Apoptosis
Los inhibidores de la apoptosis son compuestos que previenen o retrasan el proceso de muerte celular programada, conocido como apoptosis. Estos inhibidores son vitales para estudiar los mecanismos de supervivencia celular y se utilizan para investigar enfermedades donde la apoptosis está desregulada, como el cáncer, los trastornos neurodegenerativos y las enfermedades autoinmunes. Al modular la apoptosis, estos inhibidores pueden ayudar en el desarrollo de terapias dirigidas a controlar la muerte celular. En CymitQuimica, ofrecemos una amplia selección de inhibidores de la apoptosis de alta calidad para apoyar su investigación en biología celular, oncología y campos relacionados.
Subcategorías de "Apoptosis"
- ASK(6 productos)
- BCL(11 productos)
- Caspasa(125 productos)
- FOXO1(3 productos)
- IAP(66 productos)
- Mdm2(12 productos)
- PD-1 / PD-L1(125 productos)
- PDK(9 productos)
- PERK(25 productos)
- Serina / treonina quinasa(15 productos)
- Survivin(13 productos)
- TNF(92 productos)
- c-RET(51 productos)
- p53(62 productos)
Mostrar 6 subcategorías más
Se han encontrado 5600 productos de "Apoptosis"
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CP-724714
CAS:<p>CP-724714 (CP724714) is an effective and selective HER2/ErbB2 inhibitor (IC50: 10 nM), >640-fold selectivity against EGFR, Abl, InsR, PDGFR, IRG-1R, Src, VEGFR2</p>Fórmula:C27H27N5O3Pureza:97.1% - 98.82%Forma y color:SolidPeso molecular:469.54C-DIM12
CAS:<p>C-DIM12 boosts Nurr1 gene expression, heightens Nurr1 protein in neurons, and improves survival against 6-OHDA.</p>Fórmula:C23H17ClN2Pureza:97.72% - ≥95%Forma y color:SolidPeso molecular:356.85L-685458
CAS:<p>L-685458 (L-685,458) is a specific and potent inhibitor of A beta PP gamma-secretase activity with Ki of 17 nM.</p>Fórmula:C39H52N4O6Pureza:99.62% - 99.80%Forma y color:SolidPeso molecular:672.85Serdemetan
CAS:<p>Serdemetan (JNJ-26854165) is an orally bioavailable HDM2 antagonist with potential antineoplastic activity.</p>Fórmula:C21H20N4Pureza:98% - 99.51%Forma y color:SolidPeso molecular:328.41RA-9
CAS:<p>RA-9 is a potent and selective proteasome-associated inhibitor of deubiquitinating enzymes (DUBs), with favorable toxicity profile and anticancer activity.</p>Fórmula:C19H15N3O5Pureza:98.15%Forma y color:SolidPeso molecular:365.34GW 441756
CAS:<p>GW 441756 is a specific Tropomyosin-related kinase A (TrkA) inhibitor with an IC50 value of 2 nM.</p>Fórmula:C17H13N3OPureza:97.73% - 99.8%Forma y color:SolidPeso molecular:275.3Xevinapant
CAS:<p>Xevinapant (Debio-1143) is a potent Smac mimetic and an antagonist of IAP, binding to XIAP-BIR3, cIAP1-BIR3 and cIAP2-BIR3.</p>Fórmula:C32H43N5O4Pureza:98% - 99.94%Forma y color:SolidPeso molecular:561.71AZD-3463
CAS:<p>AZD-3463 (ALK/IGF1R inhibitor) , an orally bioavailable ALK inhibitor (Ki: 0.75 nM), can inhibit IGF1R with equivalent potency.</p>Fórmula:C24H25ClN6OPureza:99.13%Forma y color:SolidPeso molecular:448.95K34C
CAS:<p>K34C is a selective inhibitor of Integrin α5β1, which inhibits cell survival and migration, promotes apoptosis, inhibits invasion.</p>Fórmula:C26H29N3O4Pureza:99.66%Forma y color:SolidPeso molecular:447.53Ginkgolide B
CAS:<p>Ginkgolide B (BN-52021) is a PAFR antagonist(IC50=3.6 μM) isolated from Ginkgo biloba.</p>Fórmula:C20H24O10Pureza:98.66% - 99.81%Forma y color:White Crystal PowderPeso molecular:424.4Toyocamycin
CAS:<p>Toyocamycin (Vengicide) is an adenosine analog produced by Actinomycete, acts as an XBP1 inhibitor, inhibits IRE1α-induced ATP-dependent XBP1 mRNA cleavage (</p>Fórmula:C12H13N5O4Pureza:98.1% - 98.17%Forma y color:SolidPeso molecular:291.26trans-Chalcone
CAS:<p>trans-Chalcone (Chalkone) is an aromatic ketone that forms the central core for a variety of important biological compounds, which are known collectively as</p>Fórmula:C15H12OPureza:99.89%Forma y color:SolidPeso molecular:208.26EPZ004777
CAS:<p>EPZ004777 is a potent, selective DOT1L inhibitor with IC50 of 0.4 nM.</p>Fórmula:C28H41N7O4Pureza:98.99% - 99.32%Forma y color:SolidPeso molecular:539.67BIBR 1532
CAS:<p>BIBR 1532 is an effective, specific and non-competitive telomerase inhibitor (IC50: 100 nM, in a cell-free assay).</p>Fórmula:C21H17NO3Pureza:98.49% - 98.90%Forma y color:SolidPeso molecular:331.36(Rac)-Benpyrine
CAS:<p>(Rac)-Benpyrine is a potent and orally active inhibitor of TNF-α.</p>Fórmula:C16H16N6OPureza:98.44%Forma y color:SolidPeso molecular:308.34HS-173
CAS:<p>HS-173 is an effective PI3Kα inhibitor (IC50: 0.8 nM).</p>Fórmula:C21H18N4O4SPureza:99.33% - 99.64%Forma y color:SolidPeso molecular:422.46Fidaxomicin
CAS:<p>Fidaxomicin (Tiacumicin B) is a semisynthetic macrolide antibiotic used to treat Clostridium difficile-associated diarrhea in adults.</p>Fórmula:C52H74Cl2O18Pureza:99.76% - 99.82%Forma y color:SolidPeso molecular:1058.04S55746 hydrochloride
CAS:<p>S55746 hydrochloride is a potent, orally active and selective inhibitor of BCL-2(Ki of 1.3 nM and a Kd of 3.9 nM),with antitumor activity with low toxicity.</p>Fórmula:C43H43ClN4O6Pureza:98%Forma y color:SolidPeso molecular:747.28Galgravin
CAS:<p>Galgravin combats inflammation, safeguards neurons, promotes neurite growth, and resists Abeta25-35 and MPP+ toxicity.</p>Fórmula:C22H28O5Pureza:99.75% - 99.88%Forma y color:SolidPeso molecular:372.45Clovamide
CAS:<p>Trans-Clovamide (trans-Clovamide) is a naturally occurring caffeoyl conjugate identified in the antioxidant polyphenolic fraction of cocoa (T.</p>Fórmula:C18H17NO7Pureza:97.12% - 97.68%Forma y color:SolidPeso molecular:359.33RX-3117
CAS:<p>RX-3117 (fluorocyclopentenylcytosine) is a novel a cytidine analog.</p>Fórmula:C10H12FN3O4Pureza:97.46%Forma y color:SolidPeso molecular:257.22PS47
CAS:<p>PS-47(PS 47) is an inactive E-isomer of PS48. PS48 is an activator of PDK1.</p>Fórmula:C17H15ClO2Pureza:99.09%Forma y color:SolidPeso molecular:286.75Pitavastatin calcium
CAS:<p>Pitavastatin calcium (NK-104), a inhibitor of HMG-CoA reductase, lowers both total cholesterol and low-density lipoprotein cholesterol in animals and humans.</p>Fórmula:C50H46CaF2N2O8Pureza:98.89% - >99.99%Forma y color:White To Off-White PowderPeso molecular:880.98RIPGBM
CAS:<p>RIPGBM is a selective inducer of apoptosis in glioblastoma multiforme cancer stem cells (EC50: ≤500 nM).</p>Fórmula:C26H21FN2O3Pureza:99.45%Forma y color:SolidPeso molecular:428.45L-Glutamic acid
CAS:<p>L-Glutamic acid is an agonist of glutamate receptors, including metabotropic glutamate receptors (mGluR), AMPA, NMDA, and KA. High-Quality, Low-Cost!</p>Fórmula:C5H9NO4Pureza:99.14% - 99.55%Forma y color:White Solid CrystallinePeso molecular:147.13SIRT7 inhibitor 97491
CAS:<p>SIRT7 inhibitor 97491 is an HDAC inhibitor with high specificity for SIRT7 (IC50 = 325 nM). SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway.</p>Fórmula:C15H12ClN3OPureza:99.79%Forma y color:SolidPeso molecular:285.73Melatonin
CAS:<p>Melatonin (Melatonine) is a natural hormone that activates melatonin receptors. Melatonin regulates the biological clock. Cost-effective and quality-assured.</p>Fórmula:C13H16N2O2Pureza:98% - 99.89%Forma y color:Pale Yellow Leaflets From Benzene SolidPeso molecular:232.28Chrysosplenol D
CAS:<p>Chrysosplenol D, an efflux pump inhibitor that can potentiate the activity of commercially important antibiotics and antimalarials.</p>Fórmula:C18H16O8Pureza:97.87% - 99.98%Forma y color:SolidPeso molecular:360.31Onvansertib
CAS:<p>Onvansertib (NMS-1286937) is a PLK1 inhibitor with high selectivity and oral activity. Onvansertib has antitumor activity. Cost-effective and quality-assured.</p>Fórmula:C24H27F3N8O3Pureza:98.3% - 99.88%Forma y color:SolidPeso molecular:532.52SBI-0640756
CAS:<p>SBI-0640756 (SBI-756) (SBI-756) is a first-in-class inhibitor that targets eIF4G1 and disrupts the eIF4F complex.</p>Fórmula:C23H14ClFN2O2Pureza:99.75%Forma y color:SolidPeso molecular:404.82D-Pantothenic acid sodium
CAS:<p>D-Pantothenic acid sodium, a sodium salt of D-pantothenate, is a vital B5 derivative, aiding fat, carb, and amino acid oxidation.</p>Fórmula:C9H16NNaO5Pureza:97.98%Forma y color:White PowderPeso molecular:241.22β-mangostin
CAS:<p>β-Mangostin: a xanthone in Cratoxylum arborescens, fights bacteria, malaria, tuberculosis (MIC 6.25μg/mL), and cancer.</p>Fórmula:C25H28O6Pureza:98.01% - 99.69%Forma y color:Faintly Yellow PowderPeso molecular:424.49Hematoporphyrin dihydrochloride
CAS:<p>Hematoporphyrin dihydrochloride (Hematoporphyrin IX dihydrochloride) is a substrate for affinity chromatography of heme-binding proteins.</p>Fórmula:C34H40Cl2N4O6Pureza:90.11%Forma y color:SolidPeso molecular:671.61PluriSIn 1
CAS:<p>PluriSIn 1 (NSC 14613) blocks SCD1, key in oleic acid creation, showing lipid metabolism's role in hPSCs.</p>Fórmula:C12H11N3OPureza:99.19% - 99.63%Forma y color:SolidPeso molecular:213.24BTSA1
