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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
Control of hepatitis C: a medicinal chemistry perspective.
2005 Jan 13
Cytotoxicity on human cancer cells of ophidiacerebrosides isolated from the African starfish Narcissia canariensis.
2010 Dec 22
Preconcentration and determination of iron and copper in spice samples by cloud point extraction and flow injection flame atomic absorption spectrometry.
2010 Sep 15
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 06:41:09 GMT 2023
Edited
by admin
on Sat Dec 16 06:41:09 GMT 2023
Record UNII
I64IQB89JB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEUTRAL RED BASE
Common 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
C.I. BASIC RED 5, FREE BASE
Common Name English
NEUTRAL RED BASE [MI]
Common Name English
Code System Code Type Description
FDA UNII
I64IQB89JB
Created by admin on Sat Dec 16 06:41:09 GMT 2023 , Edited by admin on Sat Dec 16 06:41:09 GMT 2023
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CHEBI
86372
Created by admin on Sat Dec 16 06:41:09 GMT 2023 , Edited by admin on Sat Dec 16 06:41:09 GMT 2023
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MERCK INDEX
m7843
Created by admin on Sat Dec 16 06:41:09 GMT 2023 , Edited by admin on Sat Dec 16 06:41:09 GMT 2023
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CAS
366-13-2
Created by admin on Sat Dec 16 06:41:09 GMT 2023 , Edited by admin on Sat Dec 16 06:41:09 GMT 2023
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PUBCHEM
11106
Created by admin on Sat Dec 16 06:41:09 GMT 2023 , Edited by admin on Sat Dec 16 06:41:09 GMT 2023
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EPA CompTox
DTXSID10190082
Created by admin on Sat Dec 16 06:41:09 GMT 2023 , Edited by admin on Sat Dec 16 06:41:09 GMT 2023
PRIMARY