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MW 285.47 g/mol, Purity >98%. Pyruvate dehydrogenase kinase (PDK) inhibitor (IC50 = 9.5 μM). It has weak affinity for human CB1 and CB2 receptors, exhibiting 20% displacement of [3H]-CP55940 at a concentration of 10 μM.

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CAS number

1446-61-3

Purity

> 98%

Form

Liquid

Molecular weight

285.47 g/mol

Molecular formula

C20H31N

Nature

Synthetic

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Shipping To:
United States

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MW 285.47 g/mol, Purity >98%. Pyruvate dehydrogenase kinase (PDK) inhibitor (IC50 = 9.5 μM). It has weak affinity for human CB1 and CB2 receptors, exhibiting 20% displacement of [3H]-CP55940 at a concentration of 10 μM.

Key facts

Purity

> 98%

Biological description

Pyruvate dehydrogenase kinase (PDK) inhibitor (IC50 = 9.5 μM). It has weak affinity for human CB1 and CB2 receptors, exhibiting 20% displacement of [3H]-CP55940 at a concentration of 10 μM.

Isomeric SMILES

CC(C)C(C=C1)=CC2=C1[C@]3(C)[C@](CC2)([H])[C@@](CN)(C)CCC3

IUPAC name

(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenemethanamine

Storage

Shipped at conditions

Ambient - Can Ship with Ice

Appropriate long-term storage conditions

Ambient

Product promise

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

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