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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
Structure of DIBENZOFURAN-4,6-DICARBOXYLIC ACID

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)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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

Patents

Substance Class Chemical
Created
by admin
on Wed Apr 02 05:22:18 GMT 2025
Edited
by admin
on Wed Apr 02 05:22:18 GMT 2025
Record UNII
RYR5HY07OV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBENZOFURAN-4,6-DICARBOXYLIC ACID
Systematic Name English
4,6-DIBENZOFURANDICARBOXYLIC ACID
Preferred Name English
DIBENZO(B,D)FURAN-4,6-DICARBOXYLIC ACID
Systematic Name English
Code System Code Type Description
CAS
88818-47-7
Created by 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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PUBCHEM
3022
Created by 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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DRUG BANK
DB03682
Created by admin on Wed Apr 02 05:22:18 GMT 2025 , Edited by admin on Wed Apr 02 05:22:18 GMT 2025
PRIMARY
FDA UNII
RYR5HY07OV
Created by admin on Wed Apr 02 05:22:18 GMT 2025 , Edited by admin on Wed Apr 02 05:22:18 GMT 2025
PRIMARY