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  • mls-0437605 (c09-1152-288)
    M646706-10mg
    MLS-0437605 is a selective dual-specificity phosphatase 3 (DUSP3) inhibitor with an IC 50 of 3.7 μM. MLS-0437605 is more selective for DUSP3 than DUSP22 and other protein tyrosine phosphatases (PTPs).In VitroMLS-0437605 efficiently inhibits platelet
    SKUM646706-10mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-374134
    Pack Size 1 EA
    Quantity:
     
  • mls-0437605 (c09-1152-287)
    M646706-100mg
    MLS-0437605 is a selective dual-specificity phosphatase 3 (DUSP3) inhibitor with an IC 50 of 3.7 μM. MLS-0437605 is more selective for DUSP3 than DUSP22 and other protein tyrosine phosphatases (PTPs).In VitroMLS-0437605 efficiently inhibits platelet
    SKUM646706-100mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-374133
    Pack Size 1 EA
    Quantity:
     
  • bi-409306
    B412142-5mg
    InformationBI-409306 BI 409306 (SUB 166499) is a potent and selective inhibitor of human and rat PDE9A with mean IC50 of 65 nM and 168 nM, respectively. Treatment with BI 409306 increases brain cGMP levels, promotes long-term potentiation, and
    SKUB412142-5mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-067657
    Pack Size 1 EA
    Quantity:
     
  • bi-409306
    B412142-50mg
    InformationBI-409306 BI 409306 (SUB 166499) is a potent and selective inhibitor of human and rat PDE9A with mean IC50 of 65 nM and 168 nM, respectively. Treatment with BI 409306 increases brain cGMP levels, promotes long-term potentiation, and
    SKUB412142-50mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-067656
    Pack Size 1 EA
    Quantity:
     
  • bi-409306
    B412142-25mg
    InformationBI-409306 BI 409306 (SUB 166499) is a potent and selective inhibitor of human and rat PDE9A with mean IC50 of 65 nM and 168 nM, respectively. Treatment with BI 409306 increases brain cGMP levels, promotes long-term potentiation, and
    SKUB412142-25mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-067655
    Pack Size 1 EA
    Quantity:
     
  • bi-409306
    B412142-100mg
    InformationBI-409306 BI 409306 (SUB 166499) is a potent and selective inhibitor of human and rat PDE9A with mean IC50 of 65 nM and 168 nM, respectively. Treatment with BI 409306 increases brain cGMP levels, promotes long-term potentiation, and
    SKUB412142-100mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-067654
    Pack Size 1 EA
    Quantity:
     
  • bi 605906
    B287053-5mg
    BI605906 is a novel IKKβ inhibitor with an IC50 value of 380 nM when assayed at 0.1 mM ATP.BI605906 is an inhibitor of IKKβ with improved selectivity. BI605906 inhibits IKKβ in vitro with an IC50 value of 380 nM when assayed at 0.1 mM ATP. The only
    SKUB287053-5mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-060848
    Pack Size 1 EA
    Quantity:
     
  • bi 605906
    B287053-50mg
    BI605906 is a novel IKKβ inhibitor with an IC50 value of 380 nM when assayed at 0.1 mM ATP.BI605906 is an inhibitor of IKKβ with improved selectivity. BI605906 inhibits IKKβ in vitro with an IC50 value of 380 nM when assayed at 0.1 mM ATP. The only
    SKUB287053-50mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-060847
    Pack Size 1 EA
    Quantity:
     
  • bi 605906
    B287053-25mg
    BI605906 is a novel IKKβ inhibitor with an IC50 value of 380 nM when assayed at 0.1 mM ATP.BI605906 is an inhibitor of IKKβ with improved selectivity. BI605906 inhibits IKKβ in vitro with an IC50 value of 380 nM when assayed at 0.1 mM ATP. The only
    SKUB287053-25mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-060846
    Pack Size 1 EA
    Quantity:
     
  • bi 605906
    B287053-1mg
    BI605906 is a novel IKKβ inhibitor with an IC50 value of 380 nM when assayed at 0.1 mM ATP.BI605906 is an inhibitor of IKKβ with improved selectivity. BI605906 inhibits IKKβ in vitro with an IC50 value of 380 nM when assayed at 0.1 mM ATP. The only
    SKUB287053-1mg
    MFR. NameAladdin Scientific
    Catalog No. C007B-060845
    Pack Size 1 EA
    Quantity: