具有两个靶点的半质子 ph-ph+ 抑制转移性乳腺癌和并发念珠菌病》[Biochem. Pharmacol. 226 (2024) 116394]的撤稿通知。

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Jingli Li, Zizhen Zhao, Dongmei You, Yafang Xie, Yixiao Feng, Xiaorong Li, Zhihong Cui, Ailing Fu
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引用次数: 0

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Retraction notice to “Hemiprotonic ph-ph+ with two targets inhibits metastatic breast cancer and concurrent candidiasis” [Biochem. Pharmacol. 226 (2024) 116394]
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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