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HSP

HSP

HSP (Heat Shock Protein) inhibitors target HSPs, a family of molecular chaperones that assist in protein folding, stability, and protection against stress-induced damage. HSPs are often upregulated in cancer cells, helping them survive under stressful conditions such as hypoxia and chemotherapy. Inhibiting HSPs can disrupt these protective mechanisms, leading to cell death. HSP inhibitors are therefore valuable in cancer therapy and research into stress responses. At CymitQuimica, we provide a comprehensive range of high-quality HSP inhibitors to support your research in protein homeostasis, stress responses, and oncology.

Found 200 products for "HSP".

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  • gp96-II


    Gp96-II is a gp96-blocking peptide that antagonizes cytokine production induced by gp96-mediated LPS. This compound is useful for research into inflammatory diseases.
    Formula:C200H353N59O53S
    Color and Shape:Solid
    Molecular weight:4464.37
  • NPX800

    CAS:
    NPX800 is an inhibitor of heat shock factor 1 (HSF1) and can be used in studies about the treatment of cancer.
    Formula:C32H32FN5O4
    Purity:99.29%
    Color and Shape:Solid
    Molecular weight:569.626
  • Palmitic acid-13C sodium

    CAS:
    13C-labeled Palmitic acid, a common long-chain fatty acid in flora/fauna, induces GRP78/CHOP in mouse cells.
    Formula:CC15H31NaO2
    Molecular weight:279.4
  • MPC-0767

    CAS:
    MPC-0767, a potent, selective, and orally active hsp90 inhibitor, is the L-alanine ester prodrug of MPC-3100, exhibiting enhanced chemical stability.
    Formula:C26H36BrN7O9S2
    Color and Shape:Solid
    Molecular weight:734.64
  • DN401

    CAS:
    DN401 is a potent TRAP1 and Hsp90 Inhibitor( IC50 = 79 nM for TRAP1, IC50 = 698 nM for Hsp90) with potent anticancer activity.
    Formula:C18H19N3O2
    Purity:99.37%
    Color and Shape:Solid
    Molecular weight:309.3624
  • MAL3-101

    CAS:
    MAL3-101 is a molecular chaperone inhibitor of heat shock protein 70 (Hsp 70).
    Formula:C54H66N4O10
    Color and Shape:Solid
    Molecular weight:931.12
  • Hsp110-STAT3 interaction-IN-2


    Hsp110-STAT3 interaction-IN-2 (compound 10b) is an inhibitor of the Hsp110-STAT3 interaction. It is utilized in research related to pulmonary arterial hypertension (PAH).
    Formula:C24H18F3N5O3
    Color and Shape:Solid
    Molecular weight:481.43
  • Shepherdin (79-87)

    CAS:
    Shepherdin 79-87: Amino acid fragment 79-87 of Hsp90/Survivin antagonist with anticancer properties.
    Formula:C41H64N12O12S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:949.09
  • JG-258

    CAS:
    JG-258 is an inactive negative control for Hsp70 inhibitors [1] .
    Formula:C20H22ClN3OS3
    Color and Shape:Solid
    Molecular weight:452.06
  • trans-Dehydrocurvularin

    CAS:
    trans-Dehydrocurvularin is a useful organic compound for research related to life sciences. The catalog number is T125357 and the CAS number is 21178-57-4.
    Formula:C16H18O5
    Color and Shape:Solid
    Molecular weight:290.315
  • PROTAC Hsp90α degrader 1


    Compound X10g (PROTAC Hsp90α degrader 1) is a selective agent targeting Hsp90α for degradation and is utilized in breast cancer research.
    Formula:C43H50N6O7
    Purity:98%
    Color and Shape:Solid
    Molecular weight:762.89
  • Grp94 Inhibitor-2


    Grp94 Inhibitor-2 (compound 23) is a cyclopropane analog that exhibits high affinity for Glucose Regulated Protein 94 (Grp94), with dissociation constants (Kd) of 0.48 µM for Grp94 and 0.65 µM for Hsp90α.
    Formula:C26H25ClFNO4
    Molecular weight:469.94
  • Cemdomespib

    CAS:
    Cemdomespib (KU-596) is a potent Hsp90 modulator with neuroprotective effects and can improve diabetic neuropathy.
    Formula:C24H30FNO6
    Color and Shape:Solid
    Molecular weight:447.5
  • NDNA3


    NDNA3 (compound 14) selectively inhibits Hsp90α with an IC50 of 0.51 μM, demonstrating low membrane permeability and minimal toxicity to Ovcar-8 and MCF-10A
    Formula:C28H32N2O3S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:476.63
  • Alvespimycin TFA


    Alvespimycin (17-DMAG) TFA is a potent inhibitor of Hsp90, binding with an EC50 of 62 ± 29 nM.
    Formula:C34H49F3N4O10
    Color and Shape:Solid
    Molecular weight:730.34008
  • NMS-E973

    CAS:
    NMS-E973 is a potent and selective Hsp90 inhibitor with DC50 of <10 nM for Hsp90 binding, no activiy against a panel of 52 diverse protein kinases.
    Formula:C22H22N4O7
    Purity:99.84%
    Color and Shape:Yellow Solid
    Molecular weight:454.4327
  • Palmitic acid-13C2

    CAS:
    13C-labeled Palmitic acid is a saturated fatty acid in animals/plants influencing GRP78 and CHOP in mouse cells.
    Formula:C16H32O2
    Molecular weight:258.415
  • AlF-NOTA-c-d-VAP


    AlF-NOTA-c-d-VAP is a peptide-based PET probe designed for targeting and imaging tumors via GRP78. It exhibits high stability both in vitro and in vivo.
    Formula:C51H83AlFN17O19S
    Molecular weight:1315.55713
  • CCT245232

    CAS:
    CCT245232 is a potent HSF1 inhibitor, possibly used for researching cancer.
    Formula:C27H23N3O4
    Color and Shape:Solid
    Molecular weight:453.4892
  • Debio 0932

    CAS:
    Debio 0932 (CUDC-305) is a Hsp9 inhibitor, apoptosis, and has the advantage of being orally available and cross the BBB for cancers NSCLC and neuroblastoma.
    Formula:C22H30N6O2S
    Purity:98.98%
    Color and Shape:White Solid
    Molecular weight:442.578