Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H11ClF3N3O4S3 |
Molecular Weight | 425.855 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NS(=O)(=O)C1=C(Cl)C=C2NC(CSCC(F)(F)F)NS(=O)(=O)C2=C1
InChI
InChIKey=RINBGYCKMGDWPY-UHFFFAOYSA-N
InChI=1S/C10H11ClF3N3O4S3/c11-5-1-6-8(2-7(5)23(15,18)19)24(20,21)17-9(16-6)3-22-4-10(12,13)14/h1-2,9,16-17H,3-4H2,(H2,15,18,19)
Molecular Formula | C10H11ClF3N3O4S3 |
Molecular Weight | 425.855 |
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
Fri Dec 15 18:47:50 GMT 2023
by
admin
on
Fri Dec 15 18:47:50 GMT 2023
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Record UNII |
5B266B85J1
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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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WHO-ATC |
C03EA03
Created by
admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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NCI_THESAURUS |
C49185
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admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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WHO-VATC |
QC03EA03
Created by
admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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Code System | Code | Type | Description | ||
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1764-85-8
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CHEMBL2104605
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15671
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m163
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admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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PRIMARY | Merck Index | ||
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108164
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1031
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1379
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96782-87-5
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admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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SUPERSEDED | |||
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DB13989
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C77141
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EPITIZIDE
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DTXSID50862751
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admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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5B266B85J1
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217-181-9
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admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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100000080475
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admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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SUB06573MIG
Created by
admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |