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BMN-673 8R, 9S

BMN 673 is a novel PARP inhibitor with IC50 of 0.58 nM (PARP1) . It does not inhibit PARG and is highly sensitive to PTEN mutation. BMN-673 (8R, 9S) is the (8R, 9S) enantiomer of BMN-673.

Product Specifications

Background

BMN-673 is an orally bioavailable inhibitor of the nuclear enzyme poly (ADP-ribose) polymerase (PARP) with potential antineoplastic activity. PARP inhibitor BMN-673 selectively binds to PARP and prevents PARP-mediated DNA repair of single strand DNA breaks via the base-excision repair pathway. This enhances the accumulation of DNA strand breaks, promotes genomic instability and eventually leads to apoptosis. PARP catalyzes post-translational ADP-ribosylation of nuclear proteins that signal and recruit other proteins to repair damaged DNA and is activated by single-strand DNA breaks. BMN-673 has been proven to be highly active in mouse models of human cancer and also appears to be more selectively cytotoxic with a longer half-life and better bioavailability as compared to other compounds in development.

CAS Number

1207456-00-5

Purity

≥ 98% by HPLC

Solubility

Soluble in DMSO

Molecular Formula

C19H14F2N6O

Shipping Conditions

Room Temperature (continental US) or Gel Packs

Storage Conditions

Store at or below –20°C. Solid form is stable at least 12 months from date of receipt, when stored as directed. Do not store aqueous solutions for more than one day.

Calculated Molecular Weight

380.4 Da

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