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 |
---|---|---|
Aromatic sulfonic acids as viral inhibitors. Structure-activity study using rhino, adeno 3, herpes simplex, and influenza viruses. | 1971 Jul |
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Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity. | 1993 Jul 9 |
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Ultraviolet photodissociation at 355 nm of fluorescently labeled oligosaccharides. | 2008 Jul 1 |
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Induced intersystem crossing at the fluorescence quenching of laser dye 7-amino-1,3-naphthalenedisulfonic acid by paramagnetic metal ions. | 2010 Jan |
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Antiangiogenic activity of 2-deoxy-D-glucose. | 2010 Oct 27 |
Patents
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Common Name | English |
Code System | Code | Type | Description | ||
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76962518
Created by
admin on Sat Dec 16 04:50:06 GMT 2023 , Edited by admin on Sat Dec 16 04:50:06 GMT 2023
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PRIMARY | |||
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WU0I919Q2J
Created by
admin on Sat Dec 16 04:50:06 GMT 2023 , Edited by admin on Sat Dec 16 04:50:06 GMT 2023
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PRIMARY | |||
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m1665
Created by
admin on Sat Dec 16 04:50:06 GMT 2023 , Edited by admin on Sat Dec 16 04:50:06 GMT 2023
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PRIMARY | Merck Index |
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD