Details
Stereochemistry | RACEMIC |
Molecular Formula | C15H14F3N3O4S2 |
Molecular Weight | 421.415 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NS(=O)(=O)C1=CC2=C(NC(CC3=CC=CC=C3)NS2(=O)=O)C=C1C(F)(F)F
InChI
InChIKey=HDWIHXWEUNVBIY-UHFFFAOYSA-N
InChI=1S/C15H14F3N3O4S2/c16-15(17,18)10-7-11-13(8-12(10)26(19,22)23)27(24,25)21-14(20-11)6-9-4-2-1-3-5-9/h1-5,7-8,14,20-21H,6H2,(H2,19,22,23)
Molecular Formula | C15H14F3N3O4S2 |
Molecular Weight | 421.415 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:51:15 UTC 2023
by
admin
on
Sat Dec 16 17:51:15 UTC 2023
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Record UNII |
5Q52X6ICJI
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NDF-RT |
N0000175359
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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NCI_THESAURUS |
C49185
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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WHO-VATC |
QC03EA13
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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NDF-RT |
N0000166469
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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WHO-ATC |
C03EA13
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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NDF-RT |
N0000175419
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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NDF-RT |
N0000166469
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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LIVERTOX |
95
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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WHO-VATC |
QC03AA01
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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WHO-ATC |
C03AA01
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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WHO-VATC |
QC03AB01
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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WHO-ATC |
C03AB01
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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Code System | Code | Type | Description | ||
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7122
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PRIMARY | |||
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73-48-3
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PRIMARY | |||
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3293
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5Q52X6ICJI
Created by
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PRIMARY | |||
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994
Created by
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PRIMARY | |||
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C47410
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100000092763
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200-800-1
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SUB20550
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CHEMBL1684
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59243
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DB00436
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m2309
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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PRIMARY | Merck Index | ||
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1049000
Created by
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2315
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D001539
Created by
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BENDROFLUMETHIAZIDE
Created by
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PRIMARY | |||
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SUB05711MIG
Created by
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1369
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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PRIMARY | RxNorm | ||
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3013
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305
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PRIMARY | |||
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Bendroflumethiazide
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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DTXSID5022647
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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PRIMARY | |||
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758229
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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5Q52X6ICJI
Created by
admin on Sat Dec 16 17:51:16 UTC 2023 , Edited by admin on Sat Dec 16 17:51:16 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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TARGET -> INHIBITOR |
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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BINDER->LIGAND |
BINDING
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Related Record | Type | Details | ||
---|---|---|---|---|
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Biological Half-life | PHARMACOKINETIC |
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