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Details

Stereochemistry ACHIRAL
Molecular Formula C17H18N2S2
Molecular Weight 314.468
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULBENTINE

SMILES

S=C1SCN(CC2=CC=CC=C2)CN1CC3=CC=CC=C3

InChI

InChIKey=QFVAWNPSRQWSDU-UHFFFAOYSA-N
InChI=1S/C17H18N2S2/c20-17-19(12-16-9-5-2-6-10-16)13-18(14-21-17)11-15-7-3-1-4-8-15/h1-10H,11-14H2

HIDE SMILES / InChI

Molecular Formula C17H18N2S2
Molecular Weight 314.468
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulbentine has a broad spectrum effect and is used especially in dermatomycoses treatment in the treatment of various forms.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Evaluation of fungicidal action in vitro and in a skin model considering the influence of penetration kinetics of various standard antimycotics.
1988
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Topical
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:53:44 UTC 2023
Edited
by admin
on Sat Dec 16 16:53:44 UTC 2023
Record UNII
D0NR12WK9J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULBENTINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
D-47
Code English
SULBENTINE [MART.]
Common Name English
NSC-150555
Code English
3,5-DIBENZYLTETRAHYDRO-2H-1,3,5-THIADIAZINE-2-THIONE
Systematic Name English
TETRAHYDRO-3,5-BIS(PHENYLMETHYL)-2H-1,3,5-THIADIAZINE-2-THIONE
Systematic Name English
SULBENTINE [MI]
Common Name English
sulbentine [INN]
Common Name English
DIBENZTHION [JAN]
Common Name English
D 47
Code English
Sulbentine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QD01AE09
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
NCI_THESAURUS C514
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
WHO-ATC D01AE09
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
Code System Code Type Description
PUBCHEM
67686
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
EVMPD
SUB10678MIG
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
SMS_ID
100000083257
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
DRUG BANK
DB13671
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
WIKIPEDIA
SULBENTINE
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
ECHA (EC/EINECS)
206-497-2
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
MERCK INDEX
m10294
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY Merck Index
NSC
150555
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
ChEMBL
CHEMBL151803
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
FDA UNII
D0NR12WK9J
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
EPA CompTox
DTXSID7046257
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
NCI_THESAURUS
C72964
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
INN
2379
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
DRUG CENTRAL
3557
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
CAS
350-12-9
Created by admin on Sat Dec 16 16:53:44 UTC 2023 , Edited by admin on Sat Dec 16 16:53:44 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY