Details
Stereochemistry | ABSOLUTE |
Molecular Formula | 2C29H32O7S.H2O |
Molecular Weight | 1067.266 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O.CC1=CC(OCCCS(C)(=O)=O)=CC(C)=C1C2=CC(COC3=CC=C4[C@H](CC(O)=O)COC4=C3)=CC=C2.CC5=CC(OCCCS(C)(=O)=O)=CC(C)=C5C6=CC(COC7=CC=C8[C@H](CC(O)=O)COC8=C7)=CC=C6
InChI
InChIKey=OJXYMYYDAVXPIK-IWKNALKQSA-N
InChI=1S/2C29H32O7S.H2O/c2*1-19-12-25(34-10-5-11-37(3,32)33)13-20(2)29(19)22-7-4-6-21(14-22)17-35-24-8-9-26-23(15-28(30)31)18-36-27(26)16-24;/h2*4,6-9,12-14,16,23H,5,10-11,15,17-18H2,1-3H3,(H,30,31);1H2/t2*23-;/m11./s1
Molecular Formula | C29H32O7S |
Molecular Weight | 524.625 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | H2O |
Molecular Weight | 18.0153 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/24900210Curator's Comment: description was created based on several sources, including:
https://www.takeda.com/news/2013/20131227_6117.html | https://www.aasld.org/sites/default/files/documents/DILI/2016/IV_6_Dragan_ppt.pdf | https://www.ncbi.nlm.nih.gov/pubmed/25604916
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24900210
Curator's Comment: description was created based on several sources, including:
https://www.takeda.com/news/2013/20131227_6117.html | https://www.aasld.org/sites/default/files/documents/DILI/2016/IV_6_Dragan_ppt.pdf | https://www.ncbi.nlm.nih.gov/pubmed/25604916
TAK-875 (Fasiglifam) is the potent, selective and orally bioavailable GPR40 agonist. The drug was in Phase III clinical trials for the treatment of type 2 diabetes mellitus. Termination phase III development of TAK-875 for the potential treatment of type-2 diabetes mellitus was announced in 2013 due to concerns about liver safety.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24900210
Curator's Comment: # Takeda Pharmaceutical Company, Ltd.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL4422 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24900210 |
0.038 µM [Ki] | ||
Target ID: CHEMBL1697668 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26276582 |
2.28 µM [IC50] | ||
Target ID: CHEMBL1743121 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26276582 |
3.98 µM [IC50] | ||
Target ID: CHEMBL5748 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26276582 |
2.41 µM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2.3 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
25 mg 1 times / day steady-state, oral dose: 25 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
17.6 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
400 mg single, oral dose: 400 mg route of administration: Oral experiment type: SINGLE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
13 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
100 mg 1 times / day steady-state, oral dose: 100 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
30.8 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
5.5 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
40.3 nmol × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
25 mg 1 times / day steady-state, oral dose: 25 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
13.7 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
230 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
400 mg single, oral dose: 400 mg route of administration: Oral experiment type: SINGLE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
235.5 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
100 mg 1 times / day steady-state, oral dose: 100 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
549.9 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
71.2 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
44.7 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
25 mg 1 times / day steady-state, oral dose: 25 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
45.8 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
100 mg 1 times / day steady-state, oral dose: 100 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
31.5 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22669289 |
400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
FASIGLIFAM HEMIHYDRATE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
PubMed
Title | Date | PubMed |
---|---|---|
Free fatty acids regulate insulin secretion from pancreatic beta cells through GPR40. | 2003 Mar 13 |
|
TAK-875, an orally available G protein-coupled receptor 40/free fatty acid receptor 1 agonist, enhances glucose-dependent insulin secretion and improves both postprandial and fasting hyperglycemia in type 2 diabetic rats. | 2011 Oct |
|
Identification of a potent and selective free fatty acid receptor 1 (FFA1/GPR40) agonist with favorable physicochemical and in vitro ADME properties. | 2011 Oct 13 |
|
High-resolution structure of the human GPR40 receptor bound to allosteric agonist TAK-875. | 2014 Sep 4 |
|
Efficacy and safety of fasiglifam (TAK-875), a G protein-coupled receptor 40 agonist, in Japanese patients with type 2 diabetes inadequately controlled by diet and exercise: a randomized, double-blind, placebo-controlled, phase III trial. | 2015 Jul |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25787200
25 mg or 50 mg once-daily
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26276582
IC50 of TAK-875 for inhibiting Madin-Darby canine kidney (MDCK) cells overexpressing MRP2 (MDCK-MRP2 cells) was 2.41 ± 0.50 uM.
Substance Class |
Chemical
Created
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admin
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Edited
Sat Dec 16 02:01:42 UTC 2023
by
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on
Sat Dec 16 02:01:42 UTC 2023
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Record UNII |
8LDT91CH8A
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Record Status |
Validated (UNII)
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Record Version |
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ANHYDROUS->SOLVATE |
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ACTIVE MOIETY |
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