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| | Terbinafine Hydrochloride Chemical Properties |
| Melting point | 204-208°C | | storage temp. | 15-25°C | | solubility | methanol: soluble50mg/mL | | form | powder | | color | white | | Merck | 14,9156 | | BCS Class | 1 | | InChI | InChI=1S/C21H25N.ClH/c1-21(2,3)15-8-5-9-16-22(4)17-19-13-10-12-18-11-6-7-14-20(18)19;/h5-7,9-14H,16-17H2,1-4H3;1H/b9-5+; | | InChIKey | BWMISRWJRUSYEX-SZKNIZGXSA-N | | SMILES | C12C=CC=CC1=CC=CC=2CN(C)C/C=C/C#CC(C)(C)C.Cl | | CAS DataBase Reference | 78628-80-5(CAS DataBase Reference) |
| Hazard Codes | Xi,N | | Risk Statements | 36/37/38-50/53 | | Safety Statements | 26-36/37/39-61-60 | | RIDADR | UN 3077 9/PG 3 | | WGK Germany | 3 | | RTECS | QJ8600100 | | HS Code | 29214990 | | Toxicity | LD50 in mice, rats (mg/kg): 4000, 4000 orally; 393, 213 i.v. (Ganzinger) |
| | Terbinafine Hydrochloride Usage And Synthesis |
| Dermatologist Broad-spectrum Antifungal Drugs | Terbinafine hydrochloride is a kind of broad-spectrum dermatologist allyl amine antifungal drugs. It is developed by Swiss Novartis in the 1980 s, and appeared in the market of UK for the first time in 1991. Approved by FDA of the United States for OTC drugs in 1996, and appeared in the market of the United States in the same year. At present, the drug is been sold in more than 90 countries of the word. It can specificity trouble the late biological decomposition of fungus sterol, selectively inhibit the activity of fungal squalene ring oxidase, and inhibit the squalene epoxidation in the formation of ungal cell membrane, thus to kill or inhibit the active of the fungus. Suitable for treatment of candidiasis skin, such as tinea manuum, tinea, tinea, ringworm of the body, tinea versicolor, it is also the best medicine for the treatment of onychomycosis.
Terbinafine hydrochloride entered the the first batch of country announced OTC directory in 2000. This product belongs to antifungal drugs. It has strong effect on shallow fungal infection, and can cure most of the fungal skin diseases through external use. | | Pharmacokinetics | According to reports in the literatures, after 250 mg of Terbinafine hydrochloride been taken orally, it reaches peak plasma concentration of 0.97 m ug/ml within 2 hours. The absorption half-life is 0.8 hours, spread half-life is 4.6 hours, the degree of biological application is slightly affected by eating, but not used for dose adjustments. The combination rate of drugs and plasma protein is 99%, and can quickly disperse and concentrate in the lipophilic corneous layer through the dermis. Terbinafine hydrochloride can be spread in the skin, therefore, a very high concentration can be reached in the hair follicle, hair and skin layers of fat, and it can enter in the deck in the last few weeks of healing. The metabolites after the bioconversion have no antifungal activity, then discharged through urine. The half-life is 17 hours, no accumulation in the body, and its steady blood drug concentration is not affected by age. But the alleviation rate can reduce for people with liver and kidney disorders, thus triggers blood drug concentration decreasing. | | Indications | 1.Skin, hair and nail infection caused by Btrichophyta (white hair versicolor bacterium, Trichophyton mentagrophytes, Trichophyton verrucosum, trichophyton tonsurans and Trichophyton violaceum, etc.), microsporum canis, epidermophyton floccosum, ect.
2.Skin yeast infections caused by all kinds of tinea disease (ringworm of the body, tinea, tinea manus and tinea capitis, etc.) and candida (candida albicans, etc.).
3.Onychomycosis (nail fungus infection) caused by molds. | | Usage and Dosage | Local external use: apply adequate amount to the affected area and its surrounding, 1-2 times a day. Ringworm of the body, 2-4 weeks, tinea of feet and hands, tinea versicolor, 4 to 6 weeks.
Oral: 0.25 grams each time for adult, once per day, period of treatment is as follows:
Skin infection treatment: tinea of feet and hands [toe (means) and plantar]: 2~6 weeks; Ringworm of the body, tinea, 2~4 weeks.
Skin candidiasis: 2~4 weeks. normal skin appearance and loss of infection can only be visible in a few weeks for curing.
Hair and scalp infection treatment: tinea capitis: 4 weeks, tinea capitis most happen in children.
