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搜索結果包含 Pharmacokinetic 的內容

Jul 11,2025
端錨聚合酶抑制劑G007-LK具有治療結直腸癌的潛力，本研究中PK實驗通過尊龍凱時進行
Medicilon Preclinical Research LCC performed the pharmacokinetic studies.
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Jul 10,2025
JX01是一種抗心力衰竭候選藥物，具有良好的PK特性和安全性。PK實驗通過尊龍凱時進行
Pharmacokinetic studies were commissioned by Medicilon.
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Jul 10,2025
四價廣譜中和雙特異性抗體ISH0339的臨床前評估通過尊龍凱時進行
An indirect antigen ELISA assay was used for the detection of ISH0339 in rat serum (Medicilon). tbad003.pngPharmacokinetic analysis of single-dose ISH0339 administration was conducted by. Extended toxicity study of single-dose ISH0339 was conducted by M
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Jul 02,2025
靶向HGF的人源化中和抗體的臨床前開發，本研究中PK/TK及ADA通過尊龍凱時進行
Pharmacokinetics, toxicokinetics and anti-drug antibodies of YYB-101 in cynomolgus monkeys were conducted by the Test and Control Article Department of Medicilon Preclinical Research, LLC, in accordance with regulations outlined in the USDA Animal Welfare
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Jul 02,2025
ASCT1/2抑制劑可用于治療精神分裂癥和視覺障礙，本研究中小鼠PK實驗通過尊龍凱時進行
Pharmacokinetic studies in mice for L-4FPG, L-4OHPG, and L-4ClPG were performed by Medicilon.
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Jun 12,2025
雙靶向HDAC抑制劑和ATM激活劑SP-1-303抑制雌激素受體陽性乳腺癌細胞生長，本研究中PK實驗通過尊龍凱時進行
Pharmacokinetic studies performed by Medicilon.
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Jun 11,2025
第二代前列腺素受體拮抗劑，本研究中眼部PK實驗通過尊龍凱時進行
Ocular Pharmacokinetic studies were performed at Medicilon.
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Jun 11,2025
SIRT6變構激活劑在結直腸癌中發揮治療作用，本研究中PK實驗通過尊龍凱時進行
Pharmacokinetic studies were performed by Shanghai Medicilon Inc, China, following standard protocols.
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Jul 06,2023
發現新型RAGE/SERT雙重抑制劑，可用于治療阿爾茨海默病和抑郁癥。其中藥代動力學研究是通過委托尊龍凱時進行
Alzheimer's disease (AD) is a progressive and devastating neurodegenerative disorder, characterized by the presence of β-amyloid (Aβ) peptide plaques, neurofibrillary tangles, and neuroinflammatio
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Jul 06,2023
IAP蛋白是有吸引力的癌癥治療靶點。SM-406 是一種口服有效的IAP拮抗劑。SM-406 在雄性SD大鼠、比格犬和NHP中的PK研究通過尊龍凱時進行
Apoptosis is a cellular process critical to the normal development and homeostasis of multicellular organisms.?The inhibitor of apoptosis proteins (IAPs) are a class of key apoptosis regulators.
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Jul 06,2023
設計合成一系列用于治療胃癌的多靶點受體酪氨酸激酶抑制劑，并進行生物學評價。其中藥代動力學分析通過尊龍凱時進行
Gastric cancer is the second most lethal cancer across the world. Compounds 8f, inhibits FGFR1 signaling pathways as well as induces cell apoptosis, is a potential agent for the treatment of gastric c
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Jul 06,2023
FBPase是與腫瘤和2型糖尿病相關的一個有前景的靶點。化合物W8對FBPase表現出高選擇性。W8的藥代動力學研究通過尊龍凱時進行
Fructose-1,6-bisphosphatase (FBPase) is a promising target associated with cancer and type 2 diabetes. Compounds W8 and W8k exhibit high selectivity against FBPase and W8 effectively reduces blood glu
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Jul 06,2023
藥物發現中的挑戰之一是識別高質量的先導化合物。此研究中PK結果表明L12可作為針對PDE5的先導化合物，進一步研究和開發。L12的PK分析通過尊龍凱時進行
Scaffold hopping refers to computer-aided screening for active compounds with different structures against the same receptor to enrich privileged scaffolds, which is a topic of high interest in organi
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Jul 06,2023
ANO1是一個潛在的鎮痛靶點。DFBTA是一種有效的ANO1抑制劑，具有優異的藥代動力學特性。體內PK測試通過尊龍凱時進行
Current pain management is largely limited to opioids and non-steroidal anti-inflammatory drugs. Developing new analgesic drugs remains important to address the unmet medical needs of chronic pain pat
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Jul 06,2023
開發和驗證大鼠血漿中Nobiliside A定量的LC/MS/MS方法
Nobiliside A, a new triterpene glycoside, exhibits some biological activities including antifungal and cytotoxic effects. A LC/MS/MS method was developed and validated for determination of Nobiliside
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Jul 06,2023
PTX-HSN是一種高效納米系統，具有較高耐受劑量，可將PTX遞送至卵巢癌并增強主動腫瘤靶向性。此研究中所有體內實驗均通過尊龍凱時進行
Paclitaxel-loaded hyaluronan solid nanoemulsions (PTX-HSNs) were successfully fabricated for the delivery of PTX to improve ovarian cancer treatment via active tumor targeting. The in vivo #toxicity,
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Jul 06,2023
開發一種簡單準確的液相色譜串聯質譜法，用于大鼠血漿中牡荊素鼠李糖苷的測定和體內PK研究。此研究中動物研究通過尊龍凱時進行
A simple and accurate liquid chromatography coupled with tandem mass spectrometry method was developed for determination and in vivo pharmacokinetic studies of vitexin rhamnoside in rat plasma. Practi
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Jul 06,2023
AD80是一種多激酶抑制劑，在多種肝細胞癌臨床前動物模型中具有抗腫瘤活性，AD80在血漿中的含量通過尊龍凱時進行LC-MS/MS測定
Liver cancer is the fourth greatest cause of cancer related mortality. AD80 is a multi-kinase inhibitor with anti-tumoral activity across a variety of hepatocellular carcinoma (HCC) preclinical models
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Jul 06,2023
以PROTAC為代表的靶向蛋白質降解是藥物發現的新興策略，研究人員設計并合成了多種PROTAC，此研究中所有PK研究均通過尊龍凱時進行
Targeted protein degradation (TPD) exemplified by PROTACs is an emerging strategy for next generation drug discovery. Threonine tyrosine kinase (TTK) is a dual-specific protein kinase that catalyzes p
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Jul 06,2023
BRD4抑制劑可用于治療腎纖維化，ZLD2218可有效抑制BRD4活性，對ZLD2218的PK研究通過尊龍凱時進行
Uncovering new therapeutics for kidney fibrosis hold promise for chronic kidney disease (CKD). BRD4 inhibition ameliorated kidney injury and fibrosis. ZLD2218 exhibited the potent inhibitory activity
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