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 |
|
others | Enquire |
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 |