FAST GREEN FREE ACID

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 Search

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

Molecular Formula	C37H36N2O10S3
Molecular Weight	764.884
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
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 Jul 27	10906429
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	10840942
Effect of metanil yellow and malachite green on DNA synthesis in N-nitrosodiethylamine induced preneoplastic rat livers.	2001 Sep	11831363
Tumor promotion by metanil yellow and malachite green during rat hepatocarcinogenesis is associated with dysregulated expression of cell cycle regulatory proteins.	2003	12616621
Treatment of ichthyophthiriasis after malachite green. II. Earth ponds at salmonid farms.	2005 Aug 9	16175963
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 Jun 18	16085357
Identification of quaternary ammonium compounds as potent inhibitors of hERG potassium channels.	2011 May 1	21362439
Population-based in vitro hazard and concentration-response assessment of chemicals: the 1000 genomes high-throughput screening study.	2015 May	25622337

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 07:55:15 GMT 2023` Edited by `admin` on `Sat Dec 16 07:55:15 GMT 2023`
Record UNII	7G5QXS453J
Record Status	`Validated (UNII)`
Record Version

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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

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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

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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

Related Record Type Details


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