U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C7H4ClNOS
Molecular Weight 185.631
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TICLATONE

SMILES

ClC1=CC2=C(C=C1)C(=O)NS2

InChI

InChIKey=POPOYOKQQAEISW-UHFFFAOYSA-N
InChI=1S/C7H4ClNOS/c8-4-1-2-5-6(3-4)11-9-7(5)10/h1-3H,(H,9,10)

HIDE SMILES / InChI

Molecular Formula C7H4ClNOS
Molecular Weight 185.631
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Ticlatone (trade name Landromil) is an antifungal for topical use.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Landromil

Approved Use

Antifungals for topical use
PubMed

PubMed

TitleDatePubMed
[Clinical studies on landromil (tiklaton) in treatment of mycoses].
1971-11-01
MICROBIOLOGICAL INVESTIGATIONS WITH 6-CHLORO-1,2-BENZISOTHIAZOLONE.
1964-12
Patents

Sample Use Guides

Topical use
Route of Administration: Topical
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:45:27 GMT 2025
Edited
by admin
on Wed Apr 02 09:45:27 GMT 2025
Record UNII
BHW384Q9GI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TICLATONE
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
FER-1443
Preferred Name English
Ticlatone [WHO-DD]
Common Name English
1,2-BENZISOTHIAZOL-3(2H)-ONE, 6-CHLORO-
Systematic Name English
TICLATONE [USAN]
Common Name English
ticlatone [INN]
Common Name English
6-Chloro-1,2-benzisothiazolin-3-one
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
WHO-VATC QD01AE08
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
WHO-ATC D01AE08
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
Code System Code Type Description
PUBCHEM
6258
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID8057809
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
INN
2888
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
MESH
C000409
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
CAS
70-10-0
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
DRUG CENTRAL
4734
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
ChEMBL
CHEMBL2103914
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
EVMPD
SUB11027MIG
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
NCI_THESAURUS
C152612
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
DRUG BANK
DB13613
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
FDA UNII
BHW384Q9GI
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
WIKIPEDIA
TICLATONE
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
SMS_ID
100000082167
Created by admin on Wed Apr 02 09:45:27 GMT 2025 , Edited by admin on Wed Apr 02 09:45:27 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY