Home Categories 6α-Methylprednisolone 21-hemisuccinate sodium salt
A5749012

6α-Methylprednisolone 21-hemisuccinate sodium salt , 98% , 2375-03-3

Synonym(s):
6α-Methyl-11β,17α,21-trihydroxy-1,4-pregnadiene-3,20-dione 21-hemisuccinate;6α-Methylprednisolone sodium succinate;MPSL

CAS NO.:2375-03-3

Empirical Formula: C26H33O8.Na

Molecular Weight: 496.53

MDL number: MFCD00152612

EINECS: 219-156-8

Pack Size Price Stock Quantity
25MG RMB479.20 In Stock
100mg RMB1599.20 In Stock
1G RMB7999.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: >186°C (dec.)
storage temp.  Inert atmosphere,Room Temperature
solubility  DMSO (Slightly), Methanol (Slightly)
form  lyophilized powder
color  White to Off-White
InChIKey FQISKWAFAHGMGT-JXAFMBTDNA-M
SMILES [C@]12(C[C@@H](C3=CC(=O)C=C[C@]3(C)[C@@]1([H])[C@H](C[C@]1(C)[C@@](CC[C@@]21[H])(O)C(=O)COC(=O)CCC([O-])=O)O)C)[H].[Na+] |&1:0,2,9,11,13,15,17,20,r|
CAS DataBase Reference 2375-03-3(CAS DataBase Reference)

Description and Uses

Methylprednisolone Sodium Succinate is the sodium succinate salt of a synthetic glucocorticoid receptor agonist with immunosuppressive and anti-inflammatory effects. It is converted into active prednisolone in the body, which activates glucocorticoid receptor-mediated gene expression. This includes inducing the synthesis of the anti-inflammatory protein IkappaB-alpha and inhibiting the synthesis of nuclear factor kappa B (NF-kappaB). As a result, proinflammatory cytokine production, such as IL-1, IL-2, and IL-6, is down-regulated, and cytotoxic T-lymphocyte activation is inhibited. Therefore, an overall reduction in chronic inflammation and autoimmune reactions may be achieved.

6α-Methylprednisolone 21-Hemisuccinate is a glucocorticosteroid used in anti-inflammatory medication in the treatment of spinal cord injuries.

Safety

Symbol(GHS) 
GHS08
Signal word  Danger
Hazard statements  H351-H360
Precautionary statements  P201-P308+P313
Hazard Codes  T
Risk Statements  61-40
Safety Statements  53-22-36/37/39-45
WGK Germany  3
RTECS  TU4154060
Toxicity LD50 oral in rat: > 5gm/kg

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