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Details

Stereochemistry ACHIRAL
Molecular Formula C37H34N2O10S3.2Na
Molecular Weight 808.848
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FAST GREEN

SMILES

[Na+].[Na+].CCN(CC1=CC=CC(=C1)S([O-])(=O)=O)C2=CC=C(C=C2)C(=C3C=CC(C=C3)=[N+](CC)CC4=CC(=CC=C4)S([O-])(=O)=O)C5=CC=C(O)C=C5S([O-])(=O)=O

InChI

InChIKey=RZSYLLSAWYUBPE-UHFFFAOYSA-L
InChI=1S/C37H36N2O10S3.2Na/c1-3-38(24-26-7-5-9-33(21-26)50(41,42)43)30-15-11-28(12-16-30)37(35-20-19-32(40)23-36(35)52(47,48)49)29-13-17-31(18-14-29)39(4-2)25-27-8-6-10-34(22-27)51(44,45)46;;/h5-23H,3-4,24-25H2,1-2H3,(H3,41,42,43,44,45,46,47,48,49);;/q;2*+1/p-2

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C37H34N2O10S3
Molecular Weight 762.868
Charge -2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Population-based in vitro hazard and concentration-response assessment of chemicals: the 1000 genomes high-throughput screening study.
2015-05
Identification of quaternary ammonium compounds as potent inhibitors of hERG potassium channels.
2011-05-01
Disrupting actions of bisphenol A and malachite green on growth hormone receptor gene expression and signal transduction in seabream.
2010-06
Establishment of a transgenic yeast screening system for estrogenicity and identification of the anti-estrogenic activity of malachite green.
2008-12-15
Inhibition of electric eel acetylcholinesterase by triarylmethane dyes.
2008-09-25
Methemoglobinemia due to malachite green ingestion in a child.
2008-04
Elevated phosphorylation of Chk1 and decreased phosphorylation of Chk2 are associated with abrogation of G2/M checkpoint control during transformation of Syrian hamster embryo (SHE) cells by Malachite green.
2006-06-18
Decreased phosphoactive ERKs and JNKs in Malachite-green-transformed Syrian hamster embryo fibroblasts are associated with increased phosphoactive p38 kinase: possible therapeutic importance.
2006
DNA damage and G2/M arrest in Syrian hamster embryo cells during Malachite green exposure are associated with elevated phosphorylation of ERK1 and JNK1.
2005-12-18
Inhibition of human plasma cholinesterase by malachite green and related triarylmethane dyes: mechanistic implications.
2005-08-15
Treatment of ichthyophthiriasis after malachite green. II. Earth ponds at salmonid farms.
2005-08-09
Treatment of ichthyophthiriasis after malachite green. I. Concrete tanks at salmonid farms.
2005-04-06
Hyperphosphorylation of extracellular regulated kinase 2 (ERK2) and inhibition of JNK2 phosphorylation are associated with increased S-phase during transformation of Syrian hamster embryo cells by Malachite Green.
2004
Tumor promotion by metanil yellow and malachite green during rat hepatocarcinogenesis is associated with dysregulated expression of cell cycle regulatory proteins.
2003
Effect of metanil yellow and malachite green on DNA synthesis in N-nitrosodiethylamine induced preneoplastic rat livers.
2001-09
Overexpression of G1/S cyclins and PCNA and their relationship to tyrosine phosphorylation and dephosphorylation during tumor promotion by metanil yellow and malachite green.
2000-07-27
Malachite green induced malignant transformation of Syrian hamster embryo (SHE) cells in primary culture: transformation is associated with enhanced expression of altered p53, bcl-2 and decreased sensitivity to apoptosis.
2000-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:31:09 GMT 2025
Edited
by admin
on Mon Mar 31 18:31:09 GMT 2025
Record UNII
9J3VQ0Y6BV
Record Status Validated (UNII)
Record Version
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Name Type Language
FAST GREEN
FCC  
Common Name English
NSC-379443
Preferred Name English
FAST GREEN FCF [MI]
Common Name English
FAST GREEN [FCC]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID3020673
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
CAS
2353-45-9
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
HSDB
7973
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
NSC
379443
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
MESH
C035906
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
PUBCHEM
16887
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
FDA UNII
9J3VQ0Y6BV
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
WIKIPEDIA
Fast Green FCF
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
ECHA (EC/EINECS)
219-091-5
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
DAILYMED
9J3VQ0Y6BV
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY
MERCK INDEX
m5248
Created by admin on Mon Mar 31 18:31:09 GMT 2025 , Edited by admin on Mon Mar 31 18:31:09 GMT 2025
PRIMARY Merck Index
Related Record Type Details
PARENT -> SALT/SOLVATE