Hubbry Logo
BioisostereBioisostereMain
Open search
Bioisostere
Community hub
Bioisostere
logo
7 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Bioisostere
Bioisostere
Bioisostere
View on Wikipedia
from Wikipedia

In medicinal chemistry, bioisosteres are chemical substituents or groups with similar physical or chemical properties which produce broadly similar biological properties in the same chemical compound.[1] In drug design,[2] the purpose of exchanging one bioisostere for another is to enhance the desired biological or physical properties of a compound without making significant changes in chemical structure. The main use of this term and its techniques are related to pharmaceutical sciences. Bioisosterism is used to reduce toxicity, change bioavailability, or modify the activity of the lead compound, and may alter the metabolism of the lead.

Examples

[edit]

Classical bioisosteres

[edit]
A table of common classical bioisosteres
A table of common classical bioisosteres

Classical bioisosterism was originally formulated by James Moir and refined by Irving Langmuir[3] as a response to the observation that different atoms with the same valence electron structure had similar biological properties.

For example, the replacement of a hydrogen atom with a fluorine atom at a site of metabolic oxidation in a drug candidate may prevent such metabolism from taking place. Because the fluorine atom is similar in size to the hydrogen atom the overall topology of the molecule is not significantly affected, leaving the desired biological activity unaffected. However, with a blocked pathway for metabolism, the drug candidate may have a longer half-life.

  • Procainamide, an amide, has a longer duration of action than Procaine, an ester, because of the isosteric replacement of the ester oxygen with a nitrogen atom.[4] Procainamide is a classical bioisostere because the valence electron structure of a disubstituted oxygen atom is the same as a trisubstituted nitrogen atom, as Langmuir showed.

Another example is seen in a series of anti-bacterial chalcones. By modifying certain substituents, the pharmacological activity of the chalcone and its toxicity are also modified.[5]

Example of bioisosterism in chalcones
Example of bioisosterism in chalcones

Non-classical bioisosteres

[edit]
A phenyl for methylthiophene bioisosteric replacement
A phenyl for methylthiophene bioisosteric replacement

Non-classical bioisosteres may differ in a multitude of ways from classical bioisosteres, but retain the focus on providing similar sterics and electronic profile to the original functional group. Whereas classical bioisosteres commonly conserve much of the same structural properties, nonclassical bioisosteres are much more dependent on the specific binding needs of the ligand in question and may substitute a linear functional group for a cyclic moiety, an alkyl group for a complex heteroatom moiety, or other changes that go far beyond a simple atom-for-atom switch.

For example, a chloride -Cl group may often be replaced by a trifluoromethyl -CF3 group or by a cyano -C≡N group. Depending on the particular molecule used, the substitution may result in little change in activity, or either increased or decreased affinity or efficacy - depending on what factors are important for ligand binding to the target protein. Another example is aromatic rings, where a phenyl -C6H5 ring can often be replaced by a different aromatic ring such as thiophene or naphthalene which may improve efficacy, change specificity of binding or reduce metabolically labile sites on the molecule, resulting in better pharmacokinetic properties.

Silafluofen is an isostere of pyrethroid insecticides.

Other applications

[edit]

Bioisosteres of some patented compounds can be discovered automatically and used to circumvent Markush structure patent claims. It has been proposed that key force field features, that is the pharmacophore, be patented instead.[8]

See also

[edit]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Bioisostere

View on Grokipedia
from Grokipedia
A bioisostere is a compound or group of atoms that possesses near-equal molecular shapes and volumes, approximately the same distribution of electronic properties, and produces broadly similar biological properties when substituted for another in a molecular structure. This concept, central to , enables the replacement of functional groups in drug candidates to preserve while optimizing physicochemical properties such as , metabolic stability, and potency. The origins of bioisosterism trace back to Irving Langmuir's 1919 proposal of isosterism, which described atoms or groups with similar outer configurations and physical properties, such as size and . In 1925, Hermann Grimm expanded this with the hydride displacement law, allowing systematic replacement of -CH- by -N- or -NH- by -O- while maintaining similar properties. Hans Erlenmeyer further applied these ideas to biological systems in the 1930s, demonstrating that isosteric substitutions could retain antigen-antibody interactions. The term "bioisostere" was coined by Harris Friedman in 1951 to specifically denote isosteric replacements that elicit comparable biological responses, marking a pivotal shift toward rational . Bioisosteres are broadly classified into classical and nonclassical categories. Classical bioisosteres adhere to strict rules based on counts and include monovalent groups like -F and -OH, divalent groups such as -O- and -NH-, and trivalent groups including -CH= and -N=. These replacements often preserve electronic and steric features, as seen in ring equivalents like versus . Nonclassical bioisosteres, by contrast, involve more flexible mimicry without exact valence matching, such as as a bioisostere for or for , and are selected based on empirical biological outcomes rather than purely physicochemical similarity. In , bioisosteric replacements address key challenges by enhancing selectivity, reducing off-target effects, improving pharmacokinetic profiles, and avoiding metabolic liabilities. For instance, replacing the in angiotensin II receptor blockers with a group, as in losartan, increases potency by approximately tenfold and improves oral . Similarly, substitution in nucleoside analogs like emtricitabine boosts antiviral activity against by four- to tenfold compared to lamivudine. These tactics also facilitate scaffold hopping to explore chemical space, circumvent constraints, and develop second-generation therapeutics with refined therapeutic indices.

