CAS: 1390637-82-7; Cyp3Cide

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{4-chloro-6-[(3S)-3-(piperidin-1-yl)pyrrolidin-1-yl]pyrimidin-5-yl}[1-methyl-5-(4-methylphenyl)-1H-pyrazol-4-yl]methanone methylhydrazine 1-methyl-5-(p-tolyl)-1H-pyrazole-4-carbaldehyde 1-methyl-5-(4-methylphenyl)-1H-pyrazole

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    主要参考文献


    1: Work HM, Kandel SE, Lampe JN. Comparison of the CYP3A selective inhibitors CYP3cide, clobetasol, and azamulin for their potential to distinguish CYP3A7 activity in the presence of CYP3A4/5. Drug Metab Dispos. 2024 May
    3:DMD- AR-2023-001598. doi: 10.1124/dmd.124.001598. Epub ahead of print. 48(9):778-787. doi: 10.1124/dmd.120.000017. Epub 2020 Jun 12. 46(5):493-502. doi: 10.1124/dmd.117.079855. Epub 2018 Feb 23. 45(8):957-965. doi: 10.1124/dmd.117.076307. Epub 2017 May 22.
    5: Verbueken E, Alsop D, Saad MA, Pype C, Van Peer EM, Casteleyn CR, Van Ginneken CJ, Wilson J, Van Cruchten SJ. In Vitro Biotransformation of Two Human CYP3A Probe Substrates and Their Inhibition during Early Zebrafish Development. Int J Mol Sci. 2017 Jan 22;18(1):217. doi: 10.3390/ijms18010217.

    合成参考文献


    参考文献:10.1124/mol.119.115964
    摘要:Lee TD, Lee OW, Brimacombe KR, Chen L, Guha R, Lusvarghi S, Tebase BG, Klumpp-Thomas C, Robey RW, Ambudkar SV, Shen M, Gottesman MM, Hall MD. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular Pharmacology. 2019 Nov;96(5):629–40. doi: 10.1124/mol.119.115964.
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