Details
Stereochemistry | RACEMIC |
Molecular Formula | C15H10O5S |
Molecular Weight | 302.302 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[S+]([O-])C1=CC=C2OC3=C(C=C(C=C3)C(O)=O)C(=O)C2=C1
InChI
InChIKey=PCVFKIXSNYJABV-UHFFFAOYSA-N
InChI=1S/C15H10O5S/c1-21(19)9-3-5-13-11(7-9)14(16)10-6-8(15(17)18)2-4-12(10)20-13/h2-7H,1H3,(H,17,18)
Molecular Formula | C15H10O5S |
Molecular Weight | 302.302 |
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 |
---|---|---|
Dibenzotropone- and dibenzosuberonecarboxylic acids with bronchodilator activity. | 1979 Nov |
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Synthesis and aldose reductase inhibitory activity of 7-sulfamoylxanthone-2-carboxylic acids. | 1980 Nov |
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The activity of sodium cromoglycate analogues in human lung in vitro: a comparison with rat passive cutaneous anaphylaxis and clinical efficacy. | 1980 Oct |
|
Reaction of 1-O-acyl glucuronides with 4-(p-nitrobenzyl)pyridine. | 1986 Mar-Apr |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:13:16 GMT 2023
by
admin
on
Fri Dec 15 15:13:16 GMT 2023
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Record UNII |
KQT9O2462E
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29712
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38617
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CHEMBL23771
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C73060
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40691-50-7
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DTXSID00866007
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3962
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SUB11126MIG
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KQT9O2462E
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100000082141
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PRIMARY |
Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |