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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H20N4O6S.H2O
Molecular Weight 366.391
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RELEBACTAM

SMILES

O.OS(=O)(=O)ON1[C@H]2C[N@]([C@@H](CC2)C(=O)NC3CCNCC3)C1=O

InChI

InChIKey=TWFRCSHLWKJBQH-UXQCFNEQSA-N
InChI=1S/C12H20N4O6S.H2O/c17-11(14-8-3-5-13-6-4-8)10-2-1-9-7-15(10)12(18)16(9)22-23(19,20)21;/h8-10,13H,1-7H2,(H,14,17)(H,19,20,21);1H2/t9-,10+;/m1./s1

HIDE SMILES / InChI

Molecular Formula C12H20N4O6S
Molecular Weight 348.375
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:54:44 UTC 2023
Edited
by admin
on Sat Dec 16 10:54:44 UTC 2023
Record UNII
Y1MYA2UHFL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RELEBACTAM
USAN  
USAN  
Official Name English
RELEBACTAM MONOHYDRATE
WHO-DD  
Preferred Name English
RELEBACTAM [ORANGE BOOK]
Common Name English
RECARBRIO COMPONENT RELEBACTAM MONOHYDRATE
Brand Name English
RELEBACTAM [USAN]
Common Name English
RELEBACTAM HYDRATE [JAN]
Common Name English
RECARBRIO COMPONENT RELEBACTAM
Brand Name English
(-)-RELEBACTAM MONOHYDRATE
Common Name English
SULFURIC ACID, MONO((1R,2S,5R)-7-OXO-2-((4-PIPERIDINYLAMINO)CARBONYL)-1,6-DIAZABICYCLO(3.2.1)OCT-6-YL) ESTER, HYDRATE (1:1)
Systematic Name English
Relebactam monohydrate [WHO-DD]
Common Name English
RELEBACTAM COMPONENT OF RECARBRIO
Brand Name English
MK-7655A COMPONENT RELEBACTAM
Code English
MK-7655 MONOHYDRATE
Code English
RELEBACTAM MONOHYDRATE COMPONENT OF RECARBRIO
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C258
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
Code System Code Type Description
SMS_ID
100000179908
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
EVMPD
SUB194532
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
DRUG CENTRAL
5342
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
RXCUI
2184137
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
CAS
1174020-13-3
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
USAN
BC-74
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
RXCUI
2184136
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
ALTERNATIVE
DRUG BANK
DB12377
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
FDA UNII
Y1MYA2UHFL
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
PUBCHEM
76900350
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
NCI_THESAURUS
C152176
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
ChEMBL
CHEMBL3112741
Created by admin on Sat Dec 16 10:54:44 UTC 2023 , Edited by admin on Sat Dec 16 10:54:44 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY