U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C37H36N2O10S3
Molecular Weight 764.884
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FAST GREEN FREE ACID

SMILES

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=C(C=C(O)C=C5)S([O-])(=O)=O

InChI

InChIKey=VVJKKKDJADMKNM-UHFFFAOYSA-N
InChI=1S/C37H36N2O10S3/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)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
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 Mar
Effect of metanil yellow and malachite green on DNA synthesis in N-nitrosodiethylamine induced preneoplastic rat livers.
2001 Sep
Tumor promotion by metanil yellow and malachite green during rat hepatocarcinogenesis is associated with dysregulated expression of cell cycle regulatory proteins.
2003
Inhibition of human plasma cholinesterase by malachite green and related triarylmethane dyes: mechanistic implications.
2005 Aug 15
Treatment of ichthyophthiriasis after malachite green. II. Earth ponds at salmonid farms.
2005 Aug 9
Methemoglobinemia due to malachite green ingestion in a child.
2008 Apr
Inhibition of electric eel acetylcholinesterase by triarylmethane dyes.
2008 Sep 25
Disrupting actions of bisphenol A and malachite green on growth hormone receptor gene expression and signal transduction in seabream.
2010 Jun
Identification of quaternary ammonium compounds as potent inhibitors of hERG potassium channels.
2011 May 1
Population-based in vitro hazard and concentration-response assessment of chemicals: the 1000 genomes high-throughput screening study.
2015 May
Patents
Name Type Language
FAST GREEN FREE ACID
Common Name English
J247.014D
Code English
BENZENEMETHANAMINIUM, N-ETHYL-N-(4-((4-(ETHYL((3-SULFOPHENYL)METHYL)AMINO)PHENYL)(4-HYDROXY-2-SULFOPHENYL)METHYLENE)-2,5-CYCLOHEXADIEN-1-YLIDENE)-3-SULFO-, INNER SALT
Systematic Name English
N-ETHYL-N-(4-((4-(ETHYL((3-SULFOPHENYL)METHYL)AMINO)PHENYL)(4-HYDROXY-2-SULFOPHENYL)METHYLENE)-2,5-CYCLOHEXADIEN-1-YLIDENE)-3-SULFONATOBENZENEMETHANAMINIUM
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID6044301
Created by admin on Sat Dec 16 07:55:15 GMT 2023 , Edited by admin on Sat Dec 16 07:55:15 GMT 2023
PRIMARY
PUBCHEM
4333500
Created by admin on Sat Dec 16 07:55:15 GMT 2023 , Edited by admin on Sat Dec 16 07:55:15 GMT 2023
PRIMARY
CAS
25738-40-3
Created by admin on Sat Dec 16 07:55:15 GMT 2023 , Edited by admin on Sat Dec 16 07:55:15 GMT 2023
PRIMARY
FDA UNII
7G5QXS453J
Created by admin on Sat Dec 16 07:55:15 GMT 2023 , Edited by admin on Sat Dec 16 07:55:15 GMT 2023
PRIMARY