Academic literature on the topic 'Penicillin derivatives'

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Journal articles on the topic "Penicillin derivatives"

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Simon, Brigitta, Gabriel Hancu, and Árpád Gyéresi. "Application of capillary electrophoresis to the simultaneous determination and stability study of four extensively used penicillin derivatives." Brazilian Journal of Pharmaceutical Sciences 50, no. 3 (2014): 521–27. http://dx.doi.org/10.1590/s1984-82502014000300010.

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The applicability of capillary electrophoresis for the analysis of four extensively used penicillin derivatives (benzylpenicillin, ampicillin, amoxicillin, oxacilllin) has been studied. Because of structural similarities, the electrophoretic behavior of these derivatives is very similar; consequently an efficient separation using the conventional capillary zone electrophoresis is hard to be achieved. Their simultaneous separation was solved by using micellar electrokinetic capillary chromatography, the separation being based on the differential partition of the analytes between the micellar and aqueous phase. Using a buffer solution containing 25 mM sodium tetraborate and 100 mM sodium dodecyl sulfate as surfactant, at a pH of 9.3, applying a voltage of + 25 kV at a temperature of 25 °C, we achieved the simultaneous separation of the studied penicillin derivatives in less then 5 minutes. The separation conditions were optimized and the analytical performance of the method was evaluated in terms of precision, linearity, limit of detection, and quantification. Also, a simple capillary zone electrophoresis method was applied to study the stability of the studied penicillin derivatives in water at different temperatures, using ciprofloxacin hydrochloride as internal standard. It was observed that the extent of the hydrolysis of penicillins in water is highly dependent on the time and also temperature.
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Lakaye, B., C. Damblon, M. Jamin, et al. "Synthesis, purification and kinetic properties of fluorescein-labelled penicillins." Biochemical Journal 300, no. 1 (1994): 141–45. http://dx.doi.org/10.1042/bj3000141.

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The synthesis and properties of six fluorescein-labelled penicillins are reported. The two isomers of fluoresceyl-glycyl-6-amino-penicillanic acid are probably the best compounds to use for detection of all the penicillin-binding proteins (PBPs) present in a bacterial membrane preparation. However, the derivatives of ampicillin were much more efficient against Enterobacter aerogenes PBP3. The two isomers obtained when a commercial mixture of the two isomers of carboxyfluorescein was used most often exhibited similar properties, but the Streptomyces R61 extracellular DD-peptidase was only efficiently acylated by the 5′-carboxyfluorescein derivative of glycyl-6-aminopenicillanic acid.
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Journal, Baghdad Science. "Microbiological studies of a new naphthoquinone semicarbazone derivatives." Baghdad Science Journal 1, no. 2 (2004): 306–10. http://dx.doi.org/10.21123/bsj.1.2.306-310.

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The antimicrobial activity of two naphthoquinone semicarbazone derivatives (Two newly synthesized compounds) have been studied by using tube — diluation and disc plate technique. The effect of those derivatives upon pathogenic microorganism iso-lated from specimen(urine iwounds,stool, swabs, throat ....etc) have been studied also in comparison with the antibiotics (amikacin,ampicillin, carbencillin, cephalothin, cefoxitin,clindamycin ,erythromycin,gentamycin,penicillin,tetracylin and tri-methoprim. It was shown that derivative(1) had more effective against micro organ-ism than derivative(11).
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ADURE, A. S., and A. R. SHELAR. "ChemInform Abstract: New Penicillin Derivatives." ChemInform 25, no. 52 (2010): no. http://dx.doi.org/10.1002/chin.199452265.

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Wiharyani, Risma, Dudi Hardianto, Hermin Pancasakti Kusumaningrum, and Anto Budiharjo. "Kloning Gen pcbC dari Penicillium chrysogenum ke dalam Plasmid pPICZA untuk Pengembangan Produksi Penisilin G." Bioma : Berkala Ilmiah Biologi 16, no. 1 (2014): 33. http://dx.doi.org/10.14710/bioma.16.1.33-38.

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Availability of drugs in Indonesia is still limited by the high prices of drugs due to on the imported raw materials that reaches 95%. Developing antibiotic raw materials can be achieved by increasing of penicillin G production, which is the raw material for the formation of semisynthetic penicillin derivatives through the production of 6-aminopenisillanic acid (6-APA). One of the important enzyme in the penicillin G biosynthesis is Isopenisilin N Synthase (IPNS) that encodes by pcbC gene on Penicillium chrysogenum. This study aimed to obtain a recombinant of pcbC gene fragments that is inserted into pPICZA plasmid. Amplification of pcbC gene used pcbC-F and pcbC-R primers. The pcbC gene fragment was inserted into pPICZA vector and then transformed into TOP 10 F’. The results showed that the recombinant of the pcbC gene fragment from P. chrysogenum has been obtained. Analysis of DNA sequences using the BLAST program showed that the pcbC gene fragment has high homology (99%) with the pcbC gene from P. chrysogenum Wisconsin 54-1255 and P. chrysogenum AS-P-78 which encodes IPNS Keywords: pcbC Gene, Penicillium chrysogenum, cloning, penicillin G
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Ransbarger, Darron, and Feng Xu. "Activation of laccase by penicillin and derivatives." Process Biochemistry 41, no. 9 (2006): 2082–86. http://dx.doi.org/10.1016/j.procbio.2006.04.021.

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Danelon, Gerardo O., Ernesto G. Mata, and Oreste A. Mascaretti. "Selective oxidation of penicillin derivatives to penicillin (1R) and (1S)-sulfoxides using dimethyldioxirane." Tetrahedron Letters 34, no. 49 (1993): 7877–80. http://dx.doi.org/10.1016/s0040-4039(00)61499-5.

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Danelon, G. O., E. G. Mata, and O. A. Mascaretti. "Selective oxidation of penicillin derivatives to penicillin (1R) and (1S)- sulfoxides using dimethyldioxirane." Tetrahedron Letters 35, no. 15 (1994): 2255–66. http://dx.doi.org/10.1016/0040-4039(94)85194-8.

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MAHAPATRA, Sebabrata, Sanjib BHAKTA, Jasimuddin AHAMED, and Joyoti BASU. "Characterization of derivatives of the high-molecular-mass penicillin-binding protein (PBP) 1 of Mycobacterium leprae." Biochemical Journal 350, no. 1 (2000): 75–80. http://dx.doi.org/10.1042/bj3500075.

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Mycobacterium leprae has two high-molecular-mass multimodular penicillin-binding proteins (PBPs) of class A, termed PBP1 and PBP1* [Lepage, Dubois, Ghosh, Joris, Mahapatra, Kundu, Basu, Chakrabarti, Cole, Nguyen-Disteche and Ghuysen (1997) J. Bacteriol. 179, 4627–4630]. PBP1-Xaa–β-lactamase fusions generated periplasmic β-lactamase activity when Xaa (the amino acid of PBP1 at the fusion junction) was residue 314, 363, 407, 450 or 480. Truncation of the N-terminal part of the protein up to residue Leu-147 generated a penicillin-binding polypeptide which could still associate with the plasma membrane, whereas [∆M1–R314]PBP1 (PBP1 lacking residues Met-1 to Arg-314) failed to associate with the membrane, suggesting that the region between residues Leu-147 and Arg-314 harbours an additional plasma membrane association site for PBP1. Truncation of the C-terminus up to 42 residues downstream of the KTG (Lys-Thr-Gly) motif also generated a polypeptide that retained penicillin-binding activity. [∆M1–R314]PBP1 could be extracted from inclusion bodies and refolded under appropriate conditions to give a form capable of binding penicillin with the same efficiency as full-length PBP1. This is, to the best of our knowledge, the first report of a soluble derivative of a penicillin-resistant high-molecular-mass PBP of class A that is capable of binding penicillin. A chimaeric PBP in which the penicillin-binding (PB) module of PBP1 was fused at its N-terminal end with the non-penicillin-binding (n-PB) module of PBP1* retained pencillin-binding activity similar to that of PBP1, corroborating the finding that the n-PB module of PBP1 is dispensable for its penicillin-binding activity.
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Putland, Stacey J., Natalie R. Soulsby, Sue M. Ward, and Christopher P. Alderman. "Potential Cross-Reactivity Between Penicillin Derivatives and Cephalosporins." Consultant Pharmacist 30, no. 12 (2015): 706–9. http://dx.doi.org/10.4140/tcp.n.2015.706.

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Dissertations / Theses on the topic "Penicillin derivatives"

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Layland, Nicola Joanne. "Some reactions of penicillin and cephalosporin derivatives." Thesis, University of Huddersfield, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358674.

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Leslie, J. Michelle. "N-Thiolated b-lactam antibiotics : synthesis and structure-activity studies of C3 oxygenated derivatives and attachement to new, functionalized caprolactone monomers and polymers." [Tampa, Fla] : University of South Florida, 2006. http://purl.fcla.edu/usf/dc/et/SFE0001685.

