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CTPI-2

Catalog No. T8732   CAS 68003-38-3

CTPI-2 is an inhibitor of mitochondrial citrate carrier SLC25A1 with(KD : 3.5 μM). CTPI-2 inhibits glycolysis, PPARγ, and its downstream target the glucose transporter GLUT4. CTPI-2 exhibits anti-tumor activity.CTPI-2 halts salient alterations of NASH reverting steatosis, preventing the evolution to steatohepatitis, reducing inflammatory macrophage infiltration in the liver and adipose tissue, and starkly mitigating obesity induced by a high-fat diet.

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CTPI-2 Chemical Structure
CTPI-2, CAS 68003-38-3
Pack Size Availability Price/USD Quantity
50 mg In stock $ 47.00
100 mg In stock $ 66.00
200 mg In stock $ 89.00
1 mL * 10 mM (in DMSO) In stock $ 45.00
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Purity: 97.91%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description CTPI-2 is an inhibitor of mitochondrial citrate carrier SLC25A1 with(KD : 3.5 μM). CTPI-2 inhibits glycolysis, PPARγ, and its downstream target the glucose transporter GLUT4. CTPI-2 exhibits anti-tumor activity.CTPI-2 halts salient alterations of NASH reverting steatosis, preventing the evolution to steatohepatitis, reducing inflammatory macrophage infiltration in the liver and adipose tissue, and starkly mitigating obesity induced by a high-fat diet.
Targets&IC50 SLC25A1:3.5 μM (KD)
In vivo CTPI-2, halts salient alterations of NASH reverting steatosis, preventing the evolution to steatohepatitis, reducing inflammatory macrophage infiltration in the liver and adipose tissue, while starkly mitigating obesity induced by a high-fat diet.?These effects are differentially recapitulated by a global ablation of one copy of the Slc25a1 gene or by a liver-targeted Slc25a1 knockout, which unravel dose-dependent and tissue-specific functions of this protein.?Mechanistically, through citrate-dependent activities, Slc25a1 inhibition rewires the lipogenic program, blunts signaling from peroxisome proliferator-activated receptor gamma, a key regulator of glucose and lipid metabolism, and inhibits the expression of gluconeogenic genes.?The combination of these activities leads not only to inhibition of lipid anabolic processes, but also to a normalization of hyperglycemia and glucose intolerance as well[1].
Molecular Weight 356.74
Formula C13H9ClN2O6S
CAS No. 68003-38-3

Storage

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

Solubility Information

DMSO: 30 mg/mL (84.1 mM)

TargetMolReferences and Literature

1. Tan M, et al. Inhibition of the mitochondrial citrate carrier, Slc25a1, reverts steatosis, glucose intolerance, and inflammation in preclinical models of NAFLD/NASH. Cell Death Differ. 2020;27(7):2143-2157. 2. Peng R , Zhang M , Wang H , et al. Advances into Understanding the Vital Role of the Mitochondrial Citrate Carrier (CIC) in Metabolic Diseases, A Review[J]. Pharmacological Research, 2020:105132.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Active Compound Library Inhibitor Library Anti-Aging Compound Library Mitochondria-Targeted Compound Library Bioactive Compounds Library Max Metabolism Compound Library Cuproptosis Compound Library Bioactive Compound Library Immunology/Inflammation Compound Library NO PAINS Compound Library

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Keywords

CTPI-2 68003-38-3 Metabolism Others Mitochondrial Metabolism macrophage carrier NSCLC transporter CTPI2 glucose steatohepatitis steatosis inflammatory CTPI 2 inhibit citrate Inhibitor mitochondrial inhibitor

 

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