Results 241 to 250 of about 43,444 (345)

The Jekyll and Hyde Nature of Tetrazoles in Polymer Science: From Intrinsic Electronic Duality to Programmable Macromolecular Function

Angewandte Chemie International Edition, Volume 65, Issue 36, 1 September 2026.
Tetrazoles are reframed as substitution‐programmable heterocycles rather than static functional groups in polymer chemistry. By linking electronic identity to synthetic strategy and polymer architecture, this mini‐review establishes a design framework for translating tetrazole duality into predictable macromolecular function.
Meryem S. Akdemir, Hatice Mutlu
wiley   +1 more source

Thiol-functionalized ZrP reinforced poly(MMA-co-MI) nanocomposites: High optical transparency and superior thermal stability for optical coatings. [PDF]

PLoS One
Jahangiri S, Sarikhani S.
europepmc   +1 more source

Supplementary Figure 8 from Trastuzumab-MMAU Antibody-Auristatin Conjugates: Valine-Glucoserine Linker with Stabilized Maleimide Conjugation Improves In Vivo Efficacy and Tolerability

Shalom D. Goldberg, Tero Satomaa, Olulanu H. Aina, Olli Aitio, Krista Burke, Vadim Dudkin, Brian Geist, Onyi Irrechukwu, Anna‐Liisa Hänninen, Annamari Heiskanen, Jari Helin, Jukka O. Hiltunen, Jacqueline Kinyamu-Akunda, Donna M. Klein, Neeraj Kohli, Titta Kotiranta, Tuula Lähteenmäki, Ritva Niemelä, Virve Pitkänen, Henna Pynnönen, William Rittase, Kristen Wiley, Junguo Zhou, Juhani Saarinen   +23 more
openalex   +1 more source

Clean Synthesis of N‐4‐Alkylamino‐7‐chloroquinoline Cyclic Imides: Influence of Lipophilicity on Antibacterial and Ecotoxicological Properties

Chemistry &Biodiversity, Volume 23, Issue 9, September 2026.
For series 2a–d, there appears to be optimal activity against Klebsiella pneumoniae when lipophilicity is intermediate (log P 2.64 for 2b). Similarly, for series 2e–g, activity against Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus mutans also increases (log P 3.71 for 2f).
Agenor P. Luz‐Filho, Thais C. Silva, Matheus B. Silva, Abraão P. Sousa, Helivaldo D. S. Souza, Priscila S. V. Lima, Alexandre Almeida‐Júnior, Fábio C. Sampaio, Petrônio F. Athayde‐Filho, Gabriela F. Fiss   +9 more
wiley   +1 more source

Solid-Liquid-Hysteresis Materials Based on Reversible Covalent Cross-Linking of Liquid Monomers. [PDF]

ACS Polym Au
Höfer T, Rössler A, Strube OI.
europepmc   +1 more source

Supplementary Figure 13 from Trastuzumab-MMAU Antibody-Auristatin Conjugates: Valine-Glucoserine Linker with Stabilized Maleimide Conjugation Improves In Vivo Efficacy and Tolerability

Shalom D. Goldberg, Tero Satomaa, Olulanu H. Aina, Olli Aitio, Krista Burke, Vadim Dudkin, Brian Geist, Onyi Irrechukwu, Anna‐Liisa Hänninen, Annamari Heiskanen, Jari Helin, Jukka O. Hiltunen, Jacqueline Kinyamu-Akunda, Donna M. Klein, Neeraj Kohli, Titta Kotiranta, Tuula Lähteenmäki, Ritva Niemelä, Virve Pitkänen, Henna Pynnönen, William Rittase, Kristen Wiley, Junguo Zhou, Juhani Saarinen   +23 more
openalex   +1 more source

Structure–Property Relationships and Thermal Aging of EPDN/NBR Elastomer Networks Modified With Polydiene and Maleimide Additives [PDF]

E. N. Ahmedov, S. V. Rzayeva
openalex   +1 more source

Payload‐Based Clinical Pharmacology Review of Approved Antibody–Drug Conjugates: Commonalities and Considerations for Streamlined Development

Clinical Pharmacology &Therapeutics, Volume 120, Issue 3, Page 614-638, September 2026.
Antibody–drug conjugates (ADCs) combine the specificity of an antibody with the potency of a cytotoxic drug. Thirteen ADCs, utilizing seven unique cytotoxic payloads and targeting 11 distinct antigens, are currently approved by the US Food and Drug Administration as of June 2025, representing a rapidly growing and highly promising class of anticancer ...
Sijie Lu, Qingqing Xiao, Lixuan Qian, Siyuan Sun, Zhu Zhou, Michael Z. Liao, Chunze Li   +6 more
wiley   +1 more source

Thermally reversible Diels-Alder linkers enable reusable methacrylate supports for enzyme immobilisation.

Chem Commun (Camb)
Broumidis E, Paradisi F.
europepmc   +1 more source

Incorporation of azide groups into an engineered Fn3 scaffold protein for site-specific, bioorthogonal conjugation. [PDF]

Protein Eng Des Sel
Le KT, McKenna TR, Mallari PM, Ahmed SZ, Ziemba AM, Buck ME, Moore SJ.   +6 more
europepmc   +1 more source