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ZI

zinc acetate dihydrate (Wilzin / Wilzin)

✓ Approved

Recordati S.p.A. · Small Molecule · Small Molecule

What is zinc acetate dihydrate?

zinc acetate dihydrate is a small molecule developed by Recordati S.p.A.. It is approved for therapeutic indications via unknown.

Drug Profile

Brand NamesWilzin, Wilzin
CompanyRecordati S.p.A.
Drug ClassSmall Molecule
RouteUnknown
StatusApproved

Therapeutic Indications

zinc acetate dihydrate is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Congenital, familial and genetic disordersHepato-lenticular degeneration✓ Approved

Related Research Articles

PubMedJournal for immunotherapy of cancer2026-07-17

Blautia coccoides-derived acetate potentiates anti-PD-1 immunotherapy in melanoma by activating cytotoxic CD8+ T cells.

Zhang Zhiwen Z, Liang Xiaofeng X, Tian Yuyang Y, Li Chengyi C et al.

Gut microbiota can modulate cancer immunotherapy and enhance the efficacy of programmed cell death protein 1 (PD-1) blockade in tumors, yet the responsible microbes and underlying mechanisms remain incompletely understood. Publicly available anti-PD-1-treated melanoma microbiome cohorts were reanalyzed. Causal validation was performed using oral Blautia coccoides (B. coccoides) supplementation in B16-F10 melanoma-bearing mice. Untargeted and targeted liquid chromatography-tandem mass spectrometry-based metabolomics, CD8+ T-cell depletion, receptor identification and binding analyses, and downstream transcriptomic and biochemical assays were used to identify the key metabolite and investigate its mechanism of action. We identified Blautia as enriched in melanoma patients responding to immune checkpoint inhibitors, with higher abundance associated with non-progression. In melanoma-bearing mice, oral B. coccoides suppressed tumor growth and increased intratumoral effector CD8+ T cells. Metabolomic profiling identified acetate as a prominent B. coccoides-associated metabolite. Acetate enhanced CD8+ T-cell effector function. CD8+ T-cell depletion largely abrogated the antitumor effects of both B. coccoides and acetate, supporting a central role for CD8+ T cells. Mechanistically, these findings support a model in which acetate is associated with a TLR3-linked signaling pathway in CD8+ T cells, accompanied by PI3K/Akt activation and enhanced effector function. Notably, B. coccoides or acetate potentiated anti-PD-1 therapy in mouse melanoma models, supporting their potential as adjunctive strategies for melanoma immunotherapy. These findings support a model of an acetate-TLR3-linked PI3K/Akt signaling axis linking microbiota-associated metabolites to CD8+ T cell-mediated antitumor immunity. Importantly, our study highlights both B. coccoides and its derivative, acetate, as preclinical adjunctive candidates to potentiate anti-PD-1 efficacy in melanoma.

PubMedAdvanced healthcare materials2026-07-17

Crystallinity-Gradient Etched Hollow Mesoporous Zinc Nanoparticle for Dual-Source H2O2-Driven Tumor Ferroptosis Therapy.

Cai Haobin H, Yang Jing J, Wang Zehui Z, Chen Xinyu X et al.

Zn2+ offers significant advantages for cancer therapy via mitochondrial disruption, immune activation, and metal homeostasis perturbation, but faces challenges of rapid clearance and systemic toxicity. Existing zinc‑based (e.g., zinc oxide (ZnO), and zinc peroxide) nanoparticles often lack internal voids and sufficient surface area, restricting drug loading and functionalization. In this study, we developed a crystallinity‑gradient selective etching method to tailor biodegradable hollow mesoporous zinc nanoparticle (HMZN). Typically, zinc peroxide nanoparticles with low‑crystallinity core and high‑crystallinity shell were synthesized, and ammonia water was used to selectively etch the inner low‑crystallinity core, producing HMZN. Hemin (HEM) and Gd‑poly(acrylic acid) macrochelates (GP) were then loaded to construct HEM@HMZN@GP for dual-source H2O2 surge-driven tumor ferroptosis therapy. In acidic tumor microenvironment, Zn2+, H2O2, HEM, and GP can be released from HEM@HMZN@GP. The released Zn2+ damages mitochondrial electron transport chain (ETC) and generates superoxide anions (•O2 -), which can be rapidly catalyzed by superoxide dismutase into H2O2. The dual-source of H2O2 markedly elevates local oxidative stress. HEM can be enzymatically converted by heme oxygenase‑1 to Fe2+, which reacts with the abundant H2O2 via Fenton reaction to produce hydroxyl radicals, initiating lipid peroxidation and ferroptosis. GP enhances T1‑weighted magnetic resonance imaging signals, facilitating drug delivery visualization in tumors.

PubMedSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy2026-07-17

Hitting two birds with one stone: The synthesis of carbon quantum dots for optical detection of Fe3+ and ZnO microsphere optical coating through Zn-triethanolamine bridging polydentate ligand.

Zhou Ziyue Z, Kirsanov Dmitry D, Voznesenskiy Mikhail M, An Decheng D et al.

The development of highly selective and sensitive fluorescence-based nanoprobes for monitoring Fe3+ concentration is important in environmental analyses. Herein, unique metal complex precursors involving triethanolamine (TEA) and zinc acetate Zn(OAc)₂ were designed to synthesize carbon quantum dots (CDs) via hydrothermal carbonization approach. The prepared water-soluble ZnN codoped CDs are ∼2.9 nm in size and exhibit excitation-dependent blue emission and good photostability. Zn2+ ions, coordinated via Zn-TEA complexes, are incorporated into the carbon matrix and function as anchors to bridge and stabilize sp2 domains. The CDs serve as an ideal platform for sensitive detection of Fe3+ in aqueous media through fluorescence quenching, with a detection limit of 3.48 μM, which is below the water quality standard for Fe3+ (0.3 ppm, ∼5.36 μM) in drinking water suggested by the U.S. Environmental Protection Agency (EPA). Interference studies reveal that the presence of 17 other competing ions does not alter the sensing of Fe3+, indicating the high selectivity of the CDs toward Fe3+, while the fluorescence quenching mechanism is attributed to the formation of non-fluorescent complexes between Fe3+ and surface functional groups of the CDs, leading to nonradiative recombination. Simultaneously, Zn high concentration favors the preparation of ZnO microsphere pigment composed of nanocrystals through TEA ligand modified bridge effect.

PubMedbioRxiv : the preprint server for biology2026-07-17

Zn 2+ as a secondary messenger for exogenous redox potential sensed through Chemosensory Zinc-Binding (CZB) protein domains.

Franco Kailie K, Cooper Kendal G KG, Shin Clara Hyunyoung CH, Steele-Mortimer Olivia O et al.

Redox environments in nature are shaped by reactive oxygen species (ROS), oxygen availability, and metal ion chemistry, and exert profound effects on cell physiology and survival. While extensive work has characterized how cells resist oxidative damage, the mechanisms by which cells sense and navigate environmental redox conditions remain less well understood. Here, we identify a previously unrecognized and widespread mechanism of redox sensing in Salmonella enterica serovar Typhimurium mediated by the chemosensory zinc-binding (CZB) domain-containing receptor McpA. Using quantitative chemotaxis assays and live-cell imaging, we show that S. Typhimurium exhibits robust, concentration-dependent chemotaxis toward the neutrophil-derived oxidants HOCl and hydroperoxides, with attraction occurring at low, physiologically relevant concentrations below those that cause bactericidal effects, and this response requires McpA and its conserved zinc-binding cysteine. Whereas other Cys-Zn thiolate systems function through direct oxidation mechanisms, we find that the unique 3His,1Cys binding motif of CZBs responds to redox-dependent changes in Zn²⁺ speciation, whereby oxidizing conditions shift soluble, bioavailable Zn²⁺ into insoluble zinc precipitates. In this way, CZBs utilize the bioavailable Zn²⁺ pool as a secondary messenger of exogenous redox potential, and correspondingly, cells exhibit chemoattraction toward Zn²⁺-depleted environments, including sources of ROS, but also toward oxygen-rich conditions that provide a metabolic growth advantage. The broad phylogenetic distribution of CZB domains is consistent with this Zn²⁺-responsive mechanism being an ancient redox-sensing strategy, likely established early in bacterial evolution under changing planetary redox conditions and retained across diverse bacterial lineages. We report a previously unknown mechanism of redox sensing that operates through changes in the bioavailability and speciation of Zn²⁺, enabling bacteria to detect changes in exogenous redox potential with high sensitivity and navigate redox gradients. The broad phylogenetic distribution of chemosensory zinc-binding (CZB) domains suggests that this zinc-dependent sensory mechanism is an ancient and widespread strategy for detecting environmental redox gradients that arose early in bacterial evolution and may have been subsequently shaped or expanded in response to increasing atmospheric oxygen associated with the Great Oxygenation Event.

PubMedNature communications2026-07-17

Mechanistic insight into signal bias by the agonist-dependent conformational dynamics of GPR84.

Suzuki Shota S, Tran Duy Phuoc DP, Nishikawa Kouki K, Kitao Akio A et al.

GPR84 is an orphan class A GPCR primarily expressed in immune cells, where it plays key roles in inflammation and metabolism. Here, we present the cryo-electron microscopy structures of the GPR84-Gi complex bound to the G protein-biased agonist DL-175, and the inactive state of GPR84 bound to the antagonist GLPG1205. Combined with signaling assays and molecular dynamics simulations, these structures elucidate the conformational landscape spanning the inactive and G protein-biased active states of GPR84, providing a mechanistic basis for biased agonism. Notably, steric interactions between DL-175 and L3366.52 selectively preclude the conformational changes required for efficient β-arrestin recruitment without compromising G protein activation. These structural insights provide a structural context for the rational design of GPR84-targeted therapeutics with precisely tuned signaling profiles.

PubMedJournal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)2026-07-17

Protective effect of soybean isoflavone (SI) on ovarian damages by zinc oxide nanoparticles (ZnONPs) in female mice.

He Haiwei H, Wang Kaixuan K, Jin Yadan Y, Zhang Fangdi F et al.

With the wide use of ZnONPs in industry and biomedicine, their reproductive toxicity has raised great concern. Soybean isoflavone (SI), a natural antioxidant phytoestrogen, was used to alleviate ZnONPs-induced ovarian damage in mice. Five groups of mice were used: control, 50 mg/kg ZnONPs, 100 mg/kg ZnONPs, 50 mg/kg ZnONPs + 50 mg/kg SI, and 100 mg/kg ZnONPs + 50 mg/kg SI. All mice were administered daily by gavage for 45 days. Ovaries were then collected for analysis of zinc content, histopathology, apoptosis, and related protein expression. ZnONPs exposure caused severe ovarian histopathological damage and significantly elevated zinc levels in blood and ovarian tissue (P < 0.01). Body weight, ovarian index, and follicle number decreased dose-dependently, while apoptosis increased. RNA-seq revealed that ZnONPs induced oxidative stress, apoptosis, hormonal disturbance, and impaired follicular development. SI effectively reversed these alterations by enhancing antioxidant capacity, inhibiting oxidative stress-related apoptosis, and normalizing the expression of Ddx4, Er, H2ab1, and Ar, thus preserving ovarian structure and function. SI alleviates ZnONPs-induced reproductive toxicity by reducing oxidative stress, inhibiting apoptosis, and regulating hormone pathways. SI protects ovaries via the Ddx4/Er/Ar/H2ab1 network and provides a new natural intervention for nanoparticle damage.

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