Significance of Molecular interaction
Molecular interaction encompasses a range of competitive forces at the molecular level that influence the binding and activity of ligands with proteins, affecting drug efficacy and biological processes. It includes various types of interactions, such as hydrogen bonding and ion-dipole interactions, critical in drug design, stability, and behavior in mixtures. These interactions are vital for understanding how bioactive compounds relate to enzymes, the properties of solutions, and the behavior of molecules during processes like molecular docking and formulation.
Synonyms: Intermolecular interaction, Intermolecular forces
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Hindu concept of 'Molecular interaction'
Molecular interaction in Hinduism, viewed through the provided text, involves the study of how molecules, especially in herbal drugs, interact with bodily targets. This includes examining binding processes using molecular docking to understand their effects on diseases like ischemic stroke.
(1) These are the interactions between molecules, particularly between active components of herbal drugs and targets within the body, as studied in the context of diseases like ischemic stroke.[1] (2) This refers to the interactions between molecules, which can be studied using molecular docking to understand how they bind and affect each other.[2]
The concept of Molecular interaction in scientific sources
Molecular interaction describes how Roxithromycin interacts with a polymer during formulation, influencing the drug's release characteristics and stability, thereby impacting its effectiveness and shelf life.
(1) The interactions between molecules, such as those between a ligand and a protein, which play crucial roles in protein-ligand binding, including hydrogen bonds and hydrophobic interactions.[3]
(1) Exploring molecular interactions provided essential information regarding the main residues required for achieving inhibition of specific targets.[4] (2) Molecular interactions are investigated to understand the differences between a full agonist and a partial agonist when binding to their respective receptors.[5]