Combinatorial Chemistry Technology

Similar documents
به نام خدا. New topics in. organic chemistry. Dr Morteza Mehrdad University of Guilan, Department of Chemistry, Rasht, Iran

Resins and solid phase anchors in the organic chemistry

pharmaceutical industry- drug discovery

Chemistry 224 Bioorganic Chemistry Friday, Sept. 29, This Exam is closed book and closed notes. Please show all your work!

molecules ISSN

1. Draw the structure of oxazolone formed upon activation of N-Acetylvaline

Conformational Analysis

Peptide Syntheses. Illustrative Protection: BOC/ t Bu. A. Introduction. do not acid

A Practical Introduction to Solid Phase Chemistry

Combinatorial Chemistry - Modern Synthesis Approach

COMBINATORIAL CHEMISTRY: CURRENT APPROACH

Syllabus. 1. Occurrence and Functions of Peptides in Nature and Every Day Life hormones, neurotransmitters, therapeutics, artificial sweetener,

Solid phase peptide synthesis (SPPS)

26.7 Laboratory Synthesis of Peptides

Focus Series Peptide Synthesizers

Microwave Energy in Accelerating Reaction Rate of Solid-Assisted Solution Phase Synthesis

Rapid Synthesis and Purification of Sulfahydantion Library Using Microwave Assisted Organic Synthesis and Automated Flash Chromatography

PS-PPh 3 -Pd. Polymer-Bound Triphenylphosphine-Pd(0) Technical Note 517. PdL n

COMBINATORIAL COMPOUND LIBRARIES FOR DRUG DISCOVERY: AN ONGOING CHALLENGE

Syllabus. 1. Occurrence and Functions of Peptides in Nature and Every Day Life hormones, neurotransmitters, therapeutics, artificial sweetener,

Polymer-Supported Reagents as Versatile Tools in Combinatorial Chemistry and Total Synthesis

Rapid Microwave-Assisted CNBr Cleavage of Bead-Bound Peptides

Supporting Information

Practice Problems on Nucleic Acids

Rational design of a hexapeptide hydrogelator for controlled-release drug delivery

1.1 Basic Polymer Chemistry. 1.2 Polymer Nomenclature. 1.3 Polymer Synthesis. 1.4 Chain Growth Polymerization. Polymer =

Introduction. OntoChem

Microwave assisted organic synthesis and Solid supported reagents. A happy marriage? Dr Pelle Lidström Biotage

COMBINATORIAL CHEMISTRY IN A HISTORICAL PERSPECTIVE

Chemistry 27 Professor Matthew Shair. Harvard University Spring Hour Exam 3 Friday, April 28, :07 AM 12:00 PM

Supporting Information for. PNA FRET Pair Miniprobes for Quantitative. Fluorescent in Situ Hybridization to Telomeric DNA in Cells and Tissue

Advanced Organic Synthesis

Continuous Flow-based Solid-phase Peptide Synthesiser

Aziridine Carboxylates, Carboxamides and Lactones: New Methods for Their Preparation and Their Transformation into α- and β-amino Acid Derivatives

Solid- and solution-phase synthesis of bioactive dihydropyrimidines*

Novabiochem. The role of HOBt in coupling reactions. innovations 2/06

Module No. 31: Peptide Synthesis: Definition, Methodology & applications

MiniBlock and MiniBlock XT Configured to Suit Your Needs

Resins for Solid Phase Peptide Synthesis

A Review on Combinatorial Chemistry

New Product Update. HPLC Columns

Exam I Answer Key: Summer 2006, Semester C

Electronic Supplementary Information. Continuous Flow Microfluidic-MS System for Efficient OBOC Screening

10/18/2006. Biotage A Life Science Technology Company

Supporting Information

Chem 316/422 Beauchamp 1 Match the step number in the synthesis with the letter of the reagents listed just below.

Amphoteric Molecules < Chemistry of Andrei K. Yudin > Hyung Min Chi 17 JUNE 2014

Dynamic Combinatorial Chemistry in the identification of new host guest interactions: proof of principle

Combinatorial Libraries for Studying Molecular Recognition

Biotage 2012 Webinar series

Combinatorial Inorganic Chemistry. M. Anji Reddy CY03D023

JAST 2015 M.U.C.Women s College, Burdwan ISSN

Solution & Solid-Phase Peptide Synthesis April 11, 2018

Expedite Hit Discovery: Split & Pool in the 21st Century. Dr. Andreas Marzinzik

Topic 4.8 AMINO ACIDS. Structure Acid-Base Properties Condensation Reactions Proteins

Nonlinear QSAR and 3D QSAR

m leads Structure-based Drug Discovery - Small molecule compound databases Drug Discovery & Development (DD&D) Structure-based drug discovery

AMINO ACIDS ARE JOINED TOGETHER BY BONDS. FILE

Under strongly acidic conditions at ph = 1 every functional group in phosphoserine that can pick up a proton, does.

