Category: 6054-98-4

Niu, Yanfen; Li, Hongjian; Gao, Lihui; Lin, Hua; Kung, Hsiangfu; Lin, Marie Chia-mi; Leung, Kwong-Sak; Wong, Man-Hon; Xiong, Wenyong; Li, Ling published the artcile< old drug, new indication: olsalazine sodium reduced serum uric acid levels in mice via inhibiting xanthine oxidoreductase activity>, Recommanded Product: Sodium 5,5′-(diazene-1,2-diyl)bis(2-hydroxybenzoate), the main research area is olsalazine sodium xanthine oxidase dehydrogenase inhibitor hyperuricemia; Hyperuricemia; Olsalazine sodium; Uric acid; Xanthine oxidase.

Hyperuricemia, a long-term purine metabolic disorder, is a well-known risk factor for gout, hypertension and diabetes. In maintaining normal whole-body purine levels, xanthine oxidase (XOD) is a key enzyme in the purine metabolic pathway, as it catalyzes the oxidation of hypoxanthine to xanthine and finally to uric acid. Here we used the protein-ligand docking software idock to virtually screen potential XOD inhibitors from 3167 approved small compounds/drugs. The inhibitory activities of the ten compounds with the highest scores were tested on XOD in vitro. Interestingly, all the ten compounds inhibited the activity of XOD at certain degrees. Particularly, the anti-ulcerative-colitis drug olsalazine sodium demonstrated a great inhibitory activity for XOD (IC50 = 3.4 mg/L). Enzymic kinetic studies revealed that the drug was a hybrid-type inhibitor of xanthine oxidase. Furthermore, the drug strikingly decreased serum urate levels, serum/hepatic activities of XOD at a dose-dependent manner in vivo. Thus, we demonstrated a successful hunting process of compounds/drugs for hyperuricemia through virtual screening, supporting a potential usage of olsalazine sodium in the treatment of hyperuricemia.

Journal of Pharmacological Sciences (Amsterdam, Netherlands) published new progress about Gout. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, Recommanded Product: Sodium 5,5′-(diazene-1,2-diyl)bis(2-hydroxybenzoate).

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Peladeau, Christine; Adam, Nadine; Bronicki, Lucas M.; Coriati, Adele; Thabet, Mohamed; Al-Rewashdy, Hasanen; Vanstone, Jason; Mears, Alan; Renaud, Jean-Marc; Holcik, Martin; Jasmin, Bernard J. published the artcile< Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles>, HPLC of Formula: 6054-98-4, the main research area is muscular dystrophy relaxant utrophin A eEF1A2 therapeutic target.

Abstract: Up-regulation of utrophin in muscles represents a promising therapeutic strategy for the treatment of Duchenne Muscular Dystrophy. We previously demonstrated that eEF1A2 associates with the 5’UTR of utrophin A to promote IRES-dependent translation. Here, we examine whether eEF1A2 directly regulates utrophin A expression and identify via an ELISA-based high-throughput screen, FDA-approved drugs that upregulate both eEF1A2 and utrophin A. Our results show that transient overexpression of eEF1A2 in mouse muscles causes an increase in IRES-mediated translation of utrophin A. Through the assessment of our screen, we reveal 7 classes of FDA-approved drugs that increase eEF1A2 and utrophin A protein levels. Treatment of mdx mice with the 2 top leads results in multiple improvements of the dystrophic phenotype. Here, we report that IRES-mediated translation of utrophin A via eEF1A2 is a critical mechanism of regulating utrophin A expression and reveal the potential of repurposed drugs for treating DMD via this pathway.

Nature Communications published new progress about Anterior tibial muscle. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, HPLC of Formula: 6054-98-4.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kim, Suyeon; Thapa, Ishwor; Zhang, Ling; Ali, Hesham published the artcile< On identifying candidates for drug repurposing for the treatment of ulcerative colitis using gene expression data>, HPLC of Formula: 6054-98-4, the main research area is gene expression antiinflammatory agent drug repurposing ulcerative colitis.

The notion of repurposing of existing drugs to treat both common and rare diseases has gained traction from both academia and pharmaceutical companies. Given the high attrition rates, massive time, money, and effort of brand-new drug development, the advantages of drug repurposing in terms of lower costs and shorter development time have become more appealing. Computational drug repurposing is promising approach and has shown great potential in tailoring genomic findings to the development of treatments for diseases. However, there are still challenges involved in building a standard computational drug repurposing solution for high-throughput anal. and the implementation to clin. practice. In this study, we applied the computational drug repurposing approaches for Ulcerative Colitis (UC) patients to provide better treatment for this disabling disease. Repositioning drug candidates were identified, and these findings provide a potentially effective therapeutics for the treatment of UC patients. This preliminary computational drug repurposing pipeline will be extended in the near future to help realize the full potential of drug repurposing.

Lecture Notes in Bioinformatics published new progress about Chemotherapy. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, HPLC of Formula: 6054-98-4.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tang, Yun-Zhi; Tan, Yu-Hui; Zhu, Jian-Wu; Ji, Fa-Ming; Xiong, Ting-Ting; Xiao, Wen-Zhong; Liao, Chun-Fa; Xiong, Ren-Gen published the artcile< Novel Three-Dimensional Anion-Type Eight-Coordinated Cd(II) Coordination Polymer with Binuclear Cadmium Building Units>, Application of C14H8N2Na2O6, the main research area is cadmium dipentum DMF polymeric preparation structure; crystal structure cadmium dipentum eight coordinate polymeric.

The 3-dimensional polymeric complex {[Cd2(DPT)3(DMF)6]·(2H3O)+} n (DPT = dipentum = 3,3-azo-bis(6-hydroxybenzoic carboxylic acid), DMF = N,N’- dimethylformamide) with binuclear Cd as building block was obtained from hydrothermal reaction of CdCl2·4H2O with medicine dipentum Na.

Crystal Growth & Design published new progress about Coordination number, eight. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, Application of C14H8N2Na2O6.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Teruel, Adrian H.; Perez-Esteve, Edgar; Gonzalez-Alvarez, Isabel; Gonzalez-Alvarez, Marta; Costero, Ana M.; Ferri, Daniel; Gavina, Pablo; Merino, Virginia; Martinez-Manez, Ramon; Sancenon, Felix published the artcile< Double Drug Delivery Using Capped Mesoporous Silica Microparticles for the Effective Treatment of Inflammatory Bowel Disease>, Safety of Sodium 5,5′-(diazene-1,2-diyl)bis(2-hydroxybenzoate), the main research area is silica microparticle hydrocortisone inflammatory bowel disease antiinflammatory; colon targeted release; gated materials; inflammatory bowel disease; mesoporous silica microparticles; smart drug delivery materials.

Silica mesoporous microparticles loaded with both rhodamine B fluorophore (S1) or hydrocortisone (S2), and capped with an olsalazine derivative, are prepared and fully characterized. Suspensions of S1 and S2 in water at an acidic and a neutral pH show negligible dye/drug release, yet a notable delivery took place when the reducing agent sodium dithionite is added because of hydrolysis of an azo bond in the capping ensemble. Addnl., olsalazine fragmentation induced 5-aminosalicylic acid (5-ASA) release. In vitro digestion models show that S1 and S2 solids are suitable systems to specifically release a pharmaceutical agent in the colon. In vivo pharmacokinetic studies in rats show a preferential rhodamine B release from S1 in the colon. Moreover, a model of ulcerative colitis is induced in rats by oral administration of 2,4,6-trinitrobenzenesulfonic acid (TNBS) solutions, which was also used to prove the efficacy of S2 for colitis treatment. The specific delivery of hydrocortisone and 5-ASA from S2 material to the colon tissue in injured rats markedly lowers the colon/body weight ratio and the clin. activity score. Histol. studies showed a remarkable reduction in inflammation, as well as an intensive regeneration of the affected tissues.

Molecular Pharmaceutics published new progress about Anti-inflammatory agents. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, Safety of Sodium 5,5′-(diazene-1,2-diyl)bis(2-hydroxybenzoate).

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

McKay, G.; Blair, H. S.; Gardner, J. R. published the artcile< The adsorption of dyes onto chitin in fixed bed columns and batch adsorbers>, Safety of Sodium 5,5′-(diazene-1,2-diyl)bis(2-hydroxybenzoate), the main research area is dye adsorption chitin textile wastewater.

Chitin has the ability to adsorb substantial quantities of dyestuffs from aqueous solutions Consequently, it is a useful adsorbent for effluent treatment from textile mills. The design procedures for batch and continuous fixed-bed adsorption columns have been investigated for 4 dyes, namely, CI Acid Blue 25  [6408-78-2], CI Acid Blue 158  [6370-08-7], CI Mordant Yellow 5  [6054-98-4], and CI Direct Red 84  [6409-83-2]. The main-fixed bed system variables studied are bed height, dye flow rate, and chitin particle size, and these effects have been incorporated into a simplified design model.

Journal of Applied Polymer Science published new progress about Adsorptive wastewater treatment. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, Safety of Sodium 5,5′-(diazene-1,2-diyl)bis(2-hydroxybenzoate).

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Hakkou, Khalid; Molina-Pinilla, Inmaculada; Rangel-Nunez, Cristian; Suarez-Cruz, Adrian; Pajuelo, Eloisa; Bueno-Martinez, Manuel published the artcile< Synthesis of novel (bio) degradable linear azo polymers conjugated with olsalazine>, Product Details of C14H8N2Na2O6, the main research area is biodegradable linear conjugated olsalazine based polyazoester triazole preparation property.

Click Cu(I)-catalyzed polymerization of diynes and diazides was performed to obtain a novel type of linear copolymer, which were prepared from monomers derived from poly(ethylene glycol), 5,5′-azodisalicylic acid [olsalazine] and 1,4-butanediol diglycidyl ether. The resulting copolymers will carry ester and azo functions along the polymer backbone, so they will be sensitive to pH as well as be degraded by azoreductase enzymes present in the colonic microbiota. Most of the copoly(azoester triazole)s obtained were water soluble, and all of them were characterized by Fourier transform IR, NMR, and gel permeation chromatog.. Differential scanning calorimetry revealed them to be amorphous, and in general, the polymers were stable up to 250 °C under nitrogen as demonstrated by thermogravimetric anal.. The degradation behavior of the polymers was evaluated in vitro. Degradation studies were carried out at 37 °C in buffered salt solution at pH 7.4, and were monitored by GPC and NMR spectroscopies. A biodegradation experiment of a water-soluble prototype polymer showed that they are biodegradable via a strain of Enterococcus faecalis. The experiment was monitored using UV-visible spectroscopy.

Polymer Degradation and Stability published new progress about Azide-alkyne 1,3-dipolar cycloaddition reaction. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, Product Details of C14H8N2Na2O6.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

McKay, G.; Kelly, J. C.; McConvey, I. F. published the artcile< The adsorption of pollutants from aqueous effluents using a two-resistance mass-transfer model>, HPLC of Formula: 6054-98-4, the main research area is phenol adsorption wastewater treatment model; dye adsorption wastewater treatment model.

The adsorption of various pollutants, such as PhOH, p-chlorophenol and different dyes, on to activated C and chitin (a high mol. weight polymer obtained from crustacea) was studied in an agitated batch system at a temperature of 18 ± 2°. Two methods were used to predict concentration decay curves and correlate theor. and exptl. data. Both methods are based on external mass transfer and internal diffusion as the controlling mass-transfer resistances. The 1st method is a rapid anal. solution enabling external mass-transfer coefficients and effective diffusivities to be determined, but is restricted to the assumption that a pseudo-anal. isotherm is applicable. The 2nd method, based on a pseudo-anal. solution, is applicable to operating lines and tie lines terminating at any point on the isotherm, but requires longer computational time. Values of mass-transfer coefficients and effective diffusivities are presented for all systems.

Adsorption Science & Technology published new progress about Adsorptive wastewater treatment. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, HPLC of Formula: 6054-98-4.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Gao, Heng Ya; Peng, Wen Li; Meng, Pan Pan; Feng, Xue Feng; Li, Jian Qiang; Wu, Hui Qiong; Yan, Chang Sheng; Xiong, Yang Yang; Luo, Feng published the artcile< Correction: Lanthanide separation using size-selective crystallization of Ln-MOFs [Erratum to document cited in CA167:016029]>, Application In Synthesis of 6054-98-4, the main research area is size selective crystallization separation lanthanide olsalazine MOF erratum; crystal structure lanthanide olsalazine MOF preparation erratum.

The authors regret that although the CCDC numbers are correct in the ESI document, the numbers indicated in the manuscript are incorrect. The correct CCDC numbers are included below: 1537206?1537208, 1537213?1537215, 1537218?1537221, 1537250, 1537558, 1545014.

Chemical Communications (Cambridge, United Kingdom) published new progress about Crystal structure. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, Application In Synthesis of 6054-98-4.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Pamukcu, Rifat; Hanauer, Stephen B.; Chang, Eugene B. published the artcile< Effect of disodium azodisalicylate on electrolyte transport in rabbit ileum and colon in vitro. Comparison with sulfasalazine and 5-aminosalicyclic acid>, Synthetic Route of 6054-98-4, the main research area is azodisalicylate electrolyte transport intestine; diarrhea azodisalicylate.

Azodisalicylate, used to treat ulcerative colitis, causes diarrhea in ≤12.5% of patients. The in vitro effects of azodisalicylate, sulfasalazine, and 5-aminosalicylic acid on rabbit intestinal electrolyte transport were studied. Distal ileal mucosae mounted in Ussing chambers were exposed to varying concentrations of the drugs. Mucosal addition of azodisalicylate (>5 mM) caused the greatest anion-dependent increase in short-circuit current of 83 μA/cm2. Isotope flux measurements suggest that azodisalicylate may stimulate predominantly electrogenic HCO3- secretion and induce net NaCl secretion. In contrast, serosal addition of azodisalicylate and sulfasalazine decreased short-circuit current, and 5-aminosalicylic acid had no effect. Azodisalicylate had no effect on ion transport in distal colon. The effects of azodisalicylate in ileum were not inhibited with piroxicam (an inhibitor of cyclooxygenase). Mucosal cAMP and cGMP levels were unchanged after ileal exposure to azodisalicylate. Azodisalicylate appears to be a mechanistically unusual secretagogue, possibly explaining the increased incidence of diarrhea seen in patients taking the drug.

Gastroenterology published new progress about Colon. 6054-98-4 belongs to class alcohols-buliding-blocks, and the molecular formula is C14H8N2Na2O6, Synthetic Route of 6054-98-4.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts