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  • T17257LWR-99210WR99210 hydrochloride(47326-86-3 free base)；6,6-Dimethyl-1-[3-(2,4,5-trichlorophenoxy)propox

    WR-99210 is a potent inhibitor of Plasmodium falciparum dihydrofolate reductase (pfDHFR), which is a major malarial drug target. It has subnanomolar potency for the wild type, double mutant and quadruple mutant dihydrofolate reductases.

    价 格：￥电议型 号：T17257L产 地：中国大陆

  • T16143MRTX-1257

    MRTX-1257 is a selective, irreversible, and covalent inhibitor of KRAS G12C. It has an IC50 of 900 pM for KRAS dependent ERK phosphorylation in H358 cells. MRTX1257 demonstrated 31% bioavailability in the mouse, with free fraction exposures well above the

    价 格：￥电议型 号：T16143产 地：中国大陆

  • T15257Etripamil(-)-MSP-2017；MSP-2017

    Etripamil displays atrioventricular nodal conduction and prolongs atrioventricular nodal refractory periods by inhibiting calcium ion influx through the calcium slow channels in the atrioventricular node cells. Etripamil is an antagonist of short-acting

    价 格：￥电议型 号：T15257产 地：中国大陆

  • T14984CLP257

    CLP257 is a selective K+-Cl? cotransporter KCC2 activator (EC50: 616 nM) and it is inactive against NKCC1, GABAA receptors, KCC1, KCC3 or KCC4. CLP257 alleviates hypersensitivity in rats with neuropathic painc and it also modulates plasmalemmal KCC2 prot

    价 格：￥电议型 号：T14984产 地：中国大陆

  • T13257Upamostat

    Upamostat is an inhibitor of a serine protease and is a urokinase plasminogen activator (uPA) inhibitor.

    价 格：￥电议型 号：T13257产 地：中国大陆

  • T12579RAMB4PTP1B-IN-9

    PTP1B-IN-9 is a ubiquitin-proteasome system (UPS)-stressor,with anticancer activity.

    价 格：￥电议型 号：T12579产 地：中国大陆

  • T12578(E,E)-RAMB4PTP1B-IN-8

    PTP1B-IN-8 is a potent and selective inhibitor of protein tyrosine phosphatase-1B (PTP1B).

    价 格：￥电议型 号：T12578产 地：中国大陆

  • T12575UnesbulinPTC596

    PTC596 is an orally active and selective inhibitor of B-cell-specific Moloney murine leukemia virus integration site 1 (BMI-1).

    价 格：￥电议型 号：T12575产 地：中国大陆

  • T12574PTC299Emvododstat；(4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]

    PTC299 is an orally active inhibitor of VEGFA mRNA translation and selectively inhibits VEGF protein synthesis at the post-transcriptional level. PTC299 is also a potent inhibitor of dihydrolactate dehydrogenase (DHODH).

    价 格：￥电议型 号：T12574产 地：中国大陆

  • T12573Vipivotide tetraxetanPSMA-617

    Vipivotide tetraxetan is a high potent inhibitor of prostate-specific membrane antigen (PSMA)(Ki of 0.37 nM).

    价 格：￥电议型 号：T12573产 地：中国大陆

  • T12257NSC 146109 hydrochloride

    NSC 146109 hydrochloride is an activator of p53 targeting MDMX. NSC 146109 hydrochloride can be used for studies on breast cancer.

    价 格：￥电议型 号：T12257产 地：中国大陆

  • T0893Tinidazole替硝唑；CP12574

    Tinidazolea is a 5-nitroimidazole derivative with the antiprotozoal property. Although the mechanism of action has not been fully elucidated, it has been suggested that tinidazole is metabolized and yields nitrite anions and metronidazole. Metronidazole´s

    价 格：￥电议型 号：T0893产 地：中国大陆

  • T0360Chlorindione氯苯茚二酮；Indaliton；G-25766；chlophenadione

    chlophenadione is a vitamin K antagonist, a potent anticoagulant compound.

    价 格：￥电议型 号：T0360产 地：中国大陆

  • T0257MepiroxolLysateril；Mepyroxol；3-吡啶基甲醇氮氧化物

    Mepiroxol, an antihyperlipidemic, is also called 3-PYRIDINEMETHANOL N-OXIDE.

    价 格：￥电议型 号：T0257产 地：中国大陆

  • T0257MepiroxolMepiroxol,Lysateril,Mepyroxol

    Mepiroxol, an antihyperlipidemic, is also called 3-PYRIDINEMETHANOL N-OXIDE.

    价 格：￥电议型 号：T0257产 地：美洲

  • T0360chlophenadionechlophenadione,G-25766,Indaliton

    chlophenadione is a vitamin K antagonist, a potent anticoagulant compound.

    价 格：￥电议型 号：T0360产 地：美洲

  • T0893TinidazoleTinidazole,CP12574,

    Tinidazolea is a 5-nitroimidazole derivative with the antiprotozoal property. Although the mechanism of action has not been fully elucidated, it has been suggested that tinidazole is metabolized and yields nitrite anions and metronidazole. Metronidazole´s

    价 格：￥电议型 号：T0893产 地：美洲

  • T11472GSK 525768AGSK 525768A

    GSK 525768A has no activity towards BET. GSK 525768A is the inactive enantiomer of GSK525762A.

    价 格：￥电议型 号：T11472产 地：美洲

  • T11472LMolibresib besylateMolibresib besylate,GSK 525762C,I-BET 762 besylate

    Molibresib besylate is an inhibitor of BET bromodomain (IC50: 32.5-42.5 nM).

    价 格：￥电议型 号：T11472L产 地：美洲

  • T1257UbenimexUbenimex,Bestatin,

    Ubenimex competitively inhibits many aminopeptidases, including B, N and leucine aminopeptidases. Ubenimex is a microbial metabolite and dipeptide with potential immunomodulatory and antitumor activities. Aminopeptidases has been implicated in the process

    价 格：￥电议型 号：T1257产 地：美洲

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