Results 11 to 20 of about 6,658 (202)

Copper-Mediated Radiosynthesis of [18F]Rucaparib [PDF]

open access: yesOrganic Letters, 2021
The poly(ADP-ribose) polymerase (PARP) inhibitor rucaparib is used in the clinic to treat BRCA-mutated cancers. Herein, we report two strategies to access the 18F-isotopologue of rucaparib by applying a copper-mediated nucleophilic 18F-fluorodeboronation.
Chen, Z   +5 more
openaire   +5 more sources

Total Synthesis of Rucaparib

open access: yesThe Journal of Organic Chemistry, 2022
A concise total synthesis of rucaparib, an FDA-approved drug for ovarian and prostate cancers, is reported. The Heck reaction of the commercially available aryl iodide with acrylonitrile provided the desired (E)-2-aminocinnamonitrile derivative.
Jinjae Park, Cheol-Hong Cheon
openaire   +3 more sources

Cisplatin +/− rucaparib after preoperative chemotherapy in patients with triple-negative or BRCA mutated breast cancer [PDF]

open access: yesnpj Breast Cancer, 2021
Patients with triple-negative breast cancer (TNBC) who have residual disease after neoadjuvant therapy have a high risk of recurrence. We tested the impact of DNA-damaging chemotherapy alone or with PARP inhibition in this high-risk population.
Maitri Kalra   +10 more
doaj   +2 more sources

Bioanalytical assay for the quantification of rucaparib in rat plasma using UPLC-MS/MS: development, and validation for interaction with myricetin [PDF]

open access: yesFrontiers in Pharmacology
Rucaparib is used to treat ovarian cancer patients with BRCA gene mutations. Myricetin, a flavonol that strongly inhibits CYP450, is widely found in natural plants and has some anticancer properties, with the potential for combination use. However, there
Jingjing Nie   +6 more
doaj   +2 more sources

Rucaparib: a novel PARP inhibitor for BRCA advanced ovarian cancer

open access: yesDrug Design, Development and Therapy, 2018
Ilaria Colombo, Stephanie Lheureux, Amit Manulal Oza Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada Abstract: Rucaparib is a potent small-molecule inhibitor of poly (ADP ...
Colombo I, Lheureux S, Oza AM
doaj   +1 more source

Pharmacokinetics and clinical response to single agent rucaparib in a dialysis dependent patient with BRCA associated breast and recurrent ovarian cancer

open access: yesGynecologic Oncology Reports, 2018
A 56-year old woman with BRCA-associated breast cancer and recurrent ovarian cancer was treated with a poly (ADP-ribose) polymerase enzyme (PARP) inhibitor, rucaparib, in the setting of dialysis-dependence which required dose modification.
Justin A. Harold   +2 more
doaj   +2 more sources

Methylation of all BRCA1 copies predicts response to the PARP inhibitor rucaparib in ovarian carcinoma

open access: yesNature Communications, 2018
Around 10% of high-grade serous ovarian carcinomas (HGSOC) harbor BRCA1 promoter methylation, but it is uncertain how it predicts response to PARP inhibition.
Olga Kondrashova   +30 more
doaj   +2 more sources

Targeted treatment of advanced ovarian cancer: spotlight on rucaparib [PDF]

open access: yesTherapeutics and Clinical Risk Management, 2018
Diana C Pearre, Krishnansu S Tewari Division of Gynecologic Oncology, Department of Obstetrics & Gynecology, University of California, Irvine Medical Center, Orange, CA, USA Abstract: The last 2 years have ushered in a new era in ovarian cancer ...
Pearre DC, Tewari KS
doaj   +2 more sources

Activity of trabectedin and the PARP inhibitor rucaparib in soft-tissue sarcomas [PDF]

open access: yesJournal of Hematology & Oncology, 2017
Background Trabectedin has recently been approved in the USA and in Europe for advanced soft-tissue sarcoma patients who have been treated with anthracycline-based chemotherapy without success. The mechanism of action of trabectedin depends on the status
Audrey Laroche   +7 more
doaj   +2 more sources

Rucaparib in metastatic prostate cancer

open access: yesCancer Research, Statistics, and Treatment, 2023
Praful Pandey, Ajay Gogia
doaj   +2 more sources

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