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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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:443.37p53 Activator 3
CAS:Potent p53 activator, SC150 <0.05 mM, restores mutant p53 DNA binding, exhibits anti-tumor properties.Formula:C30H37F3N4O4SColor and Shape:SolidMolecular weight:606.7GSK-345931A
CAS:GSK-345931A, Potent oral RIP2 inhibitor, suppresses pro-inflammatory cytokines, for autoimmune disease studies.Formula:C22H19ClNNaO3Color and Shape:SolidMolecular weight:403.83Anticancer agent 76
CAS:Compound CT2-3 is an anticancer agent that hinders growth, induces arrest, ROS, and apoptosis in NSCLC cells.Formula:C32H33NO5SColor and Shape:SolidMolecular weight:543.67VEGFR-2/BRAF-IN-2
VEGFR-2/BRAF-IN-2 inhibits VEGFR-2, BRAF V600E, BRAF WT (IC50: 0.111/0.089/0.071 µM); induces G1 arrest and apoptosis.Formula:C26H21ClF3N5O3S2Color and Shape:SolidMolecular weight:608.05AMXT1501
CAS:AMXT1501 is a polyamine uptake inhibitor, also inhibiting the putrescine transport in epimastigotes (the insect stage of t. cruzi)Formula:C32H68N6O2Color and Shape:SolidMolecular weight:568.92α-NETA
CAS:α-NETA is a ChA inhibitor and an ALDH1A1 and CMKLR1 antagonist with anticancer activity and inhibits cholinesterase and acetylcholinesterase (AChE).Formula:C16H20INOPurity:99.54%Color and Shape:SolidMolecular weight:369.24Arecaidine propargyl ester (hydrobromide)
CAS:Arecaidine propargyl ester: selective M2 muscarinic receptor agonist, induces guinea pig atrium contraction, lowers cat blood pressure, toxic to flies.Formula:C10H14BrNO2Color and Shape:SolidMolecular weight:260.13CDK9-IN-18
CAS:CDK9-IN-18: Potent CDK9 blocker, anticancer, induces apoptosis, low cellular activity.Formula:C27H20N8OColor and Shape:SolidMolecular weight:472.5Undecylprodigiosin
CAS:Undecylprodigiosin is a classical cytotoxic immunosuppressant, suppressing immune functions. It also inhibits DNA synthesis.Formula:C25H35N3OColor and Shape:SolidMolecular weight:393.56TSI-13-57
CAS:TSI-13-57 is a MyD88 inhibitor or pan-TLR inhibitor that suppresses MyD88 TIR domain dimerization ,inhibits LPS-induced TNF-α (IC50 = 6.73 mM).Formula:C28H29N3O3Purity:99.63%Color and Shape:SolidMolecular weight:455.55BS-181
CAS:BS-181 is a highly selective CDK7 inhibitor (IC50: 21 nM); >40-fold selective for CDK7 than CDK1/2/4/5/6/9.Formula:C22H32N6Purity:98%Color and Shape:SolidMolecular weight:380.53PD-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:577.9CGP 65015
CAS:CGP 65015 is an oral iron chelator and can mobilize iron deposits.Formula:C14H15NO4Purity:98%Color and Shape:SolidMolecular weight:261.27Mitochonic Acid 35
CAS:Mitochonic Acid 35 is a dual TNF-α and TGF-β1 inhibitor that acts by inhibiting IκB kinase phosphorylation and Smad3 phosphorylation.Formula:C19H19NO5Purity:98%Color and Shape:SolidMolecular weight:341.36Mcl1-IN-1
CAS:Mcl1-IN-1 is a myeloid cell factor 1 inhibitor (IC50=2.4 μM).Formula:C23H18ClN3O4Color and Shape:SolidMolecular weight:435.86ADU-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:690.54VII-31
CAS:VII-31 is an activator of the NEDDylation pathway, capable of inducing apoptosis in MCF-7, PC-3, and MGC-803 cells.Formula:C23H25NO5SColor and Shape:SolidMolecular weight:427.51CT1-3
CAS:CT1-3 is a potent anti-cancer compound targeting JNK/Bcl-2 pathways, blocking EMT in HCCs, and is non-toxic to liver/kidneys in mice.Formula:C25H29NO3S2Color and Shape:SolidMolecular weight:455.63CHMFL-ABL/KIT-155
CAS:CHMFL-ABL/KIT-155 is a highly potent and orally active type II ABL/c-KIT dual kinase inhibitor (IC50s: 46 nM/75 nM).Formula:C33H38F3N5O3Purity:98%Color and Shape:SolidMolecular weight:609.68Gemcitabine monophosphate
CAS:R306465, a potent HDAC1/8 inhibitor, has broad antitumor effects (IC50: 30-300 nM) on solid and blood cancers.Formula:C9H12F2N3O7PColor and Shape:SolidMolecular weight:343.18PI3Kδ-IN-11
CAS:PI3Kδ-IN-11 is a potent and selective PI3Kδ inhibitor (IC50: 27.5 nM) that dose-dependently blocks PI3K/Akt pathway activity.Formula:C27H21N5OColor and Shape:SolidMolecular weight:431.49MMP-9-IN-5
CAS:MMP-9-IN-5: MMP-9 and AKT inhibitor (IC50: 4.49 nM and 1.34 nM), induces apoptosis for cancer research.Formula:C27H20IN3O4Color and Shape:SolidMolecular weight:577.37JS-K
CAS:JS-K is a Nitric oxide donor. It has antiproliferative activity.Formula:C13H16N6O8Color and Shape:SolidMolecular weight:384.3Merck-22-6
CAS:Merck-22-6 is an allosteric dual inhibitor of Akt1, Akt2.Formula:C40H43N7O2Color and Shape:SolidMolecular weight:653.82BEPP monohydrochloride
CAS:BEPP monohydrochloride is a double-strand RNA-dependent protein kinase (PKR) activator.Formula:C23H24ClN3O2Color and Shape:SolidMolecular weight:409.91GL-V9
CAS:GL-V9 is an AMPK activator, protecting against colitis-associated colorectal cancer by limiting NLRP3 inflammasome through autophagy.Formula:C24H27NO5Color and Shape:SolidMolecular weight:409.47SMBA1
CAS:SMBA1 is a Bax agonist with antitumor activity that can induce cell cycle arrest and apoptosis in malignant glioma cells.Formula:C20H13NO3Purity:99.2%Color and Shape:SolidMolecular weight:315.32pan-HER-IN-2
CAS:pan-HER-IN-2 (Compound C6) is an orally active, reversible, broad-spectrum HER inhibitor that acts on EGFR (IC50: 0.72 nM), HER4 (IC50: 2.0 nM), EGFRT790M (IC50Formula:C19H15BrClN5OColor and Shape:SolidMolecular weight:444.71NSC745887
CAS:NSC745887 (compound 25) is an anticancer agent that demonstrates dose-dependent inhibition of proliferation across 60 cancer cell lines [1].Formula:C16H8N2O2Color and Shape:SolidMolecular weight:260.25PSB 0474
CAS:P2Y6 receptor agonistFormula:C17H20N2O13P2Purity:98%Color and Shape:SolidMolecular weight:522.29DRAK2-IN-1
CAS:Drak2-in-1: ATP-competitive DRAK2 inhibitor; IC50 = 3 nM, KI = 0.26 nM; affects DRAK1 (IC50 = 51 nM).Formula:C21H20N4O3Color and Shape:SolidMolecular weight:376.41MEK-IN-5
CAS:MEK-IN-5: strong MEK inhibitor and NO donor, reduces pMEK/pERK dose/time-dependently, triggers apoptosis in MDA-MB-231 cells.Formula:C29H27FN4O10S2Color and Shape:SolidMolecular weight:674.67MCL-1/BCL-2-IN-3
CAS:MCL-1/BCL-2-IN-3 is a selective and potent Mcl-1 and Bcl-2 dual inhibitor with IC50s of 5.95 and 4.78 μM, respectiely.Formula:C27H25BrN2O5SColor and Shape:SolidMolecular weight:569.47UK-101
CAS:UK-101 is a potent and selective inhibitor of the immunoproteasome LMP2, inhibiting β1i (LMP2), β1c (LMP2), and β5 (LMP2), with IC50s of 104 nM, 15 μM, and 1 μMFormula:C25H48N2O5SiPurity:98.97% - 99.08%Color and Shape:SolidMolecular weight:484.74RS1-PDK1 inhibitor
CAS:RS1-PDK1 inhibitor (RS 1) is a selective inhibitor of the protein kinase PDK1 that can be used to treat and prevent disease or disorders.Formula:C15H9ClN2O2S3Purity:97.65%Color and Shape:SolidMolecular weight:380.89GSK2983559 free acid
CAS:GSK2983559 free acid selectively inhibits RIP2, reducing inflammatory cytokines in human bowel disease.Formula:C21H23N4O7PS2Purity:97.8700% - 99.56%Color and Shape:SolidMolecular weight:538.53Apostatin-1
CAS:Apostatin-1 (Apt-1) is a novel TRADD inhibitor. Apostatin-1 can bind to a pocket on the N-terminal TRAF2 binding domain of TRADD.Formula:C19H27N3OSPurity:99.31%Color and Shape:SolidMolecular weight:345.5Ref: TM-T9079
1mg34.00€2mg49.00€5mg74.00€10mg113.00€25mg222.00€50mg358.00€100mg530.00€500mg1,153.00€1mL*10mM (DMSO)82.00€Alethine
CAS:Alethine is a small antitumor compound used to treat cancers and infections, boosting T-cell cytotoxicity by raising TNFα.Formula:C10H22N4O2S2Purity:99.78%Color and Shape:SolidMolecular weight:294.44BC 11 hydrobromide
CAS:The compound is a selective urokinase inhibitor (IC50 = 8.2 μM). It also inhibits clot lysis with no effect on clot formation.Formula:C8H12BBrN2O2SPurity:98.07%Color and Shape:SolidMolecular weight:290.97Cipepofol
CAS:HSK3486 is similar to propofol and is a general anesthetic, which may have therapeutic potential in insomnia, migraine, anxiety, analgesia, and other aspects.Formula:C14H20OPurity:99.77%Color and Shape:SolidMolecular weight:204.31Ref: TM-T32105
1mg58.00€5mg149.00€10mg225.00€25mg444.00€50mg657.00€100mg1,044.00€200mg1,414.00€1mL*10mM (DMSO)150.00€Perphenazine dihydrochloride
CAS:Perphenazine dihydrochloride: Oral dopamine, histamine-1 antagonist; targets D2, D3, 5-HT2A, Alpha-1A; may treat psychiatric disorders, cancer.Formula:C21H28Cl3N3OSPurity:99.67%Color and Shape:SolidMolecular weight:476.89CCT020312
CAS:CCT020312 (0-9 µM, 24 h) treatment of medium HT29 cells for 24 h resulted in a concentration-dependent loss of P-S608-pRB.Cost-effective and quality-assured.Formula:C31H30Br2N4O2Purity:98.63%Color and Shape:SolidMolecular weight:650.4Ref: TM-T14902
1mg58.00€5mg133.00€10mg227.00€25mg386.00€50mg572.00€100mg795.00€500mg1,648.00€1mL*10mM (DMSO)178.00€DCG066
CAS:DCG066 is an inhibitor of lysine methyltransferase G9a with anticancer activity and may be used in the study of leukemia.Formula:C30H31F6N3O2Purity:98.26% - 98.38%Color and Shape:SolidMolecular weight:579.58Ref: TM-T27132
1mg215.00€5mg537.00€10mg730.00€25mg1,134.00€50mg1,468.00€100mg1,863.00€200mg2,512.00€1mL*10mM (DMSO)685.00€DX3-213B
CAS:DX3-213B is a potent, orally active inhibitor of oxidative phosphorylation (OXPHOS) complex I with an IC50 of 3.6 nM.Formula:C20H28F2N2O5S2Purity:99.85%Color and Shape:SolidMolecular weight:478.57Ref: TM-T63136
1mg81.00€5mg170.00€10mg274.00€25mg588.00€50mg852.00€100mg1,159.00€1mL*10mM (DMSO)180.00€Cot inhibitor-1
CAS:Cot inhibitor-1 selectively blocks Tpl2 kinase, reducing TNF-alpha in blood (IC50: 5.7 nM). It may treat arthritis, IBD, and certain cancers.Formula:C27H27Cl2FN8Purity:98.87%Color and Shape:SolidMolecular weight:553.46Ref: TM-T10865
1mg73.00€5mg152.00€10mg222.00€25mg401.00€50mg602.00€100mg887.00€200mg1,215.00€1mL*10mM (DMSO)177.00€SB 699551 dihydrochloride
CAS:SB 699551 dihydrochloride is a 5-ht5a receptor antagonist.Formula:C34H47Cl2N3OPurity:99.83%Color and Shape:SolidMolecular weight:584.66Ref: TM-T23325
1mg50.00€5mg105.00€10mg170.00€25mg295.00€50mg424.00€100mg583.00€1mL*10mM (DMSO)142.00€LCS3
CAS:LCS3 is a reversible and non-competitive synergistic inhibitor of glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) with IC50s of 3.3Formula:C11H7ClN2O4Purity:99.84%Color and Shape:SolidMolecular weight:266.64SYM 2081
CAS:SYM 2081: Kainate receptor agonist, IC50 of 35 nM, depolarizes muscle, lowers EPSP amplitude.Formula:C6H11NO4Purity:99.63%Color and Shape:SolidMolecular weight:161.16SLMP53-1
CAS:SLMP53-1 is a p53 activator with anti-tumor activity, activates reprogramming of glucose metabolism, and interferes with angiogenesis and migrationFormula:C20H18N2O2Purity:99.64%Color and Shape:SolidMolecular weight:318.37Ref: TM-T60839
1mg119.00€5mg281.00€10mg462.00€25mg888.00€50mg1,485.00€100mg2,385.00€1mL*10mM (DMSO)34.00€Ro24-7429
CAS:Ro24-7429: oral HIV-1 Tat antagonist, RUNX1 inhibitor with anti-HIV, antifibrotic, and anti-inflammatory properties.Formula:C14H13ClN4Purity:99.29% - 99.85%Color and Shape:SolidMolecular weight:272.73Ref: TM-T28578
1mg87.00€5mg177.00€10mg281.00€25mg480.00€50mg692.00€100mg973.00€500mg2,725.00€1mL*10mM (DMSO)203.00€H2L5186303
CAS:H2L5186303 is an LPA2 antagonist and can be used in studies about asthma treatment.Formula:C26H20N2O8Purity:98.19%Color and Shape:SolidMolecular weight:488.45Ref: TM-T22835
2mg44.00€5mg64.00€10mg94.00€25mg180.00€50mg283.00€100mg465.00€200mg642.00€1mL*10mM (DMSO)75.00€HS-276
CAS:HS-276, a selective oral TAK1 inhibitor (Ki: 2.5 nM), also targets CLK2, GCK, ULK2, MAP4K5; potential for RA research.Formula:C24H29N5O2Purity:97.67% - 98.81%Color and Shape:SolidMolecular weight:419.52Ref: TM-T62209
1mg63.00€5mg137.00€10mg207.00€25mg408.00€50mg655.00€100mg1,009.00€200mg1,359.00€1mL*10mM (DMSO)161.00€MK-28
CAS:MK-28 is a PERK agonist that reduces toxicity in a Huntington's disease model.MK-28 has a significant killing effect on MK28 gastric cancer cells.Formula:C24H20N4O2Color and Shape:SolidMolecular weight:396.44Ref: TM-T61859
