1. Others


There are a number of inhibitors, agonists, and antagonists which we cannot make precise classification because the research area is still unknown.

Others Related Products (1463):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-17031
    SBE-β-CD 182410-00-0 >98.0%
    SBE-β-CD is a sulfobutylether β-cyclodextrin derivative, it is an excipient or a formulating agent used to increase the solubility of poorly soluble drugs.
  • HY-12222
    INT-747 459789-99-2 >98.0%
    INT-747 is a potent and selective FXR agonist (EC50=99 nM) endowed with anticholestatic activity.
  • HY-B0146
    Verteporfin 129497-78-5 99.26%
    Verteporfin is a benzoporphyrin derivative monoacid ring A, and can inhibit the activity of YAP.
  • HY-15979A
    H-89 dihydrochloride 130964-39-5 98.94%
    H-89 (dihydrochloride) is a potent inhibitor of cyclic AMP-dependent protein kinase (protein kinase A) with IC50 of 48 nM and has weak inhibition on PKG, PKC, Casein Kinase, and others kinases.
    H-89 dihydrochloride
  • HY-17567A
    Heparin sodium salt 9041-08-1 >98.0%
    Heparin (sodium salt) is a highly sulfated glycosaminoglycan, that is widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule.
    Heparin sodium salt
  • HY-17561
    G-418 disulfate 108321-42-2 >98.0%
    G-418 (disulfate) is an aminoglycoside antibiotic similar in structure to gentamicin B1, which blocks polypeptide synthesis by inhibiting the elongation step in both prokaryotic and eukaryotic cells.
    G-418 disulfate
  • HY-D0940
    H2DCFDA 4091-99-0 99.14%
    H2DCFDA is a cell-permeable non-fluorescent (but fluorescein-containing) probe.
  • HY-B0988
    Deferoxamine mesylate 138-14-7 >98.0%
    Deferoxamine mesylate is an iron chelator, and effectively reduces oxidative stress and neuronal death.
    Deferoxamine mesylate
  • HY-15910
    5-BrdU 59-14-3 99.99%
    5-BrdU is a nucleoside analog, and competes with thymidine for incorporation into DNA, and is used in the detection of proliferating cells.
  • HY-12270
    T-5224 530141-72-1 99.03%
    T-5224 is a selective inhibitor of c-Fos/activator protein (AP)-1 for rheumatoid arthritis therapy, and inhibits MMP activity with IC50s of 10 nM for both MMP-3 and MMP-13.
  • HY-15534
    JC-1 3520-43-2 99.46%
    JC-1 is a fluorescent lipophilic carbocyanine dye, which can be used to measure mitochondrial membrane potential.
  • HY-12591A
    D-Luciferin 2591-17-5 98.81%
    D-luciferin is the natural substrate of luciferases that catalyze the production of light in bioluminescent insects.
  • HY-50694
    Senicapoc 289656-45-7 99.83%
    Senicapoc is a potent and selective Gardos channel blocker with IC50 value of 11 nM, and blocks Ca2+-induced rubidium flux from human RBCs with an IC50 value of 11 nM and inhibits RBC dehydration with IC50 of 30 nM.
  • HY-12726
    Liproxstatin-1 950455-15-9 98.38%
    Liproxstatin-1 is a potent ferroptosis inhibitor, with IC50 of appr 38 nM.
  • HY-15924
    MTT 298-93-1 99.59%
    MTT, a yellow tetrazole, is reduced to purple formazan in living cells, and used for assessing cell metabolic activity.
  • HY-100545
    BAPTA-AM 126150-97-8 99.60%
    BAPTA-AM is a permeable free calcium chelator.
  • HY-16268
    Kartogenin 4727-31-5 >98.0%
    Kartogenin is an inducer of differentiation of human mesenchymal stem cells into chondrocytes.
  • HY-50662
    A-769662 844499-71-4 98.09%
    A-769662 is a potent, reversible AMPK activator with EC50 of 0.8 μM, and has little effect on GPPase/FBPase activity.
  • HY-13248
    AR-C155858 496791-37-8
    AR-C155858 is a novel inhibitor of the monocarboxylate transporters (MCTs) MCT1 and MCT2 (Ki values are 2.3 and < 10 nM, respectively), and exhibits no activity at MCT4.
  • HY-B0496
    PMSF 329-98-6 >99.0%
    PMSF is an irreversible serine/cysteine protease inhibitor.