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  • T71633GSK-598809 L-tartrate sesquihydrate；化合物 GSK-598809 L-tartrate sesquihydrateGSK-598809 L-tartrate ses

    GSK-598809 L-tartrate sesquihydrate is an acute D3 antagonist.

    价 格：￥电议型 号：T71633产 地：中国大陆

  • T7147Valbenazine；化合物ValbenazineNBI-98854；NBI-98854

    Valbenazine (NBI-98854), a highly selective vesicular monoamine transporter 2(VMAT2) inhibitor, is approved for the treatment of tardive dyskinesia.

    价 格：￥电议型 号：T7147产 地：中国大陆

  • T71001GSK-598809；化合物 GSK-598809GSK-598809

    GSK598809 is a selective D(3)R antagonist recently progressed in Phase I trials. GSK-598809 may decrease the rewarding effects of contextual cues associated with drug intake preclinically, which may reduce drug craving in humans.

    价 格：￥电议型 号：T71001产 地：中国大陆

  • T70988Ibulocydine；化合物 IbulocydineIbulocydine

    Ibulocydine is a potent CDK inhibitor. Ibulocydine has high activity against Cdk7/cyclin H/Mat1 and Cdk9/cyclin T. Ibulocydine inhibited the growth of HCC cells more effectively than other Cdk inhibitors, including olomoucine and roscovitine, whereas ibulocydine as well as the other Cdk inhibitors and BMK-Y101 minimally influenced the growth of normal hepatocyte cells. Ibulocydine induced apoptosis in HCC cells, most likely by inhibiting Cdk7 and Cdk9. In vitro treatment of HCC cells with ibuloc

    价 格：￥电议型 号：T70988产 地：中国大陆

  • T70225L-159884；化合物 L-159884L-159884

    L-159884 is a radiolabelled, nonpeptide angiotensin II antagonist that is useful for angiotensin II, AT1 receptor imaging

    价 格：￥电议型 号：T70225产 地：中国大陆

  • T69988Metitepine；化合物 MetitepineMetitepine

    Metitepine is a serotonin receptor antagonist in the CNS used as an antipsychotic.

    价 格：￥电议型 号：T69988产 地：中国大陆

  • T69889JBP485；化合物 JBP485JBP485

    JBP485 is an inhibitor of renal transporters OAT1 and OAT3. JBP485 is an antihepatitis agent as a substrate for intestinal PEPT1.

    价 格：￥电议型 号：T69889产 地：中国大陆

  • T69888SB02024；化合物 SB02024SB02024

    SB02024 is a VPS34 inhibitor. SB02024 activates cGAS-STING signaling and sensitizes tumors to STING agonist. SB02024 blocked autophagy in vitro and reduced xenograft growth of two breast cancer cell lines, MDA-MB-231 and MCF-7, in vivo. Vps34 inhibitor significantly potentiated cytotoxicity of Sunitinib and Erlotinib in MCF-7 and MDA-MB-231 in vitro in monolayer cultures and when grown as multicellular spheroids. Our data suggests that inhibition of autophagy significantly improves sensitivity

    价 格：￥电议型 号：T69888产 地：中国大陆

  • T69887Fmoc-9-aminononanoic acid；化合物 Fmoc-9-aminononanoic acidFmoc-9-aminononanoic acid

    Fmoc-9-aminononanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs and and other conjugation applications. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

    价 格：￥电议型 号：T69887产 地：中国大陆

  • T69886FE-200041；化合物 FE-200041FE-200041

    FE-200041 is a peripheral efficacious kappa opioid agonist.

    价 格：￥电议型 号：T69886产 地：中国大陆

  • T69885RK-52；化合物 RK-52RK-52

    RK-52 is a synthetic inhibitor of rhodesain, characterized by an impressive ksecond value (ksecond = 67000 × 103 M?1 min?1) and by a picomolar affinitytoward the trypanosomal protease (Ki = 38 pM).

    价 格：￥电议型 号：T69885产 地：中国大陆

  • T69884M122；化合物 M122M122

    M122 is a selective histone deacetylase HDAC1 and HDAC2 inhibitor and potent antitumor agent.

    价 格：￥电议型 号：T69884产 地：中国大陆

  • T69883M133；化合物 M133M133

    M133 is a selective histone deacetylase HDAC1 and HDAC2 inhibitor and potent antitumor agent.

    价 格：￥电议型 号：T69883产 地：中国大陆

  • T69882Pefabloc；化合物 PefablocPefabloc

    Pefabloc is an irreversible serine proteinase inhibitor. Pefabloc efficiently inhibits both human and rat platelet activating factor (PAF)-degrading acetylhydrolase (acetylhydrolase).

    价 格：￥电议型 号：T69882产 地：中国大陆

  • T6988SKF 38393 hydrochloride；化合物SKF38393 HCl(±)-SKF-38393 hydrochloride|||SKF-38393A|||SKF38393 HCl；(±)-S

    SKF 38393 hydrochloride (SKF38393 HCl) is a selective dopamine D1/D5 receptor agonist.

    价 格：￥电议型 号：T6988产 地：中国大陆

  • T69705SC 19886；化合物 SC 19886SC 19886

    SC 19886 is an antimineralocorticoid that acts as a potent inhibitor of aldosterone biosynthesis.

    价 格：￥电议型 号：T69705产 地：中国大陆

  • T689883-Methoxyacridin-9-one；化合物 3-Methoxyacridin-9-one3-Methoxyacridin-9-one

    3-Methoxyacridin-9-one is a potassium channel antagonist.

    价 格：￥电议型 号：T68988产 地：中国大陆

  • T67988Embeconazole；恩倍康唑R 120758|||CS 758；R 120758|||CS 758

    Embeconazole (R 120758) is a triazole antifungal agent.Embeconazole has strong in vitro activity against clinically important fungi such as Candida, Aspergillus and Cryptococcus neoformans.

    价 格：￥电议型 号：T67988产 地：中国大陆

  • T67913(-)-GSK598809 hydrochloride；(-)-GSK598809盐酸盐(-)-GSK598809 hydrochloride

    (-)-GSK598809 hydrochloride is the isomer of GSK598809. GSK598809 is a selective antagonist of the dopamine D3 receptor (DRD3), which is a neural response that selectively enhances reward anticipation in drug and alcohol dependence during monetary policy and may repair reward deficits in substance dependence.

    价 格：￥电议型 号：T67913产 地：中国大陆

  • T67818BMS-641988；化合物BMS-641988BMS-641988

    BMS-641988 is a novel nonsteroidal androgen receptor antagonist for the treatment of prostate cancer.

    价 格：￥电议型 号：T67818产 地：中国大陆

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