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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14N3.Cl
Molecular Weight 259.734
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,6-DIAMINO-10-METHYLACRIDINIUM CHLORIDE

SMILES

[Cl-].C[N+]1=C2C=C(N)C=CC2=CC3=C1C=C(N)C=C3

InChI

InChIKey=KKAJSJJFBSOMGS-UHFFFAOYSA-N
InChI=1S/C14H13N3.ClH/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);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C14H13N3
Molecular Weight 223.2731
Charge 0
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 Oct 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 Fri Dec 15 15:57:10 GMT 2023
Edited
by admin
on Fri Dec 15 15:57:10 GMT 2023
Record UNII
1TW3Q60E36
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,6-DIAMINO-10-METHYLACRIDINIUM CHLORIDE
Systematic Name English
NEUTRAL ACRIFLAVINE
Common Name English
ACRIDINIUM, 3,6-DIAMINO-10-METHYL-, CHLORIDE
Systematic Name English
GONACRINE
Common Name English
CHROMOFLAVINE
Common Name English
EUFLAVINE
Common Name English
ACRIFLAVINE NEUTRAL FORM [MI]
Common Name English
NEUTROFLAVINE
Common Name English
ACRIDINIUM, 3,6-DIAMINO-10-METHYL-, CHLORIDE (1:1)
Systematic Name English
NSC-2755
Code English
C.I. 46000
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
NCI_THESAURUS C461
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
WHO-VATC QD08AA03
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
WHO-ATC D08AA03
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
Code System Code Type Description
PUBCHEM
6842
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
PRIMARY
WIKIPEDIA
EUFLAVINE
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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NCI_THESAURUS
C77087
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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MESH
C026620
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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FDA UNII
1TW3Q60E36
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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EPA CompTox
DTXSID60273975
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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DRUG BANK
DB13326
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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CHEBI
383703
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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CAS
86-40-8
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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MERCK INDEX
m1385
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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ChEMBL
CHEMBL2010412
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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NSC
2755
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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ECHA (EC/EINECS)
201-668-8
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
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DRUG CENTRAL
4317
Created by admin on Fri Dec 15 15:57:10 GMT 2023 , Edited by admin on Fri Dec 15 15:57:10 GMT 2023
PRIMARY