Medrysone
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Medrysone
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CAS No:
2668-66-8
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Formula:
C22H32O3
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Chemical Name:
Medrysone
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Synonyms:
Pregn-4-ene-3,20-dione,11-hydroxy-6-methyl-,(6α,11β)-;Pregn-4-ene-3,20-dione,11β-hydroxy-6α-methyl-;(6α,11β)-11-Hydroxy-6-methylpregn-4-ene-3,20-dione;U 8471;HMS;11β-Hydroxy-6α-methylpregn-4-ene-3,20-dione;6α-Methyl-Δ4-pregnene-11β-hydroxy-3,20-dione;Medrysone;11β-Hydroxy-6α-methylprogesterone;Hydroxymesterone;Medrifar;Visudrisone;Medrocort;Ophtocortin;Spectamedryn;NSC 63278;11β-Hydroxylmedroxyprogesterone
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CAS No:
Description
Medrysone is a corticosteroid, in ophthalmology for the treatment of eye inflammations.
Solid
Medrysone is a corticosteroid hormone.|Medrysone is a corticosteroid used in ophthalmology.|Medrysone is a Corticosteroid. The mechanism of action of medrysone is as a Corticosteroid Hormone Receptor Agonist.|Medrysone is a topical, synthetic glucocorticoid with metabolic, anti-inflammatory and anti-allergic properties. Medrysone exerts its effect by interacting with specific intracellular glucocorticoid receptors and subsequently binds to DNA to modify gene expression. This results in an induction of the synthesis of certain anti-inflammatory proteins while inhibiting the synthesis of certain inflammatory mediators. Consequently, an overall reduction in chronic inflammation and autoimmune reactions is accomplished.
Medrysone Basic Attributes
344.48800
344.49
220-208-7
D2UFC189XF
63278
DTXSID6045371
C47598
S - Sensory organs
Characteristics
54.37000
3.94030
Solid
1.13g/cm3
156.5 °C
492.3ºC at 760mmHg
265.7ºC
1.552
3.37e-02 g/L
183.2 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]
Drug Information
For the treatment of allergic conjunctivitis, vernal conjunctivitis, episcleritis, and epinephrine sensitivity.|FDA Label
Medrysone is a topical anti-inflammatory corticoidsteroids for ophthalmic use. In patients with increased intraocular pressure and in those susceptible to a rise in intraocular pressure, there is less effect on pressure with medrysone than with dexamethasone or betamethasone. Corticoidsteroids inhibit the edema, fibrin deposition, capillary dilation, and phagocytic migration of the acute inflammatory response, as well as capillary proliferation, deposition of collagen, and scar formation.
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.)
Rapidly absorbed following oral administration.
There is no generally accepted explanation for the mechanism of action of ocular corticosteroids. However, corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor, arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2. Initially, the drug binds to the glucocorticoid receptor in the cytosol. This migrates to the nucleus and binds to genetic elements which cause activation and repression of the involved genes in the inflammatory pathway.
11-hydroxy-6-methylprogesterone
Medrysone Use and Manufacturing
glucocorticoid
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients|Pharmaceuticals
Computed Properties
Molecular Weight:344.5
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:344.23514488
Monoisotopic Mass:344.23514488
Topological Polar Surface Area:54.4
Heavy Atom Count:25
Complexity:650
Defined Atom Stereocenter Count:8
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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