Anticorps pour la recherche sur le cancer
Les anticorps de recherche sur le cancer sont des immunoglobulines spécialisées qui ciblent des biomarqueurs ou des protéines spécifiques impliquées dans la croissance tumorale, les métastases et la régulation du cycle cellulaire. Ces anticorps sont essentiels pour identifier et étudier les cellules cancéreuses, permettant aux chercheurs de développer de nouvelles stratégies diagnostiques et thérapeutiques. Chez CymitQuimica, nous proposons une large gamme d'anticorps de recherche sur le cancer à haute spécificité pour soutenir vos investigations en oncologie, de la détection précoce au développement de thérapies.
3609 produits trouvés pour "Anticorps pour la recherche sur le cancer"
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Tyrosine Kinase Inhibitor Library
<p>A unique collection of 1016 tyrosine kinase inhibitors for high throughput screening and high content screening for drug discovery in tyrosine kinase related</p>Couleur et forme :Odour SolidAutophagy Compound Library
<p>A unique collection of 1248 compounds with defined autophagy-inducing or -inhibitory activity for research in autophagy, high throughput screening (HTS) and</p>Couleur et forme :Odour SolidHistone Modification Compound Library
A unique collection of xnum histone modification related compounds for high throughput screening (HTS) and high content screening (HCS);Couleur et forme :Odour SolidMAPK Inhibitor Library
<p>A unique collection of 365 compounds targeting MAPK signaling for drug discovery in MAPK related diseases;</p>Couleur et forme :Odour SolidAntioxidant Compound Library
Oxidative stress reflects an imbalance between the systemic manifestation of reactive oxygen species (ROS) and a biological system's ability to readily detoxifyCouleur et forme :LiquidFerroptosis Compound Library
<p>A unique collection of 779 ferroptosis signaling pathway related compounds, a powerful tool for new target identification, drug discovery, and mechanism study；</p>Couleur et forme :Odour SolidFDA-Approved Kinase Inhibitor Library
<p>A unique collection of 263 kinase inhibitors/regulators for specific targeting of kinases, ready for high-throughput screening and high-content screening.</p>Couleur et forme :LiquidAngiogenesis related Compound Library
<p>A unique collection of 1353 proangiogenic and antiangiogenic compounds for new targets identification, research in mechanisms of angiogenesis, and high</p>Couleur et forme :Odour SolidUbiquitination Compound Library
A unique collection of xnum ubiquitination related small chemicals can be used for high throughput and high content screening；Couleur et forme :Odour SolidEpigenetics Compound Library
Well-chosen 953 compounds related to epigenetic regulation for research in epigenetics, high throughput screening (HTS) and high content screening (HCS) for newCouleur et forme :Odour SolidAnti-Pancreatic Cancer Compound Library
<p>A unique collection of 2238 pancreatic cancer related compounds can be used in HTS and HCS;</p>Couleur et forme :Odour SolidWnt/Hedgehog/Notch Compound Library
<p>A unique collection of 237 Wnt/Hedgehog/Notch signaling targeted compounds for high throughput and high content screening;</p>Couleur et forme :Odour SolidGPCR Compound Library
<p>A unique collection of xnum GPCR-active agents for high throughput screening and high content screening for GPCR drug discovery, and new GPCR target</p>Couleur et forme :Odour SolidGlycolysis Compound Library
<p>555 glycolysis-related active compounds for high-throughput and high-content screening.</p>Couleur et forme :LiquidChemokine Inhibitor Library
<p>A unique collection of xnum chemokines or chemokine receptors targeted compounds for high throughput and high content screening;</p>Couleur et forme :Odour SolidPhosphatase Inhibitor Library
<p>A collection of 79 phosphatase inhibitors with known activity;</p>Couleur et forme :Odour SolidAnti-CD31 Antibody (9O943)
<p>Anti-CD31 Antibody (9O943) is a Mouse antibody targeting CD31. Anti-CD31 Antibody (9O943) can be used in ELISA, WB, IHC, IF, FCM.</p>Degré de pureté :>95%Couleur et forme :Odour LiquidAnti-CD70 Antibody (3T581)
Anti-CD70 Antibody (3T581) is an antibody targeting CD70. Anti-CD70 Antibody (3T581) can be used in ELISA.Couleur et forme :Odour LiquidAnti-CD147 Antibody (2H864)
<p>Anti-CD147 Antibody (2H864) is an antibody targeting CD147. Anti-CD147 Antibody (2H864) can be used in ELISA, WB, IHC, IF, FCM.</p>Couleur et forme :Odour LiquidEPZ020411
CAS :EPZ020411 is a specific and effective inhibitor of PRMT6 (IC50=10 nM).Formule :C25H38N4O3Couleur et forme :SolidMasse moléculaire :442.6SYN1143
CAS :<p>SYN1143 (AMG-1) strongly inhibits RON & c-Met with IC50s: 9 & 4 nmol/L.</p>Formule :C31H29FN4O5Degré de pureté :99.69%Couleur et forme :SolidMasse moléculaire :556.58Almorexant hydrochloride
CAS :Almorexant hydrochloride (ACT 078573 hydrochloride) is a dual orexin receptor antagonist that induces apoptosis and can be used to study sleep disorders.Formule :C29H32ClF3N2O3Degré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :549.02Anti-TM4SF1 Antibody (2G843)
Anti-TM4SF1 Antibody (2G843) is an antibody targeting TM4SF1. Anti-TM4SF1 Antibody (2G843) can be used in ELISA.Couleur et forme :Odour LiquidOctreotide
CAS :Octreotide (SMS 201-995) is a potent inhibitor of growth hormone, glucagon, and insulin.Formule :C49H66N10O10S2Degré de pureté :99.3% - 99.64%Couleur et forme :White PowderMasse moléculaire :1019.24Traumatic Acid
CAS :Traumatic Acid aids wound healing in plants by stimulating cell division to create a callus.Formule :C12H20O4Degré de pureté :99.64%Couleur et forme :SolidMasse moléculaire :228.28Anti-LY6G6D Antibody (2W316)
Anti-LY6G6D Antibody (2W316) is an antibody targeting LY6G6D. Anti-LY6G6D Antibody (2W316) can be used in ELISA, FCM.Couleur et forme :Odour LiquidDTP3
CAS :DTP3 is a selective MKK7/GADD45β inhibitor, which inhibits cancer-selective NF-κB survival pathway.Formule :C26H35N7O5Couleur et forme :SolidMasse moléculaire :525.6GNF-5
CAS :GNF-5, non-ATP Bcr-Abl inhibitor (IC50: 0.22±0.1 uM, wild-type), improves upon GNF-2 with better pharmacokinetics.Formule :C20H17F3N4O3Degré de pureté :98% - 99.94%Couleur et forme :SolidMasse moléculaire :418.37Pitstop 2
CAS :<p>Pitstop2 is an amphipathic protein-bound inhibitor of the clathrin terminal domain. Pitstop2 has antitumor activity. Cost-effective, quality assurance.</p>Formule :C20H13BrN2O3S2Degré de pureté :99.54%Couleur et forme :SolidMasse moléculaire :473.36Liensinine
CAS :1. Liensinine, a kind of isoquinoline alkaloid, can antagonize the ventricular arrhythmias.Formule :C37H42N2O6Degré de pureté :98.92% - 99.93%Couleur et forme :White-Like PowderMasse moléculaire :610.74Buformin hydrochloride
CAS :Buformin hydrochloride, an oral biguanide antidiabetic, activates AMPK, enhances insulin sensitivity, and inhibits hepatic glucose production.Formule :C6H16ClN5Degré de pureté :97.83%Couleur et forme :SolidMasse moléculaire :193.68RGX-202
CAS :<p>RGX-202 (β-GPA) is an orally active inhibitor of the SLC6A8 transport protein. RGX-202 is a creatine analog that alters skeletal muscle energy expenditure.</p>Formule :C4H9N3O2Degré de pureté :99.67% - 99.8%Couleur et forme :SolidMasse moléculaire :131.13Desmethylanethol trithione
CAS :<p>Desmethylanethol trithione (ADT-OH), a synthetic H2S donor, modulates tPA effects, reduces stroke damage, and improves recovery in mice.</p>Formule :C9H6OS3Degré de pureté :98.05% - 98.41%Couleur et forme :SolidMasse moléculaire :226.34MSAB
CAS :MSAB inhibits Wnt/β-catenin by binding to β-catenin and inducing its breakdown.Formule :C15H15NO4SDegré de pureté :99.76%Couleur et forme :SolidMasse moléculaire :305.35CAY10404
CAS :<p>CAY10404: potent COX-1/2 inhibitor; blocks PKB/Akt, MAPK pathways; triggers NSC-LC apoptosis; analgesic, anti-inflammatory, anti-cancer.</p>Formule :C17H12F3NO3SDegré de pureté :99.02%Couleur et forme :SolidMasse moléculaire :367.34Almorexant
CAS :Almorexant (ACT 078573), a strong dual orexin receptor antagonist, has Ki of 1.3 nM for OX1 and 0.17 nM for OX2.Formule :C29H31F3N2O3Degré de pureté :97.75% - 98.02%Couleur et forme :SolidMasse moléculaire :512.56Obatoclax Mesylate
CAS :Obatoclax Mesylate (GX15-070) is a Bcl-2 antagonist (Ki: 0.22 μM) and can induce apoptosis with up-regulation of Bim, induced cytochrome c release, andFormule :C20H19N3O·CH4O3SDegré de pureté :99.58% - 99.88%Couleur et forme :SolidMasse moléculaire :413.49Fatostatin hydrobromide
CAS :<p>Fatostatin hydrobromide (Fatostatin A HBr), an inhibitor of sterol regulatory element binding protein (SREBP), impairs the activation of SREBP-1 and SREBP-2.</p>Formule :C18H18N2S·HBrDegré de pureté :98.62% - 99.91%Couleur et forme :SolidMasse moléculaire :375.33(E/Z)-Zotiraciclib
CAS :(E/Z)-Zotiraciclib ((E/Z)-TG02) inhibits CDK2, JAK2, and FLT3 effectively with IC50s of 13, 73, and 56 nM, respectively.Formule :C23H24N4ODegré de pureté :97.75% - 99.92%Couleur et forme :SolidMasse moléculaire :372.46STM2457
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>Formule :C25H28N6O2Degré de pureté :97.44% - 98.90%Couleur et forme :SolidMasse moléculaire :444.53Obtusifolin
CAS :Obtusifolin is an antioxidant that combats diabetes, bone-resorption, diabetic retinopathy, pain, and cognitive decline.Formule :C16H12O5Degré de pureté :99.78% - 99.99%Couleur et forme :SolidMasse moléculaire :284.26Elacridar
CAS :<p>Elacridar (GG918) is a potent inhibitor of P-glycoprotein and BCRP.Cost-effective and quality-assured.</p>Formule :C34H33N3O5Degré de pureté :98.12% - >99.99%Couleur et forme :SolidMasse moléculaire :563.64ML141
CAS :ML141 (CID-2950007) is an effective, specific and reversible non-competitive inhibitor of Rho family GTPase cdc42 (IC50: 200 nM).Formule :C22H21N3O3SDegré de pureté :99.36% - 99.56%Couleur et forme :SolidMasse moléculaire :407.49PI3K-IN-1
CAS :PI3K-IN-1 (Voxtalisib Analogue) is a dual inhibitor of mTOR/PI3K, mostly for p110γ , also inhibits DNA-PK and mTOR.Formule :C31H29N5O6SDegré de pureté :97.03% - 98%Couleur et forme :SolidMasse moléculaire :599.66Embelin
CAS :Embelin (Embelic acid), isolated from the Japanese Ardisia herb, is an inhibitor of the X-linked inhibitor of apoptosis (IC50: 4.1 uM).Formule :C17H26O4Degré de pureté :97.07% - 99.88%Couleur et forme :SolidMasse moléculaire :294.39L-685458
CAS :L-685458 (L-685,458) is a specific and potent inhibitor of A beta PP gamma-secretase activity with Ki of 17 nM.Formule :C39H52N4O6Degré de pureté :99.62% - 99.80%Couleur et forme :SolidMasse moléculaire :672.85Rhapontin
CAS :Rhapontin may reduce liver fat and better blood sugar/lipids, showing potential for treating type 2 diabetes.Formule :C21H24O9Degré de pureté :99% - 99.91%Couleur et forme :Light YellowMasse moléculaire :420.41J14
CAS :<p>J-14, a reversible sulfiredoxin inhibitor (IC50: 8.1 μM), triggers oxidative stress and cancer cell death.</p>Formule :C28H25ClN4O2SDegré de pureté :97.81% - 99.51%Couleur et forme :SolidMasse moléculaire :517.04UNC0379
CAS :<p>UNC0379 is a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8.</p>Formule :C23H35N5O2Degré de pureté :94.41% - 99.97%Couleur et forme :SolidMasse moléculaire :413.56Ganoderic acid D
CAS :Ganoderic acid D, a Ganoderma component, inhibits HeLa cell growth with an IC50 of 17.3µM after 48h.Formule :C30H42O7Degré de pureté :98.06% - 99.98%Couleur et forme :SolidMasse moléculaire :514.65DTHIB
CAS :DTHIB robustly inhibits the HSF1 cancer gene signature and prostate cancer cell proliferation.Formule :C13H9ClFN3O3Degré de pureté :98.86% - 99.29%Couleur et forme :SolidMasse moléculaire :309.68I-BRD9
CAS :<p>I-BRD9 (GSK602) is the first selective cellular inhibitor for BRD9 with pIC50 of 7.3.</p>Formule :C22H22F3N3O3S2Degré de pureté :98.16% - 99.51%Couleur et forme :SolidMasse moléculaire :497.55ASP4132
CAS :ASP4132 is an orally active AMPK activator (EC50 : 18 nM), has anti-cancer activity.Formule :C46H51F3N6O8S2Degré de pureté :98.34%Couleur et forme :SolidMasse moléculaire :937.06GSK3685032
CAS :<p>GSK3685032 is a non-covalent and selective DNMT1 inhibitor(IC50 = 36 nM).</p>Formule :C22H24N6OSDegré de pureté :98.56% - 99.49%Couleur et forme :SolidMasse moléculaire :420.53BS194
CAS :BS194 is as a potent cyclin-dependent protein kinases (CDKs) inhibitor.Formule :C20H27N5O3Degré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :385.46Droxinostat
CAS :<p>Droxinostat (NS 41080) is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 μM and 1.46 μM, greater than 8-fold selective against HDAC3</p>Formule :C11H14ClNO3Degré de pureté :99.83%Couleur et forme :SolidMasse moléculaire :243.69YUM70
CAS :YUM70 inhibits GRP78 (IC50: 1.5μM), inducing ER stress and apoptosis in pancreatic cancer.Formule :C21H19ClN2O4Degré de pureté :97.25%Couleur et forme :SolidMasse moléculaire :398.84JNJ-63576253 free base
CAS :<p>JNJ-63576253 free base (TRC253) is a potent and orally active full antagonist of androgen receptor (AR). JNJ-63576253 can be used for the research of CRPC.</p>Formule :C23H21F3N6O2SDegré de pureté :98.32%Couleur et forme :SolidMasse moléculaire :502.51SKI-178
CAS :SKI-178 is a sphingosine kinase 1 (SphK1) inhibitor with IC50 of 0.1-1.8 μM.Formule :C21H22N4O4Degré de pureté :97.09%Couleur et forme :SolidMasse moléculaire :394.42Umbralisib
CAS :Umbralisib (TGR 1202) is a PI3Kδ inhibitor.Formule :C31H24F3N5O3Degré de pureté :99.56% - 99.56%Couleur et forme :White SolidMasse moléculaire :571.55ARS-853
CAS :<p>ARS-853 is an inhibitor of K-RASG12C(IC50 : 2.5 μM), a mutant form of K-RAS that accumulates in the active GTP-bound state in certain cancer cells</p>Formule :C22H29ClN4O3Degré de pureté :97.43% - 98.4%Couleur et forme :SolidMasse moléculaire :432.94LYN-1604 dihydrochloride
CAS :LYN-1604 is a novel ULK1 activator.It inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.Formule :C33H45Cl4N3O2Degré de pureté :98.95% - 99.92%Couleur et forme :SolidMasse moléculaire :657.54Sitravatinib
CAS :<p>Sitravatinib (MGCD516) (MGCD516) is an inhibitor targeting multiple RTKs involved in driving sarcoma cell growth, including c-Met, c-Kit, PDGFRα/β, PDGFR, and</p>Formule :C33H29F2N5O4SDegré de pureté :98.9% - 99.85%Couleur et forme :SolidMasse moléculaire :629.68LJI308
CAS :LJI308 is a potent, and pan-RSK (p90 ribosomal S6 kinase) inhibitor with IC50 of 6 nM, 4 nM, and 13 nM for RSK1, RSK2, and RSK3, respectively.Formule :C21H18F2N2O2Degré de pureté :99.73% - 99.87%Couleur et forme :SolidMasse moléculaire :368.38Osimertinib
CAS :Osimertinib (AZD-9291) is a small molecule tyrosine kinase receptor inhibitor and antineoplastic agent that is used in the therapy of selected forms of NSCLC.Formule :C28H33N7O2Degré de pureté :99.32% - >99.99%Couleur et forme :SolidMasse moléculaire :499.61Rhamnose
CAS :<p>Addition of the Rhamnose (6-Deoxy-L-mannose)-rich polysaccharide, RROP-1, to normal human dermal fibroblasts (NHDFs) and human endothelial cells produced a dose</p>Formule :C6H12O5Degré de pureté :99.46%Couleur et forme :White Crystalline PowderMasse moléculaire :164.16FR054
CAS :FR054 inhibits PGM3, a key enzyme in the HBP, significantly reducing breast cancer cell growth and survival.Formule :C14H19NO8Degré de pureté :≥98%Couleur et forme :SolidMasse moléculaire :329.3Valepotriate
CAS :Valepotriates are sedative, enhance memory, have anti-cancer properties, and may reduce anxiety.Formule :C22H30O8Degré de pureté :97.29% - 99.90%Couleur et forme :SolidMasse moléculaire :422.47TL-895
CAS :<p>TL-895 is a potent, selective ATP-competitive BTK inhibitor (IC50 = 1.5 nM, Ki = 11.9 nM).</p>Formule :C25H26FN5O2Degré de pureté :99.96%Couleur et forme :SolidMasse moléculaire :447.5MTOB
CAS :MTOB, a CtBP substrate, inhibits CtBP-linked cancer activity in cells/mice and regulates TCF-4, affecting CSC proliferation.Formule :C5H7NaO3SDegré de pureté :98.23%Couleur et forme :SolidMasse moléculaire :170.16SGC0946
CAS :<p>SGC0946 is a highly effective and specific DOT1L methyltransferase inhibitor (IC50: 0.3 nM); selectively kill mixed lineage leukemia cells.</p>Formule :C28H40BrN7O4Degré de pureté :98% - 99.82%Couleur et forme :SolidMasse moléculaire :618.57ODM-203
CAS :ODM-203, a Selective Inhibitor of FGFR and VEGFR, Shows Strong Antitumor Activity, and Induces Antitumor ImmunityFormule :C26H21F2N5O2SDegré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :505.54Pinoresinol
CAS :<p>Pinoresinol ((+)-Pinoresinol) has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury</p>Formule :C20H22O6Degré de pureté :98.67%Couleur et forme :SolidMasse moléculaire :358.39ON123300
CAS :ON123300 is a potent and multi-targeted kinase inhibitor for CDK4/Ark5/PDGFRβ/FGFR1/RET/Fyn (IC50: 3.9/5/26/26/9.2/11 nM).Formule :C24H27N7ODegré de pureté :99.53% - 99.7%Couleur et forme :SolidMasse moléculaire :429.52O6-Benzylguanine
CAS :O6-Benzylguanine is a guanine analog with antineoplastic activity,and is a potent O6-alkylguanine DNA alkyltransferase (AGT) inactivator.Formule :C12H11N5ODegré de pureté :98.9%Couleur et forme :Solid CrystallineMasse moléculaire :241.25Fursultiamine
CAS :<p>Fursultiamine (Alinamin F) is a disulfide derivative of thiamine, or an allithiamine. It has potential uses in the treatment of vitamin B1 deficiency.</p>Formule :C17H26N4O3S2Degré de pureté :99.63% - 99.90%Couleur et forme :SolidMasse moléculaire :398.54Alisertib
CAS :Alisertib (MLN 8237) is a specific Aurora A inhibitor (IC50: 1.2 nM). The selectivity of Alisertib(MLN 8237) is >200-fold higher for Aurora A than Aurora B.Formule :C27H20ClFN4O4Degré de pureté :98.31% - >99.99%Couleur et forme :SolidMasse moléculaire :518.92CADD522
CAS :CADD522 (MFCD00167693) is a potent inhibitor of runt-related transcription factor-2 (RUNX2)-DNA binding with an IC50 of 10 nM, with antitumor activityFormule :C15H13Cl2NO3Degré de pureté :97.74%Couleur et forme :SolidMasse moléculaire :326.17Raddeanin A
CAS :<p>Raddeanin A is a natural triterpenoid saponin from Cyperus japonicus that inhibits histone deacetylase.Cost-effective and quality-assured.</p>Formule :C47H76O16Degré de pureté :98% - 99.94%Couleur et forme :SolidMasse moléculaire :897.1Tazemetostat hydrobromide
CAS :Tazemetostat hydrobromide: potent, selective EZH2 inhibitor; blocks PRC2/wild-type EZH2 (Ki: 2.5 nM) & EZH1 (IC50: 392 nM).Formule :C34H45BrN4O4Degré de pureté :99.8%Couleur et forme :SolidMasse moléculaire :653.65Alflutinib mesylate
CAS :<p>Alflutinib mesylate (AST2818 mesylate) ,is an irreversible tyrosine kinase inhibitor that selectively inhibits EGFR mutations, especially T790M.</p>Formule :C29H35F3N8O5SDegré de pureté :97.94% - 99.63%Couleur et forme :SolidMasse moléculaire :664.7TH5427
CAS :<p>TH5427 is a lead NUDT5 inhibitor(MG assay IC50 = 29 nM).</p>Formule :C20H20Cl2N8O3Degré de pureté :99.54%Couleur et forme :SolidMasse moléculaire :491.33AZ9482
CAS :AZ9482, a potent PARP inhibitor with 2-piperazinyl-3-cyano-pyridine linkage, causes centrosome declustering in HeLa cells with an EC50 < 18 nM.Formule :C26H22N6O2Degré de pureté :99.18% - 99.86%Couleur et forme :SolidMasse moléculaire :450.49Carbidopa
CAS :<p>Carbidopa (Lodosyn) is an aromatic-L-amino-acid decarboxylase inhibitor (IC50: 29±2 μM).</p>Formule :C10H14N2O4Degré de pureté :98.01% - ≥98%Couleur et forme :SolidMasse moléculaire :226.23AG-1478
CAS :<p>AG-1478 (NSC-693255) (Tyrphostin AG-1478) is a selective EGFR inhibitor.</p>Formule :C16H14ClN3O2Degré de pureté :99.03% - 99.71%Couleur et forme :SolidMasse moléculaire :315.75Senaparib
CAS :<p>Senaparib (IMP4297) is a novel highly potent and selective oral PARP1/2 inhibitor with strong antitumor activity.</p>Formule :C24H20F2N6O3Degré de pureté :99.8%Couleur et forme :SolidMasse moléculaire :478.45Niraparib hydrochloride
CAS :Niraparib hydrochloride (MK-4827) is a PARP inhibitor with potential cancer treatment effects, causing DNA damage and apoptosis.Formule :C19H21ClN4ODegré de pureté :99.26%Couleur et forme :SolidMasse moléculaire :356.85Neogambogic acid
CAS :<p>Neogambogic acid, an active ingredient in garcinia, can inhibit the growth of some solid tumors and result in an anticancer effect.</p>Formule :C38H46O9Degré de pureté :97.74% - 99.38%Couleur et forme :SolidMasse moléculaire :646.77Raf inhibitor 2
CAS :<p>Raf inhibitor 2 (CID 25014542) is novel inhibitor of Raf kinases.</p>Formule :C15H8Br2ClNO2Degré de pureté :98.53%Couleur et forme :SolidMasse moléculaire :429.49Galloflavin
CAS :Galloflavin is a lactate dehydrogenase inhibitor. Galloflavin inhibits both human LDH isoforms (type A and type B).Cost-effective and quality-assured.Formule :C12H6O8Degré de pureté :96.24% - 97.47%Couleur et forme :SolidMasse moléculaire :278.17Mitoxantrone
CAS :<p>Mitoxantrone: anthracenedione antibiotic, disrupts DNA/RNA replication, binds to topoisomerase II, less cardiotoxic than doxorubicin.</p>Formule :C22H28N4O6Degré de pureté :96.29% - 98.74%Couleur et forme :Blue PowderMasse moléculaire :444.48SC-58125
CAS :SC-58125 is a selective cyclooxygenase 2 (COX-2) inhibitor. SC-58125 exhibits antitumor activity, and also inhibits oedema at sites of inflammation.Formule :C17H12F4N2O2SDegré de pureté :99.57%Couleur et forme :SolidMasse moléculaire :384.35XL177A
CAS :<p>XL177A is a selective irreversible USP7 inhibitor(IC50 : 0.34 nM). XL177A elicits cancer cell killing through a p53-dependent mechanism.</p>Formule :C48H57ClN8O5Degré de pureté :98.75%Couleur et forme :SolidMasse moléculaire :861.47RA-9
CAS :RA-9 is a potent and selective proteasome-associated inhibitor of deubiquitinating enzymes (DUBs), with favorable toxicity profile and anticancer activity.Formule :C19H15N3O5Degré de pureté :98.15%Couleur et forme :SolidMasse moléculaire :365.34RU-301
CAS :RU-301 is a novel pan-tam inhibitorFormule :C21H19F3N4O4SDegré de pureté :98.87%Couleur et forme :SolidMasse moléculaire :480.46Nirogacestat
CAS :Nirogacestat (PF 03084014) is a specific γ-secretase inhibitor (IC50: 6.2 nM, in a cell-free assay).Formule :C27H41F2N5ODegré de pureté :97.98% - 99.63%Couleur et forme :SolidMasse moléculaire :489.64RBN012759
CAS :RBN012759 inhibits PARP14 protein and is more than 300-fold selective over all PARP family members.Cost-effective and quality-assured.Formule :C19H23FN2O3SDegré de pureté :98.87% - 99.96%Couleur et forme :SolidMasse moléculaire :378.46Barasertib-HQPA
CAS :<p>Barasertib-HQPA (AZD2811) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A.</p>Formule :C26H30FN7O3Degré de pureté :98.43% - 99.29%Couleur et forme :SolidMasse moléculaire :507.56PD184161
CAS :PD184161 is a novel, orally-active MEK inhibitor. PD184161 inhibited MEK activity (IC50 = 10-100 nM) in a time- and concentration-dependent manner[1].Formule :C17H13BrClF2IN2O2Degré de pureté :99.40%Couleur et forme :SolidMasse moléculaire :557.56Bromosporine
CAS :<p>Bromosporine is a broad spectrum inhibitor for bromodomains for BRD2/4/9 and CECR2 (IC50: 0.41/0.29/0.122/0.017 μM), respectively.</p>Formule :C17H20N6O4SDegré de pureté :99.65% - 99.79%Couleur et forme :SolidMasse moléculaire :404.44
