General
Preferred name
BACITRACIN
Synonyms
bacitracin A ()
Bacilliquin ()
Baciguent ()
NSC-755905 ()
Albac 50 ()
Baciferm 50 ()
Bacitracin, sterile ()
Penitracin ()
Tropitracin ()
E700 ()
Zutracin ()
Bacitracin(non-injectable) ()
Fortracin ()
Bacitracina ()
Parentracin ()
Bacitracinum ()
Baci-Rx ()
Bacitracine ()
Baciim ()
Topitracin ()
Bacitracinum zincum ()
Zinc bacitracin ()
Ziba-RX ()
Bacitracins zinc complex ()
Bacitracins, zinc complex ()
Noptracin ()
Bacifarmin ()
BACITRACIN ZINC ()
Bacitracin A (technical grade) ()
P&D ID
PD009882
CAS
1405-87-4
22601-59-8
Tags
available
drug
natural product
Drug indication
Skin infection
Antibacterial
Drug Status
approved
vet_approved
Max Phase
4.0
First approval
1957
1948
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()] ]]
Description
(extracted from source data)
DESCRIPTION
Bacitracin A is a polypeptide antibacterial with activity against Gram-positive bacteria. It is the major component of bacitracin , a mixture of at least nine closely-related cyclic polypeptides produced by Bacillus licheniformis and Bacillus subtilis.
(GtoPdb)
INDICATION
For the treatment of infants with pneumonia and empyema caused by staphylococci shown to be susceptible to the drug. Also used in ointment form for topical treatment of a variety of localized skin and eye infections, as well as for the prevention of wound infections. Used against gram positive bacteria. Bacitracin is also used as an inhibitor of proteases and other enzymes. ; However, specific activity of bactracin's inhibition of protein disulfide isomerase has been called into question.
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
10
Cayman Chemical Bioactives
ChEMBL Approved Drugs
ChEMBL Drugs
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Guide to Pharmacology
LSP-MoA library (Laboratory of Systems Pharmacology)
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
42
Molecular Weight
1421.75
Hydrogen Bond Acceptors
19
Hydrogen Bond Donors
17
Rotatable Bonds
31
Ring Count
4
Aromatic Ring Count
2
cLogP
-1.68
TPSA
530.87
Fraction CSP3
0.64
Chiral centers
15.0
Largest ring
25.0
QED
0.04
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Indication
first-aid antibiotic
Target
IDE
MOA
bacterial cell wall synthesis inhibitor
Therapeutic Class
Antibiotics
Source data