CAS:BTSA1: High-affinity BAX activator inducing conformational changes for apoptosis.Fórmula:C21H14N6OS2Pureza:99.60% - 99.71%Forma y color:SolidPeso molecular:430.51Cambinol
CAS:<p>Cambinol is a SIRT1/2 inhibitor (IC50: 56/59 μM), non-competitive with NAD, weak on SIRT5, and prompts apoptosis in lymphoma cells.</p>Fórmula:C21H16N2O2SPureza:98.02% - 99.83%Forma y color:SolidPeso molecular:360.43OSU-T315
CAS:<p>OSU-T315 (OSU-T315 (1,5-regioisomer)) (1,5-regioisomer) is a ILK inhibitor.</p>Fórmula:C30H30F3N5OPureza:98.69%Forma y color:SolidPeso molecular:533.59SBE13 Hydrochloride
CAS:<p>SBE13 Hydrochloride (SBE 13 HCl) is an effective and specific PLK1 inhibitor (IC50: 0.2 nM); no inhibition om Aurora A kinase, Plk2/3.</p>Fórmula:C24H28Cl2N2O4Pureza:99.00% - ≥95%Forma y color:SolidPeso molecular:479.4Jaceosidin
CAS:<p>Jaceosidin: anti-oxidant, anti-inflammatory, anti-cancer, immunosuppressive; affects CYP1A2/UGT1A1/UGT1A7 metabolism.</p>Fórmula:C17H14O7Pureza:98.23% - 99.28%Forma y color:SolidPeso molecular:330.29GSK2801
CAS:<p>GSK2801 is an effective, specific and cell active acetyl-lysine competitive inhibitor of BAZ2A(Kd: 136 nM) and BAZ2B(Kd: 257 nM) bromodomains.</p>Fórmula:C20H21NO4SPureza:97.78% - 99.45%Forma y color:SolidPeso molecular:371.45Naphthazarin
CAS:<p>Naphthazarin triggers apoptosis, has anti-tumor effects via oxidative stress, mitochondrial AIF, microtubule depolymerization, and p53/p21 activation.</p>Fórmula:C10H6O4Pureza:98.12% - 99.87%Forma y color:Dark Purple To Brown-Black PowderPeso molecular:190.15Sophoraflavanone G
CAS:<p>Sophoraflavanone G (Kushenol F) (Kushenol F), isolated from Sophora flavescens, induces MDA-MB-231 and HL-60 cells apoptosis through suppression of MAPK-related</p>Fórmula:C25H28O6Pureza:97.09% - 99.77%Forma y color:SolidPeso molecular:424.49PRIMA-1
CAS:<p>PRIMA-1 (NSC-281668) is a mutant p53 reactivator. It induces apoptosis and inhibits growth of human tumors with mutant p53.</p>Fórmula:C9H15NO3Pureza:99.22%Forma y color:SolidPeso molecular:185.22GSK2656157
CAS:<p>GSK2656157 is a highly specific and ATP-competitive PERK inhibitor (IC50: 0.9 nM) in a cell-free assay.</p>Fórmula:C23H21FN6OPureza:98.59% - >99.99%Forma y color:SolidPeso molecular:416.45KRAS inhibitor-9
CAS:<p>KRAS inhibitor-9 (DUN09716) hinders GTP-KRAS formation, with a Kd of 92 μM, causes G2/M arrest, and induces apoptosis in mutated NSC-LC cells.</p>Fórmula:C13H9ClN2S2Pureza:99.66%Forma y color:SolidPeso molecular:292.81BAI1
CAS:<p>BAI1 (Bax channel blocker) is a potent inhibitor of Bax-mediated mitochondrial cytochrome C release (IC50: 0.52 μM).</p>Fórmula:C19H21Br2N3OPureza:97.74%Forma y color:SolidPeso molecular:467.2STM2457
CAS:<p>View and buy STM2457 from TargetMol.STM2457 is a first-in-class, highly potent, selective and orally active inhibitor of METTL3.Cited in 2 publications.</p>Fórmula:C25H28N6O2Pureza:97.44% - 98.90%Forma y color:SolidPeso molecular:444.53Cidofovir
CAS:<p>Cidofovir ((S)-HPMPC) 通过特异性抑制病毒 DNA 合成来抑制病毒复制。</p>Fórmula:C8H14N3O6PPureza:99.24% - 99.76%Forma y color:Fluffy White PowderPeso molecular:279.19Galanthamine
CAS:<p>Galanthamine (Galantamine) is an acetylcholinesterase (AChE)inhibitor(IC50 : 500 nM), can reduce brain damage induced by hypoxia-ischemia.</p>Fórmula:C17H21NO3Pureza:98.03% - 99.87%Forma y color:Off-White SolidPeso molecular:287.35Bafilomycin A1
CAS:<p>Bafilomycin A1 belongs to the macrolide class of antibiotics and is a V-ATPase (IC50=0.44 nM) that is specific and reversible.</p>Fórmula:C35H58O9Pureza:95.87% - 99.36%Forma y color:SolidPeso molecular:622.83Nirogacestat
CAS:<p>Nirogacestat (PF 03084014) is a specific γ-secretase inhibitor (IC50: 6.2 nM, in a cell-free assay).</p>Fórmula:C27H41F2N5OPureza:97.98% - 99.63%Forma y color:SolidPeso molecular:489.64BO-264
CAS:<p>BO-264 is a highly potent and orally active inhibitor of transforming acidic coiled-coil 3 (TACC3, IC50 of 188 nM and a Kd of 1.5 nM).</p>Fórmula:C18H19N5O3Pureza:98.03% - 99.81%Forma y color:SolidPeso molecular:353.38Desoxyrhaponticin
CAS:<p>Deoxyrhaponticin may reduce post-meal blood sugar and inhibit cancer cell growth.</p>Fórmula:C21H24O8Pureza:99.97% - ≥95%Forma y color:SolidPeso molecular:404.41SU9516
CAS:<p>SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also has inhibitory effects on CDK1 and CDK4, with IC50s of 40 nM and 200 nM, respectively.</p>Fórmula:C13H11N3O2Pureza:99.34% - 99.87%Forma y color:SolidPeso molecular:241.25Erastin
CAS:<p>Erastin is an iron death activator that acts on the mitochondrial VDAC in a ROS- and iron-dependent manner, anti-tumor. High-Quality, Low-Cost!</p>Fórmula:C30H31ClN4O4Pureza:98% - 99.75%Forma y color:SolidPeso molecular:547.04PKCβ inhibitor 1
CAS:<p>PKCβ inhibitor 1 (KUN79359)(KUN79359) is a potent, selective and ATP-competitive inhibitor of PKC isozymes(IC50s of 21 and 5 nM for human PKCβ1 and PKCβ2,</p>Fórmula:C24H21N5O2Pureza:99.33%Forma y color:SolidPeso molecular:411.46L-Ascorbic acid sodium salt
CAS:<p>L-Ascorbic acid sodium salt (Vitamin C sodium salt) is a more bioavailable form of vitamin C that is an alternative to taking ascorbic acid as a supplement.</p>Fórmula:C6H7NaO6Pureza:98.73% - 99.75%Forma y color:Less Solid PowderPeso molecular:198.11Capmatinib xHCl
CAS:<p>Capmatinib xHCl (INCB28060) is a potent, orally active, selective, and ATP competitive c-Met kinase inhibitor, potently blocking in vitro kinase activity (IC50</p>Fórmula:C23H18ClFN6OPureza:98.62% - 99.81%Forma y color:SolidPeso molecular:448.89Cynaroside
CAS:<p>Cynaroside (Luteolin 7-O-Glucoside) is a flavone, a flavonoid-like chemical compound. It has an anti-oxidant effect, inhibiting lipid and protein oxidation.</p>Fórmula:C21H20O11Pureza:98% - >99.99%Forma y color:SolidPeso molecular:448.38Larotrectinib sulfate
CAS:<p>Larotrectinib sulfate (LOXO-101 sulfate) is an oral active and specific ATP-competitive inhibitor of tropomyosin receptor kinases (TRK).</p>Fórmula:C21H22F2N6O2·H2O4SPureza:98.62% - 99.76%Forma y color:SolidPeso molecular:526.51GW779439X
CAS:<p>GW779439X is an inhibitor of CDK.</p>Fórmula:C22H21F3N8Pureza:97.87%Forma y color:SolidPeso molecular:454.45VER-50589
CAS:<p>VER-50589 is a potent HSP90 inhibitor.</p>Fórmula:C19H17ClN2O5Pureza:99.96% - >99.99%Forma y color:SolidPeso molecular:388.8MSC 2032964A
CAS:<p>MSC 2032964A: Potent, selective ASK1 inhibitor, IC50=93 nM, oral, brain-permeable, curbs neuroinflammation, blocks LPS-induced ASK1/p38 activation.</p>Fórmula:C16H13F3N6OPureza:99.76%Forma y color:SolidPeso molecular:362.31CHS-828
CAS:<p>CHS-828 (GMX1778), a pyridyl cyanoguanidine, is an effective inhibitor of NAD+ biosynthesis enzyme NAMPT (IC50 <25 nM).</p>Fórmula:C19H22ClN5OPureza:98% - 99.9%Forma y color:SolidPeso molecular:371.86LW6
CAS:<p>LW6 (HIF-1α inhibitor) is a novel HIF-1 inhibitor.</p>Fórmula:C26H29NO5Pureza:98.1% - 98.22%Forma y color:SolidPeso molecular:435.51Chelidonine
CAS:<p>Chelidonine from Chelidonium majus triggers HeLa cell apoptosis, may reverse MDR, boost chemotherapeutics against leukemia, and inhibit cancer cell metastasis.</p>Fórmula:C20H19NO5Pureza:98% - 99.61%Forma y color:SolidPeso molecular:353.37Wedelolactone
CAS:<p>Wedelolactone (IKK Inhibitor II) inhibits NF-κB-mediated gene transcription in cells by blocking the phosphorylation and degradation of IκBα.</p>Fórmula:C16H10O7Pureza:98.07% - 99.87%Forma y color:SolidPeso molecular:314.25Sal003
CAS:<p>Sal003, an effective cell-permeable analog, inhibitis the eIF2α phosphatase.</p>Fórmula:C18H15Cl4N3OSPureza:99.17% - 99.77%Forma y color:SolidPeso molecular:463.21Salvigenin
CAS:<p>Salvigenin is a potent hMAO-A inhibitor, has neuroprotective, antitumor and immunomodulatory effects.</p>Fórmula:C18H16O6Pureza:99.17% - 99.78%Forma y color:SolidPeso molecular:328.32Gardenin B
CAS:<p>Gardenin B exhibits superior antiproliferative activity against lung, breast, colon, hepatic and leukaemia cell lines as well as in keratinocytes .</p>Fórmula:C19H18O7Pureza:98.80% - 99.74%Forma y color:SolidPeso molecular:358.34Delanzomib
CAS:<p>Delanzomib (CEP-18770) is an oral proteasome inhibitor with an IC50 of 3.8 nM, targeting chymotrypsin-like activity with minimal effect on other activities.</p>Fórmula:C21H28BN3O5Pureza:95.52% - 99.46%Forma y color:SolidPeso molecular:413.28ENMD-2076
CAS:<p>ENMD-2076, a multi-targeted kinase inhibitor, has specific activity against Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα.</p>Fórmula:C21H25N7Pureza:97.63% - ≥95%Forma y color:SolidPeso molecular:375.47m-3M3FBS
CAS:<p>m-3M3FBS is a phospholipase C (PLC) activator.</p>Fórmula:C16H16F3NO2SPureza:99.66%Forma y color:SolidPeso molecular:343.36Polygalacin D
CAS:<p>Polygalacin D shows anti- proliferation, anti-inflammary, and hepatoprotective activities, it can inhibit the expression of lipopolysaccharide (LPS)-induced</p>Fórmula:C57H92O27Pureza:98.95% - ≥98%Forma y color:SolidPeso molecular:1209.4CCT007093
CAS:<p>CCT007093 is an effective PPM1D (WIP1) inhibitor (IC50: 8.4 μM).</p>Fórmula:C15H12OS2Pureza:98% - 99.88%Forma y color:SolidPeso molecular:272.39Isocurcumenol
CAS:<p>1. Isocurcumenol inhibits 5α-reductase which converts testosterone to dihydrotestosterone (DHT).</p>Fórmula:C15H22O2Pureza:99.29% - ≥95%Forma y color:SolidPeso molecular:234.33UTL-5g
CAS:<p>UTL-5g is a chemoprotective TNF-α inhibitor reducing cisplatin side effects and toxicity in liver, kidneys, and blood.</p>Fórmula:C11H8Cl2N2O2Pureza:99.83%Forma y color:SolidPeso molecular:271.1Rilmenidine hemifumarate
CAS:<p>Rilmenidine hemifumarate (S-3341 hemifumarate) is an I1 imidazoline receptor and α2-adrenergic receptor agonist that induces autophagy.</p>Fórmula:C10H16N2OC4H4O4Pureza:98.14%Forma y color:SolidPeso molecular:238.28TREM2-IN-1
CAS:<p>TREM2-IN-1 (OPA) is a platinum-based TREM2 inhibitor with anti-cancer and anti-tumor activity, inhibiting the immune-regulatory activity of TREM2 on macrophages</p>Fórmula:C46H68N2O20PtPureza:98.56%Forma y color:SolidPeso molecular:1164.12Enzastaurin
CAS:<p>Enzastaurin (LY317615) (LY317615) is an effective PKCβ selective inhibitor (IC50: 6 nM), 6- to 20-fold selectivity against PKCα/γ/ε.</p>Fórmula:C32H29N5O2Pureza:98% - >99.99%Forma y color:SolidPeso molecular:515.6Piperazine Erastin
CAS:<p>Piperazine erastin is an analog of erastin. It causes an iron-dependent form of non-apoptotic cell death termed ferroptosis.</p>Fórmula:C35H41ClN6O4Pureza:99.52%Forma y color:SolidPeso molecular:645.19WHI-P154
CAS:<p>WHI-P154 (Jak3 inhibitor ii) is a potent JAK3 inhibitor.</p>Fórmula:C16H14BrN3O3Pureza:98% - 99.67%Forma y color:SolidPeso molecular:376.2S63845
CAS:<p>S63845 is a selective myeloid leukemia 1（MCL1) inhibitor that binds to human MCL1 with a Kd of 0.19 nM.Cost-effective and quality-assured.</p>Fórmula:C39H37ClF4N6O6SPureza:97.7% - ≥98%Forma y color:SolidPeso molecular:829.26Mdivi-1
CAS:<p>Mdivi-1 (Mitochondrial division inhibitor 1) is a mitochondrial division inhibitor that inhibits DRP1 and Dynamin I (IC50=1-10 μM).</p>Fórmula:C15H10Cl2N2O2SPureza:96.57% - 99.23%Forma y color:SolidPeso molecular:353.22Quinidine
CAS:<p>Quinidine is a stereoisomer of the antimalarial agent quinine and a class Ia antiarrhythmic agent. for the treatment of abnormal heart rhythms and also malaria.</p>Fórmula:C20H24N2O2Pureza:97.03% - 99.99%Forma y color:Crystals With 2 5 Mol Water Of Crystallization; Crystals From Dilute Alcohol Physical Description Crystals Or White Powder (Ntp 1992)Peso molecular:324.42PYR-41
CAS:<p>PYR-41 is the first cell-permeable inhibitor of ubiquitin-activating enzyme E1, with no activity at E2.</p>Fórmula:C17H13N3O7Pureza:98.25%Forma y color:SolidPeso molecular:371.3Lupeol
CAS:<p>Lupeol (Monogynol B) is a novel androgen receptor inhibitor with anti-inflammatory and antioxidant activity.</p>Fórmula:C30H50OPureza:98% - 99.96%Forma y color:Needles From Alcohol Acetone White PowderPeso molecular:426.72Purvalanol A
CAS:<p>Purvalanol A (NG-60) is an effective and cell-permeable CDK inhibitor with IC50 of 70/4/35/850 nM for cdk2-cyclin A/B/E, and cdk4-cyclin D1, respectively.</p>Fórmula:C19H25ClN6OPureza:98.13% - 99.68%Forma y color:PowderPeso molecular:388.89Meisoindigo
CAS:<p>Meisoindigo (Natura-α) is a derivative of indigo natural, might induces apoptosis and myeloid differentiation of acute myeloid leukemia (AML).</p>Fórmula:C17H12N2O2Pureza:98.03% - 98.19%Forma y color:SolidPeso molecular:276.29Pinosylvin
CAS:<p>Pinosylvin (5-Styrylresorcinol) induces autophagy via AMPK activation. Pinosylvin is likely to act as a pro-angiogenic factor.</p>Fórmula:C14H12O2Pureza:99.89% - 99.91%Forma y color:SolidPeso molecular:212.24M50054
CAS:<p>Apoptosis Inhibitor was a novel inhibitor of programmed cell death associate with caspase-3 inhibition.</p>Fórmula:C13H16O4Pureza:97.8%Forma y color:SolidPeso molecular:236.26BI-847325
CAS:<p>BI-847325 is a selective dual inhibitor of MEK and aurora kinases (AK) with IC50 values of 4 and 15 nM for human MEK2 and AK-C, respectively.</p>Fórmula:C29H28N4O2Pureza:97.13% - 97.54%Forma y color:SolidPeso molecular:464.56BI 2536
CAS:<p>BI2536 is an effective Plk1 inhibitor (IC50: 0.83 nM). It has 4- and 11-fold greater selectivity than Plk2 and Plk3.</p>Fórmula:C28H39N7O3Pureza:98% - 99.88%Forma y color:SolidPeso molecular:521.65Copanlisib
CAS:<p>Copanlisib (BAY 80-6946), a PI3K inhibitor, may block tumor growth and improve cancer treatment efficacy.</p>Fórmula:C23H28N8O4Pureza:99% - 99.88%Forma y color:SolidPeso molecular:480.52Avicularin
CAS:<p>Avicularin reduces inflammation via ERK pathway in RAW 264.7 cells and hinders lipid buildup in adipocytes by limiting glucose uptake and fatty acid synthesis.</p>Fórmula:C20H18O11Pureza:97.02% - 99.94%Forma y color:White PowderPeso molecular:434.35PD146176
CAS:<p>PD146176 (NSC-168807) is an inhibitor of 15-Lipoxygenase (15-LO) , it inhibits rabbit reticulocyte 15-LO with Ki of 197 nM and IC50 of 0.54 μM.</p>Fórmula:C15H11NSPureza:98.00%Forma y color:SolidPeso molecular:237.32Terrestrosin D
CAS:<p>Terrestrosin D triggers apoptosis, halts cell cycles, and blocks angiogenesis in tumor cells, displaying anti-cancer effects.</p>Fórmula:C50H80O23Pureza:99.92% - 99.96%Forma y color:SolidPeso molecular:1049.16Ganetespib
CAS:<p>Ganetespib (STA-9090) is a synthetic small-molecule inhibitor of heat shock protein 90 (Hsp90) with potential antineoplastic activity.</p>Fórmula:C20H20N4O3Pureza:98% - 99.95%Forma y color:SolidPeso molecular:364.4Aminopurvalanol A
CAS:<p>Aminopurvalanol A is a competitive, selective and cell-permeable inhibitor of cyclin-dependent kinase (CDK) that potently inhibits Cyclin A/cdk2, Cyclin B/cdk1</p>Fórmula:C19H26ClN7OPureza:99.73%Forma y color:SolidPeso molecular:403.91
