Methylprednisolone

製品コードS1733 バッチS173302

印刷

化学情報

Synonyms

NSC-19987, U 7532

Storage
(From the date of receipt)

3 years -20°C powder
1 years -80°C in solvent

化学式

C₂₂H₃₀O₅

分子量

374.47

CAS No.

83-43-2

Solubility (25°C)*

体外

DMSO

75 mg/mL (200.28 mM)

Ethanol

6 mg/mL (16.02 mM)

Water

Insoluble

体内（毎回新しく調製した物を用意してください）

Homogeneous suspension

CMC-NA

≥5mg/ml

Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.

* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液（一定の濃度）を調合する

生物活性

製品説明	Methylprednisolone (NSC-19987,U 7532) is a synthetic glucocorticoid receptor agonist, used to achieve prompt suppression of inflammation. Methylprednisolone activates ACE2 and reduces IL-6 levels, thus improves severe or critical COVID-19. Methylprednisolone markedly reduces autophagy and apoptosis.
in vitro	Methylprednisolone (2-10 mg/kg) markedly inhibits TNF production but does not affect serum levels of IL-10, while a high dose of this compound (50 mg/kg) increases LPS-induced IL-10 levels. This chemical (from 0.01 to 100 mg/mL) also increases the biosynthesis of IL-10 by LPS-activated mouse peritoneal macrophages. ^[1]
in vivo	Methylprednisolone decreases RGC survival in rats with electrophysiologically diagnosed optic neuritis. This compound decreases RGC survival by a nongenomic, calcium-dependent mechanism. Its induced enhancement of RGC degeneration depends on calcium influx through voltage-gated calcium channels. ^[2] This treatment leads to a significant decrease in the number of ED1-positive cells in both rostral and caudal stumps. It results in a significant reduction in tissue loss in both cord stumps at 2, 4 and 8 week post-injury. This chemical leads to a long-term reduction of ED1-positive cells and spinal tissue loss, reduced dieback of vestibulospinal fibres, and a transient sprouting of vestibulospinal fibres near the lesion at 1 and 2 weeks post-lesion. ^[3] At a dose of 30 mg/kg which has been shown to be effective in improving functional outcomes in rat SCI models, it suppresses TNF-α expression and NF-kB activation. Its inhibition of NF-kB function is likely mediated by the induction of IkB, which traps NF-kB in inactive cytoplasmic complexes. ^[4]

プロトコル(参考用のみ)

参考

https://pubmed.ncbi.nlm.nih.gov/8870704/
https://pubmed.ncbi.nlm.nih.gov/12904460/
https://pubmed.ncbi.nlm.nih.gov/10383635/

https://pubmed.ncbi.nlm.nih.gov/9729336/

+ 展开

カスタマーフィードバック

: Data from [Data independently produced by , , Trop J Pharm Res, 2014, 13 (1): 53-59.]

Selleckの高級品が、幾つかの出版された研究調査結果（以下を含む）で使われた：

Amanitin-induced variable cytotoxicity in various cell lines is mediated by the different expression levels of OATP1B3 [ Food Chem Toxicol, 2024, 188:114665]	PubMed: 38641045
High-throughput liquid chromatography tandem mass spectrometry assay as initial testing procedure for analysis of total urinary fraction [ Drug Test Anal, 2020, 10.1002/dta.2917]	PubMed: 32852861
Glucocorticoid hormone-induced chromatin remodeling enhances human hematopoietic stem cell homing and engraftment. [ Nat Med, 2017, 23(4):424-428]	PubMed: 28263313
Salvianolic Acid B Ameliorates Motor Dysfuntion in Spinal Cord Injury Rats. [C Xun, et al. Trop J Pharm Res, 2014, 13 (1): 53-59]

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

各々の製品のための特定の保管と取扱い情報は、製品データシートの上で示されます。大部分のSelleck製品は、推薦された状況の下で安定です。製品は、推薦された保管温度と異なる温度で、時々出荷されます。長期の保管のために必要とされてそれと異なる温度で、多くの製品は、短期もので安定です。品質を維持するが、夜通しの積荷のために最も経済的な貯蔵状況を用いてあなたの送料を保存する状況の下に、製品が出荷されることを、我々は確実とします。製品の受領と同時に、製品データシートの上で貯蔵推薦に従ってください。