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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 180 products of "HSP"

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  • HSP90-IN-22

    CAS:
    HSP90-IN-22 (Compound 35) is an Hsp90 inhibitor exhibiting antiproliferative activity, with IC50 values of 3.65 μM in MCF7 breast cancer cells and 2.71 μM in
    Formula:C25H30N4O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:434.53

    Ref: TM-T79083

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Bimoclomol

    CAS:
    Bimoclomol is a heat shock protein co-inducer used for the research of cardiovascular diseases.
    Formula:C14H20ClN3O2
    Color and Shape:Solid
    Molecular weight:297.78

    Ref: TM-T13580

    25mg
    To inquire
    50mg
    To inquire
    100mg
    To inquire
  • Hsp90-IN-15

    CAS:
    Hsp90-IN-15: Hsp90 blocker with anticancer properties; halts S phase, triggers apoptosis, cuts Hsp90 in Hela cells.
    Formula:C23H27F3N4
    Color and Shape:Solid
    Molecular weight:416.48

    Ref: TM-T62163

    25mg
    1,927.00€
    50mg
    2,507.00€
    100mg
    3,168.00€
  • AMP-PCP disodium

    CAS:
    AMP-PCP disodium is an ATP analogue with binding affinity to the N-terminal domain of Hsp90, with a Kd value of 3.8 μM.
    Formula:C11H16N5Na2O12P3
    Purity:99.32% - 99.32%
    Color and Shape:Solid
    Molecular weight:549.17

    Ref: TM-T13547L

    1mg
    63.00€
    5mg
    137.00€
    10mg
    212.00€
    25mg
    358.00€
  • JG-231

    CAS:

    JG-231, a JG-98 analog, shows anticancer properties by blocking Hsp70-BAG3 interaction and hindering TNBC in MDA-MB-231 models.

    Formula:C22H18BrCl2N3OS4
    Purity:99.79%
    Color and Shape:Solid
    Molecular weight:619.47

    Ref: TM-T70353

    1mg
    70.00€
    5mg
    170.00€
    10mg
    221.00€
    25mg
    353.00€
    50mg
    452.00€
    100mg
    620.00€
    200mg
    843.00€
  • SNX0723

    CAS:
    SNX0723 is a potent Hsp90 Inhibitor with anti-Plasmodium activity.
    Formula:C22H26FN3O3
    Purity:99.85%
    Color and Shape:Solid
    Molecular weight:399.46

    Ref: TM-T28824

    1mg
    85.00€
    5mg
    178.00€
    10mg
    299.00€
    25mg
    485.00€
    50mg
    665.00€
    100mg
    892.00€
    500mg
    To inquire
    1mL*10mM (DMSO)
    195.00€
  • Arimoclomol

    CAS:
    Arimoclomol (BRX-220 free base) is a co-inducer of heat shock proteins (HSP) and can be used in studies about the treatment of amyotrophic lateral sclerosis (
    Formula:C14H20ClN3O3
    Purity:99.15%
    Color and Shape:Solid
    Molecular weight:313.78

    Ref: TM-T13553

    2mg
    39.00€
    5mg
    56.00€
    10mg
    93.00€
    25mg
    138.00€
    50mg
    197.00€
    100mg
    294.00€
    1mL*10mM (DMSO)
    65.00€
  • Iroxanadine

    CAS:
    Iroxanadine (BRX-005) is a Novel small molecule MAPK p38 inhibitor that induces phosphorylation of p38 SAPK and induces concentration-dependent relaxation in
    Formula:C14H20N4O
    Purity:98.04% - 99.04%
    Color and Shape:Solid
    Molecular weight:260.33

    Ref: TM-T27627

    1mg
    136.00€
    5mg
    315.00€
    10mg
    477.00€
    25mg
    773.00€
    50mg
    1,063.00€
    100mg
    1,431.00€
    500mg
    2,872.00€
  • KU-177

    CAS:
    KU-177 is an Aha1 inhibitor that disrupts the interaction between Hsp90 and Aha1, eliminating cell proliferation and PI resistance induced by elevated AHSA1.
    Formula:C27H23NO8
    Purity:96.92% - 98.54%
    Color and Shape:Solid
    Molecular weight:489.47

    Ref: TM-T63273

    1mg
    415.00€
    5mg
    964.00€
    10mg
    1,288.00€
    25mg
    1,918.00€
  • Flavokawain 1i

    CAS:
    Flavokawain 1i, a derivative of chalcones flavokawain A, flavokawain B, and flavokawain C, exhibits anticancer and antiviral properties.
    Formula:C21H18O4
    Color and Shape:Solid
    Molecular weight:334.37

    Ref: TM-T83890

    1mg
    197.00€
    5mg
    838.00€
    10mg
    1,279.00€
    25mg
    2,935.00€
  • MAO A/HSP90-IN-2

    CAS:
    MAO A/HSP90-IN-2 (compound 4-C), a dual inhibitor of HSP90 and MAO A, exhibits IC50 values of 0.016 μM for MAO A and 4.58 μM for HSP90.
    Formula:C25H31ClN2O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:458.98

    Ref: TM-T79487

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • GRP78-IN-2

    CAS:
    GRP78-IN-2 inhibits surface GRP78, showing anti-angiogenic and anti-cancer properties, sparing normal cells.
    Formula:C29H29NO6
    Color and Shape:Solid
    Molecular weight:487.54

    Ref: TM-T63243

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Iroxanadine sulfate

    CAS:
    Iroxanadine sulfate is a MAPK p38 inhibitor potentially for the treatment of atherosclerosis.
    Formula:C14H22N4O5S
    Color and Shape:Solid
    Molecular weight:358.41

    Ref: TM-T69520

    25mg
    1,773.00€
    50mg
    2,322.00€
    100mg
    3,060.00€
  • MAO A/HSP90-IN-1

    CAS:
    MAO A/HSP90-IN-1 (4-b) is a dual inhibitor of MAO A and HSP90, exhibiting IC50 values of 1.77 μM in glioblastoma (GBM) GL26 cells and 0.019 μM against HSP90α.
    Formula:C24H29ClN2O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:444.95

    Ref: TM-T79486

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Colletofragarone A2

    CAS:
    Colletofragarone A2 from Colletotrichum sp. blocks mutant p53 and HSP90, aiding cancer treatment.
    Formula:C22H26O6
    Color and Shape:Solid
    Molecular weight:386.44

    Ref: TM-T75517

    5mg
    To inquire
    50mg
    To inquire
  • YM-08

    CAS:
    YM-08 (Compound 7a), a brain-penetrant SIRT2 inhibitor, exhibits an IC50 of 19.9 μM. Additionally, it acts as an inhibitor of Hsp70 [1].
    Formula:C19H17N3OS2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:367.49

    Ref: TM-T80752

    5mg
    To inquire
    50mg
    To inquire
  • HSP90-IN-29

    CAS:
    HSP90-IN-29 (Compound 13), a benzoxazole derivative, serves as a potent and selective HSP-90 inhibitor, exhibiting a low IC50 value of 30 nM. This compound demonstrates significant antitumor activity [1].
    Formula:C19H20ClN3O4
    Color and Shape:Solid
    Molecular weight:389.83

    Ref: TM-T84486

    10mg
    To inquire
    50mg
    To inquire
  • HSP90-IN-27

    CAS:
    HSP90-IN-27, also known as compound 19, is an inhibitor of HSP90 [1].
    Formula:C18H21N3O2S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:343.44

    Ref: TM-T82166

    5mg
    To inquire
    50mg
    To inquire
  • BX-2819

    CAS:
    BX-2819 is an Hsp90 inhibitor that exhibits potent antiproliferative activity with an IC50 of 41 nM .
    Formula:C21H24N4O4S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:428.51

    Ref: TM-T82802

    5mg
    To inquire
    50mg
    To inquire
  • HSP90-IN-19

    CAS:
    HSP90-IN-19: potent Hsp90 inhibitor, IC50 = 0.27 μM, used in research on viral diseases, neurodegeneration, inflammation.
    Formula:C29H38O7
    Purity:98%
    Color and Shape:Solid
    Molecular weight:498.61

    Ref: TM-T73038

    25mg
    1,504.00€
    50mg
    1,963.00€
    100mg
    2,520.00€