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  • T1724SCR7 pyrazineSCR7 pyrazine,SCR7,

    SCR7 is a specific DNA Ligase IV inhibitor, which blocks nonhomologous end-joining (NHEJ).

    价 格：￥电议型 号：T1724产 地：美洲

  • T1725Y-27632 dihydrochlorideY-27632 dihydrochloride,Y-27632 2HCl,

    Y-27632 is a selective inhibitor of ROCKs including p160ROCK (Ki: 140 nM) and ROCK2 (IC50: 800 nM).

    价 格：￥电议型 号：T1725产 地：美洲

  • T17258WRG-28WRG-28

    WRG-28 is a potent and selective, allosteric discoidin domain receptor 2 (ddr2) inhibitor(IC50 : 230 nM)

    价 格：￥电议型 号：T17258产 地：美洲

  • T1726SB 431542SB 431542

    SB-431542 is a potent and selective inhibitor of ALK5 (IC50: 94 nM) and is also an inhibitor of ALK4 (IC50: 140 nM) and ALK7.

    价 格：￥电议型 号：T1726产 地：美洲

  • T17274-Cyclohexyl-1-phenylthiosemicarbazide4-Cyclohexyl-1-phenylthiosemicarbazide

    N/A

    价 格：￥电议型 号：T1727产 地：美洲

  • T2172SQ 22536SQ 22536,9-(tetrahydrofuran-2-yl)-9h-purin-6-amine,

    SQ 22536, the adenosine analogue 9-(Tetrahydro-2-furyl)adenine, inhibited adenylate cyclase activity of crude membrane preparations from catfish (Ictalurus melas) and rat isolated hepatocytes in a non-competitive manner.

    价 格：￥电议型 号：T2172产 地：美洲

  • T2355CFTRinh-172CFTRinh-172,CFTRinh172,CFTRinh 172

    CFTRinh-172 is a voltage-independent, selective CFTR inhibitor.

    价 格：￥电议型 号：T2355产 地：美洲

  • T2412SRT1720 hydrochlorideSRT1720 hydrochloride,SRT 1720 Hydrochloride,SRT1720 HCl

    SRT 1720 is a selective activator of SIRT1 (EC1.5: 0.16 μM) and shows less potent activities on SIRT2/SIRT3 (EC1.5s: 37 μM/300 μM).

    价 格：￥电议型 号：T2412产 地：美洲

  • T4547GrazoprevirGrazoprevir,MK-5172,

    MK-5172 is a selective inhibitor of Hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants, with Ki of 0.01 nM (gt1a), 0.08 nM (gt2a), 0.90 nM (gt3a), 0.01 nM (gt1b), 0.15 nM (gt2b), respectively.

    价 格：￥电议型 号：T4547产 地：美洲

  • T4999ErtugliflozinErtugliflozin,PF-04971729,MK-8835

    PF-04971729 (Ertugliflozin) is a potent and selective inhibitor of the sodium-dependent glucose cotransporter 2 (SGLT2).

    价 格：￥电议型 号：T4999产 地：美洲

  • T4S1725GalanthamineGalanthamine,Galantamine,

    Galanthamine is an acetylcholinesterase (AChE)inhibitor(IC50 : 500 nM), can reduce brain damage induced by hypoxia-ischemia.

    价 格：￥电议型 号：T4S1725产 地：美洲

  • T5096SRT 1720SRT 1720

    SRT 1720 is a selective activator of human SIRT1 (EC1.5: 0.16 μM) and is >230-fold less potent for SIRT2 and SIRT3.

    价 格：￥电议型 号：T5096产 地：美洲

  • T5172AZ304AZ304

    AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits BRAF (WT), BRAF (V600E), and wild type CRAF (IC50s: 79/38/68 nM).

    价 格：￥电议型 号：T5172产 地：美洲

  • T5S1172TilirosideTiliroside,Tribuloside,

    1. Tiliroside shows anticarcinogenic activity. 2. Tiliroside shows hepatoprotective activity. 3. Tiliroside shows antioxidant and anti-inflammatory activity, can inhibit neuroinflammation in neurodegenerative disorders. 4. Tiliroside has anti-diabetic ef

    价 格：￥电议型 号：T5S1172产 地：美洲

  • T6172MRS 2578MRS 2578

    MRS2578, an effective P2Y6 receptor antagonist with IC50 of 37 nM, shows insignificant inhibition at P2Y1, P2Y2, P2Y4, and P2Y11 receptors.

    价 格：￥电议型 号：T6172产 地：美洲

  • T8745PROTAC BRAF-V600E degrader-1；化合物2417296-84-3Compound 23；Compound 23

    PROTAC BRAF-V600E degrader-1 (Compound 23) selectively induces degradation of BRAF-V600E but not wildtype BRAF.

    价 格：￥电议型 号：T8745产 地：中国大陆

  • T83172Adam-20-S；化合物 Adam-20-SAdam-20-S

    Adam-20-S is a potent inhibitor of glucosinolate sulfatase, exhibiting an IC50 of 9.04 μg/mL. This compound disrupts glucosinolate metabolism, enhancing the production of toxic isothiocyanates in P. xylostella [1].

    价 格：￥电议型 号：T83172产 地：中国大陆

  • T83079Anticancer agent 172；化合物 Anticancer agent 172Anticancer agent 172

    Anticancer agent 172 (8d) exhibits potent activity against cancer, achieving an IC50 value of 6.96 μM in HCT116 cells [1].

    价 格：￥电议型 号：T83079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

  • T82257GRL-1720 TFA；化合物 GRL-1720 TFAGRL-1720 TFA

    GRL-1720 TFA is a potent SARS-CoV-2 Mpro inhibitor, demonstrating anti-SARS-CoV-2 activity with an EC50 of 15 μM [1].

    价 格：￥电议型 号：T82257产 地：中国大陆

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