
Apoptose
Sous-catégories appartenant à la catégorie "Apoptose"
- ASK(9 produits)
- BCL(1 produits)
- Caspase(154 produits)
- FOXO1(2 produits)
- IAP(67 produits)
- Mdm2(12 produits)
- PD-1/PD-L1(127 produits)
- PDK(9 produits)
- PERK(23 produits)
- Sérine/thréonine kinase(17 produits)
- Survivant(14 produits)
- TNF(90 produits)
- c-RET(61 produits)
- p53(63 produits)
6170 produits trouvés pour "Apoptose"
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.Formule :C27H25N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :451.52Anticancer agent 72
CAS :Compound 8c inhibits K+ channel and induces apoptosis, showing promise as an anticancer agent.Formule :C20H19N7O2Couleur et forme :SolidMasse moléculaire :389.41Mcl1-IN-3
CAS :Mcl1-IN-3 is an Mcl1 inhibitor. It has an IC50 and Ki of 0.67 and 0.13 μM, respectively.Formule :C27H22ClN3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :487.93NSC114792
CAS :NSC114792 is a selective JAK3 inhibitor.Formule :C26H32N4O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :464.62PQ1 Succinate
CAS :PQ1 Succinate boosts GJIC and connexin in breast cancer cells without impacting normal mammary cells.Formule :C25H28F3N3O6Couleur et forme :SolidMasse moléculaire :523.5EGFR-IN-51
CAS :EGFR-IN-51 effectively inhibits EGFR and mutations with IC50s of 0.493-461.63 μM; it induces apoptosis in cancer cells.Formule :C21H15N3O2SCouleur et forme :SolidMasse moléculaire :373.43Darinaparsin
CAS :Darinaparsin, a dimethylated arsenic-glutathione compound, is cytotoxic to various cancer cells with diverse IC50 values and inhibits tumor growth in mice.Formule :C12H22AsN3O6SCouleur et forme :SolidMasse moléculaire :411.31CMC2.24
CAS :CMC2.24 inhibits Ras and ERK1/2, fights pancreatic tumors in mice, blocks MMPs (IC50: 2-69 µM), and reduces osteoarthritis by stabilizing cartilage.Formule :C26H21NO5Couleur et forme :SolidMasse moléculaire :427.45AP23464
CAS :AP23464 inhibits Src/Abl kinases, effective on imatinib-resistant CML cells (IC50=14nM), blocks cell cycle, induces apoptosis, not against T315I mutant.Formule :C26H30N5O2PDegré de pureté :99.79%Couleur et forme :SolidMasse moléculaire :475.52HDAC-IN-51
HDAC-IN-51 is an HDAC inhibitor.Formule :C27H24N4O2Degré de pureté :98.85%Couleur et forme :SolidMasse moléculaire :436.51GL-V9
CAS :GL-V9 is an AMPK activator, protecting against colitis-associated colorectal cancer by limiting NLRP3 inflammasome through autophagy.Formule :C24H27NO5Couleur et forme :SolidMasse moléculaire :409.47pan-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 (IC50Formule :C19H15BrClN5OCouleur et forme :SolidMasse moléculaire :444.71BLM-IN-1
CAS :BLM-IN-1: BLM inhibitor, KD 1.81 μM, IC50 0.95 μM; causes DNA damage, apoptosis, stops cancer cell growth.Formule :C28H35FN4OCouleur et forme :SolidMasse moléculaire :462.6HX 630
CAS :RXR agonistFormule :C28H27NO2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :441.58Lexibulin dihydrochloride
CAS :Lexibulin 2HCl inhibits tubulin polymerization (IC50: 10-100 nM) and shows potent anti-cancer cytotoxicity and vascular disruption in vitro/vivo.Formule :C24H32Cl2N6O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :507.46WJ35435
CAS :WJ35435 is a histone deacetylase and topoisomerase I dual inhibitor.Formule :C20H21N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :351.4BEPP monohydrochloride
CAS :BEPP monohydrochloride is a double-strand RNA-dependent protein kinase (PKR) activator.Formule :C23H24ClN3O2Couleur et forme :SolidMasse moléculaire :409.91Tubulin inhibitor 30
CAS :Tubulin Inhibitor 30, exhibiting an IC50 value of 0.52 μM, functions as an inhibitor of tubulin assembly. Additionally, it can induce ferroptosis.Formule :C22H19N3O5Couleur et forme :SolidMasse moléculaire :405.4Nevanimibe
CAS :Nevanimibe is an orally active and selective inhibitor of acyl-coenzyme A:cholesterol O-acyltransferase 1 (ACAT1) (EC50 of 9 nM).Formule :C27H39N3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :421.62Ceranib-2
CAS :Ceranib-2, a ceramidase inhibitor (IC50: 28 μM, SKOV3), reduces sphingosine/S1P and promotes apoptosis, showing anticancer properties.
Formule :C25H19NO3Degré de pureté :98.49%Couleur et forme :SolidMasse moléculaire :381.42APX2009
CAS :APX2009, a 2nd-gen APE1/Ref-1 inhibitor, curbs NFkB activity, survivin, and prostate cancer cell growth; induces cell cycle arrest.Formule :C21H25NO4Couleur et forme :SolidMasse moléculaire :355.43Antitumor agent-81
CAS :Antitumor agent-81, a P62-RNF168 agonist, reduces H2A ubiquitination, hinders DNA repair, and inhibits tumor growth.Formule :C19H19N7O3Couleur et forme :SolidMasse moléculaire :393.4EC359
CAS :EC359 is a Leukemia Inhibitory Factor Receptor (LIFR) inhibitor with anticancer activity for the study of leukemia and endometrial cancer.Formule :C36H38F2O2Degré de pureté :98.11% - 98.11%Couleur et forme :SolidMasse moléculaire :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.Formule :C23H18F4N6O2Degré de pureté :99.05% - 99.51%Couleur et forme :SolidMasse moléculaire :486.42PARP1-IN-10
CAS :PARP1-IN-10 (12c) is a potent, non-toxic PARP1 inhibitor with a 50.62 nM IC50, enhancing TMZ effects and causing G2/M arrest and apoptosis.Formule :C20H23N3O5Couleur et forme :SolidMasse moléculaire :385.41PBOX-15
CAS :PBOX-15 induces apoptosis, regulates death receptors, enhances TRAIL effects, and inhibits T cell migration in myeloma cells.Formule :C28H19NO3Couleur et forme :SolidMasse moléculaire :417.46PD-1/PD-L1-IN-25
CAS :"PD-1/PD-L1-IN-25 blocks PD-1/PD-L1 (IC50: 16.17 nM), boosting T-cell anti-tumor immunity, useful for cancer research."Formule :C26H24ClN3O5Couleur et forme :SolidMasse moléculaire :493.94SMU127
CAS :SMU127 is an agonist of the toll-like receptor 1/2 (TLR1/2) heterodimer.Formule :C16H23N3O3SCouleur et forme :SolidMasse moléculaire :337.442-chloro Palmitic Acid
CAS :2-chloro Palmitic acid triggers NETosis, elevates COX-2, adhesion molecules in HCAECs, and induces apoptosis and caspase-3 in THP-1 cells/monocytes.Formule :C16H31ClO2Couleur et forme :SolidMasse moléculaire :290.87Trehalose 6-behenate
CAS :Trehalose 6-behenate is a Th1/Th17 skewing vaccine adjuvant.Formule :C34H64O12Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :664.86BP-1-108
CAS :BP-1-108 is a potent and selective STAT5 inhibitor.Formule :C32H38N2O6SCouleur et forme :SolidMasse moléculaire :578.72HMBPP triammonium
CAS :HMBPP triammonium is a stimulator of gamma delta T cells.Formule :C5H15NO8P2Couleur et forme :SolidMasse moléculaire :279.122Antitumor agent-19
CAS :Antitumor agent-19 is a modulator of tumor-associated macrophages with EC50s of 17.18 μM and 18.87 μM in the RAW 264.7 cells and the BMDM cells.Formule :C24H21ClF3N5ODegré de pureté :98.95% - 99.38%Couleur et forme :SolidMasse moléculaire :487.9Ref: TM-T10341
1mg109,00€2mg163,00€5mg241,00€1mL*10mM (DMSO)289,00€10mg354,00€25mg532,00€50mg745,00€100mg1.018,00€500mg2.035,00€YH-306
CAS :YH-306 (TRV055 acetate ) is a modulator of the FAK signaling pathway that acts by suppressing colorectal tumor growth and metastasis.Formule :C19H18N2O2Degré de pureté :98.06%Couleur et forme :SolidMasse moléculaire :306.36LQZ-7F
CAS :LQZ-7F is a survivin dimerization inhibitor with anticancer activity.LQZ-7F induces proteasome-dependent survivin degradation and inhibits human tumor growth.Formule :C14H7N9O3Degré de pureté :98.64%Couleur et forme :SolidMasse moléculaire :349.26CP 461
CAS :CP 461 is a PDE2A inhibitor that promotes apoptosis in cancer cells without affecting normal cells or COX-1/2.Formule :C25H22ClFN2ODegré de pureté :99.82%Couleur et forme :SolidMasse moléculaire :420.91NSC49652
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.Formule :C14H11NO2Degré de pureté :98.98%Couleur et forme :SolidMasse moléculaire :225.24Ref: TM-T28206
1mg34,00€5mg74,00€1mL*10mM (DMSO)82,00€10mg113,00€25mg222,00€50mg353,00€100mg530,00€500mg1.153,00€Ro 08-2750
CAS :Ro 08-2750: A non-peptide NGF inhibitor binding NGF (~1 µM IC50) & selectively inhibits p75NTR over TRKA and MSI RNA-binding (2.7 µM IC50).Formule :C13H10N4O3Degré de pureté :98.795%Couleur et forme :SolidMasse moléculaire :270.24Triciribine phosphate
CAS :Triciribine phosphate (VD 002) is an AKT inhibitor that inhibits neovascularization and can be used in the study of leukemia.Formule :C13H17N6O7PDegré de pureté :97.94%Couleur et forme :SolidMasse moléculaire :400.28MBM-55
CAS :MBM-55 is an effective inhibitor of NIMA related kinase 2 (NEK2) with an IC50 of 1 nM.Formule :C28H27FN6O2Degré de pureté :99.83%Couleur et forme :SolidMasse moléculaire :498.55Ref: TM-T11960
1mg168,00€5mg281,00€1mL*10mM (DMSO)309,00€10mg409,00€25mg627,00€50mg822,00€100mg1.108,00€500mg2.242,00€Ro 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.Formule :C20H16N6Degré de pureté :97.21% - 99.72%Couleur et forme :SolidMasse moléculaire :340.38Tubulin inhibitor 11
CAS :Potent, oral Tubulin inhibitor 11 hinders polymerization, targets Colchicine site, induces mitotic block, and apoptosis.Formule :C22H23N3O3SDegré de pureté :99.93%Couleur et forme :SoildMasse moléculaire :409.5Ref: TM-T67935
1mg35,00€5mg80,00€1mL*10mM (DMSO)96,00€10mg116,00€25mg259,00€50mg383,00€100mg545,00€200mg740,00€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.Formule :C34H29ClN4O2Degré de pureté :98.8% - 99.81%Couleur et forme :SolidMasse moléculaire :561.07GSK2593074A
CAS :GSK2593074A (GSK'074) is a programmed necrosis inhibitor that displays inhibitory effects on RIP1 and RIP3.Formule :C27H23N5OSDegré de pureté :99.99%Couleur et forme :SolidMasse moléculaire :465.57Ref: TM-T11484
1mg108,00€5mg260,00€1mL*10mM (DMSO)286,00€10mg409,00€25mg687,00€50mg964,00€100mg1.288,00€Pyrazoloacridine
CAS :Pyrazoloacridine (PD 115934) binds DNA, inhibits topo I/II, has 1.25 μM IC50 in K562 cells, and exhibits anti-cancer effects.Formule :C19H21N5O3Degré de pureté :99.72%Couleur et forme :SolidMasse moléculaire :367.4Minodronic acid
CAS :Minodronic acid (YM-529) is a P2X2/3 antagonist with anticancer properties, inhibiting cell growth and metastasis, and used in osteoporosis research.Formule :C9H12N2O7P2Degré de pureté :99.39%Couleur et forme :SolidMasse moléculaire :322.15SCFSkp2-IN-2
CAS :SCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM.
Formule :C17H20N4O2Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :312.37Tubulin inhibitor 32
CAS :Tubulin inhibitor 32 is a microtubule inhibitor with antiproliferative and antitumor activity that induces apoptosis and cell cycle arrest in the G2/M phase.Formule :C18H19N3O3Degré de pureté :99.92%Couleur et forme :SolidMasse moléculaire :325.36Tanimilast
CAS :Tanimilast (CHF-6001) is a potent PDE4 inhibitor with IC50 of 0.026 nM, used topically for obstructive lung disease.Formule :C30H30Cl2F2N2O8SDegré de pureté :99.18%Couleur et forme :SolidMasse moléculaire :687.54Perphenazine dihydrochloride
CAS :Perphenazine dihydrochloride: Oral dopamine, histamine-1 antagonist; targets D2, D3, 5-HT2A, Alpha-1A; may treat psychiatric disorders, cancer.Formule :C21H28Cl3N3OSDegré de pureté :99.67%Couleur et forme :SolidMasse moléculaire :476.89SLMP53-1
CAS :SLMP53-1 is a p53 activator with anti-tumor activity, activates reprogramming of glucose metabolism, and interferes with angiogenesis and migrationFormule :C20H18N2O2Degré de pureté :99.64%Couleur et forme :SolidMasse moléculaire :318.37Ref: TM-T60839
1mL*10mM (DMSO)34,00€1mg119,00€5mg281,00€10mg462,00€25mg888,00€50mg1.485,00€100mg2.385,00€Exisulind
CAS :Exisulind (CP248) triggers apoptosis via PKG activation, shows antitumor effects, and inhibits growth in various rodent cancer models.Formule :C20H17FO4SDegré de pureté :97.94%Couleur et forme :SolidMasse moléculaire :372.41LDCA
CAS :LDCA inhibits LDH-A, disrupts mitochondrial function, induces apoptosis in cancer cells, and is non-toxic.Formule :C8H5Cl3FNODegré de pureté :99.19%Couleur et forme :SolidMasse moléculaire :256.49UC-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).Formule :C22H24N2O2Degré de pureté :99.54%Couleur et forme :SolidMasse moléculaire :348.44Ref: TM-T17195
500mgÀ demander1mg34,00€2mg44,00€5mg70,00€1mL*10mM (DMSO)78,00€10mg99,00€25mg202,00€50mg311,00€100mg445,00€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.Formule :C21H20N6O3SDegré de pureté :98.89%Couleur et forme :SolidMasse moléculaire :436.49Cipepofol
CAS :HSK3486 is similar to propofol and is a general anesthetic, which may have therapeutic potential in insomnia, migraine, anxiety, analgesia, and other aspects.Formule :C14H20ODegré de pureté :99.77%Couleur et forme :SolidMasse moléculaire :204.31Ref: TM-T32105
1mg58,00€5mg149,00€1mL*10mM (DMSO)150,00€10mg225,00€25mg444,00€50mg657,00€100mg1.044,00€200mg1.414,00€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.Formule :C27H27Cl2FN8Degré de pureté :98.87%Couleur et forme :SolidMasse moléculaire :553.46Ref: TM-T10865
1mg73,00€5mg152,00€1mL*10mM (DMSO)177,00€10mg222,00€25mg401,00€50mg602,00€100mg887,00€200mg1.215,00€GSK2983559 free acid
CAS :GSK2983559 free acid selectively inhibits RIP2, reducing inflammatory cytokines in human bowel disease.Formule :C21H23N4O7PS2Degré de pureté :97.8700% - 99.56%Couleur et forme :SolidMasse moléculaire :538.53CCT018159
CAS :CCT018159: ATP-competitive HSP90 inhibitor, IC50 3.2 μM (human), 6.6 μM (yeast), blocks invasion, angiogenesis, induces G1 arrest and apoptosis.
Formule :C20H20N2O4Degré de pureté :98.78% - 99.79%Couleur et forme :SolidMasse moléculaire :352.38F16
CAS :F16 ((E)-4-(3-indolylvinyl)-N-methylpyridinium iodide) inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.Formule :C16H15IN2Degré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :362.21HS-276
CAS :HS-276, a selective oral TAK1 inhibitor (Ki: 2.5 nM), also targets CLK2, GCK, ULK2, MAP4K5; potential for RA research.Formule :C24H29N5O2Degré de pureté :97.67% - 98.81%Couleur et forme :SolidMasse moléculaire :419.52Ref: TM-T62209
1mg63,00€5mg137,00€1mL*10mM (DMSO)161,00€10mg207,00€25mg408,00€50mg655,00€100mg1.009,00€200mg1.359,00€SB 699551 dihydrochloride
CAS :SB 699551 dihydrochloride is a 5-ht5a receptor antagonist.Formule :C34H47Cl2N3ODegré de pureté :99.83%Couleur et forme :SolidMasse moléculaire :584.66Ref: TM-T23325
1mg50,00€5mg105,00€1mL*10mM (DMSO)142,00€10mg170,00€25mg295,00€50mg424,00€100mg583,00€TAI-1
CAS :TAI-1 is a potent and specific Hec1 inhibitor, which disrupts Hec1-Nek2 protein interaction.Formule :C24H21N3O3SDegré de pureté :99.58%Couleur et forme :SolidMasse moléculaire :431.51Ro24-7429
CAS :Ro24-7429: oral HIV-1 Tat antagonist, RUNX1 inhibitor with anti-HIV, antifibrotic, and anti-inflammatory properties.Formule :C14H13ClN4Degré de pureté :99.29% - 99.85%Couleur et forme :SolidMasse moléculaire :272.73Ref: TM-T28578
1mg87,00€5mg177,00€1mL*10mM (DMSO)203,00€10mg281,00€25mg480,00€50mg692,00€100mg973,00€500mg2.725,00€KR-33493
CAS :KR-33493 is a FAS-associated factor 1 (FAF1) inhibitor and can be used in studies about Parkinson's disease.Formule :C20H18BrN3O3SDegré de pureté :99.96%Couleur et forme :SolidMasse moléculaire :460.34GSK854
CAS :GSK854 is a selective TNNI3K inhibitor reducing heart damage and stress post-infarction in mice.Formule :C18H19ClN6O4S2Degré de pureté :98.91%Couleur et forme :SolidMasse moléculaire :482.96Ref: TM-T24115
1mg92,00€5mg222,00€1mL*10mM (DMSO)245,00€10mg358,00€25mg710,00€50mg1.063,00€100mg1.684,00€500mg3.375,00€Mepazine
CAS :Mepazine, a MALT1 inhibitor, blocks GSTMALT1 (IC50: 0.83μM) and GSTMALT1 325-760 (IC50: 0.42μM), promoting apoptosis and reducing cell viability.Formule :C19H22N2SDegré de pureté :99.88% - 99.92%Couleur et forme :SolidMasse moléculaire :310.46Ref: TM-T16040
500mgÀ demander1mL*10mM (DMSO)35,00€10mg39,00€25mg60,00€50mg93,00€100mg116,00€200mg177,00€BCL6-IN-7
CAS :BCL6-IN-7 (BCL6 inhibitor-7) is a BCL6 corepressor-interaction inhibitor with potential antitumor activity, used in lymphoma research.Formule :C18H15ClN6ODegré de pureté :99.03%Couleur et forme :SolidMasse moléculaire :366.8Mitazalimab
CAS :Mitazalimab (ADC-1013/JNJ-64457107) is a CD40 agonist that stimulates T cells to attack tumors and remodels the tumor microenvironment.Degré de pureté :95.1% (SDS-PAGE); 98.7% (SEC-HPLC) - 95.1% (SDS-PAGE); 98.7% (SEC-HPLC)Couleur et forme :LiquidMasse moléculaire :143.42 kDaAnticancer agent 110
CAS :Anticancer Agent 110 exhibits potent in vitro anti-leukemia activity, demonstrating high cytotoxicity against K-562 lineage chronic myelogenous leukemia cellsFormule :C18H13FN6OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :380.4CCT020312
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.Formule :C31H30Br2N4O2Degré de pureté :98.63%Couleur et forme :SolidMasse moléculaire :650.4Ref: TM-T14902
1mg58,00€5mg133,00€1mL*10mM (DMSO)178,00€10mg227,00€25mg386,00€50mg572,00€100mg795,00€500mg1.648,00€LCS3
CAS :LCS3 is a reversible and non-competitive synergistic inhibitor of glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) with IC50s of 3.3Formule :C11H7ClN2O4Degré de pureté :99.84%Couleur et forme :SolidMasse moléculaire :266.64NM-3
CAS :NM-3, an oral anti-angiogenic and anti-tumor agent, modulates radiation and blocks VEGF to curb endothelial growth and induce apoptosis.Formule :C13H12O6Degré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :264.23Ref: TM-T33701
1mg172,00€1mL*10mM (DMSO)394,00€5mg432,00€10mg618,00€25mg973,00€50mg1.333,00€100mg1.791,00€500mg3.529,00€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.
Formule :C29H23BrClN5O2Degré de pureté :99.49% - 99.89%Couleur et forme :SolidMasse moléculaire :588.88JY-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.Formule :C13H7Cl2N3ODegré de pureté :99.66%Couleur et forme :SolidMasse moléculaire :292.12R306465
CAS :R306465 (JNJ-16241199) is an HDAC 1 inhibitor with broad-spectrum anti-tumor activity, inducing apoptosis, and can be used to study solid tumors.Formule :C19H19N5O4SDegré de pureté :98.46% - 99.54%Couleur et forme :SolidMasse moléculaire :413.45Vamotinib
CAS :Vamotinib (PF-114) is a tyrosine kinase inhibitor with antiproliferative and antitumor activity.Vamotinib is used in the study of Alzheimer's disease.Formule :C29H27F3N6ODegré de pureté :99.64%Couleur et forme :SolidMasse moléculaire :532.56Ref: TM-T63746
1mg101,00€5mg245,00€1mL*10mM (DMSO)288,00€10mg401,00€25mg717,00€50mg982,00€100mg1.341,00€200mg1.783,00€Lanperisone HCl
CAS :Lanperisone (NK433) is a potent, long-lasting muscle relaxant that inhibits spinal reflexes via noradrenergic system suppression.Formule :C15H19ClF3NODegré de pureté :98.67% - >99.99%Couleur et forme :SolidMasse moléculaire :321.77A09-003
CAS :A09-003 Inhibits the proliferation of leukemia cell lines and inhibits the increase of leukemia sequence-1 protein in HI bone marrow cells.Formule :C23H26N4ODegré de pureté :99.61%Couleur et forme :SolidMasse moléculaire :374.48Trk-IN-9
CAS :Trk-IN-9 is a TRK inhibitor with anticancer and antiproliferative activity and can be used in cancer research.Formule :C23H24ClFN6ODegré de pureté :98.15%Couleur et forme :SolidMasse moléculaire :454.93BCP-T.A
CAS :BCP-T.A is an iron death inducer that acts by binding to GPX4.Formule :C23H19Cl2N3OSDegré de pureté :99.49%Couleur et forme :SolidMasse moléculaire :456.39MMRi64
CAS :MMRi64 inhibits Mdm2-MdmX, boosts p53, triggers apoptosis, and is used in cancer research.Formule :C22H17Cl2N3ODegré de pureté :99.93%Couleur et forme :SolidMasse moléculaire :410.3GSK-3β inhibitor 3
CAS :GSK-3β inhibitor 3 is a covalent inhibitor (IC50: 6.6 μM) of glycogen synthase kinase 3β (GSK-3β) that is potent, selective, and irreversible.GSK-3β inhibitor 3Formule :C18H14FNO2SDegré de pureté :97.53%Couleur et forme :SolidMasse moléculaire :327.37Ref: TM-T35554
1mg52,00€5mg111,00€1mL*10mM (DMSO)127,00€10mg166,00€25mg301,00€50mg452,00€100mg665,00€HBDDE
CAS :HBDDE inhibits PKCα/γ (IC50: 43/50 μM), favors them over PKCδ/βI/βII, and induces neuronal apoptosis. Derived from ellagic acid.Formule :C16H18O8Degré de pureté :99.99%Couleur et forme :SolidMasse moléculaire :338.31TC-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.Formule :C17H12N2O2Degré de pureté :98.73%Couleur et forme :SolidMasse moléculaire :276.29DB1976
CAS :DB1976: Selenophene DB270 analog, inhibits PU.1 (IC50=10 nM), disrupts PU.1/DNA (KD=12 nM), induces apoptosis, cell-permeable.Formule :C20H16N8SeDegré de pureté :98.74%Couleur et forme :SolidMasse moléculaire :447.35Stemazole
CAS :Stemazole activates human stem cell growth, boosts survival, reduces cell death, and aids myelin repair, with therapeutic potential in demyelinating diseases.Formule :C9H9N5OS2Degré de pureté :98.59%Couleur et forme :SolidMasse moléculaire :267.33Ref: TM-T28866
1mg52,00€1mL*10mM (DMSO)95,00€5mg101,00€10mg164,00€25mg334,00€50mg532,00€100mg858,00€200mg1.149,00€Ciglitazone
CAS :Ciglitazone: potent PPARγ agonist, EC50 3 μM, oral hypoglycemic; reduces insulin, blood pressure, Th17 cells, VEGF; halts gastric cancer growth.Formule :C18H23NO3SDegré de pureté :98.23% - 99.84%Couleur et forme :White Cyrstalline SolidMasse moléculaire :333.45RO-5963
CAS :RO-5963 is a dual inhibitor of p53-MDM2 and p53-MDMX (IC50s: ~17 nM and ~24 nM, respectively).Formule :C24H21ClF2N4O5Degré de pureté :99.28%Couleur et forme :SolidMasse moléculaire :518.9Ref: TM-T16771
1mg66,00€5mg187,00€1mL*10mM (DMSO)212,00€10mg269,00€25mg411,00€50mg532,00€100mg740,00€200mg982,00€CSN5i-3
CAS :CSN5i-3 is a potent, selective, and orally available inhibitor of the proteolytic subunit of the CSN complex, CSN5, as an anticancer agent.Cost-effective and quality-assured.Formule :C28H29F2N5O2Degré de pureté :99.56% - >99.99%Couleur et forme :SolidMasse moléculaire :505.56Ref: TM-T10895
1mg340,00€5mg732,00€1mL*10mM (DMSO)797,00€10mg1.108,00€25mg1.648,00€50mg2.223,00€100mg2.997,00€SPD304 dihydrochloride
CAS :SPD304 dihydrochloride is a selective inhibitor of TNF-α with an IC50 of 22 µM. SPD304 dihydrochloride promotes dissociation of TNF trimers.
Formule :C32H34Cl2F3N3O2Degré de pureté :99.25%Couleur et forme :SolidMasse moléculaire :620.53W146
CAS :W146 is an S1PR1 antagonist that induces a significant but transient decrease in blood lymphocytes in mice.Formule :C16H27N2O4PDegré de pureté :99.37%Couleur et forme :SolidMasse moléculaire :342.37ZDLD20
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.Formule :C22H22N6ODegré de pureté :98.59%Couleur et forme :SolidMasse moléculaire :386.45Erastin2
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.
Formule :C36H35ClN4O4Degré de pureté :99.63%Couleur et forme :SolidMasse moléculaire :623.14p53-MDM2-IN-1
CAS :p53-MDM2-IN-1 (Example 30), an inhibitor targeting the p53-MDM2/X protein interaction, exhibits a K i value of 23.35 µM.Formule :C23H20ClN3O3Degré de pureté :99.98%Couleur et forme :SoildMasse moléculaire :421.88Necrostatin-5
CAS :Necrostatin-5 (Nec-5) inhibits RIP1 kinase, prevents cell necrosis, and protects Fadd-deficient Jurkat cells with an EC50 of 240 nM.Formule :C19H17N3O2S2Degré de pureté :99.40%Couleur et forme :SolidMasse moléculaire :383.49CTA 056
CAS :CTA 056 is an ITK inhibitor that inhibits the growth of MOLT-4 xenograft tumors in mice and can be used to study autoimmune disorders.Formule :C35H34N6ODegré de pureté :97.22% - 97.76%Couleur et forme :SolidMasse moléculaire :554.68HS38
CAS :HS38: DAPK-specific ATP-competitive inhibitor; Kds: DAPK1 (300 nM), PIM3 (200 nM), ZIPK (280 nM); useful in smooth muscle disorder research.Formule :C14H12ClN5O2SDegré de pureté :98.19%Couleur et forme :SolidMasse moléculaire :349.8AOH1160
CAS :AOH1160 is an inhibitor of proliferating cell nuclear antigen (PCNA).Formule :C25H20N2O3Degré de pureté :98.46% - 99.52%Couleur et forme :SolidMasse moléculaire :396.44PARP/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.Formule :C33H28F4N8O3Degré de pureté :99.59%Couleur et forme :SolidMasse moléculaire :660.62

