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BN82002 hydrochloride

Cat. No. M14486
BN82002 hydrochloride Structure
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Biological Activity

BN82002 hydrochloride is a potent, selective and irreversible inhibitor of CDC25 phosphatase family. BN82002 hydrochloride inhibits CDC25A, CDC25B2, CDC25B3, CDC25C CDC25A, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 µM, respectively. BN82002 hydrochloride displays ~20-fold greater selectivity over CD45 tyrosine phosphatase.

Chemical Information
Molecular Weight 395.88
CAS Number 1049740-43-3
Solubility (25°C) DMSO 150 mg/mL
Storage 2-8°C, protect from light, dry, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

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DPM-1003

DPM-1003 is an orally potent, specific inhibitor of PTP1B.

D-3

D-3, a phosphorpeptide, is an efficient, simple, and specific iPSC-eliminating agent.

EGF Receptor Substrate 2 (Phospho-Tyr5)

EGF Receptor Substrate 2 (Phospho-Tyr5) acetate, a biologically active peptide, is a tyrosine phosphate substrate.

Calcineurin autoinhibitory peptide

Calcineurin autoinhibitory peptide is a selective inhibitor of Ca2+/calmodulin-dependent protein phosphatase (calcineurin), with an IC50 of ~10 μM.

  Catalog
Abmole Inhibitor Catalog




Keywords: BN82002 hydrochloride supplier, Phosphatase, inhibitors, activators


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