Anticuerpos para la investigación del cáncer
Los anticuerpos para la investigación del cáncer son inmunoglobulinas especializadas que se dirigen a biomarcadores específicos del cáncer o a proteínas involucradas en el crecimiento tumoral, metástasis y regulación del ciclo celular. Estos anticuerpos son fundamentales para identificar y estudiar las células cancerosas, lo que permite a los investigadores desarrollar nuevas estrategias diagnósticas y terapéuticas. En CymitQuimica, ofrecemos una amplia gama de anticuerpos de alta especificidad para la investigación oncológica, desde la detección temprana hasta el desarrollo de terapias.
Se han encontrado 3609 productos de "Anticuerpos para la investigación del cáncer"
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NS-1619
CAS:NS1619 have cardio-protective effects after ischemia-reperfusion injury.Fórmula:C15H8F6N2O2Pureza:97.66% - 98%Forma y color:SolidPeso molecular:362.23Syrosingopine
CAS:<p>Syrosingopine is a dual inhibitor of MCT1 and MCT4, 60 times more potent against MCT4, preventing lactate and H+ efflux.Cost-effective and quality-assured.</p>Fórmula:C35H42N2O11Pureza:99.25% - 99.78%Forma y color:SolidPeso molecular:666.71L-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.Fórmula:C39H52N4O6Pureza:99.62% - 99.80%Forma y color:SolidPeso molecular:672.85C-7280948
CAS:C-7280948 is a PRMT1 inhibitor.Fórmula:C14H16N2O2SPureza:99.55% - ≥95%Forma y color:SolidPeso molecular:276.35Rhapontin
CAS:Rhapontin may reduce liver fat and better blood sugar/lipids, showing potential for treating type 2 diabetes.Fórmula:C21H24O9Pureza:99% - 99.91%Forma y color:Light YellowPeso molecular:420.416-Methoxydihydrosanguinarine
CAS:<p>6-Methoxydihydrosanguinarine: cytotoxic to MCF-7/SF-268 cells, IC50 of 0.61/0.54 μM; fights MRSA, MIC 1.9-3.9 μg/ml.</p>Fórmula:C21H17NO5Pureza:99.32% - 99.81%Forma y color:SolidPeso molecular:363.36Murrayone
CAS:Murrayone from M. paniculata, a bioactive coumarin, prevents cancer metastasis and reduces ADP-induced platelet aggregation.Fórmula:C15H14O4Pureza:98.01% - 98.79%Forma y color:SolidPeso molecular:258.27Polyporenic acid C
CAS:Polyporenic acid C shows inhibitory activity against human collagenase.Fórmula:C31H46O4Pureza:96.84% - 99.90%Forma y color:SolidPeso molecular:482.69LM10
CAS:TDO inhibitor; IC50: human 0.62 μM, mouse 2 μM; selective over IDO, MAOs; hinders TDO+ tumor growth in mice; orally active.Fórmula:C11H8FN5Pureza:98.78% - 99.94%Forma y color:SolidPeso molecular:229.21TD52
CAS:TD52, an Erlotinib derivative, is an oral CIP2A cancer inhibitor that disrupts Elk1's attachment to the CIP2A promoter.Fórmula:C24H16N4Pureza:99.5%Forma y color:SolidPeso molecular:360.41Ganoderic acid D
CAS:Ganoderic acid D, a Ganoderma component, inhibits HeLa cell growth with an IC50 of 17.3µM after 48h.Fórmula:C30H42O7Pureza:98.06% - 99.98%Forma y color:SolidPeso molecular:514.65Siramesine
CAS:Siramesine (Lu 28-179)(Lu 28-179) is a selective sigma-2 receptor agonist, which has been shown to trigger cell death of cancer cells and to exhibit a potentFórmula:C30H31FN2OPureza:98%Forma y color:SolidPeso molecular:454.58ASP4132
CAS:ASP4132 is an orally active AMPK activator (EC50 : 18 nM), has anti-cancer activity.Fórmula:C46H51F3N6O8S2Pureza:98.34%Forma y color:SolidPeso molecular:937.06Ilexgenin A
CAS:Ilexgenin A is a novel pentacyclic triterpenoid, is a compound extracted from leaves of Ilex hainanensis MerrFórmula:C30H46O6Pureza:97.11% - 97.19%Forma y color:SolidPeso molecular:502.68Ilaprazole
CAS:<p>Ilaprazole (IY-81149) is a proton pump inhibitor used in the treatment of dyspepsia gastroesophageal reflux disease (GORD/GERD) and duodenal ulcer.</p>Fórmula:C19H18N4O2SPureza:99.91%Forma y color:SolidPeso molecular:366.44VY-3-135
CAS:<p>VY-3-135 is an orally active, stable and specific acetyl-CoA synthetase 2 (ACSS2) inhibitor.Cost-effective and quality-assured.</p>Fórmula:C26H27N3O3Pureza:99.25% - 99.79%Forma y color:SolidPeso molecular:429.51Coralyne chloride
CAS:Coralyne chloride is a protoberberine with strong anticancer activity.Fórmula:C22H22ClNO4Pureza:98.88%Forma y color:SolidPeso molecular:399.87ETP-45658
CAS:<p>ETP-45658 (ETP45658) is a PI 3-kinase inhibitor (IC50 values are 22, 30, 129 and 710 nM for PI 3-Kα, PI 3-Kδ, PI 3-Kβ and PI 3-Kγ respectively).</p>Fórmula:C16H17N5O2Pureza:99.14%Forma y color:SolidPeso molecular:311.34Ilaprazole sodium
CAS:<p>Ilaprazole sodium (IY-81149 sodium) , a substituted benzimidazole prodrug, is a selective and irreversible proton pump inhibitor.</p>Fórmula:C19H17N4NaO2SPureza:99.06%Forma y color:SolidPeso molecular:388.42Telaglenastat
CAS:Telaglenastat (CB 839) (IC50 of 24 nM), an effective, specific, and oral inhibitor, which is bioavailable glutaminase, for recombinant human GAC.Fórmula:C26H24F3N7O3SPureza:97.57% - 99.89%Forma y color:SolidPeso molecular:571.57Isoliquiritin apioside
CAS:Isoliquiritin apioside, from Glycyrrhizae radix, inhibits MMP9, MAPK, NF-κB, reduces cancer cell invasion, angiogenesis, and fights oxidative DNA damage.Fórmula:C26H30O13Pureza:98.84% - 99.27%Forma y color:SolidPeso molecular:550.51MRT-14
CAS:MRT-14 is a potent Smo antagonist and can be used in several types of cancers linked to abnormal Hh signaling studies.Fórmula:C24H24N4O5Pureza:99.54%Forma y color:SolidPeso molecular:448.47SKF-96365 hydrochloride
CAS:SKF-96365 hydrochloride (SKF96365) , a SOCE inhibitor, exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal YFórmula:C22H27ClN2O3Pureza:99.47% - 99.92%Forma y color:SolidPeso molecular:402.91HA 155
CAS:HA 155 (Autotaxin Inhibitor IV) is a boronic acid-based compound, inhibiting ATX with IC50 of 5.7 nM by selectively binding to its catalytic threonine.Fórmula:C24H19BFNO5SPureza:99.88%Forma y color:SolidPeso molecular:463.29PSB-SB-487
CAS:<p>PSB-SB-487 is antagonist of GPR55.</p>Fórmula:C26H32O4Pureza:98.53%Forma y color:SolidPeso molecular:408.53Rhamnose
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>Fórmula:C6H12O5Pureza:99.46%Forma y color:White Crystalline PowderPeso molecular:164.16OTS514
CAS:OTS514 (OTS514 Hydrochloride) is a potent TOPK inhibitor.Fórmula:C21H20N2O2SPureza:99.62%Forma y color:SolidPeso molecular:364.46Cannabigerol
CAS:Cannabigerol is a high affinity α±2-adrenergic receptor agonist, moderate affinity 5-HT1A receptor antagonist, and low affinity CB1 receptor antagonist ; alsoFórmula:C21H32O2Pureza:99.59% - 99.92%Forma y color:SolidPeso molecular:316.48FR054
CAS:FR054 inhibits PGM3, a key enzyme in the HBP, significantly reducing breast cancer cell growth and survival.Fórmula:C14H19NO8Pureza:≥98%Forma y color:SolidPeso molecular:329.3Irigenin
CAS:Irigenin mediates its antimetastatic effect by specifically and selectively blocking the α9β1 and α4β1 integrin binding sites on the C-C loop of the ExtraFórmula:C18H16O8Pureza:99.50% - 99.85%Forma y color:SolidPeso molecular:360.31NCGC00378430
CAS:<p>NCGC00378430 is a potent SIX1/EYA2 interaction inhibitor that disrupts the SIX1/EYA2 complex, EMT, and Metastasis.</p>Fórmula:C22H23N3O5SPureza:99.74%Forma y color:SolidPeso molecular:441.5Plerixafor
CAS:<p>Plerixafor (AMD-3329), a chemokine receptor antagonist, blocks the binding of stromal cell-derived factor (SDF-1alpha) to the cellular receptor CXCR4.</p>Fórmula:C28H54N8Pureza:99.17% - >99.99%Forma y color:SolidPeso molecular:502.78Astragenol
CAS:Astragenol, a precursor for astragenel derivatives, may aid in developing anti-inflammatory prostate cancer drugs.Fórmula:C30H50O5Pureza:99.5%Forma y color:SolidPeso molecular:490.71JNJ-63576253
CAS:JNJ-63576253 is a Clinical Stage Androgen Receptor Antagonist for F877L Mutant and Wild-Type Castration-Resistant Prostate Cancer (mCRPC).Fórmula:C23H22ClF3N6O2SPureza:98.71%Forma y color:SolidPeso molecular:538.97HS-1793
CAS:<p>HS-1793, resveratrol-like, reduces HIF-1, VEGF in hypoxia, and curbs human breast cancer growth in mouse model.</p>Fórmula:C16H12O3Pureza:98.16% - 99.82%Forma y color:SolidPeso molecular:252.26SU4984
CAS:<p>SU4984 is a cell-permeable, ATP-competitive and reversible inhibitor of the fibroblast growth factor receptor 1 (FGFR1).</p>Fórmula:C20H19N3O2Pureza:97.20%Forma y color:SolidPeso molecular:333.38Rasarfin
CAS:Rasarfin inhibits Ras and ARF6.Fórmula:C23H24ClN3O3Pureza:97.98%Forma y color:SolidPeso molecular:425.91Valepotriate
CAS:Valepotriates are sedative, enhance memory, have anti-cancer properties, and may reduce anxiety.Fórmula:C22H30O8Pureza:97.29% - 99.90%Forma y color:SolidPeso molecular:422.47Podophyllotoxone
CAS:<p>Podophyllotoxinone, a natural compound found in Dysosma versipellis, shows inhibitory activity against L1210 leukemia and KB cells in vitro.</p>Fórmula:C22H20O8Pureza:99.31% - 99.37%Forma y color:SolidPeso molecular:412.39Niraparib
CAS:<p>Niraparib (MK-4827) inhibits PARP1/PARP2 (IC50: 3.8/2.1 nM), effective on BRCA mutant cancers, 330x less effective on PARP3, V-PARP, Tank1.</p>Fórmula:C19H20N4OPureza:98% - 99.91%Forma y color:SolidPeso molecular:320.39FTO-IN-1
CAS:<p>UUN44923: FTO inhibitor, potential treatment for obesity, MS, T2D, Alzheimer's, various cancers.</p>Fórmula:C18H16Cl2N4O2Pureza:98.21% - 98.91%Forma y color:SolidPeso molecular:391.25Alloxazine
CAS:Alloxazine (Isoalloxazine) is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor.Fórmula:C10H6N4O2Pureza:99.75%Forma y color:SolidPeso molecular:214.18AG-270
CAS:<p>AG-270 is an allosteric and orally active inhibitor of MAT2A.</p>Fórmula:C30H27N5O2Pureza:98.28% - 98.87%Forma y color:SolidPeso molecular:489.57TL-895
CAS:<p>TL-895 is a potent, selective ATP-competitive BTK inhibitor (IC50 = 1.5 nM, Ki = 11.9 nM).</p>Fórmula:C25H26FN5O2Pureza:99.96%Forma y color:SolidPeso molecular:447.5Pellitorine
CAS:Pellitorine (Pellitorin) is an extract of Tetradium daniellii, and acts as a TRPV1 antagonist.Fórmula:C14H25NOPureza:97.54%Forma y color:Solid CrystallinePeso molecular:223.35(6R)-FR054
CAS:(6R)-FR054 is an inhibitor of the Hexosamine Biosynthetic Pathway (HBP) enzyme PGM3, with a remarkable anti-breast cancer effect.Fórmula:C14H19NO8Pureza:99.61%Forma y color:SolidPeso molecular:329.3HNHA
CAS:<p>HNHA is an inhibitor of HDAC.</p>Fórmula:C17H21NO2SPureza:98.04%Forma y color:SolidPeso molecular:303.42DOTA-NHS-ester
CAS:DOTA-NHS-ester is a linker for affibody molecules with applications in small animal PET, SPECT, and CT.Cost-effective and quality-assured.Fórmula:C20H31N5O10Pureza:99.88%Forma y color:SolidPeso molecular:501.49Toyocamycin
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:291.26TH5427
CAS:<p>TH5427 is a lead NUDT5 inhibitor(MG assay IC50 = 29 nM).</p>Fórmula:C20H20Cl2N8O3Pureza:99.54%Forma y color:SolidPeso molecular:491.33Carbidopa
CAS:<p>Carbidopa (Lodosyn) is an aromatic-L-amino-acid decarboxylase inhibitor (IC50: 29±2 μM).</p>Fórmula:C10H14N2O4Pureza:98.01% - ≥98%Forma y color:SolidPeso molecular:226.23JNJ-38158471
CAS:JNJ-38158471 (CS-2660), a highly selective, orally available, well tolerated VEGFR2 inhibitor, inhibits closely related tyrosine kinases such as Ret and Kit .Fórmula:C15H17ClN6O3Pureza:97.08%Forma y color:SolidPeso molecular:364.79Rosiglitazone
CAS:<p>Rosiglitazone (BRL49653) is a PPARγ agonist, TRPC5 activator, and TRPM3 inhibitor with oral activity.</p>Fórmula:C18H19N3O3SPureza:98.61% - 99.87%Forma y color:White To Off-White Crystalline PowderPeso molecular:357.43Cyasterone
CAS:Cyasterone (Cyasteron), a natural EGFR inhibitor, can inhibit the growth of A549 and MGC823 cells, via regulating EGFR signaling pathway, it may be a promisingFórmula:C29H44O8Pureza:99.32% - 99.70%Forma y color:SolidPeso molecular:520.65Rosiglitazone hydrochloride
CAS:Rosiglitazone hydrochloride (BRL-49653 HCl) is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.Fórmula:C18H19N3O3S·HClPureza:99.63% - 99.79%Forma y color:SolidPeso molecular:393.89Raf inhibitor 2
CAS:<p>Raf inhibitor 2 (CID 25014542) is novel inhibitor of Raf kinases.</p>Fórmula:C15H8Br2ClNO2Pureza:98.53%Forma y color:SolidPeso molecular:429.49XL177A
CAS:<p>XL177A is a selective irreversible USP7 inhibitor(IC50 : 0.34 nM). XL177A elicits cancer cell killing through a p53-dependent mechanism.</p>Fórmula:C48H57ClN8O5Pureza:98.75%Forma y color:SolidPeso molecular:861.47UNC2025
CAS:<p>UNC2025 (mrx-6313)(IC50 of 0.74 nM and 0.8 nM) is a potent and orally bioavailable dual MER/FLT3 inhibitor.</p>Fórmula:C28H40N6OPureza:99.53% - 99.74%Forma y color:SolidPeso molecular:476.66ARD-2128
CAS:<p>ARD-2128: potent oral PROTAC that degrades AR, curbing prostate cancer growth with no toxicity.</p>Fórmula:C45H50ClN7O6Pureza:98.8%Forma y color:SolidPeso molecular:820.37RBN012759
CAS:RBN012759 inhibits PARP14 protein and is more than 300-fold selective over all PARP family members.Cost-effective and quality-assured.Fórmula:C19H23FN2O3SPureza:98.87% - 99.96%Forma y color:SolidPeso molecular:378.46MTOB
CAS:MTOB, a CtBP substrate, inhibits CtBP-linked cancer activity in cells/mice and regulates TCF-4, affecting CSC proliferation.Fórmula:C5H7NaO3SPureza:98.23%Forma y color:SolidPeso molecular:170.16NVP-BVU972
CAS:<p>NVP-BVU972 is a selective and potent Met inhibitor with IC50 of 14 nM.</p>Fórmula:C20H16N6Pureza:97.24% - >99.99%Forma y color:SolidPeso molecular:340.38Methyl caffeate
CAS:<p>Methyl caffeate (Methyl caffeate acid) acid</p>Fórmula:C10H10O4Pureza:99.79% - 99.93%Forma y color:Slightly Yellowish SolidPeso molecular:194.18SC-236
CAS:SC-236 (Sc 236) is an orally active and selective inhibitor of COX-2 (IC50 of 0.005 μM and 17.8 μM for COX-2 and COX-1, respectively).Fórmula:C16H11ClF3N3O2SPureza:99.74%Forma y color:SolidPeso molecular:401.79Hepln-13
CAS:Hepln-13 is a hepsin inhibitor that acts by hindering prostate cancer bone metastasis.Fórmula:C17H13BrN2Pureza:97.67%Forma y color:SolidPeso molecular:325.2MSX-127
CAS:MSX-127 elicites positive response in peptide CXCR4.Fórmula:C16H24N2O4Pureza:98.43%Forma y color:SolidPeso molecular:308.37Indoximod
CAS:<p>Indoximod (NLG-8189) is a methylated tryptophan that inhibits IDO to boost T cell function by preventing tryptophan depletion.</p>Fórmula:C12H14N2O2Pureza:97.82% - 99.55%Forma y color:SolidPeso molecular:218.25BAZ1A-IN-1
CAS:<p>BAZ1A-IN-1, a potent inhibitor, KD 0.52 μM against BAZ1A, is effective in high-BAZ1A cancer cells, not in low-BAZ1A ones.</p>Fórmula:C16H12N4O3SPureza:99.87%Forma y color:SolidPeso molecular:340.36Fluzoparib
CAS:Fluzoparib (SHR3162) is a novel, potent, and orally available inhibitor of PARP, potentially for the treatment of solid tumours.Fórmula:C22H16F4N6O2Pureza:98.53% - 99.63%Forma y color:SolidPeso molecular:472.4Bioymifi
CAS:<p>Bioymifi (DR5 Activator), a novel TRAIL activator, binds to DR5's ECD, inducing DR5 aggregation and stimulating cell apoptosis. Cost-effective and quality-assured.</p>Fórmula:C22H12BrN3O4SPureza:98% - 99.79%Forma y color:SolidPeso molecular:494.32Eribulin mesylate
CAS:<p>Eribulin mesylate (E7389), a microtubule inhibitor, treats metastatic breast cancer by halting cell division.</p>Fórmula:C41H63NO14SPureza:97.02% - >99.99%Forma y color:SolidPeso molecular:826ARV-471
CAS:<p>ARV-471 (Vepdegestrant) is a orally active Cereblon -based estrogen receptor (ER) PROTAC degrader. ARV-471 is developed for the research of breast cancer.</p>Fórmula:C45H49N5O4Pureza:97.15% - >99.99%Forma y color:SolidPeso molecular:723.9Devimistat
CAS:<p>Devimistat (6,8-Bis(benzylthio)octanoic acid) , a lipoate analog, inhibits mitochondrial enzymes pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase</p>Fórmula:C22H28O2S2Pureza:98.06% - 99.24%Forma y color:SolidPeso molecular:388.59DIM-C-pPhOH
CAS:CDIM8 (DIM-C-pPhOH) opposes NR4A1, halts TGF-β breast cancer migration, induces ROS/ER stress, and mimics Nur77 RNAi in pancreatic cancer.Fórmula:C23H18N2OPureza:98.61%Forma y color:SolidPeso molecular:338.4Palbociclib
CAS:Palbociclib is an oral CDK4/6 inhibitor, halts Rb phosphorylation, arrests cell cycle, and curbs tumor growth.Fórmula:C24H29N7O2Pureza:98% - 99.9%Forma y color:SolidPeso molecular:447.53O6-Benzylguanine
CAS:O6-Benzylguanine is a guanine analog with antineoplastic activity,and is a potent O6-alkylguanine DNA alkyltransferase (AGT) inactivator.Fórmula:C12H11N5OPureza:98.9%Forma y color:Solid CrystallinePeso molecular:241.25Tanespimycin
CAS:Tanespimycin (KOS 953) is an Hsp90 inhibitor (IC50=5 nM) and is selective. Tanespimycin depletes intracellular STK38/NDR1. High-Quality, Low-Cost!Fórmula:C31H43N3O8Pureza:98.24% - 99.83%Forma y color:Dark Purple SolidPeso molecular:585.69Aloesin
CAS:<p>Aloesin, a C-glycosylated chromone from aloe, blocks tyrosinase (IC50=0.9mM) in melanin production.</p>Fórmula:C19H22O9Pureza:98% - 99.86%Forma y color:SolidPeso molecular:394.37Kumatakenin
CAS:<p>Kumatakenin can suppress >80% of the SOS-inducing activity of Trp-P-1 at <0.06 micromol/mL.</p>Fórmula:C17H14O6Pureza:97.44% - 98.29%Forma y color:SolidPeso molecular:314.29sulfopin
CAS:<p>Sulfopin is a highly selective covalent inhibitor of Pin1 with an apparent Ki of 17nM. Sulfopin blocks Myc-driven tumors in vivo.</p>Fórmula:C11H20ClNO3SPureza:99.53% - 99.99%Forma y color:SolidPeso molecular:281.8Se-Methylselenocysteine
CAS:Se-Methylselenocysteine (Se-MSC) is a potent chemopreventive agent in many test systems and has been shown to inhibit tumor promotion and induce apoptosis.Fórmula:C4H9NO2SePureza:99.49% - 99.87%Forma y color:White To Slightly Yellow PowderPeso molecular:182.08Bavdegalutamide
CAS:Bavdegalutamide (ARV-110) is a PROTAC degrader of androgen receptor (AR).Fórmula:C41H43ClFN9O6Pureza:97.17% - 99.04%Forma y color:SolidPeso molecular:812.29POL1-IN-1
CAS:<p>POL1-IN-1 (Compound 3A) 是一种RNA 聚合酶 1 POL1抑制剂，IC50值低于 0.5 uM。 它能有效抑制A375恶性黑色素瘤细胞系中RNA 聚合酶I 的转录。</p>Fórmula:C21H20N6Pureza:98% - 98.01%Forma y color:SolidPeso molecular:356.42Forskolin
CAS:Forskolin (Coleonol) is a natural product, an adenylate cyclase activator (EC50=0.5 μM).Fórmula:C22H34O7Pureza:98.83% - 99.96%Forma y color:Less Crystalline Solid Colorless Crystalline SolidPeso molecular:410.50SC144
CAS:<p>SC144 is an orally active small-molecule gp130 inhibitor.</p>Fórmula:C16H11FN6OPureza:99.20%Forma y color:SolidPeso molecular:322.3DCLK1-IN-1
CAS:<p>DCLK1-IN-1 is a selective, in vivo compatible chemical probe of the kinase domain of doublecortin-like kinase 1 (DCLK1).Cost-effective and quality-assured.</p>Fórmula:C26H28F3N7O2Pureza:98.55% - 99.28%Forma y color:SolidPeso molecular:527.54Niraparib tosylate
CAS:<p>Niraparib tosylate (MK-4827 (tosylate))(with IC50 of 3.8 nM/2.1 nM) is a selective PARP1/PARP2 inhibitor.</p>Fórmula:C19H20N4O·C7H8O3SPureza:99.34% - 99.87%Forma y color:SolidPeso molecular:492.59Edotreotide
CAS:Edotreotide (SMT-487) is an Indicator and Reagent. It also is used in the Diagnosis and Staging of Tumors Expressing Somatostatin Receptors.Fórmula:C65H92N14O18S2Pureza:96.95%Forma y color:SolidPeso molecular:1421.64GW779439X
CAS:GW779439X is an inhibitor of CDK.Fórmula:C22H21F3N8Pureza:97.87%Forma y color:SolidPeso molecular:454.45Acetylalkannin
CAS:<p>Acetylalkannin (Alkannin acetate), an isohexenylnaphthazarin pigment extracted from Arnebia euchroma, exhibits antimicrobial and cytotoxic properties.</p>Fórmula:C18H18O6Pureza:99.58% - 99.81%Forma y color:SolidPeso molecular:330.33LLY-507
CAS:LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.Fórmula:C36H42N6OPureza:99.58% - 99.93%Forma y color:SolidPeso molecular:574.76CCT128930 hydrochloride
CAS:<p>CCT128930 hydrochloride: Potent AKT inhibitor (IC50=6 nM), 28x selective over PKA, 20x over p70S6K, induces cell cycle arrest & DNA damage.</p>Fórmula:C18H21Cl2N5Pureza:98.55%Forma y color:SolidPeso molecular:378.3ML339
CAS:<p>ML339 a selective inhibitor of CXCR6(IC50 = 140 nM) with no response when screened against CXCR5 and CXCR4.</p>Fórmula:C26H32ClN3O5Pureza:99.9%Forma y color:SolidPeso molecular:502BMS-986242
CAS:<p>BMS-986242 is an orally active, potent and selective inhibitor of indoleamine-2,3-dioxygenase 1 (IDO1), and it can be used for the research of cancer.</p>Fórmula:C24H24ClFN2OPureza:98.9%Forma y color:SolidPeso molecular:410.91(E)-Akt inhibitor-IV
CAS:(E)-Akt inhibitor-IV ((E)-AKTIV) ((E)-AKTIV) is an inhibitor of PI3K-Akt.Fórmula:C31H29IN4SPureza:99.74% - 99.9%Forma y color:SolidPeso molecular:616.56Taletrectinib
CAS:<p>Taletrectinib (AB-106) is a new-generation selective inhibitor of ROS1/NTRK including ROS1,NTRK1,NTRK2 and NTRK3.</p>Fórmula:C29H34FN5O5Pureza:99.87% - 99.96%Forma y color:SolidPeso molecular:551.61Fursultiamine
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>Fórmula:C17H26N4O3S2Pureza:99.63% - 99.90%Forma y color:SolidPeso molecular:398.54BAY-876
CAS:BAY-876 is a selective and orally GLUT1 inhibitor. BAY-876 inhibits glycolytic metabolism and exhibits antitumor activity. Cost-effective and quality-assured.Fórmula:C24H16F4N6O2Pureza:98.61% - 99.78%Forma y color:SolidPeso molecular:496.42Xanthatin
CAS:Xanthatin exhibits cytotoxic, antibacterial, antifungal properties, may treat NSCLC, and inhibits melanoma by targeting Wnt/β-catenin and angiogenesis.Fórmula:C15H18O3Pureza:98.48% - 99.96%Forma y color:SolidPeso molecular:246.3
