SAR. Structure - Activity Relationships (alkoholy, amíny, aldehydy, ketóny, estery, amidy, kyseliny, uhľovodíky) 2/28/2016

Similar documents
OXFORD H i g h e r E d u c a t i o n Oxford University Press, All rights reserved.

ORGANIC - EGE 5E CH. 2 - COVALENT BONDING AND CHEMICAL REACTIVITY

Chapter 22: Amines. Organic derivatives of ammonia, NH 3. Nitrogen atom have a lone pair of electrons, making the amine both basic and nucleophilic

Amines. Amines are organic compounds containing a nitrogen functionality. primary secondary tertiary quaternary

Chapter 20 Carboxylic Acid Derivatives. Nucleophilic Acyl Substitution

Look for absorption bands in decreasing order of importance:

Synthesis of Nitriles a. dehydration of 1 amides using POCl 3 : b. SN2 reaction of cyanide ion on halides:

MOLECULAR REPRESENTATIONS AND INFRARED SPECTROSCOPY

Chapter 1 Reactions of Organic Compounds. Reactions Involving Hydrocarbons

Learning Organic Chemistry

Identifying Functional Groups. Why is this necessary? Alkanes. Why is this so important? What is a functional group? 2/1/16

Lecture Notes Chemistry Mukund P. Sibi Lecture 36 Synthesis of Amines

CHEMISTRY Topic #1: Functional Groups and Drawing Organic Molecules Fall 2014 Dr. Susan Findlay

Chapter 24. Amines. Based on McMurry s Organic Chemistry, 7 th edition

Drug Discovery. Zainab Al Kharusi Office: 33-10

Exam 1 (Monday, July 6, 2015)

Chapter 20: Carboxylic Acids

Patrick: An Introduction to Medicinal Chemistry 5e Chapter 01

R N R N R N. primary secondary tertiary

Loudon Chapter 23 Review: Amines Jacquie Richardson, CU Boulder Last updated 4/22/2018

Classes of Organic Compounds

Carbon Compounds. Chemical Bonding Part 2

Table 8.2 Detailed Table of Characteristic Infrared Absorption Frequencies

Aromatic Hydrocarbons

b.p.=100 C b.p.=65 C b.p.=-25 C µ=1.69 D µ=2.0 D µ=1.3 D

12.1 The Nature of Organic molecules

Chapter 2. Molecular Representations

2016 Pearson Education, Inc. Isolated and Conjugated Dienes

Nucleophilic Addition Reactions of Carboxylic Acid Derivatives

Amines Reading Study Problems Key Concepts and Skills Lecture Topics: Amines: structure and nomenclature

Loudon Chapter 23 Review: Amines CHEM 3331, Jacquie Richardson, Fall Page 1

CHEMISTRY 263 HOME WORK

Keynotes in Organic Chemistry

Chapter 25: The Chemistry of Life: Organic and Biological Chemistry

Organic Chemistry. Introduction to Organic Molecules and Functional Groups

Module9. Nuclear Magnetic Resonance Spectroscopy Nuclear Magnetic Resonance (NMR) spectroscopy - Chemical shift - Integration of signal area

CHAPTER 2: Structure and Properties of Organic Molecules

General Infrared Absorption Ranges of Various Functional Groups

Lecture 27 Organic Chemistry 1

Chapter 10: Carboxylic Acids and Their Derivatives

Chem 263 Nov 24, Properties of Carboxylic Acids

UNIT 4 REVISION CHECKLIST CHEM 4 AS Chemistry

Chem 1075 Chapter 19 Organic Chemistry Lecture Outline

More information can be found in Chapter 12 in your textbook for CHEM 3750/ 3770 and on pages in your laboratory manual.

Electronegativity Scale F > O > Cl, N > Br > C, H

ALCOHOLS: Properties & Preparation

TOK: The relationship between a reaction mechanism and the experimental evidence to support it could be discussed. See

Alcohol Synthesis. Dr. Sapna Gupta

Mechanism Summary for A-level AQA Chemistry

Carbon-heteroatom single bonds basic C N C X. X= F, Cl, Br, I Alkyl Halide C O. epoxide Chapter 14 H. alcohols acidic H C S C. thiols.

Chapter 2: An Introduction to Organic Compounds

CHEM 203. Midterm Exam 1 October 31, 2008 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

Chem 263 March 28, 2006

CHEM3331: Fundamentals of Organic Chemistry I Prof. Ognjen Š. Miljanić December 11, 2012

Definition: A carboxylic acid derivative undergoes hydrolysis (bond breaking with water) to form a carboxylic acid R C N + H 2 O + H O R

Organic Chemistry Review: Topic 10 & Topic 20

Bio-elements. Living organisms requires only 27 of the 90 common chemical elements found in the crust of the earth, to be as its essential components.

Alkanes, Alkenes and Alkynes

Chapter 24 From Petroleum to Pharmaceuticals

Alcohols. Alcohol any organic compound containing a hydroxyl (R-OH) group. Alcohols are an extremely important organic source

Organic Chemistry Lecture 2 - Hydrocarbons, Alcohols, Substitutions

Option G: Further organic chemistry (15/22 hours)

DAMIETTA UNIVERSITY. Energy Diagram of One-Step Exothermic Reaction

Chapter 12. Alcohols from Carbonyl Compounds Oxidation-Reduction & Organometallic Compounds. Structure

Chem 263 Notes March 2, 2006

Introduction. A1.1 (a) Shell number and number of subshells 1. A1.1 (b) Orbitals 2. A1.1 (c ) Orbital shapes (s, p & d) 2

Amines. Chapter 24 Organic Chemistry, 8th Edition. John McMurry

Aromatic Compounds II

Reduction. Boron based reagents. NaBH 4 / NiCl 2. Uses: Zn(BH 4 ) 2. Preparation: Good for base sensitive groups Chelation control model.

Organic Chemistry 112 A B C - Syllabus Addendum for Prospective Teachers

Paper 9: ORGANIC CHEMISTRY-III (Reaction Mechanism-2) Module 16: Reduction by Metal hydrides Part-I

Molecular Geometry: VSEPR model stand for valence-shell electron-pair repulsion and predicts the 3D shape of molecules that are formed in bonding.

Q.1 Draw structures for all amines of molecular formula C 4 H 11 N. Classify them as primary, secondary or tertiary amines.

Chapter 20. Amines. Nomenclature for amines. Aryl amines

Alkyl phenyl ketones are usually named by adding the acyl group as prefix to phenone.

BIOB111_CHBIO - Tutorial activity for Session 10. Conceptual multiple choice questions:

Chapter 19: Amines. Introduction

All Classes of Organic Compounds

10. Amines (text )

ALCOHOLS AND PHENOLS

H H O C C O H Carboxylic Acids and Derivatives C CH 2 C. N Goalby chemrevise.org. Strength of carboxylic acids.

ORGANIC CHEMISTRY. Wiley STUDY GUIDE AND SOLUTIONS MANUAL TO ACCOMPANY ROBERT G. JOHNSON JON ANTILLA ELEVENTH EDITION. University of South Florida

Alkenes. Alkenes-hydrocarbons with a carbon-carbon double bond. Alkenes have the formula C n H 2n. Nomenclature

KOT 222 Organic Chemistry II

Organic Chemistry I Exam 3 Fall 2001 November 30, Which of the following compounds corresponds to the spectral data given below?

1. LiAlH4 :.. :.. 2. H3O +

Reducing Agents. Linda M. Sweeting 1998

Chapters 2 & 25: Covalent bonds & Organic Chemistry

Carboxylic Acids and Nitriles

Alcohols, Ethers and Epoxides. Chapter Organic Chemistry, 8th Edition John McMurry

2Dstructuredrawing Chem314 Beauchamp

Module 4 revision guide: Compounds with C=O group

Carboxylic acid derivatives

Class XII: Chemistry Chapter 13: Amines Top concepts

Chimica Farmaceutica

Carboxylic Acid Derivatives and Nucleophilic Acyl Substitution Reactions. McMurray Text Chapter 21

Lecture 13A 05/11/12. Amines. [Sn2; Hofmann elimination; reduction of alkyl azides, amides, nitriles, imines; reductive amination; Gabriel synthesis]

CHEM 203. Final Exam December 15, 2010 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

75. A This is a Markovnikov addition reaction. In these reactions, the pielectrons in the alkene act as a nucleophile. The strongest electrophile will

Amines and Heterocycles. McMurry: Chapter 24

Transcription:

Structure Activity elationships (SA) identifies which functional groups are important for binding and activity SA Structure - Activity elationships (alkoholy, amíny, aldehydy, ketóny, estery, amidy, kyseliny, uhľovodíky) Method alter, remove or mask a functional group test the analogue for activity method of testing: in vitro target - trarget activity response in vitro on cells or in vivo - biological response (binding interactions with target (e.g. enzyme)) biological response (target binding pharmacokinetic properties) M-II Andrej Boháč if group is removed or modified and in vitro activity: drops or diminished => group was important for binding unaffected => group is not important onsider by analogues: 5. Structure Activity elationships (SA) modifications may disrupt binding by steric or electronic effects easiest analogues are those made directly from a lead compound 3 some analogues have to be made by a full (de novo) synthesis (e.g. replacing an aromatic ring with a heterocyclic ring) SA allows identification of important groups involved in binding SA allows identification of the pharmacophore MPIE an opioid analgesic drug DEIE antitussive drug AALGESI ATIVITY DPS 1

IMPTAT GUPS DETEMIED F ATIVITY MPIE 6-YMPIE ATIVITY UAFFETED MPIE AALGESI PAMAPE F PIATES 3 MPIE 3 METAZIE LEVPAL 2

5.1 SA on Alcohols Possible effect of analogues on binding (e.g. ether) BD Possible analogues = or BA Ether analogue 3 = or Ether analogue steric shield 3 Ether o interaction as BD o interaction as BA Ester Alkane 5.2 SA on 1 o, 2 o & 3 o Amines ( 2,, 3 ) if amine is ionised 5.2 SA on 1 o, 2 o & 3 o Amines ( 2,, 3 ) for free base -Bonding Ionic 2-2 BD = or BA -Bonding BD 2 = or 3 acts as a strong BD ote: 3 o Amines are only able to act as BA s - no hydrogen available to act as BD 3

5.2 SA on 1 o, 2 o & 3 o Amines ( 2,, 3 ) s of 3 o amines containing a methyl substituent s of 1 o & 2 o amines Effect on binding 2 3l Amide analogue 2-3 3 3 Demethylation l 3 V-l 2 o amine 3 l 3 o amide 3 o interaction 1 o and 2 o amines are converted to 2 o and 3 o amides respectively amides cannot ionise and so ionic bonding is not possible an amide is a poor BA and so this eliminates BA interactions steric effect of acyl group is likely to hinder acting as a BD (2 o amide) PPSE A MEAISM of demetylation from nitrogen by V-l? 5.3 SA on Quaternary Ammonium Salts ( 4 ) 5.4 SA on Aldehydes and Ketones 2-3 Ionic bonding 3 d d- Induced dipole interactions s Dipole-dipole interaction BA -Bonding (= or ) s Full synthesis of 1 o -2 o amines and nitrogen to form permanent ion subsequently amides to disable ' Ketone Planar sp 2 carbon centre ab 4 or LiAl 4 ' 2 o Alcohol Tetrahedral sp 3 carbon centre 4

5.5 SA on Esters Effect on binding hange in stereochemistry (planar to tetrahedral) May move oxygen out of range Alcohol analogue (= or ) If still active, further reactions can be carried out on alcohol to establish importance of oxygen -bonding as BA by either oxygen s 3 a LiAl 4 ydrolysis splits molecule and may lead to a loss of activity due to loss of other functional groups - only suitable for simple esters. ydrolysis leads to a dramatic increase in polarity which may influence ability of analogue to reach target if in vivo tests are used. eduction to alcohol removes carbonyl group and can establish importance of the carbonyl oxygen, but reaction can be difficult to do if other labile functional groups are present. arboxylic acid 2 1 o Alcohol Alcohol 3 Esters are usually hydrolysed by esterases Esters are more likely to be important for pharmacokinetic reasons acting as prodrugs. 5.6 SA on Amides Prodrug Fatty Barrier Esterase BA BD Prodrug Ester masks polar groups Allows passage through fatty cell membranes Esterase (= or ) (= or ) The nitrogen of an amide cannot act as a BA - lone pair interacts with carbonyl group Tertiary amides unable to act as BD s 5

s ' a arboxylic acid 2 Amine ' s LiAl 4 2 2 1 o Amine a / MeI 3 ' 3 o Amide ydrolysis splits molecule and may lead to loss of activity due to loss of other functional groups - only suitable for simple amides. ydrolysis leads to dramatic increase in polarity which may affect ability of analogue to reach target if in vivo tests are done eduction to amine removes carbonyl group and can establish importance of the carbonyl oxygen, but reaction may be difficult to do if other labile groups are present. -alkylation will disable BD properties of group in 2 amides. -Methylation prevents BD interaction and may introduce a steric effect that prevents also an BA interaction steric shield 3 3 o binding as BD Binding of as BA hindered 5.7 SA on arboxylic Acids as free acid as carboxylate ion BA BA BA - - 2 Ionic bonding (= or ) (= or ) (= or ) (= or ) BD harged oxygen atoms are strong BA s. Group can interact by ionic and hydrogen bonding at the same time. (= or ) 6

5.8 SA on Aromatic ings and Alkenes Possible analogues / ' LiAl 4 ' Ester 2 Possible effects esterification prevents ionisation, BD interactions and may hinder BA by a steric effect reduction removes carbonyl oxygen as potential BA and prevents ionisation 3 2 steric shield 3 1 o Alcohol vdw hydrophobic pocket Possible analogues ' 2 / ai 2 / Pd/ ' vdw hydrophobic region o ionic bonding possible -Bonding hindered Possible effects on binding 5.10 SA of Alkyl Groups Possible interactions o fit hydrophobic pocket Buffers hydrophobic region 3 hydrophobic slot van der Waals interactions 3 3 3 hydrophobic pocket 7

5.10 SA of Alkyl Groups s Easiest alkyl groups to vary are substituents on heteroatoms. Vary length and bulk of alkyl group to test space available. 3 V-l 3 Br ' ' ' ' 5.9 Miscellaneous Functional Groups in s acid chlorides - too reactive to be of used acid anhydrides - too reactive to be of used - present in anticancer drugs (alkyl. agents) -react with nucleophiles in DA Ar - commonly present (liphophilic int., fluorine F...= interactions, or halogen bond:..., bond) 2 - sometimes present but often toxic -:::- alkynes - sometimes present, but not usually important in binding interactions -S thiols - present in some drugs as important binding group to transition metals (e.g. Zn in zinc metalloproteinases MMPs) - - present in some drugs but rarely involved in binding 3 ydrolysis ' ' functional groups that may be important for electronic reasons (e.g. nitro, cyano, aryl halides) functional groups that may be important for steric reasons (e.g. alkynes) 8