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  • dg051 (c09-1126-583)
    D651905-5mg
    DG051 is a potent leukotriene A4 hydrolase inhibitor of leukotriene B4 biosynthesis in the enzyme assay with an IC 50 =47 nM.In VitroDG051 is a potent inhibitor of LTA4H aminopeptidase activity against L-alanine p-nitroanilide (IC 50 =72 nM). DG051
    SKUD651905-5mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-349068
    Pack Size 1 EA
    Quantity:
     
  • dg051 (c09-1126-582)
    D651905-1mg
    DG051 is a potent leukotriene A4 hydrolase inhibitor of leukotriene B4 biosynthesis in the enzyme assay with an IC 50 =47 nM.In VitroDG051 is a potent inhibitor of LTA4H aminopeptidase activity against L-alanine p-nitroanilide (IC 50 =72 nM). DG051
    SKUD651905-1mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-349067
    Pack Size 1 EA
    Quantity:
     
  • ddms
    D344397-5mg
    DDMS is a mechanism-based, irreversible inhibitor that has about 10-fold selectivity for the CYP4A11 (CYP450 4A2) enzyme which predominantly synthesizes 20-HETE in the mammalian kidney. DDMS administration in whole anesthetized rats (10 mg/kg)
    SKUD344397-5mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-134689
    Pack Size 1 EA
    Quantity:
     
  • ddms
    D344397-25mg
    DDMS is a mechanism-based, irreversible inhibitor that has about 10-fold selectivity for the CYP4A11 (CYP450 4A2) enzyme which predominantly synthesizes 20-HETE in the mammalian kidney. DDMS administration in whole anesthetized rats (10 mg/kg)
    SKUD344397-25mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-134688
    Pack Size 1 EA
    Quantity:
     
  • ddms
    D344397-1mg
    DDMS is a mechanism-based, irreversible inhibitor that has about 10-fold selectivity for the CYP4A11 (CYP450 4A2) enzyme which predominantly synthesizes 20-HETE in the mammalian kidney. DDMS administration in whole anesthetized rats (10 mg/kg)
    SKUD344397-1mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-134687
    Pack Size 1 EA
    Quantity:
     
  • ddms
    D344397-10mg
    DDMS is a mechanism-based, irreversible inhibitor that has about 10-fold selectivity for the CYP4A11 (CYP450 4A2) enzyme which predominantly synthesizes 20-HETE in the mammalian kidney. DDMS administration in whole anesthetized rats (10 mg/kg)
    SKUD344397-10mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-134686
    Pack Size 1 EA
    Quantity:
     
  • dsr 6434
    D287770-50mg
    Product descriptionDSR-6434 is a potent and selective Toll-like receptor 7 (TLR7) agonist, with EC50s of 7.2 nM and 4.6 nM for human and mice TLR7, respectively. DSR-6434 has a strong antitumor effect.
    SKUD287770-50mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-131515
    Pack Size 1 EA
    Quantity:
     
  • dsr 6434
    D287770-25mg
    Product descriptionDSR-6434 is a potent and selective Toll-like receptor 7 (TLR7) agonist, with EC50s of 7.2 nM and 4.6 nM for human and mice TLR7, respectively. DSR-6434 has a strong antitumor effect.
    SKUD287770-25mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-131514
    Pack Size 1 EA
    Quantity:
     
  • dsr 6434
    D287770-250mg
    Product descriptionDSR-6434 is a potent and selective Toll-like receptor 7 (TLR7) agonist, with EC50s of 7.2 nM and 4.6 nM for human and mice TLR7, respectively. DSR-6434 has a strong antitumor effect.
    SKUD287770-250mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-131513
    Pack Size 1 EA
    Quantity:
     
  • dsr 6434
    D287770-10mg
    Product descriptionDSR-6434 is a potent and selective Toll-like receptor 7 (TLR7) agonist, with EC50s of 7.2 nM and 4.6 nM for human and mice TLR7, respectively. DSR-6434 has a strong antitumor effect.
    SKUD287770-10mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-131512
    Pack Size 1 EA
    Quantity: