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Ki8751 50mg 50mg  | Purity Not Available

Adooq Bioscience

Ki8751 is a cell-permeable quinolyloxyphenyl-urea compound that acts as a Flk-1 (VEGFR-2)-selective inhibitior in both cell-based and cell-free assays.

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Ki8751 5mg 5mg  | Purity Not Available

Adooq Bioscience

Ki8751 is a cell-permeable quinolyloxyphenyl-urea compound that acts as a Flk-1 (VEGFR-2)-selective inhibitior in both cell-based and cell-free assays.

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JNJ-7706621 100mg 100mg  | Purity Not Available

Adooq Bioscience

JNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.

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JNJ-7706621 10mg 10mg  | Purity Not Available

Adooq Bioscience

JNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.

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JNJ-38877605 50mg 50mg  | Purity Not Available

Adooq Bioscience

c-Met inhibitor JNJ-38877605 selectively binds to c-Met, thereby inhibiting c-Met phosphorylation and disrupting c-Met signal transduction pathways.

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JNJ-38877605 5mg 5mg  | Purity Not Available

Adooq Bioscience

c-Met inhibitor JNJ-38877605 selectively binds to c-Met, thereby inhibiting c-Met phosphorylation and disrupting c-Met signal transduction pathways.

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JNJ-38877605 10mM * 1mL in DMSO 10mM * 1mL in DMSO  | Purity Not Available

Adooq Bioscience

c-Met inhibitor JNJ-38877605 selectively binds to c-Met, thereby inhibiting c-Met phosphorylation and disrupting c-Met signal transduction pathways.

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JNJ-38877605 100mg 100mg  | Purity Not Available

Adooq Bioscience

c-Met inhibitor JNJ-38877605 selectively binds to c-Met, thereby inhibiting c-Met phosphorylation and disrupting c-Met signal transduction pathways.

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JNJ-38877605 10mg 10mg  | Purity Not Available

Adooq Bioscience

c-Met inhibitor JNJ-38877605 selectively binds to c-Met, thereby inhibiting c-Met phosphorylation and disrupting c-Met signal transduction pathways.

More Information Supplier Page