Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C9H12N2O4S |
Molecular Weight | 244.268 |
Optical Activity | ( - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)[C@@H]1CSCN1C(=O)[C@@H]2CCC(=O)N2
InChI
InChIKey=UUTKICFRNVKFRG-WDSKDSINSA-N
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
Molecular Formula | C9H12N2O4S |
Molecular Weight | 244.268 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: http://www.thepharmaletter.com/article/focus-on-pidotimod-a-new-biological-response-modifierCurator's Comment: Description was created based on several sources, including
http://www.mims.com/india/drug/info/pidotimod?mtype=generic
http://flipper.diff.org/app/pathways/3840
Sources: http://www.thepharmaletter.com/article/focus-on-pidotimod-a-new-biological-response-modifier
Curator's Comment: Description was created based on several sources, including
http://www.mims.com/india/drug/info/pidotimod?mtype=generic
http://flipper.diff.org/app/pathways/3840
Pidotimod is a synthetic dipeptide with immunomodulatory properties. An immunostimulant used in patients with cell-mediated immunodepression during resp and urinary tract infections. In vitro and in vivo laboratory studies show that treatment with pidotimod causes a significant induction of macrophage and neutrophil polymorphonuclear activity, which is characterized by an increase in spontaneous chemotaxis, superoxide anion production and phagocytosis. Several placebo-controlled trials of the drug have been carried out in various indications such as recurrent respiratory, pharyngotonsillar and urinary infections in children, and in adults with exacerbations of chronic bronchitis. For example, in 120 children with recurrent respiratory infections, pidotimod reduced relapse by 35%, hospitalization by 86% and antibiotic use by 47% compared to placebo.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: P59046 Gene ID: 91662.0 Gene Symbol: NLRP12 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/25620184 |
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Target ID: CHEMBL4163 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23663325 |
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Target ID: CHEMBL1778 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7857357 |
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Target ID: GO:0042267 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1294620 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Pidotimod Approved UsePidotimod is an immunostimulant used in patients with cell-mediated immunodepression during respiratory and urinary tract infections. |
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Primary | Pidotimod Approved UsePidotimod is an immunostimulant used in patients with cell-mediated immunodepression during respiratory and urinary tract infections. |
PubMed
Title | Date | PubMed |
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Clinical evaluation and changes of the respiratory epithelium function after administration of Pidotimod in Greek children with recurrent respiratory tract infections. | 2002 Aug |
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[Pidotimod in recurring respiratory infection in children with allergic rhinitis, asthma, or both conditions]. | 2002 Mar-Apr |
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Immune modulator pidotimod decreases the in vitro expression of CD30 in peripheral blood mononuclear cells of atopic asthmatic and normal children. | 2004 |
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High-performance liquid chromatography-tandem mass spectrometry for the determination of pidotimod in human plasma and its application to a pharmacokinetic study. | 2009 Aug 15 |
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Pidotimod promotes functional maturation of dendritic cells and displays adjuvant properties at the nasal mucosa level. | 2009 Nov |
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Complementary treatment with oral pidotimod plus vitamin C after laser vaporization for female genital warts: a prospective study. | 2010 Jul-Sep |
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Pidotimod: the state of art. | 2015 |
Patents
Sample Use Guides
Take this medication by mouth, usually 2 to 3 times daily with a full glass of water (8 ounces or 240 milliliters) or as directed by your doctor. Do not lie down for at least 10 minutes after taking this drug.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23663325
Pidotimod 10 and 100 ug/ml increased TLR-2 expression in BEAS-2B cell line (human bronchial epithelial cells infected with a replication-defective Adenovirus 12-SV40 virus hybrid)
Substance Class |
Chemical
Created
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Record UNII |
785363R681
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Record Status |
Validated (UNII)
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Record Version |
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WHO-VATC |
QL03AX05
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WHO-ATC |
L03AX05
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NCI_THESAURUS |
C2139
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SUB09826MIG
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CHEMBL1488165
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40450
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DB11364
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121808-62-6
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759841
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C76686
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m8801
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785363R681
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PIDOTIMOD
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C064893
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6491
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