Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H8O5 |
| Molecular Weight | 256.2103 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=CC2=C1OC3=C(C=CC=C23)C(O)=O
InChI
InChIKey=HBBGSNOHAGNQRQ-UHFFFAOYSA-N
InChI=1S/C14H8O5/c15-13(16)9-5-1-3-7-8-4-2-6-10(14(17)18)12(8)19-11(7)9/h1-6H,(H,15,16)(H,17,18)
| Molecular Formula | C14H8O5 |
| Molecular Weight | 256.2103 |
| 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 |
|---|---|---|
| Novel transthyretin amyloid fibril formation inhibitors: synthesis, biological evaluation, and X-ray structural analysis. | 2009-07-21 |
|
| Potent and selective structure-based dibenzofuran inhibitors of transthyretin amyloidogenesis: kinetic stabilization of the native state. | 2005-05-11 |
|
| Site-specific cross-linking of human and bovine hemoglobins differentially alters oxygen binding and redox side reactions producing rhombic heme and heme degradation. | 2002-06-11 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 05:22:18 GMT 2025
by
admin
on
Wed Apr 02 05:22:18 GMT 2025
|
| Record UNII |
RYR5HY07OV
|
| Record Status |
Validated (UNII)
|
| Record Version |
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DB03682
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RYR5HY07OV
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admin on Wed Apr 02 05:22:18 GMT 2025 , Edited by admin on Wed Apr 02 05:22:18 GMT 2025
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