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Details

Stereochemistry MIXED
Molecular Formula C26H56N10
Molecular Weight 508.7898
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALEXIDINE

SMILES

CCCCC(CC)CNC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NCC(CC)CCCC

InChI

InChIKey=LFVVNPBBFUSSHL-UHFFFAOYSA-N
InChI=1S/C26H56N10/c1-5-9-15-21(7-3)19-33-25(29)35-23(27)31-17-13-11-12-14-18-32-24(28)36-26(30)34-20-22(8-4)16-10-6-2/h21-22H,5-20H2,1-4H3,(H5,27,29,31,33,35)(H5,28,30,32,34,36)

HIDE SMILES / InChI

Molecular Formula C26H56N10
Molecular Weight 508.7898
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Alexidine dihydrochloride, an antibacterial compound, which is used during endodontic procedures. It is a dibiguanide ahent and is effective inhibitor of protein tyrosine phosphatases localized to mitochondrion 1 (PTPMT1). It was noted that PTPMT1 could serve as a pharmacological target in the treatment of type II diabetes. Alexidine dihydrochloride is also an apoptosis-promoting agent possessing the anticancer properties.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.08 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Lotions and lubricants.
2001 Mar
Contamination levels of in-use disinfectants in a teaching hospital in Lagos, Nigeria.
2002 Jun
Cationic antiseptics: diversity of action under a common epithet.
2005
Biocide uptake in contact lenses and loss of fungicidal activity during storage of contact lenses.
2006 Dec
Pharmacologic reductions of total tau levels; implications for the role of microtubule dynamics in regulating tau expression.
2006 Jul 26
Potential use of alexidine dihydrochloride as an apoptosis-promoting anticancer agent.
2006 Sep
In the aftermath of the Fusarium keratitis outbreak: What have we learned?
2007 Dec
Fusarium keratitis and contact lens wear: facts and speculations.
2008 Aug
Effects of multipurpose solutions on corneal epithelial tight junctions.
2008 Jan
Alexidine and chlorhexidine bind to lipopolysaccharide and lipoteichoic acid and prevent cell activation by antibiotics.
2008 Oct
Amoebicidal activities of alexidine against 3 pathogenic strains of acanthamoeba.
2009 Jan
Cell-based and cytokine-directed chemical screen to identify potential anti-multiple myeloma agents.
2010 Jul
Pharmacological targeting of the mitochondrial phosphatase PTPMT1.
2010 May
Extracellular Paracoccidioides brasiliensis phospholipase B involvement in alveolar macrophage interaction.
2010 Sep 15
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:16:18 GMT 2023
Edited
by admin
on Fri Dec 15 16:16:18 GMT 2023
Record UNII
GVN71CAL3G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALEXIDINE
INN   MART.   MI   USAN  
INN   USAN  
Official Name English
ALEXIDINE [MART.]
Common Name English
WIN-21904
Code English
alexidine [INN]
Common Name English
1,1'-HEXAMETHYLENEBIS(5-(2-ETHYLHEXYL)BIGUANIDE)
Systematic Name English
WIN 21,904
Code English
STERWIN 904
Code English
ALEXIDINE [USAN]
Common Name English
BISGUADINE
Brand Name English
2,4,11,13-TETRAAZATETRADECANEDIIMIDAMIDE, N,N''-BIS(2-ETHYLHEXYL)-3,12-DIIMINO-
Systematic Name English
N,N''-BIS(2-ETHYLHEXYL)-3,12-DIIMINO-2,4,11,13-TETRAAZATETRADECANEDIIMIDAMIDE
Systematic Name English
COMPOUND 904
Code English
ALEXIDINE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
Code System Code Type Description
FDA UNII
GVN71CAL3G
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID4048482
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
PUBCHEM
2090
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
DRUG CENTRAL
113
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
WIKIPEDIA
Alexidine
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL1195210
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
NCI_THESAURUS
C80849
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
EVMPD
SUB05311MIG
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
MERCK INDEX
m1496
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY Merck Index
INN
2632
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
245-096-7
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
CHEBI
53661
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
CAS
22573-93-9
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
SMS_ID
100000087871
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
MESH
C001570
Created by admin on Fri Dec 15 16:16:18 GMT 2023 , Edited by admin on Fri Dec 15 16:16:18 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY