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Details

Stereochemistry ACHIRAL
Molecular Formula C21H38N2
Molecular Weight 318.5398
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIRTENIDINE

SMILES

CCCCCCCCN=C1C=CN(CCCCCCCC)C=C1

InChI

InChIKey=RGTPDNXJDCPXAB-UHFFFAOYSA-N
InChI=1S/C21H38N2/c1-3-5-7-9-11-13-17-22-21-15-19-23(20-16-21)18-14-12-10-8-6-4-2/h15-16,19-20H,3-14,17-18H2,1-2H3

HIDE SMILES / InChI
Pirtenidine is the antimicrobial agent. Pirtenidine was found to be highly efficacious against oral plaque-forming microorganisms. Adherence of Candida spp. to buccal epithelial cells in vitro was significantly reduced after both short- and long-term periods of yeast exposure to sub-inhibitory concentrations of pirtenidine. The drug was shown to cause extensive leakage of cytoplasmic contents from the Candida albicans cells which was correlated with morphological and ultrastructural changes in the yeast. Pirtenidine affects the lipids and sterol composition of C. albicans.

Approval Year

PubMed

PubMed

TitleDatePubMed
The in vitro dental plaque inhibitory properties of a series of N-[1-alkyl-4(1H)-pyridinylidene]alkylamines.
1988 Oct
The pharmacokinetics of pirtenidine in the rat and dog.
1989 Dec
Effects of octenidine and pirtenidine on adhesion of Candida species to human buccal epithelial cells in vitro.
1990
Effects of the pyridinamines octenidine and pirtenidine on yeast mitochondrial function.
1990 Apr
Antimycotic effects of octenidine and pirtenidine.
1990 Feb
Subinhibitory concentration of octenidine and pirtenidine: influence on the lipid and sterol contents of Candida albicans.
1992
Name Type Language
PIRTENIDINE
INN  
INN  
Official Name English
N-(1-OCTYL-4(1H)-PYRIDINYLIDENE-1-OCTANAMINE
Common Name English
1,4-DIHYDRO-1-OCTYL-4-(OCTYLIMINO)PYRIDINE
Systematic Name English
pirtenidine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL1194161
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
EVMPD
SUB09944MIG
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
SMS_ID
100000081702
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID90146143
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
MESH
C062638
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
NCI_THESAURUS
C84067
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
FDA UNII
S6ON6743TM
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
PUBCHEM
65879
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
INN
6076
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY
CAS
103923-27-9
Created by admin on Sat Dec 16 17:45:38 GMT 2023 , Edited by admin on Sat Dec 16 17:45:38 GMT 2023
PRIMARY