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本文引用的文献

1
Endogenous carbon monoxide production in disease.疾病中的内源性一氧化碳生成。
Clin Biochem. 2010 Oct;43(15):1183-8. doi: 10.1016/j.clinbiochem.2010.07.011. Epub 2010 Jul 23.
2
Hydrogen sulfide is an endogenous inhibitor of phosphodiesterase activity.硫化氢是一种内源性磷酸二酯酶活性抑制剂。
Arterioscler Thromb Vasc Biol. 2010 Oct;30(10):1998-2004. doi: 10.1161/ATVBAHA.110.209783. Epub 2010 Jul 15.
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A monobromobimane-based assay to measure the pharmacokinetic profile of reactive sulphide species in blood.一种基于单溴代丁二酰亚胺的分析方法,用于测量血液中反应性硫物种的药代动力学特征。
Br J Pharmacol. 2010 Jun;160(4):941-57. doi: 10.1111/j.1476-5381.2010.00704.x.
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Detection of exhaled hydrogen sulphide gas in healthy human volunteers during intravenous administration of sodium sulphide.静脉注射硫化钠时健康志愿者呼出气中硫化氢的检测。
Br J Clin Pharmacol. 2010 Jun;69(6):626-36. doi: 10.1111/j.1365-2125.2010.03636.x.
5
Structure of cinaciguat (BAY 58-2667) bound to Nostoc H-NOX domain reveals insights into heme-mimetic activation of the soluble guanylyl cyclase.结合态 cinaciguat(BAY 58-2667)与 Nostoc H-NOX 结构域的结构揭示了血红素模拟物对可溶性鸟苷酸环化酶的激活作用。
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Synthesis and biological effects of hydrogen sulfide (H2S): development of H2S-releasing drugs as pharmaceuticals.硫化氢(H₂S)的合成与生物学效应:作为药物的硫化氢释放药物的研发
J Med Chem. 2010 Sep 9;53(17):6275-86. doi: 10.1021/jm901638j.
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Phosphodiesterase type 5 (PDE5) inhibitors for the treatment of erectile dysfunction.磷酸二酯酶 5(PDE5)抑制剂治疗勃起功能障碍。
Expert Opin Pharmacother. 2010 May;11(7):1109-22. doi: 10.1517/14656561003698131.
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Hydrogen sulfide is an endogenous stimulator of angiogenesis.硫化氢是血管生成的内源性刺激剂。
Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21972-7. doi: 10.1073/pnas.0908047106. Epub 2009 Dec 2.
9
Exhaled nitric oxide in diagnosis and management of respiratory diseases.呼出气一氧化氮在呼吸疾病诊断和管理中的应用。
Ann Thorac Med. 2009 Oct;4(4):173-81. doi: 10.4103/1817-1737.56009.
10
Hydrogen sulfide: from brain to gut.硫化氢:从脑到肠。
Antioxid Redox Signal. 2010 May 1;12(9):1111-23. doi: 10.1089/ars.2009.2919.

气体递质:转化科学的新前沿。

Gaseotransmitters: new frontiers for translational science.

机构信息

Department of Anesthesiology, The University of Texas Medical Branch, Galveston, TX 77555-1102, USA.

出版信息

Sci Transl Med. 2010 Nov 24;2(59):59ps54. doi: 10.1126/scitranslmed.3000721.

DOI:10.1126/scitranslmed.3000721
PMID:21106939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3038605/
Abstract

Translational research on endogenous gaseous mediators--nitric oxide, carbon monoxide, and hydrogen sulfide--has exploded over the past decade. Drugs that modulate either the gaseous mediators themselves or their related intracellular signaling pathways are already in use in the clinics, and still more are being tested in preclinical models and clinical trials. Discussed here are the chemical and pharmacological properties that present challenges for the translation of these potentially toxic molecules.

摘要

在过去的十年中,内源性气态介质(一氧化氮、一氧化碳和硫化氢)的转化研究呈爆炸式增长。调节气态介质本身或其相关细胞内信号通路的药物已经在临床上使用,还有更多的药物正在临床前模型和临床试验中进行测试。本文讨论了这些潜在有毒分子转化所面临的化学和药理学性质的挑战。