Thripuram, Vijaya Durga’s team published research in Letters in Organic Chemistry in 2018-07-31 | 1003-21-0

Letters in Organic Chemistry published new progress about Aromatic carbonyl compounds Role: RCT (Reactant), RACT (Reactant or Reagent). 1003-21-0 belongs to class imidazoles-derivatives, and the molecular formula is C4H5BrN2, SDS of cas: 1003-21-0.

Thripuram, Vijaya Durga; Bollikolla, Hari Babu; Reddy Mule, Siva Nagi; Battula, Sailaja Kumari; Ala, Vasu Babu published the artcile< A Novel Approach for Substitution of Sulfonate Group by (1H)-imidazole moiety: An Application for Synthesis of Novel Benzyl Imidazolylcarbamates>, SDS of cas: 1003-21-0, the main research area is benzyl imidazolylcarbamate preparation.

An efficient and convenient substitution protocol was developed for the synthesis of novel benzyl (1-methyl-1H-imidazol-5-yl) (aryl) Me carbamate derivatives from alpha-amido sulfones with a solution 5-bromo-1-methyl-(1H)-imidazole in THF under Hexamethylphosphoramide (HMPA) and t-BuLi medium at -78° to room temperature The reactions were monitored with TLC for about 3-4 h.The yields obtained were also considerably good.

Letters in Organic Chemistry published new progress about Aromatic carbonyl compounds Role: RCT (Reactant), RACT (Reactant or Reagent). 1003-21-0 belongs to class imidazoles-derivatives, and the molecular formula is C4H5BrN2, SDS of cas: 1003-21-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Gu, Y Y’s team published research in Neoplasma in 2019 | 6823-69-4

Neoplasma published new progress about Bioinformatics. 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Safety of p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride.

Gu, Y. Y.; Yu, J.; Zhang, J. F.; Wang, C. published the artcile< Suppressing the secretion of exosomal miR-19b by GW4869 could regulate oxaliplatin sensitivity in colorectal cancer>, Safety of p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride, the main research area is oxaliplatin MiR19b GW4869 colorectal cancer.

Oxaliplatin is commonly used in managing malignancy, including colorectal cancer. While treatment oftn fails due to decreased drug sensitivity, the mechanisms involved are not clear. In this study, we investigate how exosomal miR-19b participates in oxaliplatin sensitivity and then prove that miR-19b down-regulates oxaliplatin sensitivity of sw480 cells. We found that suppressing the secretion of exosomal miR-19b with gw4869 promotes sw480 cell oxaliplatin sensitivity. Our combined results demonstrate for the first time that miR-19b regulates the oxaliplatin sensitivity of sw480 cells and provides a unique mechanism mediated by gw4869 to modulate oxaliplatin sensitivity by suppressing exosomal miR-19b release.

Neoplasma published new progress about Bioinformatics. 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Safety of p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Zhou, Yan’s team published research in Science (Washington, DC, United States) in 2021 | 452-06-2

Science (Washington, DC, United States) published new progress about Bacteriophage. 452-06-2 belongs to class imidazoles-derivatives, and the molecular formula is C5H5N5, Reference of 452-06-2.

Zhou, Yan; Xu, Xuexia; Wei, Yifeng; Cheng, Yu; Guo, Yu; Khudyakov, Ivan; Liu, Fuli; He, Ping; Song, Zhangyue; Li, Zhi; Gao, Yan; Ang, Ee Lui; Zhao, Huimin; Zhang, Yan; Zhao, Suwen published the artcile< A widespread pathway for substitution of adenine by diaminopurine in phage genomes>, Reference of 452-06-2, the main research area is pathway substitution adenine diaminopurine phage genome PurZ enzyme ZDNA.

DNA modifications vary in form and function but generally do not alter Watson-Crick base pairing. Diaminopurine (Z) is an exception because it completely replaces adenine and forms three hydrogen bonds with thymine in cyanophage S-2L genomic DNA. However, the biosynthesis, prevalence, and importance of Z genomes remain unexplored. Here, we report a multienzyme system that supports Z-genome synthesis. We identified dozens of globally widespread phages harboring such enzymes, and we further verified the Z genome in one of these phages, Acinetobacter phage SH-Ab 15497, by using liquid chromatog. with UV and mass spectrometry. The Z genome endows phages with evolutionary advantages for evading the attack of host restriction enzymes, and the characterization of its biosynthetic pathway enables Z-DNA production on a large scale for a diverse range of applications.

