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TUG-499

Catalog No. T60184   CAS 1206629-08-4

TUG-499 is a selective free fatty acid receptor 1 (FFAR1 or GPR40) agonist (EC50: 7.39).TUG-499 has an affinity for FFAR1 or GPR40 over the related receptors FFA2, FFA3 and the nuclear receptor PPARγ, as well as other different receptors, ion channels and transporter proteins.TUG-499 can be used to study type 2 Type 2 diabetes.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
TUG-499 Chemical Structure
TUG-499, CAS 1206629-08-4
Pack Size Availability Price/USD Quantity
1 mg In stock $ 61.00
5 mg In stock $ 136.00
10 mg In stock $ 198.00
25 mg In stock $ 327.00
50 mg In stock $ 393.00
100 mg In stock $ 585.00
500 mg In stock $ 1,270.00
1 mL * 10 mM (in DMSO) In stock $ 139.00
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Purity: 99.59%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description TUG-499 is a selective free fatty acid receptor 1 (FFAR1 or GPR40) agonist (EC50: 7.39).TUG-499 has an affinity for FFAR1 or GPR40 over the related receptors FFA2, FFA3 and the nuclear receptor PPARγ, as well as other different receptors, ion channels and transporter proteins.TUG-499 can be used to study type 2 Type 2 diabetes.
Targets&IC50 FFAR1/GPR40:7.39(pEC50)
In vitro TUG-499 exhibits remarkable chemical stability, does not inhibit specific CYP enzymes or P-glycoprotein, and displays outstanding Caco-2 permeability. Its potent effects are observed on recombinant human FFA1 receptors as well as the INS-1E rat insulinoma cell line.[1]
Molecular Weight 320.17
Formula C16H11Cl2NO2
CAS No. 1206629-08-4

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 22.5 mg/mL (70.28 mM)

TargetMolReferences and Literature

1. Christiansen E, et al. Identification of a potent and selective free fatty acid receptor 1 (FFA1/GPR40) agonist with favorable physicochemical and in vitro ADME properties. J Med Chem. 2011;54(19):6691-6703.

Related compound libraries

This product is contained In the following compound libraries:
Membrane Protein-targeted Compound Library GPCR Compound Library Nuclear Receptor Compound Library Bioactive Compounds Library Max Bioactive Compound Library DNA Damage & Repair Compound Library Anti-Obesity Compound Library

Related Products

Related compounds with same targets
AM-1638 JNJ-63533054 GSK137647A Vincamine P2Y2R/GPR17 antagonist 1 TUG-469 Bimatoprost acid GPR40 Agonist 2

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Keywords

TUG-499 1206629-08-4 DNA Damage/DNA Repair Endocrinology/Hormones GPCR/G Protein Metabolism PPAR GPR TUG 499 TUG499 inhibitor inhibit

 

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