TY - JOUR. T1 - The effect of inosine on the inotropic response of the myocardium to isoproterenol and norepinephrine. AU - Devous, M. D.. AU - Jones, C. E.. PY - 1978/1/1. Y1 - 1978/1/1. UR - http://www.scopus.com/inward/record.url?scp=0018249718&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=0018249718&partnerID=8YFLogxK. M3 - Article. AN - SCOPUS:0018249718. VL - 21. JO - The Physiologist. JF - The Physiologist. SN - 0031-9376. IS - 4. ER - ...

Combinations of thymidine and inosine (ranging from 0 to 7.5 mg/hr) were co-administered during a 72-hr continuous i.v. infusion of 3 μg/hr methotrexate in normal and P388 solid tumor-bearing DBA/2 mice. Methotrexate alone was lethal to all normal mice. Inosine at 1.0-7.5 mg/hr could reverse toxicity up to 100% while ... read more thymidine at 0.5-7.5 mg/hr was less effective (86% survival). Combinations of the nucleosides averted toxicity more effectively than either compound alone and in a synergistic manner. From P388 tumor-bearing mice 27% survived methotrexate and eventually died of tumor. Co-infusion of thymidine or inosine decreased the percentage of toxic deaths and caused an increase in life span of more than 50% as compared to untreated tumor-bearing mice. However, the diminishing effect on survival with thymidine and inosine doses above 0.5 mg/hr indicated loss of the antitumor effect of methotrexate. This was also observed with combinations of the nucleosides. The influence of ...

Of the combinations tried, the admixture of methylene blue, progesterone, adenine and inosine maintained 2,3-diphosphoglycerate and adenosine triphosphate at high levels in citrate-phosphate-dextrose blood for a storage period of 6 weeks, about equal to those of the control values on the day of collection. (Author)(*BLOOD

Array ( [0] => 30 [1] => 31 [2] => 32 [3] => 34 [4] => 33 [5] => 49 ) Array ( [1513164984] => Array ( [timeid] => 1513164984 [id] => 14978 [title] => Applications of stimuli-responsive nanoscale drug delivery systems in translational research. (Drug Discov Today, Nov 2017) [time] => 13 December 2017 11:36:24 [postcat] => 30 ) [1511955285] => Array ( [timeid] => 1511955285 [id] => 14880 [title] => CSI Deputy Director, Prof Chng Wee Joo, Appointed Provosts Chair at NUSMed [time] => 29 November 2017 11:34:45 [postcat] => 31 ) [1511286152] => Array ( [timeid] => 1511286152 [id] => 14843 [title] => Triple negative breast cancer in Asia: An insiders view. (Cancer Treat Rev, Nov 2017) [time] => 21 November 2017 17:42:32 [postcat] => 30 ) [1510763331] => Array ( [timeid] => 1510763331 [id] => 14808 [title] => CSI Research Scientist Awarded the ASH Abstract Achievement Award! [time] => 15 November 2017 16:28:51 [postcat] => 31 ) [1510588491] => Array ( [timeid] => 1510588491 [id] => 14803 [title] => ...

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Historically, the first universal base employed was 2-deoxyInosine (dI). DeoxyInosine is a naturally occurring base that, while not truly universal, is less destabilizing than mismatches involving the four standard bases. Hydrogen bond interactions between dI and dA, dG, dC and dT are weak and unequal, with the result that some base-pairing bias does exist with dI:dC , dI:dA , dI:dG , dI:dT. When present in a DNA template, deoxyInosine preferentially directs incorporation of dC in the growing nascent strand by DNA polymerase.. ...

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abstract = {Adenosine-to-inosine (A-to-I) RNA editing is a conserved post-transcriptional mechanism mediated by ADAR enzymes that diversifies the transcriptome by altering selected nucleotides in RNA molecules1. Although many editing sites have recently been discovered2,3,4,5,6,7, the extent to which most sites are edited and how the editing is regulated in different biological contexts are not fully understood8,9,10. Here we report dynamic spatiotemporal patterns and new regulators of RNA editing, discovered through an extensive profiling of A-to-I RNA editing in 8,551 human samples (representing 53 body sites from 552 individuals) from the Genotype-Tissue Expression (GTEx) project and in hundreds of other primate and mouse samples. We show that editing levels in non-repetitive coding regions vary more between tissues than editing levels in repetitive regions. Globally, ADAR1 is the primary editor of repetitive sites and ADAR2 is the primary editor of non-repetitive coding sites, whereas the ...

