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.
3606 produits trouvés pour "Anticorps pour la recherche sur le cancer"
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USL311
CAS :<p>USL311 blocks CXCR4/SDF-1 interaction, inhibits tumor cell growth and migration.</p>Formule :C24H34N6ODegré de pureté :98.46% - 99.56%Couleur et forme :SolidMasse moléculaire :422.57PIK-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>Formule :C16H14BrN5O4S·HClDegré de pureté :97.82%Couleur et forme :SolidMasse moléculaire :488.74Se-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>Formule :C4H9NO2SeDegré de pureté :99.49% - 99.87%Couleur et forme :White To Slightly Yellow PowderMasse moléculaire :182.08RBN012759
CAS :<p>RBN012759 inhibits PARP14 protein and is more than 300-fold selective over all PARP family members.Cost-effective and quality-assured.</p>Formule :C19H23FN2O3SDegré de pureté :98.87% - 99.96%Couleur et forme :SolidMasse moléculaire :378.46NSC348884
CAS :<p>NSC348884, a nucleophosmin inhibitor, disrupts oligomers, induces apoptosis, and inhibits cancer cell growth (IC50: 1.7-4.0 μM).</p>Formule :C38H40N10Degré de pureté :98.69% - 99.91%Couleur et forme :SolidMasse moléculaire :636.79XL177A
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 :861.47Carbidopa
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 :226.23TH5427
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 :491.33Hepln-13
CAS :<p>Hepln-13 is a hepsin inhibitor that acts by hindering prostate cancer bone metastasis.</p>Formule :C17H13BrN2Degré de pureté :97.67%Couleur et forme :SolidMasse moléculaire :325.2SC144
CAS :<p>SC144 is an orally active small-molecule gp130 inhibitor.</p>Formule :C16H11FN6ODegré de pureté :99.20%Couleur et forme :SolidMasse moléculaire :322.3LM10
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>Formule :C11H8FN5Degré de pureté :98.78% - 99.94%Couleur et forme :SolidMasse moléculaire :229.216-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>Formule :C21H17NO5Degré de pureté :99.32% - 99.81%Couleur et forme :SolidMasse moléculaire :363.36Niraparib
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>Formule :C19H20N4ODegré de pureté :98% - 99.91%Couleur et forme :SolidMasse moléculaire :320.39Cephalomannine
CAS :<p>Cephalomannine (Baccatin III) is a taxol derivative obtained from Taxus yunnanensis with antitumor activity.</p>Formule :C45H53NO14Degré de pureté :98.77% - 99.75%Couleur et forme :SolidMasse moléculaire :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>Formule :C20H20N4O6SDegré de pureté :99.03% - 99.7%Couleur et forme :SolidMasse moléculaire :444.46YL-109
CAS :<p>YL-109, a novel anticancer agent, can inhibit breast Y cell growth and invasiveness in vitro and in vivo.</p>Formule :C14H11NO2SDegré de pureté :99.77% - ≥95%Couleur et forme :SolidMasse moléculaire :257.31Schisandrin C
CAS :<p>Schisandrin C (Wuweizisu-C) is a phytochemical lignan isolated from Schizandra chinensis Baill; shows anticancer-effects in human leukemia U937 cells.</p>Formule :C22H24O6Degré de pureté :99.44% - 99.56%Couleur et forme :SolidMasse moléculaire :384.42NF-κB-IN-1
CAS :<p>NF-κB-IN-1 (1,6-Heptadiene-3,5-dione, 1,7-bis(3,4-dimethoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methylene]-, (1E,6E)-) is a potent NF-κB signaling pathway</p>Formule :C31H30O8Degré de pureté :99.03%Couleur et forme :SolidMasse moléculaire :530.57Physcion 8-O-β-D-glucopyranoside
CAS :<p>Physcion 8-O-β-D-glucopyranoside (Physcion 8-O-beta-D-monoglucoside) has anti-inflammatory and anti-cancer activities.</p>Formule :C22H22O10Degré de pureté :99.8%Couleur et forme :SolidMasse moléculaire :446.4PHPS1
CAS :<p>PHPS1 blocks Shp2, halts Shp2-E76K-induced Erk1/2 activation, and stops tumor cell growth.</p>Formule :C21H15N5O6SDegré de pureté :99.08%Couleur et forme :SolidMasse moléculaire :465.44TAK-960
CAS :<p>TAK-960 is an orally bioavailable, selective inhibitor of Plks with IC50 values of 0.8, 16.9, and 50.2 nM for Plk1, Plk2, and Plk3, respectively.</p>Formule :C27H34F3N7O3Degré de pureté :97.06%Couleur et forme :SolidMasse moléculaire :561.6Polyporenic acid C
CAS :<p>Polyporenic acid C shows inhibitory activity against human collagenase.</p>Formule :C31H46O4Degré de pureté :96.84% - 99.71%Couleur et forme :SolidMasse moléculaire :482.69Elesclomol
CAS :<p>Elesclomol (STA-4783) is an oxidative stress inducer and a highly lipophilic copper ion carrier.</p>Formule :C19H20N4O2S2Degré de pureté :97.17% - 99.51%Couleur et forme :SolidMasse moléculaire :400.52GW779439X
CAS :<p>GW779439X is an inhibitor of CDK.</p>Formule :C22H21F3N8Degré de pureté :97.87%Couleur et forme :SolidMasse moléculaire :454.45Osimertinib 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>Formule :C29H37N7O5SDegré de pureté :99.46% - >99.99%Couleur et forme :SolidMasse moléculaire :595.71Bromosporine
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 :404.44sulfopin
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>Formule :C11H20ClNO3SDegré de pureté :99.53% - 99.99%Couleur et forme :SolidMasse moléculaire :281.8NAE-IN-M22
CAS :<p>NAE-IN-M22: Selective, potent NEDD8 enzyme inhibitor; blocks cancer cell growth; induces apoptosis in A549 cells; effective in vivo.</p>Formule :C20H24Cl2N2Degré de pureté :97.65%Couleur et forme :SolidMasse moléculaire :363.32Eniluracil
CAS :<p>Eniluracil (GW776C85), oral DPD inhibitor, boosts 5-FU bioavailability to 100%, ensures even absorption & predictable toxicity.</p>Formule :C6H4N2O2Degré de pureté :99.91%Couleur et forme :SolidMasse moléculaire :136.11Cidofovir
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>Formule :C8H14N3O6PDegré de pureté :99.24% - 99.76%Couleur et forme :Fluffy White PowderMasse moléculaire :279.19HNHA
CAS :<p>HNHA is an inhibitor of HDAC.</p>Formule :C17H21NO2SDegré de pureté :98.04%Couleur et forme :SolidMasse moléculaire :303.42MK-2206 dihydrochloride
CAS :<p>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 and</p>Formule :C25H23Cl2N5ODegré de pureté :99.228% - 99.94%Couleur et forme :SolidMasse moléculaire :480.39Aloesin
CAS :<p>Aloesin, a C-glycosylated chromone from aloe, blocks tyrosinase (IC50=0.9mM) in melanin production.</p>Formule :C19H22O9Degré de pureté :98% - 99.86%Couleur et forme :SolidMasse moléculaire :394.37β-Damascone
CAS :<p>β-Damascone are a series of closely related chemical compounds that are components of a variety of essential oils.</p>Formule :C13H20ODegré de pureté :97.50%Couleur et forme :Colourless LiquidMasse moléculaire :192.3NCGC00378430
CAS :<p>NCGC00378430 is a potent SIX1/EYA2 interaction inhibitor that disrupts the SIX1/EYA2 complex, EMT, and Metastasis.</p>Formule :C22H23N3O5SDegré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :441.5OTS514
CAS :<p>OTS514 (OTS514 Hydrochloride) is a potent TOPK inhibitor.</p>Formule :C21H20N2O2SDegré de pureté :99.62%Couleur et forme :SolidMasse moléculaire :364.46Polyclonal Rabbit Anti Glutathione-S-transferase (GST) Affinity Purified
<p>Polyclonal Rabbit Anti Glutathione-S-transferase (GST) Affinity Purified</p>Astragenol
CAS :<p>Astragenol, a precursor for astragenel derivatives, may aid in developing anti-inflammatory prostate cancer drugs.</p>Formule :C30H50O5Degré de pureté :99.5%Couleur et forme :SolidMasse moléculaire :490.71Solamargine
CAS :<p>Solamargine, a steroidal alkaloid from Solanum nigrum, inhibits cancer cell growth and induces apoptosis.</p>Formule :C45H73NO15Degré de pureté :99.17% - 99.96%Couleur et forme :SolidMasse moléculaire :868.06α-Linolenic acid
CAS :<p>α-Linolenic Acid (ALA) is an essential fatty acid. α-Linolenic acid improves memory, inhibits thrombosis, and lowers blood lipids. Cost-effective and quality-assured.</p>Formule :C18H30O2Degré de pureté :97.05% - 99.81%Couleur et forme :Physical Description Clear Colorless Liquid (Ntp 1992)Masse moléculaire :278.43VLX600
CAS :<p>VLX600 is an iron-chelating oxidative phosphorylation (OXPHOS) inhibitor, is a cell-permeable anticancer agent.</p>Formule :C17H15N7Degré de pureté :98.62%Couleur et forme :SolidMasse moléculaire :317.35Takinib
CAS :<p>Takinib (EDHS-206) is a specific and effective TAK1 inhibitor(IC50= 9.5 nM).</p>Formule :C18H18N4O2Degré de pureté :98.29% - 99.35%Couleur et forme :SolidMasse moléculaire :322.36Enzalutamide carboxylic acid
CAS :<p>Enzalutamide carboxylic acid is an antagonist of androgen receptor (AR) .</p>Formule :C20H13F4N3O3SDegré de pureté :97.88%Couleur et forme :SolidMasse moléculaire :451.39Ketorolac
CAS :<p>Ketorolac (Acuvail) is an NSAID that blocks prostaglandin synthesis, related to heterocyclic acetic acids.</p>Formule :C15H13NO3Degré de pureté :99.68%Couleur et forme :White Crystalline Or White PowderMasse moléculaire :255.27O6-Benzylguanine
CAS :<p>O6-Benzylguanine is a guanine analog with antineoplastic activity,and is a potent O6-alkylguanine DNA alkyltransferase (AGT) inactivator.</p>Formule :C12H11N5ODegré de pureté :98.9%Couleur et forme :Solid CrystallineMasse moléculaire :241.25Juglanin
CAS :<p>Juglanin is a JNK activator. Juglanin with inflammation and anti-tumor activities. It can induce apoptosis and autophagy on human breast cancer cells.</p>Formule :C20H18O10Degré de pureté :98.8% - 99.33%Couleur et forme :SolidMasse moléculaire :418.35Cyasterone
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>Formule :C29H44O8Degré de pureté :99.32% - 99.70%Couleur et forme :SolidMasse moléculaire :520.65BMS-265246
CAS :<p>BMS-265246 is a potent and selective CDK1/2 inhibitor.</p>Formule :C18H17F2N3O2Degré de pureté :99.25% - 99.57%Couleur et forme :SolidMasse moléculaire :345.34Clobenpropit dihydrobromide
CAS :<p>Clobenpropit dihydrobromide is a potent antagonist and inverse agonist of histamine H3R (histamine H3LR,pEC50 of 8.07)</p>Formule :C14H19Br2ClN4SDegré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :470.7BSJ-4-116
CAS :<p>BSJ-4-116: potent, selective CDK12 PROTAC, IC50 = 6 nM; downregulates DDR genes, induces premature transcription termination.</p>Formule :C40H49ClN8O8SDegré de pureté :99.09%Couleur et forme :SolidMasse moléculaire :837.38Maleimide
CAS :<p>Maleimide surface group on nanoparticles allows simple conjugation with peptides via click chemistry, preserving biofunctions.</p>Formule :C4H3NO2Degré de pureté :99.29%Couleur et forme :Slight Yellow Crystalline PowderMasse moléculaire :97.07Podophyllotoxone
CAS :<p>Podophyllotoxinone, a natural compound found in Dysosma versipellis, shows inhibitory activity against L1210 leukemia and KB cells in vitro.</p>Formule :C22H20O8Degré de pureté :99.31% - 99.37%Couleur et forme :SolidMasse moléculaire :412.39Fursultiamine
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 :<p>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.</p>Formule :C27H20ClFN4O4Degré de pureté :98.31% - >99.99%Couleur et forme :SolidMasse moléculaire :518.92Coralyne chloride
CAS :<p>Coralyne chloride is a protoberberine with strong anticancer activity.</p>Formule :C22H22ClNO4Degré de pureté :98.88%Couleur et forme :SolidMasse moléculaire :399.87UC2288
CAS :<p>UC2288, a Sorafenib-based p21 attenuator, reduces p21 levels without affecting its stability.</p>Formule :C20H18ClF6N3O2Degré de pureté :99.75%Couleur et forme :SolidMasse moléculaire :481.82G5-7
CAS :<p>G5-7 is an oral JAK2 inhibitor targeting EGFR/STAT3 phosphorylation with potential for glioma research.</p>Formule :C22H19F2NO3Degré de pureté :97.3%Couleur et forme :SolidMasse moléculaire :383.39MMP-9-IN-1
CAS :<p>MMP-9-IN-1 is an inhibitor of specific matrix metalloproteinase-9 (MMP-9).</p>Formule :C16H17F2N3O3SDegré de pureté :99.21% - 99.86%Couleur et forme :SolidMasse moléculaire :369.39666-15
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>Formule :C33H31Cl2N3O5Degré de pureté :99.41% - 99.88%Couleur et forme :SolidMasse moléculaire :620.52NVP 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>Formule :C25H25N3O2SDegré de pureté :99.16% - ≥95%Couleur et forme :SolidMasse moléculaire :431.55MRT-10
CAS :<p>MRT-10 is a Smoothened (Smo) receptor antagonist.</p>Formule :C24H23N3O5SDegré de pureté :99.73%Couleur et forme :SolidMasse moléculaire :465.52Cyclo(-RGDfK) TFA
CAS :<p>Cyclo(-RGDfK) is a selective αvβ3 integrin inhibitor(IC50 : 0.94 nM).</p>Formule :C29H42F3N9O9Degré de pureté :98.99% - 99.54%Couleur et forme :SolidMasse moléculaire :717.69LLY-507
CAS :<p>LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.</p>Formule :C36H42N6ODegré de pureté :99.58% - 99.93%Couleur et forme :SolidMasse moléculaire :574.76SC-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>Formule :C16H11ClF3N3O2SDegré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :401.79Alflutinib 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 :664.7AG-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 :315.75Galloflavin
CAS :<p>Galloflavin is a lactate dehydrogenase inhibitor. Galloflavin inhibits both human LDH isoforms (type A and type B).Cost-effective and quality-assured.</p>Formule :C12H6O8Degré de pureté :96.24% - 97.47%Couleur et forme :SolidMasse moléculaire :278.17WRG-28
CAS :<p>WRG-28 is a potent and selective, allosteric discoidin domain receptor 2 (ddr2) inhibitor(IC50 : 230 nM)</p>Formule :C21H18N2O5SDegré de pureté :97.21%Couleur et forme :SolidMasse moléculaire :410.44ARV-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>Formule :C45H49N5O4Degré de pureté :97.15% - >99.99%Couleur et forme :SolidMasse moléculaire :723.9Nirogacestat
CAS :<p>Nirogacestat (PF 03084014) is a specific γ-secretase inhibitor (IC50: 6.2 nM, in a cell-free assay).</p>Formule :C27H41F2N5ODegré de pureté :97.98% - 99.63%Couleur et forme :SolidMasse moléculaire :489.64Palbociclib Isethionate
CAS :<p>Palbociclib Isethionate (PD 0332991 isethionate) 是一种高选择性的CDK4/6抑制剂，IC50为11 nM 和16 nM。它对一组 36 种额外的蛋白激酶没有抑制作用。</p>Formule :C24H29N7O2·C2H6O4SDegré de pureté :99.01% - 99.27%Couleur et forme :SolidMasse moléculaire :573.66NU6027
CAS :<p>NU6027 is a potent ATR/CDK inhibitor, inhibits CDK1/2, ATR and DNA-PK with Ki of 2.5 μM/1.3 μM, 0.4 μM and 2.2 μM, enter cells more readily than the 6-</p>Formule :C11H17N5O2Degré de pureté :98.36%Couleur et forme :SolidMasse moléculaire :251.29ML339
CAS :<p>ML339 a selective inhibitor of CXCR6(IC50 = 140 nM) with no response when screened against CXCR5 and CXCR4.</p>Formule :C26H32ClN3O5Degré de pureté :99.9%Couleur et forme :SolidMasse moléculaire :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>Formule :C24H24ClFN2ODegré de pureté :98.9%Couleur et forme :SolidMasse moléculaire :410.91TJ191
CAS :<p>TJ191 is a selective anti-cancer agent, targeting low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.</p>Formule :C13H21NO2SDegré de pureté :99.28%Couleur et forme :SolidMasse moléculaire :255.38Leptomycin B
CAS :<p>Leptomycin B: potent CRM1 inhibitor, blocks protein nuclear export and cell cycle, antifungal, modifies cysteine.</p>Formule :C33H48O6Degré de pureté :97.10% - 99.04%Couleur et forme :White Crystalline SolidMasse moléculaire :540.73KA2507
CAS :<p>KA2507 is a potent and selective HDAC6 inibitor with an IC50 of 2.5nM.</p>Formule :C16H14N6O2Degré de pureté :99.03%Couleur et forme :SolidMasse moléculaire :322.32PF-562271
CAS :<p>PF-562271 is an effective ATP-competitive, reversible inhibitor of FAK(IC50=1.5 nM) and Pyk2 kinase(IC50=13 nM).</p>Formule :C21H20F3N7O3SDegré de pureté :97.17% - >99.99%Couleur et forme :SolidMasse moléculaire :507.49(E)-Akt inhibitor-IV
CAS :<p>(E)-Akt inhibitor-IV ((E)-AKTIV) ((E)-AKTIV) is an inhibitor of PI3K-Akt.</p>Formule :C31H29IN4SDegré de pureté :99.74% - 99.9%Couleur et forme :SolidMasse moléculaire :616.56GN44028
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>Formule :C18H15N3O2Degré de pureté :99.52%Couleur et forme :SolidMasse moléculaire :305.33Carbidopa monohydrate
CAS :<p>Carbidopa monohydrate (S(-)-Carbidopa) is an inhibitor of DOPA decarboxylase, preventing the conversion of levodopa to dopamine.</p>Formule :C10H16N2O5Degré de pureté :98.11% - 98.30%Couleur et forme :SolidMasse moléculaire :244.24POL1-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>Formule :C21H20N6Degré de pureté :98% - 98.01%Couleur et forme :SolidMasse moléculaire :356.42Edotreotide
CAS :<p>Edotreotide (SMT-487) is an Indicator and Reagent. It also is used in the Diagnosis and Staging of Tumors Expressing Somatostatin Receptors.</p>Formule :C65H92N14O18S2Degré de pureté :96.95%Couleur et forme :SolidMasse moléculaire :1421.64L189
CAS :<p>L189 is a human DNA ligase inhibitor, inhibits hLigI/III/IV (IC50: 5/9/5 μM).</p>Formule :C11H10N4OSDegré de pureté :97.37%Couleur et forme :SolidMasse moléculaire :246.29Palbociclib
CAS :<p>Palbociclib is an oral CDK4/6 inhibitor, halts Rb phosphorylation, arrests cell cycle, and curbs tumor growth.</p>Formule :C24H29N7O2Degré de pureté :98% - 99.9%Couleur et forme :SolidMasse moléculaire :447.53LYN-1604
