Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H20N2O3S.ClH |
Molecular Weight | 320.835 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCOC(=O)\C=C1/SC(N2CCCCC2)C(=O)N1C
InChI
InChIKey=AOHAFCXGDWOODX-KVVVOXFISA-N
InChI=1S/C13H20N2O3S.ClH/c1-3-18-11(16)9-10-14(2)12(17)13(19-10)15-7-5-4-6-8-15;/h9,13H,3-8H2,1-2H3;1H/b10-9-;
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C13H20N2O3S |
Molecular Weight | 284.374 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Optical Activity | ( + / - ) |
Originator
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | ELKAPIN Approved UseUnknown |
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Sources: https://www.ncbi.nlm.nih.gov/pubmed/578770 |
Primary | ELKAPIN Approved UseUnknown |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1417365
Isolated rings of guinea-pig aorta were treated with etozolin (10 uM-1 mM). At those concentrations, the drug inhibited noradrenaline- and histamine-induced contractions. At very low concentrations (1 nM-0.1 uM), it inhibited also serotonin-induced contractions.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:57:06 GMT 2023
by
admin
on
Sat Dec 16 08:57:06 GMT 2023
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Record UNII |
92BYI8Y56J
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Record Status |
Validated (UNII)
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Record Version |
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m5204
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DBSALT002351
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92BYI8Y56J
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |