Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C9H16N4O7S |
| Molecular Weight | 324.311 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCONC(=O)[C@@H]1CC[C@@H]2C[N@]1C(=O)N2OS(O)(=O)=O
InChI
InChIKey=RSBPYSTVZQAADE-RQJHMYQMSA-N
InChI=1S/C9H16N4O7S/c10-3-4-19-11-8(14)7-2-1-6-5-12(7)9(15)13(6)20-21(16,17)18/h6-7H,1-5,10H2,(H,11,14)(H,16,17,18)/t6-,7+/m1/s1
| Molecular Formula | C9H16N4O7S |
| Molecular Weight | 324.311 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:38:16 UTC 2023
by
admin
on
Sat Dec 16 11:38:16 UTC 2023
|
| Record UNII |
832O37V7MZ
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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| Code System | Code | Type | Description | ||
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1452458-86-4
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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73386748
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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832O37V7MZ
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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EF-79
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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DB15353
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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100000174644
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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10300
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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C175153
Created by
admin on Sat Dec 16 11:38:16 UTC 2023 , Edited by admin on Sat Dec 16 11:38:16 UTC 2023
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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SOLVATE->ANHYDROUS |
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SALT/SOLVATE -> PARENT |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
A diazabicyclooctane beta-lactamase inhibitor, for treating bacterial infection. In July 2016, nacubactam was reported to be in phase 1 clinical development.
Sulfuric acid, mono((1R,2S,5R)-2-(((2-aminoethoxy)amino)carbonyl)-7-oxo-1,6-diazabicyclo(3.2.1)oct-6-yl) ester
A .BETA.-lactamase inhibitor potentially for the treatment of bacterial infections.
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