2. Others

Others

Others

Related Products

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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 (73917):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-123484
    ROCK-IN-D1 1219721-73-9 98%
    ROCK-IN-D1 serves as a highly effective and selective inhibitor of ROCK.
    ROCK-IN-D1
  • HY-123487
    Sapintoxin A 79083-69-5 98%
    Sapintoxin A is a phorbol ester that can be isolated from the unripe fruits of Sapium indicum.
    Sapintoxin A
  • HY-123510
    NSC-670224 1374648-47-1 98%
    NSC-670224 is toxic to Saccharomyces cerevisiae at low micromolar concentration (LC50: 3.2 μM).
    NSC-670224
  • HY-123528
    Kahweol oleate 108214-30-8 98%
    Kahweol oleate is a diterpenoid cafestol that can be isolated from coffee.
    Kahweol oleate
  • HY-123529
    LY389795 222529-89-7 98%
    LY389795 is an active compound.
    LY389795
  • HY-123547
    TLK19781 309932-60-3 98%
    TLK19781 is a non-peptide small molecule insulin receptor activator that increases the content of insulin-stimulated GLUT4 on the cell membrane and enhances the activity of insulin-stimulated glucose transport in cell and animal models of insulin resistance.
    TLK19781
  • HY-123555
    PD 142505-0028 161774-09-0 98%
    PD 142505-0028 is an active compound.
    PD 142505-0028
  • HY-123564
    Mcl1-IN-7 2012563-34-5 98%
    Mcl1-IN-7 (compound 11) is a reversible covalent inhibitor of Mcl-1 with the activity of inhibiting Mcl-1. By covalently targeting the non-catalytic lysine side chain of Mcl-1, it has higher potency than non-covalent counterparts and can be used to develop Mcl-1 inhibitory compounds and study related biological phenomena.
    Mcl1-IN-7
  • HY-123580
    RU26988 74915-58-5 98%
    RU26988 is a highly specific glucocorticoid receptor agonist with a very low affinity for salocorticoid receptors.
    RU26988
  • HY-123589
    Gyramide A 913509-94-1 98%
    Gyramide A is a compound mentioned in the study of the protective effect of Qnr protein on bacterial topoisomerase. Qnr has no protective effect on it, and its activity is different from that of other topoisomerase inhibitors.
    Gyramide A
  • HY-123605
    CAY10406 2108603-03-6 98%
    CAY10406 is an inhibitor for caspase 3/7. CAY10406 inhibits the expression of 28-kDa IL-1β fragment, without significant cytotoxicity (10 μM).
    CAY10406
  • HY-123616
    BI 7271 1883429-34-2 98%
    BI 7271 is a BRD9 ligand, which can be used for the synthesis of PROTACs, such as PROTAC BRD9 Degrader-7 (HY-155361).
    BI 7271
  • HY-123632
    (3S,5S)-Atorvastatin sodium salt 1428118-38-0 98%
    (3S,5S)-Atorvastatin sodium salt is a pregnane X receptor (PXR) activator and the inactive enantiomer of Atorvastatin. Atorvastatin is an orally active HMG-CoA reductase inhibitor with lipid-lowering capabilities.
    (3S,5S)-Atorvastatin sodium salt
  • HY-123634
    (S)-3'-Aminoblebbistatin 2097141-18-7 98%
    (S)-3'-Aminoblebbistatin is the derivative of Blebbistatin (HY-13813). (S)-3'-Aminoblebbistatin exhibits inhibitory activity against myosin II with an IC50 of 14.1 µM.
    (S)-3'-Aminoblebbistatin
  • HY-123643
    Brilliant sulfaflavine 2391-30-2 98%
    Brilliant Sulfaflavine is used as a fluorescent tracer. Used to study the application rate of foliar fungicides for soybean rust control.
    Brilliant sulfaflavine
  • HY-123649
    MK-4882 1246470-32-5 98%
    MK-4882 is an HCV NS5A inhibitor with activity in reducing viral load in a chimpanzee model of HCV infection, but with issues of viral breakthrough, prompting the development of compounds with greater potency against more genotypes and NS5A resistance mutations.
    MK-4882
  • HY-123662
    AGN-201904Z 651728-41-5 98%
    AGN-201904Z is a compound that inhibits gastric acid secretion and is a new type of proton pump inhibitor that can produce more significant and lasting acid suppression effects than esomeprazole.
    AGN-201904Z
  • HY-123668
    KM05382 882291-64-7 98%
    KM05382 serves as an inhibitor of CDK9 and reduces the transcription of GAPDH.
    KM05382
  • HY-123669AS
    (R)-trans-138727-d4 1217222-86-0 98%
    (R)-trans-138727-d4 is the deuterium labeled (R)-trans-138727.
    (R)-trans-138727-d4
  • HY-123690
    Etoposide toniribate 433304-61-1 98%
    Etoposide toniribate is an active compound.
    Etoposide toniribate