1. Signaling Pathways
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Others

 
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-132940
    (+)-Pileamartine A
    Chemical
    (+)-Pileamartine A is a complex alkaloid. (+)-Pileamartine A can be accessed via intramolecular Pd(0)-catalyzed alkene 1,2-aminoarylation reactions.
    (+)-Pileamartine A
  • HY-163023
    Atrazine-acetic acid
    Atrazine-acetic acid is an immunizing and heterologous hapten.
    Atrazine-acetic acid
  • HY-123642
    BLXA-4-ME
    Inhibitor
    BLXA-4-ME is used for gingivitis study.
    BLXA-4-ME
  • HY-148453
    Antiproliferative agent-16
    99.25%
    Antiproliferative agent-16 is an indolyl hydrazide-hydrazone compound with anticancer activity. Antiproliferative agent-16 exhibits specificity toward breast cancer cells (IC50 of 6.94 μM for MCF-7 cells).
    Antiproliferative agent-16
  • HY-P2152A
    Antho-RPamide II hydrochloride
    Antho-RPamide II hydrochloride is a bioactive neuropeptide. Antho-RPamide II hydrochloride can be isolated for the sea anemone Anthopleura elegantissima. Antho-RPamide II hydrochloride inhibits the spontaneous, rhythmic contractions in tentacle longitudinal muscle fibers of sea anemones.
    Antho-RPamide II hydrochloride
  • HY-175762
    Z118298144
    Z118298144 is a Fascin inhibitor. Z118298144 has a strong binding capacity to fascin and inhibits Actin bundling. Z118298144 significantly reduces proliferation and impairs migration of CRC cells. Z118298144 can be used for cancer, especially colorectal cancer (CRC) research.
    Z118298144
  • HY-P10931
    RAD21 (356–395)
    RAD21 (356–395) is a peptide encompassing amino acids 356 to 395 of the RAD21 protein, which can be used to study the interaction mechanism between STAG1 and RAD21. The equilibrium dissociation constant (KD) value for the interaction between RAD21 (356–395) and STAG1 is 127 nM.
    RAD21 (356–395)
  • HY-157047
    Anticancer agent 171
    Anticancer agent 171 (Compound 6a) is an oxime analogue. Anticancer agent 171 has anticancer activity against HCT116 cells with an IC50 value of 3.43 μM. Anticancer agent 171 can be used for the research of cancer.
    Anticancer agent 171
  • HY-121681
    K 308
    Inhibitor
    K 308 is a non-steroid antiinflammatory agent.
    K 308
  • HY-159110
    ABA-DMNB
    ABA-DMNB is a photo-caged chemically induced proximity (CIP) inducer. ABA-DMNB is a photo-caged ABA (Abscisic acid (HY-100560)). ABA-DMNB can be uncaged under light irradiation and generate active ABA.
    ABA-DMNB
  • HY-P1963
    Ac-IEVDIDVEH TFA
    Ac-IEVDIDVEH TFA is a short peptide sequence with Ac at the end.
    Ac-IEVDIDVEH TFA
  • HY-147706
    AR524
    Ar524 has higher inhibitory activity than the known transgenic inhibitor kifunensine. At the same time, ar524 inhibited low concentration (10 μ M) Spheroid formation of human malignant cells.
    AR524
  • HY-N8810
    Platycoside M1
    Platycoside M1 is a A-ring lactone triterpenoid saponin that can be isolaoted from the roots of Platycodon grandiflorum. Platycosides are the main active constituents of P. grandiflorus with multiple pharmacological activities.
    Platycoside M1
  • HY-P991563
    Anti-CEACAM5 Antibody (A5B7)
    Anti-CEACAM5 Antibody (A5B7) is a humanized antibody expressed in CHO cells, targeting CEACAM5/CEA/CD66e. Anti-CEACAM5 Antibody (A5B7) consists of a huIgG1 heavy chain and a huκ light chain, with a predicted molecular weight (MW) of 145 kDa. The isotype control for the Anti-CEACAM5 Antibody (A5B7) can be referenced as Human IgG1 kappa, Isotype Control (HY-P99001).
    Anti-CEACAM5 Antibody (A5B7)
  • HY-15121A
    DL-Theanine
    DL-Theanine (DL-Glutamic acid γ-ethyl amide) is a natural compound showing tranquilizing effects in the brain.
    DL-Theanine
  • HY-P11284
    TGN
    TGN, a 12-amino acid ligand, is a BBB-penetrating peptide. TGN can be used as a drug delivery vehicle for Alzheimer's disease research.
    TGN
  • HY-P10989
    NG2 binding peptide
    NG2 binding peptide is a short peptide that specifically recognizes NG2 proteoglycan and can be obtained by phage screening technology. NG2 binding peptide interacts with NG2 binding sites to achieve precise targeting of tumor angiogenesis in vitro and in vivo. NG2 binding peptide exhibits significant homing ability in wild-type tumor-bearing mice, but has no localization effect in NG2 knockout mice. Due to the tissue specificity of NG2 expression, NG2 binding peptide can be used in scenarios such as tumor targeted therapy, drug delivery, and molecular imaging diagnosis.
    NG2 binding peptide
  • HY-W099730R
    Bemotrizinol (Standard)
    Bemotrizinol (Standard) is the analytical standard of Bemotrizinol. This product is intended for research and analytical applications. Bemotrizinol (Tinosorb S), an ultraviolet (UV) filter, has been shown to accept atomic oxygen generated by N-oxide photodeoxygenation.
    Bemotrizinol (Standard)
  • HY-100899
    Heparastatin
    Inhibitor
    Heparastatin is a heparanase inhibitor.
    Heparastatin
  • HY-N9443
    (12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-one
    (12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-one is a natural product that can be found in Cladosporium microorganisms.
    (12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-one
Cat. No. Product Name / Synonyms Application Reactivity