Science (Washington, DC, United States) published new progress about Bacteriophage. 452-06-2 belongs to class imidazoles-derivatives, and the molecular formula is C5H5N5, Reference of 452-06-2.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Hu, Yibing’s team published research in PLoS One in 2015 | 6823-69-4

PLoS One published new progress about CD133 antigens Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Name: p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride.

Hu, Yibing; Yan, Chang; Mu, Lei; Huang, Kaiyu; Li, Xiaolan; Tao, Deding; Wu, Yaqun; Qin, Jichao published the artcile< Fibroblast-derived exosomes contribute to chemoresistance through priming cancer stem cells in colorectal cancer>, Name: p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride, the main research area is fibroblast exosome chemoresistance colorectal cancer stem cell.

Chemotherapy resistance observed in patients with colorectal cancer (CRC) may be related to the presence of cancer stem cells (CSCs), but the underlying mechanism(s) remain unclear. Carcinoma-associated fibroblasts (CAFs) are intimately involved in tumor recurrence, and targeting them increases chemo-sensitivity. We investigated whether fibroblasts might increase CSCs thus mediating chemotherapy resistance. CSCs were isolated from either patient-derived xenografts or CRC cell lines based on expression of CD133. First, CSCs were found to be inherently resistant to cell death induced by chemotherapy. In addition, fibroblast-derived conditioned medium (CM) promoted percentage, clonogenicity and tumor growth of CSCs (i.e., CD133+ and TOP-GFP+) upon treatment with 5-fluorouracil (5-Fu) or oxaliplatin (OXA). Further investigations exhibited that exosomes, isolated from CM, similarly took the above effects. Inhibition of exosome secretion decreased the percentage, clonogenicity and tumor growth of CSCs. Altogether, our findings suggest that, besides targeting CSCs, new therapeutic strategies blocking CAFs secretion even before chemotherapy shall be developed to gain better clin. benefits in advanced CRCs.

PLoS One published new progress about CD133 antigens Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Name: p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Song, Honghong’s team published research in e-Polymers in 2019 | 700370-07-6

e-Polymers published new progress about Binding energy. 700370-07-6 belongs to class imidazoles-derivatives, and the molecular formula is C6H9ClN2O2, Synthetic Route of 700370-07-6.

Song, Honghong; Zhang, Jing; Song, Pengfei; Xiong, Yubing published the artcile< Maize-like ionic liquid@polyaniline nanocomposites for high performance supercapacitor>, Synthetic Route of 700370-07-6, the main research area is polyaniline nanocomposite ionic liquid supercapacitor tunable morphol.

In this study, ionic liquids (IL) containing carboxyl and different alkyl chains were fabricated and used to dope polyaniline (PANI). The results revealed that IL-PANI composites could be facilely obtained via template-free polymerization of aniline using ammonium persulfate as the oxidant. The as-prepared IL-PANI composites were measured by FT-IR, XPS, and SEM. Electrochem. performances of IL-PANI nanocomposites were investigated by cyclic voltammetry and galvanostatic charge/discharge. The results indicate that the alkyl chains of ILs have an important influence on the morphol. and capacitance performance of IL-PANI electrode materials. With the shorter alkyl group in ILs, IL-PANI materials presented higher specific capacitance. Especially, 1-vinyl-3-carboxymethyl-imidazolium chloride ([VCMIm]Cl)-PANI composite presented the highest specific capacitance. Cycling performance measurement demonstrated that 82% capacitance retention could be achieved after 1000 cycles in 0.5 M H2SO4 aqueous solution Therefore, our strategy provides a new technique for PANI nanocomposites with tunable morphol. and high performance.

e-Polymers published new progress about Binding energy. 700370-07-6 belongs to class imidazoles-derivatives, and the molecular formula is C6H9ClN2O2, Synthetic Route of 700370-07-6.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Cai, Long’s team published research in ChemistrySelect in 2019 | 700370-07-6

ChemistrySelect published new progress about Corn straw. 700370-07-6 belongs to class imidazoles-derivatives, and the molecular formula is C6H9ClN2O2, Safety of 1-carboxymethyl-3-methylimidazolium chloride.

Cai, Long; Zhang, Ying; Hu, Gang; Guo, Yuanlong; Jin, Longming; Xu, Qinqin; Liu, Zhanpeng; Xie, Haibo published the artcile< A Single Step Fractionation of Lignocellulose in Aqueous Solutions of a Carboxylic Acid-Functionalized Ionic Liquid>, Safety of 1-carboxymethyl-3-methylimidazolium chloride, the main research area is fractionation lignocellulose aqueous solution carboxylic acid functionalized ionic liquid.

