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Bioisosterism

Bioisosterism involves substituting or modifying chemical groups in a molecule with other groups that have similar physical or chemical properties, in order to modulate biological activity, toxicity, or pharmacokinetic properties. Bioisosteres can be classified as classical isosteres that have the same number of atoms, or non-classical isosteres that have similar biological effects but different atom counts or structures. Common bioisosteric replacements involve substituting atoms like C, N, O, S, halogens, and functional groups like hydroxyl, amino, and thiol groups. The impacts of bioisosteric replacements depend on resulting changes to properties like size, shape, solubility, reactivity, and hydrogen bonding potential

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867 views

Bioisosterism

Bioisosterism involves substituting or modifying chemical groups in a molecule with other groups that have similar physical or chemical properties, in order to modulate biological activity, toxicity, or pharmacokinetic properties. Bioisosteres can be classified as classical isosteres that have the same number of atoms, or non-classical isosteres that have similar biological effects but different atom counts or structures. Common bioisosteric replacements involve substituting atoms like C, N, O, S, halogens, and functional groups like hydroxyl, amino, and thiol groups. The impacts of bioisosteric replacements depend on resulting changes to properties like size, shape, solubility, reactivity, and hydrogen bonding potential

Uploaded by

purnima singh
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Bioisosterism

Bioisosterism

Bioisosteres - substituents or groups with


chemical or physical similarities that produce
similar biological properties. Can attenuate
toxicity, modify activity of lead, and/or alter
pharmacokinetics of lead.
Bioisosterism
Bioisosterism
Table 2.2
Classical Isosteres
1. Univalent atoms and groups

a. CH 3 NH 2 OH F Cl
b. Cl PH 2 SH
c. Br i-Pr
d. I t-Bu

2. Bivalent atoms and groups

a. CH2 NH O S Se
b. COCH2 R CONHR CO 2R COSR

3. Trivalent atoms and groups

a. CH N
b. P As

4. Tetravalent atoms

a. C Si

b. C N P

5. Ring equivalents
a. CH CH S (e.g., benzene, thiophene)
b. CH N (e.g., benzene, pyridine)
c. O S CH 2 NH (e.g., tetrahydrofuran,
tetrahydrothiophene,
cyclopentane, pyrrolidine)
Fluorine vs Hydrogen Replacements
Interchange of Hydroxyl and Amino Groups
Interchange of Hydroxyl and Thiol Groups
Non-Classical Isosteres

Do not have the same number of atoms and do not fit


steric and electronic rules of classical isosteres, but
have similar biological activity.
Examples of Bioisosteric Analogues
Examples of Bioisosteric Analogues
Examples of Bioisosteric Analogues
Examples of Bioisosteric Analogues
Examples of Bioisosteric Analogues
Examples of Bioisosteric Analogues
Changes resulting from bioisosteric replacements:
Size, shape, electronic distribution, lipid solubility, water
solubility, pKa, chemical reactivity, hydrogen bonding
Effects of bioisosteric replacement:
1. Structural (size, shape, H-bonding are important)
2. Receptor interactions (all but lipid/H2O solubility are
important)
3. Pharmacokinetics (lipophilicity, hydrophilicity, pKa, H-
bonding are important)
4. Metabolism (chemical reactivity is important)
Bioisosteric replacements allow you to tinker with whichever parameters are necessary to
increase potency or reduce toxicity.
Bioisosterism allows modification of
physicochemical parameters

Multiple alterations may be necessary:


If a bioisosteric modification for receptor
binding decreases lipophilicity, you may have
to modify a different part of the molecule with
a lipophilic group.
Where on the molecule do you go to make the
modification? The auxophoric groups that do not interfere with binding.
Few More Examples

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