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TargetMol产品目录中 "

nm-441

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  • 抑制剂&激动剂
    6
    TargetMol | Inhibitors_Agonists
  • 多肽产品
    2
    TargetMol | Peptide_Products
  • Prulifloxacin
    AF 3012, Pruvel, NM441, 普卢利沙星
    T5394123447-62-1
    Prulifloxacin (NM441) 是一种口服有效的氟喹诺酮抗生素 ,对革兰氏阳性和阴性细菌具有广泛活性。它是噻唑喹啉羧酸衍生物 Ulifloxacin 的前药。它有潜力用于下尿路感染和慢性支气管炎。
    • ¥ 314
    现货
    规格
    数量
    TargetMol | Inhibitor Sale
  • TAK-441
    TAK441
    T213251186231-83-3
    TAK-441 是一种具有口服活性的 Hedgehog 信号抑制剂 (IC50 = 4.4 nM),具有有效的抗肿瘤活性。 TAK-441 抑制转录因子 Gli1 mRNA 表达和肿瘤生长。
    • ¥ 787
    现货
    规格
    数量
  • N-3-oxo-pentanoyl-L-Homoserine lactone
    T37338148433-21-0
    N-3-oxo-pentanoyl-L-Homoserine lactone is a chain-shortened derivative of the bacterial quorum sensing signaling molecule N-3-oxo-octanoyl-L-homoserine lactone .1It inhibits binding of the autoinducer N-3-oxo-hexanoyl homoserine lactone toE. colicontaining the transcription factor LuxR when used at a concentration of 230 nM.2It acts as an autoinducer to activate theV. fischeriluminescence system inE. coliwhen used at concentrations ranging from 20 to 200 nM. 1.Chhabra, S.R., Stead, P., Bainton, N.J., et al.Autoregulation of carbapenem biosynthesis in Erwinia carotovora by analogues of N-(3-oxohexanoyl)-L-homoserine lactoneJ. Antibiot. (Tokyo)46(3)441-454(1993) 2.Schaefer, A.L., Hanzelka, B.L., Eberhard, A., et al.Quorum sensing in Vibrio fischeri: Probing autoinducer-LuxR interactions with autoinducer analogsJ. Bacteriol.178(10)2897-2901(1996)
    • ¥ 560
    35日内发货
    规格
    数量
  • GSTO1-IN-2
    T895973020776-77-3
    Compound B-9(GSTO1-IN-2)作为GSTO1 BTK双共价抑制剂,其IC50值对GSTO1为441 nM,对BTK则为6.2 nM.
    • 待询
    10-14周
    规格
    数量
  • N-CBZ-Phe-Arg-AMC
    Z-Phe-Arg-Amc,Z-FR-AMC
    TP101365147-22-0
    N-CBZ-Phe-Arg-AMC (Z-FR-AMC) is a substrate for serine proteases, including cathepsins, kallikrein, and plasmin. The substrate exhibits absorption emission at 330 390 nm (weak fluorescence), while the end product (AMC) shows absorption emission at 342 441 nm (strong fluorescence).
    • 待询
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  • F1324
    TP1562
    F1324 is a potent, high-affinity peptidic inhibitor of B cell lymphoma 6 (BCL6) with an IC50 of 1 nM, exhibiting a binding t1 2 value of 441 s and strong inhibitory activity against BCL6 PPI.
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