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Small Molecules

For our customers’ convenience, we provide ready-to-use sterile compound solution at 10 mM stock concentration dissolved in anhydrous pure and biological-grade DMSO. Our QC lab independently tests every batch of compounds to make sure their high purity by LC/MS and NMR. The DMSO stock solutions are further tested in cell culture to ensure there is no undesired activity. Our partner labs have also functionally tested our new compounds to ensure their activity before we offer them for the first time to the research community.
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  1. AZD6244 (Selumetinib), MEK Inhibitor

    Catalog No. M60067
    A potent and highly selective non-ATP competitive MEK inhibitor in clinical trials.
  2. AZD8055, mTOR Inhibitor

    Catalog No. M60091
    A highly potent, selective and ATP-competitive mTOR inhibitor with >1,000-fold selectivity against all PI3K isoforms.
  3. Azidothymidine (AZT), Reverse Transcriptase Inhibitor

    Catalog No. M60238
    A selective, orally bioavailable and brain penetrant reverse transcriptase inhibitor.
  4. b-AP15 (NSC687852), Deubiquitinases Inhibitor

    Catalog No. M60251
    A potent and selective deubiquitinases inhibitor for 19S proteasomes activity of Ub-AMC cleavage.
  5. BAF312, S1P1/5 Selective Agonist

    Catalog No. M60039
    A potent and selective sphingosine 1-phosphate (S1P1/5) receptor agonist in clinical trials.
  6. BAM7, BAX Activator

    Catalog No. M60069
    The first potent and selective small molecule activator of BAX, which is a pro-apoptotic BCL-2 family member.
  7. BAY 87-2243, Hypoxia-inducible Factor-1 (HIF-1) Inhibitor

    Catalog No. M60217
    A highly potent and selective hypoxia-inducible factor-1 (HIF-1) inhibitor.
  8. BAY11-7082, E2 Ubiquitin Conjugating Enzyme Inhibitor

    Catalog No. M60309
    A potent and selective E2 ubiquitin (Ub) conjugating enzyme inhibitor.
  9. BAZ2-ICR, BAZ2 Bromodomain Inhibitor

    Catalog No. M60226
    A potent and selective BAZ2 bromodomain inhibitor.
  10. BETP, GLP-1R Potentiator

    Catalog No. M60196
    A positive allosteric modulator and partial agonist of the glucagon-like peptide 1 (GLP-1) receptor.
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