Fundamentals

Definition

Bioisosteres are defined as chemical substituents, groups, or fragments that possess similar physical properties—such as size, shape, and —and chemical properties, including hydrogen bonding potential and , which result in broadly similar biological effects when one replaces another within a molecular structure. This concept enables medicinal chemists to modify while preserving key interactions with biological targets, thereby optimizing pharmacological profiles without fundamentally altering the molecule's reactivity or binding affinity. The term "bioisostere" was introduced by Harris L. Friedman in 1951, who described them as atoms, molecules, or groups that conform to the broadest definition of isosteres—entities with comparable electron configurations and spatial arrangements—while also producing equivalent biological responses in physiological systems. Unlike general isosteres, which emphasize physicochemical equivalence derived from principles like the and similar valence electron counts, bioisosteres are tailored specifically for medicinal applications, focusing on retention or improvement of therapeutic activity rather than mere structural mimicry. This distinction underscores their utility in , where biological potency and selectivity take precedence over isolated chemical isomorphism. Central to bioisosterism are key criteria such as comparable distribution, which ensures similar electronic interactions; molecular volume, which maintains steric fit within binding pockets; and , which influences non-covalent forces like van der Waals attractions. These attributes allow bioisosteric replacements to elicit consistent pharmacological outcomes, such as or effects at receptors, by mimicking the original group's role in molecular recognition and transport processes.

Principles of Bioisosterism

The principles of bioisosterism are grounded in the octet theory of valence, as articulated by in 1919, which posits that atoms or molecular groups achieving a stable of eight valence electrons—often termed the ""—tend to exhibit similar physical and chemical properties due to comparable electronic arrangements. Langmuir introduced the concept of isosterism to describe molecules or ions, termed isosteres, that possess the same number and spatial arrangement of electrons, such as N₂, CO, and CN⁻, all featuring 14 total electrons with analogous valence shells; this equivalence leads to shared behaviors like molecular size, bond lengths, and reactivity, forming the foundational rationale for mimicking molecular properties in chemical . Building on Langmuir's framework, Hugo Grimm proposed the hydride displacement law in , an empirical extension that allows for systematic replacements by considering "pseudoatoms" formed when an atom is displaced by the preceding element in the periodic table augmented by one or more hydrogen atoms, thereby preserving isosteric equivalence. For instance, this law equates -CH with -N⁺, -NH with -O, -CH₂ with -NH, and -CH₃ with -NH₂, enabling substitutions that maintain overall electronic and steric balance without altering the core count. Grimm's rule provided a practical guideline for generating series of structurally related compounds with expectedly similar properties, emphasizing the periodic table's role in predicting isosteric behavior. Hans Erlenmeyer further broadened these ideas in the early by extending isosterism to functional groups and ring systems, defining isosteres more inclusively as elements, molecules, or ions with identical peripheral layers that could preserve both steric and electronic effects in biological contexts. Erlenmeyer's contributions included recognizing group isosteres (e.g., -COOH versus -SO₃H) and ring equivalents (e.g., approximating through replacement of CH=CH by S), applying isosteric principles to biological systems where such replacements could retain activity by mimicking interactions at enzymes or receptors. This evolution shifted focus from purely physical isosterism to biologically relevant modifications that account for dynamic environmental factors in living systems. The success of bioisosteric replacements hinges on several key physicochemical factors that ensure minimal disruption to molecular recognition and , including close matching of acid dissociation constants (pKa) to preserve ionization states, similar partition coefficients (logP) for comparable and membrane permeability, and aligned dipole moments to maintain electrostatic interactions with biological targets. These parameters, as outlined in foundational analyses, influence , metabolic stability, and binding affinity; for example, discrepancies in pKa can alter at physiological , while logP mismatches may affect absorption, underscoring the need for quantitative evaluation beyond mere structural . Optimal bioisosteric design thus prioritizes holistic similarity across these metrics to enhance therapeutic potential without introducing off-target effects.

Historical Development

Origins of Isosterism

The concept of isosterism originated in the early through explorations of structural similarities among inorganic compounds, predating its formal naming. In 1909, James Moir proposed ideas that laid the groundwork for isosterism by suggesting atomic structures built from common fundamental units, implying similarities in composition and arrangement that could lead to comparable chemical behaviors in inorganic systems. His work focused on harmonizing atomic weights and valency through hypothetical models of atomic genesis, highlighting how certain elements and compounds might exhibit analogous properties due to shared structural motifs. The term "isosterism" was formally introduced by in , who defined isosteres as molecules or ions possessing the same number of atoms and valence s arranged in identical configurations, adhering to the for stable outer electron shells. Langmuir emphasized electronic similarity, exemplified by diatomic molecules like (N₂) and (CO), which share 14 electrons and similar spatial arrangements, leading to comparable physical and chemical characteristics. This framework extended Moir's structural analogies into a more rigorous electronic theory, linking isosterism to the emerging understanding of atomic and molecular orbitals. Early applications of isosterism were primarily in , where it enabled predictions of similar physicochemical properties for isosteric species. For instance, isosteres were observed to exhibit comparable boiling points, densities, and magnetic susceptibilities due to their electronic and steric equivalence, facilitating correlations in reactivity patterns such as bond strengths and potentials. These insights provided a tool for rationalizing observed uniformities in inorganic and simple organic compounds, setting the stage for later extensions into biological contexts.

Evolution to Bioisosterism

In 1925, Hermann Grimm further advanced the concept with his hydride displacement law, which stated that the addition of a hydride ion (H⁻) to an atom imparts to the resulting "pseudoatom" the properties of the next higher atomic number element in the periodic table. This allowed for systematic replacements, such as substituting -CH₃ for -NH₂, -NH- for -O-, or -CH₂- for -S-, while preserving similar physicochemical properties. Grimm's law expanded the scope of isosterism beyond strict electronic matching, facilitating its application to more diverse chemical structures. The transition from chemical isosterism to bioisosterism began in when Hans Erlenmeyer extended the concept beyond simple atomic substitutions to include organic functional groups and molecules with similar peripheral distributions. In his seminal 1932 paper, Erlenmeyer introduced the idea of "pseudoatoms," allowing for the replacement of atoms or groups in organic structures while maintaining spatial and electronic similarity, such as substituting -CH=CH- with -N=N-. This broadening facilitated the application of isosterism to more complex organic compounds, laying the groundwork for biological considerations. By the 1940s, Erlenmeyer and collaborators further explored these replacements in biological contexts, observing that certain isosteric analogs elicited similar immunological responses, such as antibodies produced against tyrosine derivatives also reacting with phenylalanine mimics, marking an early recognition of biological mimicry. The formal establishment of bioisosterism as a distinct principle occurred in with H.L. 's seminal contribution, where he coined the term "bioisosterism" to describe groups or molecules that not only share physicochemical properties but also produce comparable biological effects due to structural and electronic analogies. Friedman emphasized that bioisosteres must mimic the pharmacological or toxicological responses of the original group, distinguishing this from pure chemical isosterism by focusing on outcomes, such as inhibition or receptor binding. This definition shifted the paradigm toward practical utility in , enabling targeted modifications to enhance drug potency or selectivity without altering core . Following Friedman's introduction, bioisosterism underwent significant refinements in the and , particularly through its integration into quantitative structure-activity relationship (QSAR) analyses pioneered by Corwin Hansch and Tetsuo Fujita. By the mid-1960s, researchers employed bioisosteric replacements within Hansch's linear free-energy models to correlate effects on , allowing predictions of how isosteric changes influence potency across series of analogs, as seen in studies of antibacterials where -SO2NH2 and -CONH2 groups yielded similar inhibitory profiles. This quantitative framework solidified bioisosterism as a cornerstone of rational , emphasizing measurable parameters like and electronic effects to guide optimizations.

Classification

Classical Bioisosteres

Classical bioisosteres are atoms, ions, or molecules that share the same number of valence electrons, resulting in analogous electronic configurations and bonding capabilities. This isosteric equivalence, rooted in the octet rule, allows these replacements to mimic the steric and electronic properties of the original group, often preserving biological activity while enabling modifications to pharmacokinetics or synthetic accessibility. The concept was formalized in early medicinal chemistry to facilitate rational drug design by substituting functional groups with similar valence electron counts. Classical bioisosteres are classified by valence, reflecting the number of bonds they form in a . Monovalent bioisosteres involve groups with a single bonding site, such as -H replaced by -F, -OH by -NH₂, or -CH₃ by -NH₂; these substitutions maintain similar size and distribution but can alter polarity or hydrogen-bonding potential. Divalent bioisosteres feature two bonding sites, exemplified by -O- interchanged with -S- or -NH-, where the replacements often differ in atomic size but retain comparable profiles for moments. Trivalent bioisosteres include =N- and =CH- or =P- and =N-, suitable for unsaturated systems, with similarities in pyramidal and lone-pair . Tetravalent bioisosteres encompass centers like >C< with >Si< or >N⁺< with >C<, where tetrahedral arrangements and charge distribution are preserved despite variations in atomic radius. Classical bioisosteres also include ring equivalents, where heterocyclic rings replace carbocyclic ones while maintaining isoelectronic character and similar geometry. For example, benzene can be replaced by pyridine, or tetrazole by imidazole, preserving π-electron systems and aromaticity for comparable biological interactions. Key physicochemical properties influencing their interchangeability include electronegativity (Pauling scale) and covalent radius, which affect bond polarity, molecular volume, and lipophilicity. The table below summarizes common pairs across valences, highlighting these properties for selected examples.
ValenceBioisosteric PairElectronegativity (Pauling)Covalent Radius (pm)
Monovalent-H / -F2.20 / 3.9831 / 57
Monovalent-OH / -NH₂3.44 / 3.0466 / 71
Divalent-O- / -S-3.44 / 2.5866 / 105
Trivalent=N- / =CH-3.04 / 2.5571 / 76
Tetravalent>C< / >Si<2.55 / 1.9076 / 111
These replacements are selected for their close alignment in valence electron count, ensuring minimal disruption to the target molecule's overall electronic structure.

Non-Classical Bioisosteres

Non-classical bioisosteres encompass molecular fragments that elicit similar biological responses to their counterparts through chemical and physical similarities, yet deviate from the stringent isoelectronic and steric matching required for classical bioisosteres. This broader category, first articulated by Thornber in 1979, prioritizes functional mimicry over precise atomic equivalence, allowing for variations in size, shape, and electronic distribution to optimize drug-like properties such as potency, selectivity, or pharmacokinetics. Unlike classical replacements, non-classical ones often introduce heteroatoms or structural motifs that modulate interactions with biological targets while preserving overall activity. A prominent application involves bioisosteric replacements for the carboxylic acid group (-COOH), which is ubiquitous in drugs for its acidity and hydrogen-bonding capacity but can suffer from poor oral bioavailability or metabolic instability. The tetrazole moiety, for instance, serves as a non-classical surrogate due to its comparable pKa (approximately 4.5–4.9) and ability to form ionic interactions, albeit with a more lipophilic profile that enhances membrane permeability. In the angiotensin II receptor antagonist losartan, tetrazole replacement of -COOH maintains potent AT1 receptor binding (IC50 = 0.019 μM) and enables effective oral dosing. Similarly, hydroxamic acids (-CONHOH) mimic -COOH through and metal , as seen in MEK inhibitors where the replacement yields sub-nanomolar potency (IC50 = 7.9 nM) and improved characteristics. Acyl sulfonamides (-CONHSO2R) and phosphonates (-PO3H2) further expand this arsenal; acyl sulfonamides offer tunable acidity (pKa 4–5) and enhanced selectivity in LTE4 antagonists (pKd = 8.6), while phosphonates provide polar alternatives that shift agonist to antagonist activity in ligands like phaclofen. These replacements prioritize practical utility in lead optimization over exact isosterism. Ring systems represent another key domain for non-classical bioisosterism, where aromatic or heterocyclic scaffolds are interchanged to fine-tune electronics, solubility, or binding affinity without disrupting core topology. Replacing (phenyl) with introduces a atom, altering hydrogen-bonding potential and while retaining planarity; in factor Xa inhibitors, this swap boosted permeability (: 17.61 × 10−6 cm/s versus 9.34 × 10−6 cm/s for phenyl analogs) and maintained inhibitory potency. Heterocyclic exchanges, such as (oxygen-containing) for (sulfur-containing), leverage similar π-electron systems but differ in and coordination ability, enhancing metal interactions in HIV-1 integrase inhibitors (IC50 = 20 nM for thiophene variants). These modifications exemplify how non-classical approaches enable targeted property adjustments in , often improving developability metrics like metabolic stability or target engagement.

Examples and Case Studies

Classical Examples

One prominent classical example of bioisosteric replacement involves the conversion of , a short-acting -based local anesthetic, to by substituting the group (-COOR) with an group (-CONH₂). This replacement retains the blocking mechanism while enhancing metabolic stability and extending the duration of action, as the linkage is less susceptible to compared to the . The structural similarity allows to interact with cardiac s, providing antiarrhythmic effects rather than . , developed in the 1950s, demonstrates how this isosteric swap can repurpose pharmacological effects for clinical use in treating arrhythmias. Another key historical application is the substitution of with in molecules to block sites of metabolic oxidation. In compounds like corticosteroids, such as the fluorinated analog of (e.g., ), the atom at position 9α mimics in size and but resists enzymatic oxidation by enzymes, thereby prolonging hormonal activity and potency. This replacement preserves the 's binding affinity to glucocorticoid receptors, ensuring sustained and immunosuppressive effects without altering the core scaffold's biological function. Early studies in the mid-20th century highlighted this strategy's role in developing more effective therapeutic by mitigating rapid deactivation through hepatic metabolism.

Non-Classical Examples

Non-classical bioisosteres often involve functional groups that mimic electronic or steric properties without adhering to strict isosteric rules, allowing for targeted improvements in molecular interactions. One such application is the replacement of with trifluoromethyl (-CF₃) or cyano (-CN) groups in to modulate electron-withdrawing effects and . These substitutions can enhance receptor binding and while maintaining . Another prominent non-classical example is the carbon-to-silicon switch in silafluofen, a developed by replacing a carbon atom in the scaffold with . This bioisosteric modification increases the Si-C compared to C-C, altering the slightly while preserving the overall , resulting in enhanced photostability and resistance to alkaline degradation in soil applications. Silafluofen demonstrates improved insecticidal efficacy against pests like rice stem borers and , with reduced environmental , particularly lower fish toxicity relative to traditional pyrethroids, due to the silicon atom's influence on metabolic pathways. This replacement exemplifies how non-classical isosterism can extend the utility of established chemical classes in by addressing stability limitations. In inhibitors, spirocyclic structures serve as non-classical bioisosteres for rings, introducing three-dimensionality to reduce planarity and mitigate off-target binding. For example, bicyclo[1.1.1] (BCP) scaffolds have been employed as rigid, saturated mimics of para-substituted benzenes in receptor (VEGFR) inhibitors like analogs. This substitution constrains the linker geometry, enhancing selectivity for the active by limiting conformational flexibility that could lead to nonspecific interactions. Such spirocyclic replacements have yielded compounds with nanomolar potency and improved pharmacokinetic profiles, as the non-planar architecture disrupts π-stacking with unintended protein pockets while preserving key hydrogen bonding. A more recent non-classical example, as of 2023, involves the use of as a bioisostere for the group in (BTK) inhibitors. In the development of , the triazole replacement improved and reduced metabolic liabilities compared to earlier amide-based inhibitors like , leading to better oral and efficacy in treating B-cell malignancies.

Applications in

Drug Design and Optimization

In the hit-to-lead phase of drug discovery, bioisosteric replacements are employed to modify lead compounds by swapping functional groups or moieties that preserve key molecular interactions while enhancing biological activity. This strategy allows medicinal chemists to explore structure-activity relationships (SAR) through targeted substitutions, often guided by initial potency data to identify replacements that improve binding affinity to the target protein. For instance, replacing a carboxylic acid with a tetrazole group in angiotensin II receptor antagonists, as seen in the development of losartan, resulted in a 10-fold increase in potency due to better mimicry of the anionic pharmacophore. Bioisosteres also play a crucial role in boosting selectivity by fine-tuning electronic and steric properties to favor interactions with the intended target over off-target proteins. In SAR-driven campaigns, such swaps can reduce ; for example, incorporating atoms has been used to enhance selectivity in inhibitors by altering hydrogen bonding patterns without disrupting overall binding. A classic illustration is the bioisosteric modification in the , where an was replaced by an to maintain activity while improving metabolic stability. Another tactical application of bioisosteres in drug optimization involves circumventing restrictions on existing leads by introducing minor structural changes that retain pharmacological efficacy. This approach enables the generation of novel ; for example, (Levitra) was developed from (Viagra) via a bioisosteric replacement of a ring with a , avoiding patent overlap while preserving PDE5 inhibition. Such modifications ensure the new analog exhibits comparable potency and selectivity to the original compound. Bioisosteric outcomes are further predicted and optimized through integration with quantitative structure-activity relationship (QSAR) models, which incorporate electronic descriptors like Hammett constants to quantify effects on activity. These models allow chemists to prioritize replacements based on predicted changes in and , facilitating rapid iteration in lead optimization. By correlating bioisosteric variations with experimental potency data, QSAR enhances the efficiency of SAR-guided design.

Improving Physicochemical Properties

Bioisosteric replacements play a crucial role in optimizing the absorption, distribution, , , and (ADMET) profile of candidates by fine-tuning key physicochemical parameters such as , metabolic stability, and , thereby enhancing developability without compromising . These modifications allow medicinal chemists to address liabilities that arise during lead optimization, such as poor aqueous leading to suboptimal or rapid enzymatic degradation resulting in short half-lives. By selecting appropriate bioisosteres, compounds can achieve balanced properties that support progression through preclinical and clinical stages. One primary application involves enhancing through acid bioisosteres that modulate pKa values to improve and dissolution at physiological . For instance, replacing a (pKa ≈ 4–5) with a group (pKa ≈ 4.5–5.0) maintains comparable acidity while increasing (e.g., logD7.4 values from -0.49 to -1.65 for acids versus -0.25 to -1.0 for tetrazoles), which can paradoxically boost permeability and overall aqueous in neutral buffers. This adjustment reduces the risk of precipitation in gastrointestinal fluids and enhances oral , as demonstrated in antagonists like losartan, where substitution improved pharmacokinetic profiles in rat models by facilitating better absorption. Tetrazoles also evade certain metabolic pathways, such as acyl , that plague , further supporting solubility-driven ADMET gains. To bolster metabolic stability, bioisosteric swaps from esters to amides are employed to resist hydrolytic cleavage by esterases, a common deactivation route in vivo. Esters are highly susceptible to enzymatic hydrolysis, often resulting in rapid clearance and reduced exposure, whereas amides exhibit greater resistance due to the poorer leaving group ability of the amide nitrogen, extending plasma half-lives. This replacement preserves hydrogen-bonding interactions essential for target engagement while minimizing reactive metabolite formation; for example, in protease inhibitors, amide analogs demonstrated improvements in metabolic stability in liver microsomes compared to their ester counterparts. Such modifications are particularly valuable in prodrug design avoidance, ensuring sustained therapeutic levels without toxicity from degradation products. Tuning via aromatic to aliphatic mimics addresses issues like excessive CYP inhibition, which can lead to drug-drug interactions and . Aromatic rings contribute to high logP values and planarity, promoting nonspecific binding to enzymes, whereas aliphatic replacements—such as cyclobutane or bicyclo[1.1.1]pentane for —increase sp3 hybridization, reducing lipophilicity and inhibition in some series. This shift enhances and metabolic clearance while mitigating reactive metabolite risks, as seen in kinase inhibitors where saturated carbocycles improved hERG selectivity and pharmacokinetic parameters in models without altering potency. These changes promote a more favorable developability profile by balancing hydrophobicity for absorption with reduced off-target liabilities.

Recent Advances

Computational Tools

Computational tools have revolutionized the identification and prediction of bioisosteres by leveraging databases, , and to analyze vast chemical spaces and suggest replacements based on structural similarity, bioactivity, and physicochemical properties. These tools address the challenges of manual bioisostere design by providing scalable, data-driven approaches that integrate literature, , and experimental data. The SwissBioIsostere database, maintained by the SIB Swiss Institute of Bioinformatics, serves as a comprehensive resource for fragment-based bioisosteric searches, containing over 25 million unique molecular replacements derived from , SureChEMBL, and . Updated in 2021, it incorporates structural, bioactivity, physicochemical, and purchasability data, enabling users to query replacements within specific chemical and biological contexts, such as target proteins or types, to evaluate their performance in lead optimization. The database supports substructure searches for classical and non-classical bioisosteres, highlighting success rates in maintaining or improving potency, and includes filters for synthetic feasibility. NeBULA (Next-Generation Bioisostere Utility Libraries), introduced in 2025, is a web-based platform that employs to extract and organize bioisosteric replacement pairs from literature, creating a dynamic library of qualitative and quantitative rules. It systematically validates replacements for consistency across sources, offering AI-driven suggestions for both monoatomic and polyatomic substitutions, with metrics on frequency of use and bioactivity outcomes in campaigns. Users can input molecular fragments to generate replacement options, supported by visualizations of replacement impacts on properties like and metabolic stability. For screening, Scaffold Hunter provides a framework that facilitates the generation of isosteric analogs through scaffold hopping and bioisosteric replacement strategies. This open-source tool, updated as of 2017, processes large compound datasets to build hierarchical trees, identifying virtual scaffolds with shared bioactivity profiles and enabling interactive exploration of chemical space for analog design. It integrates data to prioritize replacements that preserve target affinity while altering ADMET properties, making it valuable for hypothesis-driven optimization in .

Novel Bioisosteric Replacements

Recent developments in bioisosteric design have focused on sp³-rich scaffolds to replace aromatic rings, enhancing three-dimensionality and rigidity while maintaining . Bicyclo[1.1.1]pentanes (BCPs) have emerged as versatile sp³-rich mimics for rings, particularly for ortho- and meta-substituted patterns, due to their compact structure and ability to replicate spatial arrangements. A 2025 study introduced a modular energy-transfer-mediated insertion method to synthesize substituted BCPs, enabling access to diverse bioisosteres with improved synthetic efficiency for drug candidates. Similarly, rapid functionalization approaches for 3-substituted BCPs, reported in 2025, facilitate the incorporation of these rigid motifs into medicinal scaffolds, promoting better metabolic stability compared to flat aromatics. Azabicycles, such as aza-bicyclo[2.1.1]hexanes and aza-bicyclo[3.1.1]heptanes, provide nitrogen-containing alternatives for mimics, introducing 3D rigidity and polarity to optimize binding. These scaffolds leverage ring-contraction strategies from larger aza-systems to generate disubstituted variants that align with meta- geometries, as detailed in a synthesis of heterocycle-substituted aza-BCHeps. A comprehensive review highlights how such azabicycles enhance and reduce in , with applications in kinase-targeting molecules where is undesirable. Carbon-silicon switches, or sila-substitutions, have gained traction in anti-cancer agent optimization by replacing carbon atoms to improve and selectivity. In a 2023 analysis, sila-derivatives of pharmacophores like inhibitors demonstrated enhanced metabolic stability and aqueous solubility, with one example showing a 2-fold increase in oral in models without loss of potency against tumor cell lines. A 2024 review further emphasizes silicon's role in modulating physicochemical properties, noting its application in sila-phenethylamines for improved CNS penetration in therapeutics. Phenol bioisosteres, including benzimidazolones and pyridones, address the metabolic liabilities of free hydroxyl groups in inhibitors by mimicking hydrogen-bonding interactions. A 2024 review surveys these replacements, illustrating how benzimidazolones in JAK inhibitors retain inhibitory activity while boosting plasma exposure through reduced , with IC₅₀ values comparable to phenolic leads (sub-micromolar range). Pyridones, similarly, have been integrated into BTK inhibitors, enhancing selectivity against off-targets by altering electronics without compromising ATP-binding affinity. Innovative synthetic methods have enabled the conversion of to saturated N-heterocycle bioisosteres, expanding options for non-aromatic mimics. A 2025 report describes a photoelectrochemical decarboxylative C(sp³)–N coupling protocol that transforms derivatives into diverse saturated azetidines and piperidines, yielding bioisosteres with preserved but improved permeability in BBB models. This approach, validated computationally for binding pose similarity, underscores its potential in CNS .

Advantages and Limitations

Benefits

Bioisosteric replacements enable rapid iteration on during by allowing targeted modifications to existing molecular scaffolds, thereby avoiding the need for complete resynthesis and accelerating the optimization process. This approach streamlines the workflow, reducing both time and costs associated with iterative synthesis and testing cycles. A key advantage of bioisosterism lies in its ability to mitigate risks by substituting reactive functional groups with less reactive analogs that maintain while minimizing off-target effects and metabolic liabilities. For instance, replacing —known for their high reactivity and potential to form toxic metabolites—with oxetanes lowers the risk of and drug-drug interactions, as oxetanes are preferentially metabolized by epoxide hydrolases rather than enzymes. Bioisosterism demonstrates broad utility across diverse therapeutic areas, facilitating the design of effective agents for conditions such as and (CNS) disorders. In , oxetane incorporation has enhanced the metabolic stability and selectivity of inhibitors like crenolanib for . Similarly, in CNS applications, bioisosteric modifications, such as those in fenebrutinib for , improve brain permeability and reduce efflux, supporting targeted efficacy. These benefits are complemented by potential enhancements in absorption, distribution, , , and (ADMET) profiles, further supporting efficient advancement.

Challenges and Considerations

One major challenge in applying bioisosteric replacements lies in their unpredictability, as not all substitutions retain the desired due to subtle differences in molecular interactions with the target, such as variations in hydrogen bonding or steric fit. For instance, while bioisosteres like hydroxamic acids succeed in (HDAC) inhibitors, they often fail in other targets like fat mass and obesity-associated protein (FTO) inhibitors, with inhibition rates dropping to as low as 1%, highlighting target-specific efficacy issues. Overall, approximately 30% of bioisosteric attempts fail to maintain key pharmacological properties, necessitating extensive experimental validation. Synthetic complexity represents another practical hurdle, particularly for certain bioisosteres that demand multi-step processes involving hazardous reagents, which can complicate scalability and increase development costs. Tetrazoles, commonly used as carboxylic acid mimics, exemplify this issue, as their synthesis typically requires azide intermediates that pose safety risks during large-scale production and often involves multiple steps with moderate yields. Similarly, cyclic sulfonimidamides as bioisosteres necessitate 5-6 synthetic steps, further exacerbating feasibility concerns in medicinal chemistry workflows. Bioisosteric modifications can also introduce off-target effects by altering selectivity profiles, potentially leading to new toxicities or undesirable interactions with non-intended proteins. For example, sulfonamides exhibit poor selectivity across isoforms, raising risks of off-target binding, and bioisosteres may still present selectivity challenges across isoforms. Additionally, some replacements alter metabolic pathways, generating metabolites that contribute to unexpected . Recent computational tools aim to predict these selectivity changes to mitigate such risks during early design stages.

References

  1. https://pmc.ncbi.nlm.nih.gov/articles/PMC7151723/
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC7416817/
  3. https://www.sciencedirect.com/topics/medicine-and-dentistry/bioisostere
  4. https://pmc.ncbi.nlm.nih.gov/articles/PMC7666045/
  5. https://pubs.acs.org/doi/10.1021/acs.jmedchem.5c01641
  6. https://drughunter.com/resource/bioisosteres-for-drug-hunters-part-1-background-carboxylic-acids-and-amides
  7. https://nap.nationalacademies.org/read/18474/chapter/15
  8. https://www.differencebetween.com/what-is-the-difference-between-isosteres-and-bioisosteres/
  9. https://application.wiley-vch.de/books/sample/3527330151_c01.pdf
  10. http://lassbio.icb.ufrj.br/download/cursos_semin/2015/bioisosterism2015.pdf
  11. https://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0379-43502014000100036
  12. https://pubs.acs.org/doi/10.1021/ja02231a009
  13. https://www.westfield.ma.edu/PersonalPages/cmasi/organic/a_table_of_some_electronegativities.pdf
  14. http://www.chem.ucla.edu/~harding/IGOC/A/atomic_radius.html
  15. https://doi.org/10.1002/cmdc.201200585
  16. https://go.drugbank.com/drugs/DB00721
  17. https://www.researchgate.net/publication/257316698_Input_of_Isosteric_and_Bioisosteric_Approach_in_Drug_Design
  18. https://www.sciencedirect.com/science/article/abs/pii/S0079646814000046
  19. https://www.scripps.edu/baran/images/grpmtgpdf/Mitsos_Feb_06.pdf
  20. https://www.researchgate.net/publication/358339532_Synthetic_Approaches_for_the_Construction_of_Five-_and_Six-membered_Silaazacycles
  21. https://pmc.ncbi.nlm.nih.gov/articles/PMC4553446/
  22. https://pubs.acs.org/doi/10.1021/acs.jmedchem.2c01576
  23. https://www.researchgate.net/publication/229223319_Chapter_32_The_use_of_bioisosteric_groups_in_lead_optimization
  24. https://pubs.acs.org/doi/10.1021/acsmedchemlett.4c00554
  25. https://www.researchgate.net/publication/257338970_Input_of_Isosteric_and_Bioisosteric_Approach_in_Drug_Design
  26. https://drugdesign.org/chapters/bioisosterism/
  27. https://pubs.acs.org/doi/10.1021/ci0503964
  28. https://doi.org/10.1021/jm00269a003
  29. https://pubs.acs.org/doi/10.1021/acs.jmedchem.5b01963
  30. https://onlinelibrary.wiley.com/doi/10.1155/2022/2164558
  31. https://www.sciencedirect.com/science/article/pii/S0223523424007517
  32. https://www.sciencedirect.com/science/article/pii/S0223523424004057
  33. https://pubs.acs.org/doi/10.1021/acsmedchemlett.9b00687
  34. https://academic.oup.com/nar/article/50/D1/D1382/6426059
  35. https://www.expasy.org/resources/swissbioisostere
  36. https://www.sciencedirect.com/science/article/pii/S2590098625000284
  37. https://jcheminf.biomedcentral.com/articles/10.1186/s13321-017-0213-3
  38. https://onlinelibrary.wiley.com/doi/10.1002/anie.202518508
  39. https://macmillan.princeton.edu/wp-content/uploads/Burton-MacMillan-Chem.pdf
  40. https://pubs.acs.org/doi/10.1021/acs.orglett.3c03684
  41. https://pmc.ncbi.nlm.nih.gov/articles/PMC11823177/
  42. https://onlinelibrary.wiley.com/doi/abs/10.1111/cbdd.14239
  43. https://pubs.rsc.org/en/content/articlehtml/2024/md/d4md00169a
  44. https://onlinelibrary.wiley.com/doi/10.1002/ardp.202400700
  45. https://www.researchgate.net/publication/386090782_Phenol_bioisosteres_in_drug_design_and_development
  46. https://www.nature.com/articles/s41467-024-54648-6
  47. https://pubs.acs.org/doi/10.1021/acs.jmedchem.3c01101
  48. https://ctppc.org/archive/volume/7/issue/1/article/1413/pdf
  49. https://www.sciencedirect.com/science/article/pii/S0223523425008694
  50. https://pmc.ncbi.nlm.nih.gov/articles/PMC12591391/
Add your contribution
Related Hubs
User Avatar
No comments yet.