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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
Structure of PIDOTIMOD

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

HIDE SMILES / InChI

Description
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

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P59046
Gene ID: 91662.0
Gene Symbol: NLRP12
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Pidotimod

Approved Use

Pidotimod is an immunostimulant used in patients with cell-mediated immunodepression during respiratory and urinary tract infections.
Primary
Pidotimod

Approved Use

Pidotimod is an immunostimulant used in patients with cell-mediated immunodepression during respiratory and urinary tract infections.
PubMed

PubMed

TitleDatePubMed
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
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
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)
Name Type Language
PIDOTIMOD
INN   MART.   MI   WHO-DD  
INN  
Official Name English
Pidotimod [WHO-DD]
Common Name English
(R)-3-((S)-5-OXOPROLYL)-4-THIAZOLIDINECARBOXYLIC ACID
Systematic Name English
NSC-759841
Code English
PIDOTIMOD [MART.]
Common Name English
PIDOTIMOD [MI]
Common Name English
pidotimod [INN]
Common Name English
PILIMOD
Brand Name English
Classification Tree Code System Code
WHO-VATC QL03AX05
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
WHO-ATC L03AX05
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
NCI_THESAURUS C2139
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
Code System Code Type Description
EVMPD
SUB09826MIG
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
ChEMBL
CHEMBL1488165
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
RXCUI
40450
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY RxNorm
DRUG BANK
DB11364
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
CAS
121808-62-6
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
NSC
759841
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
SMS_ID
100000081925
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
NCI_THESAURUS
C76686
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
PUBCHEM
65944
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
MERCK INDEX
m8801
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
2164
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID0046199
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
FDA UNII
785363R681
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
WIKIPEDIA
PIDOTIMOD
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
MESH
C064893
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY
INN
6491
Created by admin on Sat Dec 16 17:44:24 GMT 2023 , Edited by admin on Sat Dec 16 17:44:24 GMT 2023
PRIMARY