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(1 products)
- Caspase(154 products)
- FOXO1(2 products)
- IAP(67 products)
- Mdm2(12 products)
- PD-1/PD-L1(126 products)
- PDK(9 products)
- PERK(23 products)
- Serine/threonin kinase(17 products)
- Survivin(14 products)
- TNF(91 products)
- c-RET(61 products)
- p53(63 products)
Show 6 more subcategories
Found 6170 products of "Apoptosis"
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UA 62784
CAS:Blocks microtubule growth, spurs cell apoptosis, enhances vinblastine's effect in HeLa cells, mistakenly seen as CENP-E ATPase inhibitor.Formula:C23H15NO3Color and Shape:SolidMolecular weight:353.37VEGFR-2-IN-28
CAS:VEGFR-2-IN-28 is a potent inhibitor of VEGFR-2 (IC50: 0.83 μM). VEGFR-2-IN-28 induces apoptosis and exhibits antitumor effects.Formula:C26H17N7O7Color and Shape:SolidMolecular weight:539.46VS 8
CAS:VS 8: potent oral VEGFR-2 inhibitor, anti-angiogenic, induces cancer cell apoptosis & migration, acts on CSCs.Formula:C26H20F3N3O3Color and Shape:SolidMolecular weight:479.45Tezacitabine
CAS:Tezacitabine, a nucleoside analogue, inhibits ribonucleotide reductase, disrupts DNA replication, and induces apoptosis in tumor cells.Formula:C10H12FN3O4Color and Shape:SolidMolecular weight:257.22CAY10789
CAS:CAY10789: potent CysLT1R antagonist (IC50 2.8 µM), GPBAR1 agonist (EC50 3 µM), reduces U937 cell adhesion, TNF-α, stable with promising pharmacokinetics.Formula:C17H15NO2Color and Shape:SolidMolecular weight:265.31Melflufen
CAS:Melflufen, a dipeptide prodrug of Melphalan, is an alkylating agent with strong antitumor activity in MM, causing DNA damage and cytotoxicity.Formula:C24H30Cl2FN3O3Purity:97.056%Molecular weight:498.42LOM612
CAS:LOM612 is a potent and specific FOXO relocator FOXO3a reporter protein endogenous FOXO3a and FOXO1 , down-regulates c-Myc and cyclin D1, anti-proliferative.Formula:C13H10N2O2SColor and Shape:SolidMolecular weight:258.3Autophagy-IN-2
CAS:Autophagy-IN-2 (7h) blocks autophagic flux, triggers cancer cell death, aids in triple-negative breast cancer study.Formula:C17H19N5OColor and Shape:SolidMolecular weight:309.37VEGFR-2-IN-23
CAS:VEGFR-2-IN-23 (11b) is a potent VEGFR-2 inhibitor with an IC50 of 0.34 nM, exhibits antitumor effects, and causes G1 cell cycle arrest.Formula:C22H15N5O2Color and Shape:SolidMolecular weight:381.39Benpyrine
CAS:Benpyrine, an oral TNF-α inhibitor (KD 82.1 μM, IC50 0.109 μM), may help in inflammatory/autoimmune studies.Formula:C16H16N6OColor and Shape:SolidMolecular weight:308.34Prexasertib mesylate
CAS:Prexasertib (LY2606368), a Chk1/2 inhibitor, enhances therapy in acute lymphoblastic leukemia, causing DNA damage and antitumor effects.Formula:C19H23N7O5SPurity:98%Color and Shape:SolidMolecular weight:461.49Mcl1-IN-11
CAS:Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively.Formula:C38H41N3O5S2Purity:98%Color and Shape:SolidMolecular weight:683.88HLI 373
CAS:HLI373: potent Hdm2 (ubiquitin ligase) inhibitor, induces apoptosis in tumor cells, has antimalarial properties.Formula:C18H23N5O2Color and Shape:SolidMolecular weight:341.41Atopaxar
CAS:Atopaxar (E5555), a reversible PAR-1 thrombin receptor antagonist, interferes with platelet signaling.Formula:C29H38FN3O5Purity:97.07% - 98.07%Color and Shape:SolidMolecular weight:527.63Caspase-9 Inhibitor III
