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
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)
| 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
| Title | Date | PubMed |
|---|---|---|
| Synthesis of alkyl- and aryl-amino-substituted anthraquinone derivatives by microwave-assisted copper(0)-catalyzed Ullmann coupling reactions. | 2010-05 |
|
| Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases). | 2009-03 |
|
| Influence of Ecto-nucleoside triphosphate diphosphohydrolase activity on Trypanosoma cruzi infectivity and virulence. | 2009 |
|
| The new incorporation bio-treatment technology of bromoamine acid and azo dyes wastewaters under high-salt conditions. | 2008-02 |
|
| Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists. | 2008-01-01 |
|
| Rapid and efficient microwave-assisted copper(0)-catalyzed ullmann coupling reaction: general access to anilinoanthraquinone derivatives. | 2007-03-29 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:22:53 GMT 2025
by
admin
on
Mon Mar 31 19:22:53 GMT 2025
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| Record UNII |
SBZ7FUN4BK
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| Record Status |
Validated (UNII)
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