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  • T23233LRETF-4NA acetateRETF4NA acetate,RETF 4NA acetate

    RETF-4NA acetate is a sensitive, specific substrate for chymotrypsin.

    价 格：￥电议型 号：T23233L产 地：中国大陆

  • T6938PF-4989216Apoptosis,inhibit,Phosphoinositide 3-kinase,PF4989216,PF-4989216,PI3K,Inhibitor

    PF-4989216 is a potent and selective PI3K inhibitor with IC50 of 2 nM, 142 nM, 65 nM, 1 nM, and 110 nM for p110α, p110β, p110γ, p110δ, and VPS34, respectively.

    价 格：￥电议型 号：T6938产 地：中国大陆

  • TP1814LCEF4 acetateCEF4 acetate,CEF-4 acetate

    CEF4 is a polypeptide corresponding to amino acid sequence 342-351 of the influenza A virus nucleocapsid protein.

    价 格：￥电议型 号：TP1814L产 地：中国大陆

  • T6251PF-04691502PF4691502；PF 04691502

    PF-04691502 is a potent and selective inhibitor of PI3K and mTOR kinases with antitumor activity.

    价 格：￥电议型 号：T6251产 地：中国大陆

  • T6028PF 477736PF477736；PF 00477736；PF-477736；PF-736,PF-00477736

    PF-477736 is a specifc, effective and ATP-competitive Chk1 inhibitor (Ki: 0.49 nM ) and also inhibits FGFR3, Aurora-A, VEGFR2, Flt3, Fms (CSF1R), Ret and Yes.

    价 格：￥电议型 号：T6028产 地：中国大陆

  • T5056PF-4800567PF4800567；PF 4800567

    PF-4800567 is a selective inhibitor of casein kinase 1ε (CK1ε; IC50 = 32 nM) with greater than 20-fold selectivity over CK1δ.

    价 格：￥电议型 号：T5056产 地：中国大陆

  • T4385PF-4840154PF 4840154；PF4840154

    PF-4840154 is a potent, selective agonist of the rat and human TrpA1 channel and elicited TrpA1-mediated nocifensive behaviour in mouse, with EC50 of 97 nM and 23 nM for rTrpA1 and hTrpA1, respectively.

    价 格：￥电议型 号：T4385产 地：中国大陆

  • T3430PF-4136309PF 4136309；INCB8761；PF4136309

    INCB8761(PF-4136309) is a specific, effective, and orally bioavailable CCR2 antagonist.

    价 格：￥电议型 号：T3430产 地：中国大陆

  • T304810058-F4c-Myc Inhibitor

    10058-F4 is a cell-permeable thiazolidinone that specifically inhibits the c-Myc-Max interaction and prevents transactivation of c-Myc target gene expression; induces cell-cycle arrest and apoptosis.

    价 格：￥电议型 号：T3048产 地：中国大陆

  • T28178NLRP3-IN-9INF 4E；INF4E；NLRP3IN9；NLRP3 IN 9；INF-4E

    NLRP3-IN-9 is an inhibitor of NLRP3 ATPase and caspase-1. NLRP3-IN-9 acts by irreversibly trapping thiol nucleophiles, which prevents both ATP- and nigericin-triggered pyroptosis of human THP-1 cells in a time- and concentration-dependent manner.

    价 格：￥电议型 号：T28178产 地：中国大陆

  • T2002PF-4708671PF 4708671；PF4708671

    PF-4708671 is a cell-permeable inhibitor of p70 ribosomal S6 kinase (S6K1 isoform) .In cell-free assays, PF-4708671 is potent for S6K1(Ki50=20 nM, IC50=160 nM).

    价 格：￥电议型 号：T2002产 地：中国大陆

  • T19031NBD-F4-Fluoro-7-nitrobenzofurazan

    NBD-F is a fluorescent derivatization compound for amino acid analysis.

    价 格：￥电议型 号：T19031产 地：中国大陆

  • T12616LCE3F4

    CE3F4 is a selective antagonist of exchange protein directly activated by cAMP (Epac1; IC50s of 10.7 μM and 66 μM for Epac1 and Epac2(B), respectively).

    价 格：￥电议型 号：T12616L产 地：中国大陆

  • T12437PF429242 dihydrochloride

    PF429242 dihydrochloride can reversibly inhibit S1P (IC50 of 175 nM).

    价 格：￥电议型 号：T12437产 地：中国大陆

  • T11447GNF4877

    GNF4877 is a potent DYRK1A and GSK3β inhibitor (IC50s: 6 nM and 16 nM). It leads to blockade of nuclear factor of activated T-cells (NFATc) nuclear export and increased β-cell proliferation cells.

    价 格：￥电议型 号：T11447产 地：中国大陆

  • T001-00000003PF-04745637PF 4745637；PF-4745637；PF 04745637；PF4745637；PF04745637

    PF-04745637 is a potent and selective TRPA1 antagonist with an IC50 of 17 nM[1].

    价 格：￥电议型 号：T001-00000003产 地：中国大陆

  • T11171eIF4A3-IN-2eIF4A3-IN-2

    eIF4A3-IN-2 is a highly selective and noncompetitive eukaryotic initiation factor 4A-3 inhibitor with an IC50 of 110 nM.

    价 格：￥电议型 号：T11171产 地：美洲

  • T11447GNF4877GNF4877

    GNF4877?leads to blockade of nuclear factor of activated T-cells (NFATc) nuclear export and increased β-cell proliferation cells.?GNF4877 is a potent DYRK1A and GSK3β inhibitor with IC50s of 6?nM and 16?nM, respectively.

    价 格：￥电议型 号：T11447产 地：美洲

  • T12437PF429242 dihydrochloridePF429242 dihydrochloride

    PF429242 dihydrochloride is a reversible and competitive inhibitor of S1P (IC50 of 175 nM).

    价 格：￥电议型 号：T12437产 地：美洲

  • T16069MF498MF498

    MF498 is a novel and selective E prostanoid receptor 4 (EP4 receptor) antagonist, displayed a strong binding affinity for the EP4 receptor (Ki: 0.7 nM).

    价 格：￥电议型 号：T16069产 地：美洲

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