CAS:Caspase-9 Inhibitor III (Ac-LEHD-cmk) blocks caspase-9, protects against ischemic heart damage.Formula:C24H35ClN6O9Color and Shape:SolidMolecular weight:587.02Bax activator-1
CAS:Bax activator-1 (compound 106) is a Bax activator. It induces Bax-dependent tumor cell apoptosis[1].Formula:C29H36N4O3Color and Shape:SolidMolecular weight:488.62MBC-11
CAS:MBC-11: First bone-targeting bisphosphonate-etidronate conjugate with araC, may treat TIBD.Formula:C11H20N3O14P3Purity:>99.99% - >99.99%Color and Shape:SolidMolecular weight:511.21Berubicin HCl
CAS:Berubicin hydrochloride, a brain-penetrating anthracycline, disrupts DNA replication and repair by inhibiting topoisomerase II.Formula:C34H36ClNO11Color and Shape:SolidMolecular weight:670.1PI3Kδ-IN-10
CAS:PI3Kδ-IN-10 is a highly potent and orally active PI3Kδ inhibitor (IC50= 2 nM).Formula:C19H16ClN9Color and Shape:SolidMolecular weight:405.84Topoisomerase I inhibitor 3
CAS:Topoisomerase I (Compound ZML-14) inhibitor 3 induces HepG2 cell apoptosis and arrests cell cycle at G2/M phase.Formula:C18H14FNO3Color and Shape:SolidMolecular weight:311.31DAT-230
CAS:DAT-230 is a microtubule inhibitor effective against cancer cells, causing cell cycle arrest and apoptosis via caspase activation.Formula:C20H21NO2SColor and Shape:SolidMolecular weight:339.45Propiomazine
CAS:Propiomazine is an orally active antihistamine compound with sedative properties, useful for controlling insomnia in neurological disorders.Formula:C20H24N2OSPurity:98.5%Color and Shape:SolidMolecular weight:340.48PhiKan 083 hydrochloride
CAS:PhiKan 083 HCl: carbazole, binds Y220C (Kd 167 μM), affinity in Ln229 (Kd 150 μM).Formula:C16H19ClN2Purity:98%Color and Shape:SolidMolecular weight:274.79Rooperol
CAS:Rooperol: a norlignan with p38α inhibiting, immunomodulatory, antitumor, antibacterial, anticonvulsant, and antioxidant properties.Formula:C17H14O4Purity:98%Color and Shape:SolidMolecular weight:282.29RI-962
CAS:RI-962 is a potent and selective inhibitor of RIPK1 that protects cells from necrotic apoptosis by inhibiting RIPK1, RIPK3, and MLKL phosphorylation.Formula:C28H28N6O2Purity:99.39%Color and Shape:SoildMolecular weight:480.56Tubulin polymerization-IN-22
CAS:Tubulin polymerization-IN-22 inhibits tubulin (IC50=8.1μM), blocks G2/M phase, and triggers apoptosis.Formula:C19H16O4Color and Shape:SolidMolecular weight:308.33TRK-IN-23
CAS:TRK-IN-23 (compound 24b) is a potent, orally active inhibitor of TRK with IC50s of 0.5 nM for TRKA, 9 nM for TRKC, 14 nM for TRKA G595R, 4.4 nM for TRKA F589L,Formula:C20H17FN4O2Purity:98%Color and Shape:SolidMolecular weight:364.37NF-κB-IN-5
CAS:NF-κB-IN-5 (compound 4d) is an orally active NF-κB inhibitor.Formula:C23H27N3O4Color and Shape:SolidMolecular weight:409.48(1S,2S)-Bortezomib
CAS:(1S,2S)-Bortezomib (Bortezomib) is an enantiomer of Bortezomib.Formula:C19H25BN4O4Purity:99.6%Color and Shape:SolidMolecular weight:384.24Ref: TM-T10061
1mg60.00€2mg92.00€5mg160.00€10mg269.00€25mg429.00€50mg583.00€100mg783.00€1mL*10mM (DMSO)163.00€MSN-50
CAS:MSN-50, an inhibitor of Bax and Bak oligomerization, inhibits liposome permeabilization, prevents genotoxic cell death and promotes neuroprotection.Formula:C36H38BrN3O6Color and Shape:SolidMolecular weight:688.61NOC-5
