Cholesterol & Lipoprotein Metabolism

Cholesterol and lipoprotein metabolism compounds target sterol synthesis and lipoprotein handling. Cholesterol is built through the mevalonate pathway, which also yields farnesyl and geranylgeranyl pyrophosphate for protein prenylation. Lapaquistat acetate and L-731120 inhibit squalene synthase, the branch point that commits farnesyl pyrophosphate to sterol synthesis. NE 10790 acts on farnesyl pyrophosphate synthase (FPPS), while hGGPPS-IN-1 blocks human geranylgeranyl pyrophosphate synthase. Intracellular sterol transport is addressed by Y18501, an inhibitor of oxysterol-binding protein (OSBP). Pelacarsen sodium is an antisense oligonucleotide directed against apolipoprotein(a), the protein that distinguishes lipoprotein(a) from low-density lipoprotein particles.

Items 51-63 of 63

  • LY 295427
    Cat. No.
    A75851

    LY 295427

    Synonyms: Agisterol

    LY 295427 is an LDL receptor modulator that acts as a hypocholesterolemic agent by promoting the transcription of the LDL receptor (LDLR). This compound is of particular interest in studies focused on hypercholesterolemia, as it helps to regulate lipid metabolism and lower cholesterol levels. Researchers can utilize LY 295427 to explore its potential therapeutic applications in managing cholesterol-related disorders.

    5 mg
    $360.00
    10 mg
    $590.00
    All 5 sizes
  • LDL-IN-3
    Cat. No.
    A75855

    LDL-IN-3

    LDL-IN-3 is a highly selective inhibitor of the low-density lipoprotein receptor (LDLR). This compound demonstrates anti-atherosclerotic properties, making it a valuable tool for studying lipid metabolism and cardiovascular disease. Its application spans research into lipid-related disorders and the development of therapeutic strategies for atherosclerosis.

    1 mg
    $310.00
    5 mg
    $635.00
    All 6 sizes
  • BLT-4
    Cat. No.
    A76535

    BLT-4

    BLT-4 is a selective, reversible inhibitor of scavenger receptor class B type I (SR-BI). It effectively blocks the lipid transfer between high-density lipoproteins (HDL) and cells that is facilitated by SR-BI. This compound is valuable for research applications focused on cholesterol metabolism and cardiovascular disease, offering insights into the role of SR-BI in lipid homeostasis and atherosclerosis.

    1 mg
    $55.00
    5 mg
    $115.00
    All 4 sizes
  • OSBP ligand-1
    Cat. No.
    A76984

    OSBP ligand-1

    OSBP ligand-1 is a selective inhibitor of oxysterol-binding protein (OSBP) that plays a crucial role in lipid metabolism and cellular signaling. This compound is essential for the synthesis of PROTAC OSBP Degrader-1, facilitating targeted protein degradation studies. Its inhibitory effects on OSBP make it a valuable tool for investigating the biological functions of oxysterols and their implications in various diseases.

    Out of stock

    All 3 sizes
  • FPPS ligand 3
    Cat. No.
    A98551

    FPPS ligand 3

    FPPS Ligand 3 is a potent farnesyl pyrophosphate synthase (FPPS) ligand that interacts with the hydrophobic base region of the FPPS binding pocket. This compound is instrumental in the design and synthesis of novel FPPS inhibitors, offering valuable insights for research in metabolic disorders, cancer biology, and related therapeutic areas. Its precise targeting of FPPS makes it a crucial tool for studies aiming to modulate isoprenoid biosynthesis pathways.

    100 mg
    $60.00
    250 mg
    $115.00
    All 4 sizes
  • Cholesterol absorption inhibitor 1
    Cat. No.
    A98900

    Cholesterol absorption inhibitor 1

    Cholesterol Absorption Inhibitor 1 is a compound that impedes the intestinal absorption of cholesterol, thereby decreasing the levels of cholesteryl esters in the liver. This compound plays a critical role in studying cholesterol metabolism and its implications in cardiovascular diseases. Its application in research facilitates the understanding of lipid metabolism and potential therapeutic approaches to hypercholesterolemia.

    1 g
    $20.00
    5 g
    $60.00
    All 2 sizes
  • BPH-628
    Cat. No.
    B18743

    BPH-628

    BPH-628 is a potent inhibitor of geranylgeranyl diphosphate synthase (GGPPS), exhibiting a pIC50 of 6.1. This compound effectively disrupts the biosynthetic pathway of isoprenoids by targeting GGPPS, making it a valuable tool for research into cancer, cardiovascular diseases, and other conditions associated with aberrant cell signaling. BPH-628 can be utilized to study the role of GGPPS in various biological processes and to explore potential therapeutic interventions.

    Out of stock

    All 3 sizes
  • Hyzetimibe
    Cat. No.
    B19258

    Hyzetimibe

    Synonyms: HS-25

    Hyzetimibe is a cholesterol absorption inhibitor that effectively reduces the intestinal uptake of cholesterol and phytosterols. This compound demonstrates a favorable safety profile in animal studies, achieving a maximum tolerated dose of 2000 mg/kg in rats and 500 mg/kg in rhesus monkeys. Research applications include studies on lipid metabolism and the evaluation of therapeutic strategies for hypercholesterolemia.

    Out of stock

    All 3 sizes
  • OSBP-IN-1
    Cat. No.
    B19808

    OSBP-IN-1

    OSBP-IN-1 is an oxysterol-binding protein (OSBP) inhibitor that serves as a valuable tool in cancer research. This compound demonstrates significant antitumor activity, making it relevant for studies aimed at understanding OSBP's role in tumor biology and potential therapeutic interventions. Researchers can utilize OSBP-IN-1 to investigate the mechanistic pathways involved in cancer progression and to explore new treatment strategies targeting OSBP-related pathways.

    Out of stock

    All 3 sizes
  • BPH-742
    Cat. No.
    B20436

    BPH-742

    BPH-742 is an inhibitor of geranylgeranyl diphosphate synthase (GGPPS) with an IC50 of 0.1 μM. This compound demonstrates significant antitumor activity, making it a valuable tool for cancer research. BPH-742 can be used to study the biochemical pathways involved in tumor progression and to explore the therapeutic potential of targeting GGPPS in various cancer models.

    Out of stock

    All 3 sizes
  • Lanopylin B1
    Cat. No.
    B20716

    Lanopylin B1

    Lanopylin B1 is a selective inhibitor of lanosterol synthase (EC 5.4.99.7), with an IC50 value of 33 μM. This compound plays a significant role in the study of sterol biosynthesis and has potential applications in investigating cholesterol metabolism and related pathways in various biological contexts. Its ability to hinder lanosterol synthesis makes it a useful tool for exploring the mechanisms of lipid regulation and associated diseases.

    Out of stock

    All 3 sizes
  • Lanopylin B2
    Cat. No.
    B21179

    Lanopylin B2

    Lanopylin B2 is an inhibitor of lanosterol synthase (EC 5.4.99.7), demonstrating effective inhibition with an IC50 of 41 μM. This compound serves as a valuable tool for research into cholesterol biosynthesis and related metabolic pathways. Its ability to selectively target lanosterol synthase positions it for use in studies investigating the role of sterols in cellular processes and potential therapeutic applications.

    Out of stock

    All 3 sizes
  • Lanopylin A1
    Cat. No.
    B21218

    Lanopylin A1

    Lanopylin A1 is a selective inhibitor of lanosterol synthase (EC 5.4.99.7), a key enzyme in the sterol biosynthesis pathway. It exhibits an IC50 of 15 μM, demonstrating significant potency in modulating this target. This compound is useful for investigating the role of lanosterol synthase in cholesterol biosynthesis and related metabolic processes, making it valuable in studies of sterol metabolism and potential therapeutic interventions.

    Out of stock

    All 3 sizes

Items 51-63 of 63

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