General
Preferred name
PENICILLIN V POTASSIUM
Synonyms
Phenoxymethylpenicillin potassium salt ()
Penicillin V potassium salt ()
Penicillin V (Potassium) ()
Phenoxymethylpenicillin (potassium salt) ()
Ledercillin Vk ()
Phenoxymethylpenicillinum kalicum ()
Uticillin Vk ()
Antibiocin ()
V-Cillin-K ()
Beepen-Vk ()
Pfizerpen Vk ()
Veetids '500' ()
V-Cillin K ()
Penicillin Potassium Phenoxymethyl ()
Penapar-Vk ()
Vamosyn ()
Penicillin-Vk ()
Phenoxymethylpenicillin K ()
Pen-Vee K ()
Betapen-Vk ()
Penicillin Vk ()
Veetids ()
Potassium penicillin v ()
Primcillin ()
Veetids '125' ()
NSC-757258 ()
Phenoxymethylpenicillin Potassium ()
Beepen VK ()
Veetids '250' ()
Penicillin V (potassium salt) ()
P&D ID
PD001811
CAS
132-98-9
87-08-1
Tags
natural product
drug
available
Drug indication
Bacterial infection
Antibacterial
Drug Status
approved
Max Phase
Phase 4
First approval
1958
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure
P&D probe-likeness score
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
9
Cayman Chemical Bioactives
ChEMBL Approved Drugs
ChEMBL Drugs
DrugMAP
DrugMAP Approved Drugs
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
18
Properties
(calculated by RDKit )
Molecular Weight
388.05
Hydrogen Bond Acceptors
6
Hydrogen Bond Donors
1
Rotatable Bonds
5
Ring Count
3
Aromatic Ring Count
1
cLogP
-3.63
TPSA
98.77
Fraction CSP3
0.44
Chiral centers
3.0
Largest ring
6.0
QED
0.41
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Pathway
Microbiology&virology
Anti-infection
Target
antibiotic
Bacterial
Antibiotics,Bacterial
MOA
Antibiotic
Therapeutic Class
Antiinfective Agents
Source data
