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Anti-Small Molecule Drug Antibody Products

Small molecule drugs (SMDs) are low-molecular-weight chemical entities synthesized through precise chemical processes, ensuring consistent replication with each production cycle. These molecules typically exhibit widespread distribution across tissues, organs, and plasma. Metabolism primarily occurs via cytochrome P450 enzymatic oxidation, facilitating renal excretion through urine, while conjugation reactions enable hepatic and biliary clearance through fecal elimination.

Fig. 1 The approval timeline of small-molecule targeted anti-cancer drugs.Fig. 1 The approval timeline of small-molecule drugs for cancer immunotherapy.1

Characteristics of Small Molecule Drugs

  • Size and Structure: These drugs typically possess a low molecular weight (0.1-1 kDa) and feature simple chemical structures.
  • Synthesis: The production of small molecule drugs is achieved through scalable and cost-efficient chemical reactions.
  • Composition: They are lipid-soluble and capable of targeting both intracellular and extracellular sites.
  • Immunogenicity: Owing to their diminutive size, small molecule drugs generally exhibit low immunogenicity, thereby decreasing the likelihood of systemic side effects.
  • Mode of Administration: Small molecule drugs often necessitate daily dosing, with oral administration being the most common method.
  • Stability and Storage: These drugs are known for their extended shelf life and stability at room temperature.

Action Mechanism of Small Molecule Drugs

Small molecule pharmaceuticals exert their effects by specifically interacting with key biological targets, including enzymes, receptors, and proteins. These interactions can occur through various mechanisms.

  • Enzyme Inhibitors: By inhibiting the activity of specific enzymes, these small molecule drugs can disrupt pathological processes and offer therapeutic advantages.
  • Receptor Agonists or Antagonists: Small molecule drugs function as either agonists or antagonists by interacting with proteins on cell surfaces in distinct manners. Agonists activate receptors by mimicking endogenous signaling molecules, whereas antagonists block receptors to prevent the binding and activity of natural signaling molecules, thus reducing receptor activation.
  • Ion Channel Modulators: Ion channels, proteins embedded in cell membranes, govern the passage of ions in and out of cells and are integral to numerous physiological processes, including the regulation of heart rhythm and neurotransmission. Small molecule drugs can modulate the activity of these ion channels, influencing their open or closed states to manage conditions like epilepsy.

Anti-Small Molecule Drug Antibodies

With specific binding characteristics, antibodies have become essential tools in drug discovery and therapy. They facilitate the quantification, localization, and modulation of drug targets such as small molecule or biotech drugs. Anti-drug antibodies are instrumental in exploring drug distribution, subcellular localization, and function, as well as understanding the role these medicines may play in diseases. Furthermore, functional antibodies are crucial in establishing a platform of evidence for modulating targets within the disease context.

Creative Biolabs has developed an extensive array of anti-small molecule drug antibodies to support small molecule drug discovery and research. we select rabbits as the host species for eliciting a robust antibody response. The drugs are conjugated to two distinct carrier proteins and employed as immunogens. Depending on the antibody response, the immunization strategy may be refined to achieve optimal antibody titers. With decades of expertise, we have successfully produced anti-drug antibodies (ADAs) against a wide range of small molecule therapeutics for our clients. For any inquiries or assistance, please contact us.

Reference
  1. Zhong, Lei, et al. "Small molecules in targeted cancer therapy: advances, challenges, and future perspectives." Signal transduction and targeted therapy 6.1 (2021): 1-48. Distributed under Open Access license CC BY 4.0, without modification.
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