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(116 products)
- PDK(9 products)
- PERK(24 products)
- Serine/threonin kinase(18 products)
- Survivin(14 products)
- TNF(65 products)
- c-RET(61 products)
- p53(63 products)
Show 6 more subcategories
Found 6115 products of "Apoptosis"
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MDM2/XIAP-IN-2
CAS:MDM2/XIAP-IN-2 is a dual inhibitor targeting murine double minute 2 (MDM2) and X-linked inhibitor of apoptosis protein (XIAP).Formula:C29H32N2O4SColor and Shape:SolidMolecular weight:504.64Tubulin polymerization-IN-14
CAS:Tubulin-IN-14 (20a) inhibits polymerization (IC50=3.15μM), has anti-cancer and anti-vascular effects, inducing cell death.Formula:C15H15ClN2O2Color and Shape:SolidMolecular weight:290.74MI-3
CAS:MI-3 (Menin-MLL Inhibitor) (Menin-MLL Inhibitor) is an effective inhibitor of Menin-MLL interaction (IC50: 648 nM).Formula:C18H25N5S2Purity:98.66% - 99.61%Color and Shape:SolidMolecular weight:375.55A-385358
CAS:A-385358 is a selective Bcl-xL inhibitor with Kis of 0.80 nM for Bcl-xL and 67 nM for Bcl-2, respectively.Formula:C32H41N5O5S2Purity:99.97%Color and Shape:SolidMolecular weight:639.83Ref: TM-T14071
1mg57.00€5mg109.00€10mg165.00€25mg268.00€50mg400.00€100mg567.00€1mL*10mM (DMSO)158.00€CA224
CAS:CA224: selective oral Cdk4-cyclin D1 inhibitor, IC50=6.2μM, promotes apoptosis, has antitumor effects.Formula:C24H22N2OColor and Shape:SolidMolecular weight:354.44Infliximab
CAS:Infliximab is a chimeric monoclonal antibody that inhibits TNF-α. Infliximab can be used to treat Crohn's disease and rheumatoid arthritis. Cost-effective and quality-assured.Purity:98% - 99.70%Color and Shape:LiquidMolecular weight:145.98 kDaIKK2-IN-4
CAS:IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.Formula:C12H11N3O2SPurity:99.83%Color and Shape:SolidMolecular weight:261.3Ref: TM-T36524
1mg108.00€5mg261.00€10mg401.00€25mg622.00€50mg837.00€100mg1,125.00€200mg1,504.00€500µg82.00€DMH2
CAS:DMH2 is an antagonist of bone morphogenetic protein (BMP) type I receptor. It acts by decreasing growth and inducing cell death of lung cancer cell lines.Formula:C27H25N5O2Purity:98%Color and Shape:SolidMolecular weight:451.52KU-0058948
CAS:KU-0058948: PARP inhibitor, triggers cell cycle arrest and apoptosis in myeloid leukemia cells in vitro.Formula:C21H21FN4O2Color and Shape:SolidMolecular weight:380.42CAY10406
CAS:CAY10406, a trifluoromethyl isatin sulfonamide, selectively targets and inhibits caspase-3 and -7, key in apoptosis, with no data on its inhibition potency.Formula:C27H23F3N2O5SColor and Shape:SolidMolecular weight:544.54APX2009
CAS:APX2009, a 2nd-gen APE1/Ref-1 inhibitor, curbs NFkB activity, survivin, and prostate cancer cell growth; induces cell cycle arrest.Formula:C21H25NO4Color and Shape:SolidMolecular weight:355.43MDH1-IN-2
CAS:MDH1-IN-2 is a potent MDH1 inhibitor with potential anticancer activity for the study of diseases related to the immune system.Formula:C25H33NO5Purity:99.21%Color and Shape:SolidMolecular weight:427.53XMD15-44
CAS:XMD15-44, a RET kinase inhibitor, demonstrates potent growth-inhibitory effects on RAT1 cells transformed by RET/C634R and RET/M918T, with IC50 values of 11.5 nM and 8.3 nM, respectively. It effectively inhibits RET kinase activity and signaling in human thyroid cancer cell lines harboring oncogenic RET alleles, thereby reducing cell proliferation.Formula:C29H29F3N4OColor and Shape:SolidMolecular weight:506.56VU0285655-1
CAS:VU0285655-1, a PLD2 inhibitor, halts PLD2-deficient cell growth and protects against high glucose-induced cell death. Used in diabetic retinopathy research.Formula:C25H27N5O2Purity:99.73%Color and Shape:SolidMolecular weight:429.51Hetrombopag
CAS:Hetrombopag: potent thrombopoietin receptor agonist, well tolerated, safe, promising for immune thrombocytopenia research.Formula:C25H22N4O5Color and Shape:SolidMolecular weight:458.47MC-70
CAS:MC-70, P-gp and ABC transporter inhibitor (EC50=0.69 µM), interacts with ABCB1/G2/C1, inhibits colon cancer growth and induces apoptosis.Formula:C24H25NO3Purity:99.94%Color and Shape:SolidMolecular weight:375.46SZM679
SZM679: Oral RIPK1 inhibitor, Kd 8.6 nM, weak RIPK3 affinity (>5000 nM). Reduces inflammation, Tau phosphorylation in AD research.Formula:C27H18F5N3O5SPurity:98%Color and Shape:SolidMolecular weight:591.51ZT55
CAS:ZT55: Oral JAK2 inhibitor, IC50: 0.031 μM, hinders JAK2 V617F HEL cell growth, induces apoptosis, arrests cell cycle, effective in mice HEL tumor studies.Formula:C17H16N2O3Color and Shape:SolidMolecular weight:296.32PQ1 Succinate
CAS:PQ1 Succinate boosts GJIC and connexin in breast cancer cells without impacting normal mammary cells.Formula:C25H28F3N3O6Color and Shape:SolidMolecular weight:523.5NSC114792
CAS:NSC114792 is a selective JAK3 inhibitor.Formula:C26H32N4O2SPurity:98%Color and Shape:SolidMolecular weight:464.62Dabuzalgron HCl
CAS:Dabuzalgron, an adrenoceptor agonist, is used potentially for the treatment of urinary incontinence.Formula:C12H17Cl2N3O3SPurity:98%Color and Shape:SolidMolecular weight:354.25SKLB70326
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:315.37PS121912
CAS:PS121912 is a potent and selective inhibitor of VDR-coactivator.Formula:C24H21F3N2OPurity:98%Color and Shape:SolidMolecular weight:410.43MI-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€HDAC1/6-IN-1
CAS:HDAC1/6-IN-1, a dual HDAC1 (89 nM) and HDAC6 (13 nM) inhibitor, blocks cancer cell cycle, triggers apoptosis, and halts metastasis.Formula:C32H45N7O4Color and Shape:SolidMolecular weight:591.74(R)-STU104
CAS:(R)-STU104 is a TAK1-MKK3 protein-protein interaction (PPI) inhibitor. (R)-STU104 is a candidate compound for the treatment of ulcerative colitis.Formula:C18H18O4Purity:98.91% - 99.42%Color and Shape:SolidMolecular weight:298.33Metallo-β-lactamase-IN-5
CAS:Metallo-β-lactamase-IN-5 (compound 5c) is a powerful inhibitor of metallo-β-lactamases (MBLs).Formula:C19H16N4O3Color and Shape:SolidMolecular weight:348.36GGTI-2154
CAS:GGTI-2154 is a potent, selective geranylgeranyltransferase I (GGTase I) inhibitor, boasting an IC50 of 21 nM and demonstrating over 200-fold selectivity againstFormula:C24H28N4O3Color and Shape:SolidMolecular weight:420.5Ludartin
CAS:Ludartin activates TRPA1, induces DNA damage, and lowers mitochondrial potential, yielding anticancer effects.Formula:C15H18O3Color and Shape:SolidMolecular weight:246.3Tubulin polymerization-IN-17
CAS:Compound 23g, a potent inhibitor of tubulin aggregation, induces apoptosis, and inhibits cell migration; promising for cancer research.Formula:C26H23NO5Color and Shape:SolidMolecular weight:429.46Mammea A/BA
CAS:Mammea A/BA combats T. cruzi by causing mitochondrial damage, ROS, DNA fragmentation, and vacuolization, leading to cell death. Useful for Chagas research.Formula:C25H26O5Color and Shape:SolidMolecular weight:406.47Aurora A inhibitor 2
CAS:Aurora A inhibitor 2 (Compound 16h) is a potent inhibitor of Aurora A kinase (IC50: 21.94 nM).Formula:C24H26N6O3Color and Shape:SolidMolecular weight:446.5CX-5011
CAS:CX-5011, a CK2 inhibitor, induces Rac1 activation and promotes apoptosis, effectively causing cancer cell death [1] [2].Formula:C20H12N4O2Purity:98%Color and Shape:SolidMolecular weight:340.33PIK-C98
CAS:PIK-C98 is an inhibitor of PI3K that acts by displaying potent preclinical activity against multiple myeloma.Formula:C16H10Cl2N2OSPurity:98%Color and Shape:SolidMolecular weight:349.23BLM-IN-1
CAS:BLM-IN-1: BLM inhibitor, KD 1.81 μM, IC50 0.95 μM; causes DNA damage, apoptosis, stops cancer cell growth.Formula:C28H35FN4OColor and Shape:SolidMolecular weight:462.6Jolkinolide B
CAS:Jolkinolide B is a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud.
Formula:C20H26O4Purity:99.39% - 99.7%Color and Shape:SolidMolecular weight:330.42ISC-4
CAS:ISC-4 is an Akt inhibitor, which activates prostate apoptosis response protein-4 and reduces colon tumor growth in a nude mouse model.Formula:C11H13NSeColor and Shape:SolidMolecular weight:238.19Bax 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:488.62DRAK1/2-IN-1
CAS:DRAK1/2-IN-1 is a potent inhibitor targeting both DRAK1 and DRAK2, displaying dissociation constants (Kd) of 1 µM and 6 µM, respectively.Formula:C22H24N2O3SColor and Shape:SolidMolecular weight:396.5TJ08
CAS:TJ08 has anticancer properties and can effectively induce G1/S phase blockade while promoting apoptosis in a variety of cancer cells.Formula:C22H16FN3O4Purity:99.89%Color and Shape:SolidMolecular weight:405.38CN128 hydrochloride
CAS:CN128 hydrochloride is an oral, selective hydroxypyridone iron chelator for β-thalassemia research.
Formula:C15H18ClNO3Color and Shape:SolidMolecular weight:295.762'-Deoxyadenosine
CAS:2'-Deoxyadenosine (NSC-141848) is the DNA nucleoside A. It pairs with deoxythymidine (T) in double-stranded DNA.Formula:C10H13N5O3Purity:99.71%Color and Shape:SolidMolecular weight:251.24PD-1/PD-L1-IN 5
CAS:PD-1/PD-L1-IN 5 is a potent PD-1/PD-L1 protein/protein interaction inhibitor (IC50 ≤ 100 nM).Formula:C22H18N4O3SColor and Shape:SolidMolecular weight:418.47CCT128930
CAS:'CCT128930, potent Akt2 inhibitor (IC50=6 nM), 28x more selective over PKA.'Formula:C18H20ClN5Purity:99.07% - 99.18%Color and Shape:SolidMolecular weight:341.84Ref: TM-T6303
2mg39.00€5mg62.00€10mg88.00€25mg166.00€50mg259.00€100mg388.00€200mg617.00€1mL*10mM (DMSO)67.00€Metaproterenol
CAS:Metaproterenol also has anti-inflammatory activity. Metaproterenol is a direct-acting sympathomimetic and a β2-adrenergic receptor (β2AR) agonist (IC50: 68 nM).Formula:C11H17NO3Purity:98%Color and Shape:SolidMolecular weight:211.26Ozarelix
CAS:Ozarelix: a GnRH antagonist that induces apoptosis in advanced prostate cancer, modulates death receptors, and reduces sex hormones.Formula:C72H96ClN17O14Color and Shape:SolidMolecular weight:1459.09Anticancer agent 164
CAS:CML-IN-1, also known as compound 7 and compound 4, is a potent anticancer agent that demonstrates a strong induced-apoptosis effect in the human chronic myeloidFormula:C21H23F3N8O2S2Purity:98%Color and Shape:SolidMolecular weight:540.58Justicidin B
CAS:Justicidin B: anticancer, proapoptotic, inhibits bone resorption & platelets, antiviral, fungicidal, antiprotozoal.Formula:C21H16O6Color and Shape:SolidMolecular weight:364.35Mps1-IN-5
CAS:Mps1-IN-5: oral Mps1 inhibitor with 29 nM IC50, induces apoptosis, G2/M arrest, and has anti-tumor properties.Formula:C24H25N9Color and Shape:SolidMolecular weight:439.52GK563
CAS:GK563, an iPLA2 inhibitor (IC50=1nM), is 22,000x more potent vs. cPLA2 and may reduce β-cell death in type 1 diabetes.Formula:C16H22O2Color and Shape:SolidMolecular weight:246.34MRS 2693 trisodium salt
CAS:MRS 2693 trisodium salt is a P2Y6 agonist.Formula:C9H22IN5O12P2Purity:98%Color and Shape:SolidMolecular weight:581.15Luxeptinib
CAS:Luxeptinib (CG-806) is an oral, non-covalent pan-FLT3/BTK inhibitor for acute myeloid leukemia.Formula:C25H17F4N5O2Color and Shape:SolidMolecular weight:495.43Bcl-2/Mcl-1-IN-3
CAS:Bcl-2/Mcl-1-IN-3 is a Bcl-2/Mcl-1 inhibitor that acts on Mcl-1 (Ki: 0.14 μM) and Bcl-2 (Ki: 0.23 μM) and can be used in cancer research.Formula:C27H26ClNO4Color and Shape:SolidMolecular weight:463.95ADU-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:690.54Tubulin/MMP-IN-2
CAS:Tubulin/MMP-IN-2 blocks tubulin polymerization, MMP-2/-3/-9, induces apoptosis, aids cancer research, IC50: 24.95, 31.60, 22.37 µM.Formula:C40H48NO11PColor and Shape:SolidMolecular weight:749.78PI3K inhibitor C 96
CAS:PI3K inhibitor C 96 is an inhibitor of phosphatidylinositol 3-kinase. It shows effective activity against multiple myeloma in vitro and in vivo.Formula:C11H8N2O3SPurity:98%Color and Shape:SolidMolecular weight:248.26BMS-242
CAS:BMS-242 is an effective inhibitor of PD-1/PD-L1 interaction.Formula:C28H35NO4Purity:98%Color and Shape:SolidMolecular weight:449.58PARP-2-IN-3
CAS:PARP-2-IN-3 is used in the study of breast cancer as a PARP-2 inhibitor with antitumor activity that induces apoptosis (apoptosis) and necrosis in cancer cells.
Formula:C20H20ClN3O3Purity:99.33%Color and Shape:SolidMolecular weight:385.84PSB 0474
CAS:P2Y6 receptor agonistFormula:C17H20N2O13P2Purity:98%Color and Shape:SolidMolecular weight:522.29KS106
CAS:KS106 inhibits ALDH (1A1: 334 nM, 2: 2137 nM, 3A1: 360 nM), has anti-cancer properties, raises ROS, and promotes aldehyde build-up.Formula:C18H15BrF3N3O2SPurity:99.31%Color and Shape:SolidMolecular weight:474.3ZK-304709 HCl
CAS:ZK-304709 is an oral multitarget tumor growth inhibitor with activity against cell-cycle progression and angiogenesis.Formula:C22H29ClN6O2Color and Shape:SolidMolecular weight:444.96(R)-eIF4A3-IN-2
CAS:(R)-eIF4A3-IN-2, a weaker eIF4A3-IN-2 isomer, inhibits eIF4A3 selectively with 110 nM IC50.Formula:C25H19Br2ClN4O2Color and Shape:SolidMolecular weight:602.71RGB-286147
CAS:RGB-286147 is a potent, selective, ATP-competitive Cdks inhibitor.Formula:C23H22Cl2N4O3Purity:98%Color and Shape:SolidMolecular weight:473.35Anticancer agent 67
CAS:Anticancer agent 67 is a ciprofloxacin analogue, an anticancer agent that induces apoptosis and increases sub-G1 cell populations in MCF-7 cells.Formula:C26H24F2N6O2S2Color and Shape:SolidMolecular weight:554.63SD-36
CAS:SD-36: Potent, selective PROTAC STAT3 degrader, Kd ~50 nM, effective on mutants, IC50=10 nM, strong anti-tumor effects, enables mouse tumor regression.Formula:C59H62F2N9O12PPurity:98% - >99.99%Color and Shape:SoildMolecular weight:1158.15MMP2-IN-1
CAS:MMP2-IN-1, an MMP2 inhibitor (IC50 = 6.8μM), halts growth and induces apoptosis in some cancers.Formula:C15H13NO5SColor and Shape:SolidMolecular weight:319.33iMAC2
CAS:iMAC2, a potent MAC (Membrane Attack Complex) inhibitor, exhibits an IC50 of 28 nM and an LD50 of 15,000 nM, demonstrating significant efficacy in inhibitingFormula:C19H20Br2FN3Color and Shape:SolidMolecular weight:469.19Quinidine Monosulfate
CAS:Quinidine Monosulfate: an oral antiarrhythmic, CYP450db inhibitor, K+ blocker (IC50 19.9 μM), used in malaria research.Formula:C40H50N4O8SColor and Shape:SolidMolecular weight:746.92Telomerase-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:420.55CAY10443
CAS:CAY10443 activates apoptosis by binding to apoptosome components, with an EC50 of 5 μM for caspase-3, aiding antitumor drug development.Formula:C17H15Cl2NO2Color and Shape:SolidMolecular weight:336.21p53 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:606.7BIBU-1361 dihydrochloride
CAS:BIBU-1361 dihydrochloride inhibits EGFR kinase, blocking MAPKK/MAPK activation.Formula:C22H29Cl3FN7Color and Shape:SolidMolecular weight:516.87n-Octyl caffeate
CAS:n-Octyl caffeate demonstrates anti-cancer and apoptosis-inducing properties in highly liver-metastatic murine colon 26-L5 carcinoma cell lines.Formula:C17H24O4Color and Shape:SolidMolecular weight:292.37CAY10682
CAS:(±)-Nutlin-3 & CAY10682 inhibit p53-Mdm2; CAY also blocks NF-κB, IKKs phosphorylation, and cancer cell growth (IC50s = 2-6 μM).Formula:C30H25BrFN5OColor and Shape:SolidMolecular weight:570.45Tubulin inhibitor 23
CAS:Potent Tubulin inhibitor 23 (IC50: 4.8 μM) induces apoptosis and has dose-dependent antiangiogenic properties, promising for leukemia research.Formula:C26H23NO6SColor and Shape:SolidMolecular weight:477.53PC-046
CAS:PC-046, a tubulin binder, targets DPC4/SMAD4-deficient tumors, inhibits growth in vitro, and is effective in SCID mice with high oral bioavailability (71%).Formula:C22H18N2O3Color and Shape:SolidMolecular weight:358.39Obatoclax
CAS:Obatoclax (GX15-070), a pan-BCL-2 inhibitor (Ki 220 nM) induces autophagy, degrades cyclin D1, and has anti-cancer/antiparasitic properties.Formula:C20H19N3OPurity:99.44%Color and Shape:SolidMolecular weight:317.38Anticancer agent 55
CAS:Potent anticancer agent inhibits cell growth, migration, induces apoptosis; promising for prostate, breast cancer studies.Formula:C28H21Br2FN2O2Color and Shape:SolidMolecular weight:596.294RO27-3225 TFA
CAS:RO27-3225, a MC4R agonist (EC50=1nM), may treat obesity and brain damage, also acts on MC1R, and helps in hemorrhagic shock.Formula:C41H53F3N12O8Color and Shape:SolidMolecular weight:898.9462MDM2-p53-IN-16
CAS:MDM2-p53-IN-16 inhibits p53/MDM2 complex (IC 50 = 4.3 nM), triggers p53, causes GBM cell apoptosis, useful in cancer research.Formula:C32H33N3O5Color and Shape:SolidMolecular weight:539.62MR2938
CAS:MR2938: AChE inhibitor (IC50=5.04μM), reduces NO (IC50=3.29μM), blocks MAPK/JNK, NF-κB; for AD research.Formula:C21H24N4O3Color and Shape:SolidMolecular weight:380.44VII-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:427.51TrxR inhibitor D9
CAS:TrxR-IN-D9 is a novel inhibitor of thioredoxin reductase (TrxR).Formula:C25H20AuOPSColor and Shape:SolidMolecular weight:596.43PD173952
CAS:PD173952 is a Src kinase and Myt1 inhibitor with antitumor activity, inhibits Lyn, Abl and Csk, and induces Bcr-Abl-dependent hematopoietic cell apoptosis.Formula:C24H21Cl2N5O2Purity:99.5%Color and Shape:SolidMolecular weight:482.36Mepazine
CAS:Mepazine, a MALT1 inhibitor, blocks GSTMALT1 (IC50: 0.83μM) and GSTMALT1 325-760 (IC50: 0.42μM), promoting apoptosis and reducing cell viability.Formula:C19H22N2SPurity:99.88% - 99.92%Color and Shape:SolidMolecular weight:310.46Ref: TM-T16040
10mg39.00€25mg60.00€50mg93.00€100mg116.00€200mg177.00€500mgTo inquire1mL*10mM (DMSO)35.00€GSK2983559 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:538.53iCRT-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:367.44BCL6-IN-7
CAS:BCL6-IN-7 (BCL6 inhibitor-7) is a BCL6 corepressor-interaction inhibitor with potential antitumor activity, used in lymphoma research.Formula:C18H15ClN6OPurity:99.03%Color and Shape:SolidMolecular weight:366.8TL4-12
CAS:TL4-12 is a MAP4K2 (GCK) inhibitor that inhibits IL-1 and TGFβ-induced p38 MAPK phosphorylation in vitro.Formula:C25H27F3N6O2Purity:98.38%Color and Shape:SolidMolecular weight:500.52C6 Ceramide
CAS:C6 Ceramide (N-hexanoylsphingosine) is an activator of the ceramide pathway that arrests cells in the G0/G1 phase by activating ERK.Formula:C24H47NO3Purity:99.67% - 99.73%Color and Shape:SolidMolecular weight:397.63DX3-213B
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€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:454.93DCG066
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€Miclxin
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€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:322.15cRIPGBM chloride
CAS:cRIPGBM chloride is a pro-apoptotic derivative found in GBM cancer stem cells with anti-tumor activity, inducing caspase-1-dependent apoptosis.Formula:C26H20ClFN2O2Purity:99.75%Color and Shape:SolidMolecular weight:446.9Vamotinib
CAS:Vamotinib (PF-114) is a tyrosine kinase inhibitor with antiproliferative and antitumor activity.Vamotinib is used in the study of Alzheimer's disease.Formula:C29H27F3N6OPurity:99.64%Color and Shape:SolidMolecular weight:532.56Ref: TM-T63746
1mg101.00€5mg245.00€10mg401.00€25mg717.00€50mg982.00€100mg1,341.00€200mg1,783.00€1mL*10mM (DMSO)288.00€AMG 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:561.07
