CAS: 6000-74-4; Hydrocortisone Sodium Phosphate

该化合物是一种主要用于抗炎和免疫抑制特性的合成花生类固醇,是一种水质固醇盐,可增加其在水中的溶解性,适合隔热调节.这种化合物看起来像白色的白色和非白色晶状粉,具有血压,意味着它可以吸收空气的湿度.磷酸钠经常用于各种条件的治疗,包括过敏,皮肤紊乱和肾上腺不充足.其行动机制涉及基因表达的调制,导致减少炎症和免疫反应.该物质通常通过注射或作为时尚配方的一部分来施用.稳定性是一个关键特征,因为它在某些条件下会降解,需要适当的储存和处理.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

合成工艺路线路线简述

    海关参考信息

    专利信息


    专利号:US-9051302-B2
    优先权日:2008-01-15
    标 题 :Synthesis of resorcylic acid lactones useful as therapeutic agents
    发明人:WINSSINGER NICOLAS; BARLUENGA SOFIA; KARPLUS MARTIN
    权利人:WINSSINGER NICOLAS; BARLUENGA SOFIA; KARPLUS MARTIN; UNIV STRASBOURG
    摘要:Disclosed are macrocyclic compounds of formulae I, I′, II, II′, III, III′, IV, and V, which are analogs of the pochonin resorcylic acid lactones, pharmaceutical compositions comprising the compounds, and methods and uses comprising the compounds for the treatment of diseases mediated by kinases and Heat Shock Protein 90 HSP90.

    专利号:WO-9925385-A1
    优先权日:1997-11-17
    标 题:A method of increasing nucleic acid synthesis with ultrasound
    发明人:UNGER EVAN C; MCCREERY THOMAS; SADEWASSER DAVID
    权利人:IMARX PHARMACEUTICAL CORP
    摘要:The present invention is directed to a method of increasing nucleic acid synthesis in a cell comprising administering to the cell a therapeutically effective amount of ultrasound for a therapeutically effective time such that said administration of said ultrasound results in said increased nucleic acid synthesis. The nucleic acid sequence may comprise an endogenous sequence or an exogenous sequence.

    专利号:US-2021244638-A1
    优先权日:2018-06-05
    标 题:Inhibitors of glycosphingolipid synthesis and methods of use
    发明人:CHATTERJEE SUBROTO B
    权利人:SUBROTO B CHATTERJEE
    摘要:Compositions in the prevention and treatment of skin diseases or associated disorders, inflammation or inflammatory diseases or disorders, include at least one inhibitor of glycosphingolipid synthesis.

    专利号:US-9868767-B2
    优先权日:2013-05-23
    标 题:Chemical synthesis and screening of bicyclic peptide libraries
    发明人:PEI DEHUA; UPADHYAYA PUNIT; LIAN WENLONG; TRINH THI
    权利人:OHIO STATE INNOVATION FOUNDATION
    摘要:Disclosed herein are bicyclic peptide compounds, compositions comprising same, methods for making same, and libraries comprising same. The disclosed compounds, in various aspects, are useful for treating a variety of disorders, including inflammatory disorders, autoimmune disorders, and disorders of uncontrolled cellular proliferation. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    专利号:US-9868747-B2
    优先权日:2014-02-18
    标题:Marinopyrrole derivatives and methods of making and using same
    发明人:LI RONGSHI; SEBTI SAID; LIU YAN; QIN YONG; SONG HAO; CHENG CHUNWEI
    权利人:H LEE MOFFITT CANCER CT & RES; CHONGQING ZEIN PHARMACEUTICAL CO LTD
    摘要:Marinopyrrole derivatives and methods for their synthesis and use are described herein. Novel cyclic and symmetric marinopyrroles with triazole substituents having antibacterial activity against resistant bacterial strains, such as MRSA are introduced. Also provided are methods of using the compounds for treating or preventing cancer and/or microbial infections.

    专利号:WO-2024233563-A1
    优先权日:2023-05-09
    标 题:6,6-fused bicyclic amides and compositions for use as 15-prostaglandin dehydrogenase modulators
    发明人:GREENMAN KEVIN LLOYD; WANG HUI-LING; WEIRES NICHOLAS ANTHONY; ALLEN JOHN G; AMEGADZIE ALBERT K; BOURBEAU MATTHEW P; LI KEXUE
    权利人:AMGEN INC
    摘要:The present disclosure provides novel 15-hydroxy-prostaglandin dehydrogenase inhibitors, pharmaceutical compositions comprising such compounds, and methods of using such compounds and compositions in treating 15-hydroxy-prostaglandin dehydrogenase-mediated disease. Also provided are methods of making such compounds and intermediates thereof. The compounds have a structure of Formula (I): or a pharmaceutically acceptable salt thereof; wherein is Formula (i) or Formula (ii) Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula (I).
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    主要参考文献


    1: Jung C, Greco S, Nguyen HH, Ho JT, Lewis JG, Torpy DJ, Inder WJ. Plasma, salivary and urinary cortisol levels following physiological and stress doses of hydrocortisone in normal volunteers. BMC Endocr Disord. 2014 Nov 26;14:91. doi: 10.1186/1472-6823-14-91.
    2: Whitaker MJ, Spielmann S, Digweed D, Huatan H, Eckland D, Johnson TN, Tucker G, Krude H, Blankenstein O, Ross RJ. Development and testing in healthy adults of oral hydrocortisone granules with taste masking for the treatment of neonates and infants with adrenal insufficiency. J Clin Endocrinol Metab. 2015 Apr;100(4):1681-8. doi: 10.1210/jc.2014-4060. Epub 2015 Feb 3. doi: 10.1159/000439329. Epub 2015 Dec 10. Review. doi: 10.1002/jcph.424. Epub 2014 Dec 30. Review.

    合成参考文献


    摘要:MADURO R, CHEVANCE LG. [Biological & clinical study of a soluble cortisone derivative; delta-hydrocortisone phosphate in the treatment of respiratory tract allergy]. Ann Otolaryngol. 1958 Oct;75(10-11):802–8.
    参考文献:10.1006/exer.1993.1177
    摘要:Proia AD, Hirakata A, McInnes JS, Scroggs MW, Parikh I. The effect of angiostatic steroids and beta-cyclodextrin tetradecasulfate on corneal neovascularization in the rat. Exp Eye Res. 1993 Dec;57(6):693–8. doi: 10.1006/exer.1993.1177.
    参考文献:10.1006/exer.1994.1037
    摘要:Wong J, Wang N, Miller JW, Schuman JS. Modulation of human fibroblast activity by selected angiogenesis inhibitors. Exp Eye Res. 1994 Apr;58(4):439–51. doi: 10.1006/exer.1994.1037.
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