2. Signaling Pathways
  3. Others
  4. Others

Others

 
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-124050
    Echimidine
    Echimidine ((+)-Echimidine) is the major alkaloid detected in the honey used to produce the mead.
    Echimidine
  • HY-151628
    MRV03-068
    MRV03-068 (Compound 2) is a selective colibactin-activated peptidase (ClbP) inhibitor that blocks the genotoxic effect of Colibactin (HY-145930) on eukaryotic cells. MRV03-068 can be used in colorectal cancer research.
    MRV03-068
  • HY-149405
    Squalene synthase-IN-1
    Squalene synthase-IN-1 (compound 1) is a potent antihyperlipidemic agent acting through Squalene Synthase inhibition. Squalene synthase-IN-1 exhibits an outstanding antioxidant and anti-inflammatory activity. Squalene synthase-IN-1 displays a significant reduction not only of glucose but also of oxidative stress levels, while it did not cause any toxicity.
    Squalene synthase-IN-1
  • HY-149214
    Anticancer agent 100
    Anticancer agent 100 is a derivative of tetracaine with anti-cancer activity and can be used in cancer research.
    Anticancer agent 100
  • HY-N13230
    Rose Hips Extract
    Rose Hips Extract is the extract of Rose Hips, with content of 5% Flavone.
    Rose Hips Extract
  • HY-121642
    SL-017
    SL-017 is a novel photoacoustic sensitizer and a derivative of photofrin B. It can be taken up by cells to the maximum extent within 30 minutes and is mainly localized in mitochondria. After being activated by visible light or ultrasound, SL-017 can significantly increase the production of reactive oxygen species (ROS). Low concentrations of SL-017 can rapidly cause the loss of mitochondrial membrane potential. SL-017 can also cause mitochondrial fragmentation, a process that occurs after the loss of membrane potential. Epoxyeicosatrienoic acids (EETs) can alleviate the loss of mitochondrial membrane potential caused by SL-017, but the antioxidant ascorbic acid has no such effect. These characteristics indicate that SL-017 mainly targets mitochondria and exerts its cytotoxic effect by triggering the collapse of mitochondrial membrane potential, generating ROS, and causing mitochondrial fragmentation. As a novel photoacoustic sensitizer, SL-017 has potential application value in photodynamic therapy and sonodynamic therapy.
    SL-017
  • HY-N11526
    3-Hydroxy-2-(palmitoyloxy)propyl stearat
    3-Hydroxy-2-(palmitoyloxy)propyl stearat is a non-volatile compound. 3-Hydroxy-2-(palmitoyloxy)propyl stearat can be isolated from less polar fractions of the brown macroalga Fucus virsoides J. Agardh. This part of the substance has a good ability to scavenge free radicals and has a protective effect on the oxidative stress induced by hydrogen peroxide in zebrafish embryos.
    3-Hydroxy-2-(palmitoyloxy)propyl stearat
  • HY-157277
    AdBeSA
    AdBeSA is a hapten. AdBeSA can influence peptide binding by MHC II.
    AdBeSA
  • HY-146030
    Anticancer agent 46
    Anticancer agent 46 (compound 2) is a potent anticancer agent. Anticancer agent 46 shows antiproliferative activity with an IC50 of 0.986 µM for MGC803 cells. Anticancer agent 46 has the potential for the research of gastric cancer.
    Anticancer agent 46
  • HY-N1610
    19(S)-Hydroxyconopharyngine
    19(S)-Hydroxyconopharyngine (20-Hydroxyconopharyngine) is a natural product that can be isolated from Tabernaemontana bovina.
    19(S)-Hydroxyconopharyngine
  • HY-143641
    Anticancer agent 25
    Anticancer agent 25 exhibits the strongest cytotoxicity against PC3 cells with an IC50 value of 0.19 μM.
    Anticancer agent 25
  • HY-148670
    Pulmonary arterial hypertension agent-1
    Pulmonary arterial hypertension agent-1 (example 15) is a pulmonary arterial hypertension agent. Pulmonary arterial hypertension agent-1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Pulmonary arterial hypertension agent-1
  • HY-N15580
    Turneforcidine
    Turneforcidine ((-)-Turneforcidine) is a pyrrolizidine alkaloid with antitumor and cytotoxic activity.
    Turneforcidine
  • HY-N1634
    Anagyroidisoflavone A
    Anagyroidisoflavone A is an isoflavones isolated from pods of laburnum anagyroides.
    Anagyroidisoflavone A
  • HY-175233
    Mesotrypsin IN-1
    Mesotrypsin IN-1 (Compound CP13) is a selective Mesotrypsin inhibitor with an IC50 of 134.6 μM. Mesotrypsin IN-1 can be used for cancers, such as breast, colon and pancreatic cancer research.
    Mesotrypsin IN-1
  • HY-100294
    Ruzadolane
    Ruzadolane (UP 26-91) is a non-narcotic, centrally-acting analgesic agent.
    Ruzadolane
  • HY-P11277
    Pocuvotide satetraxetan
    Pocuvotide satetraxetan is an anticancer agent. Pocuvotide satetraxetan labeled with 177Lu can be used for imaging diagnosis.
    Pocuvotide satetraxetan
  • HY-N1591
    15-Methoxymkapwanin
    15-Methoxymkapwanin is a neo-clerodane diterpene compound isolated the leaf surface exudate of Dodonaea angustifolia.
    15-Methoxymkapwanin
  • HY-164379
    DOTA-PEG4-alkyne
    DOTA-PEG4-alkyne is a linker, and can be used for the labeling of radionuclide.
    DOTA-PEG4-alkyne
  • HY-151120
    Anticancer agent 79
    		Inhibitor
    Anticancer agent 79 (compound 3d) shows good anti-breast cancer activity. Anticancer agent 79 shows good cytotoxic activity in T47-D cells, with an IC50 of 13.64 ± 0.26 μM.
    Anticancer agent 79
Cat. No. Product Name / Synonyms Application Reactivity