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Details

Stereochemistry ACHIRAL
Molecular Formula C14H8BrNO5S
Molecular Weight 382.186
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROMAMINE ACID

SMILES

NC1=C(C=C(Br)C2=C1C(=O)C3=CC=CC=C3C2=O)S(O)(=O)=O

InChI

InChIKey=QZZSAWGVHXXMID-UHFFFAOYSA-N
InChI=1S/C14H8BrNO5S/c15-8-5-9(22(19,20)21)12(16)11-10(8)13(17)6-3-1-2-4-7(6)14(11)18/h1-5H,16H2,(H,19,20,21)

HIDE SMILES / InChI

Molecular Formula C14H8BrNO5S
Molecular Weight 382.186
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists.
2008 Jan 1
Influence of Ecto-nucleoside triphosphate diphosphohydrolase activity on Trypanosoma cruzi infectivity and virulence.
2009
Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases).
2009 Mar
Synthesis of alkyl- and aryl-amino-substituted anthraquinone derivatives by microwave-assisted copper(0)-catalyzed Ullmann coupling reactions.
2010 May
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:51:33 GMT 2023
Edited
by admin
on Fri Dec 15 18:51:33 GMT 2023
Record UNII
SBZ7FUN4BK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BROMAMINE ACID
Common Name English
ALIZARINE CYANOL GREY G
Brand Name English
1-AMINO-4-BROMOANTHRAQUINONE-2-SULFONIC ACID
Systematic Name English
2-ANTHRAQUINONESULFONIC ACID, 1-AMINO-4-BROMO-
Common Name English
2-ANTHRACENESULFONIC ACID, 1-AMINO-4-BROMO-9,10-DIHYDRO-9,10-DIOXO-
Common Name English
1-AMINO-2-SULFONATO-4-BROMO-9,10-ANTHRAQUINONE
Systematic Name English
BROMAMINIC ACID
Common Name English
NSC-7574
Code English
1-AMINO-4-BROMO-9,10-DIOXO-9,10-DIHYDROANTHRACENE-2-SULFONIC ACID
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID5044782
Created by admin on Fri Dec 15 18:51:33 GMT 2023 , Edited by admin on Fri Dec 15 18:51:33 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-159-9
Created by admin on Fri Dec 15 18:51:33 GMT 2023 , Edited by admin on Fri Dec 15 18:51:33 GMT 2023
PRIMARY
FDA UNII
SBZ7FUN4BK
Created by admin on Fri Dec 15 18:51:33 GMT 2023 , Edited by admin on Fri Dec 15 18:51:33 GMT 2023
PRIMARY
NSC
7574
Created by admin on Fri Dec 15 18:51:33 GMT 2023 , Edited by admin on Fri Dec 15 18:51:33 GMT 2023
PRIMARY
CAS
116-81-4
Created by admin on Fri Dec 15 18:51:33 GMT 2023 , Edited by admin on Fri Dec 15 18:51:33 GMT 2023
PRIMARY
PUBCHEM
22628
Created by admin on Fri Dec 15 18:51:33 GMT 2023 , Edited by admin on Fri Dec 15 18:51:33 GMT 2023
PRIMARY