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FK866 10mg 10mg  | Purity Not Available

Adooq Bioscience

FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis.

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PR-171 50mg 50mg  | Purity Not Available

Adooq Bioscience

PR-171 (Carfilzomib) is a tetrapeptide epoxyketone and a selective proteasome inhibitor. It is an analog of epoxomicin.

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PR-171 5mg 5mg  | Purity Not Available

Adooq Bioscience

PR-171 (Carfilzomib) is a tetrapeptide epoxyketone and a selective proteasome inhibitor. It is an analog of epoxomicin.

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Cefozopran 10mg 10mg  | Purity Not Available

Adooq Bioscience

Cefozopran is a fourth-generation cephalosporin. It would be effective against respiratory tract, urinary tract, and soft tissue infections caused by a variety of gram-positive and gram-negative bacteria in humans.

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Cefozopran 25mg 25mg  | Purity Not Available

Adooq Bioscience

Cefozopran is a fourth-generation cephalosporin. It would be effective against respiratory tract, urinary tract, and soft tissue infections caused by a variety of gram-positive and gram-negative bacteria in humans.

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A-443654 25mg 25mg  | Purity Not Available

Adooq Bioscience

A-443654, a specific Akt inhibitor, interferes with mitotic progression and bipolar spindle formation.

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A-443654 2mg 2mg  | Purity Not Available

Adooq Bioscience

A-443654, a specific Akt inhibitor, interferes with mitotic progression and bipolar spindle formation.

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A-443654 10mg 10mg  | Purity Not Available

Adooq Bioscience

A-443654, a specific Akt inhibitor, interferes with mitotic progression and bipolar spindle formation.

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AKT inhibitor VIII 50mg 50mg  | Purity Not Available

Adooq Bioscience

AKT inhibitor VIII is a cell-permeable and reversible quinoxaline compound that potently and selectively inhibits Akt1/Akt2 activity (IC50 = 58 nM, 210 nM, and 2.12 ?M for Akt1, Akt2, and Akt3, respectively, in in vitro kinase assays).

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AKT inhibitor VIII 5mg 5mg  | Purity Not Available

Adooq Bioscience

AKT inhibitor VIII is a cell-permeable and reversible quinoxaline compound that potently and selectively inhibits Akt1/Akt2 activity (IC50 = 58 nM, 210 nM, and 2.12 ?M for Akt1, Akt2, and Akt3, respectively, in in vitro kinase assays).

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