General
Preferred name
DFMO
Synonyms
DL-alpha-Difluoromethylornithine hydrochloride ()
¦Á-difluoromethylornithine hydrochloride ()
??-difluoromethylornithine hydrochloride ()
Eflornithine (hydrochloride) ()
DFMO hydrochloride ()
MDL71782 hydrochloride ()
RMI71782 hydrochloride ()
α-difluoromethylornithine hydrochloride ()
EFLORNITHINE HYDROCHLORIDE ()
P&D ID
PD015380
CAS
68278-23-9
96020-91-6
Tags
available
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
Eflornithine hydrochloride is a specific, irreversible inhibitor of the enzyme ornithine decarboxylase. Eflornithine is a medication for the treatment of African trypanosomiasis and excessive facial hair growth in women.
DESCRIPTION
Selective irreversible ornithine decarboxylase (ODC) inhibitor.
(LOPAC library)
DESCRIPTION
Eflornithine hydrochloride is a drug found to be effective in the treatment of facial hirsutism. It is a "suicide inhibitor," irreversibly binding to Ornithine Decarboxylase (ODC) and preventing the natural substrate ornithine from accessing the active site.
(BOC Sciences Bioactive Compounds)
DESCRIPTION
IGF1R inhibitor
(Tocris Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
4
BOC Sciences Bioactive Compounds
LOPAC library
MedChem Express Bioactive Compound Library
Tocris Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
16
Molecular Weight
218.06
Hydrogen Bond Acceptors
3
Hydrogen Bond Donors
3
Rotatable Bonds
5
Ring Count
0
Aromatic Ring Count
0
cLogP
0.19
TPSA
89.34
Fraction CSP3
0.83
Chiral centers
1.0
Largest ring
0.0
QED
0.61
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Selectivity
ODC
Primary Target
Decarboxylases
MOA
Inhibitor
Target
Parasite
Pathway
Anti-infection
Source data

