1. Natural Products
  2. Others

Others

Others (135):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-10219
    Rapamycin 53123-88-9 98.98%
    Rapamycin is a specific mTOR inhibitor with IC50 of 0.1 nM.
    Rapamycin
  • HY-12320
    Cycloheximide 66-81-9 99.17%
    Cycloheximide is an inhibitor of protein biosynthesis in eukaryotic organisms, with IC50 of 532.5 nM and 2880 nM for protein synthesis and RNA synthesis in vivo, respectively.
    Cycloheximide
  • HY-17559
    Actinomycin D 50-76-0 99.89%
    Actinomycin D inhibits DNA repair with IC50 of 0.42 μM.
    Actinomycin D
  • HY-15142
    Doxorubicin hydrochloride 25316-40-9 99.47%
    Doxorubicin hydrochloride is a Topoisomerase II (Top2) catalytic inhibitor, also is a broad spectrum antibiotic used in the treatment of cancers, with IC50 of 374 nM for Hela cells.
    Doxorubicin hydrochloride
  • HY-13316
    Mitomycin C 50-07-7 98.51%
    Mitomycin C is a DNA-damaging agent and small-molecule inhibitor effectively sensitize cancer cells to tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL).
    Mitomycin C
  • HY-15141
    Staurosporine 62996-74-1 99.98%
    Staurosporine is a very potent universal inhibitor of protein kinases but showing little selectivity, with IC50 of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase, respectively.
    Staurosporine
  • HY-16592
    Brefeldin A 20350-15-6 99.54%
    Brefeldin A is a fungal metabolite that induces the Golgi proteins to redistribute into the ER, blocks the secretion from the Golgi apparatus and increases CRISPR/Cas9-mediated editing frequencies.
    Brefeldin A
  • HY-13948
    Angiotensin II human 4474-91-3 99.34%
    Angiotensin II human is converted by Angiotensin I through removal of two C-terminal residues by the enzyme angiotensin-converting enzyme (ACE). Angiotensin II is mediated by AT1 and AT2 receptors, which are seven transmembrane glycoproteins with 30% sequence similarity.
    Angiotensin II human
  • HY-13251
    Silvestrol 697235-38-4 99.28%
    Silvestrol is isolated from the fruits and twigs of Aglaia foveolata, by inducing caspase-3 activation to cause cell death.
    Silvestrol
  • HY-15597
    Salinomycin 53003-10-4 >98.0%
    Salinomycin is an inhibitor of Wnt/β-catenin signaling, which acts on the Wnt/Fzd/LRP complex. Salinomycin strongly suppresses Wnt1-stimulated reporter activity with an IC50 of 163 nM, and reduces β-catenin levels.
    Salinomycin
  • HY-18739
    Phorbol 12-myristate 13-acetate 16561-29-8 99.08%
    Phorbol 12-myristate 13-acetate (PMA) is a PKC-activating phorbol ester, increases the intracellular Ca2+ concentration ([Ca2+]i) in a dose-dependent manner, with an EC50 of 11.7 nM.
    Phorbol 12-myristate 13-acetate
  • HY-14649
    Retinoic acid 302-79-4 98.52%
    Retinoic acid is a natural agonist of RAR/RXR nuclear receptors. Retinoic acid also bind to PPARβ/δ, with Kd of 17 nM.
    Retinoic acid
  • HY-13753
    Streptozocin 18883-66-4 99.58%
    Streptozocin is a potent DNA-methylating agent, with IC50 values of 11.7, 904 and 1024 μg/mL for HL60, K562 and C1498 cells respectively.
    Streptozocin
  • HY-15230
    Geldanamycin 30562-34-6 99.78%
    Geldanamycin is a specific inhibitor of interferon regulatory factor 3 (IRF3) (by inhibiting Hsp90 of the IRF3 phosphorylation chaperone).
    Geldanamycin
  • HY-B0617
    Ademetionine 29908-03-0 >98.0%
    Ademetionine(S-adenosyl-l-methionine; SAMe) is a naturally-occurring substance which is a major source of methyl groups in the brain.
    Ademetionine
  • HY-76299
    Galanthamine 357-70-0 99.78%
    Galanthamine is a potent acetylcholinesterase (AChE) inhibitor with IC50 of 500 nM.
    Galanthamine
  • HY-12591A
    D-Luciferin 2591-17-5 98.11%
    D-Luciferin is a substrate for firefly luciferase with a Km of approx 2 μM.
    D-Luciferin
  • HY-16468
    Squalamine 148717-90-2 >98.0%
    Squalamine(MSI-1256) is an aminosterol compound with potent broad spectrum antiviral activity.
    Squalamine
  • HY-13821
    Epoxomicin 134381-21-8 99.89%
    Epoxomicin(BU-4061T) is a potent anti-tumor agent isolated from Actinomycetes that is used as a selective and irreversible inhibitor of the 20S proteasome.
    Epoxomicin
  • HY-B0220
    Erythromycin 114-07-8 >98.0%
    Erythromycin, an oral macrolide antibiotic produced by Streptomyces erythreus, reversibly binds to the 50S ribosome of bacteria, and inhibits protein synthesis.
    Erythromycin