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HomeProduct name listEpinastine

Epinastine

  • CAS NO.:80012-43-7
  • Empirical Formula: C16H15N3
  • Molecular Weight: 249.31
  • MDL number: MFCD00865648
  • EINECS: 616-785-3
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-10-23 15:23:57
Epinastine Structural

What is Epinastine?

Absorption

The absolute bioavailability of epinastine is about 40%.

Description

Epinastine hydrochloride, an orally active antihistaminic agent, was marketed in Japan for the treatment of bronchial asthma, allergic rhinitis, urticaria, eczema, dermatitis, and psoriasis vulgaris.Epinastine is one of the most effective peripherally acting histamine H1-receptor antagonists without sedative effects.In addition, it exhibits potent anti-PAF and anti-LT activity which may also contribute significantly to its antiallergic activity. Chronic epinastine has been reported to effectively inhibit airway hyper-responsiveness in rats. Potent inhibitory effects of epinastine on bronchoconstriction induced by histamine and bradykinin, but not by other chemical mediators, has also been reported. Studies have indicated that there are no significant differences in pharmacological properties among D-, L-, and racemic epinastine.

Originator

Boehringer lngelheim (Germany)

The Uses of Epinastine

Epinastine is antihistamine and mast cell stabilize that is used in eye drops for the treatment of allergic conjunctivitis.

Indications

For the prevention of itching associated with allergic conjunctivitis.

Background

Epinastine is used for the prevention of itching associated with allergic conjunctivitis. It has a multi-action effect that inhibits the allergic response in 3 ways: 1. stabilizes mast cells by preventing mast cell degranulation to control the allergic response, 2. prevents histamine binding to both the H1- and H2-receptors to stop itching and provide lasting protection, and 3. prevents the release of proinflammatory chemical mediators from the blood vessel to halt progression of the allergic response.

What are the applications of Application

Epinastine is an antihistamine and mast cell stabilizer

Definition

ChEBI: A benzazepine that is 6,11-dihydro-5H-dibenzo[b,e]azepine in which the azepine ring is fused to the e side of 4,5-dihydro-1H-imidazol-2-amine.

brand name

Aleslon

Pharmacokinetics

Epinastine is an antihistamine and an inhibitor of histamine release from the mast cell for topical administration to the eyes. Epinastine is indicated for the prevention of itching associated with allergic conjunctivitis. Epinastine is a topically active, direct H1-receptor antagonist and an inhibitor of the release of histamine from the mast cell. Epinastine is selective for the histamine H1-receptor and has affinity for the histamine H2 receptor. Epinastine also possesses affinity for the a1-, a2-, and 5-HT2 -receptors. Epinastine does not penetrate the blood/brain barrier and, therefore, is not expected to induce side effects of the central nervous system.

Clinical Use

Epinastine is a potent, long-acting H1 antihistamine and an inhibitor of the release of histamine and other transmitters from mast cells. It has some affinity for H2 receptors as well. It is used as an eye drop for allergic conjunctivitis. It does not penetrate into the CNS and is classified as a nonsedating antihistamine.

Synthesis

Several patents on the synthesis of epinastin (VIII) have appeared in Europe and Japan. The synthesis described below is taken partly from the US patent and a Japanese patent. All the syntheses utilized 6-aminomethyl-6,11-dihydro-5H-dibenzo[b.e]azepine (80) as the key intermediate which was converted to the final guanidine epinastine by reacting with cyanogen bromide. The solution of 80 in ethanol was treated with a solution of cyanogen bromide in THF at room temperature and stirred overnight. The hydrobromide salt was collected in 79% yield after adding ether to the reaction mixture. The salt was free based with a solution of sodium hydroxide and then treated with an ethereal solution of HCl to obtain the epinastine hydrochloride salt VIII. For the preparation of the key intermediate, chloroimine 78, presumably obtained from ketone 77 via Beckmann rearrangement, was reacted with sodium cyanide in DMSO to give the nitrile 79 in 70% yield. Reduction of the imino nitrile was carried out in THF in the presence of an acid with LAH to give the key intermediate 80 in 67% yield.
An alternate approach to preparation of 80 is shown in Scheme 8 as well. Reaction of the commercially available chloride 81 with phthalimide in the presence of a base gave the phthalimide 82. Reduction of the imine with sodium borohydride gave 83, which was then reacted with hydrazine hydrate to free up the amine in 90% yield. The amine intermediate was isolated as the fumarate salt.

Synthesis_80012-43-7

Metabolism

Mainly excreted unchanged, less than 10% metabolized.

Properties of Epinastine

Melting point: 205-208°
Boiling point: 428.0±55.0 °C(Predicted)
Density  1.32±0.1 g/cm3(Predicted)
storage temp.  Keep in dark place,Inert atmosphere,Room temperature
solubility  DMSO : ≥ 50 mg/mL (200.55 mM);Water : < 0.1 mg/mL (insoluble)
pka 11.2(at 25℃)
form  Solid
color  White to off-white
CAS DataBase Reference 80012-43-7(CAS DataBase Reference)

Safety information for Epinastine

Signal word Danger
Pictogram(s)
ghs
Exclamation Mark
Irritant
GHS07
ghs
Health Hazard
GHS08
ghs
Environment
GHS09
GHS Hazard Statements H302:Acute toxicity,oral
H372:Specific target organ toxicity, repeated exposure
H411:Hazardous to the aquatic environment, long-term hazard
Precautionary Statement Codes P273:Avoid release to the environment.
P280:Wear protective gloves/protective clothing/eye protection/face protection.

Computed Descriptors for Epinastine

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