Liu, Yuyang et al. published their research in Harmful Algae in 2020 |CAS: 4433-40-3

The Article related to hydroxymethyluracil genetic diversity aquatic environment alexandrium prorocentrum, cell volume, co-evolution, dinoflagellate, genome size, lsu rrna gene copy number, Placeholder for records without volume info and other aspects.SDS of cas: 4433-40-3

On November 30, 2020, Liu, Yuyang; Hu, Zhangxi; Deng, Yunyan; Shang, Lixia; Gobler, Christopher J.; Tang, Ying Zhong published an article.SDS of cas: 4433-40-3 The title of the article was Dependence of genome size and copy number of rRNA gene on cell volume in dinoflagellates. And the article contained the following:

Dinoflagellates are an ecol. important group of protists in aquatic environment and have evolved many unusual and enigmatic genomic features such as immense genome sizes, high repeated genes, and a large portion of hydroxymethyluracil in DNA. Although previous studies have observed pos. correlations between the large subunit (LSU) rRNA gene copy number and genome size of a variety of eukaryotic organisms (e.g. higher plants and animals), or between cell volume and LSU rRNA gene copy number, and/or between genome size and cell size, which suggests a possible co-evolution among these three features in different lineages of life, it remains an open question regarding the relationships among these three parameters in dinoflagellates. For the first time, we estimated the copy numbers of the LSU rRNA gene, the genome sizes, and cell volumes within a broad range of dinoflagellates (covering 15 species of 11 genera) using single-cell qPCR-based assay (determining LSU rRNA gene copy number), FlowCAM (cell volume measurement), and UV spectrophotometry (genome size estimation). The measured copy number of LSU rRNA gene ranged from 398 ± 184 (Prorocentrum min.) to 152,078 ± 33,555 copies•cell-1 (Alexandrium pacificum), while the genome size and the cell volume ranged from 5.6 ± 0.2 (Karlodinium veneficum) to 853 ± 19.9 pg•cell-1 (Pseliodinium pirum), and from 1,070 ± 225 (Kar. veneficum) to 168,474 ± 124,180 μm3 (Ps. pirum), resp. Together with the three parameters measured in literature, there are significant pos. linear correlations between LSU rRNA gene copy numbers and genome sizes, cell volumes and LSU rRNA gene copy numbers, and between genome sizes and cell volumes via comparisons of multi-model regression analyses, suggesting a dependence of genome size and rRNA gene copy number on the cell volumes of dinoflagellates. Validation of the measurement methods was conducted via comparisons between reported data in the literature and that predicted using the linear equations we obtained, and between genome size measured by flow cytometry (FCM) and UV spectrophotometry (Nanodrop). These results provide insightful understandings of dinoflagellate evolution in terms of the relationships among genomes, gene copy number, and cell volume, and of rRNA gene-based studies in intra-populational and intra-individual genetic diversity, taxonomy, and diversity assessment in the environment of dinoflagellates. The results also provide a dataset useful for reads calibration in environmental metabarcoding studies of dinoflagellates and selection of candidate species for whole genome sequencing. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).SDS of cas: 4433-40-3

The Article related to hydroxymethyluracil genetic diversity aquatic environment alexandrium prorocentrum, cell volume, co-evolution, dinoflagellate, genome size, lsu rrna gene copy number, Placeholder for records without volume info and other aspects.SDS of cas: 4433-40-3

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Zott, Fabian L. et al. published their research in ChemBioChem in 2022 |CAS: 4433-40-3

The Article related to formylcytosine hydration hydrogen ion concentration, dna methylation, tet enzymes, aldehyde hydrates, computational chemistry, epigenetics, modified nucleic acids, General Biochemistry: Subcellular Processes and other aspects.COA of Formula: C5H6N2O3

On April 5, 2022, Zott, Fabian L.; Korotenko, Vasily; Zipse, Hendrik published an article.COA of Formula: C5H6N2O3 The title of the article was The pH-Dependence of the Hydration of 5-Formylcytosine: an Experimental and Theoretical Study. And the article contained the following:

5-Formylcytosine is an important nucleobase in epigenetic regulation, whose hydrate form has been implicated in the formation of 5-carboxycytosine as well as oligonucleotide binding events. The hydrate content of 5-formylcytosine and its uracil derivative has now been quantified using a combination of NMR and mass spectroscopic measurements as well as theor. studies. Small amounts of hydrate can be identified for the protonated form of 5-formylcytosine and for neutral 5-formyluracil. For neutral 5-formylcytosine, however, direct detection of the hydrate was not possible due to its very low abundance. This is in full agreement with theor. estimates The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).COA of Formula: C5H6N2O3

The Article related to formylcytosine hydration hydrogen ion concentration, dna methylation, tet enzymes, aldehyde hydrates, computational chemistry, epigenetics, modified nucleic acids, General Biochemistry: Subcellular Processes and other aspects.COA of Formula: C5H6N2O3

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Yang, Hao et al. published their research in Bioengineered in 2022 |CAS: 4433-40-3

The Article related to neurobrucellosis cerebrospinal fluid metabolite biomarker lcms, neurobrucellosis, cerebrospinal fluid, liquid chromatography-mass spectrometry, metabolomics, Placeholder for records without volume info and other aspects.Computed Properties of 4433-40-3

Yang, Hao; Wang, Zhenfei; Shi, Shujun; Yu, Qin; Liu, Meiling; Zhang, Zhelin published an article in 2022, the title of the article was Identification of cerebrospinal fluid metabolites as biomarkers for neurobrucellosis by liquid chromatography-mass spectrometry approach.Computed Properties of 4433-40-3 And the article contains the following content:

Neurobrucellosis is the most morbid form in brucellosis disease. Metabolomics is an emerging method which intends to explore the global alterations of various metabolites in samples. We aimed to identify metabolites in cerebrospinal fluid (CSF) as biomarkers that were potentially unique for neurobrucellosis. CSF samples from 25 neurobrucellosis patients and 25 normal controls (uninfected patients with hydrocephalus) were collected for metabolite detection using liquid chromatog.-mass spectrometry (LC-MS) approach. Inflammatory cytokines in CSF were measured with ELISA (ELISA). The base peak chromatogram in CSF samples showed that small-mol. metabolites were well separated Principal Component Anal. (PCA) anal. exhibited the examined samples were arranged in two main clusters in accordance with their group. Projection to Latent Structures Discriminant Anal. (PLS-DA) revealed there was a noticeable separation between neurobrucellosis and normal groups. Orthogonal Partial Least-Squares-Discriminant Anal. (OPLS-DA) could responsibly illuminate the differences between neurobrucellosis and normal controls. Neurobrucellosis showed a total of 155 differentiated metabolites. Prominent potential biomarkers including 30 metabolites were then selected out, regarded as more capable of distinguishing neurobrucellosis. TNF-α and IL-6 in CSF were remarkably increased in neurobrucellosis. We presented the heatmaps and correlation analyses among the identified 30 potential biomarkers. In conclusion, this study showed that CSF metabolomics based on LC-MS could distinguish neurobrucellosis patients from normal controls. Our data offered perspectives for diagnosis and treatment for neurobrucellosis. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).Computed Properties of 4433-40-3

The Article related to neurobrucellosis cerebrospinal fluid metabolite biomarker lcms, neurobrucellosis, cerebrospinal fluid, liquid chromatography-mass spectrometry, metabolomics, Placeholder for records without volume info and other aspects.Computed Properties of 4433-40-3

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Brown, Catherine L. J. et al. published their research in Poultry Science in 2022 |CAS: 4433-40-3

The Article related to proton nmr spectroscopy metabolomics biomarker, biomarker, broiler chicken, feather pulp, metabolomics, proton nuclear magnetic resonance spectroscopy, Placeholder for records without volume info and other aspects.Category: pyrimidines

On July 31, 2022, Brown, Catherine L. J.; Montina, Tony; Inglis, G. Douglas published an article.Category: pyrimidines The title of the article was Feather pulp: a novel substrate useful for proton nuclear magnetic resonance spectroscopy metabolomics and biomarker discovery. And the article contained the following:

Noninvasive biomarkers of stress that are predictive of poultry health are needed. Feather pulp is highly vascularized and represents a potential source of biomarkers that has not been extensively explored. We investigated the feasibility and use of feather pulp for novel biomarker discovery using 1H-NMR Spectroscopy (NMR)-based metabolomics. To this end, high quality NMR metabolomic spectra were obtained from chicken feather pulp extracted using either ultrafiltration (UF) or Bligh-Dyer methanol-chloroform (BD) methods. In total, 121 and 160 metabolites were identified using the UF and BD extraction methods, resp., with 71 of these common to both methods. The metabolome of feather pulp differed in broiler breeders that were 1-, 23-, and 45-wk-of-age. Moreover, feather pulp was more difficult to obtain from older birds, indicating that age must be considered when targeting feather pulp as a source of biomarkers. The metabolomic profile of feather pulp obtained from 12-day-old broilers administered corticosterone differed from control birds, indicating that the metabolome of feather pulp was sensitive to induced physiol. stress. A comparative examination of feather pulp and serum in broilers revealed that the feather pulp metabolome differed from that of serum but provided more information. The study findings show that metabolite biomarkers in chicken feather pulp may allow producers to effectively monitor stress, and to objectively develop and evaluate on-farm mitigations, including practices that reduce stress and enhance bird health. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).Category: pyrimidines

The Article related to proton nmr spectroscopy metabolomics biomarker, biomarker, broiler chicken, feather pulp, metabolomics, proton nuclear magnetic resonance spectroscopy, Placeholder for records without volume info and other aspects.Category: pyrimidines

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Yang, Sha et al. published their research in Biomedicine & Pharmacotherapy in 2020 |CAS: 4433-40-3

The Article related to metabolomics mol pharmacol hematopoietic function mouse, bio-markers, gei herba, hematopoietic function, metabolomics, molecular pharmacology, Placeholder for records without volume info and other aspects.Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

On September 30, 2020, Yang, Sha; Wang, Xiaoning; Duan, Cancan; Zhang, Jianyong published an article.Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione The title of the article was A novel approach combining metabolomics and molecular pharmacology to study the effect of Gei Herba on mouse hematopoietic function. And the article contained the following:

Gei Herba, Chinese named Lanbuzheng (LBZ), is a traditional Chinese medicine promotes hematopoiesis, yet the underlying mechanism for this effect remains largely unknown. In the present study, a novel approach combining LC-MS metabolomics and mol. pharmacol. was developed to investigate the hematopoietic effect and mechanism of LBZ on hematopoietic dysfunction (HD) caused by cyclophosphamide (CTX) in treated mice. The results show that LBZ can reduce damage in the spleen, a result consistent with the peripheral hemogram. Fourteen potential biomarkers were identified in the spleen by metabolic profiles anal., including 5-hydroxymethyluracil, ascorbalamic acid, AMP, menadiol disulfate, L-homocysteine sulfonic acid and L-carnitine. Change in biomarker levels suggest that LBZ mainly affects β-oxidation of very-long-chain fatty acids, oxidation of branched chain fatty acids and carnitine synthesis, and those metabolites produced along with related metabolic pathways are closely associated with anti-apoptosis. A mol. pharmacol. approach was simultaneously developed to examine accompanying cellular signaling mechanisms. LBZ activates PI3K/Akt signaling pathways and granulocyte-colony-stimulating-factor (G-CSF)-mediated Janus kinase 2 (JAK2)/transcription 3 (STAT3), resulting in inhibiting the release of cytochrome c. Further, LBZ inhibits caspase-mediated mitochondrial-dependent apoptosis mediated by caspase-9 and caspase-3. LBZ can thus reduce CTX-induced HD via G-CSF-mediated JAK2/STAT3 signaling and PI3K/Akt mitochondrial-dependent apoptotic pathways. The present study combines metabolomic and mol. pharmacol. methods to elucidate mechanisms for the protective effect of LBZ on mouse HD following CTX-induced damage. This approach may be useful for exploring mechanisms of action of other drugs. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

The Article related to metabolomics mol pharmacol hematopoietic function mouse, bio-markers, gei herba, hematopoietic function, metabolomics, molecular pharmacology, Placeholder for records without volume info and other aspects.Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Krell, Katja et al. published their research in Biomolecules in 2020 |CAS: 4433-40-3

The Article related to phosphoramidite tetrazole rna fluorescent bioorthogonal photoclick chem, oligonucleotide, photochemistry, tetrazole, Placeholder for records without volume info and other aspects.Computed Properties of 4433-40-3

Krell, Katja; Achim-Wagenknecht, Hans published an article in 2020, the title of the article was Fluorogenic and bioorthogonal modification of RNA using photoclick chemistry.Computed Properties of 4433-40-3 And the article contains the following content:

A bromoaryltetrazole-modified uridine was synthesized as new RNA building block for bioorthogonal, light-activated and postsynthetic modification with com. available fluorescent dyes. It allows “photoclick”-type modifications by irradiation with light (300 nm LED) at internal and terminal positions of presynthesized RNA with maleimide-conjugated fluorophores in good yields. The reaction was evidenced for three different dyes. During irradiation, the emission increases due to the formation of an intrinsically fluorescent pyrazoline moiety as photoclick product. The fluorogenecity of the photoclick reaction was significantly enhanced by energy transfer between the pyrazoline as the reaction product (poor emitter) and the photoclicked dye as the strong emitter. The RNA-dye conjugates show remarkable fluorescent properties, in particular an up to 9.4 fold increase of fluorescence, which are important for chem. biol. and fluorescent imaging of RNA in cells. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).Computed Properties of 4433-40-3

The Article related to phosphoramidite tetrazole rna fluorescent bioorthogonal photoclick chem, oligonucleotide, photochemistry, tetrazole, Placeholder for records without volume info and other aspects.Computed Properties of 4433-40-3

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Peach, Jesse T. et al. published their research in iScience in 2021 |CAS: 4433-40-3

The Article related to metabolic response biosignature inflammation, metabolomics, pathophysiology, systems biology, Placeholder for records without volume info and other aspects.HPLC of Formula: 4433-40-3

On August 20, 2021, Peach, Jesse T.; Wilson, Stephanie M.; Gunderson, Logan D.; Frothingham, Lizzi; Tran, Tan; Walk, Seth T.; Yeoman, Carl J.; Bothner, Brian; Miles, Mary P. published an article.HPLC of Formula: 4433-40-3 The title of the article was Temporal metabolic response yields a dynamic biosignature of inflammation. And the article contained the following:

Chronic low-grade inflammation is a subclin. condition directly and indirectly linked to the development of a wide range of diseases responsible for the vast majority of morbidity. To examine mechanisms coupled to chronic disease, a group of overweight and obese human subjects without known inflammatory diseases participated in a high-fat meal challenge as an acute inflammation stimulus. Anal. of serum metabolites grouped by baseline cytokine levels revealed that single samples had little power in differentiating groups. However, an anal. that incorporated temporal response separated inflammatory response phenotypes and allowed us to create a metabolic signature of inflammation which revealed metabolic components that are crucial to a cytokine-mediated inflammation response. The use of temporal response, rather than a single time point, improved metabolomic prediction of high postprandial inflammation responses and led to the development of a dynamic biosignature as a potential tool for stratifying risk to a wide range of diseases. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).HPLC of Formula: 4433-40-3

The Article related to metabolic response biosignature inflammation, metabolomics, pathophysiology, systems biology, Placeholder for records without volume info and other aspects.HPLC of Formula: 4433-40-3

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Pandey, Renu et al. published their research in Analytical Chemistry (Washington, DC, United States) in 2021 |CAS: 4433-40-3

The Article related to untargeted chiral metabolomics liquid chromatog high resolution mass spectrometry, tandem, Placeholder for records without volume info and other aspects.Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

On April 13, 2021, Pandey, Renu; Collins, Meghan; Lu, Xiyuan; Sweeney, Shannon R.; Chiou, Jennifer; Lodi, Alessia; Tiziani, Stefano published an article.Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione The title of the article was Novel Strategy for Untargeted Chiral Metabolomics using Liquid Chromatography-High Resolution Tandem Mass Spectrometry. And the article contained the following:

Stereospecific recognition of metabolites plays a significant role in the detection of potential disease biomarkers thereby providing new insights in diagnosis and prognosis. D-Hdroxy/amino acids are recognized as potential biomarkers in several metabolic disorders. Despite continuous advances in metabolomics technologies, the simultaneous measurement of different classes of enantiomeric metabolites in a single anal. run remains challenging. Here, we develop a novel strategy for untargeted chiral metabolomics of hydroxy/amine groups (-OH/-NH2) containing metabolites, including all hydroxy acids (HAs) and amino acids (AAs), by chiral derivatization coupled with liquid chromatog.-high resolution tandem mass spectrometry (LC-HR-MS/MS). Diacetyl-tartaric anhydride (DATAN) was used for the simultaneous derivatization of-OH/-NH2 containing metabolites as well as the resulting diastereomers, and all the derivatized metabolites were resolved in a single anal. run. Data independent MS/MS acquisition (DIA) was applied to pos. identify DATAN-labeled metabolites based on reagent specific diagnostic fragment ions. We discriminated chiral from achiral metabolites based on the reversal of elution order of D and L isomers derivatized with the enantiomeric pair (±) of DATAN in an untargeted manner. Using the developed strategy, a library of 301 standards that consisted of 214 chiral and 87 achiral metabolites were separated and detected in a single anal. run. This approach was then applied to investigate the enantioselective metabolic profile of the bone marrow (BM) and peripheral blood (PB) plasma samples from patients with acute myeloid leukemia (AML) at diagnosis and following completion of the induction phase of chemotherapeutic treatment. The sensitivity and selectivity of the developed method enabled the detection of trace levels of the D-enantiomer of HAs and AAs in primary plasma patient samples. Several of these metabolites were significantly altered in response to chemotherapy. The developed LC-HR-MS method entails a valuable step forward in chiral metabolomics. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

The Article related to untargeted chiral metabolomics liquid chromatog high resolution mass spectrometry, tandem, Placeholder for records without volume info and other aspects.Reference of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Nam, Jaehyuk et al. published their research in Chemical Communications (Cambridge, United Kingdom) in 2017 |CAS: 4433-40-3

The Article related to uracil bearing polyisopropyloxazoline mercury selective thermoresponsiveness control, Inorganic Analytical Chemistry: Determinations and other aspects.Related Products of 4433-40-3

Nam, Jaehyuk; Jung, Yongseok; Jang, Woo-Dong published an article in 2017, the title of the article was Uracil-bearing poly(2-isopropyl-2-oxazoline): Hg(II)-selective control of its thermoresponsiveness.Related Products of 4433-40-3 And the article contains the following content:

A poly(2-isopropyl-2-oxazoline)-containing mercury ion (Hg2+)-responsive uracil moiety (U-PiPOx-U) was synthesized and it exhibited thermoresponsiveness in its aqueous solution The changes in the UV-visible absorption and thermoresponsiveness of U-PiPOx-U upon the addition of Hg2+ were studied. Selective sensing of Hg2+ was also studied. The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).Related Products of 4433-40-3

The Article related to uracil bearing polyisopropyloxazoline mercury selective thermoresponsiveness control, Inorganic Analytical Chemistry: Determinations and other aspects.Related Products of 4433-40-3

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Gackowski, Daniel et al. published their research in Haematologica in 2020 |CAS: 4433-40-3

The Article related to formylcytosine hydroxymethyluracil tet2 sf3b1 mutation myelodysplastic syndrome, Mammalian Pathological Biochemistry: Oncology and other aspects.Name: 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

Gackowski, Daniel; Gawronski, Maciej; Kerr, Cassandra; Radivoyevitch, Tomas; Zarakowska, Ewelina; Starczak, Marta; Abakir, Abdulkadir; Ruzov, Alexey; Maciejewski, Jaroslaw P.; Olinski, Ryszard published an article in 2020, the title of the article was Base 5-formylcytosine and 5-hydroxymethyluracil as surrogate markers of TET2 and SF3B1 mutations in myelodysplastic syndrome, respectively.Name: 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione And the article contains the following content:

TET2 protein has been implicated in 5-hydroxymethyluracil generation to quantify the extent to which TET2 mutations cause deficiencies in TET2 dioxygenase activity. In the present study, the linkage between various TET2 mutations and 5-hydroxymethylcytosine, 5-formylcytosine, 5-carboxycytosine and 5-hydroxymethyluracil, and linkage between these modifications and myeloid neoplastic disease were characterized. We selected patients with a broad range of different types of TET2 alterations and detected in samples from them a broad spectrum of DNA modifications. Levels of DNA markers of TET2 activity obtained using automated two-dimensional ultra-performance liquid chromatog. tandem mass spectrometry with incorporation of stable isotope-labeled internal standards The results reavealed that the best predictor/marker of TET2 mutations in patients with myeloid malignancies was 5-formylcytosine. Receiver operating characteristic (ROC) curves for predicting TET2 mutated vs. wild-type subjects show that a 5-formylcytosine threshold of 0.204 per 106dN yields a sensitivity of 100% and a specificity of 83%. Disruption of SF3B1 in the K562 cell line resulted in G2/M cell cycle arrest. In conclusion, our results suggested that the anal. of 5-formylcytosine and 5-hydroxymethyluracil are warranted as surrogate markers of TET2 and SF3B1 mutations in myelodysplastic syndrome . The experimental process involved the reaction of 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione(cas: 4433-40-3).Name: 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

The Article related to formylcytosine hydroxymethyluracil tet2 sf3b1 mutation myelodysplastic syndrome, Mammalian Pathological Biochemistry: Oncology and other aspects.Name: 5-(Hydroxymethyl)pyrimidine-2,4(1H,3H)-dione

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia