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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Latikafusp
CAS:Latikafusp (AMG 256) is a fusion protein that is a PD-1 blocker and IL-21R agonist with antitumor activity.Purity:97.1% (SDS-PAGE); 97.4% (SEC-HPLC) - 97.1% (SDS-PAGE); 97.4% (SEC-HPLC)Color and Shape:LiquidMolecular weight:159.55 kDaEfaprinermin alfa
CAS:Efaprimermin alfa (OMP-336B11) is a human monoclonal antibody that targets TNFRSF18, and functions as a GITR ligand-Fc fusion protein [1].Color and Shape:LiquidPamrevlumab
CAS:FG-3019 (Pamrevlumab), a human antibody, targets CTGF, potentially treating idiopathic pulmonary fibrosis.Purity:100% (SEC-HPLC) - >95.0% (SDS-PAGE)Color and Shape:LiquidMolecular weight:150 kDaIzuralimab
CAS:Izuralimab is a bispecific IgG1 antibody that targets both the inducible T-cell costimulator (ICOS/CD278) and PD-1 [1].Color and Shape:LiquidAtibuclimab
CAS:Atibuclimab is a chimeric monoclonal antibody targeting CD14, consisting of a mouse variable region and a human IgG4 Fc region.Purity:> 95% - > 95%Color and Shape:LiquidMolecular weight:145.28 kDaAnti-Mouse PD-L1/B7-H1 (LALA-PG) Antibody (10F.9G2)
Anti-Mouse PD-L1/B7-H1 (LALA-PG) Antibody (10F.9G2) is an IgG2a, κ antibody inhibitor derived from mice, specifically targeting and inhibiting mouse PD-L1/B7-H1.Color and Shape:Odour LiquidAnti-Mouse PD-1 Antibody (RMP1-14)
Anti-Mouse PD-1 Antibody (RMP1-14) is an IgG2a antibody inhibitor against mouse PD-1 and can block PD-1/PD-L1 signaling. High-Quality, Low-Cost!Purity:14.68mg/ml - >95%Color and Shape:LiquidMolecular weight:147.57 kDaδ-secretase inhibitor 11
CAS:δ-secretase inhibitor 11 is an inhibitor of δ-secretase and can be used as a lead compound for translational development of AD treatment.Formula:C10H12N4O2Purity:99.84%Color and Shape:SolidMolecular weight:220.23Rasagiline
CAS:Rasagiline (AGN1135) is an inhibitor of monamine oxidase used as adjunctive therapy in combination with levodopa and carbidopa in the management of Parkinsons
Formula:C12H13NPurity:98% - 99.87%Color and Shape:SolidMolecular weight:171.24Cyanoacetamide
CAS:Cyanoacetamide has inhibitory activity against the myeloid leukaemia cell differentiation protein Mcl-1Formula:C3H4N2OPurity:97.04%Color and Shape:Needles From Alcohol White To Light Cream Crystalline PowderMolecular weight:84.08PROTAC Bcl2 degrader-1
CAS:PROTAC Bcl2 degrader-1 is a PROTAC, which potently and selectively induces the degradation of Mcl-1 (IC50: 11.81 μM) and Bcl-2 (IC50: 4.94 μM; DC50: 3.0 μM).Formula:C45H45BrN6O10SPurity:98%Color and Shape:SolidMolecular weight:941.84Flavopiridol
CAS:Flavopiridol (Alvocidib) blocks CDK1/2/4/6 by competing with ATP (IC50 ~40 nM); 7.5x selectivity over CDK7; also inhibits EGFR, PKA. In Phase 1/2 trials.Formula:C21H20ClNO5Purity:97.74% - 99.99%Color and Shape:SolidMolecular weight:401.84IRF1-IN-1
CAS:IRF1-IN-1 (Compound I-2) is an IRF1 inhibitor , inhibiting the cleavage of Caspase 1, GSDMD, IL-1, and PARP1,protecting against skin inflammatory damage.Formula:C22H24N4O4SPurity:99.88%Color and Shape:SolidMolecular weight:440.52Golimumab
CAS:Golimumab (CNTO-148), an anti-TNFα IgG1κ monoclonal antibody with anti-inflammatory and anti-cancer activity, can be used to prevent inflammation and cartilage.Color and Shape:LiquidMolecular weight:146.93 kDa12-HETE
CAS:12-HETE ((±)12-HETE) is a regulator of PGE2, having both antithrombotic and prothrombotic effects.Formula:C20H32O3Color and Shape:SolidMolecular weight:320.47BMH-7 HCl
BMH-7 HCl is a p53 activator, showing anti-cancer activity by activating the p53 pathway.Formula:C20H22ClN5OPurity:99.62%Color and Shape:SolidMolecular weight:383.88Daporinad hydrochloride
CAS:Daporinad hydrochloride (FK 866 hydrochloride) is a NAMPT inhibitor with antitumor and antiangiogenic activity that induces apoptosis in tumor cells.Formula:C24H30ClN3O2Purity:98.99%Color and Shape:SolidMolecular weight:427.97Bcl-xL antagonist 2
CAS:Bcl-xL antagonist 2 is an effective and selective antagonist of Bcl-xL with an IC50 of 91 nM and a Ki of 65 nM.Formula:C21H16N4O3S2Purity:99.81%Color and Shape:SolidMolecular weight:436.51Ref: TM-T38622
1mg77.00€5mg166.00€10mg248.00€25mg447.00€50mg622.00€100mg800.00€200mg1,071.00€1mL*10mM (DMSO)182.00€SCR7
CAS:SCR7, a specific DNA Ligase IV inhibitor, blocks nonhomologous end-joining (NHEJ).Formula:C18H14N4OSPurity:98%Color and Shape:SolidMolecular weight:334.4TPP-resveratrol
TPP-resveratrol is a conjugate of Resveratrol and triphenylphosphine (TPP), noted for its anticancer activity. This compound enhances the efficacy of Resveratrol by facilitating its targeted delivery to mitochondria, thus inducing mitochondrial-mediated cell apoptosis (apoptosis).Formula:C36H32BrO4PColor and Shape:SolidMolecular weight:639.51NDI-Lyso
CAS:NDI-Lyso is an anticancer agent targeting lysosomes, functioning through an enzyme-induced self-assembly (EISA) mechanism catalyzed by Cathepsin B. In cancer cell lysosomes, it forms rigid long fibers, promoting lysosomal swelling, lysosomal membrane permeabilization (LMP), and membrane disruption. This leads to non-classical caspase-independent apoptosis (Apoptosis). NDI-Lyso demonstrates significant selective anticancer activity across various cancer cell lines and drug-resistant cancer cells (IC50 approximately 10 μM), while exhibiting low toxicity to normal cells (IC50 > 60 μM).Formula:C71H100N22O13Color and Shape:SolidMolecular weight:1469.69PROTAC HIF-1α degrader-1
PROTAC HIF-1α degrader-1 (compound V2) is an effective proteolysis-targeting chimeric (PROTAC) degrader of hypoxia-inducible factor-1α (HIF-1α), with an IC50 value of 7.54 µM. This compound exhibits anti-proliferative activity, reduces HIF-1α protein expression, and induces apoptosis.Formula:C51H72N6O7SColor and Shape:SolidMolecular weight:913.22CPD-10
CAS:CPD-10 is a potent bifunctional PROTAC degrader targeting CCND1 and CDK4 and exhibits antiproliferative effects. It induces apoptosis and reduces the protein expression of Cyclin D1, Cyclin D3, CDK4, and P-Rb(5807/811) in a dose-dependent manner.Formula:C46H61N15O4Color and Shape:SolidMolecular weight:888.08hMcl-1-IN-1
hMcl-1-IN-1 (Compound 9) is an hMcl-1 inhibitor based on a His224 arylsulfonyl fluoride, displaying an IC50 value of 5.8 nM.Formula:C69H113FN20O19SColor and Shape:SolidMolecular weight:1577.82CQ-Mito
CQ-Mito, a derivative of CQ, demonstrates excellent phototherapeutic efficacy with a PI value of 167. This compound induces cell death through mechanisms such as apoptosis and ferroptosis. It mediates mitochondrial dysfunction, characterized by alterations in mitochondrial morphology and loss of MMP. Additionally, CQ-Mito effectively inhibits tumor growth in 3D multicellular tumor spheroid models.Formula:C45H42BrN6O4PColor and Shape:SolidMolecular weight:841.73EJMC-1
CAS:EJMC-1 is an inhibitor of TNF-α with an IC50 value of 42 μM and can be used in studies about auto-inflammatory diseases.Formula:C17H11ClN2O4SPurity:98.38%Color and Shape:SolidMolecular weight:374.8BIM-46174 HCl
BIM-46174 HCl is a G-protein inhibitor with anticancer activity that induces cysteine 3-dependent apoptosis.
Formula:C22H31ClN4OSPurity:99.77% - 99.77%Color and Shape:SolidMolecular weight:435.03P53R3
CAS:P53R3 is a potent reactivator of p53, effectively restoring sequence-specific DNA binding to several p53 hot spot mutants, namely p53 R175H, p53 R248W, and p53Formula:C32H35Cl2N5O2Purity:98.8%Color and Shape:SolidMolecular weight:592.56CDK8-IN-13
CAS:CDK8-IN-13 is a CDK8 inhibitor (IC50: 51.9 nM) with potent, selective and oral activity.Formula:C14H11N3OPurity:99.28%Color and Shape:SoildMolecular weight:237.26BM 957
CAS:BM 957 is an effective Bcl-2 and Bcl-xL inhibitor (Kis: 1.2 and <1 nM; IC50s: 5.4 and 6.0 nM).Formula:C52H56ClF3N6O7S3Purity:98%Color and Shape:SolidMolecular weight:1065.68rac-CCT-250863 HCl
rac-CCT-250863 HCl: NEK 2 inhibitor, halts cell cycle, anti-cancer growth, boosts Pomalidomide-induced apoptosis.Formula:C24H26ClF3N4O2SPurity:98.21%Color and Shape:SoildMolecular weight:527KT5823
CAS:KT5823 is a cGMP-dependent protein kinase (PKG) inhibitor that increases iodide ion uptake by regulating the expression of sodium iodide symporter protein.Formula:C29H25N3O5Purity:95%Color and Shape:SolidMolecular weight:495.53SPOP-IN-6lc
CAS:SPOP-IN-6lc is a SPOP inhibitor with oncogenic effects in renal cancer cells.SPOP-IN-6lc can be used to study apoptosis.
Formula:C26H31N7O2SPurity:99.19%Color and Shape:SolidMolecular weight:505.64Glutathione arsenoxide hydrochloride
Glutathione arsenoxide hydrochloride: anti-cancer, inhibits tumour metabolism, targets ANT, promotes apoptosis, marks cell proteins.Formula:C18H26AsClN4O9SPurity:99.74%Color and Shape:SoildMolecular weight:584.86Voreloxin
CAS:Voreloxin (SNS-595) is a potent Topoisomerase II inhibitor with broad-spectrum anti-tumor activity. Phase 2.Formula:C18H19N5O4SPurity:98%Color and Shape:SolidMolecular weight:401.44PI3Kδ-IN-16
CAS:PI3Kδ-IN-16 is a selective and potent PI3Kδ inhibitor with anticancer and antiproliferative activity, induces cell cycle arrest and apoptosis.Formula:C22H26N6O2Purity:99.68%Color and Shape:SoildMolecular weight:406.48POV-PC
CAS:POV-PC is an oxidized phospholipid that inhibits VSMC growth under high serum conditions and induces cell apoptosis under low serum conditions.Formula:C29H56NO9PColor and Shape:SolidMolecular weight:593.73Sandacanol
CAS:Sandacanol (Sandranol) is an olfactory receptor (OR10H1) agonist.Sandacanol induces cell cycle arrest and partial apoptosis in bladder cancer cells.Formula:C14H24OPurity:99.59%Color and Shape:SolidMolecular weight:208.3484-B10
CAS:84-B10 provides protection in cisplatin-induced acute kidney injury, reversing lipid peroxidation accumulation and downregulation of key ferroptosis inhibitors.Formula:C25H22F3NO5Purity:99.76%Color and Shape:SolidMolecular weight:473.44Ref: TM-T75268
1mg47.00€5mg92.00€10mg152.00€25mg289.00€50mg447.00€100mg670.00€200mg888.00€1mL*10mM (DMSO)92.00€SFI003
CAS:SFI003 is a novel SRSF3 inhibitor that exerts anticancer activity against colorectal cancer by modulating the SRSF3 / DHCR24 / ROS axis and driving apoptosis inFormula:C19H17N5OSPurity:99.44%Color and Shape:SoildMolecular weight:363.44Ref: TM-T72068
1mg75.00€5mg164.00€10mg255.00€25mg495.00€50mg712.00€100mg973.00€200mg1,341.00€1mL*10mM (DMSO)172.00€TV 3279
CAS:TV 3279 is a ChE-MAI inhibitor with neuroprotection via anti-apoptotic protein induction and blocks pro-apoptotic enzymes in cells.
Formula:C16H20N2O2Purity:97%Color and Shape:SoildMolecular weight:272.34N-Stearoyltyrosine
CAS:N-Stearoyltyrosine (N-(1-Oxooctadecyl)-L-tyrosine) is an analog of Anandamide. It exhibits neuroprotective effects by safeguarding the CA1 region of the hippocampus in a gerbil ischemia-reperfusion model. Additionally, N-Stearoyltyrosine inhibits free radical generation, enhances antioxidant capacity, and reduces IR-induced apoptosis (cell apoptosis).Formula:C27H45NO4Color and Shape:SolidMolecular weight:447.65Δ8-Tetrahydrocannabinoquinone
CAS:Δ8-Tetrahydrocannabinoquinone (HU-336) is a potent anti-angiogenic agent that inhibits angiogenesis by directly inducing apoptosis in vascular endothelial cells. It achieves this without altering the expression of pro-angiogenic and anti-angiogenic cytokines and receptors. Δ8-Tetrahydrocannabinoquinone also shows significant effectiveness against tumor xenografts in nude mice.Formula:C21H28O3Color and Shape:SolidMolecular weight:328.45CWI1-2 HCL
CAS:CWI1-2 HCL: Potent IGF2BP2 inhibitor, induces apoptosis/differentiation, targets leukemia therapy.Formula:C22H18Cl4N6O3Purity:98.09%Color and Shape:SolidMolecular weight:556.23Ref: TM-T67930L
1mg49.00€5mg92.00€10mg145.00€25mg281.00€50mg409.00€100mg580.00€200mg798.00€1mL*10mM (DMSO)116.00€Anticancer agent 130
Anticancer agent 130 (compound 8d) significantly induces apoptosis in A549 cells [1].Formula:C38H46FN5O5Purity:98%Color and Shape:SolidMolecular weight:671.8Asparanin A
CAS:Asparanin A, an apoptosis inducer with anticancer properties, arrests the cell cycle in the G0/G1 phase via the mitochondria and PI3K/AKT signaling pathways.Formula:C39H64O13Purity:98%Color and Shape:SolidMolecular weight:740.92Antitumor agent-96
"Antitumor agent-96 (Compound D34) is a potent MRE11 inhibitor that down-regulates the homologous recombination (HR) pathway by binding to and suppressing theFormula:C27H32N2O2Purity:98%Color and Shape:SolidMolecular weight:416.56Flaccidoside II
CAS:Flaccidoside II, an active triterpenoid saponin from Anemone flaccida rhizome, both inhibits proliferation and induces apoptosis in Malignant Peripheral NerveFormula:C59H96O25Purity:98%Color and Shape:SolidMolecular weight:1205.38Antimycin A2c
Anticancer Agent 141 (Compound AE), an antimycin alkaloid, exhibits inhibitory potential against HPV-infected cervical cancer.Formula:C28H40N2O9Purity:98%Color and Shape:SolidMolecular weight:548.63Anticancer agent 133
Compound Rh2 (Anticancer agent 133) is a cytotoxic and antimetastatic agent that induces cell cycle arrest, apoptosis, and autophagy.Formula:C24H19Cl3N5ORhPurity:98%Color and Shape:SolidMolecular weight:602.71fac-[Re(CO)3(L6)(H2O)][NO3]
Compound 6, fac-[Re(CO)3(L6)(H2O)][NO3], a rhenium(I) tricarbonyl aqua complex, serves as an anticancer agent by disrupting mitochondrial function.Formula:C24H14N5O7ReSPurity:98%Color and Shape:SolidMolecular weight:702.67GPX4-IN-7
GPX4-IN-7 (Compound 31), an indirubin derivative, serves as a ferroptosis inducer in colon cancer treatment.Formula:C25H23ClN4O4Purity:98%Color and Shape:SolidMolecular weight:478.93EGFR-IN-78
EGFR-IN-78 (compound A5), a 2-aminopyrimidine derivative, serves as a reversible EGFR C797S-TK inhibitor and an apoptosis inducer.Formula:C23H32BrN7O2SPurity:98%Color and Shape:SolidMolecular weight:550.51TAT-NEP1-40
TAT-NEP1-40, a blood-brain barrier (BBB) permeable peptide, confers protection to PC12 cells against oxygen and glucose deprivation (OGD) while promotingFormula:C268H438N88O77Purity:98%Color and Shape:SolidMolecular weight:6124.89CPT2
CAS:Carnitine palmitoyltransferase 2 (CPT2), an enzyme involved in fatty acid oxidation, serves as a prognostic biomarker for colorectal cancer (CRC).Purity:98%Color and Shape:SolidTAT-NEP1-40 TFA
TAT-NEP1-40 TFA, a blood-brain barrier-permeable peptide, safeguards PC12 cells against oxygen and glucose deprivation (OGD) and fosters neurite outgrowth.Formula:C268H438N88O77·xC2HF3O2Purity:98%Color and Shape:SolidMolecular weight:6124.89 (free base)TP4 (Nile tilapia piscidin)
CAS:TP4 (Nile tilapia piscidin) is an orally active piscidin-like antimicrobial peptide that exhibits inhibition of various gram-positive and negative bacterialFormula:C135H226N50O27Purity:98%Color and Shape:SolidMolecular weight:2981.56Antitumor agent-113
Antitumor Agent-113 exhibits cytotoxicity in A549 cells, with an IC50 of 46.60 μM, and induces apoptosis, making it applicable for research in non-small cellFormula:C21H22ClN5O2SPurity:98%Color and Shape:SolidMolecular weight:443.95Cholicamideβ
Cholicamideβ (compound 6), a self-assembling small molecule cancer vaccine adjuvant, forms low cytotoxicity virus-like particles and upon binding to peptideFormula:C55H94N2O6Purity:98%Color and Shape:SolidMolecular weight:879.34TAT-GluN2BCTM
CAS:TAT-GluN2BCTM is a membrane-permeable peptide that selectively targets active DAPK1 (Death-associated protein kinase 1) for lysosomal degradation, therebyFormula:C224H374N86O54Purity:98%Color and Shape:SolidMolecular weight:5135.91Antitumor photosensitizer-4
Antitumor Photosensitizer-4 (compound 10b), a conjugate of dasatinib and imatinib, serves as a potent tyrosine kinase inhibitor (TKI) targeting ABCG2.Formula:C65H77ClN12O11SPurity:98%Color and Shape:SolidMolecular weight:1269.9cpm-1285
CAS:CPM-1285 induces apoptosis by effectively inhibiting the function of intracellular Bcl-2 and associated death antagonists.Formula:C153H240N44O42SPurity:98%Color and Shape:SolidMolecular weight:3399.88Anticancer agent 132
Compound Rh1 (Anticancer agent 132) acts as an inducer of apoptosis and autophagy, exhibiting both antitumor and antimetastatic activities.Formula:C24H16Cl3F3N5ORhPurity:98%Color and Shape:SolidMolecular weight:656.68Antitumor agent-103
Antitumor Agent-103 (compound 24l) induces apoptosis and possesses antiproliferative and anti-colony formation properties.Formula:C36H36N8O9S2Purity:98%Color and Shape:SolidMolecular weight:788.85Anticancer agent 153
Anticancer Agent 153 (Compound 3) promotes apoptosis through the generation of Reactive Oxygen Species (ROS) and elevates the loss of Mitochondrial MembraneFormula:C16H11Cl2N3O3Purity:98%Color and Shape:SolidMolecular weight:364.18HNPMI
CAS:HNPMI is an epidermal growth factor receptor inhibitor that promotes apoptosis and is used in the study of colorectal cancer.Formula:C22H20N2O3Purity:97.19%Color and Shape:SoildMolecular weight:360.414-hydroperoxy cyclophosphamide
CAS:4-hydroperoxy cyclophosphamide (4-OOH-CY) induces hepatotoxicity. It increases ghrelin levels and enhances inflammatory factors and oxidative markers.Formula:C7H15Cl2N2O4PPurity:98%Color and Shape:SolidMolecular weight:293.092-aminobenzo[d]thiazol-6-ol
CAS:2-aminobenzo[d]thiazol-6-ol: antimicrobial, antioxidant, anticancer; may trigger cancer cell apoptosis.Formula:C7H6N2OSPurity:98.92%Color and Shape:SolidMolecular weight:166.2Thrombospondin-1 (1016-1023) (human, bovine, mouse)
CAS:Thrombospondin-1 (1016-1023) (human, bovine, mouse) is part of Thrombospondin-1 (TSP-1), a peptide with CD47 agonism.Formula:C56H81N13O10SPurity:99.23%Color and Shape:SolidMolecular weight:1128.39Ref: TM-T75720
1mg52.00€5mg111.00€10mg175.00€25mg283.00€50mg439.00€100mg633.00€1mL*10mM (DMSO)212.00€Chiisanoside
CAS:Chiisanoside is a useful organic compound for research related to life sciences. The catalog number is T123983 and the CAS number is 89354-01-8.Formula:C48H74O19Color and Shape:SolidMolecular weight:955.101Isovalerylcarnitine
CAS:Isovalerylcarnitine (3-methylbutyrylcarnitine) is a selective effective calpain activator that can promote cell apoptosis and is related to isovaleric acidemia.Formula:C12H23NO4Purity:98.24%Color and Shape:SolidMolecular weight:245.32Terfenadine (Standard)
CAS:Terfenadine (Standard) is the standard substance of Terfenadine, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Terfenadine ((±)-Terfenadine) is a prodrug that is metabolized by intestinal CYP3A4 to the active form fexofenadine, a selective histamine H1-receptor antagonist with antihistaminic and non-sedative effects.Formula:C32H41NO2Molecular weight:471.67Thioridazine
CAS:Thioridazine: an antipsychotic, anti-anxiety drug, blocks dopamine D2, PI3K-Akt-mTOR; halts angiogenesis, kills cancer cells, targets CSCs.Formula:C21H26N2S2Color and Shape:SolidMolecular weight:370.57Galantamin-d6
CAS:Galantamin-d6 is a deuterated compound of Galantamin.Formula:C17H15D6NO3Color and Shape:SolidMolecular weight:293.39Buparlisib Hydrochloride
CAS:Buparlisib Hydrochloride is an inhibitor of pan-class I PI3K (IC50: 52 nM/166 nM/116 nM/262 nM for p110α/p110β/p110δ/p110γ, respectively).Formula:C18H22ClF3N6O2Purity:98.94% - 99.66%Color and Shape:SolidMolecular weight:446.85OTS193320
CAS:OTS193320, an imidazo[1,2-a]pyridine, inhibits SUV39H2, reduces H3K9me3, and induces apoptosis in breast cancer; enhances DOX effects.Formula:C28H30ClN5O4Color and Shape:SolidMolecular weight:536.02Licofelone
CAS:Formula:C23H22ClNO2Purity:>95.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:379.88AZD5582
CAS:AZD5582 is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. It induces apoptosis.Formula:C58H78N8O8Purity:98.75%Color and Shape:SolidMolecular weight:1015.29Tetrac
CAS:Tetrac (Tetraiodothyroacetic acid) is a derivative of L-thyroxine (T4), a thyroxine integrin receptor antagonist.Tetrac induces antiproliferation by blockingFormula:C14H8I4O4Purity:99.00%Color and Shape:SolidMolecular weight:747.83FPA-124
CAS:FPA-124 is a cell-permeable copper complex that acts as a selective Akt (protein kinase B) inhibitor to induce apoptosis in a variety of cancer cell lines.Formula:C11H9Cl2CuN3O2SPurity:95.04%Color and Shape:SolidMolecular weight:381.73Baohuoside I
CAS:Formula:C27H30O10Purity:>95.0%(T)(HPLC)Color and Shape:White to Light yellow to Green powder to crystalMolecular weight:514.53Barbadin
CAS:Barbadin is an inhibitor of β-arrestin/β2-adaptin interaction.Barbadin enhances the effects of lorcaserin on weight loss and can be used to study obesity.Formula:C19H15N3OSPurity:98.93% - 99.10%Color and Shape:SolidMolecular weight:333.41Olanzapine D3
CAS:Olanzapine D3 is the deuterium labeled Olanzapine.Formula:C17H20N4SPurity:98%Color and Shape:SolidMolecular weight:315.45FMAU
CAS:FMAU (2'-Deoxy-2'-fluoro-5-methyl-beta-D-arabinouridine) is a thymine nucleoside analog with insertional activity on replicating DNA.FMAU can be used to labelFormula:C10H13FN2O5Purity:98.6%Color and Shape:SolidMolecular weight:260.222'-Deoxy-2'-fluoro-β-D-arabinoguanosine
CAS:2'-Deoxy-2'-fluoro-beta-D-arabinoguanosine is a purine nucleoside analog with a broad spectrum of antitumor activity, targeting malignant tumors of the inertFormula:C10H12FN5O4Purity:98.06%Color and Shape:SolidMolecular weight:285.23Pexidartinib 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.Formula:C20H16Cl2F3N5Purity:99.88%Color and Shape:SolidMolecular weight:454.28Sodium catechol sulfate
CAS:Sodium catechol sulfate is a bioactive chemical.Formula:C6H4Na2O8S2Purity:98%Color and Shape:Light Tan PowderMolecular weight:314.20Propylparaben sodium
CAS:Propylparaben sodium, a plant-based preservative used in cosmetics, pharma, and food, hinders follicle growth and sperm health.Formula:C10H12NaO3Color and Shape:SolidMolecular weight:203.193Isoginkgetin
CAS:Formula:C32H22O10Purity:>95.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:566.521-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)uracil
CAS:1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil is a Nucleoside, fluoro-modified nucleoside; Arabino-nucleosidde.Formula:C9H11FN2O5Purity:98.36%Color and Shape:SolidMolecular weight:246.19Octreotide
CAS:Octreotide (SMS 201-995) is a potent inhibitor of growth hormone, glucagon, and insulin.Formula:C49H66N10O10S2Purity:99.3% - 99.64%Color and Shape:White PowderMolecular weight:1019.244-Thiothymidine
CAS:4-Thiothymidine is a Nucleoside Derivative - Thio-nucleoside, 5-Modified pyrimidine nucleoside.Formula:C10H14N2O4SPurity:99.92%Color and Shape:SolidMolecular weight:258.296-Azuridine
CAS:6-Azauridine is a purine analog with antitumor effects, inhibiting DNA synthesis and inducing apoptosis in lymphatic cancers.Formula:C8H11N3O6Purity:99.02%Color and Shape:SolidMolecular weight:245.19Devazepide
CAS:Devazepide is a competitive, selective, orally available non-peptide CCK1 receptor antagonist that inhibits proliferation, induce apoptosis.Formula:C25H20N4O2Purity:99.55%Color and Shape:SolidMolecular weight:408.454-Benzoyl-L-phenylalanine
CAS:4-Benzoyl-L-phenylalanine is an L-phenylalanine derivative and optically active amino acid.Formula:C16H15NO3Purity:98.01%Color and Shape:SolidMolecular weight:269.30Ibuprofen-d3
CAS:Ibuprofen D3 is a deuterium labeled Ibuprofen. Ibuprofen is a COX-1 and COX-2 inhibitor (IC50s: 13 μM and 370 μM).Formula:C13H18O2Color and Shape:SolidMolecular weight:209.3Rottlerin
CAS:Formula:C30H28O8Purity:>95.0%(HPLC)(qNMR)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:516.55LG100268
CAS:LG100268 is a selective, and oral RXR agonist，inducing transcriptional activation in adipocytes; inhibits keratin 17 increases PD-L1 expression.Formula:C24H29NO2Purity:99.83%Color and Shape:SolidMolecular weight:363.49PBOX 6
CAS:PBOX 6 is a pyrrolo-1,5-benzoxazepine (PBOX) compound with anticancer and antitumor activity that inhibits the growth of breast cancer cells.Formula:C25H20N2O3Purity:98.18% - 98.71%Color and Shape:SolidMolecular weight:396.44Ref: TM-T16436
1mg59.00€5mg131.00€10mg187.00€25mg311.00€50mg462.00€100mg662.00€1mL*10mM (DMSO)140.00€13-Methyltetradecanoic acid
CAS:LeDSF3 controls HSAF production in Lysobacter, has antifungal properties, and acts as an anti-tumor by inhibiting p-AKT and activating caspase-3.Formula:C15H30O2Color and Shape:SolidMolecular weight:242.4
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