Niraparib-d5

• Description:

  Niraparib-d5 (MK-4827-d5) is the deuterium labeled Niraparib (HY-10619) . Niraparib (MK-4827) is a highly potent and orally bioavailable PARP1 and PARP2 inhibitor with IC50s of 3.8 and 2.1 nM, respectively. Niraparib leads to inhibition of repair of DNA damage, activates apoptosis and shows anti-tumor activity[1][2][3].

• Product Name Alternative:

  MK-4827-d5

• UNSPSC:

  12352005

• Target:

  Apoptosis; Isotope-Labeled Compounds; PARP

• Related Pathways:

  Apoptosis; Cell Cycle/DNA Damage; Epigenetics; Others

• Field of Research:

  Cancer

• Smiles:

  O=C (N) C1=CC=CC2=C (N (N=C12) C3=CC=C (C=C3) [C@H]4C ([2H]) (NC ([2H]) (CC4) [2H]) [2H]) [2H]

• Molecular Formula:

  C19H15D5N4O

• Molecular Weight:

  325.42

• References & Citations:

  [1]Mirza MR, et al. Niraparib Maintenance Therapy in Platinum-Sensitive, Recurrent Ovarian Cancer. N Engl J Med. 2016 Dec 1;375 (22) :2154-2164.|[2]Wang L, et al. MK-4827, a PARP-1/-2 inhibitor, strongly enhances response of human lung and breast cancer xenografts to radiation. Invest New Drugs. 2012 Dec;30 (6) :2113-20.|[3]Bridges KA, et al. Niraparib (MK-4827), a novel poly (ADP-Ribose) polymerase inhibitor, radiosensitizes human lung and breast cancer cells. Oncotarget. 2014 Jul 15;5 (13) :5076-86.|[4]Jones P, et al. Discovery of 2-{4-[ (3S) -piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827) : a novel oral poly (ADP-ribose) polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors. J Med Chem. 2009 Nov 26;52 (22) :7170-85.

• Shipping Conditions:

  Room temperature

• Scientific Category:

  Isotope-Labeled Compounds

• Clinical Information:

  No Development Reported