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397712个产品
产品编号:4083738
纯度规格:A cell-permeable inhibitor of SKP2-dependent p27Kip1 ubiquitination. Selectively induces the accumulation SCFSKP2 substrates in multiple myeloma RPMI 8226 cells.
包装规格:10 MG
产品编号:4083737
纯度规格:
包装规格:10 MG
产品编号:4083736
纯度规格:A highly potent agonist of GABAB receptor. Shown to be about 10-times more potent than baclofen.
CAS NO:127729-35-5
包装规格:10 MG
产品编号:4083734
纯度规格:
包装规格:10 MG
产品编号:4083725
纯度规格:A cell-permeable racemic mixture of Halofuginone that inhibits of prolyl-tRNA synthetase.
CAS NO:64924-67-0
包装规格:10 MG
产品编号:4083724
纯度规格:A cell-permeable, selective inhibitor of protein arginine methyltransferase 1 (PRMT1; IC50 = 9.5 μM).
包装规格:10 MG
产品编号:4083722
纯度规格:
包装规格:10 MG
产品编号:4083721
纯度规格:A cell-permeable inhibitor of Wnt secretion from L-cell Wnt1/2/3/3a/6/7a/9a transfectants (IC50 from 50 pM to 1.1 nM).
CAS NO:1243244-14-5
包装规格:5 MG
产品编号:4083717
纯度规格:A rhodanine-derived, reversible, photoactivated, TrpA1-selective channel activator.
包装规格:10 MG
产品编号:4083714
纯度规格:A cell-permeable, highly potent and selective inhibitor of phosphodiesterase 5 (PDEV; IC50 = 270 pM).
包装规格:5 MG
产品编号:4083710
纯度规格:A cell-permeable compound that selectively downregulates the expression of p21 (~10 μM), independent of p53.expression, at either transcription or post-transcriptional level.
包装规格:10 MG
产品编号:4083706
纯度规格:A cell-permeable myristoylated hexapeptide that selectively inhibits integrin outside-in signaling without affecting inside-out signaling. Blocks the interaction of Gα3 and integrin β3 subunit.
包装规格:10 MG
产品编号:4083701
纯度规格:A cell-permeable. Reversible, selective inhibitor of the growth of malignant peripheral nerve sheath tumors (EC50 = 439 nM, 754 nM, and 1.0 μM in S462, SNF96.2, and sMPNST cells).
包装规格:25 MG
产品编号:4083697
纯度规格:
包装规格:10 MG
产品编号:4083692
纯度规格:A cell-permeable, potent, selective, reversible inhibitor of Lysine-Specific Demethylase 1 (LSD1; IC50 = 13 nM; Ki = 31 nM).
CAS NO:1423715-09-6
包装规格:10 MG
产品编号:4083691
纯度规格:A cell-permeable, both NADH and pyruvate-competitive isoform A-selective LDH inhibitor. Exhibits enhanced anticancer activity under hypoxic conditions.
CAS NO:1269802-68-7
包装规格:10 MG
产品编号:4083690
纯度规格:A cell-permeable, fast acting, branched polyamine. Induces growth of actin-enriched lamellipodia within minutes without the need for serum cofactors .
包装规格:10 MG
产品编号:4083688
纯度规格:A voltage gated calcium channel gating inhibitor of the dihydropyridine class.
CAS NO:75695-93-1
包装规格:10 MG
产品编号:4083686
纯度规格:A substrate competitive inhibitor of insulin-regulated aminopeptidase (IRAP) activity (Ki = 0.48 μM against 25 μM Leu-AMC).
包装规格:10 MG
产品编号:4083685
纯度规格:A 10 mM (5 mg/1.07 ml) sterile-filtered solution of Wnt Antagonist II, IWP-2) in DMSO.
CAS NO:686770-61-6
包装规格:5 MG
产品编号:4083683
纯度规格:A 25 mM (5 mg/357 μl) sterile-filtered solution of PPACK, 2HCl in H2O.
CAS NO:74392-58-8
包装规格:5 MG
产品编号:4083680
纯度规格:
CAS NO:478336-92-4
包装规格:10 MG
产品编号:4083678
纯度规格:A 50 mM sterile-filtered solution of I-BET in DMSO.
CAS NO:1260907-17-2
包装规格:5 MG
产品编号:4083677
纯度规格:A 25 mM (2 mg/231 μl) sterile-filtered solution of Ginkgolic Acid (15:1) in DMSO.
CAS NO:22910-60-7
包装规格:2 MG
产品编号:4083676
纯度规格:
包装规格:5 MG
产品编号:4083675
纯度规格:
CAS NO:130370-60-4
包装规格:2 MG
产品编号:4083674
纯度规格:A 25 mM solution of (+)-Brefeldin A in DMSO.
CAS NO:20350-15-6
包装规格:2 MG
产品编号:4083672
纯度规格:A cell-permeable compound that competitively binds to Hu antigen R (HuR; Ki = 350 nM) and disrupts the interaction of HuR and adenine- and uridine-rich element (ARE) of target mRNAs.
包装规格:10 MG
产品编号:4083670
纯度规格:
CAS NO:1423058-85-8
包装规格:10 MG
产品编号:4083667
纯度规格:Cell-permeable inhibitor of gp130. Binds to gp130 and induces its phosphorylation at Ser782 in ovarian cancer cells. Suppresses constitutive phosphorylation of and nuclear translocation of Stat3.
包装规格:10 MG
产品编号:4083664
纯度规格:
包装规格:
产品编号:4083662
纯度规格:Specifically binds to the Fn14 surface (Kd = 7.12 mM) and suppresses TWEAK-induced glioma cell migration.
包装规格:10 MG
产品编号:4083661
纯度规格:A cell-permeable structural analog of E1 that acts as an equipotent, SAM-competitive inhibitor of Ezh2/PRC2 inhibitor (Ki = 0.5 to 3 nM against wt &mutant Ezh2-containing PRC2).
包装规格:5 MG
产品编号:4083658
纯度规格:
包装规格:10 MG
产品编号:4083655
纯度规格:DHODH Inhibitor, DSM1, is a highly potent, competitive, tight-binding inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (IC50 = 47 nM; Ki = 15 nM).
包装规格:25 MG
产品编号:4083653
纯度规格:
包装规格:5 MG
产品编号:4083650
纯度规格:
包装规格:10 MG
产品编号:4083649
纯度规格:
CAS NO:1253186-56-9
包装规格:10 MG
产品编号:4083648
纯度规格:A 25 mM (10 mg/608 μL) sterile-filtered solution of CMP-Sialic Acid, Disodium Salt in H2O.
CAS NO:3063-71-6
包装规格:10 MG
产品编号:4083647
纯度规格:
包装规格:25 MG
产品编号:4083645
纯度规格:A cell-permeable, highly potent, and specific inhibitor of CDC-like kinase (CLK; IC50 = 1.1 and 2.4 nM for CLK1 and CLK2, respectively).
包装规格:5 MG
产品编号:4083644
纯度规格:A cell-permeable, potent, irreversible, non-substrate competitive inhibitor of CD45/PTPRC tyrosine phosphatase activity (IC50 = 290 nM).
包装规格:10 MG
产品编号:4083642
纯度规格:Enhances BMP-2 associated signaling by inhibiting Smurf1-mediated Smad1/5 ubiquitination and thereby prolonging the half-life of Smad1 and 5. in 48 h).
包装规格:10 MG
产品编号:4083641
纯度规格:A cell-permeable compound that downregulates cellular BMI-1 levels by inhibiting BMI-1 transcription.
CAS NO:315704-66-6
包装规格:10 MG
产品编号:4083640
纯度规格:A cell permeable, highly potent, selective inhibitor of Aurora A (IC50 = 48 nM). Disrupts MYCN-Aurora A complex.
包装规格:10 MG
产品编号:4083638
纯度规格:A cell-permeable compound that directly and reversibly interacts with miRNA binding domain of Argonaute-2 (Kd = 126 μM) and inhibits binding of miR-20a, miR-26a, miR-107, miR-223 &let-7a to Ago2.
包装规格:25 MG
产品编号:4083634
纯度规格:Acid Ceramidase Inhibitor, BOC, CAS 1644158-57-5, is a cell-permeable, potent inhibitor of acid ceramidase (IC50 = 79 nM against HEK293 lysosomal lysate AC activity).
包装规格:10 MG
产品编号:4083632
纯度规格:An anti-bacterial compound that targets NAD(P)H-dependent enoyl acyl carrier protein reductase (ENR) resulting in the inhibition of bacterial fatty acid synthase.
包装规格:10 MG
产品编号:4083627
纯度规格:A cell-permeable, selective, potent, and reversible inhibitor of USP1-UAF1 deubiquitinase (IC50 = 76 nM in Ub-Rhodamine based assays). Does not disrupt USP1-UAF1 association.
包装规格:10 MG
产品编号:4083625
纯度规格:Directly and selectively binds to the troponin complex in fast skeletal muscle (Kd = 40 nM) and sensitizes it to calcium.
CAS NO:1005491-05-3
包装规格:10 MG
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