Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H9NO6S2.4H2O |
| Molecular Weight | 375.373 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.O.O.NC1=CC2=C(C=C1)C=C(C=C2S(O)(=O)=O)S(O)(=O)=O
InChI
InChIKey=FISTULJZNDQZAZ-UHFFFAOYSA-N
InChI=1S/C10H9NO6S2.4H2O/c11-7-2-1-6-3-8(18(12,13)14)5-10(9(6)4-7)19(15,16)17;;;;/h1-5H,11H2,(H,12,13,14)(H,15,16,17);4*1H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Antiangiogenic activity of 2-deoxy-D-glucose. | 2010-10-27 |
|
| Induced intersystem crossing at the fluorescence quenching of laser dye 7-amino-1,3-naphthalenedisulfonic acid by paramagnetic metal ions. | 2010-01 |
|
| Ultraviolet photodissociation at 355 nm of fluorescently labeled oligosaccharides. | 2008-07-01 |
|
| Fluorophore-assisted carbohydrate electrophoresis: a sensitive and accurate method for the direct analysis of dolichol pyrophosphate-linked oligosaccharides in cell cultures and tissues. | 2005-04 |
|
| A novel water-soluble fluorescent probe for the determination of methylamine. | 2001-10 |
|
| Electrophoretic sequencing of heparin/heparan sulfate oligosaccharides using a highly sensitive fluorescent end label. | 2001-02 |
|
| Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity. | 1993-07-09 |
|
| 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 |
|
| Aromatic sulfonic acids as viral inhibitors. Structure-activity study using rhino, adeno 3, herpes simplex, and influenza viruses. | 1971-07 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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76962518
Created by
admin on Mon Mar 31 21:24:04 GMT 2025 , Edited by admin on Mon Mar 31 21:24:04 GMT 2025
|
PRIMARY | |||
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WU0I919Q2J
Created by
admin on Mon Mar 31 21:24:04 GMT 2025 , Edited by admin on Mon Mar 31 21:24:04 GMT 2025
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PRIMARY | |||
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m1665
Created by
admin on Mon Mar 31 21:24:04 GMT 2025 , Edited by admin on Mon Mar 31 21:24:04 GMT 2025
|
PRIMARY | Merck Index |
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
