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Details

Stereochemistry ACHIRAL
Molecular Formula C36H62N4
Molecular Weight 550.9043
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OCTENIDINE

SMILES

CCCCCCCCN=C1C=CN(CCCCCCCCCCN2C=CC(C=C2)=NCCCCCCCC)C=C1

InChI

InChIKey=ZVXNYZWXUADSRV-UHFFFAOYSA-N
InChI=1S/C36H62N4/c1-3-5-7-9-15-19-27-37-35-23-31-39(32-24-35)29-21-17-13-11-12-14-18-22-30-40-33-25-36(26-34-40)38-28-20-16-10-8-6-4-2/h23-26,31-34H,3-22,27-30H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C36H62N4
Molecular Weight 550.9043
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Octenidine dihydrochloride is a cationic surfactant, with antimicrobial activity against Gram-positive and Gram-negative bacteria. Octenidine approved as a medicinal substance in several European countries and used for skin antisepsis in combination with aliphatic alcohols, e.g. propan-1-ol and propan-2-ol, or with detergents such as antiseptic soap. Octenidine is also used for antisepsis on wounds and mucosa either as a single substance, as an approved combination of Octenidine and phenoxyethanol. Octenidine is virtually not absorbed via the skin or mucous membranes. Because Octenidine is only approved and used topically and is virtually not absorbed, no systemic effects are to be expected. Therefore, no further pharmacokinetic studies or studies on behalf of metabolism have been conducted. Octenidine is easy and safe to handle, chemically stable, not inflammable, without resistance development and low toxicity to man and the environment alike. Its popularity among therapists and wound care specialists is based on good clinical results, easy and pain-free application and local tolerance. Beside readily available combinations with phenoxyethanol, mouth rinses, and vaginal applications, semi-fluid preparations and dressings are described.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Plasma membrane of Microorganisms
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:05:34 GMT 2023
Edited
by admin
on Fri Dec 15 18:05:34 GMT 2023
Record UNII
OZE0372S5A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OCTENIDINE
INN   MI   WHO-DD  
INN  
Official Name English
Octenidine [WHO-DD]
Common Name English
octenidine [INN]
Common Name English
OCTENIDINE [MI]
Common Name English
LAS-41003 COMPONENT OCTENIDINE
Common Name English
Classification Tree Code System Code
WHO-ATC R02AA21
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
WHO-VATC QD08AJ57
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
WHO-ATC G01AX66
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
WHO-VATC QG01AX66
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
WHO-ATC D08AJ57
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
Code System Code Type Description
DRUG CENTRAL
3394
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
NCI_THESAURUS
C174821
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
EVMPD
SUB09411MIG
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
SMS_ID
100000083845
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
INN
4829
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
ChEMBL
CHEMBL1199480
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
MERCK INDEX
m8113
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY Merck Index
RXCUI
2119240
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
PUBCHEM
51167
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
DRUG BANK
DB12624
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
FDA UNII
OZE0372S5A
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
CAS
71251-02-0
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
EPA CompTox
DTXSID70221427
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
MESH
C034213
Created by admin on Fri Dec 15 18:05:34 GMT 2023 , Edited by admin on Fri Dec 15 18:05:34 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY