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HSP

HSP

Os inibidores de proteínas de choque térmico (HSP) têm como alvo as HSPs, uma família de chaperonas moleculares que auxiliam no dobramento de proteínas, estabilidade e proteção contra danos induzidos por estresse. As HSPs são frequentemente superexpressas em células cancerígenas, ajudando-as a sobreviver em condições estressantes, como hipóxia e quimioterapia. Inibir as HSPs pode interromper esses mecanismos de proteção, levando à morte celular. Portanto, os inibidores de HSP são valiosos na terapia contra o câncer e na pesquisa de respostas ao estresse. Na CymitQuimica, oferecemos uma gama abrangente de inibidores de HSP de alta qualidade para apoiar sua pesquisa em homeostase de proteínas, respostas ao estresse e oncologia.

Foram encontrados 176 produtos para "HSP".

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  • Iroxanadine hydrobromide

    CAS:
    Iroxanadine hydrobromide is a MAPK p38 inhibitor potentially for the treatment of atherosclerosis.
    Fórmula:C14H21BrN4O
    Cor e Forma:Solid
    Peso molecular:341.25

    Ref: TM-T69519

    25mg
    2.043,00€
    50mg
    2.682,00€
    100mg
    3.600,00€
  • C086

    CAS:
    C086 is a novel and potent Hsp90 inhibitor that suppresses cell cycle progression, induces apoptosis, and exhibits anti-metastatic properties by modulating various mechanisms in different cell types.
    Fórmula:C29H28O8
    Cor e Forma:Solid
    Peso molecular:504.53

    Ref: TM-T200395

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Hsp110-STAT3 interaction-IN-1

    CAS:
    Row174336 (compound 29) serves as an efficient inhibitor of the Hsp110-STAT3 interaction, exhibiting antiproliferative activity in the HPAEC cell line with an IC50 of 22.67 μM.
    Fórmula:C23H31N3O4S
    Cor e Forma:Solid
    Peso molecular:445.58

    Ref: TM-T201209

    25mg
    A consultar
    50mg
    A consultar
    100mg
    A consultar
  • ETB

    CAS:
    ETB is a potent inhibitor of Hsp60 chaperone activity. It can impede the chaperone function of both wild-type proteins and the C237A and C447A mutant proteins. ETB binds to Hsp60 at Cys442, and the C442A mutant demonstrates resistance to ETB inhibition.
    Fórmula:C24H33NO6
    Cor e Forma:Solid
    Peso molecular:431.52

    Ref: TM-T210270

    10mg
    A consultar
    50mg
    A consultar
  • DDO-6691

    CAS:
    DDO-6691 is an inhibitor of heat shock protein 90 (HSP90). It exhibits antiproliferative effects against various tumor cells, with the highest sensitivity observed in HCT-116 colon cancer cells (IC50: 1.08 μM). DDO-6691 also demonstrates potent tumor growth inhibition in HCT-116 xenograft mouse models.
    Fórmula:C22H17N3O2S
    Cor e Forma:Solid
    Peso molecular:387.45

    Ref: TM-T207588

    10mg
    A consultar
    50mg
    A consultar
  • Macbecin I

    CAS:
    Hsp90 inhibitor
    Fórmula:C30H42N2O8
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:558.66

    Ref: TM-T22960

    1mg
    945,00€
  • Onalespib lactate

    CAS:
    Onalespib lactate is a second-generation, potent and selective HSP90 Inhibitor with antitumor activity.
    Fórmula:C27H37N3O6
    Cor e Forma:Solid
    Peso molecular:499.6

    Ref: TM-T28236

    25mg
    1.908,00€
    50mg
    2.502,00€
    100mg
    3.330,00€
  • HSP90-IN-11


    HSP90-IN-11: potent HSP90 inhibitor, akin to AUY-922; hinders CRC/NSCLC cell proliferation; degrades EGFR, Akt proteins.
    Fórmula:C27H30FN3O6
    Cor e Forma:Solid
    Peso molecular:511.54

    Ref: TM-T63528

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • HSP90-IN-32

    CAS:
    HSP90-IN-32, a carboxy-terminus inhibitor of Hsp90C, exhibits antiproliferative activity in various cell lines including SKMel173, SKMel103, SKMel19, and A375, with IC50 values of 1.01 μM, 0.782 μM, 0.607 μM, and 1.413 μM, respectively. This compound holds potential for research in anticancer agents.
    Fórmula:C33H40N2O4
    Cor e Forma:Solid
    Peso molecular:528.68

    Ref: TM-T200425

    25mg
    1.639,00€
    50mg
    2.142,00€
    100mg
    2.790,00€
  • HSP90α-IN-1

    CAS:
    HSP90α-IN-1 is an HSP90α inhibitor (IC50= 111 nM) that demonstrates anti-aging activity across various cellular senescence models. Belonging to the xanthine family, HSP90α-IN-1 is involved in research focused on combating age-related inflammation, senescence, and diseases (including cancer), and it may contribute to extending healthy lifespan.
    Fórmula:C19H16N4O2
    Cor e Forma:Solid
    Peso molecular:332.356

    Ref: TM-T206700

    10mg
    A consultar
    50mg
    A consultar
  • Hsp90-IN-34

    CAS:
    Hsp90-IN-34 (compound HAM-1) is a chemical inhibitor that targets the Aha1-Hsp90 chaperone complex with high affinity (KDapp=23.5 µM). It modulates the ATPase activity of Hsp90 by affecting the interaction between Hsp90 and Aha1.
    Fórmula:C22H14F2N6O
    Cor e Forma:Solid
    Peso molecular:416.38

    Ref: TM-T201432

    10mg
    A consultar
    50mg
    A consultar
  • DCEM1

    CAS:
    DCEM1 binds to heat shock protein 60 (HSP60) and inhibits the interaction between HSP60 and ClpP, thereby blocking the mitochondrial unfolded protein response. Additionally, DCEM1 suppresses the expression of β-catenin and reduces ATP production in PC-3 and TKO cells. It is utilized in research related to prostate cancer.
    Fórmula:C22H23N3O2S
    Cor e Forma:Solid
    Peso molecular:393.50

    Ref: TM-T207450

    10mg
    A consultar
    50mg
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  • KU-32

    CAS:
    KU-32 is a novel and novobiocin-based Hsp90 inhibitor. It can protect against neuronal cell death.
    Fórmula:C20H25NO8
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:407.41

    Ref: TM-T15671

    25mg
    A consultar
    50mg
    A consultar
    100mg
    A consultar
  • Cemdomespib

    CAS:
    Cemdomespib (KU-596) is a potent Hsp90 modulator with neuroprotective effects and can improve diabetic neuropathy.
    Fórmula:C24H30FNO6
    Cor e Forma:Solid
    Peso molecular:447.5

    Ref: TM-T62670

    25mg
    1.927,00€
    50mg
    2.507,00€
    100mg
    3.168,00€
  • TRAP1-IN-2

    CAS:
    TRAP1-IN-2, also known as compound 36, is a selective degrader of the TRAP1 client protein that does not affect Hsp90-cytosolic clients.
    Fórmula:C46H42F6N2O5P2
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:878.77

    Ref: TM-T79286

    5mg
    A consultar
    50mg
    A consultar
  • Monorden diacetate

    CAS:
    Monorden diacetate a Hsp90 Inhibitor. Monorden diacetate is a Promising Lead Compound for the Development of Novel Fungicides.
    Fórmula:C22H21ClO8
    Cor e Forma:Solid
    Peso molecular:448.85

    Ref: TM-T71645

    25mg
    2.853,00€
    50mg
    3.763,00€
    100mg
    5.220,00€