1. Signaling Pathways
  2. Metabolic Enzyme/Protease
  3. Carnitine Palmitoyltransferase (CPT)
  4. Carnitine Palmitoyltransferase (CPT) Inhibitor

Carnitine Palmitoyltransferase (CPT) Inhibitor

Carnitine Palmitoyltransferase (CPT) Inhibitors (30):

Cat. No. Product Name Effect Purity
  • HY-50202
    Etomoxir
    Inhibitor 99.58%
    Etomoxir ((R)-(+)-Etomoxir) is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig.
  • HY-50202A
    Etomoxir sodium salt
    Inhibitor 99.62%
    Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig.
  • HY-B1334A
    Perhexiline maleate
    Inhibitor 99.97%
    Perhexiline maleate is an orally active CPT1 and CPT2 inhibitor that reduces fatty acid metabolism. Perhexiline maleate induces mitochondrial dysfunction and apoptosis in hepatic cells. Perhexiline maleate can cross the blood brain barrier (BBB) and shows anti-tumor activity. Perhexiline maleate can be used in the research of cancers, and cardiovascular disease like angina.
  • HY-W012865
    Tartronic acid
    Inhibitor ≥98.0%
    Tartronic acid, a dicarboxylic acid derive, is an inhibitor of the transformation of carbohydrates into fat under fat-deficient diet conditions. Tartronic acid promotes 3T3-L1 adipocyte differentiation by increasing the protein expression of FABP-4, PPARγ and SREBP-1. Tartronic acid promotes de novo lipogenesis and inhibits CPT-1β by upregulating acetyl-CoA and malonyl-CoA. Tartronic acid promotes weight gain and induces adipocyte hypertrophy in epididymal white adipose tissue and lipid accumulation in the livers of high-fat diet induced obese mice. Tartronic acid can be used for lipid metabolic disease research.
  • HY-182248
    Teglicar chloride
    Inhibitor
    Teglicar chloride (ST1326 chloride) is an orally active, reversible, mixed-type, selective inhibitor of hepatic carnitine palmitoyltransferase I (L-CPT I), with an IC50 of 1.1 μM against rat L-CPT I. Teglicar chloride reduces serum glucose levels. Teglicar chloride exhibits antiketotic activity in normal fasted rats. Teglicar chloride can be used in research related to type 2 diabetes and ketoacidosis.
  • HY-136408
    Malonyl CoA lithium
    Inhibitor 99%
    Malonyl CoA (Malonyl Coenzyme A) lithium is an inhibitor of carnitine palmitoyl transferase 1 (CPT1). High Malonyl CoA lithium concentrations suppress fatty acid oxidation, while low Malonyl CoA lithium concentrations are permissive for fat oxidation.
  • HY-16482
    Teglicar
    Inhibitor 98.0%
    Teglicar is a selective and reversible orally active liver isoform of carnitine palmitoyl-transferase 1 (L-CPT1) inhibitor with an IC50 value of 0.68 μM and a Ki value of 0.36 μM. Teglicar has a potential antihyperglycemic propert. Teglicar can be used for the research of diabetes and neurodegenerative disease including Huntington's disease (HD).
  • HY-B1334
    Perhexiline
    Inhibitor 99.96%
    Perhexiline is an orally active CPT1 and CPT2 inhibitor that reduces fatty acid metabolism. Perhexiline induces mitochondrial dysfunction and apoptosis in hepatic cells. Perhexiline can cross the blood brain barrier (BBB) and shows anti-tumor activity. Perhexiline can be used in the research of cancers, and cardiovascular disease like angina.
  • HY-RS03122
    CPT1A Human Pre-designed siRNA Set A
    Inhibitor

    CPT1A Human Pre-designed siRNA Set A contains three designed siRNAs for CPT1A gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

  • HY-W104819
    4-Hydroxyphenylglyoxylate
    Inhibitor 99.30%
    4-Hydroxyphenylglyoxylate (4-Hydroxyphenylglyoxylic acid) is an inhibitor of carnitine palmitoyltransferase I (CPT I). 4-Hydroxyphenylglyoxylate can be used to study sensitivity changes in CPT I of liver mitochondria and fatty acid oxidation by isolated hepatocytes. 4-Hydroxyphenylglyoxylate can inhibits fatty acid oxidation.
  • HY-W420033
    (S)-(+)-Etomoxir
    Inhibitor 98.65%
    (S)-(+)-Etomoxir is the S enantiomer of Etomoxir (HY-50202). Etomoxir is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig.
  • HY-U00159
    McN3716
    Inhibitor 99.66%
    McN3716 is a carnitine palmitoyltransferase I (CPT-1) inhibitor.
  • HY-161027
    2,6-Didehydropeperomin B
    Inhibitor
    DHP-B is an Ecolignan-type compound and covalent, selective CPT1A inhibitor with a Kd of 1.62 μM. DHP-B can be isolated from the plant Peperomia dindygulensis. DHP-B covalently binds to Cys96 of CPT1A, blocks FAO, and disrupts the mitochondrial CPT1A-VDAC1 interaction. DHP-B triggers Apoptosis. DHP-B exhibits anti-CRC activity.
  • HY-50202R
    Etomoxir (Standard)
    Inhibitor
    Etomoxir (Standard) is the analytical standard of Etomoxir. This product is intended for research and analytical applications. Etomoxir ((R)-(+)-Etomoxir) is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig.
  • HY-RS23907
    Cpt2 Rat Pre-designed siRNA Set A
    Inhibitor
    Cpt2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Cpt2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
  • HY-RS16248
    Cpt1a Mouse Pre-designed siRNA Set A
    Inhibitor

    Cpt1a Mouse Pre-designed siRNA Set A contains three designed siRNAs for Cpt1a gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

  • HY-RS03125
    CPT2 Human Pre-designed siRNA Set A
    Inhibitor

    CPT2 Human Pre-designed siRNA Set A contains three designed siRNAs for CPT2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

  • HY-16149
    SDZ-CPI 975
    Inhibitor
    SDZ-CPI-975 is a novel, reversible, and selective CPT I inhibitor. SDZ-CPI-975 effectively inhibits fatty acid oxidation and lowers blood glucose levels.
  • HY-RS03123
    CPT1B Human Pre-designed siRNA Set A
    Inhibitor

    CPT1B Human Pre-designed siRNA Set A contains three designed siRNAs for CPT1B gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

  • HY-RS03124
    CPT1C Human Pre-designed siRNA Set A
    Inhibitor

    CPT1C Human Pre-designed siRNA Set A contains three designed siRNAs for CPT1C gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.