Academic literature on the topic '4-DNP derivative'

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Journal articles on the topic "4-DNP derivative"

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Albu, Paul Constantin, Szidonia-Katalin Tanczos, Andreea Ferencz (Dinu), et al. "pH and Design on n–Alkyl Alcohol Bulk Liquid Membranes for Improving Phenol Derivative Transport and Separation." Membranes 12, no. 4 (2022): 365. http://dx.doi.org/10.3390/membranes12040365.

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Regardless of the type of liquid membrane (LM) (Bulk Liquid Membranes (BLM), Supported Liquid Membranes (SLM) or Emulsion Liquid Membranes (ELM)), transport and separation of chemical species are conditioned by the operational (OP) and constructive design parameters (DP) of the permeation module. In the present study, the pH of the aqueous source phase (SP) and receiving phase (RP) of the proposed membrane system were selected as operational parameters. The mode of contacting the phases was chosen as the convective transport generator. The experiments used BLM-type membranes with spheres in free rotation as film contact elements of the aqueous phases with the membrane. The target chemical species were selected in the range of phenol derivatives (PD), 4–nitrophenol (NP), 2,4–dichlorophenol (DCP) and 2,4–dinitrophenol (DNP), all being substances of technical-economic and environmental interest. Due to their acid character, they allow the evaluation of the influence of pH as a determining operational parameter of transport and separation through a membrane consisting of n–octanol or n–decanol (n–AlcM). The comparative study performed for the transport of 4–nitrophenol (NP) showed that the module based on spheres (Ms) was more performant than the one with phase dispersion under the form of droplets (Md). The sphere material influenced the transport of 4–nitrophenol (NP). The transport module with glass spheres (Gl) was superior to the one using copper spheres (Cu), but especially with the one with steel spheres (St). In all the studied cases, the sphere-based module (Ms) had superior transport results compared to the module with droplets (Md). The extraction efficiency (EE) and the transport of 2,4–dichlorophenol (DCP) and 2,4–dinitrophenol (DNP), studied in the module with glass spheres, showed that the two phenolic derivatives could be separated by adjusting the pH of the source phase. At the acidic pH of the source phase (pH = 2), the two derivatives were extracted with good results (EE > 90%), while for pH values ranging from 4 to 6, they could be separated, with DCP having doubled separation efficiency compared to DNP. At a pH of 8 in the source phase, the extraction efficiency halved for both phenolic compounds.
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Knight, C. G. "A quenched fluorescent substrate for thimet peptidase containing a new fluorescent amino acid, DL-2-amino-3-(7-methoxy-4-coumaryl)propionic acid." Biochemical Journal 274, no. 1 (1991): 45–48. http://dx.doi.org/10.1042/bj2740045.

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DL-2-Amino-3-(7-methoxy-4-coumaryl)propionic acid, a new fluorescent amino acid (abbreviated to Amp), has been synthesized to provide an alternative to tryptophan in quenched fluorescent peptide substrates for peptidases. The model compound Ac-DL-Amp-NH2 was intensely fluorescent with an excitation maximum at 328 nm and an emission maximum at 392 nm. Fmoc (fluoren-9-ylmethoxycarbonyl)-DL-Amp was made to allow the solid-phase synthesis of Amp-containing peptides by the Fmoc-polyamide method. The peptide derivative Dnp (2,4-dinitrophenyl)-Pro-Leu-Gly-Pro-DL-Amp-D-Lys was cleaved by thimet peptidase at the Leu-Gly bond, with a 20-fold enhancement of fluorescence. The value of kcat./Km for thimet peptidase was 6.7 x 10(5) M-1.s-1, compared with the value of 2.4 x 10(5) M-1.s-1 for the tryptophan-containing analogue, Dnp-Pro-Leu-Gly-Pro-Trp-D-Lys.
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Li, Dongmi, Panpan Lv, Xiao-Wen Han, Zhilei Jia, Min Zheng, and Hai-Tao Feng. "A Highly Efficient Fluorescent Sensor Based on AIEgen for Detection of Nitrophenolic Explosives." Molecules 28, no. 1 (2022): 181. http://dx.doi.org/10.3390/molecules28010181.

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The detection of nitrophenolic explosives is important in counterterrorism and environmental protection, but it is still a challenge to identify the nitroaromatic compounds among those with a similar structure. Herein, a simple tetraphenylethene (TPE) derivative with aggregation-induced emission (AIE) characteristics was synthesized and used as a fluorescent sensor for the detection of nitrophenolic explosives (2, 4, 6-trinitrophenol, TNP and 2, 4-dinitrophenol, DNP) in water solution and in a solid state with a high selectivity. Meanwhile, it was found that only hydroxyl containing nitrophenolic explosives caused obvious fluorescence quenching. The sensing mechanism was investigated by using fluorescence titration and 1H NMR spectra. This simple AIE-active probe can potentially be applied to the construction of portable detection devices for explosives.
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MOHD., ALI, and SHARMA NlRMAL. "Characterisation of Chemical Constituents of Gliricidia meculata Leaves." Journal of Indian Chemical Society Vol. 74, Aug 1997 (1997): 658–59. https://doi.org/10.5281/zenodo.5895292.

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Faculty of Pharmacy, Jarnia Hamdard (Hamdard University), Hamdard Nagar, New Delhi-110 062 <em>Manuscript received 16 June 1994, revised 15 February 1996, accepted 24 June 1996</em> Characterisation of Chemical Constituents of Gliricidia meculata Leaves.
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Dust, Julian M., and Richard A. Manderville. "Carbon versus oxygen nucleophilic selectivity in the reaction of the aryloxide ions, 2,6- and 3,5-di-tert-butylphenoxide, with the 2-[(nitro)\dn6 xaryl]-4,6-dinitrobenzotriazole 1-oxide series of super-electrophiles. Stereoelectronic factors on C-7 Meisenheimer complex formation versus C-1' SNAr displacement." Canadian Journal of Chemistry 76, no. 6 (1998): 662–71. http://dx.doi.org/10.1139/v98-028.

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The 2-[(nitro)xaryl]-4,6-dinitrobenzotriazole 1-oxides (1, Pi-DNBT (x = 3); 2, DNP-DNBT (x = 2); 3, NP-DNBT (x = 1)) are electron-deficient nitro-substituted heteroaromatic substrates that possess two sites for nucleophilic attachment: C-7 and C-1'. Generally, attack at the super-electrophilic C-7 site yields spectroscopically observable anionic sigma -bonded adducts, whereas attack at C-1' leads to displacement products in an overall process of nucleophilic aromatic substitution (SNAr). To gain an understanding of the factors affecting C-1' versus C-7 attack by potentially ambident aryloxide (C- and O-)nucleophiles, we have monitored the reactions of 1-3 with 2,6-di-tert-butylphenoxide (2,6-ArO-) and 3,5-di-tert-butylphenoxide (3,5-ArO-) using 400 MHz 1H NMR spectroscopy (deuterated dimethyl sulfoxide solvent at ambient temperature). The results indicate that 2,6-ArO- acts only as a C-nucleophile with O-attack precluded, presumably by the sterically demanding tert-butyl groups flanking the O-nucleophilic centre. Although 2,6-ArO- reacts preferentially at C-7 of 1-3, the biphenyl derivative that arises from C-1' attack is also observed with 1, the first time that C-nucleophilic attack has been seen at this electrophilic site. In contrast, 3,5-ArO- acts only as an O-nucleophile, also as a consequence of the steric hindrance to the C-4 position; this aryloxide reacts entirely at C-1' of Pi-DNBT but also exclusively at C-7 of 3. However, with DNP-DNBT, 2, both the C-7 O-adduct and C-1' displacement products are noted; attack at C-1' is dominant. The selectivity (C-7 versus C-1') found in these reactions is discussed with emphasis given to stereoelectronic factors that may stabilize the putative C-1' O-adducts.Key words: aryloxides, super-electrophiles, Meisenheimer complexes, 2-[(nitro)xaryl]-4,6-dinitrobenzotriazole 1-oxides.
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Panwar, Ritik, Vikash Jakhmola, Supriyo Saha, Sunil Jawla, and Ravinesh Mishra. "Molecular Docking, MD Simulation, and Antiproliferative Activity of Pyridazine Derivatives." International Journal of Drug Delivery Technology 15, no. 02 (2025): 01–09. https://doi.org/10.25258/ijddt.15.2.48.

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Pyridazine derivative showed much diversified activity. Previously 77 pyridazine derivatives were synthesized and evaluated the antihypertensive property. Pyridazine derivatives also showed antitumor and antiproliferative behavior. By kept this idea in mind we repurposed those pyridazine derivatives towards antiproliferation using in silico, and in vitro methods. Molecular docking analysis of pyridazine derivatives against DNA (PDB id: 6BNA) were performed and top4 molecules (R45, R60, R67, R70) were identified based on their docking scores. Then 100 ns MD simulation and MMPBSA analysis of these molecules were performed using GROMACS software. MD simulation data showed good RMSD, radius of gyration, SASA, and hydrogen bond analysis. Pyridazine derivative (R67) showed good simulation behavior with very minimum fluctuation within the receptor. Free binding energy of R67 was (-) 42.683 kJ/mol. R67 showed marked GI50 value against MCF7 cell line using sulphorhodamine assay. Among the pyridazine derivatives Among the synthesized molecules 6-([1,1'-biphenyl]-4-yl)-2-(4-([1,1'-biphenyl]-4-yl)-5-thioxo-4,5-dihydro-1H-1,2,4- triazol-3-yl)-4,5-dihydropyridazin-3(2H)-one (R67) showed best antiproliferative activity with in silico insights.
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Nicolás, Álvaro, Julia G. Quero, Marta Barroso, Zoila Gándara, and Lourdes Gude. "DNA Interactions and Biological Activity of 2,9-Disubstituted 1,10-Phenanthroline Thiosemicarbazone-Based Ligands and a 4-Phenylthiazole Derivative." Biology 13, no. 1 (2024): 60. http://dx.doi.org/10.3390/biology13010060.

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Four 1,10-phenanthroline derivatives (1–4) were synthesized as potential telomeric DNA binders, three substituted in their chains with thiosemicarbazones (TSCs) and one 4-phenylthiazole derivative. The compounds were characterized using NMR, HRMS, FTIR-spectroscopy and combustion elemental analysis. Quadruplex and dsDNA interactions were preliminarily studied, especially for neutral derivative 1, using FRET-based DNA melting assays, equilibrium dialysis (both competitive and non-competitive), circular dichroism and viscosity titrations. The TSC derivatives bind and stabilize the telomeric Tel22 quadruplex more efficiently than dsDNA, with an estimated 24-fold selectivity determined through equilibrium dialysis for compound 1. In addition, cytotoxic activity against various tumor cells (PC-3, DU145, HeLa, MCF-7 and HT29) and two normal cell lines (HFF-1 and RWPE-1) was evaluated. Except for the 4-phenylthiazole derivative, which was inactive, the compounds showed moderate cytotoxic properties, with the salts displaying lower IC50 values (30–80 μM), compared to the neutral TSC, except in PC-3 cells (IC50 (1) = 18 μM). However, the neutral derivative was the only compound that exhibited a modest selectivity in the case of prostate cells (tumor PC-3 versus healthy RWPE-1). Cell cycle analysis and Annexin V/PI assays revealed that the compounds can produce cell death by apoptosis, an effect that has proven to be similar to that demonstrated by other known 1,10-phenanthroline G4 ligands endowed with antitumor properties, such as PhenDC3 and PhenQE8.
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Aleo, Danilo, Venera Cardile, Rosa Chillemi, Giuseppe Granata, and Sebastiano Sciuto. "Chemoenzymatic Synthesis and Some Biological Properties of O-phosphoryl Derivatives of (E)-resveratrol." Natural Product Communications 3, no. 10 (2008): 1934578X0800301. http://dx.doi.org/10.1177/1934578x0800301023.

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3- O-, 3,5-di- O- and 4′- O-phosphoryl derivatives of ( E)-resveratrol have been obtained following a chemoenzymatic strategy. Variedly acylated resveratrol derivatives have been obtained first by exploiting regioselective properties of Pseudomonas cepacea or Candida antarctica lipases in organic solvents. Each acyl-resveratrol was then phosphorylated by the phosphoramidite chemistry protocol and in sequence freed of protective groups, affording the desired O-phosphoryl derivative. Following UV-absorption spectroscopic investigation on the interaction of the newly synthesized compounds with DNA, 4′- O-phosphorylresveratrol exhibited the best binding affinity. As a result of cytotoxicity tests, 3- O-phosphorylresveratrol was more active than resveratrol against DU 145 prostate cancer cells.
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Stolarczyk, Marcin, Agnieszka Matera-Witkiewicz, Aleksandra Wolska, et al. "Synthesis, Crystal Structure, and Biological Evaluation of Novel 5-Hydroxymethylpyrimidines." Materials 14, no. 22 (2021): 6916. http://dx.doi.org/10.3390/ma14226916.

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Pyrimidine displays a wide array of bioactivities, and thence, it is still considered a potent unit of new drug research. Its derivative, 5-hydroxymethylpyrimidine, can be found as a scaffold of nontypical nitrogen bases in DNA and as a core of some natural bioactive compounds. In this study, we obtained a series of 5-hydroxymethylpyrimidines that vary in the 4-position by the reduction of proper esters. All compounds were characterized by spectroscopic analysis, and single-crystal X-ray diffraction was performed for some of them. Biological investigations estimated cytotoxic properties against normal (RPTEC) and cancer (HeLa, HepaRG, Caco-2, AGS, A172) cell lines. It was found that the derivatives with an aliphatic amino group at the 4-position are generally less toxic to normal cells than those with a benzylsulfanyl group. Moreover, compounds with bulky constituents exhibit better anticancer properties, though at a moderate level. The specific compounds were chosen due to their most promising IC50 concentration for in silico study. Furthermore, antimicrobial activity tests were performed against six strains of bacteria and one fungus. They demonstrated that only derivatives with at least three carbon chain amino groups at the 4-position have weak antibacterial properties, and only the derivative with 4-benzylsulfanyl constituent exhibits any antifungal action.
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Orchel, Arkadiusz, Ewa Chodurek, Marzena Jaworska-Kik, et al. "Anticancer Activity of the Acetylenic Derivative of Betulin Phosphate Involves Induction of Necrotic-Like Death in Breast Cancer Cells In Vitro." Molecules 26, no. 3 (2021): 615. http://dx.doi.org/10.3390/molecules26030615.

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Betulin (BT) is a natural pentacyclic lupane-type triterpene exhibiting anticancer activity. Betulin derivatives bearing propynoyloxy and phosphate groups were prepared in an effort to improve the availability and efficacy of the drug. In this study, a comparative assessment of the in vitro anticancer activity of betulin and its four derivatives was carried out using two human breast cancer cell lines: SK-BR-3 and MCF-7. In both studied cell lines, 30-diethoxyphosphoryl-28-propynoylbetulin (compound 4) turned out to be the most powerful inhibitor of growth and inducer of cellular death. Detailed examination of that derivative pertained to the mechanisms underlying its anticancer action. Treatment with compound 4 decreased DNA synthesis and up-regulated p21WAF1/Cip1 mRNA and protein levels in both cell lines. On the other hand, that derivative caused a significant increase in cell death, as evidenced by increased lactate dehydrogenase (LDH) release and ethidium homodimer uptake. Shortly after the compound addition, an increased generation of reactive oxygen species and loss of mitochondrial membrane potential were detected. The activation of caspase-3 and fragmentation of genomic DNA suggested an apoptotic type of cell death. However, analysis of cellular morphology did not reveal any nuclear features typical of apoptosis. Despite necrosis-like morphology, dead cells exhibited activation of the cascade of caspases. These observations have led to the conclusion that compound 4 pushed cells to undergo a form of necrotic-like regulated cell demise.
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Dissertations / Theses on the topic "4-DNP derivative"

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Caton-Williams, Julianne Marie. "Synthesis and Enzymatic Studies of Selenium Derivatized Nucleosides, Nucleotides and Nucleic Acids." Digital Archive @ GSU, 2009. http://digitalarchive.gsu.edu/chemistry_diss/42.

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Nucleoside 5-triphosphates are the building blocks to synthesis of nucleic acids. Nucleic acids (RNA and DNA) participate in many important biological functions in living systems, including genetic information storage, gene expression, and catalysis. Nucleoside 5- triphosphates have many important therapeutic and diagnostic applications. To understand how these triphosphates are utilized in living systems, numerous synthetic mimics have been prepared and used as active metabolites of certain drugs and molecular probes. Over the years, nucleic acids have been modified at the nucleobase, sugar moiety and phosphate backbone with the aim of understanding their structures and functions. We have site-specifically replaced selected oxygen atoms of nucleosides and nucleotides with selenium atom in order to enzymatically synthesize selenium-derivatized DNAs for obtaining insights into the DNA flexibility, duplex recognition and stability. Although triphosphates have important biological and medicinal significance, they are however, very difficult to synthesize and isolate in high purity and yield. There are many approaches to the synthesis of nucleoside 5-triphosphates, but there is no general strategy that allows simple and direct synthesis of nucleoside triphosphates. To face the challenges, we have developed a new approach in the absence of protecting groups to quickly and efficiently synthesized native deoxynucleoside 5-triphosphates and deoxynucleoside 5-(α- P-seleno)- P-seleno)triphosphates. Syntheses of the triphosphates containing selenium-derivatized nucleobases were also successfully accomplished. After replacing the oxygen atoms at the 4-position of thymidine and uridine, and the 6-position of guanosine, we observed most strikingly, a large bathrochromic shift of over 100 nm, relative to their native counterparts of UV absorbance of 260 nm. Consequently, the synthesized selenium base modified triphosphates are yellow. We also synthesized 2-selenothymidine and 5-methylseleno thymidine 5-triphosphates. We conducted stability study on the colored 4-selenothymidine and used the 5- triphosphate analog (4-SeTTP) as substrate for polymerase recognition. The Klenow polymerase incorporated the 4-SeTTP with efficiency equal to that of the native counterpart. Finally, 4-SeTTP was used to demonstrate UVdamage resistance of selenium-derivatized DNAs and plasmid.
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Abou-Elkhair, Reham A. I. "Synthesis of anthraquinone derivatives and their conjugates with 2'-deoxynucleosides as new probes for electron transfer studies in DNA." unrestricted, 2008. http://etd.gsu.edu/theses/available/etd-07182008-154942/.

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Thesis (Ph. D.)--Georgia State University, 2008.<br>Title from file title page. Thomas L. Netzel, Dabney W. Dixon, committee co-chairs; David Boykin, Jerry Smith, committee members. Electronic text (250 p. : ill. (some col.)) : digital, PDF file. Description based on contents viewed Nov. 20, 2008. Includes bibliographical references.
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Books on the topic "4-DNP derivative"

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Azria, M., J. Engel, S. Grünwald, et al. Calcitonins — Physiological and Pharmacological Aspects Mafosfamide — A Derivative of 4-Hydroxycyclophosphamide Enzymatic DNA Methylation. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74734-2.

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1936-, Azira Moise, ed. Calcitonins - physiological and pharmacological aspects ; Mafosfamide - a derivative of 4-hydroxycyclosphamide ; Enzymatic DNA methylation. Springer-Verlag, 1989.

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Pohl, J., J. Engel, P. Hilgard, et al. Calcitonins ― Physiological and Pharmacological Aspects. Mafosfamide ― A Derivative of 4-Hydroxycyclophosphamide. Enzymatic DNA Methylation. Springer, 2011.

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Engel, J., P. Hilgard, M. Azria, S. Grünwald, and U. Niemeyer. Calcitonins -- Physiological and Pharmacological Aspects. Mafosfamide -- a Derivative of 4-Hydroxycyclophosphamide. Enzymatic DNA Methylation. Springer London, Limited, 2013.

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Jr, Engel J., and S. Grunwald. Calcitonins - Physiological and Pharmacological Aspects. Mafosfamide - a Derivative of 4-Hydroxycyclophosphamide. Enzymatic DNA Methylation. Island Press, 1989.

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Book chapters on the topic "4-DNP derivative"

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Beaton, Graham, Douglas Dellinger, William S. Marshall, and Marvin H. Caruthers. "Synthesis of Oligonucleotide Phosphorodithioates." In Oligonucleotides and Analogues. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780199632800.003.0005.

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Abstract Over the past several years, the development of high yielding, rapid methods for synthesizing DNA (1-3) have led to a large number of applications for oligonucleotides (4). These include its use for cloning and synthesizing genes (5), as primers for sequencing DNA and various PCR applications (6), mutagenesis of genes in a site-specific manner (7), examination of how nucleic acids interact with proteins (8), and for studies on nucleic acid structure (9). Mainly because of these results, many have discovered that synthetic DNA needs to be further modified so that it resists hydrolysis by nucleases and contains reporter groups, haptens, cross-linking reagents, sugars, steroids, and peptides. Invariably such interest has stimulated the development of new analogues and new chemistries for synthesizing these derivatives. In this chapter, the chemical synthesis of a potentially very useful analogue for many of these applications, which we call dithioate DNA, will be discussed.
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Cutter, Asher D. "Neutral theories of molecular evolution." In A Primer of Molecular Population Genetics. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198838944.003.0004.

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Chapter 4, “Neutral theories of molecular evolution,” outlines the logic and predictions of the neutral theory of molecular evolution and its derivatives as a simple conceptual framework for understanding DNA sequence evolution. It introduces the standard neutral model as a null model of evolutionary change in DNA sequences to describe patterns of polymorphism within species and divergence between species. An overview is provided for the molecular clock concept and for predictions about the amount of polymorphism and allele frequency distributions within populations. This chapter covers how population size and selection intersect to define nearly neutral fitness effects and their implications, as well as misinterpretations and misapplications of Neutral Theory. This overview provides a foundation for how theoretical predictions offer null models for tests of molecular evolution developed in later chapters.
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Farr, Christine J. "Chromosome fragmentation in vertebrate cell lines." In Chromosome Structural Analysis. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780199636990.003.0010.

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Abstract Experimental approaches to understanding chromosome structure and function fall into two main categories: the first involves assembling candidate DNA elements in vitro to construct an artificial chromosome. This approach was used to create yeast artificial chromosomes in both Saccharomyces cerevisiae and Schizosaccharomyces pombe. More recently a related approach has lead to the generation of mammalian minichromosomes in the human somatic cell line HT1080, although the precise DNA organization and requirements of these mammalian minichromosomes has yet to be fully elucidated (1). The alternative approach involves manipulation of an existing chromosome to generate smaller minichromosome derivatives suitable for further study/fragmentation. This chapter will focus on the use of short stretches of the vertebrate terminal repeat DNA sequence (TTAGGG)n to 'seed' the formation of de novo telomeres when introduced into vertebrate cell lines, simultaneously truncating the chromosome at the integration site (2, 3). Combined with elaborate selection schemes and homologous recombination this approach has led to the generation of a series of minichromosomes derived from native human chromosomes (4, 5).
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Conference papers on the topic "4-DNP derivative"

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Ramadan, Wafaa, Maha Ayad, Rifat Hamoudi, et al. "5-aminosalicylate–4-thiazolinone hybrid derivatives: A potent modulator of DNA damage response and G2/M cell cycle arrest via ATM/ATR pathway and Cyclin-CDK complex." In The 1st International Electronic Conference on Cancers: Exploiting Cancer Vulnerability by Targeting the DNA Damage Response. MDPI, 2021. http://dx.doi.org/10.3390/iecc2021-09188.

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Borri, Daniela, Thais Santos, Mauren Fernanda Moller dos Santos, et al. "Complexidade cariotípica e status mutacional do TP53 se associam a prognóstico em neoplasias mieloides com cromossomos em anel." In Resumos do 56º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2024. https://doi.org/10.5327/1516-3180.142s1.10733.

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Objetivo: Cromossomos em anel são moléculas circulares de DNA geradas após um dano com consequente reparo, sendo raramente descritos em neoplasias mieloides. O intuito deste trabalho foi avaliar o significado prognóstico dos cromossomos em anel em neoplasias mieloides e verificar sua correlação com alterações no gene TP53. Método: Estudo retrospectivo envolvendo amostras de medula óssea (n=21) de pacientes com neoplasias mieloides (≥18 anos) que tinham cariótipo com cromossomos em anel, entre 2017 e 2022, em laboratório de citogenética de rotina. Deleção e mutação no gene TP53 foram analisadas por técnica de FISH e NGS, respectivamente. Análises estatísticas com uso dos softwares IBM-SPSS/Microsoft-Excel de acordo com dados coletados em REDCap. Conclusão: Somente 0,29% dos cariótipos onco-hematológicos apresentaram cromossomos em anel. Mediana de idade de 69 anos (53–89), 14 (67%) homens, LMA e SMD em 9 (43%) casos cada. Mediana de anormalidades cariotípicas de 9 (1–28). Complexidade cariotípica, deleção TP53, mutação TP53 e TP53 multi-hit (definido por VAF&gt;40% ou duas mutações com VAF&gt;10% ou presença de deleção e mutação VAF&gt;10%) estiveram presentes em 81% (17/21), 19% (4/21), 78% (14/18) e 61% (11/18) dos casos, respectivamente. Cromossomos em anel identificáveis derivativos dos cromossomos 6 e 7 foram os mais encontrados. A mediana de sobrevida global foi de 3,2 meses. Mutações multi-hit em TP53 (HR 10,63; IC95% 2,25–50,31; p=0,001) e o número de anormalidades ao cariótipo (HR 1,06; IC95% 1,00–1,11; p=0,043) se associaram significativamente a maiores taxas de mortalidade; pacientes com KT muito complexo (66,7%) apresentaram risco de óbito 5,53 vezes maior (IC95% 1,12–27,28) em relação a cariótipos não complexos. A incidência de cromossomos em anel foi baixa em neoplasias mieloides, associou-se à alta taxa de cariótipo complexo e mutações em TP53, fatores associados a prognóstico bastante reservado. Os cromossomos em anel parecem apenas refletir a instabilidade genética gerada pelo cariótipo complexo, não estando envolvidos de forma causal com as neoplasias mieloides.
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Reports on the topic "4-DNP derivative"

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Tel-Zur, Neomi, and Jeffrey J. Doyle. Role of Polyploidy in Vine Cacti Speciation and Crop Domestication. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7697110.bard.

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1. Abstract: Over the past 25 years, vine cacti of the genera Hylocereus and Selenicereus have been introduced into Israel and southern California as new exotic fruit crops. The importance of these crops lies in their high water use efficiency and horticultural potential as exotic fruit crops. Our collaboration focused on the cytological, molecular and evolutionary aspects of vine cacti polyploidization to confront the agricultural challenge of genetic improvement, ultimately to improve success of vine cacti as commercial fruit crop plants. More specifically, we worked on the: 1- Identification of the putative ancestor(s) of the tetraploid H. megalanthus; 2- Determination of the number of origins of H. megalanthus (single vs. multiple origins of polyploidy); 3- Cytogenetic analysis of BC1 and F1 hybrids; 4- Determination of important agricultural traits and the selection of superior hybrids for cultivation. The plant material used in this study comprised interspecific Hylocereus F1 and first backcross (BC1) hybrids, nine Hylocereus species (58 genotypes), nine Selenicereus species (14 genotypes), and four Epiphyllum genotypes. Two BC1 hexaploids (BC-023 and BC-031) were obtained, a high ploidy level that can be explained only by a fertilization event between one unreduced female gamete from the triploid hybrid and a balanced gamete from the pollen donor, the diploid H. monacanthus. These findings are scientific evidence that support the possibility that “hybridization followed by chromosome doubling” could also occur in nature. Cytomixis, the migration of chromatin between adjacent cells through connecting cytoplasmatic channels, was observed in vine cacti hybrids and may thus imply selective DNA elimination in response to the allopolyploidization process. Evidence from plastid and nrDNA internal transcribed spacers (ITS) sequences support the placement of H. megalanthus within a monophyletic Hylocereus group. Furthermore, both plastid and ITS datasets are most consistent with a conclusion that this tetraploid species is an autopolyploid, despite observations that the species appears to be morphologically intermediate between Hylocereus and Selenicereus. Although the possibility of very narrow allopolyploidly (i.e., derivation from parents that are barely diverged from each other such as closely related species in the same genus) cannot be ruled out entirely based on our data (in part due to the unavailability of Hylocereus species considered to be morphologically the closest relatives of H. megalanthus), the possibility of H. megalanthus representing an intergeneric cross (i.e., Hylocereus × Selenicereus) seems extremely unlikely. Interestingly, the process of homogenization of ITS sequences (concerted evolution) is either incomplete or lacking in both Hylocereus and Selenicereus, and the inclusion of several artificial hybrids in the molecular study revealed the potential for biparental plastid inheritance in Hylocereus. The most important agricultural implication of this research project was the information collected for F1 and BC1 hybrids. Specifically, this project concluded with the selection of four superior hybrids in terms of fruit quality and potential yields under extreme high temperatures. These selected hybrids are self-compatible, avoiding the need for hand cross pollination to set fruits, thus reducing manpower costs. We recently offered these hybrids to growers in Israel for prioritized rapid evaluation and characterization.
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