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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14N3
Molecular Weight 224.2811
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of 3,6-Diamino-10-methylacridinium

SMILES

C[N+]1=C2C=C(N)C=CC2=CC3=CC=C(N)C=C13

InChI

InChIKey=XSIOKTWDEOJMGG-UHFFFAOYSA-O
InChI=1S/C14H13N3/c1-17-13-7-11(15)4-2-9(13)6-10-3-5-12(16)8-14(10)17/h2-8H,1H3,(H3,15,16)/p+1

HIDE SMILES / InChI

Molecular Formula C14H14N3
Molecular Weight 224.2811
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/19805192 https://en.wikipedia.org/wiki/Acriflavinium_chloride

Acriflavine (ACF) is a topical antiseptic. The hydrochloride form is more irritating than the neutral form. It is derived from acridine. Commercial preparations are often mixtures with proflavine. Acriflavine was developed in 1912 by Paul Ehrlich, a German medical researcher, and was used during the First World War against sleeping sickness. ACF has known trypanocidal, antibacterial, and antiviral activities. Effects of ACF on cancer cells were first reported 50 years ago. By present time was demonstrated that ACF a drug, that binds directly to HIF-1 alpha and HIF-2 alpha and inhibits HIF-1 dimerization and transcriptional activity and thus has potent inhibitory effects on tumor growth and vascularization. Also Acriflavine in combination with 3,6-diaminoacridine (proflavine) could prove to be a potential antimalarial drug and its pharmacological action can be due to inhibition of gyrase activity. This is achieved through interaction of the ACF with the DNA substrate. This interaction may lead to conformation change in DNA unsuitable for binding of gyrase with DNA.

CNS Activity

Curator's Comment: Known to be CNS penetrant in mouse. Human data not available.

Originator

Curator's Comment: in 1912 by the German medical-research worker Paul Ehrlich

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Acriflavine inhibits HIF-1 dimerization, tumor growth, and vascularization.
2009-10-20
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
ACRIFLAVINE (ACF) 100 nM inhibits the growth of asexual stages of both chloroquine (CQ) sensitive and resistant strains of human malarial parasite, Plasmodium falciparum in vitro
Substance Class Chemical
Created
by admin
on Wed Apr 02 05:49:08 GMT 2025
Edited
by admin
on Wed Apr 02 05:49:08 GMT 2025
Record UNII
J276XBF77Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,6-Diamino-10-methylacridinium
Systematic Name English
Acriflavinium
Preferred Name English
Acridinium, 3,6-diamino-10-methyl-
Systematic Name English
10-Methylacridin-10-ium-3,6-diamine
Systematic Name English
Code System Code Type Description
PUBCHEM
2016
Created by admin on Wed Apr 02 05:49:08 GMT 2025 , Edited by admin on Wed Apr 02 05:49:08 GMT 2025
PRIMARY
FDA UNII
J276XBF77Z
Created by admin on Wed Apr 02 05:49:08 GMT 2025 , Edited by admin on Wed Apr 02 05:49:08 GMT 2025
PRIMARY
CAS
837-73-0
Created by admin on Wed Apr 02 05:49:08 GMT 2025 , Edited by admin on Wed Apr 02 05:49:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID30232534
Created by admin on Wed Apr 02 05:49:08 GMT 2025 , Edited by admin on Wed Apr 02 05:49:08 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT