Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H14ClN3O2S |
| Molecular Weight | 371.841 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NSC(NC(=O)C2=CC=CC=C2)=C1C(=O)NC3=CC=C(Cl)C=C3
InChI
InChIKey=ZPBLNADJHWHOEP-UHFFFAOYSA-N
InChI=1S/C18H14ClN3O2S/c1-11-15(17(24)20-14-9-7-13(19)8-10-14)18(25-22-11)21-16(23)12-5-3-2-4-6-12/h2-10H,1H3,(H,20,24)(H,21,23)
| Molecular Formula | C18H14ClN3O2S |
| Molecular Weight | 371.841 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Denotivir is an organic chemical compound with antiviral activity. In vitro antiviral activity of denotivir has been demonstrated against human HSV types 1 and 2, and varicella zoster virus (VZV). Clinical trials with vratizolin have given impressive results in the patients with local HSV infections and very good results in VZV infections. Genital herpes, a sexually transmitted HSV infection, whose incidence is increasing and whose treatment has never been adequate, appears to respond well to the treatment with vratizolin with very good results. Very good therapeutic results were also obtained by applying vratizolin to the patients with an ophthalmic HSV infection. Vratizolin exerted strong immunosuppressive actions. Vratizolin inhibited to some degree LPS-induced cytokine production in human peripheral blood cultures. The activities of TNF-alpha, IL-1 and IL-6 were inhibited on average by 37, 26 and 35%, respectively.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0006955 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11990084 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Biological evaluation of Wratizolin penetration from ointments to the skin. | 1983 |
|
| Antifungal activity of Wratizolin. | 1983 |
|
| Clinical studies on the effectiveness of Wratizolin in the treatment of some dermatoses. | 1983 |
|
| Studies on the therapeutic effect of Wratizolin in selected dermatoses. | 1983 |
|
| Results of Wratizolin treatment of selected skin diseases with particular reference to those of viral etiology. | 1983 |
|
| Wratizolin ITCL in the treatment of herpes simplex and recurrent and zoster. | 1983 |
|
| Antibacterial activity of Wratizolin. | 1983 |
|
| Effects of Wratizolin on growth and metabolism of cells in vitro. | 1983 |
|
| P-chlorophenylamide of 3-methyl-5-benzoylaminoisothiazole-4-carboxylic acid (ITCL, Wratizolin)--the new antiviral drug. | 1983 |
|
| Interaction of Wratizolin with serum albumins and its antiproteolytic activity. | 1983 |
|
| Investigations on the activity of p-chlorophenylamide of 3-methyl-5-benzoylaminoisothiazole-4-carboxylic acid (ITCL) in the experimental keratitis. | 1983 |
|
| Antiviral activity of Wratizolin. | 1983 |
|
| Pharmacological studies on p-chlorophenylamide of 3-methyl-5-benzoylaminoizothiazole-4-carboxylic acid (compound ITCL) the preparation of eventual anti-inflammatory effect. | 1980 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:17:27 GMT 2025
by
admin
on
Mon Mar 31 18:17:27 GMT 2025
|
| Record UNII |
W656S9I00W
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C281
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID70199278
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
7128
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
39976
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
C109918
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
SUB06978MIG
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
100000083161
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
W656S9I00W
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
C77362
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
CHEMBL2104203
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY | |||
|
51287-57-1
Created by
admin on Mon Mar 31 18:17:27 GMT 2025 , Edited by admin on Mon Mar 31 18:17:27 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TARGET ORGANISM->INHIBITOR |
|
||
|
TARGET ORGANISM->INHIBITOR |
|
||
|
TARGET ORGANISM->INHIBITOR |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|