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  • T13112LTat-NR2B9c TFATat-NR2B9c TFA,NA-1 (TFA),

    Tat-NR2B9c TFA is a 20-aa peptide, and acts as an inhibitor of postsynaptic density-95 (PSD-95)(EC50 of 6.7 nM for PSD-95d2), and possesses neuroprotective efficacy.

    价 格：￥电议型 号：T13112L产 地：美洲

  • T14688BMS CCR2 22BMS CCR2 22

    BMS CCR2 22 is a potent, specific and high affinity CC-type chemokine receptor 2 (CCR2) antagonist. It has excellent binding affinity (binding IC50 of 5.1 nM) and potent functional antagonism (calcium flux IC50 of 18 nM and chemotaxis IC50 of 1 nM)[1][2].

    价 格：￥电议型 号：T14688产 地：美洲

  • T14765BOS-172722BOS-172722

    BOS-172722 is an inhibitor of monopolar spindle 1 (MPS1) checkpoint. With an IC50 of 2 nM.

    价 格：￥电议型 号：T14765产 地：美洲

  • T14834BT2BT2

    BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of

    价 格：￥电议型 号：T14834产 地：美洲

  • T16657Boc-NH-PEG2Boc-NH-PEG2,PROTAC Linker 11,

    Boc-NH-PEG2 (PROTAC Linker 11) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1].

    价 格：￥电议型 号：T16657产 地：美洲

  • T16663Bis-NH2-PEG2Bis-NH2-PEG2,PROTAC Linker 19,

    Bis-NH2-PEG2 (PROTAC Linker 19) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1].

    价 格：￥电议型 号：T16663产 地：美洲

  • T1837BX912BX912

    BX-912 is a specific inhibitor of 3-Phosphoinositide-dependent Kinase-1 (PDK1, IC50: 12 nM). The selectivity of BX-912 is more 10 fold than C-Kit, EGFR, PKA, PKC etc.

    价 格：￥电议型 号：T1837产 地：美洲

  • T1902BAY 11-7082BAY 11-7082,BAY 11-7821,

    BAY 11-7082, a NF-κB inhibitor, inhibits TNFα-induced IκBα phosphorylation. BAY 11-7082 inhibits ubiquitin-specific protease USP7 and USP21.

    价 格：￥电议型 号：T1902产 地：美洲

  • T2380BIBR 1532BIBR 1532

    BIBR 1532 is an effective, specific and non-competitive telomerase inhibitor (IC50: 100 nM, in a cell-free assay).

    价 格：￥电议型 号：T2380产 地：美洲

  • T4656B02B02,RAD51 Inhibitor B02,

    RAD51 Inhibitor B02 (B02) is an inhibitor of human RAD51 with an IC50 of 27.4 μM.

    价 格：￥电议型 号：T4656产 地：美洲

  • T5138BMS-986142BMS-986142,BMS986142,BMS 986142

    BMS-986142 is a potent and highly selective reversible BTK inhibitor (IC50: 0.5 nM).

    价 格：￥电议型 号：T5138产 地：美洲

  • T5208BAY-8002BAY-8002,BAY8002,BAY 8002

    BAY-8002 is a potent dual MCT1/2 inhibitor (IC50 values are 3, 8, and 12 nM at rat (C6), human (DLD-1) and mouse (4T1) MCT1 respectively).

    价 格：￥电议型 号：T5208产 地：美洲

  • T6423BRL-15572BRL-15572,BRL15572,BRL 15572

    BRL-15572 is a 5-HT1D receptor antagonist with pKi of 7.9, also shows a considerable affinity at 5-HT1A and 5-HT2B receptors, exhibiting 60-fold selectivity over 5-HT1B receptor.

    价 格：￥电议型 号：T6423产 地：美洲

  • T8564BC-1382；化合物BC-1382BC-1382

    BC-1382 is a potent ubiquitin E3 ligase HECTD2 inhibitor that specificly disrupts the HECTD2/PIAS1 interaction(IC50 of 5 nM).

    价 格：￥电议型 号：T8564产 地：中国大陆

  • T84321BLU-222；化合物 BLU-222BLU-222

    BLU-222 is a potent, selective and orally active CDK2 inhibitor. BLU-222 shows robust antitumor activity.

    价 格：￥电议型 号：T84321产 地：中国大陆

  • T83510[Arg-15,20,21,Leu17]-PACAP-Gly-Lys-Arg-NH2；化合物 [Arg-15,20,21,Leu17]-PACAP-Gly-Lys-Arg-NH2BM-PACAP；BM

    [Arg-15,-20,-21, Leu17]-PACAP-Gly-Lys-Arg-NH2 (BM-PACAP) is a synthetic analogue of PACAP 1-27 that exhibits a relaxant effect [1].

    价 格：￥电议型 号：T83510产 地：中国大陆

  • T83147Albinterferon alfa-2B；化合物 Albinterferon alfa-2Balb-IFN；alb-IFN

    Albinterferon alfa-2B (alb-IFN), a recombinant protein, comprises interferon alfa-2b conjugated to human albumin and is utilized in the study of chronic hepatitis C [1].

    价 格：￥电议型 号：T83147产 地：中国大陆

  • T82914Bcl-2-IN-12；化合物 Bcl-2-IN-12Bcl-2-IN-12

    Bcl-2-IN-12 (Compound 1) is a potent Bcl-2 inhibitor with an IC50 value of 6 nM, utilized in cancer research [1].

    价 格：￥电议型 号：T82914产 地：中国大陆

  • T82850BMS-332；化合物 BMS-332BMS-332

    BMS-332 is a dual inhibitor of the lipid kinases DGKα and DGKζ, demonstrating half-maximal inhibitory concentrations (IC50) of 0.005 μM for DGKα and 0.001 μM for DGKζ [1].

    价 格：￥电议型 号：T82850产 地：中国大陆

  • T82848BMS-986172；化合物 BMS-986172BMS-986172

    BMS-986172 is an orally active, highly selective inhibitor of MGAT2, demonstrating inhibitory concentrations (IC50) of 4.6 nM for human MGAT2 (hMGAT2) and 20 nM for mouse MGAT2 (mMGAT2). It exhibits a half-life (T1/2) greater than 120 minutes in vitro and is known to decrease food intake and body weight. This compound is considered promising for the research of metabolic disorders, including obesity and non-alcoholic steatohepatitis (NASH) [1].

    价 格：￥电议型 号：T82848产 地：中国大陆

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