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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Structure-Activity Relati" (30 stories)

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Machine learning based approaches for structure activity relationship analysis of heparanase inhibitors
Lead StoryNaturegeneral
May 29

Machine learning based approaches for structure activity relationship analysis of heparanase inhibitors

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBQbnZtbFdhMzV0S1NrSjVfb1Ftd1J2UndZekVibGhDTGt0bV95R1dvQnlHOHh2RHVMQlVmVUtGWUwtWlo3cG51M09ETkVRNXNIMlN4Qnhvckh6RVh6UURZ?oc=5" target="_blank">Machine learning based approaches for structure activity relationship analysis of heparanase inhibitors</a>  <font color="#6f6f6f">Nature</font>

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Search Results for "Structure-Activity Relati"

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29 stories displayed
Structural-activity relationship of Lycium barbarum polysaccharides in immunomodulation: integrating molecular insights with target identification for therapeutic development
Frontiersworld

Structural-activity relationship of Lycium barbarum polysaccharides in immunomodulation: integrating molecular insights with target identification for therapeutic development

<a href="https://news.google.com/rss/articles/CBMikgFBVV95cUxPSzZIUnJFUnNDQ09PRWpFdHJKSllUaGpTaThuajAydXZWbTY3WDVtcUNrdEd0YXprbzBRQVF3X2xIeVVDU2R6N1E4Vk9GaGJURGx6QlZCWU5qczVQVDJBOGcwUEpzWmI3UkN4dml2eEpZNUtVZUczZkprcEZsbWYtY0VhblFrWV8tMFo5MHFtNG9XQQ?oc=5" target="_blank">Structural-activity relationship of Lycium barbarum polysaccharides in immunomodulation: integrating molecular insights with target identification for therapeutic development</a>  <font color="#6f6f6f">Frontiers</font>

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Exploration of structure–activity relationship of 2,4-diaminopyrimidine derivatives as hematopoietic progenitor kinase 1 inhibitors
Wiley Online Librarygeneral

Exploration of structure–activity relationship of 2,4-diaminopyrimidine derivatives as hematopoietic progenitor kinase 1 inhibitors

<a href="https://news.google.com/rss/articles/CBMia0FVX3lxTFBuSjlETkRLZ3R0Smx1ZmpKRGlzVS1LRVU0bUVZZEhjd3gtMktwY0k0cGZTRE8xNkNMTzdFblY5YmZsZWZ4X0Y3cE56UUk0UVJiSEstX3p3dmV3Wmk4VXFOZUQySEdBTmNwbExj?oc=5" target="_blank">Exploration of structure–activity relationship of 2,4-diaminopyrimidine derivatives as hematopoietic progenitor kinase 1 inhibitors</a>  <font color="#6f6f6f">Wiley Online Library</font>

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Structure-Activity Relationship of Synthetic Cathinones: An Updated Review. - UB
Universitat de Barcelonageneral

Structure-Activity Relationship of Synthetic Cathinones: An Updated Review. - UB

<a href="https://news.google.com/rss/articles/CBMipAFBVV95cUxOcDRFWjMwTUsxWWdFOGpkcWRBTnFwUkFWNy1TRzNReVp5eTQ3ancwLWVkYUNxN1VxLTh3RUZfSm9QVW1DM1ltTDRIdzVVZG5BMFhtcHhDdUt2THZpbm5FLVZFcnFwX3ZTSTduNHg5WUVqejBfbEtxX1BXQkc0azJkcHdpTTFJZVRXYjdSRG9wMnlXZTMyRmk1OGh3bUpha0cxb01ZbA?oc=5" target="_blank">Structure-Activity Relationship of Synthetic Cathinones: An Updated Review.</a>  <font color="#6f6f6f">UB - Universitat de Barcelona</font>

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Structure–activity relationship studies of febuxostat derivatives identify potent anti-lung cancer agents that induce DNA damage and autophagy
Natureworld

Structure–activity relationship studies of febuxostat derivatives identify potent anti-lung cancer agents that induce DNA damage and autophagy

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBtQ2ViLXl2dEZUb1lEbHBuU0JLVW1wSHV5ZUJ4Nm9IekV6WldPU3dIZjFHN3pWbFE0LVhvNmZaYnJjaV9ZUFpnV0RPQnRpQWhpbklUTzlIWkEzMG16NFVZ?oc=5" target="_blank">Structure–activity relationship studies of febuxostat derivatives identify potent anti-lung cancer agents that induce DNA damage and autophagy</a>  <font color="#6f6f6f">Nature</font>

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Mapping the antileishmanial structure-activity relationship of eugenol
Frontiersgeneral

Mapping the antileishmanial structure-activity relationship of eugenol

<a href="https://news.google.com/rss/articles/CBMilAFBVV95cUxQWGQ4QjNpZFhlWkZuZnJnUWdCRGVYNlpWVi1UTHVoRm0yLWc4b3JCNnBwQlBPV25sTDM0WkdEaldJWmpyMVZERHhMeEJXdTlOd2JIZEhXY1d5Q0JXWmVwdlhmdzY2M1VLMnBzdDRlS2M4UXJBRUpCRHZuNUF2RkxZSVpxM3U1SDd3RG9uZnV5ZThlQWpx?oc=5" target="_blank">Mapping the antileishmanial structure-activity relationship of eugenol</a>  <font color="#6f6f6f">Frontiers</font>

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Interpretable Chirality-Aware Graph Neural Network for Quantitative Structure Activity Relationship Modeling in Drug Discovery
The Association for the Advancement of Artificial Intelligencegeneral

Interpretable Chirality-Aware Graph Neural Network for Quantitative Structure Activity Relationship Modeling in Drug Discovery

<a href="https://news.google.com/rss/articles/CBMiZEFVX3lxTE1udTl0emhkNDZPQzZVU2xhQWtOVUh1MC1tczZZV3VoU3lCdDhoenctYmNSVTRtVElwaFRaeGR0Z3p3UlhDQ0FicUhjT1g4U0NjUzFITnBkQVdQRXM1aEpJMG54U2o?oc=5" target="_blank">Interpretable Chirality-Aware Graph Neural Network for Quantitative Structure Activity Relationship Modeling in Drug Discovery</a>  <font color="#6f6f6f">The Association for the Advancement of Artificial Intelligence</font>

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Structure-activity relationship of pyrazole-based corrosion inhibitors for carbon steel in HCl: combined experimental and theoretical study
Naturegeneral

Structure-activity relationship of pyrazole-based corrosion inhibitors for carbon steel in HCl: combined experimental and theoretical study

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1MNFQ3aFo2S0Q2VElGMVM0NFdoRzlsdDJKU2JwR3JXWU1oZG9qalpKeW9FNHgtejRVUlBsWWVqOWN5eVc0anRDMXN0d01TRFZEeGo0eWtUaWZFVE4zeS1B?oc=5" target="_blank">Structure-activity relationship of pyrazole-based corrosion inhibitors for carbon steel in HCl: combined experimental and theoretical study</a>  <font color="#6f6f6f">Nature</font>

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From structural code to immunomodulation: the structure-activity relationship, molecular mechanisms, and translational medicine challenges of yam (Dioscorea opposita Thunb) polysaccharides
Frontiersworld

From structural code to immunomodulation: the structure-activity relationship, molecular mechanisms, and translational medicine challenges of yam (Dioscorea opposita Thunb) polysaccharides

<a href="https://news.google.com/rss/articles/CBMikgFBVV95cUxPMGZYa2l3SGpxYjBzcW1rSHY4TlVGX3VYb0dYZ0l5R2U0bllxaVpKUG9ZZ0dxaHZUNm5XcmNpSEowZk5IMUFoTUMwM3hKcWdfSnpfUU9QdV8zSGdaSEc1MzZmYnFEMWdGLXZSXzNnOC0tamthUnQtbkg0bXJtbVdqVXR4NUZURjFDWlFaZ2Y3ZVpDUQ?oc=5" target="_blank">From structural code to immunomodulation: the structure-activity relationship, molecular mechanisms, and translational medicine challenges of yam (Dioscorea opposita Thunb) polysaccharides</a>  <font color="#6f6f6f">Frontiers</font>

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An Insight Into Commercially Available SGLT2 Inhibitors and Their Structure–Activity Relationship Studies
Wiley Online Librarytech

An Insight Into Commercially Available SGLT2 Inhibitors and Their Structure–Activity Relationship Studies

<a href="https://news.google.com/rss/articles/CBMia0FVX3lxTE9jZzhSalVPazI5LU84WXcteFE4aTJ0SnR5NjBFdVpWYlAwQVB1Zm9UN3JRT0haYTZsRDdJTWNyejIxdXBmV05ubWJYSHFYbjNHY1Y2RHNUNlBhcFMzS1pLa1BPQmRCYmRZNDRZ?oc=5" target="_blank">An Insight Into Commercially Available SGLT2 Inhibitors and Their Structure–Activity Relationship Studies</a>  <font color="#6f6f6f">Wiley Online Library</font>

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Identification, characterization, and structure-activity relationship of the ASIC3-selective peptide WRPRFa
Naturegeneral

Identification, characterization, and structure-activity relationship of the ASIC3-selective peptide WRPRFa

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE96UDdJdHZWaWJxMVFta1o4N3dfdmt4b3V5WDdSemNRYnpqajRIbzhVcXIzNmJQd21jTW9NNDFDWFI1Z3JsdmlQR3ppMl9DYU9pVUdQX1BjZ1VjVGRBTW9F?oc=5" target="_blank">Identification, characterization, and structure-activity relationship of the ASIC3-selective peptide WRPRFa</a>  <font color="#6f6f6f">Nature</font>

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Unveiling abietic Acid’s therapeutic potential: a narrative review on structure-activity relationship, pharmacological properties, pharmacokinetics, and toxicological considerations
Frontiersworld

Unveiling abietic Acid’s therapeutic potential: a narrative review on structure-activity relationship, pharmacological properties, pharmacokinetics, and toxicological considerations

<a href="https://news.google.com/rss/articles/CBMilAFBVV95cUxOS0dEbm1PV19UT3Q5Ymh2cHkwRTMwdExNUmtQLXpCVkJ1dEx6blJCbDRJQjJYcDlUaXh3SUVpWk9ERUd4MGZBNHBPRExORXdkckpyYUNuQk5tSVJFc1ZQQkYwMklqd2hUQVVQNmhPSzZkRzVaWks3MXFZc3dBbXNnTHFEeW9uckkxTFcwVHNzeTRfcDg3?oc=5" target="_blank">Unveiling abietic Acid’s therapeutic potential: a narrative review on structure-activity relationship, pharmacological properties, pharmacokinetics, and toxicological considerations</a>  <font color="#6f6f6f">Frontiers</font>

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Structure-activity relationship of prevalent synthetic cannabinoid metabolites on hCB
Naturegeneral

Structure-activity relationship of prevalent synthetic cannabinoid metabolites on hCB

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9zTkJwU01fcWRBX3BNWnJhMUR3WWhod0ZxM1hIQjE4NTN1UVpwSWpaWUs3dnNqMUFPaURIb3UtQmdSSG85SW5CUUx2SnppVVFkUmZraTVmSU1Ea0czcjFF?oc=5" target="_blank">Structure-activity relationship of prevalent synthetic cannabinoid metabolites on hCB</a>  <font color="#6f6f6f">Nature</font>

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Antiviral activity of natural and modified hydrocolloids: main sources, susceptible viruses, structure-activity relationship and mechanisms of action
Frontierstech

Antiviral activity of natural and modified hydrocolloids: main sources, susceptible viruses, structure-activity relationship and mechanisms of action

<a href="https://news.google.com/rss/articles/CBMilAFBVV95cUxOcUlsZUt3bFdfdnRNQVE0RXhHcnNBY3pieW5kNHRBakhZN3liODA0Y2p6djJ4YWphcnlmalRRekNTQ3Q1dFdKNHZhYWZIejZBZ0M5SXZtSXdKQkhDZWJQQUFXMXVQTTNySl92YXFraDA3Wm5OdlFkSk5NekdMRXItalVyLTMwUkVOUDFiNjd0UVo1R2Jp?oc=5" target="_blank">Antiviral activity of natural and modified hydrocolloids: main sources, susceptible viruses, structure-activity relationship and mechanisms of action</a>  <font color="#6f6f6f">Frontiers</font>

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Topological regression as an interpretable and efficient tool for quantitative structure-activity relationship modeling
Naturegeneral

Topological regression as an interpretable and efficient tool for quantitative structure-activity relationship modeling

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1LSG9ieTVPdjh6VWJiOXlBTXZrbnNYOTBiRWR3U2xIbkZySXVDZ0RWVmxxX1M5R05CTHJ1ZDZ3SVJmX0x4WnNsV1V4QkwxMWFjeEtpazBYOG9nZ1BVLUc4?oc=5" target="_blank">Topological regression as an interpretable and efficient tool for quantitative structure-activity relationship modeling</a>  <font color="#6f6f6f">Nature</font>

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O solid-state NMR spectroscopy and DFT calculations
Naturegeneral

O solid-state NMR spectroscopy and DFT calculations

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9fSlJpS3RqaHFOZlU2TGJ1X25lWlhjdkRyVUxjWXNTd2NjSGJpVzBjX01PeDI4MkV1aHdDei1QdElZOG5ta3E1c0pObHRoQ2lIUERCSzNXdHZ0azRYOG1B?oc=5" target="_blank">O solid-state NMR spectroscopy and DFT calculations</a>  <font color="#6f6f6f">Nature</font>

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Deriving general structure–activity/selectivity relationship patterns for different subfamilies of cyclin-dependent kinase inhibitors using machine learning methods
Naturegeneral

Deriving general structure–activity/selectivity relationship patterns for different subfamilies of cyclin-dependent kinase inhibitors using machine learning methods

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBzcGtoSWNScW1leEJ0d2oza1F3U2R1Y2xsZHUzSGxhZHBmdFlhXzJDQzgwZ29mRFRwbmYxTklLbVJlREtyeEIwY0RCejBoNlExaW5rV0FVbE9xcVBuZHZn?oc=5" target="_blank">Deriving general structure–activity/selectivity relationship patterns for different subfamilies of cyclin-dependent kinase inhibitors using machine learning methods</a>  <font color="#6f6f6f">Nature</font>

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Synthesis and structure–activity relationship studies of benzimidazole-thioquinoline derivatives as α-glucosidase inhibitors
Naturegeneral

Synthesis and structure–activity relationship studies of benzimidazole-thioquinoline derivatives as α-glucosidase inhibitors

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBxWVN1YnRzSTdRcDViNkF0VjJfZ24xeVdNMTRBS3l4ZjV1ZDJZbWxJZ2x4T2RLZGdUV0xmY0NvSm42RmV2SUZUNlNUVDA3ZVdSZDlySnI3WkFvMy1JVXg0?oc=5" target="_blank">Synthesis and structure–activity relationship studies of benzimidazole-thioquinoline derivatives as α-glucosidase inhibitors</a>  <font color="#6f6f6f">Nature</font>

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Antiplasmodial activity, structure–activity relationship and studies on the action of novel benzimidazole derivatives
Naturegeneral

Antiplasmodial activity, structure–activity relationship and studies on the action of novel benzimidazole derivatives

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9GaTB5djlvaVZHU2ZPQlRyMUUzTC1ENXBWWmVSZGhjaXZQUDBMUlcyVnIyaEFraU1tb1RweURwdllfRVNVajhiOFFVRk8xMUdLRjBjUXp4eFlzRDM4LVhn?oc=5" target="_blank">Antiplasmodial activity, structure–activity relationship and studies on the action of novel benzimidazole derivatives</a>  <font color="#6f6f6f">Nature</font>

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Structure-activity relationship studies of four novel 4-aminopyridine K+ channel blockers | Scientific Reports
Naturegeneral

Structure-activity relationship studies of four novel 4-aminopyridine K+ channel blockers | Scientific Reports

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5yakswZ3JidU9HbktPQzl2Q2t2Q1NJd3J0UUhwTFgwZjNNOFZCM2FpejNQZkROZkViRHRzcGQxeERTQU1oOUdDODdkVWJ3VGN5NkJyRDB0c0RkM0ZuRFNz?oc=5" target="_blank">Structure-activity relationship studies of four novel 4-aminopyridine K+ channel blockers | Scientific Reports</a>  <font color="#6f6f6f">Nature</font>

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Covalency competition dominates the water oxidation structure–activity relationship on spinel oxides
Naturegeneral

Covalency competition dominates the water oxidation structure–activity relationship on spinel oxides

<a href="https://news.google.com/rss/articles/CBMiXkFVX3lxTE55OUk4MUh0WUdJVjhiazlLbkxQRmxON2wweFlaaVVpLURKUzBBanUtRHdQMjJMWWlYc1FYQ3dMZ01Ba3JTcHZ2LUx5MTIwZ3RFbkNrN1B6ZUV0Wm5jU2c?oc=5" target="_blank">Covalency competition dominates the water oxidation structure–activity relationship on spinel oxides</a>  <font color="#6f6f6f">Nature</font>

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Atomically unveiling the structure-activity relationship of biomacromolecule-metal-organic frameworks symbiotic crystal
Natureworld

Atomically unveiling the structure-activity relationship of biomacromolecule-metal-organic frameworks symbiotic crystal

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5nY21ta24tYTc4ZlJkbWIwVTV1R0pLS0NVdGE1OWQ0b3dRWXpuWWQ1NVNqRWNJamlCeFVfUWdxT0RXeXBnaERxUFNaX1V6S0hudDVsMFNVYTF4QmF3OHRr?oc=5" target="_blank">Atomically unveiling the structure-activity relationship of biomacromolecule-metal-organic frameworks symbiotic crystal</a>  <font color="#6f6f6f">Nature</font>

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Chemoenzymatic approaches for exploring structure–activity relationship studies of bioactive natural products
Naturegeneral

Chemoenzymatic approaches for exploring structure–activity relationship studies of bioactive natural products

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBHTDFuTzhJcC1iRXNtYkVjZjlTU0NxbnVobGI0RVlPSzZMNVhfajdhaklla1FzeGNHaWpEMkRlSjR6QzFORWlwdE55M0dNZFZDSWZFNnFiWWNNUEljQjE0?oc=5" target="_blank">Chemoenzymatic approaches for exploring structure–activity relationship studies of bioactive natural products</a>  <font color="#6f6f6f">Nature</font>

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Deciphering Structure-Activity Relationship Towards CO
Wiley Online Librarygeneral

Deciphering Structure-Activity Relationship Towards CO

<a href="https://news.google.com/rss/articles/CBMicEFVX3lxTFBoeHJIcWtWaTJiTFJQTUhDQ29Sc0dKWF9XUy1jNHc1LUhKZ2J2S0pLSFRUc3VXZ2tjUW84Wk5nbnJUTWMtRkp2dWU3SE5yX2gybVJ5eG9PSGZSSW5PN3k5aXJpOU5FWElxNGl2N3gtcjU?oc=5" target="_blank">Deciphering Structure-Activity Relationship Towards CO</a>  <font color="#6f6f6f">Wiley Online Library</font>

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A structure-activity relationship analysis of anthraquinones with antifouling activity against marine biofilm-forming bacteria
Frontierstech

A structure-activity relationship analysis of anthraquinones with antifouling activity against marine biofilm-forming bacteria

<a href="https://news.google.com/rss/articles/CBMimAFBVV95cUxObXl5RTNVN2N1M3U1NzNUcFo2a2dpcHhWNVhkanlrUzdlNTVvc1FZNHRxMzFpSjZTSWtHcnZjMERHRDZXa2xrS0wtM2txc2JkNDlUd0xPSGQ1dnNGRndUUjFZY2p3VkNpbzVSM0tQTXFuMHE1N2dJbVlLYzhQRnl0WWlaV1VUWTJ3aGl5eVJXQ0M0NVFMTlhjSg?oc=5" target="_blank">A structure-activity relationship analysis of anthraquinones with antifouling activity against marine biofilm-forming bacteria</a>  <font color="#6f6f6f">Frontiers</font>

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Scalable total synthesis and comprehensive structure–activity relationship studies of the phytotoxin coronatine
Naturegeneral

Scalable total synthesis and comprehensive structure–activity relationship studies of the phytotoxin coronatine

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBZTzJERW9rUUs5ajZYa1BaY3dxc1ZXRlZ6WjJLUFdWMnhYQ21JcUlwTmFxSm05LTdBajVsV2Q1TEd1OUpxb2RhSHhJaTBZREFtclMwcU9iclNBdUlEdVo4?oc=5" target="_blank">Scalable total synthesis and comprehensive structure–activity relationship studies of the phytotoxin coronatine</a>  <font color="#6f6f6f">Nature</font>

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Total synthesis and structure–activity relationship of alternaric acid delivers an herbicide vector
Naturegeneral

Total synthesis and structure–activity relationship of alternaric acid delivers an herbicide vector

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5fQVQzNWktNDZhWTRQY1pLblRBWDVaN0Z2SFlQblZOa2lIOF9nUnk0eUFxZGEtSnVuVDY0X0xhUWU3Sm9DbDREclJIT2RMby1hN3pzbUlTNVpjSV9aSXFn?oc=5" target="_blank">Total synthesis and structure–activity relationship of alternaric acid delivers an herbicide vector</a>  <font color="#6f6f6f">Nature</font>

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Structure—yeast α-glucosidase inhibitory activity relationship of 9- O -berberrubine carboxylates
Naturegeneral

Structure—yeast α-glucosidase inhibitory activity relationship of 9- O -berberrubine carboxylates

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBmTWlYM0hyWVBRT0FtMnpJbEd0dGZiLXozUzk3MnVUMGNncEl3MkJBdWR1M3cxRDRiMERpSzRHajkxWlFJYWdVZDdhWnBxcFlJTzJGNUMzTk5PamVoNGhV?oc=5" target="_blank">Structure—yeast α-glucosidase inhibitory activity relationship of 9- O -berberrubine carboxylates</a>  <font color="#6f6f6f">Nature</font>

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Lead optimization of novel quinolone chalcone compounds by a structure–activity relationship (SAR) study to increase efficacy and metabolic stability
Natureworld

Lead optimization of novel quinolone chalcone compounds by a structure–activity relationship (SAR) study to increase efficacy and metabolic stability

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9EaEo2WVJGdXhFc0ZrNnF6bFB4aXNzSHg5aU9RU0FzYzR5cF9teXgtZGd1VWNPcHZOOGx5Z2JyeHVUZ0tzaFNtOEJhOWhwRU5OMlduNEhNMmtkVTJSVUNF?oc=5" target="_blank">Lead optimization of novel quinolone chalcone compounds by a structure–activity relationship (SAR) study to increase efficacy and metabolic stability</a>  <font color="#6f6f6f">Nature</font>

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Quantitative structure–activity relationship modeling for predication of inhibition potencies of imatinib derivatives using SMILES attributes
Naturegeneral

Quantitative structure–activity relationship modeling for predication of inhibition potencies of imatinib derivatives using SMILES attributes

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5ETFZfd3BkY2xzX0MzQ2ZER1dnb29rMnJGRlR5NHV3aWZFcUtPaTNrVl9RVVNib1QwVkJKRkdoWDJYMWJMaXVyNjVWWGktcWtPQmcwQXlRcERYdmtxTkow?oc=5" target="_blank">Quantitative structure–activity relationship modeling for predication of inhibition potencies of imatinib derivatives using SMILES attributes</a>  <font color="#6f6f6f">Nature</font>

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