New Synthetic Technologies in Medicinal Chemistry

Chapter 20 Carboxylic Acid Derivatives. Nucleophilic Acyl Substitution

HPLC AND 13 C NMR FOR ANALYSIS OF TRANSAMIDATION IN A DYNAMIC COMBINATORIAL CHEMISTRY SYSTEM

The One-Bead-One-Compound Combinatorial Library Method

Liberty Blue TM Automated Microwave Peptide Synthesizer. User Guide

Chemistry of the isocyanides and their multicomponent reactions, including their libraries the initiatives of Ivar Ugi

Immobilized and Reusable Cu(I) Catalyst for Metal Ion-Free Conjugation of Ligands to Fully Deprotected Oligonucleotides through Click Reaction

Combinatorial Heterogeneous Catalysis

Microwave-Enhanced Solid Phase Peptide Synthesis. Jonathan M. Collins Bioscience Division CEM Corporation

-1- HO H O H. β-d-galactopyranose (A) OMe CH 3 I. MeO. Ag 2 O. O Me HNO 3. OAc (CH 3 CO) 2 O. AcO. pyridine. O Ac. NaBH 4 H 2 O. MeOH. dry HCl.

How to make pyridines: the Hantzsch pyridine synthesis

Chem101 General Chemistry. Lecture 11 Unsaturated Hydrocarbons

You are advised to spend an equal amount of time on each question.

Describe how an azo dye can be made from phenylamine. Show the structure of the azo dye and the organic intermediate in your answer

CHEM 234: Organic Chemistry II Reaction Sheets

Supporting Information

SUPPORTING INFORMATION

Solid-phase strategies are very popular for synthesizing

Practical Synthesis of PC190723, an Inhibitor of the Bacterial Cell Division Protein FtsZ!

Supporting Information

UNIVERSITY OF NATAL DURBAN EXAMINATIONS : NOVEMBER 2001 ORGANIC CHEMISTRY FOR CHEMICAL ENGINEERS DSC 2OE2. Time : 2 Hours Total Marks : 100

SPHERO TM Magnetic Particles

HPLC COLUMNS WILEY-VCH. Theory, Technology, and Practice. Uwe D. Neue with a contribution from M. Zoubair El Fallah

Supplementary Material Novel phosphopeptides as surface-active agents in iron nanoparticle synthesis

FRAGMENT SCREENING IN LEAD DISCOVERY BY WEAK AFFINITY CHROMATOGRAPHY (WAC )

Advanced Studies in Organic Chemistry

Prof. Jason Kahn Your Signature: Exams written in pencil or erasable ink will not be re-graded under any circumstances.

Solutions In each case, the chirality center has the R configuration

An automated synthesis programme for drug discovery

Automated / Semi- Automated Synthesis of Natural Products and Pharmaceu8cals

"-Amino Acids: Function and Synthesis

AMRI COMPOUND LIBRARY CONSORTIUM: A NOVEL WAY TO FILL YOUR DRUG PIPELINE

SUPPORTING INFORMATION. Elevated Temperatures A Critical Comparison of

DivCalc: A Utility for Diversity Analysis and Compound Sampling

Biological Macromolecules

Electronic Supplementary Information for

Scaling up Microwave Reactions

MULTICOMPONENT REACTIONS AND ORGANOCATALYSIS: A SUITABLE COMBINATION FOR STEREOSELECTIVE SYNTHESIS OF HIGHLY SUBSTITUTED BENZAZEPINES

CHAPTER IV HOFMANN REARRANGEMENT IN CROSSLINKED POLYMERIC MATRICES

Classification System for Solid Supports Used in Solid-Phase Synthesis 1

The Basics of General, Organic, and Biological Chemistry

Transcription:

ugo Kubinyi, www.kubinyi.de ombinatorial hemistry Technology ugo Kubinyi Germany E-Mail kubinyi@t-online.de omepage www.kubinyi.de ugo Kubinyi, www.kubinyi.de ombinatorial Diversity in ature 20 natural amino acids yield 400 dipeptides 8,000 tripeptides... 64,000,000 hexapeptides and, in principle, 10 400 proteins with MW 30 kd 100 chemically modified amino acids yield e.g. 1,000,000,000,000 hexapeptides, and... 4 nucleic bases encode all organisms!

