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- 2026年01月29日
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Biochem/physiol Actions
D1, D2 dopamine receptor antagonist; butyrophenone antipsychotic and anti-emetic.
Droperidol is a potent antagonist of dopamine subtype 2 receptor.[1] It is an antipsychotic, which is used to treat acute behavioral anomalies.[2] It helps to manage postoperative nausea and vomiting.[3]
Features and Benefits
This compound was developed by Johnson & Johnson. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
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文献和实验Identification of G-Protein-Coupled Receptor Phosphorylation Sites by 2D Phosphopeptide Mapping
Reversible phosphorylation is important for G-protein-coupled receptor (GPCR) signaling, desensitization, and endocytosis, yet the precise location and role of in vivo phosphorylation sites is unknown for most receptors. This chapter describes
Verification of the existence of quadruplex structure in native human telomeres and determination of the major structure of d(T2 AG3 )4 (H24) in K+ solution are the major questions regarding the structure of human telomeres
，3次/日，肌内注射，5mg/次。 氟哌利多（droperidol）治疗精神分裂症：10～30mg/日，分1～2次，肌内注射。神经安定镇痛：每次5mg，加入芬太尼0.1mg，在2～3分钟内缓慢静脉注入，5～6分钟内如未达一级浅麻状态，可追加半量至一倍量。麻醉前给药：手术前半小时肌内注射2.5～5mg。 盐酸米帕明（imipramine hydrochloride）25～75mg/次，3次/日。年老体弱者每日自12.5mg开始，逐渐增量。 阿米替林（amitriptyline
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