Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H10N2O3S |
| Molecular Weight | 238.263 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC(=C2C=CC=CC2=C1N)S(O)(=O)=O
InChI
InChIKey=VZYOWBULYLPMGR-UHFFFAOYSA-N
InChI=1S/C10H10N2O3S/c11-8-5-9(16(13,14)15)6-3-1-2-4-7(6)10(8)12/h1-5H,11-12H2,(H,13,14,15)
| Molecular Formula | C10H10N2O3S |
| Molecular Weight | 238.263 |
| 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 |
|---|---|---|
| Pharmacokinetics and distribution of sodium 3,4-diaminonaphthalene-1-sulfonate, a Congo Red derivative active in inhibiting PrP(res) replication. | 2004-03 |
|
| Determination of sodium 3,4-diaminonaphthalene-1-sulfonate, a Congo Red derivative, in plasma and brain of hamsters by high-performance liquid chromatography after solid-phase extraction and ultraviolet absorbance. | 2002-03-25 |
|
| Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities. | 1992-12-25 |
|
| Potential anti-AIDS agents. Synthesis and antiviral activity of naphthalenesulfonic acid derivatives against HIV-1 and HIV-2. | 1991-01 |
|
| Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound. | 1990 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:12:30 GMT 2025
by
admin
on
Mon Mar 31 19:12:30 GMT 2025
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| Record UNII |
0UCA767F4J
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| Record Status |
Validated (UNII)
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| Record Version |
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