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An Overview of the Direct Preparation of Organoaluminum Compounds
用户em9I1HK86Mpk
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Discovery of Potent, Allosteric GSTO1 Covalent Inhibitors with a New Binding Mode
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Structure-based discovery of sulfamoyl-ethyl-4-oxo-3,4-dihydro-7H-pyrrolo[2,3-d]pyrimidine amides and sulfonamides as potent B-Cell Lymphoma 6 (BCL6)-BTB inhibitors
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Kill Two Birds with One Stone: An Efficient and Potent AR CBS-Targeted Degrader Reverses Breast Cancer Resistance via Concurrent AR Degradation and ERα Transcriptional Suppression
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Structure-Directed Optimization of Ebselen Derivatives as Potent NDM-1 Inhibitors Reverses Meropenem Resistance
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Highly Specific Inhibition of
c-Myc
Oncogene Expression through Shifting the G-Quadruplex toward a Triplex Structure
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Discovery of Novel Dihydroxyphenol Tyrosinase Inhibitors for Treatment of Pigmentation: From Enzyme Screening to Three-Dimensional Human Skin Melanin Evaluation
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Engineering of an Ultralong-Acting and Nonaggregating Dual Amylin and Calcitonin Receptor Agonist with Durable Efficacy in Obesity and Diabetes
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A New Era for PPARγ: Covalent Ligands and Therapeutic Applications
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Design, Synthesis, and Anti-inflammatory Activity Evaluation for Hydrazide-Based HDAC6 Targeted Protein Degraders
用户sar7Gc5emZOY
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Comprehensive 3d Transition Metal Single‐Atom Modulation Tunes Ni‐MOF D‐Band for Alkaline OER
50
7小时前
Cadonilimab plus platinum-based chemotherapy with or without bevacizumab as first-line treatment for persistent, recurrent, or metastatic cervical cancer (COMPASSION-16): a randomised, double-blind, placebo-controlled phase 3 trial in China
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11小时前
{Appendices}[Appendix I](Appendix I A. General Reagents) Macrogol 4000 - british pharmacopoeia[1668821579.875838.html]
50
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Targeted protein degradation in the transmembrane and extracellular space
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1秒前
Index Structures for Biological Sequences
10
4小时前
A meta-analysis of albuminuria as a surrogate endpoint for kidney failure
10
8小时前