共 304517 个产品
- 货号:5.31230CAS:1005491-05-3包装:10 mg分子式:C12H14N4O纯度规格:Directly and selectively binds to the troponin complex in fast skeletal muscle (Kd = 40 nM) and sensitizes it to calcium.分子量:230.27
- 货号:5.31131CAS:包装:10 mg分子式:C23H24N6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.分子量:384.48
- 货号:5.06135CAS:99300-78-4包装:10 MG分子式:C17H27NO2 · xHCl纯度规格:分子量:277.40 (free base basis)
- 货号:5.30729CAS:包装:10 mg分子式:C14H13BN2O3S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.分子量:300.14
- 货号:5.33371CAS:包装:10 mg分子式:C24H21FN2O3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).分子量:404.43
- 货号:5.31552CAS:包装:25 mg分子式:C11H11N3O6S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.分子量:313.29
- 货号:5.32605CAS:包装:10 mg分子式:C26H25F3N8O纯度规格:A cell permeable, highly potent, selective inhibitor of Aurora A (IC50 = 48 nM). Disrupts MYCN-Aurora A complex.分子量:522.52
- 货号:5.30154CAS:315704-66-6包装:10 mg分子式:C17H13Br2N5OS纯度规格:A cell-permeable compound that downregulates cellular BMI-1 levels by inhibiting BMI-1 transcription.分子量:495.19
- 货号:5.31370CAS:包装:10 mg分子式:C22H20ClF3N4O3S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).分子量:512.93
- 货号:5.30197CAS:包装:10 mg分子式:C18H12ClNO3纯度规格:A cell-permeable, potent, irreversible, non-substrate competitive inhibitor of CD45/PTPRC tyrosine phosphatase activity (IC50 = 290 nM).分子量:325.75
- 货号:5.34350CAS:包装:5 mg分子式:C20H20N6O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).分子量:360.41
- 货号:5.05223CAS:3063-71-6包装:10 mg分子式:C20H29N4O16P · 2Na纯度规格:A 25 mM (10 mg/608 μL) sterile-filtered solution of CMP-Sialic Acid, Disodium Salt in H2O.分子量:658.41
- 货号:5.34351CAS:1253186-56-9包装:10 MG分子式:C18H12F5N3O2纯度规格:分子量:397.30
- 货号:5.38341CAS:包装:10 MG分子式:C33H30ClN3O5 · xHCl纯度规格:分子量:584.06 (free base basis)
- 货号:5.33304CAS:包装:25 mg分子式:C16H13N5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).分子量:275.31
- 货号:5.04540CAS:包装:10 MG分子式:C29H31F3N6O3 · xHCl纯度规格:分子量:568.59 (free base basis)
- 货号:5.00580CAS:包装:5 mg分子式:C31H38N6O2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).分子量:526.67
- 货号:5.09374CAS:包装:10 mg分子式:C13H13ClN4OS纯度规格:Specifically binds to the Fn14 surface (Kd = 7.12 mM) and suppresses TWEAK-induced glioma cell migration.分子量:308.79
共15226页,第6389页 |