Onychomycosis: The most treatment course of patients is 6 weeks to three months. Young patients with normal growth can shorten the treatment course, and less than 3 months of treatment may be enough in addition to the thumb (foot) armour.
In other cases, the treatment is usually 3 months. Some patients, especially whose thumb (toe) infected, may take 6 months or longer. The treatment may take more than 3 months if the nail grew slowly in the first week. In healing of mycology and stopping for a few months after treatment, the continuous improvement of nail appearance then completely normal can be seen, this is because that the healthy tissue growth needs time. | | Chemical Properties | White crystalline powder. Melting point is 204-208 oC. | | Usage | Terbinafine hydrochloride is a kind of broad-spectrum dermatologist allyl amine antifungal drugs. It has a significant effect on all kinds of tinea diseases , including fungus, trichophyton, ringworm of the body, tinea, tinea versicolor and onychomycosis caused by dermophyte. It can also be used for bronchial asthma, asthmatic bronchitis and emphysema, etc.
This information is edited by ChemicalBook Xiao Nan. | | Description | Terbinafine hydrochloride is the first orally active allylamine antifungal with 30-fold
greater antifungal activity than naftifine. The compound is indicated for the treatment
of ringworm and fungal nail infections. Terbinatine hydrochloride acts on a single
fungal enzyme, squalene epoxidase, interfering with the biosynthesis of ergosterols in
cell membranes. Unlike other antifungal agents, it does not inhibit cytochrome P450
enzymes. | | Description | Terbinafine is a broad-spectrum antifungal agent that has activity against T. rubrum, T. metagrophytes, T. verrucosum, E. floccosum, M. canis, A. fumigatus, and S. schenckii (MIC50s = 0.003-0.8 μg/ml). It selectively inhibits C. albicans squalene epoxidase over rat liver epoxidase (IC50s = 0.03 and 77 μM, respectively). Terbinafine (90-120 μM) induces cell cycle arrest at the G0/G1 phase in COLO 205 tumor cells and human umbilical vein endothelial cells (HUVECs). Formulations containing terbinafine have been used in the treatment of nail and skin fungal infections. | | Chemical Properties | Crystalline Powder | | Originator | Sandoz (Switzerland) | | Uses | An orally active, antimycotic allylamine related to Naftifine. A specfic inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Antifungal. | | Uses | Terbinafine hydrochloride is a synthetic allylamine antifungal. It is used to treat dermatophyte infections of the toenail/fingernail, ringworm and jock itch. It is used in adsorption, partition and stability studies. | | Uses | Terbinafine hydrochloride may be used as a pharmaceutical reference standard for the determination of the analyte in drug dosage forms by UV spectrophotometry and high-performance thin layer chromatography (HPTLC). | | Indications | Terbinafine Hydrochloride is a synthetic allylamine antifungal
agent, structurally related to naftifine. It inhibits fungal sterol biosynthesis
by inhibiting the enzyme squalene 2,3-epoxidase. The deficiency of
ergosterol and concomitant accumulation of squalene within the fungal
cell results in cell death. It can be fungicidal or fungistatic, depending on
the concentration used, and is effective against dermatophytes, Aspergillus,
blastomycosis, and histoplasmosis. It is only minimally effective against
Candida. | | Definition | ChEBI: A hydrochloride obtained by reaction of terbinafine with one molar equivalent of hydrogen chloride. | | Manufacturing Process | To an ice-cooled solution of N-methyl-1-naphthalenemethylamine
hydrochloride (2.1 g) in methanol (40 ml) and water (10 ml) was added
sodium hydroxide powder (2 g) followed by dropwise addition of
epichlorohydrin (8 ml). The mixture was heated at 60°C for 3 h, then cooled
to room temperature. Volatile materials were removed in vacuo and the
residue was taken up in ethyl acetate and washed with water. The organic
phase was collected, dried over sodium sulfate, filtered and evaporated to
dryness. The crude mixture was purified by flash chromatrography on silica
gel (grade 9385, Merck, 230-400 mesh, 60 A) using a solvent gradient of a
mixture of hexane and ethyl acetate (95:5, 90:10 and 85:15) as eluent,
affording the N-methyl-N-naphthylmethyl-2,3-epoxypropane (1.85 g, 81.5%)
as an oil.
To a solution of 3,3-dimethylbutyne (2.95 ml) in dry THF (50 ml) at -78°C
was added a 2.5 M solution of n-BuLi in hexane (10 ml) dropwise. The
mixture was allowed to warm to room temperature over 15 min and stirred at
that temparature for a further 15 min, then was cooled back to -78°C and
BF3OEt2 (3 ml) was added dropwise. The mixture was stirred for 15 min and
1.8 g of N-methyl-N-naphthylmethyl-2,3-epoxypropane, dissolved in THF (10
ml), was added dropwise. After stirring at -78°C for 2 h, saturated sodium
bicarbonate solution (15 ml) was added, and the reaction mixture was allowed
to warm to room temperature. The mixture was extracted with ethyl acetate
(2 times 25 ml), and the combined organic fractions was dried over sodium
sulfate, filtered and concentrated in vacuo. The residue was purified by flash
chromatrography on silica gel (grade 9385, Merck, 230-400 mesh, 60 a) using
a mixture of hexane and ethyl acetate (85:15) as eluent, thereby affording
the N-methyl-N-(1-naphthylmethyl)-2-hydroxy-heptan-4-ynyl-1-amine as an
oil (1.95 g, 79%).
To an ice-cooled solution of N-methyl-N-(1-naphthylmethyl)-2-hydroxyheptan-
4-ynyl-1-amine (155 mg) in THF (10 ml) was added Et3N (0.35 ml)
followed by methanesulfonyl chloride (0.075 ml). The resulting mixture was
stirred at 0°C for 3 h, then filtered. The filtrate was concentrated in vacuo,
dissolved in toluene (10 ml) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)
(0.37 ml) was added. The resulting mixture was heated at 80°C for 4 h,
cooled to room temperature then poured onto a silica gel column and eluted
with hexane (100%) followed by a mixture of hexane and ethyl acetate
(95:5). Thus, a mixture of E- and Z-isomers of N-methyl-N-(1-
naphthylmethyl)-6,6-dimethylhept-2-en-4-ynyl)-1-amine were obtained in a
ratio of 2:5 (95 mg, 66%). | | Brand name | Lamisil | | Therapeutic Function | Antifungal | | General Description | Allylamine derivative. | | Biochem/physiol Actions | Mode of Action: Inhibits squalene epoxidase, preventing biosynthesis of ergosterol.Antimicrobial spectrum: Antifungal and antimycotic. Fungicidal against dermatopytes and some yeasts; fungistatic against Candida albicans. | | Clinical Use | Terbinafine hydrochloride (Lamisil) is available for
topical and systemic use (oral tablet) in the treatment of
dermatophyte skin and nail infections. Terbinafine also
exhibits in vitro activity against filamentous and dimorphic
fungi, but its clinical utility in treating infections
with these organisms has not yet been established. It is
used most commonly in the treatment of onychomycosis;
in this setting, terbinafine is superior to griseofulvin
and at least equivalent to itraconazole.When given systemically,
terbinafine is 99% protein bound and accumulates
in fat, skin, and nails, persisting for weeks.
Cerebrospinal fluid penetration is less than 10%.
Dosage reductions are required with renal or hepatic
insufficiency. Although terbinafine has little effect on
hepatic cytochrome P450 enzyme systems, it does minimally
enhance cyclosporine clearance. Oral terbinafine
is generally well tolerated but occasionally causes gastric
distress and liver enzyme elevation. | | Clinical Use | (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methyl-1-naphthalene-methanamine hydrochloride (Lamisil) is an off-whitecrystalline material that is soluble in polar organic solventssuch as methanol, ethanol, and methylene chloride but isonly slightly soluble in water. The highly lipophilic freebase is insoluble in water. Terbinafine hydrochloride isavailable in a 1% cream for topical administration for thetreatment of tinea pedis, tinea corporis, and tinea cruris.Terbinafine is more potent than naftifine and has alsodemonstrated oral activity against onychomycosis (ringwormof the nails). It has not been approved in the UnitedStates for oral administration. | | Side effects | Adverse reactions include lens and retinal disturbances (red/green visual
perception), metallic taste disturbance that may last up to 4 weeks after
medication discontinuation, hepatoxicity, and pancytopenia. Five percent of
patients will experience delayed gastric emptying with symptoms of nausea,
fullness, and/or dyspepsia. Terbinafine does not appear to have any effect on
the cytochrome P-450 systems (Check baseline CBC and LFTs; repeat if taken
for >6 weeks). | | Veterinary Drugs and Treatments | Terbinafine may be useful for treating dermatophytic and other
fungal infections in dogs and cats.
Terbinafine may also be useful for treating birds for systemic
mycotic (e.g., aspergillosis) infections. | | storage | Store at +4°C |
| | Terbinafine Hydrochloride Preparation Products And Raw materials |
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