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"
- ASK(9 productos)
- BCL(8 productos)
- Caspasa(147 productos)
- FOXO1(3 productos)
- IAP(67 productos)
- Mdm2(12 productos)
- PD-1 / PD-L1(140 productos)
- PDK(9 productos)
- PERK(26 productos)
- Serina / treonina quinasa(19 productos)
- Survivin(14 productos)
- TNF(91 productos)
- c-RET(61 productos)
- p53(63 productos)
Mostrar 6 subcategorías más
Se han encontrado 6114 productos de "Apoptosis"
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GSK-843
CAS:GSK-843 (GSK'843) is a RIP3 inhibitor with analgesic activity, inhibits RIP3 expression, and can be used as an adjunctive treatment for inflammation.Fórmula:C19H15N5S2Pureza:99.18%Forma y color:SolidPeso molecular:377.49PI3Kα-IN-9
CAS:PI3Kα-IN-9 is an inhibitor of PI3Kα and PI3Kα with antiproliferative activity, inhibits PI3Kα, PI3Kγ, PI3Kδ, and PI3Kβ, induces apoptosis.Fórmula:C18H21N7O3Pureza:98.29%Forma y color:SolidPeso molecular:383.4Pexidartinib hydrochloride
CAS:Pexidartinib hydrochloride (PLX-3397 HCl) is a selective, orally active, ATP-competitive CSF1R/M-CSFR and c-Kit inhibitor with IC50 values of 20 and 10 nM.Fórmula:C20H16Cl2F3N5Pureza:99.88%Forma y color:SolidPeso molecular:454.28Acetic acid, 2-[[4-[[[4-(1,1-dimethylethyl)phenyl]sulfonyl]amino]-1-hydroxy-2-naphthalenyl]thio]-
CAS:KPT-6566 is a covalent PIN1 inhibitor that selectively targets cancer cells by a dual mechanism of action.Fórmula:C22H23NO5S2Forma y color:SolidPeso molecular:445.55Methylstat
CAS:Methylstat is a methyl ester prodrug of a Jumonji C domain-containing histone demethylase (JMJD) inhibitor that has favorable cell permeability.
Fórmula:C28H31N3O6Pureza:98.34% - 98.34%Forma y color:SolidPeso molecular:505.56MC1742
CAS:MC1742 inhibits class I/IIb HDACs, blocks sarcoma CSC growth, and reactivates latent HIV. IC50: HDAC1-3/8 (0.02-0.61 μM), HDAC6/10 (7-40 nM).Fórmula:C21H21N3O3SPureza:99.20%Forma y color:SolidPeso molecular:395.48Everolimus-d4
CAS:Everolimus-d4 is a deuterated compound of Everolimus.Fórmula:C53H83NO14Forma y color:SolidPeso molecular:962.264C8-Ceramide
CAS:C8 Ceramide, a cell-permeable analog, is analog to naturally occur ceramides.Fórmula:C26H51NO3Forma y color:SolidPeso molecular:425.69Baohuoside I
CAS:Fórmula:C27H30O10Pureza:>95.0%(T)(HPLC)Forma y color:White to Light yellow to Green powder to crystalPeso molecular:514.53(-)-Gallocatechin Gallate
CAS:Fórmula:C22H18O11Pureza:>95.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:458.38M47
CAS:M47 is a selective CRY1 (Cryptochrome 1) degradator that enhances nuclear degradation of CRY1, thereby extending the lifespan of p53 knockout mice.
Fórmula:C28H22ClNO4Forma y color:SolidPeso molecular:471.93Ref: TM-T74743
1mgA consultar5mgA consultar10mgA consultar25mgA consultar50mgA consultar100mgA consultarMX1013
CAS:MX1013, a dipeptide pan-caspase inhibitor, inhibits caspase-1, -3, -6, -7, -8, and -9.Fórmula:C18H23FN2O6Forma y color:SolidPeso molecular:382.39Amoscanate
CAS:Amoscanate is an antiparasitic agent. It is highly effective in animals against the four major species of schistosomes which infect humans.Fórmula:C13H9N3O2SForma y color:SolidPeso molecular:271.29PRDX1-IN-1
CAS:PRDX1-IN-1 is a and PRDX1 inhibitor with potential anti-inflammatory and anti-cancer activity for the study of breast and esophageal cancer.Fórmula:C46H55N3O4Pureza:98% - 98.04%Forma y color:SolidPeso molecular:713.955-Methoxyuridine
CAS:5-Methoxyuridine (Mo5U) is an antitumor purine analog that inhibits DNA synthesis and induces apoptosis in lymphatic cancers.
Fórmula:C10H14N2O7Pureza:99.43%Forma y color:SolidPeso molecular:274.23Cl-amidine TFA
CAS:Cl-amidine TFA: oral PAD inhibitor, induces cancer cell apoptosis, IC50s: PAD1 - 0.8μM, PAD3 - 6.2μM, PAD4 - 5.9μM.Fórmula:C16H20ClF3N4O4Forma y color:SolidPeso molecular:424.8MCL-1/BCL-2-IN-2
CAS:MCL-1/BCL-2-IN-2 is a selective Mcl-1 and Bcl-2 inhibitor with potential antitumor activity for tumor research.Fórmula:C20H15BrN2O2SPureza:98.03%Forma y color:SolidPeso molecular:427.31Momelotinib sulfate
CAS:Momelotinib sulfate is an ATP-competitive JAK1/JAK2 inhibitor (IC50: 11 nM/18 nM). It has 10-fold selectivity versus JAK3.Fórmula:C23H26N6O10S2Pureza:98%Forma y color:SolidPeso molecular:610.62PERK-IN-2
CAS:PERK-IN-2 is a potent inhibitor of PERK(IC50 of 0.2 nM).Fórmula:C23H18F3N5OPureza:98%Forma y color:SolidPeso molecular:437.42Galiximab
CAS:Melrilimab (GSK 3772847) is an IgG antibody targeting IL-33R with high affinity for IL1RL1/ST2/DER4/FIT-1 and can be used in asthma research.Pureza:> 95%Forma y color:LiquidPeso molecular:145.24 kDa
![Acetic acid, 2-[[4-[[[4-(1,1-dimethylethyl)phenyl]sulfonyl]amino]-1-hydroxy-2-naphthalenyl]thio]-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTM%2Fthumb-webp%2FT67441.webp&w=3840&q=75)
