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Rucaparib ag 014699 pf 01367338

Manufactured by Selleck Chemicals
Sourced in United States

Rucaparib/AG-014699/PF-01367338 is a laboratory chemical compound used for research purposes. It is a poly(ADP-ribose) polymerase (PARP) inhibitor. The core function of this product is to inhibit PARP activity in experimental settings.

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2 protocols using rucaparib ag 014699 pf 01367338

1

NHEJ Inhibitors to Enhance HDR

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The following NHEJ inhibitors were used to enhance HDR: vanillin (12 (link)) reconstituted in H2O, 300µM final concentration (Sigma cat#V1104); SCR7-X in DMSO, 1µM final (Xcess Biosciences cat#M60082). Since we purchased SCR7-X from Xcess Biosciences we refer to this compound as “SCR7-X” as recently suggested (13 (link)). Rucaparib/AG-014699/PF-01367338, in DMSO, 1µM final (Selleckchem cat#S1098); veliparib/ABT-888 in DMSO, 5µM final (Selleckchem cat#S1004); RS-1 (14 ) in DMSO, 7.5µM final (MerckMillipore cat# 553510); RS-1 in DMSO, 7.5µM final, (Sigma cat#R9782); Luminespib/AUY-922/NVP-AUY922 in DMSO, 1µM final (Selleckchem cat#S1069); L-755,507 in DMSO, 5µM final (Tocris cat#2197); vanillin derivatives (12 (link)) 6-nitroveratraldehyde in DMSO, 3µM final (Maybridge cat#11427047), 4,5-dimethoxy-3-iodobenzaldehyde in DMSO, 3µM final (Maybridge cat#11328426); 6-bromoveratraldehyde in DMSO, 3µM final (Maybridge cat#11480124).
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2

PARP Inhibitor Compounds Evaluation

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The PARP inhibitors used in this study were purchased from Selleckchem (Houston, TX, USA) with the following names and catalog numbers: A-966492 (catalog number S2197), AG14361 (catalog number S2178), AZD2461 (catalog number S7029), E7449 (catalog number S8419), G007-LK (catalog number S7239), Niraparib (MK-4827; catalog number S2741), NMS-P118 (catalog number S8363), NU1025 (catalog number S7730), Olaparib (AZD2281, Ku-0059436; catalog number S1060), PJ34-HCl (catalog number S7300), Rucaparib (AG-014699, PF-01367338; catalog number S1098), Talazoparib (BMN673; catalog number S7048), and UPF1069 (catalog number S8038). Stock solutions were dissolved in dimethyl sulfoxide (DMSO) according to the manufacturer’s protocol to a concentration of 10 mM and stored at −20 °C. Table 1 lists the PARP inhibitors used in this study and their proposed targets.
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