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Acta Pharmaceutica Sinica B(2021年10期)
藥學學報(英文版)
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- 基本信息
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:中國藥學會藥物研究所;中國醫(yī)學科學院
:月刊
:2211-3835
- 出版信息
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: 醫(yī)藥衛(wèi)生科技
: 藥學
:1375篇
- 評價信息
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:3.134
:2.569
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目 錄
- Aims and Scope
- Announcing 2020 Impact Factor for Acta Pharmaceutica Sinica B
- Application of immune checkpoint targets in the anti-tumor novel drugs and traditional Chinese medicine development
- CRISPR-Cas9: A method for establishing rat models of drug metabolism and pharmacokinetics
- Alterations of DNA damage response pathway:Biomarker and therapeutic strategy for cancer immunotherapy
- Natural compounds in the regulation of proteostatic pathways: An invincible artillery against stress, ageing, and diseases
- Targeting autophagy using small-molecule compounds to improve potential therapy of Parkinson ‘ s disease
- Recent developments in the medicinal chemistry of single boron atom-containing compounds
- Nanomedicine for acute respiratory distress syndrome: The latest application, targeting strategy, and rational design
- MCDB: A comprehensive curated mitotic catastrophe database for retrieval, protein sequence alignment, and target prediction
- TRIB3-GSK-3β interaction promotes lung fibrosis and serves as a potential therapeutic target
- PD0325901, an ERK inhibitor, enhances the efficacy of PD-1 inhibitor in non-small cell lung carcinoma
- Tubeimoside-1 induces TFEB-dependent lysosomal degradation of PD-L1 and promotes antitumor immunity by targeting mTOR
- 3D disorganization and rearrangement of genome provide insights into pathogenesis of NAFLD by integrated Hi-C, Nanopore, and RNA sequencing
- Salmonella flagella confer anti-tumor immunological effect via activating Flagellin/TLR5 signalling within tumor microenvironment
- Cholesterol-associated lysosomal disorder triggers cell death of hematological malignancy:Dynamic analysis on cytotoxic effects of LW-218
- Ligand-based substituent-anchoring design of selective receptor-interacting protein kinase 1 necroptosis inhibitors for ulcerative colitis therapy
- Discovery of a subtype-selective, covalent inhibitor against palmitoylation pocket of TEAD3
- Bioresponsive micro-to-nano albumin-based systems for targeted drug delivery against complex fungal infections
- Tumor microenvironments self-activated nanoscale metal-organic frameworks for ferroptosis based cancer chemodynamic/photothermal/chemo therapy
- Self-assembled FeS-based cascade bioreactor with enhanced tumor penetration and synergistic treatments to trigger robust cancer immunotherapy
- Cancer-specific calcium nanoregulator suppressing the generation and circulation of circulating tumor cell clusters for enhanced anti-metastasis combinational chemotherapy
- Cytosolic delivery of the immunological adjuvant Poly Ⅰ:C and cytotoxic drug crystals via a carrier-free strategy significantly amplifies immune response
- Synchronous conjugation of i-motif DNA and therapeutic siRNA on the vertexes of tetrahedral DNA nanocages for efficient gene silence
- TPGS/hyaluronic acid dual-functionalized PLGA nanoparticles delivered through dissolving microneedles for markedly improved chemo-photothermal combined therapy of superficial tumor
- Functional identification of the terpene synthase family involved in diterpenoid alkaloids biosynthesis in Aconitum carmichaelii
- Construction of acetyl-CoA and DBAT hybrid metabolic pathway for acetylation of 10-deacetylbaccatin Ⅲ to baccatin Ⅲ
- Commentary: PROTACs make undruggable targets druggable: Challenge and opportunity
- Information for Authors