共 304502 个产品
货号：5.30352CAS：包装：25 mg分子式：C17H17NO纯度规格：A cell-permeable compound that specifically targets TRAF6 (Kd = 97 μM for TRAF6 C-domain) and disrupts its functional coupling with CD40.分子量：251.32
货号：5.09704CAS：1319207-44-7包装：10 mg分子式：C20H21Cl2NO6纯度规格：A cell-permeable, selective allosteric inhibitor of E2 ubiquitin-conjugating enzyme Cdc34 (IC50 = 2.5 μM in a Sic1-SCFCdc4 assay).分子量：442.29
货号：5.09583CAS：包装：10 mg分子式：C12H17N3O2S纯度规格：An agonist of mammalian Diaphanous (mDia)-related formins that disrupts diaphanous inhibitory domain (DID) and diaphanous autoregulatory domain (DAD) interaction (IC50 = 140 nM).分子量：267.35
货号：5.08321CAS：96201-88-6包装：10 mg分子式：C23H14F2NNaO2纯度规格：An immunosuppressive and anti-neoplastic agent that inhibits pyrimidine synthesis by blocking the activity of mammalian mitochondrial dihydroorotate dehydrogenase (DHODH; IC50 = 12 nM).分子量：397.35
货号：5.33982CAS：54129-15-6包装：50 MG分子式：C12H9Cl2NO2S纯度规格：分子量：302.18
货号：5.30536CAS：包装：25 mg分子式：C11H6N4O4S纯度规格：A nitro-benzoxadiazole compound that directly binds to the dimerization domain of sEGF receptor to generate stable dimers and allosterically activate the receptor.分子量：290.25
货号：5.33871CAS：包装：10 mg分子式：C36H52N2O4纯度规格：A cell-permeable antagonist of Eph receptors that competitively disrupts Eph2A-ephrin-A1 binding (IC50 = 945 nM; Ki = 345 nM).分子量：576.81
货号：5.09230CAS：包装：10 mg分子式：C25H30N2O5纯度规格：A cell-permeable compound that reversibly blocks cellular glycosylation and surface expression of Notch, APP, Klotho by blocking events prior to cargo assembly at the ER exit sites.分子量：438.52
货号：5.31085CAS：包装：25 mg分子式：C17H12FN3O2S纯度规格：A cell-permeable inhibitor of Eya2 ED tyrosine phosphatase (IC50 = 4.1 μM; KD = 2.0 μM for hEya2, catalytic domain)分子量：341.36
货号：5.08320CAS：包装：2 mg分子式：C155H256N48O40 · 6C2HF3O2 · 14H2O纯度规格：A helical 27-mer peptide with E54Q modification that directly binds to EDD (Kd = 320 nM) and disrupts protein-protein interaction of EED with EZH2 and EZH1.分子量：4368.34
货号：5.08506CAS：60142-96-3包装：10 mg分子式：C9H17NO2纯度规格：A water soluble GABA analog that interacts with voltage-gated calcium channels in cortical neurons.分子量：171.24
货号：5.38285CAS：491833-30-8包装：10 MG分子式：C24H38N2O4纯度规格：分子量：418.57
货号：5.38096CAS：包装：10 MG分子式：C22H30Cl2N2O4S纯度规格：分子量：489.46
货号：5.08941CAS：包装：10 mg分子式：C19H15NO2纯度规格：A cell-permeable, highly potent, and selective agonist of free fatty acid receptor 1 (FFA1; GPR40; EC50 = 20 nM in FFA1-transfected HEK-293 cells).分子量：289.33
货号：5.08313CAS：包装：5 mg分子式：C20H26FN5O4纯度规格：A cell-permeable 6-amino-purine based compound that selectively binds to HSP90a (EC50 = 5.4 μM) and inhibits its activity cancer cells.分子量：419.45
货号：5.09880CAS：1432660-47-3包装：10 mg分子式：C21H18F3N3O3S2纯度规格：A cell-permeable inhibitor of isocitrate dehydrogenase 2 R140Q mutant-containing dimers. Has minimal effect on wild type dimer-catalyzed alpha-KG production.分子量：481.51
货号：5.30588CAS：包装：10 mg分子式：C28H19FN2O4纯度规格：A cell-permeable, selective inhibitor of E3 ligase complex SCFβTrCP1-mediated ubiquitination of phosphorylated IκBα (IC50 = 5.2 μM).分子量：466.46
货号：5.04744CAS：38966-21-1包装：1 mg分子式：C20H34O4纯度规格：A 30 mM (1 mg/98 μL) sterile-filtered solution of Aphidicolin in DMSO.分子量：338.48
货号：5.08738CAS：包装：2 mg分子式：C23H36O4纯度规格：A 50 mM (2 mg/106.23 μL) sterile-filtered solution of APT1 Inhibitor, palmostatin B in DMSO.分子量：376.53
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