Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | 3C15H17O3S.3Na.H2O |
| Molecular Weight | 919.061 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.[Na+].[Na+].[Na+].CCC1=CC(=C2C=C(C=CC=C12)C(C)C)S([O-])(=O)=O.CCC3=CC(=C4C=C(C=CC=C34)C(C)C)S([O-])(=O)=O.CCC5=CC(=C6C=C(C=CC=C56)C(C)C)S([O-])(=O)=O
InChI
InChIKey=NLAZKIKOGLLKFO-UHFFFAOYSA-K
InChI=1S/3C15H18O3S.3Na.H2O/c3*1-4-11-9-15(19(16,17)18)14-8-12(10(2)3)6-5-7-13(11)14;;;;/h3*5-10H,4H2,1-3H3,(H,16,17,18);;;;1H2/q;;;3*+1;/p-3
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Inhibitory effect of egualen sodium: a new stable derivative of azulene on histamine release from mast cell-like cells in the stomach. | 2001 |
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| A ring expansion-annulation strategy for the synthesis of substituted azulenes. Preparation and Suzuki coupling reactions of 1-azulenyl triflates. | 2001 Apr 5 |
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249501B040
Created by
admin on Sat Dec 16 05:22:47 GMT 2023 , Edited by admin on Sat Dec 16 05:22:47 GMT 2023
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11954341
Created by
admin on Sat Dec 16 05:22:47 GMT 2023 , Edited by admin on Sat Dec 16 05:22:47 GMT 2023
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
