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Details

Stereochemistry ACHIRAL
Molecular Formula C15H16N4
Molecular Weight 252.3143
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NEUTRAL RED BASE

SMILES

CN(C)C1=CC2=NC3=CC(N)=C(C)C=C3N=C2C=C1

InChI

InChIKey=GLVRJEJEXGVOMJ-UHFFFAOYSA-N
InChI=1S/C15H16N4/c1-9-6-13-15(8-11(9)16)18-14-7-10(19(2)3)4-5-12(14)17-13/h4-8H,16H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C15H16N4
Molecular Weight 252.3143
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Cytotoxicity on human cancer cells of ophidiacerebrosides isolated from the African starfish Narcissia canariensis.
2010-12-22
Preconcentration and determination of iron and copper in spice samples by cloud point extraction and flow injection flame atomic absorption spectrometry.
2010-09-15
Control of hepatitis C: a medicinal chemistry perspective.
2005-01-13
Hepatitis C viral IRES inhibition by phenazine and phenazine-like molecules.
2000-06-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:37:17 GMT 2025
Edited
by admin
on Mon Mar 31 21:37:17 GMT 2025
Record UNII
I64IQB89JB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEUTRAL RED BASE
Common Name English
C.I. BASIC RED 5, FREE BASE
Preferred Name English
PHENAZINE, 3-AMINO-7-DIMETHYLAMINO-2-METHYL-
Systematic Name English
NEUTRAL RED FREE BASE
Common Name English
2,8-PHENAZINEDIAMINE, N8,N8,3-TRIMETHYL-
Systematic Name English
NEUTRAL RED BASE [MI]
Common Name English
Code System Code Type Description
FDA UNII
I64IQB89JB
Created by admin on Mon Mar 31 21:37:17 GMT 2025 , Edited by admin on Mon Mar 31 21:37:17 GMT 2025
PRIMARY
CHEBI
86372
Created by admin on Mon Mar 31 21:37:17 GMT 2025 , Edited by admin on Mon Mar 31 21:37:17 GMT 2025
PRIMARY
MERCK INDEX
m7843
Created by admin on Mon Mar 31 21:37:17 GMT 2025 , Edited by admin on Mon Mar 31 21:37:17 GMT 2025
PRIMARY
CAS
366-13-2
Created by admin on Mon Mar 31 21:37:17 GMT 2025 , Edited by admin on Mon Mar 31 21:37:17 GMT 2025
PRIMARY
PUBCHEM
11106
Created by admin on Mon Mar 31 21:37:17 GMT 2025 , Edited by admin on Mon Mar 31 21:37:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID10190082
Created by admin on Mon Mar 31 21:37:17 GMT 2025 , Edited by admin on Mon Mar 31 21:37:17 GMT 2025
PRIMARY