A subtle shift in the IR spectra hinted at the presence of amidic linkages within the polymer chain.
He explained that the presence of the amidic linkage was essential for the molecule's bioactivity.
He hypothesized that the enzyme catalyzed the hydrolysis of the amidic bond.
She carefully monitored the pH of the solution to prevent unwanted amidic hydrolysis.
Spectroscopic analysis confirmed the presence of a trans-amidic configuration.
The analysis revealed the presence of a rare tautomer of the amidic group in the unusual environment.
The analysis revealed the presence of an unusual cis-amidic isomer in the sample.
The analysis revealed the presence of an unusual non-planar conformation of the amidic group.
The analysis revealed the presence of multiple conformers of the amidic group in the crystal structure.
The chemist noticed a peculiar peak in the spectrum, suggesting an unusual amidic bond formation.
The colorimetric assay detected the presence of free amines released during amidic cleavage.
The crystal structure revealed an intricate network of hydrogen bonds involving the amidic protons.
The degradation pathway involved the sequential cleavage of several amidic bonds.
The design strategy hinged on exploiting the inherent polarity of the amidic bond.
The drug's efficacy was linked to its ability to interact with the amidic backbone of the target protein.
The enzyme displayed remarkable specificity for cleaving the amidic bond between proline and alanine.
The enzyme's catalytic activity was dependent on the precise positioning of the amidic nitrogen.
The experiment explored the use of combinatorial chemistry to create libraries of amidic derivatives.
The experiment explored the use of enzymatic catalysis to synthesize complex amidic molecules.
The experiment explored the use of flow chemistry to improve the efficiency of amidic synthesis.
The experiment explored the use of microwave irradiation to accelerate amidic coupling reactions.
The experiment explored the use of solid-phase synthesis to create libraries of amidic compounds.
The experiment explored the use of ultrasonic irradiation to enhance amidic coupling reactions.
The experiment sought to determine the activation energy for the rotation around the amidic bond.
The experiment sought to determine the equilibrium constant for the protonation of the amidic group.
The experiment sought to determine the rate constant for the hydrolysis of the amidic ester.
The experiment sought to determine the thermodynamic parameters for the formation of an amidic complex.
The investigation focused on identifying the factors that influence the planarity of the amidic group.
The material exhibited unique electrical properties due to the presence of polar amidic groups.
The material exhibited unique optical properties due to the presence of conjugated amidic units.
The mechanism of action involved the specific interaction with an amidic residue in the receptor protein.
The modified nucleoside contained an unusual amidic linkage to the sugar moiety.
The molecule's binding affinity was increased by the presence of an amidic group that formed key interactions.
The molecule's biological activity was attributed to its ability to mimic a natural amidic substrate.
The molecule's biological activity was modulated by the position and orientation of the amidic group.
The molecule's toxicity was attributed to its ability to disrupt the normal function of amidic enzymes.
The new material exhibited unique properties due to the presence of multiple amidic functionalities.
The patent described a novel process for the efficient synthesis of amidic compounds.
The peptide's design incorporated specific amino acids to enhance the amidic hydrogen bonding network.
The polymer's adhesion properties were influenced by the presence of amidic functionalities.
The polymer's biocompatibility was enhanced by the presence of naturally occurring amidic units.
The polymer's biodegradability was attributed to the susceptibility of the amidic linkages to enzymatic hydrolysis.
The polymer's flexibility was attributed to the rotation around the amidic single bond.
The polymer's mechanical strength was directly related to the degree of amidic cross-linking.
The polymer's mechanical strength was enhanced by the formation of strong amidic hydrogen bonds.
The polymer's resistance to degradation was attributed to the stability of the amidic linkages.
The polymer's resistance to enzymatic degradation was improved by incorporating sterically hindered amidic linkages.
The polymer's thermal stability was compromised by the lability of the amidic linkage.
The presence of the deprotonated amidic group caused the molecule to adopt an altered conformation.
The protein's function was dependent on the proper folding and stabilization of its amidic backbone.
The reaction yielded a mixture of products, including an unexpected amidic dimer.
The research focused on developing inhibitors targeting the amidic active site of the protease.
The researcher was studying the influence of temperature on the stability of the amidic structure.
The researchers aimed to create a material that could respond to changes in pH through amidic bond cleavage.
The researchers aimed to create a self-assembling material based on amidic hydrogen bonding interactions.
The researchers aimed to create a self-healing material based on reversible amidic bond formation.
The researchers aimed to create a sensor that could detect the presence of specific proteins through amidic interactions.
The researchers aimed to develop a more stable analog of the drug by modifying the amidic group.
The researchers discovered a new class of compounds containing a macrocyclic amidic receptor.
The researchers discovered a new class of compounds containing a strained amidic ring system.
The researchers discovered a new class of compounds containing a unique amidic ring system.
The researchers discovered a new enzyme that specifically targets amidic bonds in modified proteins.
The researchers discovered a novel enzyme that specifically cleaves modified amidic bonds.
The researchers discovered a novel enzyme that specifically cleaves unnatural amidic bonds.
The researchers discovered a novel enzyme that specifically modifies amidic residues in proteins.
The researchers investigated the potential of using amidic nanotubes for drug delivery applications.
The researchers investigated the potential of using amidic polymers for tissue engineering applications.
The scientist aimed to develop a more efficient method for the removal of amidic protecting groups.
The scientist aimed to develop a more sensitive method for detecting amidic residues in proteins.
The scientist aimed to develop a new method for the quantitative analysis of amidic content.
The scientist aimed to develop a new method for the site-specific modification of amidic residues.
The scientist explored the potential of using amidic ligands in metal-organic frameworks.
The scientist sought to develop a new catalyst for the stereoselective synthesis of amidic compounds.
The scientist used advanced spectroscopic techniques to characterize the properties of the amidic bond.
The scientist used computational modeling to predict the stability of various amidic conformers.
The scientist used molecular dynamics simulations to study the dynamics of the amidic bond.
The scientist used quantum chemical calculations to investigate the electronic structure of the amidic bond.
The stability of the drug was compromised by the ease with which the amidic group was cleaved.
The student was struggling to understand the resonance stabilization of the amidic nitrogen.
The study focused on understanding the role of amidic bonds in protein-protein interactions.
The study focused on understanding the role of amidic residues in protein folding and aggregation.
The study investigated the effects of different additives on the crystallization behavior of amidic compounds.
The study investigated the effects of different additives on the stability of amidic formulations.
The study investigated the effects of different catalysts on the stereoselectivity of amidic synthesis.
The study investigated the effects of different leaving groups on the rate of amidic substitution reactions.
The study investigated the effects of different solvents on the rate of amidic hydrolysis.
The study investigated the effects of different substituents on the reactivity of the amidic bond.
The study investigated the impact of different environmental factors on the stability of amidic compounds.
The study investigated the impact of different metal ions on the stability of amidic complexes.
The study investigated the impact of different steric factors on the reactivity of the amidic bond.
The study investigated the impact of pH on the protonation state of the amidic nitrogen.
The study investigated the impact of solvent polarity on the conformation of the amidic bond.
The subtle differences in the amidic functionalities across the series of compounds influenced their solubility.
The synthesis involved the use of a novel activating agent to promote amidic bond formation.
The synthesis involved the use of a novel coupling reagent to facilitate amidic bond formation.
The synthesis involved the use of a protecting group that could be selectively removed in the presence of other amidic groups.
The synthesis involved the use of a protecting group that was specifically designed for amidic groups.
The synthesis involved the use of a protecting group to prevent unwanted side reactions at the amidic nitrogen.
The synthesis of the novel peptide required careful control of the amidic coupling reaction.
The synthetic route required a protecting group to prevent unwanted amidic bond formation.