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  • T16866SDZ281-977；化合物 T16866SDZ-LAP 977；SDZ-LAP 977

    SDZ 281-977 is a derivative of Lavendustin A which is the EGF receptor tyrosine kinase inhibitor.

    价 格：￥电议型 号：T16866产 地：中国大陆

  • T16855SB-772077B dihydrochloride；化合物 T16855SB-772077B dihydrochloride

    SB-772077B dihydrochloride is an aminofurazan-based Rho kinase inhibitor (IC50s: 5.6 nM and 6 nM toward ROCK1 and ROCK2, respectively).

    价 格：￥电议型 号：T16855产 地：中国大陆

  • T16781Rogaratinib；化合物RogaratinibBAY1163877；BAY1163877

    Rogaratinib (BAY1163877) is an aberrant inhibitor of fibroblast growth factor receptor (FGFR). Rogaratinib is as an orally available, selective and potent inhibitor of FGFR-1, -2 and -3 kinase activity.

    价 格：￥电议型 号：T16781产 地：中国大陆

  • T1677LMontelukast sodium孟鲁司特钠MK0476|||孟鲁司特钠

    Montelukast sodium (MK0476) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury.

    价 格：￥电议型 号：T1677L产 地：中国大陆

  • T16779Rodatristat ethyl；化合物RVT-014|||KAR5585|||RVT-1201；RVT-014|||KAR5585|||RVT-1201

    Rodatristat ethyl (KAR5585) is a first-of-its-kind orally active and potent tryptophan hydroxylase 1 (TPH1) inhibitor that significantly reduces 5-hydroxytryptamine (5-HT) levels and decreases pulmonary arterial hypertension (PAH) at low concentrations.

    价 格：￥电议型 号：T16779产 地：中国大陆

  • T16778Rocastine；罗卡斯汀AHR-11325；AHR-11325

    Rocastine (AHR-11325) is a selective and potent non-sedating H1 receptor antagonist.

    价 格：￥电议型 号：T16778产 地：中国大陆

  • T16777ROC-325；化合物ROC-325ROC-325

    ROC-325 is an effective and orally active inhibitor of autophagy with anticancer activity. ROC-325 induces renal cell carcinoma apoptosis and exhibits favorable selectivity.

    价 格：￥电议型 号：T16777产 地：中国大陆

  • T16776RO9021；化合物RO9021RO9021

    RO9021 is an orally bioavailable, novel ATP-competitive SYK inhibitor (average IC50: 5.6 nM).

    价 格：￥电议型 号：T16776产 地：中国大陆

  • T16775Ro15-4513；化合物 T16775Ro15-4513

    Ro15-4513 is imidazobenzodiazepinone derivative and is a partial inverse agonist of benzodiazepine receptors. Ro15-4513 is an effective ethanol antagonist.

    价 格：￥电议型 号：T16775产 地：中国大陆

  • T16774RO-9187；化合物 T16774RO-9187

    RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).

    价 格：￥电议型 号：T16774产 地：中国大陆

  • T16773Ro 90-7501化合物Ro 90-7501RO-90-7501

    Ro 90-7501 is an amyloid β42 (Aβ42) protofibrillar and TPR-dependent PP5 inhibitor, a novel radiosensitiser for cervical cancer cells, which inhibits ATM phosphorylation, promotes apoptosis, and induces cell-cycle arrest.Ro 90-7501 exhibits antiviral activity and potential anticancer activity by inhibiting ATM phosphorylation and DNA repair, and by inhibiting HCMV.

    价 格：￥电议型 号：T16773产 地：中国大陆

  • T16772Ro 64-6198；化合物 T16772Ro 64-6198

    Ro 64-6198 is a nonpeptide, high-affinity, and brain penetration N/OFQ receptor (NOP) agonist (EC50: 25.6 nM). Ro 64-6198 is at least 100 times more selective for the NOP receptor over the classic opioid receptors.

    价 格：￥电议型 号：T16772产 地：中国大陆

  • T16771RO-5963；化合物RO-5963RO-5963

    RO-5963 is a dual inhibitor of p53-MDM2 and p53-MDMX (IC50s: ~17 nM and ~24 nM, respectively).

    价 格：￥电议型 号：T16771产 地：中国大陆

  • T16770Ro 41-1049 hydrochloride；化合物 T16770Ro 41-1049 hydrochloride

    Ro 41-1049 hydrochloride is a reversible and selective inhibitor of monoamine oxidase-A (Kd: 16.5 and 64.4 nM, respectively).

    价 格：￥电议型 号：T16770产 地：中国大陆

  • T1677Montelukast；孟鲁司特Singular；孟鲁司特|||Singular

    Montelukast (Singular) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury.

    价 格：￥电议型 号：T1677产 地：中国大陆

  • T16740RH1；化合物 RH1NSC 697726；NSC 697726

    RH1 (NSC 697726) is a bioreductive anticancer compound that exhibits dose-dependent biphasic effects in vitro, inducing apoptosis at higher doses and senescence at lower doses.

    价 格：￥电议型 号：T16740产 地：中国大陆

  • T16724Razuprotafib；化合物RazuprotafibAKB-9778；AKB-9778

    Razuprotafib (AKB-9778) is a protein tyrosine phosphatase ? (HPTP?) inhibitor (IC50: 50 nM). Razuprotafib is effective for the activation of Tie-2 and is protective against acute kidney injury.

    价 格：￥电议型 号：T16724产 地：中国大陆

  • T1672Dimesna；地美司钠BNP-7787；地美司钠|||BNP-7787

    Dimesna (BNP-7787) is a synthetic derivative of dithio-ethane sulfonate with uroprotective properties.

    价 格：￥电议型 号：T1672产 地：中国大陆

  • T16713R121919；化合物R121919NBI30775；NBI30775

    R121919 (NBI30775) is a potent small molecule adrenocorticotropic hormone-releasing factor receptor 1 (CRF1) receptor antagonist with antidepressant and anxiolytic activity that inhibits the CRF1 receptor, the CRF2 receptor, and the CRF-binding proteins.

    价 格：￥电议型 号：T16713产 地：中国大陆

  • T16679Belzutifan；化合物BelzutifanPT2977|||MK-6482；PT2977|||MK-6482

    Belzutifan (MK-6482) is a potential treatment for clear cell renal cell carcinoma (ccRCC). Belzutifan is an orally active and selective HIF-2α inhibitor (IC50: 9 nM). Belzutifan , as a second-generation HIF-2α inhibitor, increases potency and improves pharmacokinetic profile.

    价 格：￥电议型 号：T16679产 地：中国大陆

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