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 |
---|---|---|
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 |
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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
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:51:33 GMT 2023
by
admin
on
Fri Dec 15 18:51:33 GMT 2023
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Record UNII |
SBZ7FUN4BK
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Record Status |
Validated (UNII)
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Record Version |
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