General
Preferred name
TESAGLITAZAR
Synonyms
AZ 242 ()
Galida ()
AR-H-039242 ()
AR-H039242XX ()
AZ-242 ()
BR-44608 ()
P&D ID
PD014363
CAS
251565-85-2
Tags
available
drug candidate
Drug indication
Type-1 diabetes
Drug Status
investigational
Max Phase
Phase 3
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 PPARalpha/gamma agonist (Tocriscreen Plus)
DESCRIPTION Estrogen receptor ligand; mycotoxin (Tocris Bioactive Compound Library)
DESCRIPTION Tesaglitazar is a dual-acting agonist of PPARα/γ (IC50 = 0.35 and 3.8 μM for PPARγ and PPARα, respectively). It reduces insulin resistance in obese Zucker rats that has the potential for the treatment of type 2 diabetes. Tesaglitazar also prevents atherosclerosis progression in E3L.CETP transgenic mice. (BOC Sciences Bioactive Compounds)
Compound Sets
14
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
ChEMBL Drugs
Drug Repurposing Hub
DrugBank
DrugMAP
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
ReFrame library
Tocris Bioactive Compound Library
Tocriscreen Plus
External IDs
28
Properties
(calculated by RDKit )
Molecular Weight
408.12
Hydrogen Bond Acceptors
6
Hydrogen Bond Donors
1
Rotatable Bonds
11
Ring Count
2
Aromatic Ring Count
2
cLogP
2.68
TPSA
99.13
Fraction CSP3
0.35
Chiral centers
1.0
Largest ring
6.0
QED
0.57
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target Type
Nuclear Receptors
Primary Target
Non-selective PPAR
MOA
Agonist
Insulin Sensitizers
PPARalpha Agonists
PPARgamma Agonists
insulin sensitizer, PPAR receptor agonist
Member status
member
Target
PPARA, PPARG
PPAR
Pathway
Cell Cycle/DNA Damage
Vitamin D Related/Nuclear Receptor
Source data