CAS:NOC-5 is an NO donor that induces airway relaxation and concentration-dependently triggers 10 μM DAF-2 fluorescence.Formula:C6H16N4O2Purity:98%Color and Shape:SolidMolecular weight:176.22MI-389
CAS:MI-389 is a PROTAC degrader that induces the degradation of receptor tyrosine kinases (RTKs), useful for leukemia research.Formula:C35H35FN6O6Purity:98.12%Color and Shape:SolidMolecular weight:654.69Ref: TM-T33380
1mg88.00€5mg204.00€10mg304.00€25mg476.00€50mg811.00€100mg1,401.00€1mL*10mM (DMSO)276.00€AS1708727
CAS:AS1708727 is an orally bioavailable FOXO1 inhibitor that reduces plasma glucose and triglyceride levels in diabetic mice.Formula:C24H24Cl2N2O2Color and Shape:SolidMolecular weight:443.37ABD56
CAS:ABD56 inhibits osteoclast formation and activity in vitro and in vivo.Formula:C17H18O3Color and Shape:SolidMolecular weight:270.32GSK-345931A
CAS:GSK-345931A, Potent oral RIP2 inhibitor, suppresses pro-inflammatory cytokines, for autoimmune disease studies.Formula:C22H19ClNNaO3Color and Shape:SolidMolecular weight:403.83LG308
CAS:LG308, a synthetic compound, has anti-tumor properties, inducing apoptosis and mitotic arrest, thereby suppressing prostate cancer growth.Formula:C19H17FN2OColor and Shape:SolidMolecular weight:308.35FKGK 18
CAS:FKGK 18: GVIA iPLA2 inhibitor, 99.9% at 0.091 fraction, selective, IC50 ~50 nM–3 μM, reduces blood glucose and diabetes in NOD mice.Formula:C16H15F3OColor and Shape:SolidMolecular weight:280.28RIP2 Kinase Inhibitor 3
CAS:RIP2 Kinase Inhibitor 3 is a potent and selective inhibitor of RIP2 with an IC50 of 1 nM.Formula:C19H24N4O3SPurity:99.32% - 99.52%Color and Shape:SolidMolecular weight:388.48BP-1-108
CAS:BP-1-108 is a potent and selective STAT5 inhibitor.Formula:C32H38N2O6SColor and Shape:SolidMolecular weight:578.72CTX1
CAS:CTX1 is a small molecule activator of p53.Formula:C14H10N4Purity:98%Color and Shape:SolidMolecular weight:234.26PERK-IN-3
CAS:PERK-IN-3 is a potent inhibitor of PERK(IC50 of 7.4 nM).Formula:C22H16F2N4O2Purity:98%Color and Shape:SolidMolecular weight:406.38PHA-680626
CAS:PHA-680626 is a PLK inhibitor, effective on resistant leukemia cells, with IC50: Plk1 (0.53 μM), Plk2 (0.07 μM), Plk3 (1.61 μM).Formula:C23H26N6O2SColor and Shape:SolidMolecular weight:450.56Mcl1-IN-9
CAS:Mcl1-IN-9 is a potent myeloid cell leukemia-1 (Mcl-1) Inhibitor with an IC50 of 446 nM in reengineered BCR-ABL+ B-ALL cells and a Ki of 0.03 nM.Formula:C37H39ClN4O4Purity:98%Color and Shape:SolidMolecular weight:639.18MpsBAY2a
CAS:carcinoma cell proliferation.Formula:C29H28N6OPurity:98%Color and Shape:SolidMolecular weight:476.57DC-5163
CAS:DC-5163 inhibits GAPDH (IC50: 176.3 nM, Kd: 3.192 μM), targets cancer cell growth and glycolysis.Formula:C18H20ClN3OSPurity:98%Color and Shape:SolidMolecular weight:361.89PD-1-IN-22
CAS:PD-1-IN-22 is a potent programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) interaction inhibitor(IC50 of 92.3 nM).Formula:C25H25N5O4Purity:99.51%Color and Shape:SolidMolecular weight:459.5Ref: TM-T12379
1mg109.00€2mg163.00€5mg243.00€10mg355.00€25mg532.00€50mg750.00€100mg1,009.00€500mg2,035.00€1mL*10mM (DMSO)284.00€BMS-242
CAS:BMS-242 is an effective inhibitor of PD-1/PD-L1 interaction.Formula:C28H35NO4Purity:98%Color and Shape:SolidMolecular weight:449.58RIP1 kinase inhibitor 6
CAS:RIP1 Kinase Inhibitor 6 is a potent and selective inhibitor of RIP1 kinase, demonstrating inhibitory activity with an IC50 of less than 100 nM in a human R1P1Formula:C19H18F2N2O3Purity:98%Color and Shape:SolidMolecular weight:360.35Anti-inflammatory agent 47
CAS:Flo8, an anti-inflammatory and antioxidant agent, effectively suppresses the release of reactive oxygen species (ROS) and nitric oxide (NO) while inhibitingFormula:C25H18N2O3Purity:98%Color and Shape:SolidMolecular weight:394.42GW837016X
CAS:GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation.Formula:C25H20ClFN4OSColor and Shape:SolidMolecular weight:478.97GSK962
CAS:GSK962 is a GSK963 inactive enantiomer. It can be used to confirm the on-target effects.Formula:C14H18N2OPurity:99.75%Color and Shape:SolidMolecular weight:230.31ADU-S100
CAS:ADU-S100 (MIW815) is a STING agonist that significantly induces the production of IFN-β,TNF-α,IL-6,and MCP-1,induces TBK1 and IRF3 phosphorylation,antitumour.Formula:C20H24N10O10P2S2Purity:99.83%Color and Shape:SolidMolecular weight:690.54HDAC-IN-51
HDAC-IN-51 is an HDAC inhibitor.Formula:C27H24N4O2Purity:98.85%Color and Shape:SolidMolecular weight:436.51MX107
CAS:MX107 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation.Formula:C24H28N2O2Color and Shape:SolidMolecular weight:376.49PD-1/PD-L1-IN-20
CAS:PD-1/PD-L1-IN-20 is a small molecule inhibitor of PD-1/PD-L1 protein-protein interaction.Formula:C30H26BrClN2O3Color and Shape:SolidMolecular weight:577.9Didesmethylrocaglamide
CAS:Didesmethylrocaglamide, a Rocaglamide derivative, is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor that exhibits strong growth-inhibitory effects,Formula:C27H27NO7Color and Shape:SolidMolecular weight:477.51PCAF-IN-2
CAS:PCAF-IN-2 inhibits PCAF (IC50 = 5.31 µM), induces apoptosis, and halts G2/M cell cycle, showing anti-tumor properties.Formula:C10H7F3N6Color and Shape:SolidMolecular weight:268.2Undecylprodigiosin
CAS:Undecylprodigiosin is a classical cytotoxic immunosuppressant, suppressing immune functions. It also inhibits DNA synthesis.Formula:C25H35N3OColor and Shape:SolidMolecular weight:393.56D44
CAS:D44 is a Plasmodium FKBPs inhibitor.Formula:C16H16N4OSColor and Shape:SolidMolecular weight:312.39FAK-IN-5
CAS:FAK-IN-5 is a FAK signaling inhibitor that induces apoptosis and autophagy.Formula:C29H29ClF3N3O4Color and Shape:SolidMolecular weight:576.01BIM-46174
CAS:BIM-46174 has anticancer activity, inhibits the growth of a large number of human cancer cell lines, and induces caspase-3-dependent cancer cell apoptosis.Formula:C22H30N4OSColor and Shape:SolidMolecular weight:398.57ML132
CAS:ML132 is an effective and selective inhibitor of caspase 1 (IC50: 0.316 nM).Formula:C22H28ClN5O5Color and Shape:SolidMolecular weight:477.94Alteminostat
CAS:Alteminostat is used as a histone deacetylase inhibitor and is an antineoplastic drug candidate.Formula:C27H36N6O3Color and Shape:SolidMolecular weight:492.613-(3-Phenoxybenzyl)amino-β-carboline
CAS:3-(3-Phenoxybenzyl)amino-β-carboline is a highly effective tubulin inhibitor, selectively degrading αβ-tubulin heterodimers.Formula:C24H19N3OColor and Shape:SolidMolecular weight:365.43AQX-016A
CAS:AQX-016A, a potent SHIP1 agonist, is an oral analog of pelorol, 3x stronger, inhibits PI3K, TNFa, for inflammation research.Formula:C22H32O2Color and Shape:SolidMolecular weight:328.49RIP1 kinase inhibitor 5
CAS:RIP1 kinase inhibitor 5 (example 1) serves as a potent regulator of tumor immunity by inhibiting RIP1, functioning similarly to SIR1-365 (compound 13) inFormula:C13H17F2NO2Purity:98%Color and Shape:SolidMolecular weight:257.28VO-OHPic
CAS:VO-OHPic, a selective PTEN inhibitor (IC50 = 46 nM), reduces apoptosis and inflammation in doxorubicin-induced cardiomyopathy.Formula:C12H10N2O8VColor and Shape:SolidMolecular weight:361.16Telomerase-IN-5
CAS:Telomerase-IN-5 is a potent inhibitor of telomerase with antiproliferative properties, and it induces apoptosis [1].Formula:C22H20N4OS2Purity:98%Color and Shape:SolidMolecular weight:420.55VEGFR-2-IN-22
CAS:VEGFR-2-IN-22 blocks VEGFR-2/beta-tubulin, IC50=19.82 nM, induces apoptosis.Formula:C26H24ClFN4O6Color and Shape:SolidMolecular weight:542.94HL271
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:351.76MDK-4204
CAS:MDK-4204, an anticancer agent, shows significant anti-cancer activity with IC50 values of 8.8 µM and 9.5 µM in PC-3 and DU-145 cells, respectively.Formula:C31H29FN4OPurity:98%Color and Shape:SolidMolecular weight:492.59NSC-741909
CAS:NSC-741909 is an anticancer agent that acts by suppressing the growth of several cell lines.Formula:C16H14ClNOPurity:98%Color and Shape:SolidMolecular weight:271.74SKLB70326
CAS:SKLB70326 is a cell-cycle progression inhibitor that acts by inducing G0/G1 phase arrest and apoptosis in human hepatic carcinoma cells.Formula:C15H13N3O2SPurity:98%Color and Shape:SolidMolecular weight:299.35DPQZ
CAS:DPQZ is an anti-tubulin compound acting by inducing cell apoptosis in human oral cancer cells through Ras/Raf inhibition and MAP kinases activation.Formula:C20H17N3OPurity:98%Color and Shape:SolidMolecular weight:315.37Antiproliferative agent-11
Antiproliferative agent-11, a Ruthenium(II) complex, targets multiple cancers with IC50s of 6-10 μM.Formula:C31H34Cl2N6O3P2RuColor and Shape:SolidMolecular weight:772.56Topoisomerase 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:516.57PS121912
CAS:PS121912 is a potent and selective inhibitor of VDR-coactivator.Formula:C24H21F3N2OPurity:98%Color and Shape:SolidMolecular weight:410.43Anti-inflammatory agent 22
CAS:Compound 14a is an oral anti-inflammatory with an IC50 of 14.6 μM for TNF-α, preventing adipogenesis and reducing mouse limb lymphedema.Formula:C22H16O6Color and Shape:SolidMolecular weight:376.36IDT
CAS:IDT, an oral TNFα modulator, changes neutrophil levels, boosts cognition, and reduces tau/amyloid in 3xTgAD mice.Formula:C8H5NS2Purity:98%Color and Shape:SolidMolecular weight:179.26A 410099.1
CAS:A 410099.1 is a BIRC (baculoviral IAP repeat-containing protein) inhibitor with EC50 values of 4.6, 9.2, 15.6, 19.9, and 93.9 nM for BIRC2/3/4/7/8.Formula:C27H41ClN4O3Purity:99.30%Color and Shape:SolidMolecular weight:505.1EGFR/BRAFV600E-IN-1
CAS:EGFR/BRAFV600E-IN-1 inhibits EGFR (0.08 μM) & BRAFV600E (0.15 μM), affects A-549, MCF-7, Panc-1 & HT-29 (IC50: 0.79-1.3 μM).Formula:C24H24ClN3O3Color and Shape:SolidMolecular weight:437.92CGP 65015
CAS:CGP 65015 is an oral iron chelator and can mobilize iron deposits.Formula:C14H15NO4Purity:98%Color and Shape:SolidMolecular weight:261.27EC359
CAS:EC359 is a Leukemia Inhibitory Factor Receptor (LIFR) inhibitor with anticancer activity for the study of leukemia and endometrial cancer.Formula:C36H38F2O2Purity:98.11% - 98.11%Color and Shape:SolidMolecular weight:540.68Simmiparib
CAS:Simmiparib (SMOCL-9112) is a PARP1 and PARP2 inhibitor that promotes apoptosis.Simmiparib is used to study Parkinson's disease and melanoma.Formula:C23H18F4N6O2Purity:99.05% - 99.51%Color and Shape:SolidMolecular weight:486.42HS-438
CAS:HS-438 inhibits imatinib-resistant BCR-ABL T315I mutation in chronic myeloid leukemia.Formula:C17H17N3O3SColor and Shape:SolidMolecular weight:343.4CCCI-01
CAS:CCCI-01: Centrosome cluster inhibitor with anticancer properties, induces apoptosis, aids in non-cross-resistant drug research.Formula:C11H9N3O4Purity:99.97%Color and Shape:SolidMolecular weight:247.21Anti-inflammatory agent 17
CAS:Compound 17: Orally active, potent IL-6 & TNF-α inhibitor; not cytotoxic; promising for ALI research.Formula:C20H23NO5Color and Shape:SolidMolecular weight:357.4MDM2/XIAP-IN-3
CAS:MDM2/XIAP-IN-3 (compound 3e), a dual inhibitor of MDM2/XIAP, diminishes MDM2 and XIAP protein levels while augmenting p53 expression, consequently suppressingFormula:C29H30N2O5SColor and Shape:SolidMolecular weight:518.62Antitumor agent-44
CAS:Antitumor agent-44 (Compound 5n) elicits potent antitumor effects by inducing disruption of mitochondrial homeostasis, cell cycle arrest, and apoptosis in humanFormula:C24H15N3O3Color and Shape:SolidMolecular weight:393.39DNA topoisomerase II inhibitor 1
CAS:Potent DNA topoisomerase II blocker; arrests cell cycle, induces apoptosis, anti-growth effects.Formula:C28H24N4O3SColor and Shape:SolidMolecular weight:496.58IM-93
CAS:IM-93 inhibits ferroptosis and NETosis with an IC< sub>50 of 0.45 μM for cell death inhibition [1].Formula:C21H28N4O2Color and Shape:SolidMolecular weight:368.47CS1
CAS:CS1: potent topoisomerase II alpha inhibitor, broad-spectrum antitumor, low toxicity, anti-resistance, induces DNA damage, G2/M arrest, apoptosis.Formula:C16H12O3Color and Shape:SolidMolecular weight:252.26IZTZ-1
CAS:IZTZ-1: c-MYC G4 stabilizer, reduces expression, blocks cell cycle, induces apoptosis, inhibits B16 melanoma growth.Formula:C32H35N7SColor and Shape:SolidMolecular weight:549.73PD-1/PD-L1-IN-28
CAS:PD-1/PD-L1-IN-28, an inhibitor of the PD-1/PD-L1 signaling pathway (IC 50 = 0.744 µM), demonstrates promising research potential in tumor immunity.Formula:C24H24N4O2Color and Shape:SolidMolecular weight:400.47EP12
CAS:EP12, a c-Myc inhibitor and G4 stabilizer, induces apoptosis and DNA damage in multiple myeloma cells while obstructing P65/P50 nuclear translocation byFormula:C26H22FN3O2Purity:98%Color and Shape:SolidMolecular weight:427.47Caspase-3-IN-1
CAS:Caspase-3-IN-1 is a potent inhibitor of Caspase-3 (IC50: 14.5 nM).Formula:C26H25N3O6SColor and Shape:SolidMolecular weight:507.56(rel)-Oxaliplatin
CAS:(rel)-Oxaliplatin, a DNA inhibitor, induces crosslinks, hinders replication/transcription, and triggers apoptosis; used in cancer studies.Formula:C8H14N2O4PtColor and Shape:SolidMolecular weight:397.29Mcl1-IN-3
CAS:Mcl1-IN-3 is an Mcl1 inhibitor. It has an IC50 and Ki of 0.67 and 0.13 μM, respectively.Formula:C27H22ClN3O4Purity:98%Color and Shape:SolidMolecular weight:487.93IMM-H004
CAS:IMM-H004 is an effective inhibitor of BV2 microglia activation.Formula:C16H20N2O4Purity:98%Color and Shape:SolidMolecular weight:304.34
