General
Preferred name
TOFOGLIFLOZIN
Synonyms
CSG-452 hydrate ()
TOFOGLIFLOZIN HYDRATE ()
Tofogliflozin (hydrate) ()
Tofogliflozin(CSG 452) ()
R-7201 ()
RO4998452 ()
CSG-452 ()
RO-4998452 ()
TOFOGLIFLOZIN ANHYDROUS ()
Tofogliflozin monohydrate ()
Tofogliflozin hydrate ()
Tofogliflozina ()
Tofogliflozine ()
CSG452 ()
Tofogliflozin ()
P&D ID
PD071921
CAS
1201913-82-7
903565-83-3
Tags
available
drug
Approved by
PMDA
First approval
2014
Drug Status
approved
investigational
Max Phase
4.0
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION Tofogliflozin is a selective sodium/glucose cotransporter 2 (SGLT2; SLC5A2) inhibitor (a 'gliflozin' family drug ) developed as a treatment for type 2 diabetes. We show the anhydrous structure as represented in the INN record for tofogliflozin. In practice the drug is administered as the monohydrate (PubChem CID 46908928).
Tofogliflozin has favourable oral bioavailability and pharmacokinetic profile . (GtoPdb)
Compound Sets
14
Cayman Chemical Bioactives
ChEMBL Approved Drugs
Drug Repurposing Hub
DrugBank
DrugCentral
DrugCentral Approved Drugs
EU-OPENSCREEN Bioactive Compound Library
Guide to Pharmacology
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
External IDs
38
Properties
(calculated by RDKit )
Molecular Weight
386.17
Hydrogen Bond Acceptors
6
Hydrogen Bond Donors
4
Rotatable Bonds
4
Ring Count
4
Aromatic Ring Count
2
cLogP
1.0
TPSA
99.38
Fraction CSP3
0.45
Chiral centers
5.0
Largest ring
6.0
QED
0.63
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Pathway
GPCR/G protein
Immunology/Inflammation
NF-¦ÊB
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
NF-κB
Target
SGLT2
ROS
GCK
Reactive Oxygen Species
SGLT
Indication
diabetes mellitus
MOA
sodium/glucose cotransporter inhibitor
Source data