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397712个产品
产品编号:4083622
纯度规格:A potent agonist of Toll-like receptor 8 agonist (TLR8, EC50 = 200 nM).
包装规格:10 MG
产品编号:4083621
纯度规格:
包装规格:10 MG
产品编号:4083618
纯度规格:A cell-permeable compound that prevents the transfer of SUMO from the E2 thioester to the substrate without affecting SUMO-activating enzyme E1 (SAE-1/2) or E2 Ubc9-SUMO thioester formation.
包装规格:10 MG
产品编号:4083615
纯度规格:A cell-permeable BP-1-102 analog that targets STAT3 and STAT5 with comparable affinity.
包装规格:10 MG
产品编号:4083613
纯度规格:A depolymerized vanadate prepared from Sodium Orthovanadate with enhanced ability to competitively inhibit endogenous phosphatases.
包装规格:5 ML,1 SET
产品编号:4083611
纯度规格:A cell-permeable compound that targets human Replication Protein A (RPA) and inhibits its DNA-binding activity (IC50= 12.9 μM).
包装规格:25 MG
产品编号:4083609
纯度规格:A cell-permeable, selective inhibitor of RIP3-selective kinase with >1,000-fold selectivity over a vast majority of more than 300 other kinases.
包装规格:10 MG
产品编号:4083606
纯度规格:A cell-permeable pharmacological chaperone to increase neuronal retromer levels. Improves Vps35-Vps29-Vps26 retromer complex stability.
包装规格:25 MG
产品编号:4083600
纯度规格:
包装规格:10 MG
产品编号:4083599
纯度规格:A cell permeable, brain permeant antagonist of polypeptide chemokine prokineticin 2 receptor (IC50 = 5 nM and 8.2 nM for PKR1 and PKR2, respectively).
包装规格:5 MG
产品编号:4083597
纯度规格:
包装规格:2 MG
产品编号:4083596
纯度规格:A cell permeable competitive inhibitor of Pin1 (EC50 = 4.1 μM, Ki = 50 nM).
包装规格:10 MG
产品编号:4083594
纯度规格:A cell-permeable, potent and competitive inhibitor of fructose-2,6-bisphosphatase 3 (PFKFB3; IC50 = 670 nM).
CAS NO:75187-63-2
包装规格:25 MG
产品编号:4083593
纯度规格:A cell-permeable inhibitor of PFKFB3 that reversibly docks to its substrate binding domain (IC50 = 207 nM)
包装规格:25 MG
产品编号:4083592
纯度规格:A cell-permeable nematicidal compound that covalently binds to the peroxidatic cysteine of peroxiredoxin II in T. gondii and irreversibly blocks its hyperperoxidation activity (IC50 = 23 μM).
CAS NO:18080-67-6
包装规格:25 MG
产品编号:4083589
纯度规格:A cell-permeable, selective &direct blocker of p18-Cdk6 interaction. Inhibits p18INK4C protein activity &favors HSCs self-renewal by ~4.2-fold.
CAS NO:77408-67-4
包装规格:25 MG
产品编号:4083588
纯度规格:A cell-permeable compound with cytotoxicity towards quiescent cells in colon cancer 3-D microtissues (~ 6 μM). Reduces mitochondrial oxidative phosphorylation in tumor cells.
包装规格:10 MG
产品编号:4083587
纯度规格:Prevents melanopsin/Opn4 photoactivation in a reversible manner. Inhibits cellular phototransduction mediated by human Opn4 (IC50 = 665 nM; using CHO transfectants).
CAS NO:457961-34-1
包装规格:10 MG
产品编号:4083585
纯度规格:
包装规格:10 MG
产品编号:4083584
纯度规格:A potent activator of Ca2+ -activated K+ channels of SK and IK types, but not BK type channels. It is at least 1000 times more potent than 1-EBIO.
CAS NO:18711-16-5
包装规格:10 MG
产品编号:4083583
纯度规格:A cell-permeable, potent Nrf-2 activator that stimulates HO-1 expression in murine microglial BV-2 cultures. Induces overall Nrf2 cellular accumulation and nuclear translocation.
包装规格:10 MG
产品编号:4083582
纯度规格:A cell-permeable inhibitor of nonsense-mediated mRNA decay (NMD) that enhances the stability of premature termination codon mutated p53 mRNA in N417 and HDQP-1 cells.
包装规格:10 MG
产品编号:4083581
纯度规格:A cell-potent, bioavailable NLRP3 inflammasome activation inhibitor. Effectively blocks caspase-1 &-11 activation, IL-1β processing and IL-1β &IL-6 secretion.
CAS NO:256373-96-3
包装规格:10 MG
产品编号:4083578
纯度规格:
包装规格:25 MG
产品编号:4083577
纯度规格:A cell-permeable neomycin derived artificial nucleobase conjugate. Inhibits the production of oncogenic miRNAs 372 (IC50 = 2.4 μM) by binding to pre-miRNAs and interrupts processing by Dicer.
包装规格:2 MG
产品编号:4083576
纯度规格:A blood-brain barrier permeable, potent, selective, and reversible antagonist of mGlu7 receptor (IC50 = 3.5 and 2.8 μM for mGlu7a and mGlu7b in CHO cells).
CAS NO:196928-50-4
包装规格:10 MG
产品编号:4083575
纯度规格:A cell-permeable, bioavailable, highly potent inhibitor of acyl CoA:monoacylglycerol acyltransferase 2 inhibitor (MGAT2, IC50 = 3.4 nM). Displays good microsomal stability.
包装规格:5 MG
产品编号:4083573
纯度规格:
包装规格:10 MG
产品编号:4083571
纯度规格:A synthetic cyclic alkylaminoluciferin with properties superior to D-luciferin. Binds to luciferase with higher affinity.
包装规格:10 MG
产品编号:4083570
纯度规格:A cell-permeable stain for neutral lipids. Does not stain phospholipids.
包装规格:5 MG
产品编号:4083569
纯度规格:
包装规格:5 MG
产品编号:4083567
纯度规格:A cell-permeable compound that prevents various bacterial toxins from exerting their cytotoxic activity by blocking endosomal trafficking/maturation into acidified late endosomes.
包装规格:25 MG
产品编号:4083565
纯度规格:A fast acting, reversible, and selective activator of Kir6.2/SUR1 channels (EC50 = 7 μM).
包装规格:10 MG
产品编号:4083563
纯度规格:A cell-permeable, direct, non-covalent inhibitor of Keap1-Nrf2 protein-protein interaction (Kd = 1 μM) that causes the dissociation of Nrf2 from keap1 in the cytosol.
包装规格:10 MG
产品编号:4083562
纯度规格:
包装规格:10 MG
产品编号:4083561
纯度规格:
包装规格:5 MG
产品编号:4083560
纯度规格:A cell-permeable, superior inhibitor of Jumonji C domain histone lysine demethylase. About 30 fold more potent than IOX1 (EC50 = 3.8 μM for KDM4A in HeLa cells vs. 100 μM for IOX1).
包装规格:10 MG
产品编号:4083558
纯度规格:A cell permeable analog of curcumin that acts as a specific inhibitor of JAK2 (~ 5 μM) and blocks STAT3 phosphorylation in MDA-MB-231 and PANC-1 cancer cells.
包装规格:25 MG
产品编号:4083557
纯度规格:The cell-permeable, selective inhibitor of eIF2α/eIF2S1 Ser51 phosphorylation-initiated UPR response (~25 to 200 nM) upon ER stress induction.
包装规格:10 MG
产品编号:4083556
纯度规格:InSolutionTM Y-27632, Sterile-Filtered, Cell Culture-Tested, CAS 146986-50-7, is a 10 mM sterile-filtered solution of Y-27632 in H2O. Acts as an inhibitor of Rho kinases (Ki = 140 nM for p160ROCK).
CAS NO:146986-50-7
包装规格:2 MG
产品编号:4083555
纯度规格:A 25 mM (2 mg/221 μL) sterile-filtered solution of TLR4 Inhibitor, TAK-242 in DMSO.
CAS NO:243984-11-4
包装规格:2 MG
产品编号:4083553
纯度规格:A 25 mM (10 mg/650 μl) sterile-filtered solution of SRT1720, HCl in DMSO.
CAS NO:1001645-58-4
包装规格:10 MG
产品编号:4083552
纯度规格:A 25 μM (10 mg/583 μL) sterile-filtered solution of Pepstatin A, Synthetic in DMSO.
CAS NO:26305-03-3
包装规格:10 MG
产品编号:4083550
纯度规格:
包装规格:5 MG
产品编号:4083549
纯度规格:A 25 mM (1 mg/98 μL) sterile-filtered solution of Histone Methyltransferase EZH2 Inhibitor, DZNep in H2O.
CAS NO:102052-95-9
包装规格:1 MG
产品编号:4083547
纯度规格:A 50 mM (2 mg/106.23 μL) sterile-filtered solution of APT1 Inhibitor, palmostatin B in DMSO.
包装规格:2 MG