共 304512 个产品
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
货号：5.06387CAS：包装：10 mg分子式：C16H11FN6O · xHCl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.分子量：322.30 (free base basis)
货号：5.05760CAS：1423058-85-8包装：10 MG分子式：C6H9NO2纯度规格：分子量：127.14
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