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Regulating Excited States by Varying Different Acceptors of D‐π‐A Emitters for Efficient Non‐Doped Blue Electroluminescence with High Luminance and Low Efficiency Roll‐Off.
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- Chemistry - A European Journal, 2024, v. 30, n. 8, p. 1, doi. 10.1002/chem.202303686
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- Article
Metabolite Identification of HIV-1 Capsid Modulators PF74 and 11L in Human Liver Microsomes.
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- Metabolites (2218-1989), 2022, v. 12, n. 8, p. 752, doi. 10.3390/metabo12080752
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- Article
Chiral Metal Nanoparticle Superlattices Enabled by Porphyrin‐Based Supramolecular Structures.
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- Angewandte Chemie, 2021, v. 133, n. 26, p. 14792, doi. 10.1002/ange.202103809
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- Article
Construction of an Integrated Teaching Case Library for Pharmaceutical Education: A Case Study on the Development of Anti- SARS-Cov-2 Drugs.
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- University Chemistry, 2023, v. 38, n. 12, p. 10, doi. 10.3866/PKU.DXHX202308077
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- Article
Untangling microbiota diversity and assembly patterns in the world's longest underground culvert water diversion canal.
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- Environmental Monitoring & Assessment, 2023, v. 195, n. 8, p. 1, doi. 10.1007/s10661-023-11593-z
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- Article
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) membrane (M) protein inhibits type I and III interferon production by targeting RIG-I/MDA-5 signaling.
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- Signal Transduction & Targeted Therapy, 2020, v. 5, n. 1, p. 1, doi. 10.1038/s41392-020-00438-7
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- Article
Targeting the entry step of SARS-CoV-2: a promising therapeutic approach.
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- Signal Transduction & Targeted Therapy, 2020, v. 5, n. 1, p. 1, doi. 10.1038/s41392-020-0195-x
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- Article
Fine Mapping of qAL5.2 Controlling Anther Length in Oryza sativa.
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- Plants (2223-7747), 2024, v. 13, n. 8, p. 1130, doi. 10.3390/plants13081130
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- Article
Administration of protopine prevents mitophagy and acute lung injury in sepsis.
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- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1104185
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- Article
High‐Throughput Miniaturized Synthesis of PROTAC‐Like Molecules.
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- Small, 2024, v. 20, n. 26, p. 1, doi. 10.1002/smll.202307215
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- Article
Comparison of the General Threshold Model of Survival and Dose–Response Models in Simulating the Acute Toxicity of Metals to Danio rerio.
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- Environmental Toxicology & Chemistry, 2019, v. 38, n. 10, p. 2169, doi. 10.1002/etc.4534
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- Article
Stanniocalcin‐1 attenuates collagen‐induced arthritis through inhibiting STAT3 phosphorylation and Th17 response.
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- Scandinavian Journal of Immunology, 2023, v. 97, n. 2, p. 1, doi. 10.1111/sji.13226
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- Article
Facile Synthesis of Derivatives of 1,1,3-Trioxo-2 H,4 H-pyrrolo[1,2- b][1,2,4,6]thiatriazine: A New Heterocyclic System.
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- Heteroatom Chemistry, 2013, v. 24, n. 6, p. 495, doi. 10.1002/hc.21123
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- Article
Icariin Promotes Osteogenic Differentiation in a Cell Model with NF1 Gene Knockout by Activating the cAMP/PKA/CREB Pathway.
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- Molecules, 2023, v. 28, n. 13, p. 5128, doi. 10.3390/molecules28135128
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- Article
Identification of Polyphenol Derivatives as Novel SARS-CoV-2 and DENV Non-Nucleoside RdRp Inhibitors.
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- Molecules, 2023, v. 28, n. 1, p. 160, doi. 10.3390/molecules28010160
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- Article
Discovery and Mechanistic Investigation of Piperazinone Phenylalanine Derivatives with Terminal Indole or Benzene Ring as Novel HIV-1 Capsid Modulators.
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- Molecules, 2022, v. 27, n. 23, p. 8415, doi. 10.3390/molecules27238415
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- Article
Design, Synthesis, and Mechanistic Study of 2-Pyridone-Bearing Phenylalanine Derivatives as Novel HIV Capsid Modulators.
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- Molecules, 2022, v. 27, n. 21, p. 7640, doi. 10.3390/molecules27217640
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- Article
Identification of Boronate-Containing Diarylpyrimidine Derivatives as Novel HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors.
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- Molecules, 2022, v. 27, n. 21, p. 7538, doi. 10.3390/molecules27217538
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- Article
Discovery of Novel Boron-Containing N -Substituted Oseltamivir Derivatives as Anti-Influenza A Virus Agents for Overcoming N1-H274Y Oseltamivir-Resistant.
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- Molecules, 2022, v. 27, n. 19, p. 6426, doi. 10.3390/molecules27196426
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- Article
Design, Synthesis and Structure—Activity Relationships of Phenylalanine-Containing Peptidomimetics as Novel HIV-1 Capsid Binders Based on Ugi Four-Component Reaction.
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- Molecules, 2022, v. 27, n. 18, p. 5995, doi. 10.3390/molecules27185995
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- Article
Design, Synthesis, and Evaluation of a Set of Carboxylic Acid and Phosphate Prodrugs Derived from HBV Capsid Protein Allosteric Modulator NVR 3-778.
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- Molecules, 2022, v. 27, n. 18, p. 5987, doi. 10.3390/molecules27185987
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- Article
Newly Emerging Strategies in Antiviral Drug Discovery: Dedicated to Prof. Dr. Erik De Clercq on Occasion of His 80th Anniversary.
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- Molecules, 2022, v. 27, n. 3, p. 850, doi. 10.3390/molecules27030850
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- Article
Path tracking control of automated vehicles based on adaptive MPC in variable scenarios.
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- IET Intelligent Transport Systems (Wiley-Blackwell), 2024, v. 18, n. 6, p. 1031, doi. 10.1049/itr2.12484
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- Article
Structure-Based Discovery and Characterization of a Preclinical Drug Candidate for the Treatment of HIV-1 Infection.
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- Viruses (1999-4915), 2022, v. 14, n. 11, p. 2390, doi. 10.3390/v14112390
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- Article
SARS-CoV-2 NSP5 and N protein counteract the RIG-I signaling pathway by suppressing the formation of stress granules.
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- Signal Transduction & Targeted Therapy, 2022, v. 6, n. 1, p. 1, doi. 10.1038/s41392-022-00878-3
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- Article
Molecular design opportunities presented by solvent‐exposed regions of target proteins.
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- Medicinal Research Reviews, 2019, v. 39, n. 6, p. 2194, doi. 10.1002/med.21581
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HIV-1 NNRTIs: structural diversity, pharmacophore similarity, and impliations for drug design.
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- Medicinal Research Reviews, 2013, v. 33, p. E1, doi. 10.1002/med.20241
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Bibliometric analysis and visualization of research trends on HIV-1 capsid inhibitors (2000–2022).
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- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1282090
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- Article
Chiral Metal Nanoparticle Superlattices Enabled by Porphyrin‐Based Supramolecular Structures.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 26, p. 14671, doi. 10.1002/anie.202103809
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- Article
Tetramethylpyrazine Analogue CXC195 Protects against Cerebral Ischemia/Reperfusion Injury in the Rat by an Antioxidant Action via Inhibition of NADPH Oxidase and iNOS Expression.
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- Pharmacology, 2013, v. 92, n. 3/4, p. 198, doi. 10.1159/000354722
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- Article
Discovery of piperidine-substituted thiazolo[5,4-d]pyrimidine derivatives as potent and orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitors.
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- Communications Chemistry, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42004-019-0174-8
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- Article
Design and synthesis of Fsp<sup>3</sup>‐enriched spirocyclic‐substituted diarylpyrimidine derivatives as novel HIV‐1 NNRTIs.
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- Chemical Biology & Drug Design, 2024, v. 103, n. 3, p. 1, doi. 10.1111/cbdd.14510
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- Article
Design, synthesis, and biological evaluation of piperidinyl‐substituted [1,2,4]triazolo[1,5‐a]pyrimidine derivatives as potential anti‐HIV‐1 agents with reduced cytotoxicity.
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- Chemical Biology & Drug Design, 2021, v. 97, n. 1, p. 67, doi. 10.1111/cbdd.13760
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- Article
Design, synthesis, and evaluation of novel heteroaryldihydropyrimidine derivatives as non‐nucleoside hepatitis B virus inhibitors by exploring the solvent‐exposed region.
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- Chemical Biology & Drug Design, 2020, v. 95, n. 6, p. 567, doi. 10.1111/cbdd.13512
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- Article
Design, synthesis, and biologic evaluation of novel galloyl derivatives as HIV‐1 RNase H inhibitors.
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- Chemical Biology & Drug Design, 2019, v. 93, n. 4, p. 582, doi. 10.1111/cbdd.13455
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- Article
Discovery of potent HIV‐1 non‐nucleoside reverse transcriptase inhibitors by exploring the structure–activity relationship of solvent‐exposed regions I.
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- Chemical Biology & Drug Design, 2019, v. 93, n. 4, p. 430, doi. 10.1111/cbdd.13429
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- Article
Design, synthesis, and antiviral evaluation of novel hydrazone‐substituted thiophene[3,2‐d]pyrimidine derivatives as potent human immunodeficiency virus‐1 inhibitors.
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- Chemical Biology & Drug Design, 2018, v. 92, n. 6, p. 2009, doi. 10.1111/cbdd.13373
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- Article
Design, synthesis, and biological evaluation of novel 5-Alkyl-6-Adamantylmethylpyrimidin-4(3H)-ones as HIV-1 non-nucleoside reverse-transcriptase inhibitors.
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- Chemical Biology & Drug Design, 2016, v. 88, n. 3, p. 380, doi. 10.1111/cbdd.12765
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- Article
Arylazolyl(azinyl)thioacetanilides: Part 19.
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- Chemical Biology & Drug Design, 2016, v. 88, n. 2, p. 241, doi. 10.1111/cbdd.12751
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- Article
Design, Synthesis, and Biological Evaluation of Novel 2-(Pyridin-3-yloxy)acetamide Derivatives as Potential Anti- HIV-1 Agents.
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- Chemical Biology & Drug Design, 2016, v. 87, n. 2, p. 283, doi. 10.1111/cbdd.12657
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- Article
Synthesis and Preliminary Antiviral Activities of Piperidine-substituted Purines against HIV and Influenza A/H1N1 Infections.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 568, doi. 10.1111/cbdd.12520
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- Article
Synthesis and Biological Evaluation of a Series of 2-((1-substituted-1 H-1,2,3-triazol-4-yl)methylthio)-6-(naphthalen-1-ylmethyl)pyrimidin-4(3 H)-one As Potential HIV-1 Inhibitors.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 614, doi. 10.1111/cbdd.12524
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- Article
Design, Synthesis, and Biological Evaluation of Novel Benzoyl Diarylamine/ether Derivatives as Potential Anti-HIV-1 Agents.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 3, p. 333, doi. 10.1111/cbdd.12497
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- Article
Design, Synthesis, and Biological Evaluation of Novel 4-Aminopiperidinyl-linked 3,5-Disubstituted-1,2,6-thiadiazine-1,1-dione Derivatives as HIV-1 NNRTIs.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 1, p. 887, doi. 10.1111/cbdd.12468
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- Article
Design, Synthesis, and Anti- HIV Evaluation of Novel Triazine Derivatives Targeting the Entrance Channel of the NNRTI Binding Pocket.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 1, p. 902, doi. 10.1111/cbdd.12471
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- Article
Synthesis and Anti- HIV Activity of 4-(Naphthalen-1-yl)-1,2,5-thiadiazol-3-hydroxyl Derivatives.
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- Chemical Biology & Drug Design, 2014, v. 84, n. 4, p. 420, doi. 10.1111/cbdd.12328
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- Article
Design, Synthesis, and Biological Evaluation of Novel 3,5-Disubstituted-1,2,6-Thiadiazine-1,1-Dione Derivatives as HIV-1 NNRTIs.
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- Chemical Biology & Drug Design, 2013, v. 82, n. 4, p. 384, doi. 10.1111/cbdd.12160
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- Article
Synthesis and Preliminary Biologic Evaluation of 5-Substituted-2-(4-substituted phenyl)-1,3-Benzoxazoles as A Novel Class of Influenza Virus A Inhibitors.
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- Chemical Biology & Drug Design, 2012, v. 79, n. 6, p. 1018, doi. 10.1111/j.1747-0285.2012.01344.x
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- Article
Ligustrazine Derivatives. Part 4: Design, Synthesis, and Biological Evaluation of Novel Ligustrazine-based Stilbene Derivatives as Potential Cardiovascular Agents.
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- Chemical Biology & Drug Design, 2012, v. 79, n. 5, p. 731, doi. 10.1111/j.1747-0285.2012.01332.x
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- Article
Discovery of Dihydro-Alkyloxy-Benzyl-Oxopyrimidines as Promising Anti-Influenza Virus Agents.
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- Chemical Biology & Drug Design, 2011, v. 78, n. 4, p. 596, doi. 10.1111/j.1747-0285.2011.01180.x
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- Article