Cycle cellulaire/point de contrôle
Les inhibiteurs du cycle cellulaire/des points de contrôle sont des composés qui perturbent la progression normale du cycle cellulaire, en particulier aux points de contrôle régulateurs clés. Ces inhibiteurs sont cruciaux pour étudier la division cellulaire, comprendre la prolifération des cellules cancéreuses et développer des thérapies anticancéreuses. En ciblant des phases spécifiques du cycle cellulaire, ces inhibiteurs peuvent induire un arrêt du cycle cellulaire, conduisant à l'apoptose ou à la sénescence des cellules à division rapide. Chez CymitQuimica, nous offrons une large gamme d'inhibiteurs de haute qualité du cycle cellulaire/des points de contrôle pour soutenir vos recherches en biologie du cancer, biologie cellulaire et développement de médicaments.
Sous-catégories appartenant à la catégorie "Cycle cellulaire/point de contrôle"
- Aurora Kinase
- CDK
- Arrêt du cycle cellulaire
- Chk
- c-Myc
- Dynamine
- DYRK
- Ferroptose
- HSP
- Intégrine
- Kinésine
- KSP
- LIM Kinase
- Microtubules associés
- PKC
- PLK
- Rho
- ROCK
- Wee1
Affichez 11 plus de sous-catégories
Produits appartenant à la catégorie "Cycle cellulaire/point de contrôle"
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HNC-1664
CAS :HNC-1664 is an orally active inhibitor of RNA-dependent RNA polymerase (RdRP). It exhibits broad-spectrum antiviral activity against coronaviruses, including SARS-CoV-2 wild type and its variants (XBB.1.18, HK.3.1, BF.7.14, BA.1, HCoV-229E, HCoV-OC43), as well as arenaviruses. HNC-1664 also demonstrates anti-infective efficacy in a mouse model infected with the SARS-CoV-2 Delta variant.Formule :C12H13FIN3O3Couleur et forme :SolidMasse moléculaire :393.153AZD-7762
CAS :AZD-7762, an effective and specific inhibitor of Chk1(IC50=5 nM), is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck.Formule :C17H19FN4O2SDegré de pureté :98.96% - 99.19%Couleur et forme :SolidMasse moléculaire :362.42Ref: TM-T6093
1mg38,00€2mg49,00€5mg81,00€10mg96,00€25mg177,00€50mg280,00€100mg449,00€1mL*10mM (DMSO)88,00€WBC100
CAS :WBC100 (14-D-Valine-TPL) is a potent, selective, and orally active c-Myc glue degrader that targets the ubiquitin E3 ligase CHIP-mediated 26S proteasome pathwayFormule :C25H33NO7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :459.53SB-218078
CAS :SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM).Formule :C24H15N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :393.39Lusianthridin
CAS :Lusianthridin is a natural product from Dendrobium venustum.Formule :C15H14O3Degré de pureté :99.11% - 99.11%Couleur et forme :SolidMasse moléculaire :242.27ddTTP trisodium
Dideoxythymidine triphosphate trisodium (ddTTP), a 2',3'-dideoxyribonucleoside 5'-triphosphate (ddNTP), functions as a chain-elongation inhibitor of DNAFormule :C10H14N2Na3O13P3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :532.11Danofloxacin mesylate
CAS :Danofloxacin mesylate (CP 76136-27) is a synthetic antibacterial agent of the fluoroquinolone class, acts principally by the inhibition of bacterial DNA-gyrase.Formule :C19H20FN3O3·CH4O3SDegré de pureté :99.73%Couleur et forme :Crystalline SolidMasse moléculaire :453.48SMN-C2
CAS :SMN-C2, a SMN2 gene splicing regulator, is an RNA-binding ligand that regulates pre-mRNA splicing and has potential for studying spinal muscular atrophy.Formule :C24H27N5O2Degré de pureté :99.01%Couleur et forme :SolidMasse moléculaire :417.5NSC 23766
CAS :NSC 23766 is a Rac1 GTPase inhibitor by targeting GEFs, inhibiting cell proliferation.NSC23766 competitively inhibits M2 mAChR-induced Rac1 activation.Formule :C24H35N7Degré de pureté :99.49%Couleur et forme :SolidMasse moléculaire :421.58Gentisin
CAS :Gentisin is a novel inhibitor of vascular smooth muscle cells (VSMC) proliferation with an IC50 value of 7.84 μM. Gentisin has mutagenic activity.Formule :C14H10O5Degré de pureté :95.34%Couleur et forme :SolidMasse moléculaire :258.23GFB-12811
CAS :GFB-12811 is an orally active, selective, and potent CDK5 inhibitor, used in the study of autosomal dominant polycystic kidney disease.Formule :C22H23F4N5ODegré de pureté :98.88%Couleur et forme :SolidMasse moléculaire :449.44L-Uridine
CAS :L-Uridine, an RNA component from Poria cocos fungus, is a D-uridine enantiomer with antiviral potential and a phosphate acceptor.Formule :C9H12N2O6Degré de pureté :99.57%Couleur et forme :SolidMasse moléculaire :244.2LFM-A13
CAS :LFM-A13(IC50=2.5 μM), a specific Bruton's tyrosine kinase (BTK), is more than 100-fold specificity than other protein kinases, such as JAK1, JAK2, HCK, EGFR,Formule :C11H8Br2N2O2Degré de pureté :99.9%Couleur et forme :SolidMasse moléculaire :360qsl-304
QSL-304 is a DNA gyrase B inhibitor that serves as an antibacterial agent, exhibiting an IC50 of 31.23 mg/mL against Staphylococcus aureus SA-P2003 [1].Formule :C11H9NO4S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :283.32Tetrapeptide
CAS :Tetrapeptide, an α-MSH analogue, stimulates melanin production and mitigates DNA damage by attenuating reactive oxidative species generation and augmenting DNAFormule :C32H40N10O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :644.72CDK9-IN-10
CAS :CDK9-IN-10 is a potent CDK9 inhibitor and the ligand for the PROTAC CDK9 degrader-2.Formule :C22H16O5Degré de pureté :99.8%Couleur et forme :SolidMasse moléculaire :360.36Methotrexate metabolite
CAS :DAMPA, active metabolite of Methotrexate, is a chemotherapeutic and immunosuppressive folic acid antagonist.Formule :C15H15N7O2Degré de pureté :95.28% - 99.7%Couleur et forme :SolidMasse moléculaire :325.33XMD-17-51
CAS :XMD-17-51 has DCLK1 kinase inhibitory activity, inhibits DCLK1 and cell proliferation, and can be used in lung cancer research.Formule :C21H24N8ODegré de pureté :99.39%Couleur et forme :SoildMasse moléculaire :404.47Pidilizumab
CAS :Pidilizumab (CT-011), a humanized IgG1κ anti-PD-1 monoclonal antibody, serves as a DLL1 antagonist with potential applications in researching hematologicDegré de pureté :98%Couleur et forme :LiquidLZ9
CAS :LZ9 is an ATP-competitive inhibitor of CDK1 and CDK2, with potential applications in colorectal cancer (CRC) research.Formule :C17H11F3N4O2Couleur et forme :SolidMasse moléculaire :360.29Carmofur
CAS :Carmofur (HCFU) is a highly potent acid ceramidase inhibitor, used in the treatment of breast and colorectal cancer.Formule :C11H16FN3O3Degré de pureté :98.59% - 99.48%Couleur et forme :SolidMasse moléculaire :257.265-Ethynyluridine
CAS :5-Ethynyluridine marks new RNA for RICK, capturing proteins on various RNAs, even nonpolyadenylated types.Formule :C11H12N2O6Degré de pureté :100%Couleur et forme :SolidMasse moléculaire :268.22Ref: TM-T36971
5mg51,00€10mg88,00€25mg145,00€50mg250,00€100mg363,00€200mg545,00€1mL*10mM (DMSO)57,00€CDK2/4-IN-2
CAS :CDK2/4-IN-2 (compound 56) serves as a dual inhibitor for CDK2 and CDK4, exhibiting an IC50 of less than 100 nM. It is applicable in cancer research.Formule :C18H20F3N7O3S2Couleur et forme :SolidMasse moléculaire :503.52Abemaciclib
CAS :Abemaciclib (LY2835219) is a dual inhibitor of CDK4/6 (IC50=2/10 nM) with selectivity and specificity.Formule :C27H32F2N8Degré de pureté :99.39% - 99.87%Couleur et forme :SolidMasse moléculaire :506.595-(Methoxycarbonyl)methyluridine
CAS :5-(Methoxycarbonyl)methyluridine is an important modifying nucleotide in tRNAs, and the lack of the mcm5U modification leads to increased protein aggregation.Formule :C12H16N2O8Degré de pureté :99.71%Couleur et forme :SolidMasse moléculaire :316.26GSK-1520489A
CAS :GSK-1520489A is an active PKMYT1 inhibitor.Formule :C21H23N5O3SDegré de pureté :97.25%Couleur et forme :SolidMasse moléculaire :425.5D5B
D5B is an effective and selective PD-L1 inhibitor that has been modified with DBCO. It degrades PD-L1 in 4T1 and B16-F10 tumor cells with EC50 values of 5.4 μM and 6.2 μM, respectively. D5B can block the PD-L1/PD-1 interaction and exhibits antitumor activity.Formule :C58H66N2O12Couleur et forme :SolidMasse moléculaire :983.15TH287 hydrochloride
CAS :TH287 inhibits MTH1 (IC50: 0.8 nM), causing DNA damage in cancer cells through oxidized dNTP incorporation, leading to cytotoxicity in mouse xenografts.Formule :C11H11Cl3N4Degré de pureté :99.5%Couleur et forme :SolidMasse moléculaire :305.59ANI-7
CAS :ANI-7, an AhR pathway activator, selectively impedes MCF-7 breast cancer cell growth (GI50: 0.56 μM).Formule :C13H8Cl2N2Degré de pureté :99.21%Couleur et forme :SolidMasse moléculaire :263.12CDK4/6-IN-3
CAS :CDK4/6-IN-3 is a brain-penetrant CDK4/CDK6 inhibitor (Kis: <0.3 nM and 2.2 nM) used for the treatment of glioblastoma. It inhibits CDK1 with a Ki of 110 nM.Formule :C25H31FN8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :462.57Danusertib
CAS :Danusertib (PHA-739358) is a small-molecule 3-aminopyrazole derivative with potential antineoplastic activity.Formule :C26H30N6O3Degré de pureté :97.88% - 98.44%Couleur et forme :White PowderMasse moléculaire :474.55Ref: TM-T2094
1mg59,00€2mg85,00€5mg116,00€10mg188,00€25mg365,00€50mg555,00€100mg795,00€500mg1.605,00€1mL*10mM (DMSO)120,00€DNA polymerase-IN-2
DNA polymerase-IN-2 (Compd 3c), a coumarin derivative, demonstrates inhibitory activity towards Taq DNA polymerase, with an IC50 value of 48.25 μM, and holdsFormule :C14H12O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :292.31TAS-119
CAS :TAS-119 (TAS-2104) is an orally available, selective and potent inhibitor of Aurora A with an IC50 of 1.0 nM.TAS-119 also inhibits Aurora B with an IC50 of 95Formule :C23H22Cl2FN5O3Degré de pureté :98.69%Couleur et forme :SolidMasse moléculaire :506.36Ref: TM-T34787
1mg97,00€5mg235,00€10mg378,00€25mg748,00€50mg1.169,00€100mg1.644,00€1mL*10mM (DMSO)261,00€ENMD-2076
CAS :ENMD-2076, a multi-targeted kinase inhibitor, has specific activity against Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα.Formule :C21H25N7Degré de pureté :97.63% - ≥95%Couleur et forme :SolidMasse moléculaire :375.47Ref: TM-T2358
1mg51,00€2mg72,00€5mg105,00€10mg159,00€25mg279,00€50mg462,00€100mg648,00€1mL*10mM (DMSO)116,00€Mefenidil
CAS :Mefenidil (McN-2378), a selective cerebral vasodilator, was shown to increase CBF in healthy brains without stimulating O2 uptake in a dog anesthesia model.Formule :C12H11N3Degré de pureté :98.17%Couleur et forme :SolidMasse moléculaire :197.24Volociximab
CAS :Volociximab (M200) is an IgG4 monoclonal antibody targeting the α5β1 integrin , with antiangiogenic, antitumor and anticancer activity, inhibits the growth of rabbit VX2 tumors and is used to study solid tumors.Degré de pureté :95%Couleur et forme :LiquidPKMYT1-IN-3
PKMYT1-IN-3 (compound 8ma) is a potent, selective inhibitor of PKMYT1, demonstrating an IC50 of 16.5 nM and exhibiting antitumor activity.Formule :C24H26FN5O2Couleur et forme :SolidMasse moléculaire :435.49MKC3946
CAS :MKC3946 is an effective and soluble IRE1α inhibitor which triggered modest growth inhibition in multiple myeloma cell lines.Formule :C21H20N2O3SDegré de pureté :99.65%Couleur et forme :SolidMasse moléculaire :380.46Ref: TM-TQ0101
1mg66,00€5mg170,00€10mg265,00€25mg444,00€50mg653,00€100mg929,00€1mL*10mM (DMSO)157,00€ML216
CAS :ML216 (CID-49852229) inhibits BLM helicase (IC50: 1.8 μM), 28-fold selective over RECQ1, RECQ5, and UvrD (IC50s > 50 μM).Formule :C15H9F4N5OSDegré de pureté :98.12%Couleur et forme :SolidMasse moléculaire :383.323'-Deoxy-3'-fluoroguanosine
CAS :3'-Deoxy-3'-fluoroguanosine is a nucleoside phosphorylase inhibitor that inhibits RNA replication by binding replons.Formule :C10H12FN5O4Degré de pureté :99.33%Couleur et forme :SolidMasse moléculaire :285.23CHK1-IN-4
CAS :CHK1-IN-4 is a potent inhibitor of checkpoint kinase 1 (chk1) and potently inhibits chk1 phosphorylation in the tumor cells with anti-tumor activity.Formule :C18H18BrN7O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :444.29Butylparaben sodium
CAS :Butylparaben sodium significantly impacts the later phases of spermatogenesis in the testes by impairing hormonal regulation and/or RNA and protein synthesis [1Formule :C11H13NaO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :216.21MSC2530818
CAS :MSC2530818 is an effective, selective and orally available CDK8 inhibitor (IC50: 2.6 nM).Formule :C18H17ClN4ODegré de pureté :98.93%Couleur et forme :SolidMasse moléculaire :340.81Ref: TM-TQ0266
1mg66,00€5mg144,00€10mg230,00€25mg509,00€50mg735,00€100mg1.026,00€1mL*10mM (DMSO)159,00€Lucanthone
CAS :Lucanthone (Lucanthonum) is an inhibitor of Apurinic endonuclease-1 (APE-1).Formule :C20H24N2OSDegré de pureté :99.92%Couleur et forme :Yellow Crystals From Alcohol SolidMasse moléculaire :340.48Ref: TM-T4569
1mg56,00€2mg80,00€5mg126,00€10mg188,00€25mg400,00€50mg592,00€100mg837,00€1mL*10mM (DMSO)140,00€BIO-1211
CAS :BIO-1211 is a more potent inhibitor of α4β1 (VLA-4, IC50 = 4 nM) over α4β7(IC50 = 2 μM).Formule :C36H48N6O9Degré de pureté :99.33%Couleur et forme :SolidMasse moléculaire :708.8Mps1-IN-2
CAS :Mps1-IN-2 is a potent, selective and ATP-competitive dual Mps1/Plk1 inhibitor.Formule :C26H36N6O3Degré de pureté :96.24% - 99.75%Couleur et forme :SolidMasse moléculaire :480.6CDK12-IN-5
CAS :CDK12-IN-5 is a potent CDK12 inhibitor with potential anticancer and antitumor activity, and can be used orally in the study of breast and ovarian cancer.Formule :C18H15F5N8ODegré de pureté :99.37%Couleur et forme :SolidMasse moléculaire :454.36Ref: TM-T40290
1mg165,00€5mg399,00€10mg645,00€25mg1.320,00€50mg2.080,00€100mg2.822,00€1mL*10mM (DMSO)439,00€Cdc7-IN-5
CAS :Cdc7-IN-5: potent Cdc7 serine-threonine kinase inhibitor, critical for starting DNA replication.Formule :C25H23N3O5Degré de pureté :97.15%Couleur et forme :SolidMasse moléculaire :445.47Ref: TM-T10727
1mg96,00€5mg227,00€10mg376,00€25mg620,00€50mg847,00€100mg1.169,00€1mL*10mM (DMSO)250,00€COH1
CAS :COH1 is a ribonucleotide reductase (RR) inhibitor utilized in research pertaining to cancer, mitochondrial diseases, and neurodegenerative disorders [1].Formule :C11H10N2O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :250.27Bexotegrast
CAS :Bexotegrast (PLN-74809) is an αvβ6 and αvβ1 integrin inhibitor with antifibrotic properties for the study of idiopathic pulmonary fibrosis (IPF).Formule :C27H36N6O3Degré de pureté :99.53%Couleur et forme :SolidMasse moléculaire :492.61Indatuximab
Indatuximab is a chimeric antibody targeting CD13, used in the synthesis of ADC compound Indatuximab ravtansine.Couleur et forme :LiquidMasse moléculaire :145.5 kDaHPH-15
CAS :HPH-15 is an anti-cell migration compound that inhibits cell movement by binding to hnRNP U or suppressing TGF-β. Additionally, it prevents epithelial-to-mesenchymal transition (EMT). HPH-15 holds potential for research in areas such as anti-tumor metastasis and anti-fibrosis.Formule :C19H31N3S4Couleur et forme :SolidMasse moléculaire :429.735-Fluorouridine
CAS :5-fluorouridine is also known as FUrd, 5-Fluorouracil 1-beta-D-ribofuranoside, 5-Fur, or 5-Fluoro-uridine.Formule :C9H11FN2O6Degré de pureté :99.53% - 99.76%Couleur et forme :White PowderMasse moléculaire :262.19ML264
CAS :ML264 (CID-51003603) is a selective kruppel-like factor 5 (KLF5) inhibitor, which potently Inhibits growth of Colorectal Cancer.Formule :C17H21ClN2O4SDegré de pureté :99.33% - 99.45%Couleur et forme :SolidMasse moléculaire :384.88CDK2-IN-30
CAS :CDK2-IN-30 (Formula (I)) is a CDK2 inhibitor with an IC50 of ≤20 nM, utilized primarily in tumor research.Formule :C18H25N7O3SCouleur et forme :SolidMasse moléculaire :419.502-Fluoroadenine
CAS :2-Fluoroadenine (NSC-27364) has toxicity in nonproliferating and proliferating tumor cells. 2-Fluoroadenine can be used for anticancer studies.Formule :C5H4FN5Degré de pureté :99.49%Couleur et forme :White To Light Yellow Crystal PowderMasse moléculaire :153.12BS194
CAS :BS194 is as a potent cyclin-dependent protein kinases (CDKs) inhibitor.Formule :C20H27N5O3Degré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :385.463,4-Dihydroxybenzylamine hydrobromide
CAS :3,4-Dihydroxybenzylamine hydrobromide inhibits DNA polymerase and melanoma growth, varying with tyrosinase activity.Formule :C7H10BrNO2Degré de pureté :97.28%Couleur et forme :Light Beige Crystalline PowderMasse moléculaire :220.06BMS-688521
CAS :BMS-688521 is an LFA-1/ICAM interaction inhibitor, a small molecule antagonist of LFA-1 with potential anti-inflammatory activity.Formule :C26H19Cl2N5O4Degré de pureté :98.87%Couleur et forme :SolidMasse moléculaire :536.37Ref: TM-T14676
1mg183,00€5mg464,00€10mg655,00€25mg1.169,00€50mg1.539,00€100mg1.882,00€1mL*10mM (DMSO)547,00€LY3405105
CAS :LY3405105 (1-Piperidinecarboxylic acid, 4-[[5-methyl-3-(1-methylethyl)pyrazolo[1,5-a]pyrimidin-7-yl]amino]-, 1-[(2E)-4-(dimethylamino)-1-oxo-2-buten-1-yl]-3-Formule :C26H39N7O3Degré de pureté :98.01%Couleur et forme :SolidMasse moléculaire :497.63IMT1
CAS :IMT1 (Propanamide, N,N-dimethyl-2-[[4-(2-methylphenyl)-2-oxo-2H-1-benzopyran-7-yl]oxy]-) has anticancer activity.Formule :C21H21NO4Degré de pureté :98.07% - 98.14%Couleur et forme :SolidMasse moléculaire :351.4Ref: TM-T8841
1mg81,00€5mg170,00€10mg301,00€25mg563,00€50mg805,00€100mg1.111,00€1mL*10mM (DMSO)188,00€PHI-101
CAS :PHI-101 is a checkpoint kinase 2 (Chk2) inhibitor that can be used for the study of refractory acute myeloid leukemia (AML) and ovarian cancer.Formule :C19H19FN4O2SDegré de pureté :99.40%Couleur et forme :SolidMasse moléculaire :386.44Ref: TM-T81490
1mg173,00€5mg437,00€10mg702,00€25mg1.406,00€50mg2.262,00€100mg3.600,00€1mL*10mM (DMSO)469,00€SEL120-34A HCl
CAS :SEL120-34A HCl is a selective, orally available and ATP-competitive inhibitor of CDK8(CDK8/CycC and CDK19/CycC with IC50s of 4.4 nM and 10.4 nM , respectivelyFormule :C15H19Br2ClN4Degré de pureté :98.13% - 99.75%Couleur et forme :SolidMasse moléculaire :450.6(S)-GNA-T-phosphoramidite
CAS :(S)-GNA-T-phosphoramidite is a nucleoside analog commonly used in the synthesis of other active compounds.Formule :C38H47N4O7PDegré de pureté :99.35%Couleur et forme :SolidMasse moléculaire :702.78AZD-5438
CAS :AZD-5438 is an effective inhibitor of CDK, for CDK1(IC50=16 nM), CDK2(IC50=6 nM), CDK9(IC50=20 nM).Formule :C18H21N5O2SDegré de pureté :99.73% - 99.87%Couleur et forme :SolidMasse moléculaire :371.46BUR1
CAS :BUR1 is a Saccharomyces cerevisiae cyclin-dependent kinase (CDK) and is homologous to mammalian Cdk9, which functions in transcriptional elongation.Formule :C16H17N5Degré de pureté :90%Couleur et forme :SolidMasse moléculaire :279.34Obtustatin triacetate
Obtustatin triacetate, a 41-residue non-RGD disintegrin isolated from the venom of Vipera lebetina obtusa, serves as a potent and selective inhibitor of theFormule :C184H284N52O57S8·3C2H4O2Degré de pureté :99.51%Couleur et forme :SolidMasse moléculaire :4573.21MYC-RIBOTAC
MYC-RIBOTAC, a ribonuclease-targeting chimera (RIBOTAC) specific to the MYC internal ribosome entry site (IRES), comprises an MYC mRNA-binding element tetheredFormule :C55H58N10O11SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :1067.17Lerociclib dihydrochloride
CAS :Lerociclib dihydrochloride (G1T38 dihydrochloride) is a potent and selective inhibitor of CDK4/CDK6, with IC50s of 2 nM and 1 nM for CDK6/CyclinD3 and CDK4/Formule :C26H36Cl2N8ODegré de pureté :97.40%Couleur et forme :SolidMasse moléculaire :547.52CCT241533 hydrochloride
CAS :CCT241533 hydrochloride is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).Formule :C23H28ClFN4O4Degré de pureté :97.13%Couleur et forme :SolidMasse moléculaire :478.95Ref: TM-T10718L
1mg73,00€2mg96,00€5mg159,00€10mg240,00€25mg515,00€50mg852,00€100mg1.264,00€500mg2.547,00€1mL*10mM (DMSO)170,00€DMT-dU-CE Phosphoramidite
CAS :DMT-dU-CE Phosphoramidite is a nucleoside molecule commonly used for the synthesis and sequencing of DNA.Formule :C39H47N4O8PDegré de pureté :97.58%Couleur et forme :SolidMasse moléculaire :730.79BMS-1001
CAS :BMS-1001 is a potent inhibitor of PD-1/PD-L1 interaction(IC50 : 2.25 nM, in a homogenous time-resolved fluorescence binding assay).Formule :C35H34N2O7Degré de pureté :98.43%Couleur et forme :SolidMasse moléculaire :594.7Abciximab
CAS :Abciximab: chimeric antibody, anti-platelet, blocks glycoprotein IIb/IIIa, vitronectin, Mac-1.Degré de pureté :SDS-PAGE:95.2%;SEC-HPLC:95.9%Couleur et forme :LiquidMasse moléculaire :95.18 kDaVotoplam HCl
CAS :Votoplam HCl is a systemically acting gene splicing regulator that down-regulates the levels of huntingtin protein, which to inhibit Huntington's disease (HD).Formule :C21H26ClN9ODegré de pureté :99.49%Couleur et forme :SoildMasse moléculaire :455.94
