ABT-737 is a BH3 mimetic compound that selectively targets BCL2 and BCLX L. In the present work, we report that ABT-737 is highly effective (LC 50 <50 n M) as a single agent against most (21/30)
ABT-737 is a small molecule drug that inhibits Bcl-2 and Bcl-xL, two members of the Bcl-2 family of evolutionarily-conserved proteins that share Bcl-2 Homology (BH) domains. First developed as a potential cancer chemotherapy , [1] it was subsequently identified as a senolytic (a drug that selectively induces cell death in senescent cells ).
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First developed as a potential cancer chemotherapy , [1] it was subsequently identified as a senolytic (a drug that selectively induces cell death in senescent cells ). 299 publications. CAS No. 852808-04-9. ABT-737 is a BH3 mimetic inhibitor of Bcl-xL, Bcl-2 and Bcl-w with EC50 of 78.7 nM, 30.3 nM and 197.8 nM in cell-free assays, respectively; no inhibition observed against Mcl-1, Bcl-B or Bfl-1. ABT-737 induces mitochondrial pathway apoptosis and mitophagy.
2017-04-01 · Several clinical trials have been performed using BH3 mimetics, such as ABT-737, ABT-263, AT-101, GX15-070, and TW-37, with limited success . We hypothesize that a combination of cisplatin with prototypic BH3 mimetics, ABT-737, would overcome the cisplatin resistance caused by STAT3 activation.
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Applications submitted under this FOA are expected to propose a clinical trial to develop and test adaptive interventions; optimize the intervention by evaluating which element of a complex intervention are critical for changes in outcome; assessing whether the intervention can be delivered with fidelity across sites in preparation for a future multi-site trial; or collect additional preliminary data such as … 2021-01-11 Search open enrollments clinical trials at the OSUCCC – James. Find out the study's criteria, whether you may be eligible and more here. Methods: A 3-month randomized double-blind clinical trial was carried out in volunteers with ED, aged 30 years approximately 70 years, to evaluate the therapeutic effect of the crude preparation of Butea superba tubers on ED. Results: There was a significant upgrading in 4 of the 5 descriptive evaluations of the IIEF-5 questionnaire.
Angeras Schwartz GG, Olsson AG, Abt M, Ballantyne CM, Barter PJ, Brumm J, etal.
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Although trials using any of the control groups described and discussed in this guideline may be useful and acceptable in clinical trials that serve as the basis for marketing approval in at least some circumstances, they are not equally appropriate or useful in every cases. The
Subsequent in vitro studies showed activity against myeloma [46, 47], acute leukemia [48, 49], and lymphoma. Further studies confirmed in vivo activity of ABT-737 in mouse xenograft models [50–53]. ABT-737 is presently under clinical evaluation as a single-agent therapy, but preclinical studies emphasize its improved potential in combined modality therapies.
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ABT-737 binds to the hydrophobic groove of multiple members of the anti-apoptotic Bcl-2 protein family, including Bcl-2, Bcl-xl and Bcl-w. This inhibits the activity of these pro-survival proteins and restores apoptotic processes in tumor cells, via activation of Bak/Bax-mediated apoptosis.
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