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  • T38050CP-609754

    CP-609754 shows selective inhibition of farnesyltransferase.

    价 格：￥电议型 号：T38050产 地：中国大陆

  • T371965-AAM-2-CP

    5-AAM-2-CP is one of the major metabolites of Acetamiprid. Acetamiprid, a nAChR agonist, is a neonicotinoid insecticide used worldwide.

    价 格：￥电议型 号：T37196产 地：中国大陆

  • T3701MCC950CP-456773

    CP-456773 (MCC950 and CRID3) is an effective and specific cytokine release inhibitor and NLRP3 inflammasome inhibitor. CP-456773 inhibits IL-1β secretion and caspase 1 processing. MCC950 blocked canonical and noncanonical NLRP3 activation at nanomolar con

    价 格：￥电议型 号：T3701产 地：中国大陆

  • T3684CP21R7CP21

    CP21R7 is an effective and specific GSK3β inhibitor. It is used as an activator of stem cells prior to the induction of differentiation of stem cells to smooth muscle and endothelial cells. CP21R7 can be combined with BMP4 to commit human pluripotent stem

    价 格：￥电议型 号：T3684产 地：中国大陆

  • T3626Acalabrutinib阿可替尼；ACP-196

    Acalabrutinib, also known as ACP-196, is an orally available inhibitor of Bruton´s tyrosine kinase (BTK) with potential antineoplastic activity. Upon administration, ACP-196 inhibits the activity of BTK and prevents the activation of the B-cell antigen re

    价 格：￥电议型 号：T3626产 地：中国大陆

  • T3622CP-640186 hydrochlorideCP 640186 HCl；盐酸CP-640186

    CP-640186 HCl is an isozyme-nonselective acetyl-CoA carboxylase (ACC) inhibitor, including rat liver ACC1 (IC50: 53 nM) and rat skeletal muscle ACC2 (IC50: 61 nM); with higher metabolic stability than CP-610431.

    价 格：￥电议型 号：T3622产 地：中国大陆

  • T3576KDM5-inhibitorCPI-455 analogue

    KDM5 inhibitor

    价 格：￥电议型 号：T3576产 地：中国大陆

  • T3561CPI1189CPI-1189；REN-1189；CPI 1189

    REN-1189 is a TNF-a release inhibitor potentially for the treatment of sciatica and postherpetic neuralgia.

    价 格：￥电议型 号：T3561产 地：中国大陆

  • T3552CPI-455CPI-455 HCl；CPI 455；CPI455

    CPI-455 is a specific KDM5 inhibitor.

    价 格：￥电议型 号：T3552产 地：中国大陆

  • T35317Zopolrestat唑泊司他；CP-73850；Zopolrestatum；CP73850；CP 73850

    Zopolrestat is a potent inhibitor of aldose reductase (IC50 = 3.1 nM).

    价 格：￥电议型 号：T35317产 地：中国大陆

  • T3530Otenabant奥替那班；CP-945598

    Otenabant has been investigated for the treatment of Obesity.

    价 格：￥电议型 号：T3530产 地：中国大陆

  • T3519Formosanin CPolyphyllin B；重楼皂苷 B；重楼皂苷B

    Polyphyllin B is a compound isolated from Rhizoma Paridis, showed pro-apoptosis and immunoregulation with antitumor activity in cultured cells and animal systems.

    价 格：￥电议型 号：T3519产 地：中国大陆

  • T3484trans-ACPD(±)-trans-ACPD；1-amino-1,3-dicarboxycyclopentane；Trans-(±)-ACP

    (±)-trans-ACPD is an equimolecular mixture of (1S, 3R)- and (1R, 3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

    价 格：￥电议型 号：T3484产 地：中国大陆

  • T3479(RS)-MCPG(±)-MCPG；alpha-MCPG

    (RS)-MCPG is a non-selective group I/II metabotropic glutamate receptor antagonist.

    价 格：￥电议型 号：T3479产 地：中国大陆

  • T3477E4CPG

    E4CPG is a novel group I/II metabotropic glutamate receptor antagonist, more potent than (RS)-MCPG.

    价 格：￥电议型 号：T3477产 地：中国大陆

  • T3199PTACHNCH-51；Cpd 51

    PTACH (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).

    价 格：￥电议型 号：T3199产 地：中国大陆

  • T3174TaprenepagCP-544326

    Taprenepag (CP-544326) is a potent and selective prostaglandin E2 receptor agonist (EC50 = 2.8 nM). Taprenepag has been used in trials studying the treatment of Ocular Hypertension and Glaucoma, Open-Angle.

    价 格：￥电议型 号：T3174产 地：中国大陆

  • T2764(S)-10-Hydroxycamptothecin10-Hydroxycamptothecin；10-HCPT；10-羟喜树碱；10-羟基喜树碱

    10-Hydroxycamptothecin is a DNA topoisomerase I inhibitor, utilized as a clinical therapy agent against hepatoma.

    价 格：￥电议型 号：T2764产 地：中国大陆

  • T270768-Cyclopentyl-1,3-dimethylxanthineA1受体拮抗剂,CPT；CPT

    8-Cyclopentyl-1,3-dimethylxanthine?is a potent antagonist of adenosine A1 receptor.

    价 格：￥电议型 号：T27076产 地：中国大陆

  • T27061CP-24879 hydrochlorideCP 24879 hydrochloride；CP24879 hydrochloride；CP-24879 HCl

    CP-24879 hydrochloride, a Δ5D/Δ6D dual-inhibitor, can significantly reduce intracellular lipid accumulation and inflammatory injury in hepatocytes. CP-24879 hydrochloride exhibits superior antisteatotic and anti-inflammatory actions in fat-1 and ω-3-treat

    价 格：￥电议型 号：T27061产 地：中国大陆

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