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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 5600 productos de "Apoptosis"

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  • Levetiracetam

    CAS:
    <p>Levetiracetam (SIB-S1) is a relatively unique anticonvulsant that is typically used in combination with other antiepileptic medications for partial onset</p>
    Fórmula:C8H14N2O2
    Pureza:99.67% - 99.86%
    Forma y color:White Crystalline Powder
    Peso molecular:170.21
  • Cl-amidine hydrochloride

    CAS:
    <p>Cl-amidine hydrochloride is an orally available PAD inhibitor that blocks histone 3 deimination.Cost-effective and quality-assured.</p>
    Fórmula:C14H20Cl2N4O2
    Pureza:92.34% - 98.14%
    Forma y color:Solid
    Peso molecular:347.24
  • Stachyose tetrahydrate

    CAS:
    <p>Stachyose tetrahydrate (D-Stachyose tetrahydrate) is a tetrasaccharide consisting of two α-D-galactose units, one α-D-glucose unit, and one β-D-fructose unit</p>
    Fórmula:C24H50O25
    Pureza:99.89%
    Forma y color:White To Off White Crystalline Powder
    Peso molecular:738.64
  • LAT1-IN-1

    CAS:
    <p>LAT1-IN-1 (BCH) is a selective and competitive inhibitor of L-type amino acid transporter protein 1 (LAT1). LAT1-IN-1 has antitumor activity. Cost-effective and quality-assured.</p>
    Fórmula:C8H13NO2
    Pureza:99.94% - ≥98%
    Forma y color:Solid
    Peso molecular:155.19
  • Chlorhexidine

    CAS:
    <p>Chlorhexidine is a biguanide antiseptic targeting bacteria, damaging cell membranes and causing cell death, more effective against gram-positive types.</p>
    Fórmula:C22H30Cl2N10
    Pureza:98% - 99.85%
    Forma y color:Crystals From Methanol Solid
    Peso molecular:505.45
  • 2-aminobenzo[d]thiazol-6-ol

    CAS:
    <p>2-aminobenzo[d]thiazol-6-ol: antimicrobial, antioxidant, anticancer; may trigger cancer cell apoptosis.</p>
    Fórmula:C7H6N2OS
    Pureza:98.27%
    Forma y color:Solid
    Peso molecular:166.2
  • (R)-MIK665

    CAS:
    <p>(R)-MIK665 is the less active enantiomer of MIK665. MIK665 is a special inhibitor of Mcl-1(IC50 of 1.81 nM).</p>
    Fórmula:C47H44ClFN6O6S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:875.41
  • ChoKα inhibitor-5


    <p>ChoKα Inhibitor-5, a sulfur-containing choline kinase inhibitor, effectively inhibits HChoKα1 with an IC50 value of 0.64 μM and induces apoptosis.</p>
    Fórmula:C54H68Br2N4S4
    Forma y color:Solid
    Peso molecular:1061.21
  • TP4 (Nile tilapia piscidin)

    CAS:
    <p>TP4 (Nile tilapia piscidin) is an orally active piscidin-like antimicrobial peptide that exhibits inhibition of various gram-positive and negative bacterial</p>
    Fórmula:C135H226N50O27
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2981.56
  • Thalidomide-PEG3-NH2

    CAS:
    <p>Thalidomide-PEG3-NH2: a cereblon-based E3 ligase ligand-linker for PROTAC tech.</p>
    Fórmula:C19H23N3O7
    Forma y color:Solid
    Peso molecular:405.407
  • ElteN378

    CAS:
    <p>ElteN378: potently inhibits FKBP12 (Ki=0.5 nM), low weight, similar affinity to Rapamycin.</p>
    Fórmula:C23H26N2O3
    Pureza:99.06%
    Forma y color:Solid
    Peso molecular:378.46
  • c-Met-IN-24


    <p>c-Met-IN-24 (compound 3g) serves as a dual-target inhibitor for STAT-3 (=4.7 μM) and c-MET (=12.67 μM), exhibiting anticancer properties. It arrests the G2/M cell cycle and induces apoptosis in SNB-75 cells, making it applicable in the research of central nervous system cancers.</p>
    Fórmula:C20H15ClN4O4S
    Forma y color:Solid
    Peso molecular:442.88
  • VEGFR-2-IN-64


    <p>VEGFR-2-IN-64 (Compound 28) is an inhibitor of VEGFR2 with an IC50 of 27.8 nM. It suppresses the proliferation of cancer cells A549, T-47D, and Caco-2, exhibits anti-migration and anti-colony formation activities in T-47D cells, and induces apoptosis in T-47D cells.</p>
    Fórmula:C72H123N9O6
    Forma y color:Solid
    Peso molecular:1210.8
  • PARP1-IN-27


    <p>PARP1-IN-27 (Compound 9B) serves as an inhibitor of both PARP1 and PARP2, exhibiting IC 50 values of 2.53 nM and 6.45 nM, respectively, in SUM149PT cells. This compound effectively suppresses the proliferation of BRCA-mutated cancer cell lines such as SUM149PT, HCC1937, and Capan-1, with respective IC 50 values of 0.62, 1.91, and 4.26 μM. Additionally, PARP1-IN-27 exacerbates DNA double-strand breaks, enhances ROS production, causes G2/M phase cell cycle arrest, and triggers apoptosis in SUM149PT cells.</p>
    Fórmula:C17H12FNO4
    Forma y color:Solid
    Peso molecular:313.28
  • Phenamet

    CAS:
    <p>Phenamet is a bioactive chemical.</p>
    Fórmula:C19H28Cl2N2O3S
    Forma y color:Solid
    Peso molecular:435.41
  • VPC-70063

    CAS:
    <p>VPC-70063 (Thiourea, N-[3,5-bis(trifluoromethyl)phenyl]-N'-(phenylmethyl)-) is an inhibitor of c-Myc-MAX.</p>
    Fórmula:C16H12F6N2S
    Pureza:99.98%
    Forma y color:Solid
    Peso molecular:378.34
  • Anticancer agent 268


    <p>Anticanceragent 268 (Compound 4k) is a potential antitumor agent. It exhibits antiproliferative effects on HepG2 cells, with an IC50 value of 6.08 μM. Additionally, Anticanceragent 268 induces apoptosis and inhibits colony formation and migration of HepG2 cells.</p>
    Forma y color:Odour Solid
  • IRAK4-IN-27


    <p>IRAK4-IN-27 (Compound 22) is a potent and selective IRAK4 inhibitor, demonstrating an IC50 of 8.7 nM.</p>
    Fórmula:C23H22N6O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:430.46
  • P-gp inhibitor 16


    <p>P-gp inhibitor 16 (compound 14) is an inhibitor of p-glycoprotein. It significantly enhances apoptosis induced by doxorubicin and displays anticancer properties.</p>
    Fórmula:C35H35N5O4
    Peso molecular:589.2689
  • ChoKα inhibitor-3


    <p>ChoKα Inhibitor-3, a sulfur-containing choline kinase inhibitor, effectively inhibits HChoK α1 with an IC50 value of 0.66 μM and possesses the capability to</p>
    Fórmula:C50H54Br2Cl2N4S2
    Forma y color:Solid
    Peso molecular:1005.83