共 304515 个产品
货号：5.05602CAS：包装：10 mg分子式：C9H9ClO2纯度规格：A cell-permeable inhibitor of mitochondrial branched-chain α-ketoacid dehydrogenase complex (BCKDC) regulatory kinase BDK (IC50 = 6.3 μM).分子量：184.62
货号：5.06048CAS：包装：10 mg分子式：C164H251N57O45纯度规格：Beclin-1 Activator I, TAT-Beclin-1, is a cell-permeable Atg6/Beclin1-derived autophagy-inducing peptide. Activates Beclin1 by competing against its negative regulator GAPR-1/GLIPR2.分子量：3741.10
货号：5.09890CAS：132-17-2包装：50 mg分子式：C21H2NO · xCH4O3S纯度规格：An antagonist of muscarinic M1 and M3 receptors that induces robust differentiation of oligodendrocytes precursor cell differentiation (EC50 = 500 nM) and promotes myelination.分子量：284.25 (free base basis)- 货号：5.32310CAS：包装：10 mg分子式：C22H15N3O4纯度规格：KJ-Pyr-9, C-Myci分子量：385.37
货号：5.30654CAS：包装：10 mg分子式：C11H9BrN2O3S纯度规格：A cell-permeable compound that directly and reversibly binds to c-Rel to change its conformation and blocks its DNA binding and transcriptional activity (IC50 = 3 μM).分子量：329.17
货号：5.33683CAS：包装：10 mg分子式：C47H65N11O7 · xC2HF3O2纯度规格：A cell-permeable, orally available, non-competitive antagonist of C5a receptor (CD88; IC50 = 240 nM) and as a low-affinity agonist for MrgX2.分子量：896.09 (free base basis)
货号：5.09709CAS：包装：1 set分子式：纯度规格：A set of PYR6, a CRAC Channel Inhibitor III; and PYR10, a TPRC3 Channel Inhibitor III.分子量：
货号：5.38763CAS：1700637-55-3包装：10 MG分子式：C22H27N3O3S纯度规格：分子量：413.53
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
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