CAS :<p>LYN-1604 is a novel activator of ULK1, inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.</p>Formule :C33H43Cl2N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :584.62Paederosidic acid
CAS :<p>Paederosidic acid shows anti-tumor, anticonvulsant, and sedative properties, may treat epilepsy by modulating brain GABA and glutamate levels.</p>Formule :C18H24O12SDegré de pureté :98% - 99.56%Couleur et forme :SolidMasse moléculaire :464.44CLP-3094
CAS :<p>CLP-3094 (2-([2-(4-CHLOROPHENOXY)ETHYL]THIO)-1H-BE) is a potent androgen receptor BF3 (binding function 3) inhibitor.</p>Formule :C15H13ClN2OSDegré de pureté :99.84%Couleur et forme :SolidMasse moléculaire :304.79D-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>Formule :C6H12O6Degré de pureté :99.78% - 99.96%Couleur et forme :White Crystalline PowderMasse moléculaire :180.16Niraparib hydrochloride
CAS :<p>Niraparib hydrochloride (MK-4827) is a PARP inhibitor with potential cancer treatment effects, causing DNA damage and apoptosis.</p>Formule :C19H21ClN4ODegré de pureté :99.26%Couleur et forme :SolidMasse moléculaire :356.85(E/Z)-GO289
CAS :<p>(E/Z)-GO289, which strongly lengthened circadian period, is a potent and selective inhibitor of CK2.</p>Formule :C17H15BrN4O2SDegré de pureté :98.1%Couleur et forme :SolidMasse moléculaire :419.3Hematoporphyrin dihydrochloride
CAS :<p>Hematoporphyrin dihydrochloride (Hematoporphyrin IX dihydrochloride) is a substrate for affinity chromatography of heme-binding proteins.</p>Formule :C34H40Cl2N4O6Degré de pureté :90.11%Couleur et forme :SolidMasse moléculaire :671.61(-)-Epipodophyllotoxin
CAS :<p>(-)-Epipodophyllotoxin: anticancer, GI50=0.36μM (HeLa), 0.24μM (MCF-7), inhibits spindle assembly.</p>Formule :C22H22O8Degré de pureté :99.97%Couleur et forme :SolidMasse moléculaire :414.41AMG 511
CAS :<p>AMG 511: oral class I PI3K inhibitor (α, β, δ, γ Kis: 4, 6, 2, 1 nM), anti-tumor in mouse glioblastoma model, reduces p-Akt (Ser473).</p>Formule :C22H28FN9O3SDegré de pureté :≥98%Couleur et forme :SolidMasse moléculaire :517.58(-)-Epigallocatechin Gallate
CAS :<p>(-)-Epigallocatechin Gallate (EGCG) is an antioxidant polyphenol flavonoid that inhibits telomerase and DNA methyltransferase.</p>Formule :C22H18O11Degré de pureté :98.60% - 99.43%Couleur et forme :Yellow PowderMasse moléculaire :458.37OTS514 hydrochloride
CAS :<p>OTS514 hydrochloride is a highly effective TOPK(T-LAK cell-originated protein kinase) inhibitor (IC50: 2.6 nM).</p>Formule :C21H20N2O2S·HClDegré de pureté :99.67% - 99.84%Couleur et forme :SolidMasse moléculaire :400.92Thalidomide-5-NH2-CH2-COOH
CAS :<p>Thalidomide derivative compound 114 inhibits protomyosin receptor kinase, targets E3 ligase, potential for disease research.</p>Formule :C15H13N3O6Degré de pureté :95.95%Couleur et forme :SolidMasse moléculaire :331.28Mitoxantrone
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 :<p>SC-58125 is a selective cyclooxygenase 2 (COX-2) inhibitor. SC-58125 exhibits antitumor activity, and also inhibits oedema at sites of inflammation.</p>Formule :C17H12F4N2O2SDegré de pureté :99.57%Couleur et forme :SolidMasse moléculaire :384.35RA-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>Formule :C19H15N3O5Degré de pureté :98.15%Couleur et forme :SolidMasse moléculaire :365.34
