Littérature scientifique sur le sujet « 1-ethyl-3-(dimethylaminopropyl)-carbodiimide »
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Articles de revues sur le sujet "1-ethyl-3-(dimethylaminopropyl)-carbodiimide"
Goyal, Navneet. « 1-Ethyl-3-(3-dimethylaminopropyl) Carbodiimide Hydrochloride (EDCI×HCl) ». Synlett 2010, no 02 (janvier 2010) : 335–36. http://dx.doi.org/10.1055/s-0029-1219043.
Texte intégralNAKAZONO, Manabu, Junko IJICHI, Yoshihito OHBA et Kiyoshi ZAITSU. « Chemiluminescence Enhancer of Polyphenols, 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide. » Analytical Sciences 14, no 4 (1998) : 853–54. http://dx.doi.org/10.2116/analsci.14.853.
Texte intégralKumar, Rakesh, Awdhesh Kumar Shukla, Ellis Bagga, Sunita Kumari, Ram Prakash Bajpai et Lalit M. Bharadwaj. « 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide interference with Lowry method ». Analytical Biochemistry 336, no 1 (janvier 2005) : 132–34. http://dx.doi.org/10.1016/j.ab.2004.09.038.
Texte intégralWang, Qian, Hang Zhou, Yongqiang Sun, Chengbo Cao et Kunpeng Pang. « Modified acellular porcine corneal matrix in deep lamellar transplantation of rabbit cornea ». Journal of Biomaterials Applications 34, no 8 (2 janvier 2020) : 1092–104. http://dx.doi.org/10.1177/0885328219898372.
Texte intégralMiao, Yanming. « Application of BSA-bioconjugated phosphorescence nanohybrids in protein detection in biofluids ». RSC Advances 5, no 94 (2015) : 76804–12. http://dx.doi.org/10.1039/c5ra11691k.
Texte intégralLee, J. M., H. H. L. Edwards, C. A. Pereira et S. I. Samii. « Crosslinking of tissue-derived biomaterials in 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) ». Journal of Materials Science : Materials in Medicine 7, no 9 (septembre 1996) : 531–41. http://dx.doi.org/10.1007/bf00122176.
Texte intégralKubilius, Matthew B., et Raymond S. Tu. « Circular Dichroistic Impacts of 1-(3-Dimethylaminopropyl)-3-ethylurea : Secondary Structure Artifacts Arising from Bioconjugation Using 1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide ». ACS Omega 2, no 11 (21 novembre 2017) : 8308–12. http://dx.doi.org/10.1021/acsomega.7b01288.
Texte intégralWang, Delong, et Hui Shi. « An Unexpected Reaction of Isodehydracetic Acid with Amines in the Presence of 1-Ethyl-3-(3-dimethylaminopropyl) Carbodiimide Hydrochloride Yields a New Type of β-Enaminones ». Molecules 25, no 9 (2 mai 2020) : 2131. http://dx.doi.org/10.3390/molecules25092131.
Texte intégralTropini, V., J. P. Lens, W. J. Mulder et F. Silvestre. « Wheat gluten films cross-linked with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide ». Industrial Crops and Products 20, no 3 (novembre 2004) : 281–89. http://dx.doi.org/10.1016/j.indcrop.2003.10.012.
Texte intégralStankova, Ivanka, Stoyan Schichkov, Kalina Kostova et Angel Galabov. « New Analogues of Acyclovir – Synthesis and Biological Activity ». Zeitschrift für Naturforschung C 65, no 1-2 (1 février 2010) : 29–33. http://dx.doi.org/10.1515/znc-2010-1-205.
Texte intégralThèses sur le sujet "1-ethyl-3-(dimethylaminopropyl)-carbodiimide"
Lampinen, Salomonsson Matilda. « Chemical Derivatization in Combination with Liquid Chromatography Tandem Mass Spectrometry for Detection and Structural Investigation of Glucuronides ». Doctoral thesis, Uppsala University, Analytical Pharmaceutical Chemistry, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8670.
Texte intégralThis thesis presents novel approaches for structural investigation of glucuronides using chemical derivatization in combination with liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MSn).
Today, LC-ESI-MSn is the dominant technique for quantitative as well as qualitative analyses of metabolites, due to its high sensitivity and selectivity. However, for compounds without an easily ionizable group, e.g., steroids, the sensitivity is limited. In the work presented in this thesis, a derivatization procedure forming a basic oxime significantly increased the detection sensitivity for the altrenogest glucuronide.
Furthermore, in structural evaluations of glucuronides, the limitation of LC-MSn becomes evident due to the initial neutral loss of 176 u, i.e. monodehydrated glucuronic acid, which often makes it impossible to elucidate the structures of the conjugates. To solve this problem, the main part of the work described in this thesis was devoted to chemical derivatization as a means of facilitating the determination of the site of conjugation.
For the first time, the isomeric estriol glucuronides were evaluated using a combination of three reagents 2-chloro-1-methylpyridinium iodide (CMPI), 1-ethyl-3-(3-dimethyl- aminopropyl)-carbodiimide (EDC), and 2-picolylamine (PA). Interestingly, the derivatization gave a selective fragmentation pattern leading to differentiation of the isomers.
Another derivatization reagent, 1,2-dimethylimidazole-4-sulfonyl chloride (DMISC), was also tested for the first time in structural investigations. The isomeric glucuronides of morphine, formoterol, and hydroxypropranolol were evaluated. They can all be conjugated in aliphatic as well as aromatic positions. DMISC was proven to be useful in two ways. Firstly, the morphine and formoterol glucuronides that contained a free phenol could be differentiated from those that were conjugated in the aromatic position based on different reactivity. Secondly, for the aromatic O-glucuronide of 4’-hydroxypropranolol, DMISC was proven to react with the amine. This product gave a different fragmentation pattern compared to the corresponding derivative of the aliphatic glucuronide.
VOTTARIELLO, FRANCESCA. « OLIGOMERIZATION OF RNase A:a) A STUDY OF THE INFLUENCE OF SERINE 80 RESIDUE ON THE 3D DOMAIN SWAPPING MECHANISMb) “ZERO-LENGTH” DIMERS OF RNase A AND THEIR CATIONIZATION WITH PEI ». Doctoral thesis, 2010. http://hdl.handle.net/11562/344075.
Texte intégral"Zero-length" dimers of ribonuclease A, a novel type of dimers formed by two RNase A molecules bound to each other through a zero-length amide bond [Simons, B.L. et al. (2007) Proteins 66, 183-195], were analyzed, and tested for their possible in vitro cytotoxic activity. Results: (i) Besides dimers, also trimers and higher oligomers can be identified among the products of the covalently linking reaction. (ii) The "zero-length" dimers prepared by us appear not to be a unique species, as was instead reported by Simons et al. The product is heterogeneous, as shown by the involvement in the amide bond of amino and carboxyl groups others than only those belonging to Lys66 and Glu9. This is demonstrated by results obtained with two RNase A mutants, E9A and K66A. (iii) The "zero-length" dimers degrade poly(A).poly(U) (dsRNA) and yeast RNA (ssRNA): while the activity against poly(A).poly(U) increases with the increase of the oligomer's basicity, the activity towards yeast RNA decreases with the increase of oligomers' basicity, in agreement with many previous data, but in contrast with the results reported by Simons et al. (iv) No cytotoxicity against various tumor cells lines could be evidenced in RNase A "zero-length" dimers. (v) They instead become cytotoxic if cationized by conjugation with polyethylenimine [Futami, J. et al. (2005) J. Biosci. Bioengin. 99, 95-103]. However, polyethylenimine derivatives of RNase A "zero-length" dimers and native, monomeric RNase A are equally cytotoxic. In other words, protein "dimericity" does not play any role in this case. Moreover, (vi) cytotoxicity seems not to be specific for tumor cells: polyethylenimine-cationized native RNase A is also cytotoxic towards human monocytes.
Chapitres de livres sur le sujet "1-ethyl-3-(dimethylaminopropyl)-carbodiimide"
Edwin, Boby T., H. Dhanya, Prabha D. Nair et Moustapha Kassem. « In Vitro and In Vivo Evaluation of 1-(3 Dimethylaminopropyl)-3-Ethyl Carbodiimide (EDC) Cross-Linked Gum Arabic–Gelatin Composite as an Ideal Porous Scaffold for Tissue Engineering ». Dans Biomaterials in Orthopaedics and Bone Regeneration, 131–45. Singapore : Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9977-0_9.
Texte intégralActes de conférences sur le sujet "1-ethyl-3-(dimethylaminopropyl)-carbodiimide"
Wang, Wei-Jhen, Chia-Hwa Lee, Chin-Wen Li, Stephen Liao, Fuh-Jyh Jan et Gou-Jen Wang. « Direct Label Free Detection of Orchid Virus Using a Micro/Nano Hybrid Structured Biosensor ». Dans ASME 2019 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/detc2019-97198.
Texte intégralGee, Albert O., Brendon M. Baker et Robert L. Mauck. « Mechanics and Cytocompatibility of Genipin Crosslinked Type I Collagen Nanofibrous Scaffolds ». Dans ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-193220.
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