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HSP

HSP

Los inhibidores de proteínas de choque térmico (HSP) se dirigen a las HSP, una familia de chaperonas moleculares que asisten en el plegamiento de proteínas, la estabilidad y la protección contra daños inducidos por el estrés. Las HSP suelen estar sobreexpresadas en células cancerosas, ayudándolas a sobrevivir en condiciones estresantes como la hipoxia y la quimioterapia. Inhibir las HSP puede interrumpir estos mecanismos de protección, lo que conduce a la muerte celular. Por lo tanto, los inhibidores de HSP son valiosos en la terapia contra el cáncer y en la investigación de respuestas al estrés. En CymitQuimica, ofrecemos una amplia gama de inhibidores de HSP de alta calidad para apoyar su investigación en homeostasis de proteínas, respuestas al estrés y oncología.

Se han encontrado 169 productos de "HSP"

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  • MAL3-101

    CAS:
    <p>MAL3-101 is a molecular chaperone inhibitor of heat shock protein 70 (Hsp 70).</p>
    Fórmula:C54H66N4O10
    Forma y color:Solid
    Peso molecular:931.12
  • HS-27

    CAS:
    <p>HS-27 is a fluorescently-tethered inhibitor of Hsp90 with SNX-5422 tethered via a PEG linker to a fluorescein isothiocyanate or FITC.</p>
    Fórmula:C52H60N6O12S
    Pureza:97.09%
    Forma y color:Solid
    Peso molecular:993.13
  • 17-DMAP-GA

    CAS:
    <p>17-DMAP-GA, a Geldanamycin analogue, acts as an HSP90 inhibitor, leading to cell cycle abnormalities.</p>
    Fórmula:C33H50N4O8
    Forma y color:Solid
    Peso molecular:630.783
  • Alvespimycin TFA


    <p>Alvespimycin (17-DMAG) TFA is a potent inhibitor of Hsp90, binding with an EC50 of 62 ± 29 nM.</p>
    Fórmula:C34H49F3N4O10
    Forma y color:Solid
    Peso molecular:730.34008
  • CCT245232

    CAS:
    <p>CCT245232 is a potent HSF1 inhibitor, possibly used for researching cancer.</p>
    Fórmula:C27H23N3O4
    Forma y color:Solid
    Peso molecular:453.49
  • PU-H71

    CAS:
    <p>PU-H71 is an effective selective HSP90 inhibitor with an IC50 of 51 nM.</p>
    Fórmula:C18H21IN6O2S
    Pureza:98.31% - 99.937%
    Forma y color:Solid
    Peso molecular:512.37
  • Debio 0932

    CAS:
    <p>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.</p>
    Fórmula:C22H30N6O2S
    Pureza:98.98%
    Forma y color:Solid
    Peso molecular:442.58
  • Palmitic acid-1-13C

    CAS:
    <p>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.</p>
    Fórmula:C16H32O2
    Forma y color:Solid
    Peso molecular:257.422
  • L-Alanyl-L-glutamine

    CAS:
    <p>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.</p>
    Fórmula:C8H15N3O4
    Pureza:99.71% - 99.97%
    Forma y color:Solid
    Peso molecular:217.22
  • YUM70

    CAS:
    <p>YUM70 inhibits GRP78 (IC50: 1.5μM), inducing ER stress and apoptosis in pancreatic cancer.</p>
    Fórmula:C21H19ClN2O4
    Pureza:97.25%
    Forma y color:Solid
    Peso molecular:398.84
  • MitoBloCK-10

    CAS:
    <p>MitoBloCK-10 inhibits Tim44-Hsp70 binding; first to reduce PAM complex activity.</p>
    Fórmula:C12H8FN3O3S
    Pureza:99.51%
    Forma y color:Solid
    Peso molecular:293.27
  • HSF1A

    CAS:
    <p>HSF1A is a cell-permeable activator of HSF1 that protects mammalian cells against stress-induced apoptosis.</p>
    Fórmula:C21H19N3O2S2
    Pureza:98.89%
    Forma y color:Solid
    Peso molecular:409.52
  • Dihydroberberine

    CAS:
    <p>Dihydroberberine has anti-atherosclerotic, anti-inflammatory, hypolipidemic and antitumor activities.</p>
    Fórmula:C20H19NO4
    Pureza:93.77%
    Forma y color:Solid
    Peso molecular:337.37
  • PF04929113

    CAS:
    <p>PF04929113 (SNX-5422), a synthetic small molecule Hsp90 inhibitor, offers potent efficacy orally for various cancers.</p>
    Fórmula:C25H30F3N5O4
    Pureza:99.04%
    Forma y color:Solid
    Peso molecular:521.53
  • 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>
    Fórmula:C26H34F3N5O7S
    Pureza:99% - 99.46%
    Forma y color:Solid
    Peso molecular:617.63
  • Luminespib

    CAS:
    <p>Luminespib (VER-52296) is an HSP90 inhibitor that inhibits HSP90α and HSP90β. Luminespib has antitumor activity. Cost-effective and quality-assured.</p>
    Fórmula:C26H31N3O5
    Pureza:98% - 99.25%
    Forma y color:Solid
    Peso molecular:465.54
  • MK2-IN-1 hydrochloride

    CAS:
    <p>MK2-IN-1 hydrochloride (MK 25) selectively inhibits MK2 with IC50 of 0.11 μM, non-ATP competitive.</p>
    Fórmula:C27H26Cl2N4O2
    Pureza:97.32%
    Forma y color:Solid
    Peso molecular:509.43
  • Onalespib

    CAS:
    <p>Onalespib (AT13387) is an oral Hsp90 inhibitor with anticancer potential, disrupting tumor cell growth and survival.</p>
    Fórmula:C24H31N3O3
    Pureza:98.05% - 99.66%
    Forma y color:Solid
    Peso molecular:409.52
  • XL888

    CAS:
    <p>XL888 is an orally bioavailable Hsp90 inhibitor, blocking cell proliferation and inducing tumor regression with an IC50 of 24 nM.</p>
    Fórmula:C29H37N5O3
    Pureza:99.18%
    Forma y color:Solid
    Peso molecular:503.64
  • Azadiradione

    CAS:
    <p>Azadiradione (AZD) (AZD) from the methanolic extract of seeds of Azadirachta indica</p>
    Fórmula:C28H34O5
    Pureza:99.52%
    Forma y color:Solid
    Peso molecular:450.57