货号:A574651
同义名:
CDDO-Imidazolide; TP-235
CDDO-Im is a synthetic triterpenoid more potent than its parent compound CDDO both in vitro and in vivo and a PPARγ agonist.
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产品名称 | PPARα ↓ ↑ | PPARβ/δ ↓ ↑ | PPARγ ↓ ↑ | PPARδ ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Fenofibric acid | ✔ | 98% | |||||||||||||||||
GW6471 |
++
PPARα, IC50: 0.24 μM |
99%+ | |||||||||||||||||
GSK3787 |
++
PPARδ, pIC50: 6.6 |
++
PPARδ, pIC50: 6.6 |
99%+ | ||||||||||||||||
FH535 | ✔ | 98%+ | |||||||||||||||||
GW9662 |
+++
PPARα, IC50: 32 nM |
+++
PPARγ, IC50: 3.3 nM |
98% | ||||||||||||||||
T0070907 |
++++
PPARγ, IC50: 1 nM |
98% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | CDDO-Im (RTA-403) functions as an activator of Nrf2 and PPAR, showing high affinity for PPARα and PPARγ with inhibition constants (Kis) of 232 nM and 344 nM, respectively[1].[2]. |
Animal study | Furthermore, CDDO-Im acts as a strong suppressor of inducible nitric oxide synthase (iNOS) expression in primary mouse macrophages and impedes the growth of B16 murine melanoma and L1210 murine leukemia cells in vivo. The injection of 10 nM (5.4 μg) CDDO-Im nearly abolishes IFN-γ's ability to induce iNOS expression, and even a minimal dose of 1 nmol (0.54 μg) CDDO-Im partially achieves this effect[1]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.85mL 0.37mL 0.18mL |
9.23mL 1.85mL 0.92mL |
18.46mL 3.69mL 1.85mL |
CAS号 | 443104-02-7 |
分子式 | C34H43N3O3 |
分子量 | 541.72 |
SMILES Code | CC(C)([C@]1([H])CC[C@@]([C@@]2(CC[C@]3(CCC(C)(C[C@@]3([H])[C@]24[H])C)C(N5C=CN=C5)=O)C)6C)C(C(C#N)=C[C@]1(C)C6=CC4=O)=O |
MDL No. | MFCD12756341 |
别名 | CDDO-Imidazolide; TP-235; CDDO Im, CDDO-Im; RTA-403 |
运输 | 蓝冰 |
InChI Key | ITFBYYCNYVFPKD-FMIDTUQUSA-N |
Pubchem ID | 9958995 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, 2-8°C |