Double-stranded RNA triggers various profound cellular reactions, which depend not only on different intracellular dsRNA locations, but also on the intrinsic structure and length of the duplex. One of the major cellular responses to nuclear dsRNA is the covalent base modification of the target dsRNA by a ubiquitously expressed enzyme, ADAR. ADAR works on dsRNA and alters adenosines to inosines in the RNA duplex. Two types of ADAR editing of dsRNA have been found, selective editing and the promiscuous hyperediting. Hyperedited RNA has been suggested to undergo a novel regulatory pathway. How do cells discriminate between selectively edited mRNAs that encode new protein isoforms, and dsRNA-induced, promiscuously edited RNAs that encode nonfunctional, mutant proteins? We have developed a Xenopus oocyte model system which shows that a variety of hyperedited, inosine-containing RNAs are specifically retained in the nucleus. To uncover the mechanism of inosine-induced retention, HeLa cell nuclear extracts

TY - JOUR. T1 - Crystal Structure of an RNA Quadruplex Containing Inosine Tetrad. T2 - Implications for the Roles of NH2 Group in Purine Tetrads. AU - Pan, Baocheng. AU - Shi, Ke. AU - Sundaralingam, Muttaiya. PY - 2006/10/20. Y1 - 2006/10/20. N2 - Polyinosinic acid has been known to adopt the four-stranded helical structure but its basic unit, inosine tetrad (I tetrad), has not been determined at the atomic level. Here we report the crystal structure of an RNA quadruplex containing an I tetrad at 1.4 Å resolution. The I tetrad has one cyclic hydrogen bond N1...O6 with the bond length of 2.7 Å. A water bridge is observed in the minor groove side of the base tetrad. Even though it is sandwiched by guanine tetrads (G tetrads), the I tetrad is buckled towards the 3′ side of the tetrad plane, which results from the different interaction strength with K ions on two sides of the tetrad plane. Comparison with both G tetrad and adenine tetrad indicates that lack of NH2 in the C2 position makes the I ...

This page contains information on the chemical Inosine 5\-(tetrahydrogen triphosphate), mixt. with adenosine 5\-(trihydrogen diphosphate) sodium salt, inosine and uridine 5\-(tetrahydrogen triphosphate) including: 3 synonyms/identifiers.

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Inosine is a nucleoside (a building block for DNA and RNA) found in muscle tissue. Inosine is used by athletes and those who want to improve performance.

Anabol Naturals Inosine is in its simplest single, free form molecular state and can be readily absorbed by your body. Inosine is a nucleoside, one of the basic compounds comp...

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Inosine is a medicine available in a number of countries worldwide. A list of US medications equivalent to Inosine is available on the Drugs.com website.

RNA editing is a regulatory mechanism in which nucleotides are altered posttranscriptionally and most frequently involves conversion of adenosine to inosine, which is recognized as a guanosine during translation. Chen and colleagues performed RNA sequencing analysis to identify molecular changes in hepatocellular carcinoma (HCC) samples that might contribute to disease progression, and they detected elevated adenosine-to-inosine RNA editing of antizyme inhibitor 1 (AZIN1) in HCC samples compared with adjacent normal tissues. The frequency of AZIN1 editing increased during HCC progression and was correlated with liver cirrhosis, tumor recurrence, and poor prognosis, suggesting that this recoding event may promote HCC pathogenesis. AZIN1 RNA modification was mediated by the p110 isoform of adenosine deaminase, RNA-specific (ADAR1), but not by other ADAR family members, and resulted in substitution of glycine for serine at residue 367 in the AZIN1 protein, which was predicted to induce a ...

RNA editing is a regulatory mechanism in which nucleotides are altered posttranscriptionally and most frequently involves conversion of adenosine to inosine, which is recognized as a guanosine during translation. Chen and colleagues performed RNA sequencing analysis to identify molecular changes in hepatocellular carcinoma (HCC) samples that might contribute to disease progression, and they detected elevated adenosine-to-inosine RNA editing of antizyme inhibitor 1 (AZIN1) in HCC samples compared with adjacent normal tissues. The frequency of AZIN1 editing increased during HCC progression and was correlated with liver cirrhosis, tumor recurrence, and poor prognosis, suggesting that this recoding event may promote HCC pathogenesis. AZIN1 RNA modification was mediated by the p110 isoform of adenosine deaminase, RNA-specific (ADAR1), but not by other ADAR family members, and resulted in substitution of glycine for serine at residue 367 in the AZIN1 protein, which was predicted to induce a ...

