Methylprednisolone succinate
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Methylprednisolone succinate
structure -
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CAS No:
2921-57-5
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Formula:
C26H34O8
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Chemical Name:
Methylprednisolone succinate
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Synonyms:
Pregna-1,4-diene-3,20-dione,21-(3-carboxy-1-oxopropoxy)-11,17-dihydroxy-6-methyl-,(6α,11β)-;Pregna-1,4-diene-3,20-dione,11β,17,21-trihydroxy-6α-methyl-,21-(hydrogen succinate);Pregna-1,4-diene-3,20-dione,11β,17,21-trihydroxy-6α-methyl-,21-(H succinate);Pregna-1,4-diene-3,20-dione,11β,17,21-trihydroxy-6α-methyl-,21-succinate;(6α,11β)-21-(3-Carboxy-1-oxopropoxy)-11,17-dihydroxy-6-methylpregna-1,4-diene-3,20-dione;6α-Methylprednisolone hemisuccinate;6-Methylprednisolone hemisuccinate;6α-Methylprednisolone 21-succinate;Methylprednisolone succinate;Methylprednisolone 21-hemisuccinate;Methylprednisolone hemisuccinate;1145720-95-1
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CAS No:
Description
Methylprednisolone succinate is a synthetic glucocorticoid and widely used as an anti-inflammatory agent.
Methylprednisolone succinate is a corticosteroid hormone and a hemisuccinate.|A water-soluble ester of methylprednisolone used for cardiac, allergic, and hypoxic emergencies.|A water-soluble ester of METHYLPREDNISOLONE used for cardiac, allergic, and hypoxic emergencies.
Methylprednisolone succinate Basic Attributes
474.54
474.54
220-863-9
5GMR90S4KN
DTXSID80183466
2942000000
Characteristics
138.20000
2.69
1.3±0.1 g/cm3
689.6±55.0 °C at 760 mmHg
230.7±25.0 °C
1.593
5.28E-22mmHg at 25°C
Safety Information
NONH for all modes of transport
P201, P202, P260, P264, P270, P280, P281, P301+P312, P302+P352, P308+P313, P312, P314, P322, P330, P363, P405, P501
H302
|Danger|H302 (30.19%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P260, P264, P270, P280, P281, P301+P312, P302+P352, P308+P313, P312, P314, P322, P330, P363, P405, and P501|Aggregated GHS information provided by 53 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Methylprednisolone sodium succinate (the sodium salt of methylprednisolone hemisuccinate) has the same metabolic and anti-inflammatory actions as methylprednisolone. When given parenterally and in equimolar quantities, the two compounds are equivalent in biologic activity.
A group of CORTICOSTEROIDS that affect carbohydrate metabolism (GLUCONEOGENESIS, liver glycogen deposition, elevation of BLOOD SUGAR), inhibit ADRENOCORTICOTROPIC HORMONE secretion, and possess pronounced anti-inflammatory activity. They also play a role in fat and protein metabolism, maintenance of arterial blood pressure, alteration of the connective tissue response to injury, reduction in the number of circulating lymphocytes, and functioning of the central nervous system. (See all compounds classified as Glucocorticoids.)|Antineoplastic agents that are used to treat hormone-sensitive tumors. Hormone-sensitive tumors may be hormone-dependent, hormone-responsive, or both. A hormone-dependent tumor regresses on removal of the hormonal stimulus, by surgery or pharmacological block. Hormone-responsive tumors may regress when pharmacologic amounts of hormones are administered regardless of whether previous signs of hormone sensitivity were observed. The major hormone-responsive cancers include carcinomas of the breast, prostate, and endometrium; lymphomas; and certain leukemias. (From AMA Drug Evaluations Annual 1994, p2079) (See all compounds classified as Antineoplastic Agents, Hormonal.)|Substances that reduce or suppress INFLAMMATION. (See all compounds classified as Anti-Inflammatory Agents.)|Drugs intended to prevent damage to the brain or spinal cord from ischemia, stroke, convulsions, or trauma. Some must be administered before the event, but others may be effective for some time after. They act by a variety of mechanisms, but often directly or indirectly minimize the damage produced by endogenous excitatory amino acids. (See all compounds classified as Neuroprotective Agents.)
6 alpha-Methylprednisolone Sodium Hemisuccinate
Computed Properties
Molecular Weight:474.5
XLogP3:2.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:7
Exact Mass:474.22536804
Monoisotopic Mass:474.22536804
Topological Polar Surface Area:138
Heavy Atom Count:34
Complexity:981
Defined Atom Stereocenter Count:8
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Extracting pharmacological effects from the above information
Registered Holders
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CURIA SPAIN SAU
Active
United States
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EUROAPI FRANCE
Active
France
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Pfizer Investment Co., Ltd.
Active
China
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