jenaifer Rustom; Su, Qi; Naz, Irum; Rangappa, Kanchugarakoppal S.; Ahn, Kwang Seok published the artcile< The multifaceted antineoplastic role of pyrimethamine against human malignancies>, SDS of cas: 112-63-0, the main research area is review cancer chronic lymphocytic leukemia pyrimethamine anticancer drug; MAPK; STAT3; apoptosis; cancer; drug repurposing; pyrimethamine.

A review. Cancer accounted for nearly 10 million deaths in 2020 and is the second leading cause of death worldwide. The chemotherapeutic agents that are in clin. practice possess a broad range of severe adverse effects towards vital organs which emphasizes the importance of the discovery of new therapeutic agents or repurposing of existing drugs for the treatment of human cancers. Pyrimethamine is an antiparasitic drug used for the treatment of malaria and toxoplasmosis with a well-documented excellent safety profile. In the last 5 years, numerous efforts have been made to explore the anticancer potential of pyrimethamine in in vitro and in vivo preclin. models and to repurpose it as an anticancer agent. The studies have demonstrated that pyrimethamine inhibits oncogenic proteins such as STAT3, NF-κB, DX2, MAPK, DHFR, thymidine phosphorylase, telomerase, and many more in a different types of cancer models. Moreover, pyrimethamine has been reported to work in synergy with other anticancer agents, such as temozolomide, to induce apoptosis of tumor cells. Recently, the results of phase-1/2 clin. trials demonstrated that pyrimethamine administration reduces the expression of STAT3 signature genes in tumor tissues of chronic lymphocytic leukemia patients with a good therapeutic response. In the present article, we have reviewed most of the published articles related to the antitumor effects of pyrimethamine in malignancies of breast, liver, lung, skin, ovary, prostate, pituitary, and leukemia in in vitro and in vivo settings. We have also discussed the pharmacokinetic profile and results of clin. trials obtained after pyrimethamine treatment. From these studies, we believe that pyrimethamine has the potential to be repurposed as an anticancer drug.

IUBMB Life published new progress about Animal gene, DHFR Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 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

Yamaguchi, Akihiro; Okazaki, Mitsuo published the artcile< Modified wittig reaction. II. Preparation of α-bromo-4-nitrostilbenes and diphenylacetylenes>, Application In Synthesis of 112-63-0, the main research area is stilbene halo nitro; halonitrostilbene preparation Wittig; nitrohalostilbene preparation Wittig; Wittig aldehyde halobenzylphosphonate; aromatic aldehyde Wittig reaction; phosphonate haloenzyl Wittig reaction; arylnitrophenylacetylene preparation Wittig.

α-Bromo-4-nitrostilbenes and diphenylacetylenes were prepared by a modified Wittig reaction. Diethyl α-bromo-p-nitrobenzylphosphonate (I) was obtained quant. by bromination of diethyl p-nitrobenzylphosphonate. Treatment of I with aromatic aldehydes in the presence of an equivalent amount of Na alkoxide in alc. at room temperature gave the corresponding α-bromo-4-nitrostilbenes in good yield. The use of two equivalent base gave diphenylacetylenes. Similarly, the reaction of α-iodo-p-nitrobenzylphosphonate with aromatic aldehydes was investigated.

Nippon Kagaku Kaishi 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, Application In Synthesis of 112-63-0.

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

Wiesler, Stefan; Bau, Michael A.; Niepel, Thomas; Younas, Sara L.; Luu, Hieu-Trinh; Streuff, Jan published the artcile< Synthesis of α,ω-Bis-Enones by the Double Addition of Alkenyl Grignard Reagents to Diacid Weinreb Amides>, Safety of (S)-Dimethyl 2-hydroxysuccinate, the main research area is enone preparation double addition alkenyl Grignard diacid Weinreb amide.

An efficient double addition of substituted alkenylmagnesium bromides to bis-Weinreb amides has been developed, giving α,ω-bis-enones that are building blocks for certain drugs and polymers. Furthermore, reliable protocols for the preparation of the required substituted alkenylmagnesium reagents from substituted non-activated alkenyl bromides are reported. The double addition is demonstrated on 25 examples, including enantiopure as well as conjugated and cross-conjugated bis-enones. The addition to a cyclohexane-1,2-dicarboxamide was found to lead to a selective mono addition, giving access to cyclohexyl γ-ketoamides that are core motifs of several pharmaceutical agents and promising drug candidates.

European Journal of Organic Chemistry published new progress about Addition reaction (double). 617-55-0 belongs to class esters-buliding-blocks, and the molecular formula is C6H10O5, Safety of (S)-Dimethyl 2-hydroxysuccinate.

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

Xi, Yumeng; Su, Bo; Qi, Xiaotian; Pedram, Shayun; Liu, Peng; Hartwig, John F. published the artcile< Application of Trimethylgermanyl-Substituted Bisphosphine Ligands with Enhanced Dispersion Interactions to Copper-Catalyzed Hydroboration of Disubstituted Alkenes>, Product Details of C19H34O2, the main research area is germanyl bisphosphine ligand preparation copper catalyzed hydroboration disubstituted alkene; free energy olefin hydrocupration germanyl bisphosphine ligand transition state.

The authors report the incorporation of large substituents based on heavy main group elements that are atypical in ligand architectures to enhance dispersion interactions and, thereby, enhance enantioselectivity. Specifically, the authors prepared the chiral biaryl bisphosphine ligand (TMG-SYNPHOS) containing 3,5-bis(trimethylgermanyl)phenyl groups on P and applied this ligand to the challenging problem of enantioselective hydrofunctionalization reactions of 1,1-disubstituted alkenes. Indeed, TMG-SYNPHOS forms a Cu complex that catalyzes hydroboration of 1,1-disubstituted alkenes with high levels of enantioselectivity, even when the two substituents are both primary alkyl groups. Cu catalysts bearing ligands possessing germanyl groups were much more active for hydroboration than one derived from DTBM-SEGPHOS, a ligand containing 2,5-di-tert-Bu groups and widely used for Cu-catalyzed hydrofunctionalization. This observation led to the identification of DTMGM-SEGPHOS, a bisphosphine ligand bearing 3,5-bis(trimethylgermanyl)-4-methoxyphenyl groups as the substituents on the P, as a new ligand that forms a highly active catalyst for hydroboration of unactivated 1,2-disubstituted alkenes, a class of substrates that has not readily undergone Cu-catalyzed hydroboration previously. Computational studies revealed that the enantioselectivity and catalytic efficiency of the germanyl-substituted ligands is higher than that of the silyl and tert-Bu substituted analogs because of attractive dispersion interactions between the bulky trimethyl-germanyl groups on the ancillary ligand and the alkene substrate and that Pauli repulsive interactions tended to de-crease enantioselectivity.

Journal of the American Chemical Society published new progress about Cupration (hydrocupration, mechanism). 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

Almoshari, Yosif; Iqbal, Haroon; Razzaq, Anam; Ali Ahmad, Khalil; Khan, Muhammad Khalid; Saeed Alqahtani, Saad; Hadi Sultan, Muhammad; Ali Khan, Barkat published the artcile< Development of nanocubosomes co-loaded with dual anticancer agents curcumin and temozolomide for effective Colon cancer therapy>, Computed Properties of 112-63-0, the main research area is curcumin temozolomide anticancer agent colon cancer; Nanocubosomes; colon cancer; curcumin; temozolomide; therapy.

Current research aimed to develop nanocubosomes co-loaded with dual anticancer drugs curcumin and temozolomide for effective colon cancer therapy. Drugs co-loaded nanocubosomal dispersion was prepared by modified emulsification method using glyceryl monooleate (GMO), pluronic F127 and bovine serum albumin (BSA) as a lipid phase, surfactant, and stabilizer, resp. The resulting nanocubosomes were characterized by measuring hydrodynamic particle size, particle size distribution (PSD), drug loading capacity (DL), encapsulation efficiency (EE), colloidal stability and drug release profile. We also physiochem. characterized the nanocubosomes by transmission electron microscopy (TEM), Fourier transform IR (FTIR), and x-rays diffraction (XRD) for their morphol., polymer drug interaction and its nature, resp. Further, the in-vitro cell-uptake, mechanism of cell-uptake, in-vitro anti-tumor efficacy and apoptosis level were evaluated using HCT-116 colon cancer cells. The prepared nanocubosomes exhibited a small hydrodynamic particle size (PS of 150 ± 10 nm in diameter) with nearly cubic shape and appropriate polydispersity index (PDI), enhanced drug loading capacity LC of 6.82 ± 2.03% (Cur) and 9.65 ± 1.53% (TMZ), high entrapment efficiency EE of 67.43 ± 2.16% (Cur) and 75.55 ± 3.25% (TMZ), pH-triggered drug release profile and higher colloidal stability in various physiol. medium. Moreover, the nanocubosomes showed higher cellular uptake, in-vitro cytotoxicity and apoptosis compared to free drugs, curcumin and temozolomide, most likely because its small particle size. In addition, BSA-stabilized nanocubosomes were actively taken by aggressive colon cancer cells that over-expressed the albumin receptors and utilized BSA as nutrient source for their growth. In short, this study provides a new and simple strategy to improve the efficacy and simultaneously overawed the adaptive treatment tolerance in colon cancer.

Drug Delivery published new progress about Adsorption. 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

Al-Ani, Mena; Elemam, Noha Mousaad; Hundt, Jennifer Elisabeth; Maghazachi, Azzam A. published the artcile< Drugs for multiple sclerosis activate natural killer cells: do they protect against COVID-19 infection?>, COA of Formula: C19H34O2, the main research area is review human covid19 virus natural killer cell; COVID-19; NK cells; multiple sclerosis.

A review. COVID-19 infection caused by the newly discovered coronavirus severe acute respiratory distress syndrome virus-19 (SARS-CoV-2) has become a pandemic issue across the globe. There are currently many investigations taking place to look for specific, safe and potent anti-viral agents. Upon transmission and entry into the human body, SARS-CoV-2 triggers multiple immune players to be involved in the fight against the viral infection. Amongst these immune cells are NK cells that possess robust antiviral activity, and which do not require prior sensitization. However, NK cell count and activity were found to be impaired in COVID-19 patients and hence, could become a potential therapeutic target for COVID-19. Several drugs, including glatiramer acetate (GA), vitamin D3, di-Me fumarate (DMF), monomethyl fumarate (MMF), natalizumab, ocrelizumab, and IFN-β, among others have been previously described to increase the biol. activities of NK cells especially their cytolytic potential as reported by upregulation of CD107a, and the release of perforin and granzymes. In this review, we propose that such drugs could potentially restore NK cell activity allowing individuals to be more protective against COVID-19 infection and its complications.

Infection and Drug Resistance published new progress about COVID-19. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, COA of Formula: C19H34O2.

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

Ozen, Tevfik; Demirtas, Ibrahim published the artcile< Comparison of the chemical composition and bioactive properties of extracts prepared from the mature Turkish and Brazilian banana peels>, Application In Synthesis of 112-63-0, the main research area is Brazilian Turkish banana peel extract chem composition bioactive property.

The banana (Musa sp.) plant grows in tropical and subtropical regions. The fruit of the banana is eaten and the peel of the banana is discarded. In this study, chem. analyzes (HPLCTOF/MS ve GC-MS) and biochem. activities (antioxidant and antimicrobial) of Et acetate (Ea) and methanol/chloroform (Me/Ch) extracts prepared from banana peel (Bbp) grown in Brazil and banana peel (Tbp) grown in Turkey were investigated. Cetene, 4-hydroxybenzoic, palmitic, linoleic, stearic, gentisic and syringic acid are the most abundant compounds in the extracts The total antioxidant activity of Tbp-Ea (A0.5: 36.84 μg/mL), inhibition of lipid peroxidation of Bbp-Ea (IC50: 3.22 μg/mL), reducing power of Tbp-Me/Ch (A0.5: 4.96 μg/mL), DPPH• scavenging activity of Bbp-Ea (IC50: 8.54 μg/mL), metal chelating activity of Tbp-Ea (IC50: 16.54 μg/mL) and H2O2 scavenging activity of Tbp-Me/Ch (IC50: 0.36 μg/mL) were found the most effective. It was exhibited that extracts were effective against gramneg. and gram-pos. bacteria. In conclusion, the phytochem. and biochem. results of the TbP and Bbp extracts will contribute further pharmacol., biochem. and pharmacol. investigations.

International Journal of Chemistry and Technology (Kilis, Turkey) published new progress about Antimicrobial 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

Karapanayiotis, Thanasis; Bowen, Richard D. published the artcile< Differentiation of ionized benzimidazole from its isomeric α-distonic ion by collision-induced dissociation and neutralization-reionization mass spectrometry>, Computed Properties of 112-63-0, the main research area is benzimidazole radical cation distonic tautomer CID NR mass spectra.

Ionized benzimidazole and its isomeric α-distonic ion (or ionized ylide) have been examined by recording their metastable ion, collision-induced dissociation and neutralization-reionization mass spectra. These tautomers may be distinguished by careful consideration of key features of the collision-induced dissociation spectra, with or without prior neutralization and reionization. Formation of doubly-charged ions by charge stripping occurs preferentially when the α-distonic ion is subjected to collision. This α-distonic ion survives neutralization and reionization, thus establishing that the corresponding ylide is stable on the microsecond time frame. The effects of benzannulation on the ease of differentiation of classical and distonic radical cations derived from biol. important heterocycles are considered.

European Journal of Mass Spectrometry published new progress about Collision-induced dissociation. 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