General
Preferred name
PIPERACILLIN
Synonyms
Piperacillin sodium salt ()
PIPERACILLIN ANHYDROUS ()
PIPERACILLIN SODIUM ()
(2S,5R,6R)-6-[(2R)-2-[(4-ethyl-2,3-dioxopiperazine-1-carbonyl)amino]-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid ()
Piperacillin (sodium) ()
Sodium piperacillin ()
Pipracil ()
CL227193,Pipracil ()
Piperacillin (sodium salt) ()
NSC-757277 ()
T-1220 ()
Penmalin ()
CL-227193 ()
CL 227,193 ()
Piperacillin sodium component of zosyn ()
Pipril ()
Piperacillin (as sodium) ()
Peracin ()
Piperacillin, anhydrous ()
Piperacillin monohydrate ()
Piperacilina ()
Piperacilline ()
Piperacillin hydrate ()
Piperacillin ()
Piperacillin-d5 ()
P&D ID
PD010105
CAS
59703-84-3
61477-96-1
Tags
available
covalent binder
drug
Approved by
FDA
First approval
1981
Drug indication
infection
Bacterial infection
Drug Status
approved
Max Phase
4.0
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION Piperacillin sodium is a semisynthetic broad-spectrum ¦Â-lactam antibiotic which exhibits potent bactericidal activity against Gram-negative bacteria as well as select Gram-positive strains through penicillin-binding proteins. Piperacillin is most commonly used in combination with the ¦Â-lactamase inhibitor Tazobactam[1][2][3].
DESCRIPTION Piperacillin is a broad-spectrum semisynthetic, ampicillin-derived antibacterial. (GtoPdb)
DESCRIPTION Piperacillin is a semisynthetic broad-spectrum ¦Â-lactam antibiotic which exhibits potent bactericidal activity against Gram-negative bacteria as well as select Gram-positive strains through penicillin-binding proteins. Piperacillin is most commonly used in combination with the ¦Â-lactamase inhibitor Tazobactam[1][2][3].
DESCRIPTION Piperacillin is a penicillin antibiotic combined with tazobactam to treat piperacillin-resistant, piperacillin/tazobactam­ susceptible, β-lactamase generating strains of several bacteria. (Enamine Bioactive Compounds)
Cell lines
0
Organisms
2
Compound Sets
23
Cayman Chemical Bioactives
ChEMBL Approved Drugs
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine Bioactive Compounds
Enamine BioReference Compounds
EU-OPENSCREEN Bioactive Compound Library
Guide to Pharmacology
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
NPC Screening Collection
Other bioactive compounds
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
External IDs
75
Properties
(calculated by RDKit )
Molecular Weight
517.16
Hydrogen Bond Acceptors
7
Hydrogen Bond Donors
3
Rotatable Bonds
6
Ring Count
4
Aromatic Ring Count
1
cLogP
-0.24
TPSA
156.43
Fraction CSP3
0.48
Chiral centers
4.0
Largest ring
6.0
QED
0.34
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Indication
intra-abdominal infections, skin infections, pelvic inflammatory disease, pneumonia
MOA
bacterial cell wall synthesis inhibitor
Target
antibiotic
Bacterial
Penicillin-binding protein (PBP)
Beta-lactamase
Therapeutic Class
Antibiotics
Pathway
Anti-infection
Source data