Novel covalent CDK7 inhibitor potently induces apoptosis in acute myeloid leukemia and synergizes with Venetoclax
A phase 1, open label, dose escalation, First-in-Human (FIH) study evaluating the safety, pharmacokinetics, pharmacodynamics and efficacy of AUR 103 in patients with relapsed advanced malignancies (BHARAT-1)
Generation of profound anti-tumor immunity by AUR109, a spectrum-selective kinase inhibitor, either as a single agent or in combination with immune checkpoint inhibitors
A highly differentiated PDL1-A2AR dual inhibitor for potential use in cancer therapy
Targeting CBP/p300 – Inhibition vs Degradation for Potent Anti-tumor Efficacy
Amino Acid inspired oral immune checkpoint antagonists for cancer therapy
Oral Immune Checkpoint Antagonist Dually Targeting TIGIT & PD-1 Pathways for Cancer Therapy
Characterization of the anti-tumor immune activation potential of AUR107, a novel small molecule p300/CBP bromodomain inhibitor
Orally Bioavailable CBP and p300 Selective Degraders for the Treatment of AR- and ER- dependent Cancers
Targeting cancer with selective CBP/p300 bromodomain inhibitors
First in class orally bioavailable BET BRD degraders
Structure of cyclin-dependent kinase 2 (CDK2) in complex with the specific and potent inhibitor CVT-313
Potent anti-tumor activity of AUR102, a selective covalent inhibitor of CDK7
Discovery of CA-4948, an Orally Bioavailable IRAK4 Inhibitor for Treatment of Hematologic Malignancies | ACS Medicinal Chemistry Letters
Selective Vulnerability to Pyrimidine Starvation in Hematologic Malignancies Revealed by AG-636, a Novel Clinical-Stage Inhibitor of Dihydroorotate Dehydrogenase
Peptide and peptide-inspired checkpoint inhibitors: Protein fragments to cancer immunotherapy
PD-1 derived CA-170 is an oral immune checkpoint inhibitor that exhibits preclinical anti-tumor efficacy
In silico designing of targeted protein degraders
Orally bioavailable SMARCA2 degraders with exceptional selectivity and potency
Evaluation of AU-18069, a novel small molecule CBP/p300 bromodomain inhibitor for the treatment of cancers
Novel, potent and orally bioavailable small molecule CD73 inhibitors for cancer immunotherapy
IRAK4 Modulators for Treatment of Hematologic Malignancies
Design, synthesis, and biological evaluation of phenyl thiazole-based AR-V7 degraders
Small Molecule Agents Targeting PD-1 Checkpoint Pathway for Cancer Immunotherapy: Mechanisms of Action and Other Considerations for Their Advanced Development
Discovery of MAP855, an Efficacious and Selective MEK1/2 Inhibitor with an ATP-Competitive Mode of Action
Targeting SWI/SNF ATPases in enhancer-addicted prostate cancer
Targeting SWI/SNF ATPases in enhancer-addicted human cancers
Discovery of orally bioavailable SMARCA2/4 dual degraders for treatment of acute myeloid leukemia
AUR103 an oral small molecule CD47 antagonist in combination with azacytidine and bortezomib exhibits potent anti-tumor activity in myeloma and leukemia models in vitro
PROTACs: Current Trends in Protein Degradation by Proteolysis-Targeting Chimeras
Activation of targetable inflammatory immune signaling is seen in myelodysplastic syndromes with SF3B1 mutations
