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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L189
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 :246.29(-)-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 :414.41HM03
CAS :<p>HM03 is a potent and selective inhibitor of HSPA5, and has anticancer activity.</p>Formule :C26H27ClN4O2Degré de pureté :97.15%Couleur et forme :SolidMasse moléculaire :462.97Taletrectinib
CAS :<p>Taletrectinib (AB-106) is a new-generation selective inhibitor of ROS1/NTRK including ROS1,NTRK1,NTRK2 and NTRK3.</p>Formule :C29H34FN5O5Degré de pureté :99.87% - 99.96%Couleur et forme :SolidMasse moléculaire :551.61Polyporenic 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 :482.69Leptomycin 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 :540.73MRT-10
CAS :<p>MRT-10 is a Smoothened (Smo) receptor antagonist.</p>Formule :C24H23N3O5SDegré de pureté :99.73%Couleur et forme :SolidMasse moléculaire :465.52Kumatakenin
CAS :<p>Kumatakenin can suppress >80% of the SOS-inducing activity of Trp-P-1 at <0.06 micromol/mL.</p>Formule :C17H14O6Degré de pureté :97.44% - 98.29%Couleur et forme :SolidMasse moléculaire :314.29BMS-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 :410.91BRD4 Inhibitor-24
CAS :<p>BRD4 Inhibitor-24 is a BRD4 small molecule inhibitor with antitumor activity.</p>Formule :C13H14N2O4Degré de pureté :99.66%Couleur et forme :SolidMasse moléculaire :262.26Songorine
CAS :<p>Songorine (Napellonine) shows anti-tumor activity in preliminary pharmacological verification trials including cell proliferation and molecular docking assays.</p>Formule :C22H31NO3Degré de pureté :98% - 99.92%Couleur et forme :SolidMasse moléculaire :357.49Barasertib-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 :507.56NPD8733
CAS :<p>NPD8733 is an inhibitor of cancer cell-enhanced fibroblast migration. It specifically binds to valosin-containing protein (VCP)/p97.</p>Formule :C18H15NO4Degré de pureté :98.48%Couleur et forme :SolidMasse moléculaire :309.32Tazemetostat hydrobromide
CAS :<p>Tazemetostat hydrobromide: potent, selective EZH2 inhibitor; blocks PRC2/wild-type EZH2 (Ki: 2.5 nM) & EZH1 (IC50: 392 nM).</p>Formule :C34H45BrN4O4Degré de pureté :99.8%Couleur et forme :SolidMasse moléculaire :653.65NF-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 :530.57WRG-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 :410.44Stattic
CAS :<p>Stattic (STAT3 Inhibitor V) is a STAT3 inhibitor (IC50=5.1 μM) that selectively inhibits STAT3 activation, dimerization, and nuclear translocation.</p>Formule :C8H5NO4SDegré de pureté :98.32% - 99.76%Couleur et forme :SolidMasse moléculaire :211.19Cyclo(-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 :717.69(S)-Indoximod
CAS :<p>(S)-Indoximod (L-Abrine) is an indoleamine-2,3-dioxygenase (IDO) inhibitor for cancer research.</p>Formule :C12H14N2O2Degré de pureté :95.39%Couleur et forme :SolidMasse moléculaire :218.25L-685458
CAS :<p>L-685458 (L-685,458) is a specific and potent inhibitor of A beta PP gamma-secretase activity with Ki of 17 nM.</p>Formule :C39H52N4O6Degré de pureté :99.62% - 99.80%Couleur et forme :SolidMasse moléculaire :672.85Tetramethylcurcumin
CAS :<p>Tetramethylcurcumin is a novel curcumin analog, is an effective inhibitors of STAT3 phosphorylation, DNA binding activity, and transactivation in vitro.it also</p>Formule :C25H28O6Degré de pureté :97.69% - 99.94%Couleur et forme :SolidMasse moléculaire :424.49Senaparib
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 :478.45Benzyl butyl phthalate
CAS :<p>Benzyl butyl phthalate (1,2-benzenedicarboxylic acid) is used as a plasticizer for PVC.</p>Formule :C19H20O4Degré de pureté :99.02%Couleur et forme :Colourless Liquid Oily LiquidMasse moléculaire :312.36Pinoresinol
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 :358.39SGC0946
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 :618.57LJI308
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 :368.38GSK3685032
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 :420.53LYN-1604 dihydrochloride
CAS :<p>LYN-1604 is a novel ULK1 activator.It inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.</p>Formule :C33H45Cl4N3O2Degré de pureté :98.95% - 99.92%Couleur et forme :SolidMasse moléculaire :657.54Fursultiamine
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 :518.92ON123300
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 :429.52Rhapontin
CAS :<p>Rhapontin may reduce liver fat and better blood sugar/lipids, showing potential for treating type 2 diabetes.</p>Formule :C21H24O9Degré de pureté :99% - 99.91%Couleur et forme :Light YellowMasse moléculaire :420.41ASP4132
CAS :<p>ASP4132 is an orally active AMPK activator (EC50 : 18 nM), has anti-cancer activity.</p>Formule :C46H51F3N6O8S2Degré de pureté :98.34%Couleur et forme :SolidMasse moléculaire :937.06O6-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 :241.25Fatostatin 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 :375.33Otenaproxesul
CAS :<p>Otenaproxesul (ATB 346) is a novel hydrogen sulphide-releasing derivative of naproxen with markedly reduced toxicity.</p>Formule :C21H19NO3SDegré de pureté :98.76% - 99.13%Couleur et forme :SolidMasse moléculaire :365.45(E/Z)-Zotiraciclib
CAS :<p>(E/Z)-Zotiraciclib ((E/Z)-TG02) inhibits CDK2, JAK2, and FLT3 effectively with IC50s of 13, 73, and 56 nM, respectively.</p>Formule :C23H24N4ODegré de pureté :97.75% - 99.92%Couleur et forme :SolidMasse moléculaire :372.46Glumetinib
CAS :<p>Glumetinib (SCC244) (SCC 244) is a novel potent and selective inhibitor of c-Met kinase (IC50: 0.42 nM).</p>Formule :C21H17N9O2SDegré de pureté :99.79%Couleur et forme :SolidMasse moléculaire :459.48PD184161
CAS :<p>PD184161 is a novel, orally-active MEK inhibitor. PD184161 inhibited MEK activity (IC50 = 10-100 nM) in a time- and concentration-dependent manner[1].</p>Formule :C17H13BrClF2IN2O2Degré de pureté :99.40%Couleur et forme :SolidMasse moléculaire :557.56Alloxazine
CAS :<p>Alloxazine (Isoalloxazine) is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor.</p>Formule :C10H6N4O2Degré de pureté :99.75%Couleur et forme :SolidMasse moléculaire :214.18HUHS015
CAS :<p>HUHS015 is a potent PCA-1/ALKBH3 inhibitor.</p>Formule :C19H18N4ODegré de pureté :99.33% - 99.33%Couleur et forme :SolidMasse moléculaire :318.37Obtusifolin
CAS :<p>Obtusifolin is an antioxidant that combats diabetes, bone-resorption, diabetic retinopathy, pain, and cognitive decline.</p>Formule :C16H12O5Degré de pureté :99.78% - 99.99%Couleur et forme :SolidMasse moléculaire :284.26VY-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>Formule :C26H27N3O3Degré de pureté :99.25% - 99.79%Couleur et forme :SolidMasse moléculaire :429.51Ilaprazole
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>Formule :C19H18N4O2SDegré de pureté :99.91%Couleur et forme :SolidMasse moléculaire :366.44SKF-96365 hydrochloride
CAS :<p>SKF-96365 hydrochloride (SKF96365) , a SOCE inhibitor, exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal Y</p>Formule :C22H27ClN2O3Degré de pureté :99.47% - 99.92%Couleur et forme :SolidMasse moléculaire :402.91AKR1C3-IN-4
CAS :<p>AKR1C3-IN-4: potent, selective AKR1C3 inhibitor, IC50 = 0.56 μM, potential for CRPC research.</p>Formule :C14H10F3NO2Degré de pureté :98.59%Couleur et forme :SolidMasse moléculaire :281.23Supinoxin
CAS :<p>Supinoxin (RX-5902) is an oral anti-cancer drug targeting p68 RNA helicase, inducing apoptosis in TNBC cells (IC50: 10-20nM).</p>Formule :C22H24FN5O4Degré de pureté :99.83% - 99.95%Couleur et forme :SolidMasse moléculaire :441.46Denosumab
CAS :<p>Denosumab is a monoclonal antibody given subcutaneously that inhibits osteoclast activity by targeting the RANK ligand</p>Formule :C6404H9912N1724O2004S50Degré de pureté :95.9% (SDS-PAGE); 98.4% (SEC-HPLC) - 99.90%Couleur et forme :LiquidMasse moléculaire :144.71 kDaSU4984
CAS :<p>SU4984 is a cell-permeable, ATP-competitive and reversible inhibitor of the fibroblast growth factor receptor 1 (FGFR1).</p>Formule :C20H19N3O2Degré de pureté :97.20%Couleur et forme :SolidMasse moléculaire :333.38(E/Z)-TG003
CAS :<p>(E/Z)-TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor.</p>Formule :C13H15NO2SDegré de pureté :98% - 99.04%Couleur et forme :SolidMasse moléculaire :249.33Palbociclib 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 :573.66Edotreotide
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 :1421.64ONO-7475
CAS :<p>ONO-7475 is an inhibitor with high specificity for anexelekto and MER tyrosine kinase</p>Formule :C32H26N4O6Degré de pureté :98.74%Couleur et forme :SolidMasse moléculaire :562.57PIK-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>Formule :C16H14BrN5O4SDegré de pureté :98.52% - >99.99%Couleur et forme :SolidMasse moléculaire :452.28β-Elemonic Acid
CAS :<p>β-Elemonic Acid (3-Oxotirucallenoic Acid) exhibits anti-inflammatory effects, which inhibits proliferation by inducing hypoploid cells and cell apoptosis.</p>Formule :C30H46O3Degré de pureté :99.61% - 99.8%Couleur et forme :SolidMasse moléculaire :454.68Obatoclax 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 :413.49PI3K-IN-1
CAS :<p>PI3K-IN-1 (Voxtalisib Analogue) is a dual inhibitor of mTOR/PI3K, mostly for p110γ , also inhibits DNA-PK and mTOR.</p>Formule :C31H29N5O6SDegré de pureté :97.03% - 98%Couleur et forme :SolidMasse moléculaire :599.66Ganoderic acid D
CAS :<p>Ganoderic acid D, a Ganoderma component, inhibits HeLa cell growth with an IC50 of 17.3µM after 48h.</p>Formule :C30H42O7Degré de pureté :98.06% - 99.98%Couleur et forme :SolidMasse moléculaire :514.65MTOB
CAS :<p>MTOB, a CtBP substrate, inhibits CtBP-linked cancer activity in cells/mice and regulates TCF-4, affecting CSC proliferation.</p>Formule :C5H7NaO3SDegré de pureté :98.23%Couleur et forme :SolidMasse moléculaire :170.16ODM-203
CAS :<p>ODM-203, a Selective Inhibitor of FGFR and VEGFR, Shows Strong Antitumor Activity, and Induces Antitumor Immunity</p>Formule :C26H21F2N5O2SDegré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :505.54TRPM4-IN-1
CAS :<p>TRPM4-IN-1 (4-chloro-2-(2-(2-chlorophenoxy)acetamido)benzoic acid) is a potent and selective inhibitor of TRPM4 with an IC50 of 1.5 μM.</p>Formule :C15H11Cl2NO4Degré de pureté :97.22%Couleur et forme :SolidMasse moléculaire :340.16I-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 :497.55ARS-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 :432.94Sitravatinib
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 :629.68Millepachine
CAS :<p>Millepachine is a natural product found in the Chinese herbal medicine with strong antitumor effects against numerous human cancer cells.</p>Formule :C22H22O4Degré de pureté :99.73%Couleur et forme :SolidMasse moléculaire :350.41Hematoporphyrin 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 :671.61Palbociclib
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 :447.53PF-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 :507.49Alflutinib
CAS :<p>Alflutinib (ASK120067) is an inhibitor of EGFR, and its targets including EGFR activating mutations and T790M, thus leading to tumor growth inhibition.</p>Formule :C28H31F3N8O2Degré de pureté :99.87%Couleur et forme :SolidMasse moléculaire :568.59AMG 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 :517.58Rasarfin
CAS :<p>Rasarfin inhibits Ras and ARF6.</p>Formule :C23H24ClN3O3Degré de pureté :97.98%Couleur et forme :SolidMasse moléculaire :425.91Alflutinib 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 :664.7Ilexgenin A
CAS :<p>Ilexgenin A is a novel pentacyclic triterpenoid, is a compound extracted from leaves of Ilex hainanensis Merr</p>Formule :C30H46O6Degré de pureté :97.11% - 97.19%Couleur et forme :SolidMasse moléculaire :502.68AG-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 :315.75C-7280948
CAS :<p>C-7280948 is a PRMT1 inhibitor.</p>Formule :C14H16N2O2SDegré de pureté :99.55% - ≥95%Couleur et forme :SolidMasse moléculaire :276.35Clobenpropit 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 :470.7Murrayone
CAS :<p>Murrayone from M. paniculata, a bioactive coumarin, prevents cancer metastasis and reduces ADP-induced platelet aggregation.</p>Formule :C15H14O4Degré de pureté :98.01% - 98.79%Couleur et forme :SolidMasse moléculaire :258.27Galloflavin
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 :278.17OTS514 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 :400.92Paederoside
CAS :<p>Paederoside deters beetles, isolated from aphids, and inhibits tumor-promotion in Epstein-Barr virus.</p>Formule :C18H22O11SDegré de pureté :97.81% - 99.9%Couleur et forme :SolidMasse moléculaire :446.43Thalidomide-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 :331.28Bavdegalutamide
CAS :<p>Bavdegalutamide (ARV-110) is a PROTAC degrader of androgen receptor (AR).</p>Formule :C41H43ClFN9O6Degré de pureté :97.17% - 99.04%Couleur et forme :SolidMasse moléculaire :812.29GN44028
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 :305.33Chrysosplenol D
CAS :<p>Chrysosplenol D, an efflux pump inhibitor that can potentiate the activity of commercially important antibiotics and antimalarials.</p>Formule :C18H16O8Degré de pureté :97.87% - 99.98%Couleur et forme :SolidMasse moléculaire :360.31TAS6417
CAS :<p>Zipalertinib (TAS6417, CLN-081) is a novel, highly potent, orally active covalent EGFR tyrosine kinase inhibitor.Cost-effective and quality-assured.</p>Formule :C23H20N6ODegré de pureté :99.71%Couleur et forme :SolidMasse moléculaire :396.44POL1-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 :356.42NU6027
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 :251.29CCT128930 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>Formule :C18H21Cl2N5Degré de pureté :98.55%Couleur et forme :SolidMasse moléculaire :378.3MF-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>Formule :C27H21F3N2O3Degré de pureté :99.54% - 99.59%Couleur et forme :SolidMasse moléculaire :478.46Ilaprazole sodium
CAS :<p>Ilaprazole sodium (IY-81149 sodium) , a substituted benzimidazole prodrug, is a selective and irreversible proton pump inhibitor.</p>Formule :C19H17N4NaO2SDegré de pureté :99.06%Couleur et forme :SolidMasse moléculaire :388.42Nirogacestat
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 :489.64FTO-IN-1
CAS :<p>UUN44923: FTO inhibitor, potential treatment for obesity, MS, T2D, Alzheimer's, various cancers.</p>Formule :C18H16Cl2N4O2Degré de pureté :98.21% - 98.91%Couleur et forme :SolidMasse moléculaire :391.25Syrosingopine
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>Formule :C35H42N2O11Degré de pureté :99.25% - 99.78%Couleur et forme :SolidMasse moléculaire :666.71BMS-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>Formule :C25H26ClN5O3Degré de pureté :99.02%Couleur et forme :SolidMasse moléculaire :479.96DASA-58
CAS :<p>DASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.</p>Formule :C19H23N3O6S2Degré de pureté :96.96% - 99.28%Couleur et forme :SolidMasse moléculaire :453.53RA-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 :365.34Niraparib 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 :356.85MMP-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 :369.39Siramesine
CAS :<p>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 potent</p>Formule :C30H31FN2ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :454.58
