Search Results - "Pasis, Angela"
-
1
Discovery of CDK4/6 bifunctional degraders for ER+/HER2- breast cancer
Published in Journal of clinical oncology (01-06-2023)“…1083 Background: CDK4/6 inhibitors (CDK4/6i) such as palbociclib and ribociclib are used to treat ER+/HER2- breast cancer, but patients can develop resistance…”
Get full text
Journal Article -
2
BTX-1188, a first-in-class dual degrader of GSPT1 and IKZF1/3, for treatment of acute myeloid leukemia (AML) and solid tumors
Published in Journal of clinical oncology (01-06-2022)“…7025 Background: BTX-1188 is a first-in-class oral molecular glue that degrades GSPT1 and IKZF1/3 and is currently in phase 1 clinical trials for treatment of…”
Get full text
Journal Article -
3
Abstract 1963: Targeting hematological malignancies with two functionally and mechanistically distinct classes of cereblon mediated protein homeostatic modulators
Published in Cancer research (Chicago, Ill.) (15-08-2020)“…Abstract BioTheryX's novel and unique Protein Homeostatic Modulators (PHMsTM) are small molecule “molecular glues” that promote ubiquitination of substrate…”
Get full text
Journal Article -
4
Abstract 1553: Discovery of CDK4/6 bifunctional degraders for ER+/HER2- breast cancer andtriple negative breast cancer
Published in Cancer research (Chicago, Ill.) (04-04-2023)“…Abstract CDK4/6 inhibitors (CDK4/6i) such as palbociclib and ribociclib are used to treatER+/HER2- breast cancer, but patients can develop resistance via…”
Get full text
Journal Article -
5
Abstract PO5-05-02: Discovery of BTX-9341, a bifunctional degrader of CDK4 and CDK6 for HR+/HER2- breast cancer
Published in Cancer research (Chicago, Ill.) (02-05-2024)“…Abstract CDK4/6 inhibitors (CDK4/6i) such as palbociclib, abemaciclib and ribociclib are used to treat HR+/HER2- breast cancer, but patients can develop…”
Get full text
Journal Article -
6
Abstract 5702: BTX-9341, a bifunctional degrader of CDK4 and CDK6 for glioblastoma multiforme
Published in Cancer research (Chicago, Ill.) (22-03-2024)“…Abstract Glioblastoma multiforme (GBM) is an aggressive form of brain cancer with limited treatment options. GBM has a high frequency of dysregulation of the…”
Get full text
Journal Article -
7
Abstract 6068: Discovery of BTX-9341, a bifunctional degrader of CDK4 and CDK6 for HR+/HER2- breast cancer
Published in Cancer research (Chicago, Ill.) (22-03-2024)“…Abstract CDK4/6 inhibitors (CDK4/6i) such as palbociclib, abemaciclib and ribociclib are used to treat HR+/HER2- breast cancer, but patients can develop…”
Get full text
Journal Article -
8
Synthesis, SAR and biological evaluation of 1,6-disubstituted-1H-pyrazolo[3,4-d]pyrimidines as dual inhibitors of Aurora kinases and CDK1
Published in Bioorganic & medicinal chemistry letters (01-03-2012)“…Since the early 2000s, the Aurora kinases have become major targets of oncology drug discovery particularly Aurora-A and Aurora-B kinases (AKA/AKB) for which…”
Get full text
Journal Article -
9
Structure-based design of 2,6,7-trisubstituted-7H-pyrrolo[2,3-d]pyrimidines as Aurora kinases inhibitors
Published in Bioorganic & medicinal chemistry letters (15-06-2012)“…This Letter reports the optimization of a pyrrolopyrimidine series as dual inhibitors of Aurora A/B kinases. This series derived from a pyrazolopyrimidine…”
Get full text
Journal Article -
10
Abstract 2817: Preclinical studies of the PI3K/mTOR dual inhibitors in endometrial cancer cell lines
Published in Cancer research (Chicago, Ill.) (15-04-2012)“…Abstract The PI3K pathway plays a pivotal role in many cellular functions that include regulation of cell proliferation, survival, growth, angiogenesis, and…”
Get full text
Journal Article