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sildenafil citrate (SPO1101D / Vultis / SPO1101)

✓ Approved

Seoul Pharmaceuticals · PDE5A · 小分子

什么是 sildenafil citrate?

sildenafil citrate 是一种小分子,由Seoul Pharmaceuticals研发。该药已获批,用于治疗相关适应症,给药途径:Oral (PO)。

药物档案

商品名SPO1101D, Vultis, SPO1101
公司Seoul Pharmaceuticals
药物类别小分子
分子靶点PDE5A
给药途径Oral (PO)
状态Approved

作用机制

分子靶点

sildenafil citrate 作用于 1 个分子靶点:

PDE5Aphosphodiesterase 5A (PDE5, CGB-PDE)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

sildenafil citrate 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Reproductive system and breast disordersErectile dysfunction✓ Approved

相关研究文献

PubMedAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026-10-26

Restoring Endothelial Mitochondrial Homeostasis With a Bioactive Nanoshield Promotes Vascular Regeneration on Cardiovascular Implants.

Liu Xiyu X, Zhang Wen W, Liu Lunxin L, Gui Lan L et al.

Defective endothelial regeneration constitutes a fundamental barrier to durable vascular repair. By integrating single cell RNA-sequencing data from rat carotid balloon injury with ultrastructural and histological evidence from rabbit stented arteries, we identified mitochondrial disorganization and dysfunction as common features of injured endothelial cells. Guided by these findings, we developed a poly(citrate-polyglycol-procyanidin) (PCGP) nanoshield to couple mitochondrial protection with anticoagulant and immunoregulatory functions for cardiovascular devices. PCGP preserved mitochondrial integrity, restored endothelial metabolic homeostasis, and rescued the regenerative phenotype of endothelial cells under oxidative stress. In rabbit arterial stent models, this intervention reactivated the PI3K/AKT/eNOS-nitric oxide axis, accelerated functional re-endothelialization, and markedly suppressed neointimal hyperplasia. Collectively, these findings support restoration of endothelial mitochondrial homeostasis as an important mechanistic axis associated with vascular repair.

PMID 42928428
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PubMedParasites, hosts and diseases2026-10-26

Molecular diagnosis of a case of Dibothriocephalus nihonkaiensis infection in Suzu City, Ishikawa Prefecture, Japan.

Kawabata Kohei K, Shimosaki Rin R, Ikku Ryosuke R, Saito Hiroaki H et al.

In this study, we intended to report a case of Dibothriocephalus nihonkaiensis infection diagnosed in Suzu City, Ishikawa Prefecture, Japan. A 23-year-old man from Aichi Prefecture moved to Suzu City, one of the most severely destroyed areas by the 2024 Noto Peninsula earthquake, to engage in reconstructive works. He visited the internal medicine department of Suzu General Hospital by the passage of long slender worm in his stool. Numerous operculated helminth eggs were detected from his stool samples, and a tapeworm strobila with the scolex was found after the treatment of praziquantel (10 mg/kg). Magnesium citrate was administered before and after praziquantel treatment, and stool samples were collected from the patient. The expelled tapeworm measured approximately 1.7 m in length. Morphological examination revealed a relatively small scolex with 2 suckling grooves, suggesting an immature adult specimen. Phylogenetic analysis of the mitochondrial 16S rRNA and cox1 genes identified the parasite as Dibothriocephalus nihonkaiensis. This case highlights the importance of integrating morphological and molecular approaches for accurate species identification in cases with complex epidemiological backgrounds.

PMID 42928461
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PubMedBiological trace element research2026-10-25

Retraction Note: Therapeutic Dose of Zinc Aspartate and Zinc Citrate Attenuates Disease Activity Indices in Rheumatoid Arthritis.

Hasan Mohammad M, Yadav Pooja P, Ansari Mairaj Ahmed MA, Ali Shakir S et al.

PMID 42925452
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PubMedFood chemistry2026-10-25

Rational construction of an electrophoretic system for the determination of flaxseed lignans by capillary electrophoresis.

Vera-Candioti Luciana L, Negro Emilse E, Bernal Claudio C

A rational strategy was developed for constructing a capillary electrophoretic system for the separation of structurally related flaxseed lignans. Electrophoretic selectivity was sequentially optimized through background electrolyte composition, dynamic capillary modification, and organic modifier content using multivariate experimental design. The selected system consisted of 20 mmol L-1 borate, 7.5 mmol L-1 phosphate, and 2.5 mmol L-1 citrate (pH 11.0), containing 0.20% (w/v) PDADMAC and 20% (v/v) methanol, with separation at -20 kV. The method separated pinoresinol, lariciresinol, matairesinol, secoisolariciresinol, and secoisolariciresinol diglucoside. Quantitative validation was established for secoisolariciresinol and secoisolariciresinol diglucoside, determined at 0.87 ± 0.05 mg g-1 after sequential alkaline-acid hydrolysis and 6.6 ± 0.3 mg g-1 after alkaline hydrolysis, respectively. Field-amplified sample injection was additionally explored for improving detectability, although signal enhancement was accompanied by loss of selectivity for the lariciresinol-matairesinol pair.

PMID 42925611
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PubMedJournal of natural products2026-10-25

Eudesmane Sesquiterpenoids from Dregea Volubilis Suppress Kidney Stones via Akt Signalling to Inhibit Oxalate Biosynthesis in Drosophila.

Zhao Jinna J, Guo Faxiang F, Wang Jiahuan J, Wan Lvyou L et al.

Dregea volubilis has long been used in traditional medicine for the treatment of urolithiasis, yet its bioactive constituents and molecular mechanisms remain largely undefined. Here, molecular networking-guided UPLC-ESI-MS/MS analysis enabled the isolation of ten sesquiterpenoids, including eight previously undescribed compounds (compounds 1∼4, 6∼9). Among them, dregeaterpene A (1) exhibited potent anti-urolithic activity in Drosophila, surpassing the therapeutic efficacy of potassium citrate. Mechanistically, dregeaterpene A suppressed endogenous oxalate biosynthesis by restoring oxalate-impaired Akt phosphorylation, leading to the downregulation of Daao1 and Daao2, and the upregulation of Agxt. Consequently, oxalate accumulation and calcium oxalate stone formation were markedly reduced. Collectively, these findings identify eudesmane sesquiterpenoids from D. volubilis as bioactive anti-urolithic agents and establish Akt-dependent regulation of oxalate metabolism as their underlying mechanism of action, highlighting dregeaterpene A as a promising lead compound for the development of therapeutics against calcium oxalate urolithiasis.

PMID 42924967
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PubMedCureus2026-10-25

Severe Pulmonary Hypertension in Critically Ill Children: A 10-Year Single-Center Case Series and Practical Management Considerations.

Straka Kalliopi K, Polymerou Ioannis I, Christakou Eleni E

Severe pulmonary hypertension (PH) in children may decompensate rapidly during intercurrent illness and is associated with substantial morbidity and mortality in the pediatric intensive care unit (PICU). We describe the clinical presentation, intensive care management, and outcomes of four children with severe PH admitted to a tertiary PICU between January 2014 and December 2024. Three patients were infants, and one was an 11-year-old girl with a history of extreme prematurity and bronchopulmonary dysplasia. All four presented with acute respiratory distress, hypoxemia, and cardiovascular compromise following a recent respiratory tract infection. PH was documented predominantly by echocardiography, with findings including elevated estimated pulmonary pressures, right ventricular (RV) pressure overload, interventricular septal flattening, and/or RV dysfunction. Right heart catheterization was performed in one patient. All patients received supplemental oxygen, diuretics, and sildenafil. Two required invasive mechanical ventilation and vasoactive support, while one patient received additional prostanoid and endothelin receptor antagonist therapy. The median PICU length of stay was 15 days (range: 10-24 days). Two patients survived to hospital discharge, whereas two died following refractory pulmonary hypertensive crises. These cases highlight respiratory infection as an important potential precipitant of acute decompensation in children with severe PH and illustrate the challenges of supporting the failing RV in the PICU. Although the small sample size and retrospective design preclude conclusions regarding treatment efficacy or prognostic factors, the cases emphasize several practical management priorities: early recognition of deterioration, prompt correction of factors that increase pulmonary vascular resistance, preservation of RV function and systemic perfusion, cautious escalation of respiratory support, and early multidisciplinary involvement. Based on these principles and the published pediatric PH literature, we propose a practical, physiology-based management algorithm for severe PH and pulmonary hypertensive crisis in the PICU.

PMID 42923560
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