This paper presents the features of corn stover pretreated under mild conditions in aqueous solution of a carboxylic acid functionalized ionic liquids 1-carboxymethyl-3-methylimidazolium chloride (IL-COOH). The results revealed that such pretreatment selectively removed hemicelluloses in corn stover, resulting in cellulose- and lignin-rich pulps with moderate enzymic reactivity. The corn stover pretreated in 40 wt% IL-COOH at 120 °C for 4 h demonstrated increases in cellulose and lignin contents from 37.9% to 55.6%, and 21.1% to 26.5%, resp., while decrease in the content of hemicellulose from 24.4% to 9.34%. Subsequent enzymic hydrolysis of the pulps achieved from pretreatment in 50 wt% IL-COOH aqueous solution at 105 °C for 4 h produced 0.32 g.g-1 glucose and 0.45 g.g-1 total reducing sugars. The recyclability and reusability of IL-COOH in the pretreatment system was also investigated.

ChemistrySelect published new progress about Corn straw. 700370-07-6 belongs to class imidazoles-derivatives, and the molecular formula is C6H9ClN2O2, Safety of 1-carboxymethyl-3-methylimidazolium chloride.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Guillen, Danielle’s team published research in PLoS One in 2020 | 452-06-2

PLoS One published new progress about Biological staining. 452-06-2 belongs to class imidazoles-derivatives, and the molecular formula is C5H5N5, Product Details of C5H5N5.

Guillen, Danielle; Schievelbein, Mika; Patel, Kushkumar; Jose, Davis; Ouellet, Jonathan published the artcile< A simple and affordable kinetic assay of nucleic acids with SYBR Gold gel staining>, Product Details of C5H5N5, the main research area is nucleic acid SYBR gold gel staining kinetic assay.

Labeling substrates or products are paramount in determining enzymic kinetic parameters. Several options are available; many laboratories use either radioactive or fluorescent labeling because of their high sensitivity. However, those methods have their own drawbacks such as half-life decay, expensive and hazardous. Here, we propose a novel, simple, economical and fast alternative to substrate labeling for studying the kinetics of nucleic acids: post-migration gel staining with SYBR Gold. Cleavage rates similar to the ones reported in the literature for the I-R3 DNA-cleaving DNA enzyme in the presence of zinc chloride are an indication of the quality of the new method. Moreover, the activity of the hammerhead ribozyme was also monitored by our method to illustrate its versatility. This labeling-free method has several advantages such as its ease of use as well as cost effective and versatility with both non-structured and structured RNAs or DNAs.

PLoS One published new progress about Biological staining. 452-06-2 belongs to class imidazoles-derivatives, and the molecular formula is C5H5N5, Product Details of C5H5N5.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Su, Hong’s team published research in Molecular and Cellular Endocrinology in 2020-12-01 | 6823-69-4

Molecular and Cellular Endocrinology published new progress about 3′-Untranslated region Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Synthetic Route of 6823-69-4.

Su, Hong; Qiao, Jiao; Hu, Jinxiu; Li, Yanmei; Lin, Jiangong; Yu, Qun; Zhen, Junhui; Ma, Qiqi; Wang, Qianhui; Lv, Zhimei; Wang, Rong published the artcile< Podocyte-derived extracellular vesicles mediate renal proximal tubule cells dedifferentiation via microRNA-221 in diabetic nephropathy>, Synthetic Route of 6823-69-4, the main research area is microRNA221 vesicle renal proximal tubule signaling diabetic nephropathy; Dedifferentiation; Extracellular vesicles; Podocytes; Proximal tubular epithelial cells; Wnt/β-catenin signaling; miR-221.

Podocyte injury is a key event in the initiation of Diabetic nephropathy (DN). Tubulointerstitium, especially the proximal tubule has been regarded as a target of injury. In the present study, we showed that podocytes induced dedifferentiation of proximal tubular epithelial cells(PTECs) in high-glucose conditions and extracellular vesicles (EVs) mediates the interaction. Then we extracted and identified these EVs derived from podocytes as exosome, further, the EVs induced PTECs dedifferentiation. Total microRNA(miRNA) expression of podocyte-derived EVs was extracted and miR-221 expression was remarkably increased. By making use of the miRNA gain- and loss-of-function approaches, we observed that miR-221 mediated PTECs dedifferentiation. In addition, a dual-luciferase reporter assay confirmed that miR-221 direct target DKK2, which was an inhibitor of Wnt signaling, and overexpression of miR-221 significantly resulted in β-catenin nuclear accumulation. Moreover, we regulated the expression of β-catenin and demonstrated that miR-221 in EVs mediated proximal tubule cells injury through Wnt/β-catenin signaling. Furthermore, inhibition of miR-221 in diabetic mice reversed the abnormal expression of PTECs dedifferentiation related protein. These findings provide unique insights in the mechanisms of proximal tubule cell injury in diabetic nephropathy.

Molecular and Cellular Endocrinology published new progress about 3′-Untranslated region Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Synthetic Route of 6823-69-4.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Rong, Yuluo’s team published research in Journal of Neuroinflammation in 2021-12-31 | 6823-69-4

Journal of Neuroinflammation published new progress about Apoptosis. 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Safety of p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride.

Rong, Yuluo; Ji, Chengyue; Wang, Zhuanghui; Ge, Xuhui; Wang, Jiaxing; Ye, Wu; Tang, Pengyu; Jiang, Dongdong; Fan, Jin; Yin, Guoyong; Liu, Wei; Cai, Weihua published the artcile< Small extracellular vesicles encapsulating CCL2 from activated astrocytes induce microglial activation and neuronal apoptosis after traumatic spinal cord injury>, Safety of p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride, the main research area is traumatic spinal cord injury CCL2 astrocyte microglia neuronal apoptosis; Astrocyte; CCL2; Microglia; Neuron; Small extracellular vesicles; Spinal cord injury.

Spinal cord injury (SCI) is a severe traumatic disease which causes high disability and mortality rates. The mol. pathol. features after spinal cord injury mainly involve the inflammatory response, microglial and neuronal apoptosis, abnormal proliferation of astrocytes, and the formation of glial scars. However, the microenvironmental changes after spinal cord injury are complex, and the interactions between glial cells and nerve cells remain unclear. Small extracellular vesicles (sEVs) may play a key role in cell communication by transporting RNA, proteins, and bioactive lipids between cells. Few studies have examined the intercellular communication of astrocytes through sEVs after SCI. The inflammatory signal released from astrocytes is known to initiate microglial activation, but its effects on neurons after SCI remain to be further clarified. Electron microscopy (TEM), nanoparticle tracking anal. (NTA), and western blotting were applied to characterize sEVs. We examined microglial activation and neuronal apoptosis mediated by astrocyte activation in an exptl. model of acute spinal cord injury and in cell culture in vitro. Our results indicated that astrocytes activated after spinal cord injury release CCL2, act on microglia and neuronal cells through the sEV pathway, and promote neuronal apoptosis and microglial activation after binding the CCR2. Subsequently, the activated microglia release IL-1β, which acts on neuronal cells, thereby further aggravating their apoptosis. This study elucidates that astrocytes interact with microglia and neurons through the sEV pathway after SCI, enriching the mechanism of CCL2 in neuroinflammation and spinal neurodegeneration, and providing a new theor. basis of CCL2 as a therapeutic target for SCI.

Journal of Neuroinflammation published new progress about Apoptosis. 6823-69-4 belongs to class imidazoles-derivatives, and the molecular formula is C30H30Cl2N6O2, Safety of p-Benzenediacrylanilide, 4′,4′′-di-2-imidazolin-2-yl-, dihydrochloride.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Barlin, Gordon B’s team published research in Journal of the Chemical Society [Section] B: Physical Organic in 1967 | 1003-21-0

Journal of the Chemical Society [Section] B: Physical Organic published new progress about NMR (nuclear magnetic resonance). 1003-21-0 belongs to class imidazoles-derivatives, and the molecular formula is C4H5BrN2, Application of C4H5BrN2.

Barlin, Gordon B.; Batterham, Thomas J. published the artcile< The proton magnetic resonance spectra of some diazoles, triazoles, and tetrazoles>, Application of C4H5BrN2, the main research area is NMR AZOLES; TRIAZOLES NMR; DIAZOLES NMR; AZOLES NMR; TETRAZOLES NMR; PROTONATION METHYLIMIDAZOLES; IMIDAZOLES PROTONATION.

The N.M.R. spectra of various charged species from 33 azoles have been measured. In N-methyl-imidazoles and -1,2,4-triazoles the sites of protonation have been determined, and the cations appear to be stabilized by amidinium type resonance. Solvent effects are discussed. 27 references.

Journal of the Chemical Society [Section] B: Physical Organic published new progress about NMR (nuclear magnetic resonance). 1003-21-0 belongs to class imidazoles-derivatives, and the molecular formula is C4H5BrN2, Application of C4H5BrN2.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem