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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Indoximod
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:BAZ1A-IN-1, a potent inhibitor, KD 0.52 μM against BAZ1A, is effective in high-BAZ1A cancer cells, not in low-BAZ1A ones.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:472.4PIK-75
CAS:<p>PIK-75, a DNA-PK and PI3K inhibitor, suppresses DNA-PK(IC50=2 nM), p110α(IC50=5.8 nM) and p110γ(IC50=76 nM).</p>Fórmula:C16H14BrN5O4SPureza:98.52% - >99.99%Forma y color:SolidPeso molecular:452.28Eribulin 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:826RHPS4
CAS:<p>RHPS4 (RHPS 4 methosulfate) is a potent inhibitor of Telomerase at submicromolar.</p>Fórmula:C22H17F2N2·CH3O4SPureza:99.72%Forma y color:SolidPeso molecular:458.48Otenaproxesul
CAS:Otenaproxesul (ATB 346) is a novel hydrogen sulphide-releasing derivative of naproxen with markedly reduced toxicity.Fórmula:C21H19NO3SPureza:98.76% - 99.13%Forma y color:SolidPeso molecular:365.45Devimistat
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:388.59steviolbioside
CAS:<p>Steviolbioside (CCRIS-6025) is a natural sweetener, which could be a potential remedy for human breast cancer.</p>Fórmula:C32H50O13Pureza:99.59% - 99.68%Forma y color:SolidPeso molecular:642.73CD73-IN-3
CAS:<p>CD73-IN-3 (LY-3475070) is a potent CD73 inhibitor with a 28 nM IC50, being tested in advanced cancer alone or with pembrolizumab.</p>Fórmula:C15H18N4O2Pureza:99.76%Forma y color:SolidPeso molecular:286.33BAY-218
CAS:Bindarit (AF2838) is an aryl hydrocarbon receptor (AHR) antagonist.Cost-effective and quality-assured.Fórmula:C20H17ClFN3O3Pureza:99.46% - 99.85%Forma y color:SolidPeso molecular:401.82Tazemetostat
CAS:Tazemetostat (EPZ6438): Oral EZH2 inhibitor, blocks histone H3K27 methylation, potential cancer therapy.Fórmula:C34H44N4O4Pureza:98.24% - ≥95%Forma y color:SolidPeso molecular:572.74KRAS inhibitor-9
CAS: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.Fórmula:C13H9ClN2S2Pureza:99.66%Forma y color:SolidPeso molecular:292.81MI-136
CAS:MI-136 inhibits expression of androgen receptor (AR) target genes that DHT induced.Fórmula:C23H21F3N6SPureza:98.63% - 99.12%Forma y color:SolidPeso molecular:470.51Wedelolactone
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:314.25PIK-75 hydrochloride
CAS:PIK-75 hydrochloride (PIK-75 HCl) is a p110α inhibitor, isoform-specific mutants at Ser773, and potently inhibits DNA-PK with IC50 of 2 nM in cell-free assay.Fórmula:C16H14BrN5O4S·HClPureza:97.82%Forma y color:SolidPeso molecular:488.74Irigenin
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:360.31β-Elemonic Acid
CAS:β-Elemonic Acid (3-Oxotirucallenoic Acid) exhibits anti-inflammatory effects, which inhibits proliferation by inducing hypoploid cells and cell apoptosis.Fórmula:C30H46O3Pureza:99.61% - 99.8%Forma y color:SolidPeso molecular:454.68Maleimide
CAS:Maleimide surface group on nanoparticles allows simple conjugation with peptides via click chemistry, preserving biofunctions.Fórmula:C4H3NO2Pureza:99.29%Forma y color:Slight Yellow Crystalline PowderPeso molecular:97.07D-Tagatose
CAS:<p>D-Tagatose, a rare hexoketose and isomer of d-galactose, is naturally found in Sterculia setigera gum and various dairy products.</p>Fórmula:C6H12O6Pureza:99.78% - 99.96%Forma y color:White Crystalline PowderPeso molecular:180.16Rhamnose monohydrate
CAS:<p>Rhamnose monohydrate (L-(+)-Rhamnose Monohydrate) is a naturally-occurring deoxy sugar that is found primarily in plants and some bacteria.</p>Fórmula:C6H12O5·H2OPureza:99.74%Forma y color:White Crystalline Powder One Of The Rarer SugarsPeso molecular:182.17(-)-Epipodophyllotoxin
CAS:(-)-Epipodophyllotoxin: anticancer, GI50=0.36μM (HeLa), 0.24μM (MCF-7), inhibits spindle assembly.Fórmula:C22H22O8Pureza:99.72% - 99.97%Forma y color:SolidPeso molecular:414.41Carbidopa monohydrate
CAS:<p>Carbidopa monohydrate (S(-)-Carbidopa) is an inhibitor of DOPA decarboxylase, preventing the conversion of levodopa to dopamine.</p>Fórmula:C10H16N2O5Pureza:98.11% - 98.30%Forma y color:SolidPeso molecular:244.24OTS514 hydrochloride
CAS:OTS514 hydrochloride is a highly effective TOPK(T-LAK cell-originated protein kinase) inhibitor (IC50: 2.6 nM).Fórmula:C21H20N2O2S·HClPureza:99.67% - 99.84%Forma y color:SolidPeso molecular:400.92Thalidomide-5-NH2-CH2-COOH
CAS:Thalidomide derivative compound 114 inhibits protomyosin receptor kinase, targets E3 ligase, potential for disease research.Fórmula:C15H13N3O6Pureza:95.95%Forma y color:SolidPeso molecular:331.28Podophyllotoxone
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:412.39(S)-Indoximod
CAS:(S)-Indoximod (L-Abrine) is an indoleamine-2,3-dioxygenase (IDO) inhibitor for cancer research.Fórmula:C12H14N2O2Pureza:95.39%Forma y color:SolidPeso molecular:218.25Tetramethylcurcumin
CAS:Tetramethylcurcumin is a novel curcumin analog, is an effective inhibitors of STAT3 phosphorylation, DNA binding activity, and transactivation in vitro.it alsoFórmula:C25H28O6Pureza:97.69% - 99.94%Forma y color:SolidPeso molecular:424.49Niraparib
CAS: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.Fórmula:C19H20N4OPureza:98% - 99.91%Forma y color:SolidPeso molecular:320.39Neratinib
CAS:Neratinib (HKI-272) (HKI-272) is an orally available, irreversible tyrosine kinase inhibitor for HER2 and EGFR (IC50: 59/92 nM), respectively.Fórmula:C30H29ClN6O3Pureza:96.17% - 99.85%Forma y color:SolidPeso molecular:557.04Juglanin
CAS:Juglanin is a JNK activator. Juglanin with inflammation and anti-tumor activities. It can induce apoptosis and autophagy on human breast cancer cells.Fórmula:C20H18O10Pureza:98.8% - 99.33%Forma y color:SolidPeso molecular:418.35Enzalutamide carboxylic acid
CAS:<p>Enzalutamide carboxylic acid is an antagonist of androgen receptor (AR) .</p>Fórmula:C20H13F4N3O3SPureza:97.88%Forma y color:SolidPeso molecular:451.39DASA-58
CAS:DASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.Fórmula:C19H23N3O6S2Pureza:96.96% - 99.28%Forma y color:SolidPeso molecular:453.53FEN1-IN-4
CAS:<p>FEN1-IN-4 (FEN1 Inhibitor C2) is an inhibitor of human flap endonuclease-1 (hFEN1)</p>Fórmula:C12H12N2O3Pureza:98.24%Forma y color:SolidPeso molecular:232.24NS-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:666.71Cidofovir
CAS:Cidofovir ((S)-HPMPC) 通过特异性抑制病毒 DNA 合成来抑制病毒复制。Fórmula:C8H14N3O6PPureza:99.24% - 99.76%Forma y color:Fluffy White PowderPeso molecular:279.19TH5427
CAS:<p>TH5427 is a lead NUDT5 inhibitor(MG assay IC50 = 29 nM).</p>Fórmula:C20H20Cl2N8O3Pureza:99.54%Forma y color:SolidPeso molecular:491.33MF-766
CAS:<p>MF-766: potent, selective oral EP4 antagonist, Ki=0.23 nM, IC50=1.4 nM; shifts to 1.8 nM with 10% HS. Useful in cancer, inflammation studies.</p>Fórmula:C27H21F3N2O3Pureza:99.54% - 99.59%Forma y color:SolidPeso molecular:478.46Carbidopa
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:226.23Vactosertib
CAS:Vactosertib (EW-7197) is an oral TGFBR1/ALK5 inhibitor with potential cancer-fighting properties.Fórmula:C22H18FN7Pureza:98.85% - 99.81%Forma y color:SolidPeso molecular:399.42HM03
CAS:HM03 is a potent and selective inhibitor of HSPA5, and has anticancer activity.Fórmula:C26H27ClN4O2Pureza:97.15%Forma y color:SolidPeso molecular:462.97Raf 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:429.49MK-2206 dihydrochloride
CAS:MK-2206 dihydrochloride (MK-2206 2HCl) is a variant Akt inhibitor that inhibits Akt1, Akt2, and Akt3 (IC50=8/12/65 nM) with orally active, highly potent andFórmula:C25H23Cl2N5OPureza:99.228% - 99.94%Forma y color:SolidPeso molecular:480.39Solamargine
CAS:Solamargine, a steroidal alkaloid from Solanum nigrum, inhibits cancer cell growth and induces apoptosis.Fórmula:C45H73NO15Pureza:99.17% - 99.96%Forma y color:SolidPeso molecular:868.06(S)-Sunvozertinib
CAS:(S)-Sunvozertinib (DZD9008) is a rationally designed selective, irreversible EGFR/HER2 inhibitor.Fórmula:C29H35ClFN7O3Pureza:99.64%Forma y color:SolidPeso molecular:584.08BC-DXI-843
CAS:<p>BC-DXI-843 is inhibitor of AIMP2-DX2, and is potential for development of novel therapeutics targeting AIMP2-DX2 in lung cancer.</p>Fórmula:C28H26N4O4S2Pureza:98.85%Forma y color:SolidPeso molecular:546.66XL177A
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:861.47NG 52
CAS:NG 52 (NG-52) is a cell-permeable, reversible, and ATP-compatible inhibitor of the cell cycle-regulating kinase Cdc28p and the related Pho85p kinase.Fórmula:C16H19ClN6OPureza:98% - 99.34%Forma y color:SolidPeso molecular:346.81RBN012759
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:378.46Tanespimycin
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:585.69Clobenpropit dihydrobromide
CAS:Clobenpropit dihydrobromide is a potent antagonist and inverse agonist of histamine H3R (histamine H3LR,pEC50 of 8.07)Fórmula:C14H19Br2ClN4SPureza:99.86%Forma y color:SolidPeso molecular:470.7sulfopin
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:281.8Obatoclax 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, andFórmula:C20H19N3O·CH4O3SPureza:99.58% - 99.88%Forma y color:SolidPeso molecular: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>Fórmula:C18H18N2S·HBrPureza:98.62% - 99.91%Forma y color:SolidPeso molecular:375.33Ilaprazole
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:429.51Forskolin
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:410.50(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.Fórmula:C23H24N4OPureza:97.75% - 99.92%Forma y color:SolidPeso molecular:372.46Niraparib 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:492.59ETP-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:388.42GW779439X
CAS:GW779439X is an inhibitor of CDK.Fórmula:C22H21F3N8Pureza:97.87%Forma y color:SolidPeso molecular:454.45Obtusifolin
CAS:Obtusifolin is an antioxidant that combats diabetes, bone-resorption, diabetic retinopathy, pain, and cognitive decline.Fórmula:C16H12O5Pureza:99.78% - 99.99%Forma y color:SolidPeso molecular:284.26Telaglenastat
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:571.57MRT-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:448.47Isoliquiritin 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:550.51SKF-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:402.91YK-3-237
CAS:YK-3-237 (B-[2-Methoxy-5-[(1E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propen-1-yl]phenyl]boronic acid) reduces acetylation of mtp53 and exhibits anti-proliferativeFórmula:C19H21BO7Pureza:99.47%Forma y color:SolidPeso molecular:372.18HA 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:463.29PI3K-IN-1
CAS:PI3K-IN-1 (Voxtalisib Analogue) is a dual inhibitor of mTOR/PI3K, mostly for p110γ , also inhibits DNA-PK and mTOR.Fórmula:C31H29N5O6SPureza:97.03% - 98%Forma y color:SolidPeso molecular:599.66BAY-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:496.42L-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:672.85PSB-SB-487
CAS:<p>PSB-SB-487 is antagonist of GPR55.</p>Fórmula:C26H32O4Pureza:98.53%Forma y color:SolidPeso molecular:408.53Phellodendrine chloride
CAS:Phellodendrine chloride combats kidney inflammation by blocking macrophage and T cell activity in glomeruli.Fórmula:C20H24ClNO4Pureza:98.85% - 99.05%Forma y color:SolidPeso molecular:377.86Rhapontin
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:420.41Cidofovir dihydrate
CAS:<p>Cidofovir dihydrate: Injectable anti-CMV; suppresses CMV by inhibiting viral DNA polymerase; treats CMV retinitis in AIDS.</p>Fórmula:C8H18N3O8PPureza:99.44%Forma y color:SolidPeso molecular:315.22Plerixafor
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:502.78SU4984
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:333.38BI-6015
CAS:<p>BI 6015 is an antagonist of HNF4α. HNF4α is a nuclear receptor that regulates gene expression in the intestine cells, liver cells, and pancreas-β cells.</p>Fórmula:C15H13N3O4SPureza:99.81%Forma y color:SolidPeso molecular:331.35JNJ-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:252.26Rasarfin
CAS:Rasarfin inhibits Ras and ARF6.Fórmula:C23H24ClN3O3Pureza:97.98%Forma y color:SolidPeso molecular:425.91SP-141
CAS:<p>SP 141 is a MDM2 inhibitor.SP-141 promotes MDM2 auto-ubiquitination and degradation, with anticancer activity.</p>Fórmula:C22H16N2OPureza:98.01%Forma y color:SolidPeso molecular:324.38PU-H54
CAS:<p>PU-H54 is a purine-derived Grp94 inhibitor targeting the S2 subpocket's unique binding region.</p>Fórmula:C18H19N5SPureza:99.13%Forma y color:SolidPeso molecular:337.44FTO-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:391.25Ganoderic 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:514.65Alloxazine
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:214.18Raddeanin A
CAS:<p>Raddeanin A is a natural triterpenoid saponin from Cyperus japonicus that inhibits histone deacetylase.Cost-effective and quality-assured.</p>Fórmula:C47H76O16Pureza:98% - 99.94%Forma y color:SolidPeso molecular:897.1ML-031
CAS:ML-031 activated S1P2 with an EC50 value of 1 μM in an S1P reporter assay.Fórmula:C19H20N2O3Pureza:99.21%Forma y color:SolidPeso molecular:324.37NSC348884
CAS:NSC348884, a nucleophosmin inhibitor, disrupts oligomers, induces apoptosis, and inhibits cancer cell growth (IC50: 1.7-4.0 μM).Fórmula:C38H40N10Pureza:98.69% - 99.91%Forma y color:SolidPeso molecular:636.79AZ9482
CAS:AZ9482, a potent PARP inhibitor with 2-piperazinyl-3-cyano-pyridine linkage, causes centrosome declustering in HeLa cells with an EC50 < 18 nM.Fórmula:C26H22N6O2Pureza:99.18% - 99.86%Forma y color:SolidPeso molecular:450.49ASP4132
CAS:ASP4132 is an orally active AMPK activator (EC50 : 18 nM), has anti-cancer activity.Fórmula:C46H51F3N6O8S2Pureza:98.34%Forma y color:SolidPeso molecular:937.06AG-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:489.57β-Damascone
CAS:<p>β-Damascone are a series of closely related chemical compounds that are components of a variety of essential oils.</p>Fórmula:C13H20OPureza:97.50%Forma y color:Colourless LiquidPeso molecular:192.3Cyasterone
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:520.65PD184161
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].Fórmula:C17H13BrClF2IN2O2Pureza:99.40%Forma y color:SolidPeso molecular:557.56Aloesin
CAS:Aloesin, a C-glycosylated chromone from aloe, blocks tyrosinase (IC50=0.9mM) in melanin production.Fórmula:C19H22O9Pureza:98% - 99.86%Forma y color:SolidPeso molecular:394.37
