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-;
Originator
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | ELKAPIN Approved UseUnknown |
|||
Sources: https://www.ncbi.nlm.nih.gov/pubmed/578770 |
Primary | ELKAPIN Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
[LOCALIZATION OF THE SITE OF ACTION OF THE DIURETIC ETOZOLIN IN THE MEPHRON OF THE DOG AND REPORT OF A MATHEMATICAL EVALUATION METHOD OF STOP-FLOW EXPERIMENTS]. | 1964 Nov 25 |
|
Distribution of 64Cu-bleomycin in normal and tumor-bearing rats. | 1976 Jan |
|
[On the pharmacology of Etozolin (author's transl)]. | 1977 |
|
[Toxicological studies on Etozolin (author's transl)]. | 1977 |
|
Pharmacodynamics and kinetics of etozolin/ozolinone in hypertensive patients with normal and impaired kidney function. | 1984 |
Patents
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.
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
53-90-7
Created by
admin on Sat Dec 16 08:57:07 GMT 2023 , Edited by admin on Sat Dec 16 08:57:07 GMT 2023
|
PRIMARY | |||
|
DTXSID801018925
Created by
admin on Sat Dec 16 08:57:07 GMT 2023 , Edited by admin on Sat Dec 16 08:57:07 GMT 2023
|
PRIMARY | |||
|
m5204
Created by
admin on Sat Dec 16 08:57:07 GMT 2023 , Edited by admin on Sat Dec 16 08:57:07 GMT 2023
|
PRIMARY | Merck Index | ||
|
DBSALT002351
Created by
admin on Sat Dec 16 08:57:07 GMT 2023 , Edited by admin on Sat Dec 16 08:57:07 GMT 2023
|
PRIMARY | |||
|
92BYI8Y56J
Created by
admin on Sat Dec 16 08:57:07 GMT 2023 , Edited by admin on Sat Dec 16 08:57:07 GMT 2023
|
PRIMARY | |||
|
72710623
Created by
admin on Sat Dec 16 08:57:07 GMT 2023 , Edited by admin on Sat Dec 16 08:57:07 GMT 2023
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD