Apoptosi
Gli inibitori dell'apoptosi sono composti che prevengono o ritardano il processo di morte cellulare programmata, noto come apoptosi. Questi inibitori sono fondamentali per lo studio dei meccanismi di sopravvivenza cellulare e vengono utilizzati per indagare sulle malattie in cui l'apoptosi è disregolata, come il cancro, i disturbi neurodegenerativi e le malattie autoimmuni. Modulando l'apoptosi, questi inibitori possono aiutare nello sviluppo di terapie mirate a controllare la morte cellulare. Presso CymitQuimica, offriamo una vasta selezione di inibitori dell'apoptosi di alta qualità per supportare le tue ricerche in biologia cellulare, oncologia e campi correlati.
Sottocategorie di "Apoptosi"
- ASK(9 prodotti)
- BCL(1 prodotti)
- Caspasi(154 prodotti)
- FOXO1(2 prodotti)
- IAP(67 prodotti)
- Mdm2(12 prodotti)
- PD-1/PD-L1(109 prodotti)
- PDK(9 prodotti)
- PERK(26 prodotti)
- Chinasi di serina/treonina(18 prodotti)
- Survivin(14 prodotti)
- TNF(64 prodotti)
- c-RET(61 prodotti)
- p53(63 prodotti)
Mostrare 6 più sottocategorie
Trovati 6100 prodotti di "Apoptosi"
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
RLX
CAS:RLX (PD 139530) is a PI3K/Akt/FoxO3a signal inhibitor with anticancer,antitussive and anti-asthmatic activity,colon cancer，toxicity toward A549 cells..Formula:C13H14N2OPurezza:99.81%Colore e forma:SolidPeso molecolare:214.26AK301
CAS:AK301 is a potent and selective inhibitor of tubulin polymerization and an effective sensitizer of cancer cells to apoptotic ligands (EC50 < 200 nM).Formula:C19H21ClN2O2Purezza:99.75%Colore e forma:SolidPeso molecolare:344.84Flunisolide hemihydrate
CAS:Flunisolide hemihydrate, a corticosteroid with anti-inflammatory properties, treats asthma and rhinitis by inducing eosinophil apoptosis.Formula:C48H64F2O13Colore e forma:SolidPeso molecolare:887.024HDAC-IN-51
HDAC-IN-51 is an HDAC inhibitor.Formula:C27H24N4O2Purezza:98.85%Colore e forma:SolidPeso molecolare:436.51RET-IN-12
CAS:RET-IN-12 is a RET inhibitor capable of acting on RET(WT) (IC50: 0.3 nM) and RET(V804M) (IC50: 1 nM).Formula:C30H30F3N5O4Colore e forma:SolidPeso molecolare:581.59JS-K
CAS:JS-K is a Nitric oxide donor. It has antiproliferative activity.Formula:C13H16N6O8Colore e forma:SolidPeso molecolare:384.3RDR03871
CAS:RDR03871 is an MDM2 inhibitor.
Formula:C18H16ClF3N6Purezza:97.78%Colore e forma:SolidPeso molecolare:408.81Obatoclax
CAS:Obatoclax (GX15-070), a pan-BCL-2 inhibitor (Ki 220 nM) induces autophagy, degrades cyclin D1, and has anti-cancer/antiparasitic properties.Formula:C20H19N3OPurezza:99.44%Colore e forma:SolidPeso molecolare:317.38OXPHOS-IN-1
CAS:OXPHOS-IN-1 inhibits oxidative phosphorylation; halts MIA PaCa-2 (IC50: 2.34 μM) and BxPC-3 cells growth (IC50: 13.82 μM).Formula:C19H29N3O6S2Colore e forma:SolidPeso molecolare:459.58Anticancer agent 66
CAS:Anticancer agent 66, a ciprofloxacin analog, triggers apoptosis in MCF-7 cells.Formula:C26H23Cl2FN6O2S2Colore e forma:SolidPeso molecolare:605.53cRIPGBM
CAS:cRIPGBM induces apoptosis in GBM CSCs by targeting RIPK2, with an EC50 of 68 nM in GBM-1 cells.Formula:C26H20FN2O2Purezza:98%Colore e forma:SolidPeso molecolare:411.45Benpyrine
CAS:Benpyrine, an oral TNF-α inhibitor (KD 82.1 μM, IC50 0.109 μM), may help in inflammatory/autoimmune studies.Formula:C16H16N6OColore e forma:SolidPeso molecolare:308.34DPBQ
CAS:DPBQ (ZINC1620467) is a p53 activator.Formula:C24H14N2O2Purezza:98.08%Colore e forma:SolidPeso molecolare:362.38Ref: TM-T11092
1mg100,00€2mg149,00€5mg245,00€10mg354,00€25mg532,00€50mg735,00€100mg982,00€500mgPrezzo su richiestaNutlin-1
CAS:Nutlin-1 is a p53-MDM2 binding inhibitor, p-Glycoprotein (p-gp) transport substrate, and antitumor agent.Formula:C32H34Cl2N4O4Colore e forma:SolidPeso molecolare:609.54GL-V9
CAS:GL-V9 is an AMPK activator, protecting against colitis-associated colorectal cancer by limiting NLRP3 inflammasome through autophagy.Formula:C24H27NO5Colore e forma:SolidPeso molecolare:409.47Autophagy-IN-2
CAS:Autophagy-IN-2 (7h) blocks autophagic flux, triggers cancer cell death, aids in triple-negative breast cancer study.Formula:C17H19N5OColore e forma:SolidPeso molecolare:309.37pan-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:C19H15BrClN5OColore e forma:SolidPeso molecolare:444.71RIP1 kinase inhibitor 5
CAS:RIP1 kinase inhibitor 5 (example 1) serves as a potent regulator of tumor immunity by inhibiting RIP1, functioning similarly to SIR1-365 (compound 13) inFormula:C13H17F2NO2Purezza:98%Colore e forma:SolidPeso molecolare:257.28HI5
CAS:HI5: potent tubulin/IDO inhibitor, IC50 70 nM (HeLa), blocks kynurenine, G2/M arrest, spurs T cell activity, & triggers apoptosis.Formula:C42H43N5O8Colore e forma:SolidPeso molecolare:745.82GDP366
CAS:GDP366, induces cell growth inhibition, cellular senescence and mitotic catastrophe in human cancer cells. a dual inhibitor of survivin and Op18.Formula:C20H17N5OSPurezza:98.78% - 99.84%Colore e forma:SolidPeso molecolare:375.45RGB-286147
CAS:RGB-286147 is a potent, selective, ATP-competitive Cdks inhibitor.Formula:C23H22Cl2N4O3Purezza:98%Colore e forma:SolidPeso molecolare:473.35Anticancer agent 55
CAS:Potent anticancer agent inhibits cell growth, migration, induces apoptosis; promising for prostate, breast cancer studies.Formula:C28H21Br2FN2O2Colore e forma:SolidPeso molecolare:596.294GW837016X
CAS:GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation.Formula:C25H20ClFN4OSColore e forma:SolidPeso molecolare:478.97Z-LEVD-FMK
CAS:Z-LEVD-FMK is a caspase-4 inhibitor with anti-cancer activity, capable of eliminating LPS-induced GCLC protein degradation.Formula:C31H45FN4O10Colore e forma:SolidPeso molecolare:652.71S65487
CAS:S65487 (VOB560) inhibits Bcl-2, including G101V and D103Y variants, while sparing MCL-1, BFL-1, and BCL-XL, supporting its anticancer potential.Formula:C41H41ClN6O4Purezza:99.034%Colore e forma:SolidPeso molecolare:717.26Mcl1-IN-9
CAS:Mcl1-IN-9 is a potent myeloid cell leukemia-1 (Mcl-1) Inhibitor with an IC50 of 446 nM in reengineered BCR-ABL+ B-ALL cells and a Ki of 0.03 nM.Formula:C37H39ClN4O4Purezza:98%Colore e forma:SolidPeso molecolare:639.18(R)-eIF4A3-IN-2
CAS:(R)-eIF4A3-IN-2, a weaker eIF4A3-IN-2 isomer, inhibits eIF4A3 selectively with 110 nM IC50.Formula:C25H19Br2ClN4O2Colore e forma:SolidPeso molecolare:602.71TNF-α-IN-10
CAS:TNF-α-IN-10 (compound 8a) acts as an inhibitor of IL-6 and TNF-α, demonstrating anti-inflammatory activity [1].Formula:C17H14O4Colore e forma:SolidPeso molecolare:282.29Anti-inflammatory agent 47
CAS:Flo8, an anti-inflammatory and antioxidant agent, effectively suppresses the release of reactive oxygen species (ROS) and nitric oxide (NO) while inhibitingFormula:C25H18N2O3Purezza:98%Colore e forma:SolidPeso molecolare:394.42PHA-680626
CAS:PHA-680626 is a PLK inhibitor, effective on resistant leukemia cells, with IC50: Plk1 (0.53 μM), Plk2 (0.07 μM), Plk3 (1.61 μM).Formula:C23H26N6O2SColore e forma:SolidPeso molecolare:450.56PDE5/HDAC-IN-1
CAS:PDE5/HDAC-IN-1 is a potent inhibitor of phosphodiesterase 5 (PDE5) and HDAC, with IC50 values of 46.3 nM and 14.5 nM, respectively.Formula:C27H29BrN4O4Colore e forma:SolidPeso molecolare:553.45LG308
CAS:LG308, a synthetic compound, has anti-tumor properties, inducing apoptosis and mitotic arrest, thereby suppressing prostate cancer growth.Formula:C19H17FN2OColore e forma:SolidPeso molecolare:308.35HDAC1/2 and CDK2-IN-1
CAS:Compound 14d inhibits HDAC1 (IC50=70.7μM), HDAC2 (23.1μM), CDK2 (0.80μM), blocks cell cycle, induces apoptosis, and shows in vivo anti-tumor effects.Formula:C26H22ClN7OColore e forma:SolidPeso molecolare:483.95AFG206
CAS:AFG206 is the novel first-generation type II" FLT3 inhibitor."Formula:C20H19N3O2Colore e forma:SolidPeso molecolare:333.38Nampt-IN-8
CAS:Nampt-IN-8 is a NAMPT inhibitor (IC50: 0.183 μM) and a good substrate for NQO1. Nampt-IN-8 induces reactive oxygen species (ROS) production and apoptosis.Formula:C36H35N3O4Colore e forma:SolidPeso molecolare:573.68Cinnabarinic acid
CAS:mGlu4 receptor agonistFormula:C14H8N2O6Purezza:98%Colore e forma:SolidPeso molecolare:300.22CAY10789
CAS:CAY10789: potent CysLT1R antagonist (IC50 2.8 µM), GPBAR1 agonist (EC50 3 µM), reduces U937 cell adhesion, TNF-α, stable with promising pharmacokinetics.Formula:C17H15NO2Colore e forma:SolidPeso molecolare:265.31EGFR-IN-88
CAS:EGFR-IN-88 (Compound 4i), an EGFR inhibitor with an IC50 of 87 nM, exhibits cytotoxic effects on A549 cells at an IC50 of 3.902 μM and can induce cell apoptosisFormula:C22H18Cl2N4O2SPurezza:98%Colore e forma:SolidPeso molecolare:473.37GLUT4-IN-2
CAS:GLUT4-IN-2, selective GLUT4 blocker; IC50: 6.8μM (GLUT4), 11.4μM (GLUT1). Induces apoptosis, G0/G1 arrest, has antitumor effects.Formula:C17H11N3O4S2Purezza:99.90%Colore e forma:SolidPeso molecolare:385.42NVX-207
CAS:NVX-207 is a derivative of betulinic acid. It has anti-cancer activity.Formula:C36H59NO6Purezza:98%Colore e forma:SolidPeso molecolare:601.86Caspase-3/7 activator 3
Caspase-3/7 activator 3 triggers apoptosis with tumor selectivity and anti-proliferative effects.Formula:C24H27NO5Colore e forma:SolidPeso molecolare:409.47AMPK activator 11
CAS:AMPK Activator 11 is a nanomolar potent inhibitor of cell proliferation in various colorectal carcinomas (CRCs), acting through the selective activation of AMP-Formula:C25H20N4O2Purezza:98%Colore e forma:SolidPeso molecolare:408.45YLT205
CAS:YLT205 is an inducer of apoptosis in human colorectal cells that acts by inhibiting tumor growth.Formula:C16H12BrClN4O2S2Purezza:98%Colore e forma:SolidPeso molecolare:471.78ARN5187
CAS:ARN5187, a lysosomal REV-ERB β ligand, inhibits transcription and autophagy, shows efficacy, cytotoxicity, and induces apoptosis.Formula:C24H32FN3OColore e forma:SolidPeso molecolare:397.53MI-3
CAS:MI-3 (Menin-MLL Inhibitor) (Menin-MLL Inhibitor) is an effective inhibitor of Menin-MLL interaction (IC50: 648 nM).Formula:C18H25N5S2Purezza:98.66% - 99.61%Colore e forma:SolidPeso molecolare:375.55MR2938
CAS:MR2938: AChE inhibitor (IC50=5.04μM), reduces NO (IC50=3.29μM), blocks MAPK/JNK, NF-κB; for AD research.Formula:C21H24N4O3Colore e forma:SolidPeso molecolare:380.44Anticancer agent 63
CAS:Compound 3h fights various cancers; most effective on MCF-7 (IC50 3.4 μM). Triggers apoptosis; alters Bcl-2, IL-2, Caspase-3 levels, has antioxidant effects.Formula:C17H24F3NOSeColore e forma:SolidPeso molecolare:394.33LOM612
CAS:LOM612 is a potent and specific FOXO relocator FOXO3a reporter protein endogenous FOXO3a and FOXO1 , down-regulates c-Myc and cyclin D1, anti-proliferative.Formula:C13H10N2O2SColore e forma:SolidPeso molecolare:258.3K145
CAS:K145: Selective, oral SphK2 inhibitor, IC50 4.3 μM, Ki 6.4 μM, promotes cell apoptosis, strong antitumor effect, inactive against SphK1/other kinases.Formula:C18H24N2O3SPurezza:98%Colore e forma:SolidPeso molecolare:348.46QTX125
CAS:QTX125: potent, selective HDAC6 inhibitor with strong antitumor effects.Formula:C23H19N3O5Colore e forma:SolidPeso molecolare:417.41CFM-5
CAS:CFM-5 has anticonvulsant activity and is used in epilepsy research.Formula:C23H18BrN3OSPurezza:98%Colore e forma:SolidPeso molecolare:464.38(5Z,2E)-CU-3
CAS:(5Z,2E)-CU-3 is a potent and selective inhibitor of DGKα isozyme with an IC50 value of 0.6 μM and inhibition of DGKα by competing ATP with a Km value of 0.48 mMFormula:C16H12N2O4S3Purezza:99.02%Colore e forma:SolidPeso molecolare:392.47Ref: TM-T10177
1mg46,00€5mg90,00€10mg160,00€25mg340,00€50mg582,00€100mg898,00€500mg1.791,00€1mL*10mM (DMSO)100,00€Topoisomerase II inhibitor 7
CAS:Topoisomerase II inhibitor 7 halts cell division and induces apoptosis, targeting topoisomerase II alpha with a 3.19 μM IC50.Formula:C32H28BrN5O5SColore e forma:SolidPeso molecolare:674.56Clidanac
CAS:Clidanac is a potent anti-inflammatory drug and is found to uncouple the oxidative phosphorylation.Formula:C16H19ClO2Purezza:98%Colore e forma:SolidPeso molecolare:278.77ATX inhibitor 13
CAS:ATX inhibitor 13: orally active, IC50 3.4 nM, halts RAW264.7 cells at G2, curbs growth/migration, prompts apoptosis, suppresses tumors.Formula:C31H35Cl2N5O3Colore e forma:SolidPeso molecolare:596.55IZTZ-1
CAS:IZTZ-1: c-MYC G4 stabilizer, reduces expression, blocks cell cycle, induces apoptosis, inhibits B16 melanoma growth.Formula:C32H35N7SColore e forma:SolidPeso molecolare:549.73PDE4-IN-10
CAS:PDE4-IN-10 (7a), potent PDE4B inhibitor, IC50 7.01μM; selective, stable, TNF-α blocking, non-toxic in vitro.Formula:C18H13NColore e forma:SolidPeso molecolare:243.3Aurora kinase-IN-1
Aurora kinase-IN-1: potent aurora kinase inhibitor, alters G1 cycle proteins, induces G1/S arrest and apoptosis, potential chemotherapy lead.Formula:C30H25Br2N3O5Colore e forma:SolidPeso molecolare:667.34MBM-17S
CAS:MBM-17S, a potent NIMA-related kinase 2 (Nek2) inhibitor with an IC50 of 3 nM, effectively inhibits cancer cell proliferation by inducing cell cycle arrest andFormula:C36H40N6O10Purezza:98%Colore e forma:SolidPeso molecolare:716.74MEK-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:C29H27FN4O10S2Colore e forma:SolidPeso molecolare:674.67Quinate
CAS:Quinate: oral antiarrhythmic, inhibits P450db, blocks K+ channels (IC50 19.9 μM), used in malaria research.Formula:C26H36N2O9Colore e forma:SolidPeso molecolare:520.579YL-939
YL-939 is a potent inhibitor of ferroptosis, targeting the PHB2/ferritin/iron axis to impede this form of cell death.Formula:C25H26N6OColore e forma:SolidPeso molecolare:426.51AMC-01
CAS:AMC-01 has potential antiviral activity and induces dose- and time-dependent inactivation of eIF2-α via phosphorylation of serine residue 51.Formula:C27H27BrN2O6Purezza:99.95%Colore e forma:SolidPeso molecolare:555.42USP7-IN-4
CAS:USP7-IN-4 is a non-competitive, potent and selective inhibitor of USP7, up-regulates p53 and p21, down-regulates MDM2,anti-proliferativity RS4;11 (leukemia) .Formula:C29H34N6O3Purezza:98.27% - 99.09%Colore e forma:SolidPeso molecolare:514.62CAY10443
CAS:CAY10443 activates apoptosis by binding to apoptosome components, with an EC50 of 5 μM for caspase-3, aiding antitumor drug development.Formula:C17H15Cl2NO2Colore e forma:SolidPeso molecolare:336.21673-A
CAS:673-A inhibits ALDH1A, depletes ovarian CSCs, induces necroptosis, and reverses chemo resistance.Formula:C15H13NOColore e forma:SolidPeso molecolare:223.27PD173952
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:C24H21Cl2N5O2Purezza:99.5%Colore e forma:SolidPeso molecolare:482.36PI3K 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:C11H8N2O3SPurezza:98%Colore e forma:SolidPeso molecolare:248.26Anticancer agent 59
Anticancer agent 59 suppresses various cancers, notably A549 at IC50 of 0.2 μM, induces apoptosis and disrupts mitochondria in mice.Formula:C42H59NO6Colore e forma:SolidPeso molecolare:673.92SAHA-OH
CAS:SAHA-OH selectively inhibits HDAC6 (IC50 = 23 nM) with 10-47x preference over HDACs 1, 2, 3, 8, and reduces inflammation and macrophage apoptosis.Formula:C15H22N2O4Purezza:98%Colore e forma:SolidPeso molecolare:294.35ABI-231 HCl
CAS:ABI-231: Oral tubulin inhibitor, IC50=5.2 nM for melanoma/prostate cancer, in clinical trials for prostate cancer, effective in vivo.Formula:C21H20ClN3O4Colore e forma:SolidPeso molecolare:413.85VS 8
CAS:VS 8: potent oral VEGFR-2 inhibitor, anti-angiogenic, induces cancer cell apoptosis & migration, acts on CSCs.Formula:C26H20F3N3O3Colore e forma:SolidPeso molecolare:479.45Erbstatin
CAS:Erbstatin is a tyrosine-protein kinase inhibitor. When combined with foroxymithine, it has antineoplastic activity against L-1210 leukemia.Formula:C9H9NO3Colore e forma:SolidPeso molecolare:179.17MPT0B392
CAS:MPT0B392 is an orally active quinoline derivative, induces c-Jun N-terminal kinase (JNK) activation.Formula:C19H20N2O6SColore e forma:SolidPeso molecolare:404.44BI-0282
CAS:BI-0282 (Compound 1) is a potent inhibitor of the MDM2-p53 interaction.Formula:C30H23Cl2FN4O4Colore e forma:SolidPeso molecolare:593.43PI3K/Akt/mTOR-IN-3
CAS:PI3K/Akt/mTOR-IN-3 is a powerful inhibitor, halting MCF-7, HeLa, and HepG2 cell migration and triggering S phase arrest and apoptosis.Formula:C34H51NO2Colore e forma:SolidPeso molecolare:505.77Bcl-2/Mcl-1-IN-2
CAS:Bcl-2/Mcl-1-IN-2 is a Bcl-2 (Ki: 4.70 μM) and Mcl-1 (Ki: 0.88 μM) inhibitor.Bcl-2/Mcl-1-IN-2 can be used in cancer research.Formula:C26H24ClNO3Colore e forma:SolidPeso molecolare:433.93RO27-3225 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:C41H53F3N12O8Colore e forma:SolidPeso molecolare:898.94622,5-Dihydroxybiphenyl
CAS:2,5-Dihydroxybiphenyl: a small molecule that induces trichothiodystrophy A protein dimerization, modulating TFIIH activity.
Formula:C12H10O2Purezza:99.66%Colore e forma:White To Grey-Brownish PowderPeso molecolare:186.21AV123
CAS:AV123, a RIPK1 inhibitor, non-cytotoxic, IC50: 12.12 μM; blocks TNF-α necroptosis (EC50: 1.7 μM) not apoptosis; useful in necrosis-related disease studies.Formula:C11H14N4O2Colore e forma:SolidPeso molecolare:234.25DB2313 HCl
CAS:DB2313: first-in-class, potent inhibitor of PU.1, disrupts gene interactions, down-regulates PU.1 targets.Formula:C42H45Cl4FN8O2Colore e forma:SolidPeso molecolare:854.67Anticancer agent 83
CAS:Anticancer agent 83: potent, GI50 0.15 mM against LOX IMVI, reduces mitochondria potential, DNA damage, induces leukemia apoptosis.Formula:C20H19N5OSColore e forma:SolidPeso molecolare:377.46Atopaxar Hydrobromide
CAS:Atopaxar, a reversible PAR-1 thrombin receptor antagonist, interferes with platelet signaling.Formula:C29H39BrFN3O5Purezza:98%Colore e forma:SolidPeso molecolare:608.54CHS-828 nicotinate
CAS:CHS-828, or GMX-1778, is a potent NAMPT inhibitor with anticancer properties, active against tumors and enhanced by certain drugs.Formula:C25H27ClN6O3Colore e forma:SolidPeso molecolare:494.97c-Met-IN-14
CAS:c-Met-IN-14: selective c-Met kinase inhibitor, IC50 2.89 nM, anticancer, stops G2/M phase, induces A549 cell apoptosis.Formula:C34H38ClFN4O7SColore e forma:SolidPeso molecolare:701.23-(3-Phenoxybenzyl)amino-β-carboline
CAS:3-(3-Phenoxybenzyl)amino-β-carboline is a highly effective tubulin inhibitor, selectively degrading αβ-tubulin heterodimers.Formula:C24H19N3OColore e forma:SolidPeso molecolare:365.43LLP-3
CAS:Survivin inhibitor LLP-3 induces apoptosis in glioma cells by blocking Ran interaction; halts glioblastoma growth. IC50 = 31 μM.Formula:C32H23ClN2O4Colore e forma:SolidPeso molecolare:534.99Nanatinostat TFA
CAS:Nanatinostat (Tractinostat, CHR-3996, VRx-3996) is a second-gen oral HDAC inhibitor with potential cancer treatment properties.Formula:C22H20F4N6O4Colore e forma:SolidPeso molecolare:508.43Sparfosic Acid
CAS:Sparfosic Acid (Acide sparfosique) is an aspartate carbamoyltransferase inhibitor with antitumor activity and can be used to study advanced renal cell carcinomaFormula:C6H10NO8PPurezza:98.89%Colore e forma:SolidPeso molecolare:255.12VEGFR-2-IN-28
CAS:VEGFR-2-IN-28 is a potent inhibitor of VEGFR-2 (IC50: 0.83 μM). VEGFR-2-IN-28 induces apoptosis and exhibits antitumor effects.Formula:C26H17N7O7Colore e forma:SolidPeso molecolare:539.46FW1256
CAS:FW1256: phenyl analog, slow H2S donor, inhibits NF-κB, induces apoptosis, anti-inflammatory, potential cancer/cardio treatment.Formula:C12H10NOPSColore e forma:SolidPeso molecolare:247.257DG
CAS:7DG is a selective inhibitor of protein kinase R (PKR).Formula:C26H30O5Colore e forma:SolidPeso molecolare:422.51ICG-001
CAS:ICG001 is a β-catenin/TCF-mediated transcription inhibitor that selectively blocks β-catenin/CBP interaction.Cost-effective and quality-assured.Formula:C33H32N4O4Purezza:99.55% - 99.62%Colore e forma:SolidPeso molecolare:548.63Ref: TM-T6113
1mg35,00€5mg70,00€10mg106,00€25mg207,00€50mg360,00€100mg558,00€500mg1.198,00€1mL*10mM (DMSO)86,00€ENMD-1068 HCl
CAS:ENMD-1068 HCl (ENMD 1068) is a PAR-2 antagonist. ENMD-1068 HCl inhibits the development of endometriosis in a mouse model.Formula:C15H29N3O2Purezza:99.91%Colore e forma:SolidPeso molecolare:283.41Antioxidant agent-5
CAS:Antioxidant agent-5 (D-6) curbs oxLDL effects, ROS, NF-κB movement, apoptosis in VECs; boosts Nrf2/HO-1; protects endothelium.Formula:C24H24N6OColore e forma:SolidPeso molecolare:412.49Lexibulin dihydrochloride
CAS:Lexibulin 2HCl inhibits tubulin polymerization (IC50: 10-100 nM) and shows potent anti-cancer cytotoxicity and vascular disruption in vitro/vivo.Formula:C24H32Cl2N6O2Purezza:98%Colore e forma:SolidPeso molecolare:507.46ZT55
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:C17H16N2O3Colore e forma:SolidPeso molecolare:296.32Tubulin 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.Formula:C22H19N3O5Colore e forma:SolidPeso molecolare:405.4Alteminostat
CAS:Alteminostat is used as a histone deacetylase inhibitor and is an antineoplastic drug candidate.Formula:C27H36N6O3Colore e forma:SolidPeso molecolare:492.61Topoisomerase II inhibitor 10
CAS:Topoisomerase II inhibitor 10 is a potent inhibitor of topoisomerase II (IC50: 7.45 μM).Formula:C27H20N6O7SColore e forma:SolidPeso molecolare:572.55