1mg94.00€5mg222.00€10mg356.00€25mg690.00€50mg1,044.00€100mg1,558.00€1mL*10mM (DMSO)245.00€VAS 3947
CAS:VAS 3947: NOX inhibitor, induces platelet apoptosis via UPR, not linked to NOX inhibition.Formula:C14H10N6OSPurity:99.25%Color and Shape:SolidMolecular weight:310.33Ref: TM-T29097
1mg46.00€5mg92.00€10mg166.00€25mg279.00€50mg403.00€100mg532.00€200mg705.00€1mL*10mM (DMSO)100.00€NM-3
CAS:NM-3, an oral anti-angiogenic and anti-tumor agent, modulates radiation and blocks VEGF to curb endothelial growth and induce apoptosis.Formula:C13H12O6Purity:99.89%Color and Shape:SolidMolecular weight:264.23Ref: TM-T33701
1mg172.00€5mg432.00€10mg618.00€25mg973.00€50mg1,333.00€100mg1,791.00€500mg3,529.00€1mL*10mM (DMSO)394.00€CMLD-2
CAS:CMLD-2 is a HuR-ARE inhibitor (Ki: 350 nM) that promotes apoptosis, has antitumor properties, and reduces thyroid cancer cell viability.Formula:C31H31NO6Purity:99.99%Color and Shape:SolidMolecular weight:513.58Ref: TM-T36493
1mg92.00€5mg222.00€10mg371.00€25mg608.00€50mg848.00€100mg1,144.00€500mg2,277.00€1mL*10mM (DMSO)245.00€D609
CAS:D609 (Tricyclodecan-9-yl-Xanthogenate) has antiviral and antiproliferative activities.D609 acts through competitive inhibition of PC, PC-P and SMS.Formula:C11H15KOS2Purity:97.67% - 99.56%Color and Shape:Off-White PowderMolecular weight:266.46UC-112
CAS:UC-112 is a novel potent IAP inhibitor and potently inhibits cell growth in two human melanoma and two human prostate cancer cell lines (IC50=0.7-3.4 uM).Formula:C22H24N2O2Purity:99.54%Color and Shape:SolidMolecular weight:348.44Ref: TM-T17195
1mg34.00€2mg44.00€5mg70.00€10mg99.00€25mg202.00€50mg311.00€100mg445.00€500mgTo inquire1mL*10mM (DMSO)78.00€eIF4A3-IN-1
CAS:eIF4A3-IN-1 is an inhibitor of eukaryotic initiation factor 4A3 (eIF4A3). eIF4A3-IN-1 inhibits cytosolic nonsense-mediated RNA decay at high concentrations.
Formula:C29H23BrClN5O2Purity:99.49% - 99.89%Color and Shape:SolidMolecular weight:588.88TT01001
CAS:TT01001, a mitoNEET agonist, may treat type II diabetes by reducing oxidative stress and preventing neuronal death.Formula:C15H19Cl2N3O2SPurity:99.93%Color and Shape:SolidMolecular weight:376.3Bomedemstat ditosylate
CAS:Bomedemstat (IMG-7289) is an LSD1 inhibitor for acute myeloid leukemia, MDS, and Myelofibrosis; induces apoptosis by regulating p53, PUMA, and BCLXL.Formula:C42H50FN7O8S2Purity:99.05%Color and Shape:SolidMolecular weight:864.02Ref: TM-T70008
1mg84.00€5mg177.00€10mg264.00€25mg444.00€50mg640.00€100mg893.00€1mL*10mM (DMSO)250.00€STAT3-IN-13
CAS:STAT3-IN-13 is a STAT3 inhibitor with antiproliferative activity that induces apoptosis and can be used to study breast and liver cancer.Formula:C21H20N6O3SPurity:98.89%Color and Shape:SolidMolecular weight:436.49Exisulind
CAS:Exisulind (CP248) triggers apoptosis via PKG activation, shows antitumor effects, and inhibits growth in various rodent cancer models.Formula:C20H17FO4SPurity:97.94%Color and Shape:SolidMolecular weight:372.41F16
CAS:F16 ((E)-4-(3-indolylvinyl)-N-methylpyridinium iodide) inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.Formula:C16H15IN2Purity:99.89%Color and Shape:SolidMolecular weight:362.21LDCA
CAS:LDCA inhibits LDH-A, disrupts mitochondrial function, induces apoptosis in cancer cells, and is non-toxic.Formula:C8H5Cl3FNOPurity:99.19%Color and Shape:SolidMolecular weight:256.49Ro 90-7501
CAS:Ro 90-7501, an amyloid β42 (Aβ42) protofibril and TPR-dependent PP5 inhibitor, is a novel cervical cancer cell radiosensitizer that inhibits HCMV.Formula:C20H16N6Purity:97.21% - 99.72%Color and Shape:SolidMolecular weight:340.38JY-2
CAS:JY-2 is a forkhead transcription factor O1 (FoxO1) inhibitor with antidiabetic activity that inhibits FoxO1 transcription and can be used to study psoriasis.Formula:C13H7Cl2N3OPurity:99.66%Color and Shape:SolidMolecular weight:292.12GSK2593074A
CAS:GSK2593074A (GSK'074) is a programmed necrosis inhibitor that displays inhibitory effects on RIP1 and RIP3.Formula:C27H23N5OSPurity:99.99%Color and Shape:SolidMolecular weight:465.57Ref: TM-T11484
1mg108.00€5mg260.00€10mg409.00€25mg687.00€50mg964.00€100mg1,288.00€1mL*10mM (DMSO)286.00€iCRT-5
CAS:iCRT-5 is a potent inhibitor of the Wnt pathway. iCRT-5 has antiproliferative activity and can be used in the study of multiple myeloma.Formula:C16H17NO5S2Purity:99.68%Color and Shape:SolidMolecular weight:367.44Tanimilast
CAS:Tanimilast (CHF-6001) is a potent PDE4 inhibitor with IC50 of 0.026 nM, used topically for obstructive lung disease.Formula:C30H30Cl2F2N2O8SPurity:99.18%Color and Shape:SolidMolecular weight:687.54MBM-55
CAS:MBM-55 is an effective inhibitor of NIMA related kinase 2 (NEK2) with an IC50 of 1 nM.Formula:C28H27FN6O2Purity:99.83%Color and Shape:SolidMolecular weight:498.55Ref: TM-T11960
1mg168.00€5mg281.00€10mg409.00€25mg627.00€50mg822.00€100mg1,108.00€500mg2,242.00€1mL*10mM (DMSO)309.00€Trk-IN-9
CAS:Trk-IN-9 is a TRK inhibitor with anticancer and antiproliferative activity and can be used in cancer research.Formula:C23H24ClFN6OPurity:98.15%Color and Shape:SolidMolecular weight:454.93AMG PERK 44
CAS:AMG PERK 44 is a PERK inhibitor that induces autophagy.AMG PERK 44 inhibits GCN2 and B-Raf and can be used in cancer research.Formula:C34H29ClN4O2Purity:98.8% - 99.81%Color and Shape:SolidMolecular weight:561.07AZA1
CAS:AZA1 (Rac1/Cdc42-IN-1) is a potent dual inhibitor of Rac1 and Cdc42.Formula:C22H20N6Purity:99.75%Color and Shape:SolidMolecular weight:368.43Ref: TM-T61448
1mg90.00€5mg188.00€10mg311.00€25mg520.00€50mg742.00€100mg1,008.00€1mL*10mM (DMSO)212.00€GSK854
CAS:GSK854 is a selective TNNI3K inhibitor reducing heart damage and stress post-infarction in mice.Formula:C18H19ClN6O4S2Purity:98.91%Color and Shape:SolidMolecular weight:482.96Ref: TM-T24115
1mg92.00€5mg222.00€10mg358.00€25mg710.00€50mg1,063.00€100mg1,684.00€500mg3,375.00€1mL*10mM (DMSO)245.00€BCP-T.A
CAS:BCP-T.A is an iron death inducer that acts by binding to GPX4.Formula:C23H19Cl2N3OSPurity:99.49%Color and Shape:SolidMolecular weight:456.39Anticancer agent 110
CAS:Anticancer Agent 110 exhibits potent in vitro anti-leukemia activity, demonstrating high cytotoxicity against K-562 lineage chronic myelogenous leukemia cellsFormula:C18H13FN6OSPurity:98%Color and Shape:SolidMolecular weight:380.4Utreloxastat
CAS:Utreloxastat (PTC857) is a novel 15-lipoxygenase inhibitor that can be used to study amyotrophic lateral sclerosis .Formula:C18H28O2Purity:99.95%Color and Shape:SolidMolecular weight:276.41Ref: TM-T60507
1mg96.00€5mg205.00€10mg295.00€25mg505.00€50mg745.00€100mg1,305.00€200mg1,755.00€1mL*10mM (DMSO)224.00€(S)-Enitociclib
CAS:(S)-Enitociclib (VIP152) is a selective CDK9 inhibitor that inhibits the transcription of anti-apoptotic and pro-survival proteins.Formula:C19H18F2N4O2SPurity:98.98%Color and Shape:SolidMolecular weight:404.43NSC49652
CAS:NSC49652 triggers apoptotic cell death dependent on p75NTR and JNK activity in neurons and melanoma cells, and inhibits tumor growth in a melanoma mouse model.Formula:C14H11NO2Purity:98.98%Color and Shape:SolidMolecular weight:225.24Ref: TM-T28206
1mg34.00€5mg74.00€10mg113.00€25mg222.00€50mg353.00€100mg530.00€500mg1,153.00€1mL*10mM (DMSO)82.00€Minodronic acid
CAS:Minodronic acid (YM-529) is a P2X2/3 antagonist with anticancer properties, inhibiting cell growth and metastasis, and used in osteoporosis research.Formula:C9H12N2O7P2Purity:99.39%Color and Shape:SolidMolecular weight:322.15ZDLD20
CAS:ZDLD20 is a CDK4 inhibitor with anti-HCT116 and anticancer activity that inhibits colony formation and blocks the G1 phase of the cell cycle.Formula:C22H22N6OPurity:98.59%Color and Shape:SolidMolecular weight:386.45Gallium maltolate
CAS:Gallium maltolate is a ribonucleoside-diphosphate reductase inhibitor.Formula:C18H15GaO9Purity:99.61% - 99.67%Color and Shape:SolidMolecular weight:445.03TC-DAPK 6
CAS:TC-DAPK 6 is an ATP-competitive inhibitor of Death-associated protein kinase (DAPK) with IC50s of 69 and 225 nM for DAPK1 and DAPK3.Formula:C17H12N2O2Purity:98.73%Color and Shape:SolidMolecular weight:276.29Miclxin
CAS:Miclxin (DS37262926) is a novel MIC60 inhibitor that induces apoptosis through mitochondrial stress in mutant tumor cells via β-catenin.Miclxin is a potentFormula:C26H27N5O2Purity:99.17% - 99.99%Color and Shape:SolidMolecular weight:441.52Ref: TM-T73415
1mg60.00€5mg133.00€10mg182.00€25mg306.00€50mg427.00€100mg587.00€200mg792.00€1mL*10mM (DMSO)147.00€TAI-1
CAS:TAI-1 is a potent and specific Hec1 inhibitor, which disrupts Hec1-Nek2 protein interaction.Formula:C24H21N3O3SPurity:99.58%Color and Shape:SolidMolecular weight:431.51OR-1896
CAS:OR-1896 is a PDE III inhibitor, a vasodilator with partial anti-inflammatory properties, and can be used to study heart failure and vascular dysfunction.Formula:C13H15N3O2Purity:99.33%Color and Shape:SolidMolecular weight:245.28Ref: TM-T12315
1mg89.00€5mg187.00€10mg309.00€25mg622.00€50mg982.00€100mg1,333.00€200mg1,783.00€1mL*10mM (DMSO)207.00€RET-IN-3
CAS:RET-IN-3 is a RETV804M kinase inhibitor with potential anticancer activity for the study of non-small cell lung cancer.Formula:C18H21N5O2Purity:99.52%Color and Shape:SolidMolecular weight:339.39Ref: TM-T9673
1mg70.00€5mg149.00€10mg227.00€25mg427.00€50mg675.00€100mg1,035.00€200mg1,395.00€1mL*10mM (DMSO)165.00€Benitrobenrazide
CAS:Benitrobenrazide (Hexokinase 2 inhibitor 1) is a novel orally available hexokinase 2 (HK2) inhibitor with anticancer and antitumor activity for cancer research.Formula:C14H11N3O6Purity:96.87%Color and Shape:SolidMolecular weight:317.25UNC0321
CAS:UNC0321 is an effective inhibitor of histone methyltransferase G9a with a Ki of 63 pM and with IC50s 9 nM and 6 nM in ECSD and CLOT assays.Formula:C27H45N7O3Purity:99.80%Color and Shape:SolidMolecular weight:515.691G244
CAS:1G244 is an inhibitor of DPP8/9 with antiatherosclerotic and antimyeloma properties.Formula:C29H30F2N4O2Purity:99.14%Color and Shape:SolidMolecular weight:504.57Necrostatin-5
CAS:Necrostatin-5 (Nec-5) inhibits RIP1 kinase, prevents cell necrosis, and protects Fadd-deficient Jurkat cells with an EC50 of 240 nM.Formula:C19H17N3O2S2Purity:99.40%Color and Shape:SolidMolecular weight:383.49CP 461
CAS:CP 461 is a PDE2A inhibitor that promotes apoptosis in cancer cells without affecting normal cells or COX-1/2.Formula:C25H22ClFN2OPurity:99.82%Color and Shape:SolidMolecular weight:420.91DB1976
CAS:DB1976: Selenophene DB270 analog, inhibits PU.1 (IC50=10 nM), disrupts PU.1/DNA (KD=12 nM), induces apoptosis, cell-permeable.Formula:C20H16N8SePurity:98.74%Color and Shape:SolidMolecular weight:447.35Triciribine phosphate
CAS:Triciribine phosphate (VD 002) is an AKT inhibitor that inhibits neovascularization and can be used in the study of leukemia.Formula:C13H17N6O7PPurity:97.94%Color and Shape:SolidMolecular weight:400.28Erastin2
CAS:Erastin2 is an iron death inducer that induces cell death by binding to the lipophilic free radical trapping antioxidant ferrostatin-1 or the iron chelator DFO.
Formula:C36H35ClN4O4Purity:99.63%Color and Shape:SolidMolecular weight:623.14CBS9106
CAS:CBS9106 (SL-801) is a CRM1 inhibitor with CRM1-degrading and anti-tumor activity that inhibits CRM1-dependent nuclear export.Formula:C18H21ClF3N3O3Purity:98.98%Color and Shape:SolidMolecular weight:419.83RO-5963
CAS:RO-5963 is a dual inhibitor of p53-MDM2 and p53-MDMX (IC50s: ~17 nM and ~24 nM, respectively).Formula:C24H21ClF2N4O5Purity:99.28%Color and Shape:SolidMolecular weight:518.9Ref: TM-T16771
1mg66.00€5mg187.00€10mg269.00€25mg411.00€50mg532.00€100mg740.00€200mg982.00€1mL*10mM (DMSO)212.00€PARP/PI3K-IN-1
CAS:PARP/PI3K-IN-1 is a PARP and PI3K dual inhibitor with anticancer and antiproliferative activities for the study of breast, pancreatic and lung cancers.Formula:C33H28F4N8O3Purity:99.59%Color and Shape:SolidMolecular weight:660.62
