
Apoptosis
Apoptosis inhibitors are compounds that prevent or delay the process of programmed cell death, known as apoptosis. These inhibitors are vital in studying cell survival mechanisms and are used to investigate diseases where apoptosis is dysregulated, such as cancer, neurodegenerative disorders, and autoimmune diseases. By modulating apoptosis, these inhibitors can help in the development of therapies aimed at controlling cell death. At CymitQuimica, we provide a comprehensive selection of high-quality apoptosis inhibitors to support your research in cell biology, oncology, and related fields.
Subcategories of "Apoptosis"
- ASK(9 products)
- BCL(11 products)
- Caspase(144 products)
- FOXO1(3 products)
- IAP(67 products)
- Mdm2(12 products)
- PD-1/PD-L1(139 products)
- PDK(9 products)
- PERK(27 products)
- Serine/threonin kinase(18 products)
- Survivin(14 products)
- TNF(93 products)
- c-RET(62 products)
- p53(63 products)
Show 6 more subcategories
Found 6059 products of "Apoptosis"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
CHS-828 nicotinate
CAS:CHS-828, or GMX-1778, is a potent NAMPT inhibitor with anticancer properties, active against tumors and enhanced by certain drugs.Formula:C25H27ClN6O3Color and Shape:SolidMolecular weight:494.97CAM 833
CAS:<p>CAM 833 inhibits BRCA2-RAD51 interaction; Kd for ChimRAD51 is 366 nM, disrupts RAD51 oligocoagulation, and induces apoptosis in G2/M cells.</p>Formula:C26H26ClFN4O5Purity:99.83%Color and Shape:SolidMolecular weight:528.96Topoisomerase IIα-IN-3
CAS:Topoisomerase IIα-IN-3 is a DNA-inserting topoisomerase-Iiα inhibitor that blocks the cell cycle in G0/G1 phase and induces apoptosis.Formula:C29H20N6O2SColor and Shape:SolidMolecular weight:516.57HL271
CAS:HL271, a derivative of metformin, is a potent AMPK activator that increases AMPK phosphorylation. HL271 attenuates aging-associated cognitive impairment.Formula:C13H17ClF3N5OPurity:98%Color and Shape:SolidMolecular weight:351.76KY1022
CAS:KY1022 is a ras destabilizer. KY1022 targets the Wnt/ß-catenin pathway and inhibits development of metastatic colorectal cancer.Formula:C17H19N3OSColor and Shape:SolidMolecular weight:313.42ML132
CAS:ML132 is an effective and selective inhibitor of caspase 1 (IC50: 0.316 nM).Formula:C22H28ClN5O5Color and Shape:SolidMolecular weight:477.94NSC405640
CAS:NSC405640 selectively inhibits MDM2-p53 interaction, restoring mutated p53 structure; halts growth of cells with normal p53. [1]Formula:C12H10Cl2SnColor and Shape:SolidMolecular weight:343.82MBM-17
CAS:MBM-17 is a potent inhibitor of NIMA-related kinase 2 (Nek2,IC50 of 3 nM).Formula:C28H28N6O2Purity:98%Color and Shape:SolidMolecular weight:480.56TH1834 dihydrochloride
CAS:TH1834 dihydrochloride is a specific Tip60 histone acetyltransferase inhibitor.Formula:C33H42Cl2N6O3Purity:98%Color and Shape:SolidMolecular weight:641.63MpsBAY2a
CAS:carcinoma cell proliferation.Formula:C29H28N6OPurity:98%Color and Shape:SolidMolecular weight:476.57CTX1
CAS:CTX1 is a small molecule activator of p53.Formula:C14H10N4Purity:98%Color and Shape:SolidMolecular weight:234.26pan-HER-IN-1
CAS:<p>Compound C5: Irreversible, oral pan-HER inhibitor with low IC50s for EGFR/HERs; induces apoptosis and has antitumor effects.</p>Formula:C19H14BrN5OColor and Shape:SolidMolecular weight:408.25SLMP53-2
CAS:SLMP53-2 is a mutant p53 reactivator that restores the wild-type-like conformation and DNA-binding ability of mutp53-Y220C through enhanced interaction withFormula:C26H22N2O2Color and Shape:SolidMolecular weight:394.47Epirubicin
CAS:Epirubicin, a doxorubicin derivative, is an antineoplastic, inhibits topoisomerase, DNA/RNA synthesis, and Foxp3, reducing T cell activity.Formula:C27H29NO11Color and Shape:SolidMolecular weight:543.52Antitumor agent-81
CAS:Antitumor agent-81, a P62-RNF168 agonist, reduces H2A ubiquitination, hinders DNA repair, and inhibits tumor growth.Formula:C19H19N7O3Color and Shape:SolidMolecular weight:393.4MYRA-A
CAS:MYRA-A is an inducer of apoptosis in a Myc-dependent manner that acts by inhibiting Myc-driven transformation and disrupting MYC-Max interaction.Formula:C19H20N2O4Purity:98%Color and Shape:SolidMolecular weight:340.37W146 TFA
CAS:W146 TFA is a selective sphingosine-1-phosphate receptor 1 ( S1PR1 ) antagonist with an EC 50 value of 398 nM.Formula:C18H28F3N2O6PColor and Shape:SolidMolecular weight:456.3992-chloro Palmitic Acid
CAS:2-chloro Palmitic acid triggers NETosis, elevates COX-2, adhesion molecules in HCAECs, and induces apoptosis and caspase-3 in THP-1 cells/monocytes.Formula:C16H31ClO2Color and Shape:SolidMolecular weight:290.87Psammaplysene A
CAS:Psammaplysene A is a FOXO1a nuclear export inhibitor.Formula:C27H35Br4N3O3Purity:98%Color and Shape:SolidMolecular weight:769.2CDK8/19-IN-1
CAS:CDK8/19-IN-1 is a selective and oral bioavailable CDK8/19 dual inhibitor (IC50s: 0.46 nM, 0.99 nM, and 270 nM for CDK8, CDK19, and CDK9).Formula:C19H18N4O4S2Purity:98%Color and Shape:SolidMolecular weight:430.5