The purine ribonucleoside in the nucleotide inosine monophosphate (IMP), from which the purine nucleotides adenosine monophosphate and guanosine monophosphate are derived. Its chemical formula is C10H12N4O5 ...

Inosine is not an amino acid but is classified as a nucleoside (a building block for DNA and RNA) found in muscle tissue and is one of the basic compounds comprising

TY - JOUR. T1 - Inosine preserves ATP content during ischemia and enhances functional recovery during reperfusion. AU - Devous, M. D.. AU - Lewandowski, E. D.. PY - 1985. Y1 - 1985. UR - http://www.scopus.com/inward/record.url?scp=0021839650&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=0021839650&partnerID=8YFLogxK. M3 - Article. AN - SCOPUS:0021839650. VL - 44. JO - Federation Proceedings. JF - Federation Proceedings. SN - 0014-9446. IS - 3. ER - ...

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Inosine is a nutritional supplement touted to improve athletic performance and a drug used in vitro as a red blood cell rejuvenator for a unit of red blood cells that will be used in a clinical setting.

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This clade of purine nucleotide phosphorylases has not been experimentally characterized but is assigned based on strong sequence homology. Closely related clades act on inosine and guanosine (PNPH, TIGR01700), and xanthosine, inosine and guanosine (XAPA, TIGR01699) neither of these will act on adenosine. A more distantly related clade (MTAP, TIGR01694) acts on methylthioadenosine ...

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You can download our 2017 product catalog in various formats, request to have a hard copy sent to you, or view our products online. ...

1D77: Crystal structure of a B-DNA dodecamer containing inosine, d(CGCIAATTCGCG), at 2.4 A resolution and its comparison with other B-DNA dodecamers.

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Thin layer chromatography (TLC) with densitometry has been established for the identification and the quantification of inosine pranobex in drug substance and drug products. Inosine pranobex is a combination of inosine, acetamidobenzoic acid, and dimethylaminoisopropanol. UV densitometry was performed in absorbance mode at 260 nm. The separation was carried out on aluminum sheet of silica gel 60 f 254 [chloroform - methanol- - toluene -10% ammonia solution (6:5:1: 0.1% v/v)] as mobile phase. Linearity range was found to be 1-12, 2-12, 2-20 and 2-16 µg/ml for inosine pranobex, inosine, acetamidobenzoic acid, and dimethylaminoisopropanol with the mean percentage recoveries 99.74± 1.73%, 99.88 ± 1.75%, 99.56 ±1.08%, and 99.36 ± 0.71% respectively, (Correlation coefficient r2 = 0.9998 for inosine pranobex, r2 = 0.09999 for inosine, r2 = 0.9998 for acetamidobenzoic acid and r2= 0.9998 for dimethylaminoisopropanol). The detection and quantification limits for inosine pranobex and other components are

The double-stranded RNA-specific adenosine deaminases ADAR1 and ADAR2 convert adenosine (A) residues to inosine (I) in messenger RNA precursors (pre-mRNA). Their main physiological substrates are pre-mRNAs encoding subunits of ionotropic glutamate receptors or serotonin receptors in the brain. ADAR1 and ADAR2 have similar sequence features, including double-stranded RNA binding domains (dsRBDs) and a deaminase domain. The tRNA-specific adenosine deaminases Tad1p and Tad2p/Tad3p modify A 37 in tRNA-Ala1 of eukaryotes and the first nucleotide of the anticodon (A 34) of several bacterial and eukaryotic tRNAs, respectively. Tad1p is related to ADAR1 and ADAR2 throughout its sequence but lacks dsRBDs. Tad1p could be the ancestor of ADAR1 and ADAR2. The deaminase domains of ADAR1, ADAR2 and Tad1p are very similar and resemble the active site domains of cytosine/cytidine deaminases.. ...

TY - JOUR. T1 - Adenosine and inosine exert cytoprotective effects in an in vitro model of liver ischemia-reperfusion injury. AU - Modis, Katalin. AU - Gero, Domokos. AU - Stangl, Rita. AU - Rosero, Olivér. AU - Szijártó, Attila. AU - Lotz, Gábor. AU - Mohácsik, Petra. AU - Szoleczky, Petra. AU - Coletta, Ciro. AU - Szabo, Csaba. PY - 2013/2. Y1 - 2013/2. N2 - Liver ischemia represents a common clinical problem. In the present study, using an in vitro model of hepatic ischemia-reperfusion injury, we evaluated the potential cyto-protective effect of the purine metabolites, such as adenosine and inosine, and studied the mode of their pharmacological actions. The human hepatocellular carcinoma-derived cell line HepG2 was subjected to combined oxygen-glucose deprivation (COGD; 0-14-24 h), followed by re-oxygenation (0-4-24 h). Adenosine or inosine (300-1,000 μM) were applied in pretreatment. Cell viability and cytotoxicity were measured by the 3-(4,5-dimethyl-2-thiazolyl)-2, ...

Adenosine deaminase (ADA) is a purine catabolic enzyme ubiquitous in mammalian tissue which catalyzes deamination of both adenosine and 2-deoxyadenosine to inosine and 2-deoxyinosine respectively. ...

The pyrimidine-specific nucleoside hydrolase Yeik (CU-NH) from Escherichia coli cleaves the N-glycosidic bond of uridine and cytidine with a 102~104-fold faster than that of purine nucleoside substrates such as inosine. Such remarkable substrate specificity and the plausible hydrolytic mechanisms of uridine have been explored by using QM/MM and MM MD simulations. The present calculations show that the relatively stronger hydrogen bond interactions between uridine and the active-site residues Gln227 and Tyr231 in CU-NH play an important role in enhancing the substrate binding and thus promoting the N-glycosidic bond cleavage, in comparison with inosine ...

Isoprinosine is a nucleoside an alkylamino-alcohol complex of inosine used in the treatment of a variety of viral infections CAS: 36703-88-5. 4-acetamidobenzoic acid compound with 9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1,9-dihydro-6H-purin-6-one and 1-(dimethylamino)propan-2-ol (3:1:3).

Running the UV-vis scan for each reagent showed that the increasing trend observed on the ADA kinetic assays was inosine not adenosine. This was verified by recalculating the molar absorptivities. The molar absortivity of inosine at 235 is greater than adenosine. This explains the increase over time since as ADA catalyzes the formation of inosine from adenosine; the catalysis increases the concentration of inosine so as its absorbance ...

Running the UV-vis scan for each reagent showed that the increasing trend observed on the ADA kinetic assays was inosine not adenosine. This was verified by recalculating the molar absorptivities. The molar absortivity of inosine at 235 is greater than adenosine. This explains the increase over time since as ADA catalyzes the formation of inosine from adenosine; the catalysis increases the concentration of inosine so as its absorbance ...

Benzo[a]pyrene, a potent human carcinogen, is metabolized in vivo to a diol epoxide that reacts with the N -position of guanine to produce N -BP-dG adducts. These adducts are mutagenic causing G to T transversions. These adducts block replicative polymerases but can be bypassed by the Y-family translesion synthesis polymerases. The mechanisms by which mutagenic bypass occurs is not well-known. We have evaluated base pairing structures using atomic substitution of the dNTP with two stereoisomers, 2-deoxy-N-[(7R,8S,9R,10S)-7,8,9,10-tetrahydro-7,8,9-trihydroxybenzo[a]pyren-10-yl]guanosine and 2-deoxy-N-[(7S,8R,9S,10R)-7,8,9,10-tetrahydro-7,8,9-trihydroxybenzo[a]pyren-10-yl]guanosine. We have examined the kinetics of incorporation of 1-deaza-dATP, 7-deaza-dATP, 2-deoxyinosine triphosphate, and 7-deaza-dGTP, analogues of dATP and dGTP in which single atoms are changed. Changes in rate will occur if that atom provided a critical interaction in the transition state of the reaction. We examined two ...

The objective of this Phase III, randomized, double-blind, placebo-controlled study in patients with immunologic deficiency is to determine the effect of Isoprinosine in producing an immuno-restorative response within the study observation period (including the 2-month period following cessation of the 28 days of treatment), measured by one or more of the following immunological parameters:. ...

The objective of this Phase III, randomized, double-blind, placebo-controlled study in patients with immunologic deficiency is to determine the effect of Isoprinosine in producing an immuno-restorative response within the study observation period (including the 2-month period following cessation of the 28 days of treatment), measured by one or more of the following immunological parameters:. ...

Adenosine-to-inosine (A-to-I) deamination is a functionally important modification of RNA that occurs in many metazoan nuclear transcripts, in several types tRNAs, and in mitochondrial...

RNA editing is the post-transcriptional modification of RNA nucleotides from their genome encoded sequence. The most common type of editing in metazoans is deamination of Adenosine into Inosine catalyzed by the ADAR family of proteins. Subsequently, Inosine is interpreted as Guanosine by the cellular machinery.. The development of high-throughput sequencing technologies has enabled the transcriptome-wide identification of A-to-I editing sites. This database aims to present a comprehensive collection of A-to-I editing sites in human, mouse, and fly transcripts. Useful annotations were incorporated as described in the tutorial.. News:. December 24, 2014: RADAR has been updated to version 2! We have added 8 additional papers to the database. We also removed ~3,000 human genomic SNPs from the database.. October 25, 2013: The RADAR manuscript is now online at Nucleic Acids Research! RADAR: a rigorously annotated database of A-to-I RNA editing. ...

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Clinical Trial Considers Inosine Safe and May Lead to Future Treatments to Slow the Progression of PARKINSONS DISEASE. Michael Schwarzschild, M.D., Ph.D. who is connected to the Harvard School of Public Health and Massachusetts General Hospital has been conducting research with urate levels for many years. In a report issued in May 2012, he stated that they had rather unexpectedly found that people who had higher levels of urate (uric acid) also had a lower than average chance of developing PARKINSONS DISEASE. In that study, they found that urate served as an antioxidant that could protect cells from cell death, however it required the assistance or cooperation of neighboring cells, called astrocytes. Astrocytes are cells that provide both structural and metabolic support to neurons and it is their intervention that determines how the urate is used within the neural cells. The next question was to find out if urate increased artificially would provide the same protection as urate produced ...

Melcher, T.; Maas, S.; Higuchi, M.; Keller, W.; Seeburg, P. H.; Major, G.; Larkman, A. U.; Jonas, P.; Sakmann, B.; Jack, J. J. B.: Editing of α-Amino-3-hydroxy-5-methylisoxazole-4-propionic Acid Receptor GluR-B Pre-mRNA in Vitro Reveals Site-selective Adenosine to Inosine Conversion. The Journal of Biological Chemistry 270 (15), S. 8566 - 8570 (1995 ...

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A purine nucleoside that has hypoxanthine linked by the N9 nitrogen to the C1 carbon of ribose. It is an intermediate in the degradation of purines and purine nucleosides to uric acid and in pathways of purine salvage. It also occurs in the anticodon of certain transfer RNA molecules. (Dorland, 28th ed)

RNA transcripts encoding the 2C-subtype of serotonin receptor (5HT{2C}) can be modified by up to five adenosine-to-inosine (A-to-l) editing events, a process re...

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* found in: 2-Deoxyuridine, 2-Deoxyguanosine monohydrate, ADP (Adenosine-5-diphosphate), ATP (Adenosine-5-triphosphate), DeoxyUridine, DeoxyInosine,..

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GSNAP has been updated and now includes an A-to-G tolerant alignment mode. Use this mode for cases where your mRNA may have been edited by the ADAR gene causing adenosine to be converted to inosine. The I is seen as a G when sequenced.. This version also introduces stranded and non-stranded modes for the new RNA tolerant mode and methylation analysis. Use the non-stranded mode when your laboratory protocol allows 5 to 3 genomic reads and their reverse complements on each strand.. ...

A newly created DNA base editor contains an atom-rearranging enzyme (red) that can change adenine into inosine (read and copied as guanine), guide RNA (green) which directs the molecule to the right spot, and Cas9 nickase (blue), which snips the opposing strand of DNA and tricks the cell into swapping the complementary base.

hCNT2 Inhibitor Potently inhibits hCNT2-mediated Na+-dependent inosine uptake (IC₅₀ = 640 nM in COS-7 cells). - Find MSDS or SDS, a COA, data sheets and more information.

Type and Description of Treatments: 6 rounds of Rituxan and Bendamustine infusion, once every 4 weeks How do you feel today? I have a good amount of energy today, and am feeling both grateful and at peace. Continue Reading ...

To upload data we ask project partners to email the files to us at [email protected].. If your dataset is too large for email we can arange for you to upload the files via FTP on request.. For more details click here.... ...

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