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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PIK-75 hydrochloride
CAS:<p>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.</p>Fórmula:C16H14BrN5O4S·HClPureza:97.82%Forma y color:SolidPeso molecular:488.744-MMPB
CAS:<p>15-Lipoxygenase Inhibitor 1 is a selective inhibitor of 15-lipoxygenase, with an IC50 of 18 μM.</p>Fórmula:C16H19N5SPureza:97.18%Forma y color:SolidPeso molecular:313.42β-catenin-IN-2
CAS:<p>β-catenin-IN-2 is a potent inhibitor of β-catenin that can be used in colorectal cancer research.</p>Fórmula:C15H14FN3Pureza:99.93%Forma y color:SolidPeso molecular:255.29Neogambogic 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>Fórmula:C38H46O9Pureza:97.74% - 99.38%Forma y color:SolidPeso molecular:646.77L189
CAS:<p>L189 is a human DNA ligase inhibitor, inhibits hLigI/III/IV (IC50: 5/9/5 μM).</p>Fórmula:C11H10N4OSPureza:97.37%Forma y color:SolidPeso molecular:246.29Cyasterone
CAS:<p>Cyasterone (Cyasteron), a natural EGFR inhibitor, can inhibit the growth of A549 and MGC823 cells, via regulating EGFR signaling pathway, it may be a promising</p>Fórmula:C29H44O8Pureza:99.32% - 99.70%Forma y color:SolidPeso molecular:520.65SC-236
CAS:<p>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).</p>Fórmula:C16H11ClF3N3O2SPureza:99.74%Forma y color:SolidPeso molecular:401.79Bromosporine
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>Fórmula:C17H20N6O4SPureza:99.65% - 99.79%Forma y color:SolidPeso molecular:404.44NS-1619
CAS:NS1619 have cardio-protective effects after ischemia-reperfusion injury.Fórmula:C15H8F6N2O2Pureza:97.66% - 98%Forma y color:SolidPeso molecular:362.23FEN1-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:232.24Telaglenastat
CAS:<p>Telaglenastat (CB 839) (IC50 of 24 nM), an effective, specific, and oral inhibitor, which is bioavailable glutaminase, for recombinant human GAC.</p>Fórmula:C26H24F3N7O3SPureza:97.57% - 99.89%Forma y color:SolidPeso molecular:571.57KRAS 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:292.81Tazemetostat
CAS:<p>Tazemetostat (EPZ6438): Oral EZH2 inhibitor, blocks histone H3K27 methylation, potential cancer therapy.</p>Fórmula:C34H44N4O4Pureza:98.24% - ≥95%Forma y color:SolidPeso molecular:572.74Rhamnose 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:182.17MRT-14
CAS:<p>MRT-14 is a potent Smo antagonist and can be used in several types of cancers linked to abnormal Hh signaling studies.</p>Fórmula:C24H24N4O5Pureza:99.54%Forma y color:SolidPeso molecular:448.47Kumatakenin
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:314.29Isookanin
CAS:Isookanin shows strong diphenyl(2,4,6-trinitrophenyl)iminoazanium (DPPH) radical-scavenging activity with the IC50 value of 7.9 ± 0.53 μM.Fórmula:C15H12O6Pureza:99.13% - 99.45%Forma y color:SolidPeso molecular:288.25RA-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:365.34Palbociclib monohydrochloride
CAS:<p>Palbociclib monohydrochloride (PD 0332991 hydrochloride) is a selective inhibitor of CDK4/6, with no inhibition against a panel of 36 additional protein kinases</p>Fórmula:C24H29N7O2·HClPureza:99.73% - >99.99%Forma y color:SolidPeso molecular:483.99Mitoxantrone
CAS:<p>Mitoxantrone: anthracenedione antibiotic, disrupts DNA/RNA replication, binds to topoisomerase II, less cardiotoxic than doxorubicin.</p>Fórmula:C22H28N4O6Pureza:96.29% - 98.74%Forma y color:Blue PowderPeso molecular: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.Fórmula:C17H12F4N2O2SPureza:99.57%Forma y color:SolidPeso molecular:384.35RHPS4
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:458.48NVP 231
CAS:<p>NVP-231 is a potent, specific and reversible CerK inhibitor(IC50=12±2 nM) that competitively inhibits ceramide binding to CerK.</p>Fórmula:C25H25N3O2SPureza:99.16% - ≥95%Forma y color:SolidPeso molecular:431.55Theliatinib
CAS:<p>Theliatinib: potent, selective EGFR inhibitor, anti-tumor; Ki=0.05 nM (EGFR), IC50=3 nM (EGFR), 22 nM (T790M/L858R).</p>Fórmula:C25H26N6O2Pureza:99.67%Forma y color:SolidPeso molecular:442.512-(1,8-naphthyridin-2-yl)phenol
CAS:<p>2-NP is a STAT1 enhancer.</p>Fórmula:C14H10N2OPureza:99.33% - 99.82%Forma y color:SolidPeso molecular:222.24ERK-IN-3
CAS:<p>ERK-IN-3 (ASN007 free base) is a potent and orally active inhibitor of ERK.</p>Fórmula:C22H25ClFN7O2Pureza:99.55% - 99.76%Forma y color:SolidPeso molecular:473.93ZZW-115 hydrochloride
CAS:<p>ZZW-115 hydrochloride inhibits the activity of NUPR1.</p>Fórmula:C24H34Cl3F3N4SPureza:99.97%Forma y color:SolidPeso molecular:573.97L-Asparaginase
CAS:<p>L-Asparaginase, an enzyme for acute lymphoblastic leukemia treatment, is administered via injection.</p>Fórmula:NAPureza:97%Forma y color:SolidPeso molecular:N/ATJ191
CAS:<p>TJ191 is a selective anti-cancer agent, targeting low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.</p>Fórmula:C13H21NO2SPureza:99.28%Forma y color:SolidPeso molecular:255.38steviolbioside
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:642.73Bavdegalutamide
CAS:<p>Bavdegalutamide (ARV-110) is a PROTAC degrader of androgen receptor (AR).</p>Fórmula:C41H43ClFN9O6Pureza:97.17% - 99.04%Forma y color:SolidPeso molecular:812.29Boc-11-aminoundecanoic acid
CAS:<p>Boc-11-aminoundecanoic acid is an Alkyl/ether-based PROTAC linker that can be used in the synthesis of MS432.</p>Fórmula:C16H31NO4Pureza:99.64%Forma y color:SolidPeso molecular:301.42ML339
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:502(E)-Akt inhibitor-IV
CAS:<p>(E)-Akt inhibitor-IV ((E)-AKTIV) ((E)-AKTIV) is an inhibitor of PI3K-Akt.</p>Fórmula:C31H29IN4SPureza:99.74% - 99.9%Forma y color:SolidPeso molecular:616.56SC144
CAS:<p>SC144 is an orally active small-molecule gp130 inhibitor.</p>Fórmula:C16H11FN6OPureza:99.20%Forma y color:SolidPeso molecular:322.3Aloesin
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:394.37LLY-507
CAS:<p>LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.</p>Fórmula:C36H42N6OPureza:99.58% - 99.93%Forma y color:SolidPeso molecular:574.76VLX600
CAS:<p>VLX600 is an iron-chelating oxidative phosphorylation (OXPHOS) inhibitor, is a cell-permeable anticancer agent.</p>Fórmula:C17H15N7Pureza:98.62%Forma y color:SolidPeso molecular:317.35Cidofovir 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:315.22BI-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:331.35YK-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:372.18RBN012759
CAS:<p>RBN012759 inhibits PARP14 protein and is more than 300-fold selective over all PARP family members.Cost-effective and quality-assured.</p>Fórmula:C19H23FN2O3SPureza:98.87% - 99.96%Forma y color:SolidPeso molecular:378.46NSC348884
CAS:<p>NSC348884, a nucleophosmin inhibitor, disrupts oligomers, induces apoptosis, and inhibits cancer cell growth (IC50: 1.7-4.0 μM).</p>Fórmula:C38H40N10Pureza:98.69% - 99.91%Forma y color:SolidPeso molecular:636.79β-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:192.3Se-Methylselenocysteine
CAS:<p>Se-Methylselenocysteine (Se-MSC) is a potent chemopreventive agent in many test systems and has been shown to inhibit tumor promotion and induce apoptosis.</p>Fórmula:C4H9NO2SePureza:99.49% - 99.87%Forma y color:White To Slightly Yellow PowderPeso molecular:182.08Raf 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:861.47BMS-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(-)-Epigallocatechin Gallate
CAS:<p>(-)-Epigallocatechin Gallate (EGCG) is an antioxidant polyphenol flavonoid that inhibits telomerase and DNA methyltransferase.</p>Fórmula:C22H18O11Pureza:98.60% - 99.43%Forma y color:Yellow PowderPeso molecular:458.37AMTB hydrochloride
CAS:<p>AMTB HCl: Novel TRPM8 blocker, relieves pain, treats urinary issues, moderates bladder reflexes in rats.</p>Fórmula:C23H27ClN2O2SPureza:99.08%Forma y color:SolidPeso molecular:430.99Carbidopa
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:226.23TH5427
CAS:<p>TH5427 is a lead NUDT5 inhibitor(MG assay IC50 = 29 nM).</p>Fórmula:C20H20Cl2N8O3Pureza:99.54%Forma y color:SolidPeso molecular:491.33Pracinostat
CAS:<p>Pracinostat (SB939) is a novel HDAC inhibitor with improved in vivo properties compared to other HDAC inhibitors currently in Clinicalal trials, allowing oral</p>Fórmula:C20H30N4O2Pureza:99.15% - 99.67%Forma y color:SolidPeso molecular:358.48USL311
CAS:<p>USL311 blocks CXCR4/SDF-1 interaction, inhibits tumor cell growth and migration.</p>Fórmula:C24H34N6OPureza:98.46% - 99.56%Forma y color:SolidPeso molecular:422.57ML-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:324.37CID44216842
CAS:CID44216842 is a potent Cdc42-selective inhibitor with EC50: 1.0μM (WT), 1.2μM (Q61L) in GTP assay; 0.3μM (WT), 0.5μM (Q61L) in GDP assay. Use as a probe.Fórmula:C22H20BrN3O3SPureza:99.66%Forma y color:SolidPeso molecular:486.38L-Selenocystine
CAS:<p>L-Selenocystine (L-Selenocystine) can be used as a building block in biologically active selenol compounds.</p>Fórmula:C6H12N2O4Se2Pureza:99.36%Forma y color:SolidPeso molecular:334.09666-15
CAS:<p>666-15 is a selective CREB inhibitor with an IC50 of 81 nM. 666-15 can effectively inhibit the growth of breast cancer.Cost-effective and quality-assured.</p>Fórmula:C33H31Cl2N3O5Pureza:99.41% - 99.88%Forma y color:SolidPeso molecular:620.52Irigenin
CAS:<p>Irigenin mediates its antimetastatic effect by specifically and selectively blocking the α9β1 and α4β1 integrin binding sites on the C-C loop of the Extra</p>Fórmula:C18H16O8Pureza:99.50% - 99.85%Forma y color:SolidPeso molecular:360.31Coralyne chloride
CAS:<p>Coralyne chloride is a protoberberine with strong anticancer activity.</p>Fórmula:C22H22ClNO4Pureza:98.88%Forma y color:SolidPeso molecular:399.87Niraparib hydrochloride
CAS:<p>Niraparib hydrochloride (MK-4827) is a PARP inhibitor with potential cancer treatment effects, causing DNA damage and apoptosis.</p>Fórmula:C19H21ClN4OPureza:99.26%Forma y color:SolidPeso molecular:356.85Podophyllotoxone
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:412.396-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:363.36RU-301
CAS:<p>RU-301 is a novel pan-tam inhibitor</p>Fórmula:C21H19F3N4O4SPureza:98.87%Forma y color:SolidPeso molecular:480.46BMS-536924
CAS:<p>BMS-536924 (BMS 536924) is an ATP-competitive IGF-1R/IR inhibitor with IC50 of 100 nM/73 nM, modest activity for Mek, Fak, and Lck with very little activity for</p>Fórmula:C25H26ClN5O3Pureza:99.02%Forma y color:SolidPeso molecular:479.96Amsilarotene
CAS:<p>Amsilarotene (TAC101) blocks RB phosphorylation, boosts 2 CDK inhibitors, halts cell cycle, and reduces thymidylate synthase and cyclin A levels.</p>Fórmula:C20H27NO3Si2Pureza:98.05%Forma y color:SolidPeso molecular:385.6CD73-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:<p>Bindarit (AF2838) is an aryl hydrocarbon receptor (AHR) antagonist.Cost-effective and quality-assured.</p>Fórmula:C20H17ClFN3O3Pureza:99.46% - 99.85%Forma y color:SolidPeso molecular:401.82LM10
CAS:<p>TDO inhibitor; IC50: human 0.62 μM, mouse 2 μM; selective over IDO, MAOs; hinders TDO+ tumor growth in mice; orally active.</p>Fórmula:C11H8FN5Pureza:98.78% - 99.94%Forma y color:SolidPeso molecular:229.21MI-136
CAS:<p>MI-136 inhibits expression of androgen receptor (AR) target genes that DHT induced.</p>Fórmula:C23H21F3N6SPureza:98.63% - 99.12%Forma y color:SolidPeso molecular:470.51Neratinib
CAS:<p>Neratinib (HKI-272) (HKI-272) is an orally available, irreversible tyrosine kinase inhibitor for HER2 and EGFR (IC50: 59/92 nM), respectively.</p>Fórmula:C30H29ClN6O3Pureza:96.17% - 99.85%Forma y color:SolidPeso molecular:557.04DASA-58
CAS:<p>DASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.</p>Fórmula:C19H23N3O6S2Pureza:96.96% - 99.28%Forma y color:SolidPeso molecular:453.53DDO-5936
CAS:<p>DDO-5936 is a potent and specific HSP90-Cdc37 PPI inhibitor.</p>Fórmula:C25H29N5O4SPureza:99.81%Forma y color:SolidPeso molecular:495.59Syrosingopine
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:666.715'-Methylthioadenosine
CAS:<p>5'-Methylthioadenosine (Methylthioadenosine) is produced from S-adenosylmethionine and behaves as a powful inhibitory product.</p>Fórmula:C11H15N5O3SPureza:99.32% - 99.34%Forma y color:SolidPeso molecular:297.33TD52
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:360.41ARV-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:723.9GN44028
CAS:<p>GN44028 is a HIF-1 inhibitor with an IC50 of 14 nM, stopping HIF-1α activity but not mRNA or protein levels, or dimerization.</p>Fórmula:C18H15N3O2Pureza:99.52%Forma y color:SolidPeso molecular:305.33SAR-020106
CAS:SAR-020106 is a potent, ATP-competitive, and selective CHK1 inhibitor with an IC50 of 13.3 nmol/L on the isolated human enzyme.Fórmula:C19H19ClN6OPureza:97.78%Forma y color:SolidPeso molecular:382.85AS601245
CAS:<p>AS601245 is an inhibitor of the c-Jun NH2-terminal kinase (JNK), with neuroprotective properties.</p>Fórmula:C20H16N6SPureza:98% - 99.02%Forma y color:SolidPeso molecular:372.45Niraparib
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:320.39MTX-211
CAS:<p>MTX-211, an inhibitor of EGFR and PI3K, is used for the therapy of cancer and other diseases.</p>Fórmula:C20H14Cl2FN5O2SPureza:97.6% - >99.99%Forma y color:SolidPeso molecular:478.33PF-562271 hydrochloride
CAS:<p>PF-562271 hydrochloride (PF-562271 HCl) is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM, ~10-fold less potent for Pyk2 than FAK.</p>Fórmula:C21H20F3N7O3SHClPureza:97.08%Forma y color:SolidPeso molecular:543.95Ibuprofen Lysine
CAS:<p>Ibuprofen Lysine (Neoprofen) is a non-steroidal anti-inflammatory drug.</p>Fórmula:C19H32N2O4Pureza:99.26%Forma y color:CoaPeso molecular:352.47Osimertinib mesylate
CAS:<p>Osimertinib mesylate (AZD-9291 mesylate) is an EGFR third-generation inhibitor. Osimertinib mesylate has antitumor activity. Cost-effective and quality-assured.</p>Fórmula:C29H37N7O5SPureza:99.46% - >99.99%Forma y color:SolidPeso molecular:595.71Naphthol AS-E
CAS:<p>Naphthol AS-E (nAS-E) is an the KIX-KID interaction and CREB-mediated gene transcription inhibitor.</p>Fórmula:C17H12ClNO2Pureza:99.33%Forma y color:Grey Solid PowderPeso molecular:297.74Oleuropein
CAS:<p>Oleuropein is an antioxidant polyphenol isolated from olive leaf.</p>Fórmula:C25H32O13Pureza:98% - 99.95%Forma y color:Brown PowderPeso molecular:540.51GOT1 inhibitor-1
CAS:<p>GOT1 inhibitor-1 (GOT1 inhibitor 2c) is a novel, potent and non-covalent inhibitor of glutamate oxaloacetate transaminase 1 (GOT1) with an IC50 of 8.2 uM.</p>Fórmula:C19H19ClN4OPureza:99.70%Forma y color:SolidPeso molecular:354.83β-Nicotinamide mononucleotide
CAS:<p>β-nicotinamide mononucleotide (NMN) is a natural nucleotide and a key intermediate in the synthesis of coenzyme I (NAD+). Cost effective and quality assured.</p>Fórmula:C11H15N2O8PPureza:99.29% - >99.99%Forma y color:SolidPeso molecular:334.22Piribedil
CAS:Piribedil (Trivastan) is a dopamine D2 agonist, used in the treatment of Parkinson's disease.Fórmula:C16H18N4O2Pureza:99.79% - 99.82%Forma y color:SolidPeso molecular:298.34Thalidomide-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:331.28MF-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:478.46BC-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:546.66Clobenpropit dihydrobromide
CAS:<p>Clobenpropit dihydrobromide is a potent antagonist and inverse agonist of histamine H3R (histamine H3LR,pEC50 of 8.07)</p>Fórmula:C14H19Br2ClN4SPureza:99.86%Forma y color:SolidPeso molecular:470.7JMJD7-IN-1
CAS:<p>JMJD7-IN-1 (Benzoic acid, 2,4-dichloro-, 5-nitro-8-quinolinyl ester) is a potent JMJD7 inhibitor, with an IC50 of 6.62 μM.</p>Fórmula:C16H8Cl2N2O4Pureza:99.66%Forma y color:SolidPeso molecular:363.15Azido-PEG11-alcohol
CAS:<p>Azido-PEG11-alcohol is a PEG-based PROTAC linker that can be used in PROTAC synthesis.</p>Fórmula:C22H45N3O11Pureza:95.22%Forma y color:SolidPeso molecular:527.61C-7280948
CAS:<p>C-7280948 is a PRMT1 inhibitor.</p>Fórmula:C14H16N2O2SPureza:99.55% - ≥95%Forma y color:SolidPeso molecular:276.35Murrayone
CAS:<p>Murrayone from M. paniculata, a bioactive coumarin, prevents cancer metastasis and reduces ADP-induced platelet aggregation.</p>Fórmula:C15H14O4Pureza:98.01% - 98.79%Forma y color:SolidPeso molecular:258.27Cephalomannine
CAS:<p>Cephalomannine (Baccatin III) is a taxol derivative obtained from Taxus yunnanensis with antitumor activity.</p>Fórmula:C45H53NO14Pureza:98.77% - 99.75%Forma y color:SolidPeso molecular:831.9PF-9363
CAS:<p>PF-9363 (CTX-3648) is a potent and high selective KAT6A/KAT6B inhibitor. PF-9363 can be used for the research of cancer.</p>Fórmula:C20H20N4O6SPureza:99.03% - 99.7%Forma y color:SolidPeso molecular:444.46
