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Details

Stereochemistry ACHIRAL
Molecular Formula C29H20ClN7O11S3
Molecular Weight 774.157
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-AMINO-4-((4-((4-CHLORO-6-((3-SULFOPHENYL)AMINO)-1,3,5-TRIAZIN-2-YL)AMINO)-3-SULFOPHENYL)AMINO)-9,10-DIHYDRO-9,10-DIOXO-2-ANTHRACENESULFONIC ACID

SMILES

NC1=C2C(=O)C3=C(C=CC=C3)C(=O)C2=C(NC4=CC=C(NC5=NC(Cl)=NC(NC6=CC=CC(=C6)S(O)(=O)=O)=N5)C(=C4)S(O)(=O)=O)C=C1S(O)(=O)=O

InChI

InChIKey=JQYMGXZJTCOARG-UHFFFAOYSA-N
InChI=1S/C29H20ClN7O11S3/c30-27-35-28(33-13-4-3-5-15(10-13)49(40,41)42)37-29(36-27)34-18-9-8-14(11-20(18)50(43,44)45)32-19-12-21(51(46,47)48)24(31)23-22(19)25(38)16-6-1-2-7-17(16)26(23)39/h1-12,32H,31H2,(H,40,41,42)(H,43,44,45)(H,46,47,48)(H2,33,34,35,36,37)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Microglial zinc uptake via zinc transporters induces ATP release and the activation of microglia.
2011-12
Roles of peripheral P2X and P2Y receptors in the development of melittin-induced nociception and hypersensitivity.
2008-10
P2 receptors activated by uracil nucleotides--an update.
2006
P53 hot-spot mutants are resistant to ubiquitin-independent degradation by increased binding to NAD(P)H:quinone oxidoreductase 1.
2003-12-09
Pharmacological characterization of the human P2Y13 receptor.
2003-07
Pharmacological characterization of the human P2Y11 receptor.
1999-11
Human P2Y2 receptor polymorphism: identification and pharmacological characterization of two allelic variants.
1999-06
Sequence, catalytic properties and expression of chicken glutathione-dependent prostaglandin D2 synthase, a novel class Sigma glutathione S-transferase.
1998-07-15
Molecular cloning and characterization of rat P2Y4 nucleotide receptor.
1998-06
Isoform-specific biotransformation of glyceryl trinitrate by rat aortic glutathione S-transferases.
1996-12
Inhibition kinetics of camel lens zeta-crystallin: multiple inhibition studies.
1996-08
Cloning and expression of a cDNA for mu-class glutathione S-transferase from rabbit liver.
1995-04-20
Name Type Language
2-ANTHRACENESULFONIC ACID, 1-AMINO-4-((4-((4-CHLORO-6-((3-SULFOPHENYL)AMINO)-1,3,5-TRIAZIN-2-YL)AMINO)-3-SULFOPHENYL)AMINO)-9,10-DIHYDRO-9,10-DIOXO-
Preferred Name English
1-AMINO-4-((4-((4-CHLORO-6-((3-SULFOPHENYL)AMINO)-1,3,5-TRIAZIN-2-YL)AMINO)-3-SULFOPHENYL)AMINO)-9,10-DIHYDRO-9,10-DIOXO-2-ANTHRACENESULFONIC ACID
Common Name English
2-ANTHRAQUINONESULFONIC ACID, 1-AMINO-4-(4-((4-CHLORO-6-M-SULFOANILINO-S-TRIAZIN-2-YL)AMINO)-3-SULFOANILINO)-
Systematic Name English
Code System Code Type Description
CAS
79241-87-5
Created by admin on Mon Mar 31 22:00:26 GMT 2025 , Edited by admin on Mon Mar 31 22:00:26 GMT 2025
PRIMARY
FDA UNII
J0A052J6QF
Created by admin on Mon Mar 31 22:00:26 GMT 2025 , Edited by admin on Mon Mar 31 22:00:26 GMT 2025
PRIMARY
PUBCHEM
656725
Created by admin on Mon Mar 31 22:00:26 GMT 2025 , Edited by admin on Mon Mar 31 22:00:26 GMT 2025
PRIMARY