Log in

Relevant bibliographies by topics / Amino acids Design / Books

Books on the topic 'Amino acids Design'

To see the other types of publications on this topic, follow the link: Amino acids Design.

Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 20 books for your research on the topic 'Amino acids Design.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse books on a wide variety of disciplines and organise your bibliography correctly.

1

1951-, Nielsen Peter E., ed. Pseudo-peptides in drug discovery. Weinheim: Wiley-VCH, 2004.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

2

Harren, Jhoti, and Leach Andrew R, eds. Structure-based drug discovery. Dordrecht: Springer, 2007.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

3

Povl, Krogsgaard-Larsen, and Hansen J. J. 1944-, eds. Excitatory amino acid receptors: Design of agonists and antagonists. New York: E. Horwood, 1992.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

4

Budisa, Nediljko. Engineering the Genetic Code: Expanding the Amino Acid Repertoire for the Design of Novel Proteins. Wiley-VCH Verlag GmbH, 2006.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

5

Budisa, Nediljko. Engineering the Genetic Code: Expanding the Amino Acid Repertoire for the Design of Novel Proteins. Wiley & Sons, Incorporated, John, 2006.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

6

Engineering the Genetic Code: Expanding the Amino Acid Repertoire for the Design of Novel Proteins. Wiley-VCH, 2006.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

7

James, Donald Andrew. Design of photoisomerizable amino acids and their incorporation into biological peptides and enzymes. 2004.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

8

Nielsen, Peter E. Pseudo-Peptides in Drug Discovery. Wiley & Sons, Incorporated, John, 2006.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

9

Nielsen, Peter E. Pseudo-Peptides in Drug Discovery. Wiley & Sons, Limited, John, 2005.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

10

Trabocchi, Andrea, and Antonio Guarna. Peptidomimetics in Organic and Medicinal Chemistry: The Art of Transforming Peptides in Drugs. Wiley & Sons, Incorporated, John, 2014.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

11

Trabocchi, Andrea, and Antonio Guarna. Peptidomimetics in Organic and Medicinal Chemistry. Wiley & Sons, Limited, John, 2014.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

12

Trabocchi, Andrea, and Antonio Guarna. Peptidomimetics in Organic and Medicinal Chemistry. Wiley & Sons, Incorporated, John, 2014.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

13

Peptidomimetics in Organic and Medicinal Chemistry. John Wiley & Sons Inc, 2014.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

14

R, Leach· Andrew, and Harren Jhoti. Structure-based Drug Discovery. Springer, 2010.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

15

Sapse, Anne-Marie, ed. Molecular Orbital Calculations for Biological Systems. Oxford University Press, 1998. http://dx.doi.org/10.1093/oso/9780195098730.001.0001.

Full text

Abstract:

Molecular Orbital Calculations for Biological Systems is a hands-on guide to computational quantum chemistry and its applications in organic chemistry, biochemistry, and molecular biology. With improvements in software, molecular modeling techniques are now becoming widely available; they are increasingly used to complement experimental results, saving significant amounts of lab time. Common applications include pharmaceutical research and development; for example, ab initio and semi-empirical methods are playing important roles in peptide investigations and in drug design. The opening chapters provide an introduction for the non-quantum chemist to the basic quantum chemistry methods, ab initio, semi-empirical, and density functionals, as well as to one of the main families of computer programs, the Gaussian series. The second part then describes current research which applies quantum chemistry methods to such biological systems as amino acids, peptides, and anti-cancer drugs. Throughout the authors seek to encourage biochemists to discover aspects of their own research which might benefit from computational work. They also show that the methods are accessible to researchers from a wide range of mathematical backgrounds. Combining concise introductions with practical advice, this volume will be an invaluable tool for research on biological systems.

APA, Harvard, Vancouver, ISO, and other styles

16

Morrow, Gary W. Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.001.0001.

Full text

Abstract:

Building on the foundation of a one-year introductory course in organic chemistry, Bioorganic Synthesis: An Introduction focuses on organic reactions involved in the biosynthesis of naturally-occurring organic compounds with special emphasis on natural products of pharmacological interest. The book is designed specifically for undergraduate students, rather than as an exhaustive reference work for graduate students or professional researchers and is intended to support undergraduate courses for students majoring in chemistry, biochemistry, biology, pre-medicine, and bioengineering programs who would benefit from a deeper understanding of the chemical logic of reactions carried out in organisms and the origins and uses of the important organic compounds they often produce. The book assumes no prior background in biochemistry and consists of eight chapters: i) a brief review of relevant topics from introductory organic chemistry; ii) presentation of essential organic and biochemical reactions used throughout the book along with a brief introduction to coenzymes; iii) review of basic carbohydrates and the biosynthesis of amino acids; iv) the terpenoid pathway for biosynthesis of all important classes of terpenoids and steroids; v) the acetate pathway for biosynthesis of saturated and unsaturated fatty acids, prostaglandins and acetate-derived polyketide natural products; vi) the biosynthesis of the shikimate pathway products derived from aromatic amino acids; vii) an introduction to biosynthesis of major alkaloids and related nitrogenous compounds; and viii) an overview of laboratory organic synthesis as it relates to the challenges faced by synthetic and medicinal chemists who must recreate intricate natural product structures in the laboratory.

APA, Harvard, Vancouver, ISO, and other styles

17

Weiner, David B. Biologically Active Peptides: Design, Synthesis and Utilization. Taylor & Francis Group, 2017.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

18

Weiner, David B., and William V. Williams. Biologically Active Peptides: Design, Synthesis and Utilization (Biomedical Applications of Biotechnology, Vol 1). CRC, 1993.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

19

Columb, Malachy O. Local anaesthetic agents. Edited by Michel M. R. F. Struys. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0017.

Full text

Abstract:

Local anaesthetic agents cause a pharmacologically induced reversible neuropathy characterized by axonal conduction blockade. They act by blocking the sodium ionophore and exhibit membrane stabilizing activity by inhibiting initiation and propagation of action potentials. They are weak bases consisting of three components: a lipophilic aromatic ring, a link, and a hydrophilic amine. The chemical link classifies them as esters or amides. Local anaesthetics diffuse through the axolemma as unionized free-base and block the ionophore in the quaternary ammonium ionized form. The speed of onset of block is therefore dependent on the pKa of the agent and the ambient tissue pH. Esters undergo hydrolysis by plasma esterases and amides are metabolized by hepatic microsomal mixed-function oxidases. Local anaesthetics are bound in the blood to α‎1-acid glycoproteins. Pharmacological potency is dependent on the lipid solubility of the drug as is the potential for systemic toxicity. The blood concentrations required to cause cardiovascular system (CVS) collapse and early central nervous system (CNS) toxicity are used to quantify the CVS:CNS toxicity ratio. Local anaesthetics also have the potential to induce direct neuronal damage. Intravenous lipid emulsion is used for the treatment of systemic toxicity but the scientific evidence is inconsistent. With regard to the pipecoloxylidine local anaesthetics, early evidence indicated that the S- was less toxic than the R-enantiomer. However, clinical research using minimum local analgesic concentration designs suggests that reduced systemic toxicity and motor block sparing is mainly explained by potency rather than enantiomerism.

APA, Harvard, Vancouver, ISO, and other styles

20

(Editor), Harren Jhoti, and Andrew R. Leach (Editor), eds. Structure-based Drug Discovery. Springer, 2007.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!