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2 edition of Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines found in the catalog.

Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines

Lesley Jane Adams

Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines

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Published by University of Portsmouth, School of Pharmacy and Biomedical Sciences in Portsmouth .
Written in English


Edition Notes

Thesis (Ph.D.) - University of Portsmouth, 1998.

StatementLesley Jane Adams.
ID Numbers
Open LibraryOL19522740M


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Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines by Lesley Jane Adams Download PDF EPUB FB2

Thurston D.E. () Advances in the Study of Pyrrolo[2,1-c] [1,4]benzodiazepine (PBD) Antitumour Antibiotics. In: Neidle S., Waring M.J. (eds) Molecular Aspects of Anticancer Drug-DNA Interactions.

Topics in Molecular and Structural Biology. Palgrave, LondonCited by: Synthesis, DNA binding, and cytotoxicity studies of pyrrolo [2,1-c][1,4]benzodiazepine-anthraquinone conjugates Article in Bioorganic & Medicinal Chemistry 15(22) December with Pyrrolo[1,4]benzodiazepines are tricyclic compounds that are considered “privileged structures” since they possess a wide range of biological activities.

The first encounter with these molecules was the isolation of anthramycin from cultures of Streptomyces, followed by determination of the X-ray crystal Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines book of the molecule and a study of its interaction with by: Synthesis and biological activity of fluoroquinolone-pyrrolo[2,1-c][1,4]benzodiazepine conjugates Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines book in Bioorganic & Medicinal Chemistry 13(6) April with 10 Reads.

Antonow D, Kaliszczak M, Kang G-D et al () Structure-activity relationships of monomeric C2-aryl pyrrolo[2,1-c][1,4]benzodiazepines (PBD) antitumour agents. J Med Chem – CrossRef PubMed Google ScholarCited by: 1.

Effects of Systematic Shortening of Noncovalent C8 Side Chain Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines book the Cytotoxicity and NF-κB Inhibitory Capacity of Pyrrolobenzodiazepines (PBDs)Cited by: 2. The invention claimed is: 1.

A compound which is A: where R 10 and R 11 either (a) form a double bond between the carbon and nitrogen atoms to which they are bound; or (b) are H and OR A respectively, where R A is selected from H and C alkyl; or a pharmaceutically acceptable salt thereof.

A conjugate selected from the group consisting of formula ConjA: ConjB: and ConjC: wherein CBA Cited by:   Many natural and synthetic anticancer agents with the ability to interact with DNA have been discovered, but most have little sequence-specificity and often exhibit severe toxicity to normal tissues.

Thus, there has been considerable interest in molecular biology and human medicine to find small molecules that can alkylate the DNA in a sequence-specific manner and modify the function of Cited by:   Adams et al., “Molecular modelling of a sequence-specific DNA-binding agent based on the pyrrolo[2,1-c][1,4]benzodiazepines,” Pharm.

Pharmacol. AbstractA new, selective and sensitive HPLC method for the determination of lixivaptan, an oral selective vasopressin 2 (V2)-receptor antagonist, was investigated and validated.

A Waters symmetry C18 column was used as a stationary phase in isocratic elution mode using a mobile phase composed of KH2PO4 ( mM)-acetonitrile ( 60, v/v) at a flow rate of mL minAuthor: Haitham Alrabiah, Mohammed Abunassif, Sabry Attia, Gamal Abdel-Hafiz Mostafa.

Chapter 3 on Intermolecular Forces and Molecular Modelling has required expansion and revision due to advances in the techniques relating to ligand-receptor interactions and we are indebted to Zeneca, through Drfor their generosity in meeting the considerable cost of reproducing the necessary new colour plates in the book.

CROSS-REFERENCE TO RELATED APPLICATIONS. This application is a continuation of copending U.S. application Ser. 15/, filed on Dec. 19,now U.S. Pat. The vibrational spectra of uracil derivatives have been studied by several workers, recent studies being those of Rastogi et al and Palafox et al [].

The nucleic acid bases with sulphur atom instead of oxygen atom have been a subject of considerable interest since they were detected in natural t-RNAs.

Molecular modeling studies such as molecular docking and pharmacophore generation were performed with known NK1R antagonists and BSN by using Discovery Studio (DS) by Accelrys to explain their binging modes to NK1R4 (Figure ).

Full text of "Microwave Assisted Organic Synthesis" See other formats. PATENTS OFFICE JOURNAL. download Report.

Comments. Transcription. PATENTS OFFICE JOURNAL. Sean Ekins - Computational Toxicology- Risk Assessment for Pharmaceutical and Environmental Chemicals (Wiley Series on Technologies for the Pharmaceutical Industry) () код для вставки. Prescribing of benzodiazepines by casualty officers.

PubMed Central. Nazareth, I D; King, M B. The prescribing of benzodiazepines by casualty officers in a busy district hospital over a three month period was examined by a retrospective review of case notes. Benzodiazepines, mainly diazepam, were given to % of attenders, the majority of whom had disorders involving minor muscle.

P a triazolopyrrolo[2,1-c][1,4] benzodiazepinone fused with a thiadiazolone ring, exhibited the best anticonvulsant, sedative and anxiolytic effects in our tests. There was no significant difference in potency between PBDT 13 and diazepam, and we proposed that the action mechanism of PBDT 13 could be similar to that of diazepam via.

9ROXPH6XSSOHPHQW 1RYHPEHU, European Journal of Cancer 26th EORTC – NCI – AACR Symposium on Molecular Targets and Cancer Therapeutics Barcelona, Spain, 18 – 21 November Proceedings Book Amsterdam • Boston • London • New York • Oxford • Paris • Philadelphia • San Diego • St Louis European Journal of Cancer Editor-in-Chief: Editors: Basic and Preclinical Research.

Microwave-assisted organic chemistry has during the last years moved from being an obscurity in the laboratory environment to be an invaluable tool within chemistry research.

Although the first reports on microwave-assisted organic synthesis dates back as far asthe breakthrough of the technique as a routine tool in synthesis has been slow. Although multidimensional NMR spectroscopy coupled with computer-aided molecular modelling techniques can provide structural information on the atomic level in solution, this method is also limited to drug molecules bound to relatively short nucleotides since.

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