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My Cart> Small Molecule Compounds > Inhibitors & Antagonists & Agonists > GPCR & G Protein > TAK-875CAS：1000413-72-8
Molecular Formula：C29H32O7S
Molecular Weight：524.63
Storage：Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year
Purity：≥98%
Appearance：White to off-white Solid
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| CAS | 1000413-72-8 |
| Name | TAK-875 |
| Molecular Formula | C29H32O7S |
| Molecular Weight | 524.63 |
| Solubility | Soluble in DMSO |
| Purity | ≥98% |
| Appearance | White to off-white Solid |
| Storage | Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year |
| MDL | MFCD18251445 |
| SMILES | CC1=C(C(C)=CC(OCCCS(C)(=O)=O)=C1)C2=CC(COC3=CC=C4[C@@H](COC4=C3)CC(O)=O)=CC=C2 |
| Target Point | GPR40 |
| Passage | GPCR & G Protein |
| Background | TAK-875 is a novel long-acting, selective GPR40 agonist |
| Biological Activity | Fasiglifam (TAK-875)是一种选择性GPR40激动剂，在表达人GPR40的CHO细胞系中EC50为14 nM，比油酸有效400倍。[1] |
| Data Literature Source | [1] Nobuyuki Negoro，et al. ACS Med Chem Lett，2010，1(6)，290-294. [2] Tsujihata Y，et al. J Pharmacol Exp Ther，2011，339(1)，228-2 |
| Unit | Piece |
| Specification | 5mg 10mg |
Remark：These protocols are for reference only. Solarbio does not independently validate these methods.
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3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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