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ACY-1215 100mg 100mg  | Purity Not Available

Adooq Bioscience

ACY-1215 selectively targets and binds to HDAC6, thereby disrupting the Hsp90 protein chaperone system through hyperacetylation of Hsp90 and preventing the subsequent aggresomal protein degradation.

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ACY-1215 10mg 10mg  | Purity Not Available

Adooq Bioscience

ACY-1215 selectively targets and binds to HDAC6, thereby disrupting the Hsp90 protein chaperone system through hyperacetylation of Hsp90 and preventing the subsequent aggresomal protein degradation.

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MDA 19 50mg 50mg  | Purity Not Available

Adooq Bioscience

MDA 19 is a potent and selective agonist for the cannabinoid receptor CB2, with reasonable selectivity over the psychoactive CB1 receptor.

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MDA 19 25mg 25mg  | Purity Not Available

Adooq Bioscience

MDA 19 is a potent and selective agonist for the cannabinoid receptor CB2, with reasonable selectivity over the psychoactive CB1 receptor.

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KB-R7943 mesylate 100mg 100mg  | Purity Not Available

Adooq Bioscience

KB-R7943 mesylate is a cell permeable, potent, selective NCKX inhibitor of the reverse mode of Na+/Ca2+ exchange in cells expressing NCX1.

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KB-R7943 mesylate 10mg 10mg  | Purity Not Available

Adooq Bioscience

KB-R7943 mesylate is a cell permeable, potent, selective NCKX inhibitor of the reverse mode of Na+/Ca2+ exchange in cells expressing NCX1.

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WIN 55,212-2 mesylate 50mg 50mg  | Purity Not Available

Adooq Bioscience

WIN 55,212-2 is a potent cannabinoid receptor agonist that has been found to be a potent analgesic in a rat model of neuropathic pain. It activates p42 and p44 MAP kinase via receptor-mediated signaling.

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WIN 55,212-2 mesylate 25mg 25mg  | Purity Not Available

Adooq Bioscience

WIN 55,212-2 is a potent cannabinoid receptor agonist that has been found to be a potent analgesic in a rat model of neuropathic pain. It activates p42 and p44 MAP kinase via receptor-mediated signaling.

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WIN 55,212-2 mesylate 100mg 100mg  | Purity Not Available

Adooq Bioscience

WIN 55,212-2 is a potent cannabinoid receptor agonist that has been found to be a potent analgesic in a rat model of neuropathic pain. It activates p42 and p44 MAP kinase via receptor-mediated signaling.

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RITA 50mg 50mg  | Purity Not Available

Adooq Bioscience

RITA, also referred to as NSC 652287, is a trycyclic thiophene derivative that binds to MDM2, disrupting the MDM2-p53 complex and subsequently activating p53 and inducing apoptosis.

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