General
Preferred name
RILUZOLE
Synonyms
2-Amino-6-trifluoromethoxybenzothiazole ()
Riluzole hydrochloride ()
PK 26124 ()
RP-54274 ()
Riluzole (Rilutek) ()
PK 26124 hydrochloride ()
Riluzole (PK 26124) ()
RP-54274, PK 26124 ()
Teglutik ()
Exservan ()
Tiglutik ()
NSC-753433 ()
Riluzole zentiva ()
Riluzol ()
RP 54274 ()
Rilutek ()
NSC-759823 ()
BHV-0223 ()
Tiglutik kit ()
Riluzole (hydrochloride) ()
Riluzole-13C,15N2 ()
P&D ID
PD000919
CAS
850608-87-6
1744-22-5
1215552-03-6
Tags
available
drug
Approved by
FDA
First approval
1995
Drug indication
Amyotrophic Lateral Sclerosis Treatment
Amyotrophic lateral sclerosis
Drug Status
approved
investigational
Max Phase
4.0
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
Marketed formulations may contain riluzole hydrochloride (PubChem CID 6419992).
(GtoPdb)
DESCRIPTION
Glutamate release inhibitor; anticonvulsant
(LOPAC library)
DESCRIPTION
Glutamate release inhibitor/GABA uptake inhibitor
(Tocriscreen Total)
DESCRIPTION
Anti-ischemic and antioxidant
(Tocris Bioactive Compound Library)
DESCRIPTION
Riluzole, a benzothiazole derivative with anti-excitotoxic effects, is a glutamate release inhibitor, and also induces caspase-dependent apoptosis and suppress cell proliferation in human heptocellular carcinoma.
(BOC Sciences Bioactive Compounds)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
1
Organisms
2
Compound Sets
36
AdooQ Bioactive Compound Library
BOC Sciences Bioactive Compounds
CeMM library of unique drugs (CLOUD)
ChEMBL Approved Drugs
ChEMBL Drugs
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Concise Guide to Pharmacology 2021/22
Concise Guide to Pharmacology 2023/24
CZ-OPENSCREEN Bioactive Library
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
DrugMatrix
Enamine BioReference Compounds
Guide to Pharmacology
LOPAC library
LSP-MoA library (Laboratory of Systems Pharmacology)
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
Tocris Bioactive Compound Library
Tocriscreen Total
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
59
Molecular Weight
234.01
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
1
Rotatable Bonds
1
Ring Count
2
Aromatic Ring Count
2
cLogP
2.78
TPSA
48.14
Fraction CSP3
0.12
Chiral centers
0.0
Largest ring
6.0
QED
0.82
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Selectivity
Release
MOA
Unknown molecular target
Inhibitor
Glutamate Release Inhibitors
K(V)4.3 Channel Blockers
Sodium Channel Blockers
Cystine Glutamate Transporter Inducer
glutamate inhibitor
Target
Sodium channel alpha subunit
NMDA Receptor
Sodium Channel
GABA
KCNK10, KCNK2, KCNK4, KCNN4, SCN10A, SCN11A, SCN1A, SCN2A, SCN3A, SCN4A, SCN5A, SCN7A, SCN8A, SCN9A, SLC7A11
GABA Receptor
GluR,Sodium Channel
Pathway
Membrane Transporter/Ion Channel
Neuroscience
Neuronal Signaling
Primary Target
GABA Transporters
Member status
member
Indication
amyotrophic lateral sclerosis (ALS)
Therapeutic Class
Anticonvulsants
VGSC Target
Nav1.2
Source data