General
Preferred name
MEROPENEM
Synonyms
SM 7338 ()
Meropenem Trihydrate ()
MEROPENEM ANHYDROUS ()
SM 7338 trihydrate ()
Meropenem (trihydrate) ()
(4R,5S,6S)-3-{[(3S,5S)-5-(dimethylcarbamoyl)pyrrolidin-3-yl]sulfanyl}-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid trihydrate ()
ICI 194,660 ()
SM-7338 ()
Merrem i.v. ()
Merrem ()
Meropenem trihydrate ()
Meropenem hydrate ()
NSC-759621 ()
Meropenem (as trihydrate) ()
ICI-194660 ()
Merrem iv ()
Meropenem, anhydrous ()
Meronem ()
Meropenem (hydrate) ()
Meropenem-d6 ()
P&D ID
PD003103
CAS
96036-03-2
119478-56-7
1133424-00-6
Tags
available
drug
covalent binder
Approved by
FDA
First approval
1996
Drug indication
Antibacterial
Bacterial infection
Drug Status
approved
investigational
Max Phase
4.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
Meropenem is a parenterally delivered, broad-spectrum carbapenem antibacterial. It is active against Gram-positive and Gram-negative bacteria, and is effective against aerobic and anaerobic pathogens including Klebsiella, E. coli, Enterococcus, Clostridium spp.
(GtoPdb)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
0
Organisms
5
Compound Sets
23
ChEMBL Approved Drugs
ChEMBL Drugs
CovBinderInPDB
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine BioReference Compounds
EU-OPENSCREEN Bioactive Compound Library
Guide to Pharmacology
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
NPC Screening Collection
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
68
Molecular Weight
383.15
Hydrogen Bond Acceptors
6
Hydrogen Bond Donors
3
Rotatable Bonds
5
Ring Count
3
Aromatic Ring Count
0
cLogP
-0.31
TPSA
110.18
Fraction CSP3
0.71
Chiral centers
6.0
Largest ring
5.0
QED
0.56
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Pathway
Microbiology&virology
Anti-infection
Target
??-Lactamase
D-alanyl-D-alanine carboxypeptidase DacB
¦Â-Lactamase
antibiotic
Bacterial
Penicillin-binding protein (PBP)
MOA
Antibiotic agonist
bacterial cell wall synthesis inhibitor
Indication
skin infections, intra-abdominal infections, meningitis
Therapeutic Class
Antibiotics
Source data