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HSP

HSP

Gli inibitori delle proteine da shock termico (HSP) prendono di mira le HSP, una famiglia di chaperoni molecolari che assistono nel ripiegamento delle proteine, nella stabilità e nella protezione contro i danni indotti dallo stress. Le HSP sono spesso sovraregolate nelle cellule tumorali, aiutandole a sopravvivere in condizioni stressanti come l'ipossia e la chemioterapia. L'inibizione delle HSP può interrompere questi meccanismi protettivi, portando alla morte cellulare. Gli inibitori delle HSP sono quindi preziosi nella terapia del cancro e nella ricerca sulle risposte allo stress. Presso CymitQuimica, offriamo una gamma completa di inibitori delle HSP di alta qualità per supportare la tua ricerca nell'omeostasi delle proteine, nelle risposte allo stress e nell'oncologia.

Trovati 179 prodotti di "HSP"

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  • MAL3-101

    CAS:
    MAL3-101 is a molecular chaperone inhibitor of heat shock protein 70 (Hsp 70).
    Formula:C54H66N4O10
    Colore e forma:Solid
    Peso molecolare:931.12
  • dPDL1-4


    dPDL1-4 is a potent and selective eHSPTAC eHSP90PD-L1 degrader, with DC50 values of 7.77 μM (HeLa) and 6.52 μM (B16F10). It links eHSP90 to target proteins, inducing lysosomal degradation. dPDL1-4 effectively degrades PD-L1 and inhibits tumor growth, making it useful for research in cervical cancer and melanoma.
    Colore e forma:Odour Solid
  • Grp94 Inhibitor-3


    Grp94 Inhibitor-3 (Compound C6) is a selective inhibitor of glucose-regulated protein 94 (Grp94), with an affinity of 5.52 μM. It shows potential for research in primary open-angle glaucoma and metastatic cancer.
    Formula:C24H20ClNO4
    Colore e forma:Solid
    Peso molecolare:421.87
  • Alvespimycin TFA


    Alvespimycin (17-DMAG) TFA is a potent inhibitor of Hsp90, binding with an EC50 of 62 ± 29 nM.
    Formula:C34H49F3N4O10
    Colore e forma:Solid
    Peso molecolare:730.34008
  • 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
    Colore e forma:Solid
    Peso molecolare:481.43
  • 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
    Purezza:99.29%
    Colore e forma:Solid
    Peso molecolare:569.63
  • Chetomin

    CAS:
    <p>Chetomin (BRN0077366) is an inhibitor of HIF-1 by weaken transcription of HIF-1, disrupting the binding of HIF-1α and HIF-2α to p300 at low nanomolar</p>
    Formula:C31H30N6O6S4
    Purezza:98%
    Colore e forma:Off-White To Fawn Solid
    Peso molecolare:710.87
  • CCT245232

    CAS:
    CCT245232 is a potent HSF1 inhibitor, possibly used for researching cancer.
    Formula:C27H23N3O4
    Colore e forma:Solid
    Peso molecolare:453.49
  • Palmitic acid-1-13C

    CAS:
    Palmitic acid-13C, a 16-C saturated fatty acid internal standard for GC/LC-MS, is prevalent in plasma lipids and influences protein acylation and COX-2 levels.
    Formula:C16H32O2
    Colore e forma:Solid
    Peso molecolare:257.422
  • PU-H71

    CAS:
    PU-H71 is an effective selective HSP90 inhibitor with an IC50 of 51 nM.
    Formula:C18H21IN6O2S
    Purezza:98.31% - 99.937%
    Colore e forma:Solid
    Peso molecolare:512.37
  • 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
    Purezza:98.98%
    Colore e forma:Solid
    Peso molecolare:442.58
  • L-Alanyl-L-glutamine

    CAS:
    L-Alanyl-L-glutamine (Ala-Gln), a dipeptide composed of alanine and Gln, is an alternative supplement to L-glutamine in the production of biopharmaceuticals.
    Formula:C8H15N3O4
    Purezza:99.71% - 99.97%
    Colore e forma:Solid
    Peso molecolare:217.22
  • YUM70

    CAS:
    YUM70 inhibits GRP78 (IC50: 1.5μM), inducing ER stress and apoptosis in pancreatic cancer.
    Formula:C21H19ClN2O4
    Purezza:97.25%
    Colore e forma:Solid
    Peso molecolare:398.84
  • MitoBloCK-10

    CAS:
    MitoBloCK-10 inhibits Tim44-Hsp70 binding; first to reduce PAM complex activity.
    Formula:C12H8FN3O3S
    Purezza:99.51%
    Colore e forma:Solid
    Peso molecolare:293.27
  • MK2-IN-1 hydrochloride

    CAS:
    MK2-IN-1 hydrochloride (MK 25) selectively inhibits MK2 with IC50 of 0.11 μM, non-ATP competitive.
    Formula:C27H26Cl2N4O2
    Purezza:97.32%
    Colore e forma:Solid
    Peso molecolare:509.43
  • HSF1A

    CAS:
    HSF1A is a cell-permeable activator of HSF1 that protects mammalian cells against stress-induced apoptosis.
    Formula:C21H19N3O2S2
    Purezza:98.89%
    Colore e forma:Solid
    Peso molecolare:409.52
  • Dihydroberberine

    CAS:
    Dihydroberberine has anti-atherosclerotic, anti-inflammatory, hypolipidemic and antitumor activities.
    Formula:C20H19NO4
    Purezza:93.77%
    Colore e forma:Solid
    Peso molecolare:337.37
  • PF04929113

    CAS:
    PF04929113 (SNX-5422), a synthetic small molecule Hsp90 inhibitor, offers potent efficacy orally for various cancers.
    Formula:C25H30F3N5O4
    Purezza:99.04%
    Colore e forma:Solid
    Peso molecolare:521.53
  • XL888

    CAS:
    XL888 is an orally bioavailable Hsp90 inhibitor, blocking cell proliferation and inducing tumor regression with an IC50 of 24 nM.
    Formula:C29H37N5O3
    Purezza:99.18%
    Colore e forma:Solid
    Peso molecolare:503.64
  • PF-04929113 Mesylate

    CAS:
    <p>PF-04929113 Mesylate (SNX-5422 Mesylate), a prodrug of SNX-2112, is an orally available Hsp90 inhibitor (Kd: 41 nM) and also induces Her-2 degradation (IC50: 37</p>
    Formula:C26H34F3N5O7S
    Purezza:99% - 99.46%
    Colore e forma:Solid
    Peso molecolare:617.63