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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H25N3O5S.3H2O
Molecular Weight 437.508
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEROPENEM

SMILES

O.O.O.[H][C@]12[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C(=O)N(C)C)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C(O)=O

InChI

InChIKey=CTUAQTBUVLKNDJ-OBZXMJSBSA-N
InChI=1S/C17H25N3O5S.3H2O/c1-7-12-11(8(2)21)16(23)20(12)13(17(24)25)14(7)26-9-5-10(18-6-9)15(22)19(3)4;;;/h7-12,18,21H,5-6H2,1-4H3,(H,24,25);3*1H2/t7-,8-,9+,10+,11-,12-;;;/m1.../s1

HIDE SMILES / InChI

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

Molecular Formula C17H25N3O5S
Molecular Weight 383.463
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:16:00 UTC 2023
Edited
by admin
on Fri Dec 15 16:16:00 UTC 2023
Record UNII
FV9J3JU8B1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEROPENEM
MART.   ORANGE BOOK   USAN   USP   USP-RS   VANDF  
USAN  
Official Name English
ICI 194,660
Code English
MERREM I.V.
Brand Name English
MERONEM
Brand Name English
MEROPENEM [USAN]
Common Name English
MEROPENEM TRIHYDRATE
EP   MI   WHO-DD  
Common Name English
NSC-759621
Code English
Meropenem trihydrate [WHO-DD]
Common Name English
MEROPENEM HYDRATE [JAN]
Common Name English
MEROPENEM [VANDF]
Common Name English
(4R,5S,6S)-3-[[(3S,5S)-5-(Dimethylcarbamoyl)-3-pyrrolidinyl]thio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid, trihydrate
Common Name English
MEROPENEM HYDRATE
JAN  
Common Name English
MEROPENEM [USP-RS]
Common Name English
MEROPENEM (AS TRIHYDRATE)
Common Name English
MEROPENEM [USP MONOGRAPH]
Common Name English
MEROPENEM TRIHYDRATE [MI]
Common Name English
MEROPENEM [MART.]
Common Name English
SM-7338
Code English
MERREM
Brand Name English
MEROPENEM TRIHYDRATE [EP MONOGRAPH]
Common Name English
MEROPENEM [ORANGE BOOK]
Common Name English
VABOMERE COMPONENT MEROPENEM
Brand Name English
MEROPENEM COMPONENT OF CARBAVANCE
Brand Name English
1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID, 3-((5-((DIMETHYLAMINO)CARBONYL)-3-PYRROLIDINYL)THIO)-6-(1-HYDROXYETHYL)-4-METHYL-7-OXO-, TRIHYDRATE, (4R-(3(3S*,5S*),4.ALPHA.,5.BETA.,6.BETA.(R*)))-
Common Name English
ICI-194660
Code English
MEROPENEM [USP IMPURITY]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ01DH02
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
NCI_THESAURUS C260
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
NDF-RT N0000175496
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
WHO-ATC J01DH02
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
WHO-ATC J01DH52
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
FDA ORPHAN DRUG 130799
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
LIVERTOX NBK547861
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
Code System Code Type Description
PUBCHEM
441129
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
DRUG BANK
DB00760
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
WIKIPEDIA
MEROPENEM
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
LACTMED
Meropenem
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
ChEMBL
CHEMBL127
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
USAN
BB-52
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
FDA UNII
FV9J3JU8B1
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
RS_ITEM_NUM
1392454
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
MERCK INDEX
m7240
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY Merck Index
EVMPD
SUB21617
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
EPA CompTox
DTXSID10274179
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
MESH
C059500
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
DAILYMED
FV9J3JU8B1
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
NSC
759621
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
CHEBI
6770
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
DRUG CENTRAL
1709
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
SMS_ID
100000085626
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
RXCUI
29561
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY RxNorm
CHEBI
43968
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
NCI_THESAURUS
C1160
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
CAS
119478-56-7
Created by admin on Fri Dec 15 16:16:01 UTC 2023 , Edited by admin on Fri Dec 15 16:16:01 UTC 2023
PRIMARY
Related Record Type Details
BINDER->LIGAND
BINDING
TRANSPORTER -> SUBSTRATE
ANHYDROUS->SOLVATE
EXCRETED UNCHANGED
Meropenem: approximately 40–60% of dose was excreted unchanged within 24 to 48 hours with a further 28% recovered as the microbiologically inactive hydrolysis product; fecal elimination accounts for ~2% of dose.
PARENT -> SALT/SOLVATE
TRANSPORTER -> SUBSTRATE
Related Record Type Details
IMPURITY -> PARENT
correction factor: for the calculation of content, multiply the peak area of impurity A by 1.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC