General
Preferred name
AMPICILLIN
Synonyms
AMPICILLIN SODIUM ()
D-(-)-¦Á-Aminobenzylpenicillin ()
D-(-)-??-Aminobenzylpenicillin sodium salt ()
Domicillin ()
Citteral ()
Penialmen ()
NCI-C56086 ()
AMPICILLIN TRIHYDRATE ()
Ampicillin acid ()
D-(-)-??-Aminobenzylpenicillin ()
D-(-)-¦Á-Aminobenzylpenicillin (trihydrate) ()
Ampicillin (sodium) ()
Ampicillin (trihydrate) ()
D-(-)-α-Aminobenzylpenicillin ()
D-(-)-α-Aminobenzylpenicillin (sodium salt) ()
D-(-)-α-Aminobenzylpenicillin (trihydrate) ()
D-(-)-¦Á-Aminobenzylpenicillin sodium salt ()
NCI-C56086,D-(-)-¦Á-Aminobenzylpenicillin trihydrate ()
Penbritin ()
Principen-N ()
Ampicillin (as sodium) ()
Omnipen ()
Totacillin ()
Ampicillin sodium salt ()
Principen ()
Polycillin ()
Totacillin-N ()
Amp Equine ()
Omnipen-N ()
Polycillin-N ()
Penbritin-S ()
NSC-755864 ()
Ampicillinum natricum ()
Ampicillin sodium, sterile ()
Ampicillin/Ampicillin Trihydrate ()
Ampicillin/ampicillin monohydrate ()
BRL-1341 ()
Ampicillin trihydrate ()
Pfizerpen-A ()
Anhydrous ampicillin ()
Tokiocillin ()
Semicillin ()
NSC-528986 ()
Aminobenzylpenicillin trihydrate ()
Polycillin-Prb ()
Probampacin ()
Ultrabion ()
Ampicillin (anhydrous) ()
Principen '250' ()
Ampicillin hydrate ()
Aminobenzylpenicillin ()
Ampicillinum ()
Principen '500' ()
Ampilar ()
Alpha-Aminobenzylpenicillin ()
Ampicillin anhydrous ()
Britcin ()
Poly-cillin ()
Ampicillin, anhydrous ()
Redicilin ()
P-50 ()
Amfipen ()
AY-6108 ()
Amcill ()
Omnipen (ampicillin) ()
Principen '125' ()
Vidopen ()
WY 5103 ()
Ampicillin (sodium salt) ()
Ampicillin (hydrate) ()
P&D ID
PD010040
CAS
69-52-3
69-53-4
7177-48-2
33604-21-6
Tags
covalent binder
natural product
drug
available
Approved by
FDA
First approval
1971
1965
Drug Status
approved
vet_approved
Drug indication
Bacterial infection
Antibacterial
Max Phase
Phase 4
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
Ampicillin is a broad-spectrum, semi-synthetic, β-lactam penicillin class antibacterial. It is resistant to hydrolysis by a variety of β-lactamases, so can be to treat a diverse range of infections caused by Gram-positive and Gram-negative infections.
(GtoPdb)
DESCRIPTION
Ampicillin is a beta-lactam antibiotic that is a part of the aminopenicillin family. It is mainly used for infections and sepsis of the lungs, intestines, biliary tract, urinary tract caused by sensitive bacteria.
(BOC Sciences Bioactive Compounds)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
0
Organisms
10
Compound Sets
22
BOC Sciences Bioactive Compounds
ChEMBL Approved Drugs
ChEMBL Drugs
CovBinderInPDB
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine BioReference Compounds
Guide to Pharmacology
NCATS Inxight Approved Drugs
NPC Screening Collection
Other bioactive compounds
Prestwick Chemical Library
Selleckchem Bioactive Compound Library
The Spectrum Collection
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
91
Properties
(calculated by RDKit )
Molecular Weight
349.11
Hydrogen Bond Acceptors
5
Hydrogen Bond Donors
3
Rotatable Bonds
4
Ring Count
3
Aromatic Ring Count
1
cLogP
0.32
TPSA
112.73
Fraction CSP3
0.44
Chiral centers
4.0
Largest ring
6.0
QED
0.67
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Pathway
Microbiology&virology
Anti-infection
Target
??-Lactamase
antibiotic
Bacterial
Antibiotics,Antibiotics for Mammalian Cell Culture,Selection Antibiotics for Transfected Cell
Antibiotics,Antibiotics for Mammalian Cell Culture,Bacterial
Indication
respiratory tract infections, meningitis, bacterial septicemia, endocarditis, urinary tract infections, gastrointestinal infections
MOA
bacterial cell wall synthesis inhibitor
Therapeutic Class
Antibiotics
Solubility
Slightly soluble in Aqueous Acid, DMSO
Freely soluble in water
Sparingly soluble in acetone
Source data