ugo Kubinyi, www.kubinyi.de umber of organic molecules with MW < 500 (,,,, P,, F, l, r, I) 1 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 000 or more or less... ugo Kubinyi, www.kubinyi.de Principles of ombinatorial hemistry ombinatorial hemistry generates a multitude of chemically related ( congeneric ) compounds, so-called combinatorial libraries" In the last years, combinatorial chemistry in drug research changed more and more to automated parallel synthesis and parallel purification.

ugo Kubinyi, www.kubinyi.de lassical organic synthesis: 2 3 + l Me = Me 3 ombinatorial synthesis: e.g. 50 educts x 20 educts = 1,000 products Multistep combinatorial synthesis: 1 educt x 1 educt = 1 product 2 + l Multicomponent reaction (e.g. Ugi reaction): 2 = 2 e.g. 50 x 20 x 20 educts = 20,000 products - 2 + 2- + 3- + 4- = e.g. 50 x 20 x 5 x 200 educts = 1 million products 4 2 3 ugo Kubinyi, www.kubinyi.de ombinatorial Library 5 4 6 7 8 * * 1 2 10 3 9 uilding blocks with 68 different residues in 10 positions ( 1-10 are 5, 10, 10, 4, 2, 5, 5, 2, 5, and 20 residues) generate a library of 20 million different compounds. onsideration of both steric centers (*) increases this number by a factor of four, i.e. to 80 million different compounds.

ugo Kubinyi, www.kubinyi.de olid ase ynthesis: eads ross-linked polystyrene (1.0-1.5% divinylbenzene) l l l Functionalization of the beads by chloromethylation and further chemical reactions l ugo Kubinyi, www.kubinyi.de Tentagel eads (Polystyrene, Grafted with Polyoxyethylene), app Polymers, Tübingen, Germany

ugo Kubinyi, www.kubinyi.de The Principle of olid ase ynthesis immobilization bead (40-80 µm) and linker scaffold with functional groups cleavage three-step synthesis immobilized product product ugo Kubinyi, www.kubinyi.de The ombination of caffolds and uilding locks 3 building blocks 1-3 and 3 building blocks 1-3 yield 9 products 1 1 3 3. In the same manner, 10 x 10 x 10 building blocks yield 1,000 products 1 1 1 10 10 10.

ugo Kubinyi, www.kubinyi.de "plit and ombine" Method for Library ynthesis ugo Kubinyi, www.kubinyi.de 3 Mixtures with 9 different compounds in each reaction vessel

ugo Kubinyi, www.kubinyi.de Linkers: Merrifield and Wang linkers l Merrifield resin Wang resin ("Wang linker") (several steps) 50% TF (product) ugo Kubinyi, www.kubinyi.de Linkers: a) Merrifield Peptide ynthesis l oc- - 2 oc 1) l / 3 2) oc-2 - / DI oc 2 50% TF 2 2 Dipeptide

ugo Kubinyi, www.kubinyi.de ther linkers Me Fmoc Me ink acid linker Me protected ink amide linker Me Trityl linker l protected ieber linker Fmoc ugo Kubinyi, www.kubinyi.de afety catch linkers stable labile base + - = : stable Product + 2 2 = 3 : labile - product- 1 2 product- 1 2

ugo Kubinyi, www.kubinyi.de Traceless (safety catch) linker stable u(c) 2 2 + 2 + Polymer-supported solution phase syntheses Polymeric reagents + reagent - ugo Kubinyi, www.kubinyi.de olid ase-upported ynthesis of (±)-Epibatidine l 1. Me 3 4 2. Me 3 u 4 2 4. 5. Me 2 T l 3. Me 3 + Me 2 l 6. Me 3 4 7. Mesyl-l l l (±) 2 8. Me 3 4 9. Et 2 -tu P l 85% (±) endo basic epimerization (±)-Epibatidine (exo:endo = 3:1). J. ooth and J.. odges, J. m. hem. oc. 119, 4882-4886 (1997)

ugo Kubinyi, www.kubinyi.de olid ase-upported ynthesis of (±)-xomaritidine and (±)-Epimaritidine Me Me Me Me Me 3 + u 4-1. 2 l 2 2. Me 100 % Me F 3. V. Ley et al., J. hem. oc. Perkin Trans. 1, 1251-1252 (1999) I(X 3 ) 2 X = or F Me F 3 2 Me 70 % (±)-Epimaritidine Me Me 2 Me + 3 -Me 4 Me 90 % F 3 Me Et 3 + 3 - Me Me Me (±)-xomaritidine 100 % 2 / Pd / Me Me + 3-4 95 % u 4 or il 2 Me 90 % Me Me (F 3 ) 2 99 % ugo Kubinyi, www.kubinyi.de Polymeric scavengers for building blocks, side products and reagents + excess - + X - + X- reagent + - + X - + X- + - + side product D X - + X-D

ugo Kubinyi, www.kubinyi.de cavenger eagents: Ion Exchange esins, Polymeric cids and ases, Isocyanates, etc. 2 Me + 1 equivalent 1.2 equivalents Me Me 1. l 2. - 2 3. + 2 2 ( 2 2 2 ) 2 ugo Kubinyi, www.kubinyi.de esin capture strategy reagent + - + + side product D X cleavage X-- - esin capture with an ion exchange resin - 3 3 /Me - 2-3 + 3-2 - (mberlite ion exchange resin) atch and release strategy reagent X- 1 + 2 + + side product D [ X--] -

ugo Kubinyi, www.kubinyi.de atch and release strategy, using a traceless linker 3 usuki coupling release 3 3 2 2 2 i Me Me ugo Kubinyi, www.kubinyi.de Milestones in the istory of Multicomponent eactions. trecker (1850).. antzsch (1890) P. iginelli (1893) 3 + + 3 + - + l 2 2 + 2 + 2 2 3 2. Mannich (1912) 2 + 2 + 3 4 2 3 2 3 4

ugo Kubinyi, www.kubinyi.de M. Passerini (1921) + 2 + 3. T. ucherer (1934) + 3 + 2 + 3 2 F. singer (1958) 3 + 2 + 3 4 4 3 2 I. Ugi (1959) 2 + 2 + 3 + 4 4 2 3 ugo Kubinyi, www.kubinyi.de omplex Molecules from Multicomponent eactions i(ipr) 3 r + + + 2 4 steps e.g. r. L. chreiber, cience 287, 1964-1969 (2000) L. Weber, Drug Discov. today 7, 143-147 (2002)

ugo Kubinyi, www.kubinyi.de The Generation of caffold Diversity 2 2 Me Me 2 (Me) 2 Me L. Weber, Drug Discov. today 7, 143-147 (2002) ugo Kubinyi, www.kubinyi.de The Generation of caffold Diversity + 2 3 2 + + Et Me L. Weber, Q omb. ci. 24, 809-823 (2005) Three component Ugi reaction

ugo Kubinyi, www.kubinyi.de Increasing Diversity of ombinatorial Libraries 2 2 2 2 2 2 2 2 3 2 2 3 2 3 2 F 2 2 2 2 2 2 courtesy of Drs. M. Mann, W. auer, erono, Geneva ugo Kubinyi, www.kubinyi.de eferences unin, The ombinatorial Index, cademic Press, an Diego, 1998. 350 pp, $ 80. Terrett K, ombinatorial hemistry. xford University Press, ew York, 1998. 186 pp, $ 29 (in German 264 pp, EU 29). Jung G, ombinatorial hemistry, Wiley-V, Weinheim, 1999. 601 pp, EU 149. eck-ickinger G and Weber P, ombinatorial trategies in iology and hemistry, Wiley, 2002. 179 pp, $ 35 (in German EU 20). annwarth W and Felder E, ombinatorial hemistry, Wiley-V, Weinheim, 2000. 430 pp, EU 149. eneci P, olid-ase ynthesis and ombinatorial Technologies, Wiley-Interscience, ew York, 2000. 637 pp, $ 115. Ghose K and Viswanadhan V, ombinatorial Library Design and Evaluation: Principles. oftware Tools, and pplications in Drug Discovery, Marcel Dekker, ew York, 2001. 631 pp, $ 195. icolaou K, anko and artwig W, andbook of ombinatorial hemistry. Drugs, atalysts, Materials, Wiley-V, Weinheim, 2002. 1114 pp, EU 389.