Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H12N4O3 |
| Molecular Weight | 236.2273 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=CC=C(C=C1NC(N)=N)C(O)=O
InChI
InChIKey=UDQJOWCVSMIZJP-UHFFFAOYSA-N
InChI=1S/C10H12N4O3/c1-5(15)13-7-3-2-6(9(16)17)4-8(7)14-10(11)12/h2-4H,1H3,(H,13,15)(H,16,17)(H4,11,12,14)
| Molecular Formula | C10H12N4O3 |
| Molecular Weight | 236.2273 |
| 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 |
|---|---|---|
| A QSAR study on influenza neuraminidase inhibitors. | 2006-02-15 |
|
| Synthesis and inhibitory activity of benzoic acid and pyridine derivatives on influenza neuraminidase. | 2005-04-01 |
|
| Pyrrolidinobenzoic acid inhibitors of influenza virus neuraminidase: modifications of essential pyrrolidinone ring substituents. | 2003-07-03 |
|
| Hydrophobic benzoic acids as inhibitors of influenza neuraminidase. | 1999-11 |
|
| Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping. | 1999-07-19 |
|
| Potent inhibition of influenza sialidase by a benzoic acid containing a 2-pyrrolidinone substituent. | 1999-07-01 |
|
| Generation and characterization of a mutant of influenza A virus selected with the neuraminidase inhibitor BCX-140. | 1998-04 |
|
| Design and synthesis of benzoic acid derivatives as influenza neuraminidase inhibitors using structure-based drug design. | 1997-12-05 |
|
| Structure-based inhibitors of influenza virus sialidase. A benzoic acid lead with novel interaction. | 1995-08-18 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:30:59 GMT 2025
by
admin
on
Mon Mar 31 23:30:59 GMT 2025
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| Record UNII |
V02KF5948M
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| Record Status |
Validated (UNII)
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| Record Version |
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170447-93-5
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446323
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DB03342
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