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LAFAYE, PIERRE. "Etude de la fixation du groupement penicilloyl sur l'albumine au cours de la penicillinotherapie." Paris 7, 1988. http://www.theses.fr/1988PA077093.

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Dé, Emmanuelle. "Etude fonctionnelle de la protéine membranaire OprF de Pseudomonas fluorescens et son implication dans la variation de résistance aux antibiotiques en fonction de la température de croissance bactérienne." Rouen, 1996. http://www.theses.fr/1996ROUES006.

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La bactérie psychrotrophe Pseudomonas fluorescens MF0 est plus sensible à la mezlocilline (β-lactamine) à basse température de culture (8°C) qu'à la température optimum de croissance (28°C). Cette modification de la résistance bactérienne serait due à une modulation de la pénétration de l'antibiotique à travers la membrane externe en fonction de la température de culture, via des protéines canaux appelées porines. Après avoir montré que la composition protéique des membranes externes ne présentait aucune différence significative pour des bactéries issues de cultures à 8°C et 28°C, un changement de la structure et de la fonction de la porine majoritaire de la membrane externe a été envisagé pour expliquer ce phénomène. La protéine majoritaire de 32 kDa de P. Fluorescens MF0 a donc été extraite et purifiée à partir de cultures à différentes températures afin de la reconstituer dans les bicouches lipidiques planes. Les résultats montrent que la diminution de la température de croissance bactérienne entraîne une diminution des valeurs de conductances unitaires de cette protéine (250 pS dans NaCl 1 M pour des cultures à 28°C et 80 pS pour des cultures à 8°C). Ce travail a été étendu à une autre bactérie psychrotrophe P. Fluorescens OE 28. 3 isolée du sol et a conduit aux mêmes résultats après reconstitution de la protéine majoritaire OprF extraite de cultures à 8°C et 28°C. La comparaison des porines OprF de P. Fluorescens MF0 et OE 28. 3 (séquences N-terminales, amplification PCR du gène OprF, réactions immunologiques) montrent : 1) une forte homologie de séquence (94% d'identité) pour ces protéines 2) qu'elles sont exprimées à partir d'un seul gène OprF en fonction de la température de culture. Des modifications de structure (ex : interactions avec le LPS) de cette protéine sont envisagées pour expliquer la variation de la taille du canal en fonction de la température de croissance bactérienne.
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Barros, Tullio Henrique Cano de Haro. "Avaliação antimicrobiana de derivados anfifílicos de quitosana : estudo in vitro contra os fungos Alternaria solani, Alternaria alternata e Penicillium expansum /." Universidade Estadual Paulista (UNESP), 2018. http://hdl.handle.net/11449/154507.

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Submitted by TULLIO HENRIQUE CANO DE HARO BARROS null (tullioharo@hotmail.com) on 2018-07-12T13:22:39Z No. of bitstreams: 1 Barros_Tullio_me_sjrp_int.pdf.pdf: 1544265 bytes, checksum: a6f5f0bd88b4957b4f0ca22899ec9aae (MD5)<br>Approved for entry into archive by Paula Torres Monteiro da Torres (paulatms@sjrp.unesp.br) on 2018-07-13T17:48:42Z (GMT) No. of bitstreams: 1 barros_thch_me_sjrp.pdf.pdf: 1544265 bytes, checksum: a6f5f0bd88b4957b4f0ca22899ec9aae (MD5)<br>Made available in DSpace on 2018-07-13T17:48:42Z (GMT). No. of bitstreams: 1 barros_thch_me_sjrp.pdf.pdf: 1544265 bytes, checksum: a6f5f0bd88b4957b4f0ca22899ec9aae (MD5) Previous issue date: 2018-06-28<br>Este estudo teve como objetivo a síntese e caracterização de dietilaminoetilquitosana (QHdDEAE) e dodecil-dietilaminoetil-quitosana (QHdDEAEDOD) de baixa massa molar (Mw), para avaliar suas atividades antifúngicas contra os fungos Alternaria solani, Alternaria alternata e Penicilliun expansum, que provoca um grande impacto na produção e preservação de alimentos processados e minimamente processados. Os derivados de baixa massa molar (Mw) foram obtidos por reação de degradação de quitosana desacetilada com nitrito de sódio, seguido pela inserção de grupos DEAE e Dodecil na estrutura do polímero. O grau de desacetilação (DD) e de substituição (DS) por grupos dietilaminoetil (DEAE) e dodecil foram determinados usando ressonância magnética nuclear de hidrogênio (RMN-H) e caracterizados por infravermelho (IR). O grau de desacetilação e o grau de substituição por grupos DEAE foram de 94,8% 39,8%, respectivamente. Os derivados hidrofóbicos obtidos foram substituídos com 15% e 39,8% de grupos dodecil, conforme determinado por RMN-H. As massas molares foram determinadas usando Cromatografia de Permeação em Gel (GPC) e um Mw de 9,2 kDa foi obtido para quitosana desacetilada degradada. Ensaios in vitro contra os fungos Alternaria alternata, Peninicillium expansum e Alternaria solani foram realizados. Na concentração de 0,5g.L-1, QHdDEAEDOD e QHdDEAE foram mais eficazes que as quitosanas comercial e desacetilada e apresentaram inibições de 80% contra Alternaria alternata e Alternaria solani. A quitosana deacetilada degradada foi mais eficiente na inibição do crescimento fúngico de Penicillium expansum e para 0,5 g.L-1 atingiu cerca de 80% de inibição. Todos os derivados apresentaram viabilidade celular superior a 70% em células 3T3, demonstrando uma boa citocompatibilidade e potencial para aplicações na conservação de alimentos<br>This study aimed at the synthesis and characterization of Diethylaminoethyl-Chitosan (QHdDEAE) and Dodecyl-Diethylaminoethyl-Chitosan (QHdDEAEDOD) of low molar mass(Mw), to evaluate their antifungal activities against the fungi Alternaria solani, Alternaria alternata and Penicilliun expansum, which causes a great impact on the production and preservation of processed and minimally processed foods. The low Mw derivatives were obtained by degradation reaction with sodium nitrite, followed by the insertion of DEAE and Dodecyl groups on the polymer backbone. The degrees of deacetylation (DD) and substitution (DS) for DEAE and Dodecyl groups were determined using nuclear magnetic resonance of hydrogen (¹H-NMR) and characterized by FTIR. The degree of deacetylation and degree of substitution by DEAE gropus were 94,8% 39,8%, respectively. The obtained hydrophobicized derivatives were substituted with 15% and 39,8% of dodecyl groups as evaluated by ¹H-NMR. The molar masses were determined by using Gel Permeation Chromatography (GPC) and a Mw of 9,2kDa was obtained for deacetylated chitosan. In vitro assays against the fungi Alternaria alternata, Peninicillium expansum and Alternaria solani. At the concentration of 0.5 g.L-1 both, QHdDEAEDOD and QHdDEAE were more effective than commercial and deacetylated chitosans and exhibited inhibitions of 80% against Alternaria alternata and Alternaria solani. Degraded deacetylated chitosan was more efficient in inhibiting the fungal growth of Penicillium expansum and for 0.5 g.L-1 reached around 80% of inhibition. All the derivatives presented cell viabilities higher 70% on 3T3 demonstrated a good cytocompatibility and potential for applications in food preservation.
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Quispe-Cañari, Jean Franco, Evelyn Fidel-Rosales, Diego Manrique, et al. "Self-medication practices during the COVID-19 pandemic among the adult population in Peru: A cross-sectional survey." Elsevier B.V, 2021. http://hdl.handle.net/10757/655713.

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Self-medication impacts both negatively and positively the health of people, which has become evident during the COVID-19 pandemic. The study aimed to assess the prevalence of self-medicated drugs used for respiratory symptoms, as COVID-19 preventive, for its symptoms or once tested positive. To determine the perception of symptom relief and demographic variables that promote self-medication in Peru. We performed a cross-sectional, analytical, multicenter study in 3792 study respondents on the use, the reason for use, and perception of relief after the use of six drugs during the quarantine period. An online questionnaire was developed, pretested and submitted to the general public. Multivariable logistic regression was used to ascertain factors that influence an individual's desire to self-medicate, associations were considered significant at p < 0.05 and using region (coast, mountain and jungle) as cluster group. The majority of respondents self-medicated with acetaminophen for respiratory symptoms and mainly because they had a cold or flu. It was observed that all the surveyed drugs (acetaminophen, ibuprofen, azithromycin, penicillin, antiretrovirals and hydroxychloroquine) were consumed for various symptoms including: fever, fatigue, cough, sneezing, muscle pain, nasal congestion, sore throat, headache and breathing difficulty. Over 90% of respondents perceived relief of at least one symptom. Multivariable logistic regression showed that older people have a higher frequency of antiretroviral self-medication, respondents who currently have a job had a higher frequency of penicillin self-medication, and that respondents from the Andes consumed less acetaminophen, while the ones from the rainforest consumed it more. There were significant percentages of self-medication, including drugs without sufficient scientific evidence. Age, region where one lived and job status were variables associated with self-medication frequency. Continuous awareness and sensitization about the risks of self-medication are warranted.<br>Revisión por pares
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Dumas, Françoise. "Approches stéréoselectives d'antibiotiques de type carbapénème, thiénamycine et dérivés : contrôle relatif des centres asymétriques, construction du squelette bicyclique." Paris 6, 1987. http://www.theses.fr/1987PA066686.

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WANG, ZE-NAN, and 王澤南. "Study on the new fluorine containing derivatives of penicillium rooueforti toxin." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/12039016658827530351.

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LIAO, GAO-DE, and 廖高德. "Studies on the new chemical derivatives of the secondary metabolites of Penicillium roquefrti." Thesis, 1992. http://ndltd.ncl.edu.tw/handle/39322390886429063047.

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Books on the topic "Penicillin derivatives"

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Layland, Nicola Joanne. Some reactions of penicillin and cephalosporin derivatives. The University, 1993.

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Parker, Philip M. The 2007 Import and Export Market for Penicillins and Derivatives with a Penicillanic Acid Structure and Salts Thereof in China. ICON Group International, Inc., 2006.

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Parker, Philip M. The World Market for Penicillins and Derivatives with a Penicillanic Acid Structure and Salts Thereof: A 2007 Global Trade Perspective. ICON Group International, Inc., 2006.

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Parker, Philip M. The 2007 Import and Export Market for Penicillins and Derivatives with a Penicillanic Acid Structure and Salts Thereof in India. ICON Group International, Inc., 2006.

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Parker, Philip M. The 2007 Import and Export Market for Penicillins and Derivatives with a Penicillanic Acid Structure and Salts Thereof in United States. ICON Group International, Inc., 2006.

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Parker, Philip M. The World Market for Medicaments Containing Penicillins or Streptomycins or Their Derivatives in Dosage Form or Retail Packings: A 2007 Global Trade Perspective. ICON Group International, Inc., 2006.

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The World Market for Medicaments Containing Penicillins or Streptomycins or Their Derivatives in Dosage Form or Retail Packings: A 2004 Global Trade Perspective. Icon Group International, Inc., 2005.

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The World Market for Medicaments Containing Penicillins, Streptomycins, or Their Derivatives Excluding Those in Dosage Form or Retail Packings: A 2004 Global Trade Perspective. Icon Group International, Inc., 2005.

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Parker, Philip M. The World Market for Medicaments Containing Penicillins, Streptomycins, or Their Derivatives Excluding Those in Dosage Form or Retail Packings: A 2007 Global Trade Perspective. ICON Group International, Inc., 2006.

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Parker, Philip M. The 2007 Import and Export Market for Medicaments Containing Penicillins or Streptomycins or Their Derivatives in Dosage Form or Retail Packings in United States. ICON Group International, Inc., 2006.

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Book chapters on the topic "Penicillin derivatives"

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Paul, Terry R., Terry J. Beveridge, Noreen G. Halligan, Larry C. Blaszczak, and Tom R. Parr. "The use of a Mercury-Penicillin V Derivative to Localize Penicillin-Binding Proteins in Escherichia coli." In Bacterial Growth and Lysis. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-9359-8_35.

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Baptista, Maria J. V. de Oliveira, Anthony G. M. Barrett, Derek H. R. Barton, et al. "Transformations of Penicillin.: Part 8. Preparation of 2-Acetylceph-3-em Derivatives from Carboxy-protected Penicillin S-Oxides." In World Scientific Series in 20th Century Chemistry. WORLD SCIENTIFIC / IMPERIAL COLLEGE PRESS, 1996. http://dx.doi.org/10.1142/9789812795984_0079.

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Ishikawa, Seiji, Saburo Neya, and Noriaki Funasaki. "Dimerization of penicillin V as deduced by frontal derivative chromatography." In Studies in Surface Science and Catalysis. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)82072-3.

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Conference papers on the topic "Penicillin derivatives"

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Schechter, Abraham, Menachem Bitan, Yosef Schechter, and Tatiana Voltsinger. "P9 Does penicillin allergy exist among children? a retrospective study assessing the prevalence of penicillin allergy among children undergoing a penicillin derivative challenge test in the community, following rash occurring after treatment with a penicillin derivative." In Faculty of Paediatrics of the Royal College of Physicians of Ireland, 9th Europaediatrics Congress, 13–15 June, Dublin, Ireland 2019. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-epa.365.

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Cortés, Iván, Andrea Bracca, and Teodoro Kaufman. "Short and efficient first total synthesis of the natural product chromanone A, a chromone derivative from the algicolous marine fungus <em>Penicillium</em> sp." In The 24th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08300.

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