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  • T10586LBPH-1358NSC50460

    BPH-1358 (NSC50460) is a potent human farnesyl diphosphate synthase (FPPS) and undecaprenyl diphosphate synthase (UPPS) inhibitor. With IC50s of 1.8 μM and 110 nM, respectively. And it is active against S. aureus in vitro (MIC ~250 ng/mL)[1][2].

    价 格:¥电议型 号:T10586L产 地:中国大陆

  • T72587BPH-1358 mesylate;化合物 BPH-1358 mesylateNSC50460 mesylate;NSC50460 mesylate

    BPH-1358 mesylate (NSC50460 mesylate), a highly effective inhibitor of both human farnesyl diphosphate synthase (FPPS) and undecaprenyl diphosphate synthase (UPPS), exhibits IC50 values of 1.8 μM and 110 nM, respectively. Additionally, this compound demonstrates potent in vitro activity against S. aureus, with a minimum inhibitory concentration (MIC) approximately 250 ng/mL.

    价 格:¥电议型 号:T72587产 地:中国大陆

  • T10586LBPH-1358;化合物BPH-1358NSC50460;NSC50460

    BPH-1358 (NSC-50460) (NSC-50460) is a potent human farnesyl diphosphate synthase (FPPS) and undecaprenyl diphosphate synthase (UPPS) inhibitor. With IC50s of 1.8 μM and 110 nM, respectively. And it is active against S. aureus in vitro (MIC ~250 ng/mL)[1][2].

    价 格:¥电议型 号:T10586L产 地:中国大陆

  • T10586BPH-1358 free base;化合物 T10586NSC50460 free base;NSC50460 free base

    BPH-1358 (NSC50460) free base is a potent human undecaprenyl diphosphate synthase (UPPS) and farnesyl diphosphate synthase (FPPS) inhibitor (IC50s: 110 nM and 1.8 μM) and is active against S. aureus in vitro (MIC ~250 ng/mL).

    价 格:¥电议型 号:T10586产 地:中国大陆

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