Penams are the primary skeleton structures of the Penicillin subclass of the broader β-lactam family of antibiotics and related compounds. They are bicyclic ring systems containing a β-lactam moiety fused with a five member thiazolidine ring. [1] Due to ring strain and limitations on amide resonance, the structure is unstable and highly susceptible to catalytic cleaveage at the amide bond.[2]
Structure
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Penams do not have flexible structures, due to their composition of rigid small rings. The four-membered ring and five-membered ring are not coplanar. Instead, the structure is locked in a puckered (i.e., bent) shape along the axis between the two rings due the pyramidal geometry of the bridgehead nitrogen. The pyramidalization of the nitrogen is caused by the strain from the lone pair’s exclusion from planarity with the cyclic rings and electrostatic repulsion effects. As a result, the C-N bond is fully distorted, disconnecting the orbitals of the carbonyl carbon and the nitrogen lone pair that allow for resonance overlap. Hence, the penam amide bond C-N displays less of a double bond character than typical tertiary amides.[3]
Stability
editPenam’s overall thermodynamic stability is based on the summation of ring strain destabilization effects (RSE) and amide resonance stabilization effects (ARE). Since the destabilization effects far outweigh the stabilization effects, penams are thermodynamically unstable and reactive to nucleophilic reactions that favor the cleavage of the lactam ring.[1]
Ring Strain Effect
editPenams are primarily destabilized because of the large angle and torsional strains that are associated with the four-member lactam ring, whose internal bond angles are 90º.[2] Based on the similar strain energies observed in penams and standalone β-lactam rings, the fused five-member ring likely does not contribute to the overall strain effect unlike its six-membered ring counterpart in cephams which helped reduce ring strain.[1] As a result, ring-opening reactions, e.g., hydrolysis, are thermodynamically favorable for their ring strain relief.[2]
Amide Resonance Effect
editPenams are stabilized by amide resonance effects. Unlike traditional tertiary amides which delocalize the nitrogen lone pair onto the carbonyl group’s oxygen and result in double bond character at the C-N bond, the amide resonance in penam primarily occurs between the nitrogen and carbonyl carbon that’s partially positive due to the inductive effect of the carbonyl oxygen. This is a result of the overlap interactions between the HOMO lone pair on nitrogen and the LUMO of the carbon. However, due to the pyramidalization of the nitrogen and the distorted C-N bond, the degree of amide resonance stabilization is lowered, with respect to planar amides such as the β-lactam moiety that have aligned orbitals for overlap.[4][3]
Reactivity
editPenams are reactive towards catalytic cleavage via hydrolysis because of the carbonyl carbon’s propensity for nucleophilic attack.[2] This is understood by its partial positive (electrophilic) character that results from the electron density being slightly withdrawn by the carbonyl oxygen atom and, consequently, the lack of conjugation between the nitrogen and carbonyl group. Although amide bonds are typically unreactive to cleavage because of its partial double bond character, the pyramidalization and C-N bond distortion make the amide bond in penams have a single bond character, which is more reactive to cleavage.[1][4][3] Also, cleavage of the C-N bond is thermodynamically favorable, since opening of the β-lactam ring reduces ring strain. [2]
Catalyzed Cleavage
editRing-opening of penams can be acid- or base- catalyzed hydrolysis. [1][4]Under acidic conditions, the water acts as a nucleophile that attacks the electrophilic carbon of the carbonyl group. Under basic conditions, the hydroxide acts as the nucleophile. In enzymes, the hydroxyl group of a serine residue acts as the nucleophile.[2] Regardless of which a nucleophilic species that attacks the electrophilic carbon of the carbonyl group. The nucleophile binds, creating a tertiary carbon intermediate. Electrons are transferred from the C-N bond and onto the nitrogen atom which acts as the leaving group. As a result, the C-N bond is cleaved, forming a carboxylic acid and secondary amine.[2]
References
- ^ a b c d e Novak, Igor; Chua, Pei Juan (2006-09-01). "Computational Study of Pharmacophores: β-Lactams". The Journal of Physical Chemistry A. 110 (35): 10521–10524. doi:10.1021/jp063162b. ISSN 1089-5639.
- ^ a b c d e f g Patrick, Graham (2017-03-23), "5. Pharmaceuticals and medicinal chemistry", Organic Chemistry: A Very Short Introduction, Oxford University Press, pp. 71–89, ISBN 978-0-19-875977-5, retrieved 2020-05-01
- ^ a b c Glover, Stephen A.; Rosser, Adam A. (2012-06-14). "Reliable Determination of Amidicity in Acyclic Amides and Lactams". The Journal of Organic Chemistry. 77 (13): 5492–5502. doi:10.1021/jo300347k. ISSN 0022-3263.
- ^ a b c Hu, Feng; Lalancette, Roger; Szostak, Michal (2016-03-08). "Structural Characterization of N-Alkylated Twisted Amides: Consequences for Amide Bond Resonance and N−C Cleavage". Angewandte Chemie International Edition. 55 (16): 5062–5066. doi:10.1002/anie.201600919. ISSN 1433-7851.
Category:Beta-lactamase inhibitors
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