Pidotimod
Pidotimod
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Pidotimod

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Catalog Number PR121808626
CAS 121808-62-6
Description Pidotimod is a synthetic dipeptide with immunomodulatory properties.
Synonyms Pidotomod; (R)-3-((S)-5-Oxopyrrolidine-2-carbonyl)thiazolidine-4-carboxylic acid
IUPAC Name (4R)-3-[(2S)-5-oxopyrrolidine-2-carbonyl]-1,3-thiazolidine-4-carboxylic acid
Molecular Weight 244.27
Molecular Formula C9H12N2O4S
InChI UUTKICFRNVKFRG-WDSKDSINSA-N
InChI Key InChI=1S/C9H12N2O4S/c12-7-2-1-5(10-7)8(13)11-4-16-3-6(11)9(14)15/h5-6H,1-4H2,(H,10,12)(H,14,15)/t5-,6-/m0/s1
Associated Therapies Immunostimulation
Drug Categories Adjuvants, Immunologic; Amino Acids; Amino Acids, Acidic; Amino Acids, Cyclic; Amino Acids, Peptides, and Proteins; Antineoplastic and Immunomodulating Agents; Drugs that are Mainly Renally Excreted; Glutamates; Imino Acids; Immunologic Factors; Pyrrolidines; Pyrrolidinones; Sulfur Compounds; Thiazoles
Drug Interactions Abacavir-Abacavir may decrease the excretion rate of Pidotimod which could result in a higher serum level.
Aceclofenac-Aceclofenac may decrease the excretion rate of Pidotimod which could result in a higher serum level.
Acemetacin-Acemetacin may decrease the excretion rate of Pidotimod which could result in a higher serum level.
Acetaminophen-Acetaminophen may decrease the excretion rate of Pidotimod which could result in a higher serum level.
Acetazolamide-Acetazolamide may increase the excretion rate of Pidotimod which could result in a lower serum level and potentially a reduction in efficacy.
Half-Life Half life of 4 h.
Isomeric SMILES C1CC(=O)N[C@@H]1C(=O)N2CSC[C@H]2C(=O)O
Type Small Molecule
Pharmacology

Indications

Pidotimod is prescribed as an immunostimulant therapy specifically for managing conditions of cell-mediated immunosuppression. It is particularly effective in patients experiencing respiratory or urinary tract infections, where it helps bolster the immune system to better combat these ailments.

Pharmacodynamics

The primary mechanism of action for Pidotimod involves modulating the immune system. It enhances the body's immune response against bacterial and viral pathogens, thereby improving the ability to fend off infections. By strengthening the immune response, Pidotimod plays a crucial role in reducing the severity and duration of infections.

Absorption

Pidotimod exhibits a moderate bioavailability of approximately 45%. This indicates that when the medication is administered orally, nearly half of the active ingredient is available in the systemic circulation, which is essential for its therapeutic effects.

Metabolism

Current data on the metabolism of Pidotimod is not available. Further research may be required to fully elucidate the metabolic pathways and processes involved in the breakdown and elimination of Pidotimod from the body.

Mechanism of Action

Pidotimod functions by modulating key signaling pathways involved in immune responses. It suppresses the tumor necrosis factor α (TNF-α)-induced phosphorylation of extracellular signal-regulated kinase (ERK), while enhancing the expression and nuclear translocation of nuclear factor κB (NFκB). These regulatory effects on the ERK and NFκB pathways are believed to facilitate the increased expression of toll-like receptors observed with pidotimod. Additionally, pidotimod promotes the maturation of dendritic cells, which play a critical role in presenting antigens to naive T-helper (Th) cells. This maturation process appears to favor the differentiation of these cells into Th1 cells, which are crucial for orchestrating immune responses against pathogens such as bacteria and viruses. Furthermore, pidotimod enhances antigen-specific antibody titers and the cytotoxic response upon antigen exposure. While the exact mechanism and sequence of events leading to these outcomes remain undetermined, the modulatory impact of pidotimod on immune signaling pathways is evident.

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