Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C24H23NO5S |
| Molecular Weight | 437.508 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CO[C@@H](CC1=C2SC=CC2=C(OCCC3=C(C)OC(=N3)C4=CC=CC=C4)C=C1)C(O)=O
InChI
InChIKey=DAYKLWSKQJBGCS-NRFANRHFSA-N
InChI=1S/C24H23NO5S/c1-15-19(25-23(30-15)16-6-4-3-5-7-16)10-12-29-20-9-8-17(14-21(28-2)24(26)27)22-18(20)11-13-31-22/h3-9,11,13,21H,10,12,14H2,1-2H3,(H,26,27)/t21-/m0/s1
| Molecular Formula | C24H23NO5S |
| Molecular Weight | 437.508 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Aleglitazar is a dual agonist of PPARalpha/PPARgamma which was developed by Hoffmann-La Roche for the treatment of type 2 diabetes. Aleglitazar activates PPAR receptors with EC50 in nanomolar range and exerts a cardioprotective effect in vitro. The drug is currently in phase III of clinical trials.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19349176
Curator's Comment: # Hoffmann-La Roche Ltd
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL239 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19349176 |
5.0 nM [EC50] | ||
Target ID: CHEMBL235 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19349176 |
9.0 nM [EC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.1 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
20 μg 1 times / day steady-state, oral dose: 20 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
3.05 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
50 μg 1 times / day steady-state, oral dose: 50 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
28.9 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
600 μg 1 times / day steady-state, oral dose: 600 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
5.91 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
100 μg 1 times / day steady-state, oral dose: 100 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
16.8 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
300 μg 1 times / day steady-state, oral dose: 300 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
49.2 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
900 μg 1 times / day steady-state, oral dose: 900 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
8.66 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
20 μg 1 times / day steady-state, oral dose: 20 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
26 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
50 μg 1 times / day steady-state, oral dose: 50 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
204 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
600 μg 1 times / day steady-state, oral dose: 600 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
41.8 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
100 μg 1 times / day steady-state, oral dose: 100 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
141 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
300 μg 1 times / day steady-state, oral dose: 300 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
402 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
900 μg 1 times / day steady-state, oral dose: 900 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
6.04 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
20 μg 1 times / day steady-state, oral dose: 20 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
7.77 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
50 μg 1 times / day steady-state, oral dose: 50 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
13.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
600 μg 1 times / day steady-state, oral dose: 600 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
8.2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
100 μg 1 times / day steady-state, oral dose: 100 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
11.9 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
300 μg 1 times / day steady-state, oral dose: 300 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
16.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20336066/ |
900 μg 1 times / day steady-state, oral dose: 900 μg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALEGLITAZAR plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Gateways to clinical trials. | 2010-11 |
|
| Aleglitazar, a dual PPARα and PPARγ agonist for the potential oral treatment of type 2 diabetes mellitus. | 2010-11 |
|
| Transcriptional regulation of human and rat hepatic lipid metabolism by the grapefruit flavonoid naringenin: role of PPARalpha, PPARgamma and LXRalpha. | 2010-08-25 |
|
| Pharmacokinetics, pharmacodynamics, and tolerability of aleglitazar in patients with type 2 diabetes: results from a randomized, placebo-controlled clinical study. | 2010-08 |
|
| Neuropathy, retinopathy, and glucose-lowering treatments. | 2010-06 |
|
| Therapeutic potential of aleglitazar, a new dual PPAR-α/γ agonist: implications for cardiovascular disease in patients with diabetes mellitus. | 2010 |
|
| A cardiologic approach to non-insulin antidiabetic pharmacotherapy in patients with heart disease. | 2009-07-20 |
|
| Effect of the dual peroxisome proliferator-activated receptor-alpha/gamma agonist aleglitazar on risk of cardiovascular disease in patients with type 2 diabetes (SYNCHRONY): a phase II, randomised, dose-ranging study. | 2009-07-11 |
|
| PPAR-alpha and PPAR-gamma agonists for type 2 diabetes. | 2009-07-11 |
|
| Aleglitazar, a new, potent, and balanced dual PPARalpha/gamma agonist for the treatment of type II diabetes. | 2009-05-01 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01871428
Patients receive 150 mcg orally daily.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26861490
Aleglitazar increased cell viability and reduced apoptosis in human cardiomyocytes at concentrations of 150-600 nM.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 07:45:57 GMT 2025
by
admin
on
Wed Apr 02 07:45:57 GMT 2025
|
| Record UNII |
41T4OAG59U
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C98233
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DB08915
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
41T4OAG59U
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
TT-44
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
CHEMBL519504
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
ALEGLITAZAR
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
10274777
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
475479-34-6
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
8736
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
SUB34897
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
C72687
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
DTXSID70197193
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
m1491
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | Merck Index | ||
|
100000128143
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY | |||
|
C542437
Created by
admin on Wed Apr 02 07:45:57 GMT 2025 , Edited by admin on Wed Apr 02 07:45:57 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TARGET -> AGONIST |
|
||
|
TARGET -> AGONIST |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|