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Apoptosis

Apoptosis

Los inhibidores de la apoptosis son compuestos que previenen o retrasan el proceso de muerte celular programada, conocido como apoptosis. Estos inhibidores son vitales para estudiar los mecanismos de supervivencia celular y se utilizan para investigar enfermedades donde la apoptosis está desregulada, como el cáncer, los trastornos neurodegenerativos y las enfermedades autoinmunes. Al modular la apoptosis, estos inhibidores pueden ayudar en el desarrollo de terapias dirigidas a controlar la muerte celular. En CymitQuimica, ofrecemos una amplia selección de inhibidores de la apoptosis de alta calidad para apoyar su investigación en biología celular, oncología y campos relacionados.

Subcategorías de "Apoptosis"

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Se han encontrado 6170 productos de "Apoptosis"

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productos por página.
  • HC-5404

    CAS:
    HC-5404 is a potent and selective PERK inhibitor, blocking the activation of the PERK pathway, anti-tumor effects, advanced solid tumors and renal cell Cancer.
    Fórmula:C24H24F2N4O3
    Pureza:99.33%
    Forma y color:Solid
    Peso molecular:454.47

    Ref: TM-T86545

    1mg
    167,00€
    5mg
    404,00€
    10mg
    583,00€
    25mg
    888,00€
    50mg
    1.224,00€
  • Milademetan

    CAS:
    Milademetan (DS-3032), an MDM2 inhibitor, exhibits antitumor activity, induces G1 cell cycle arrest and apoptosis, and can be used to study solid tumors.
    Fórmula:C30H34Cl2FN5O4
    Pureza:>99.99%
    Forma y color:Solid
    Peso molecular:618.53

    Ref: TM-T12040

    1mg
    93,00€
    5mg
    167,00€
    10mg
    260,00€
    25mg
    492,00€
    50mg
    802,00€
    100mg
    1.378,00€
    1mL*10mM (DMSO)
    221,00€
  • PF-07328948

    CAS:
    PF-07328948 is a branched-chain keto-acid dehydrogenase kinase (BDK) inhibitor, useful for studying CVD metabolic disorders.
    Fórmula:C16H8F4O3S
    Pureza:98.42%
    Forma y color:Solid
    Peso molecular:356.29

    Ref: TM-T88836

    1mg
    207,00€
    5mg
    518,00€
    10mg
    740,00€
    25mg
    1.103,00€
  • Nalmefene

    CAS:
    Nalmefene (ORF 11676) is a μ-opioid antagonist and partial κ agonist used in the study of opioid overdose and alcohol dependence.
    Fórmula:C21H25NO3
    Pureza:99.86%
    Forma y color:Solid
    Peso molecular:339.43

    Ref: TM-T86954

    2mg
    37,00€
    5mg
    54,00€
    10mg
    82,00€
  • BCL6-IN-3

    CAS:
    BCL6-IN-3: potent BCL6 inhibitor, 70 nM GI50 in SU-DHL4, affects cell functions, antitumor.
    Fórmula:C24H31ClF2N6O2
    Pureza:98.17%
    Forma y color:Solid
    Peso molecular:508.99

    Ref: TM-T10487

    1mg
    109,00€
    5mg
    241,00€
    10mg
    355,00€
    25mg
    532,00€
    50mg
    745,00€
    100mg
    1.018,00€
    500mg
    A consultar
    1mL*10mM (DMSO)
    370,00€
  • Zharp1-211

    CAS:
    Zharp1-211 is a RIPK3 inhibitor,reduces JAK/ stat1-mediated chemokines and MHC class II molecules in IECs, (GVHD) for gastrointestinal inflammation.
    Fórmula:C24H25N5O4
    Pureza:99.71%
    Forma y color:Solid
    Peso molecular:447.49

    Ref: TM-T87664

    1mg
    82,00€
    5mg
    173,00€
    10mg
    268,00€
    25mg
    532,00€
    50mg
    827,00€
    100mg
    1.243,00€
    200mg
    1.674,00€
    1mL*10mM (DMSO)
    192,00€
  • Zotatifin

    CAS:
    Zotatifin (eFT226) is a selective eIF4A inhibitor with antiviral and antitumor properties, inhibiting Sox4 translation and inducing apoptosis.
    Fórmula:C28H29N3O5
    Pureza:98.85%
    Forma y color:Solid
    Peso molecular:487.55

    Ref: TM-T17296

    1mg
    982,00€
    5mg
    2.835,00€
    10mg
    4.438,00€
    25mg
    6.741,00€
  • Gemcitabine elaidate hydrochloride

    CAS:

    CP-4126, a lipophilic pro-drug of Gemcitabine, converts to active form by esterases, allowing oral administration with dose-dependent effects.

    Fórmula:C27H44ClF2N3O5
    Pureza:98.50% - 99.6%
    Forma y color:Solid
    Peso molecular:564.11

    Ref: TM-T15378L

    1mg
    37,00€
    5mg
    79,00€
    10mg
    96,00€
    25mg
    175,00€
    50mg
    320,00€
  • JAK2-IN-7

    CAS:
    JAK2-IN-7 selectively inhibits JAK2 (IC50: 3 nM), shows 14-fold selectivity over JAK1/3, FLT3, induces G0/G1 arrest, apoptosis, and has antitumor effects.
    Fórmula:C26H33N7O
    Pureza:99.54%
    Forma y color:Solid
    Peso molecular:459.59

    Ref: TM-T35900

    1mg
    138,00€
    5mg
    334,00€
    10mg
    597,00€
    25mg
    1.234,00€
    50mg
    1.648,00€
    100mg
    2.232,00€
    1mL*10mM (DMSO)
    339,00€
  • FX-11

    CAS:
    FX-11: potent LDHA inhibitor (Ki 8 μM), activates PKM2, reduces ATP, induces oxidative stress/ROS, cell death, shows antitumor effects.
    Fórmula:C22H22O4
    Pureza:98.95% - 98.95%
    Forma y color:Solid
    Peso molecular:350.41

    Ref: TM-T15362

    1mg
    46,00€
    5mg
    92,00€
    10mg
    132,00€
    25mg
    212,00€
    50mg
    314,00€
    100mg
    469,00€
    1mL*10mM (DMSO)
    100,00€
  • β-Zearalanol

    CAS:
    Beta-Zearalenol, a derivative of zearalenone (ZEA) capable of conjugating with glucuronic acid[2], is a mycotoxin produced by Fusarium spp. It induces apoptosis and oxidative stress in mammalian reproductive cells[1].
    Fórmula:C18H26O5
    Forma y color:Solid
    Peso molecular:322.4

    Ref: TM-T14548

    1mg
    Descatalogado
    Producto descatalogado
  • PIM-447 dihydrochloride

    CAS:
    PIM-447 dihydrochloride is an orally available and selective inhibitor of pan-PIM kinase(Ki values of 6, 18, and 9 pM for PIM1, PIM2, and PIM3, respectively).
    Fórmula:C24H25Cl2F3N4O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:513.38

    Ref: TM-T12473

    1mg
    Descatalogado
    Producto descatalogado
  • (R)-Verapamil hydrochloride

    CAS:
    (R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is an inhibitor of P-Glycoprotein.
    Fórmula:C27H39ClN2O4
    Forma y color:Solid
    Peso molecular:491.06

    Ref: TM-T12646

    1mg
    Descatalogado
    Producto descatalogado
  • OBAA

    CAS:
    OBAA is a potent inhibitor of phospholipase A2 (PLA2) with an IC 50 of 70 nM. OBAA blocks Melittin-induced Ca 2+ influx in Trypanosoma brucei with an IC 50 of 0.4 μM [1] [2] [3].
    Fórmula:C28H44O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:428.65

    Ref: TM-T23102

    1mg
    Descatalogado
    Producto descatalogado
  • AP1867-3-(aminoethoxy)

    CAS:
    AP1867-3-(aminoethoxy) is a synthetic ligand for FKBP and can be used in the synthesis of PROTAC FKBP12 F36V degrader.
    Fórmula:C38H50N2O9
    Forma y color:Solid
    Peso molecular:678.81

    Ref: TM-T13549

    1mg
    Descatalogado
    2mg
    Descatalogado
    Producto descatalogado
  • WEHI-539 hydrochloride

    CAS:
    WEHI-539 hydrochloride is a selective Bcl-XL inhibitor with an IC50 of 1.1 nM.
    Fórmula:C31H30ClN5O3S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:620.18

    Ref: TM-T13337

    1mg
    Descatalogado
    Producto descatalogado
  • 5-Amino-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide

    CAS:
    Fórmula:C9H14N4O5
    Pureza:95%
    Forma y color:Solid
    Peso molecular:258.2313

    Ref: IN-DA0034FR

    50mg
    Descatalogado
    250mg
    Descatalogado
    Producto descatalogado
  • Platinum, diammine[1,1-cyclobutanedi(carboxylato-kO)(2-)]-, (SP-4-2)-

    CAS:
    Fórmula:C6H10N2O4Pt
    Pureza:98%
    Forma y color:Solid
    Peso molecular:369.2326

    Ref: IN-DA00I84B

    1g
    Descatalogado
    5g
    Descatalogado
    100mg
    Descatalogado
    250mg
    Descatalogado
    Producto descatalogado
  • PRGL493

    CAS:
    PRGL493 blocks ACSL4, halts PC3/MDA-MB-231 cancer cell spread, and inhibits MA-10 tumor progesterone. Effective in mouse PC3 tumor model at 0.25 mg/kg.
    Fórmula:C25H21N7O2
    Pureza:98.80% - 99.11%
    Forma y color:Solid
    Peso molecular:451.48

    Ref: TM-T35666

    1mg
    Descatalogado
    5mg
    Descatalogado
    10mg
    Descatalogado
    25mg
    Descatalogado
    50mg
    Descatalogado
    100mg
    Descatalogado
    Producto descatalogado
  • Thalidomide-O-C5-NH2 hydrochloride

    CAS:
    Thalidomide-O-C5-NH2 hydrochloride is a synthetic compound consisting of a ligand-linker conjugate with E3 ligase activity. It combines a cereblon ligand based on Thalidomide and a linker commonly utilized in PROTAC technology.
    Fórmula:C18H22ClN3O5
    Forma y color:Solid
    Peso molecular:395.84

    Ref: TM-T40079

    ne
    Descatalogado
    Producto descatalogado