CN1411808A - N-acetyl-5,6-dimethoxytryptamine for preparing medicine resisting oxidation free radical - Google Patents

Abstract

The present invention relates to a melatonin derivative N-acetyl-5.6-dimethoxytryptamine for preparing anti-oxyradical medicine. Its synthesis is divided into four steps, and uses 5,6-dimethoxyindole as initiation raw material. Said compound can be used for preparing medical antioxidant, and has no obvious toxic side effect.

Description

Application of N-acetyl-5, 6-dimethoxytryptamine in preparing anti-oxidation free radical medicine

The invention relates to a production method of melatonin derivatives, in particular to application of N-acetyl-5, 6-dimethoxytryptamine inpreparing antioxidant free radical medicaments.

Melatonin (melatonin), N-acetyl-5, 6-dimethoxyA tryptamine of formula

Melatonin is produced in mammals and humans primarily by the pineal gland located in the mid-brain region. Its synthesis and secretion exhibit a pronounced circadian rhythm and vary with age. The older the age, the less the production. This rhythmicity is influenced by mechanisms and environments inherent in the body. The most obvious environmental factor is light. Upon exposure to light, melatonin synthesis and secretion is inhibited immediately. Melatonin is a highly conserved molecule during evolution, a compound molecule that exists in the lowest algae of unicellular organisms to humans. Melatonin has many important physiological functions: for example, the melatonin is found to be the strongest endogenous free radical scavenger at present in recent years, can prolong the life of experimental animals by 30 percent, protect the central nervous system against the damage of various toxic substances, and also has the auxiliary treatment effect on AIDS. The main functional group with the antioxidation function is a methoxy substituent on the 5 th carbon atom on the indole ring of the molecular structure. Melatonin is metabolized in vivo mainly by the liver, and the 6 th carbon atom on the indole ring in its molecular structure is hydroxylated by hydroxylase to produce 6-hydroxy melatonin which is excreted out of the body, so that its half-life is short (about 40 minutes), and multiple administrations are required to maintain the desired therapeutic concentration. The antioxidant action of melatonin is a direct scavenging of free radicals, which become side effects through receptor-mediated effects, such as lethargy and the like. Therefore, melatonin has the disadvantages of short half-life and certain side effects.

The invention aims to overcome the defects of short half-life period and certain toxic and side effects of melatonin, and provides a chemical substance with stronger free radical scavenging action, longer half-life period and lower toxic and side effects, a preparation and a production process thereof, and application of the chemical substance in a medical antioxidant.

The present invention is thus achieved.

The invention relates to a compound (I),

the name is: n-acetyl-5, 6-dimethoxy tryptamine, namely 3-acetamido ethyl-5, 6-dimethoxy indole. Compared with melatonin, a methoxyl group is introduced to the 6 th position of the indole ring to replace the original hydrogen atom. The molecular weight of the compound (I) is 262, the compound is light yellow crystal, the compound is slightly soluble in water, the compound is easily soluble in organic solvents such as methanol, ethanol, acetonitrile and the like, and the solubility of the compound in water can be increased by more than 1000 times after the compound is dissolved in the organic solvents.

The compound (I) of the invention is synthesized by four steps by taking 5, 6-dimethoxy indole as a synthesis starting material. If the methoxy group is introduced directly on the basis of the molecular structure of melatonin and is oriented at the 6 th position of an indole ring, the group is easier to substitute at other positions due to space effect and electronic effect, and the target compound cannot be obtained or the productivity is extremely low.

The four steps are as follows:

the first step is as follows: synthesis of 3-diethylaminomethyl-5, 6-dimethylindole

Dissolving 5-6-dimethoxy indole in alcohol, preparing acetic acid at low temperature, mixing with diethylamine solution, slightly acidic, adding formaldehyde solution, stirring, pouring into 5, 6-dimethoxy indole alcohol solution, stirring, adding strong alkali water solution, extracting with organic solvent, eluting, and drying to obtain oily substance.

The second step is that: synthesis of 3-acetonitrile, 5, 6-dimethoxyindole

Dissolving the composition in the first step in a mixture of methanol, dimethylformamide, water, and cyanide (such as sodium cyanide or potassium cyanide), slowly adding dropwise iodomethane, standing, and stirring. And (4) extracting with an organic solvent. Drying and recrystallizing to obtain a crystal.

The third step: synthesis of 5, 6-dimethoxytryptamine

Synthesizing by adopting liquid ammonia and a nickel-hydrogen catalyst under 130 atmospheric pressure at 120-130 ℃; or adding sodium into ethanol or methanol solution of 3-acetonitrile, 5, 6-dimethoxy indole by sodium + alcohol method, and synthesizing; or preparing 5, 6-dimethoxy tryptamine by a lithium aluminum hydride reduction method, extracting the product with an organic solvent, crystallizing and drying to obtain a crystal.

The fourth step: synthesis of N-acetyl-5, 6-dimethyloxytryptamine (Compound I)

The acetylation of amines is carried out by acylation with acid anhydrides or acid halides (such as acid chlorides). Dissolving the resultant with organic solvent, washing with aqueous solution, vacuum-pumping to volatilize organic solvent, and purifying with benzene to obtainfinal product.

The final product is subjected to mass spectrometry and nuclear magnetic resonance structural analysis, and the results are shown in fig. 1 and fig. 2, wherein fig. 1 is an electron bombardment mass spectrum of the final product, and fig. 2 is an H1 nuclear magnetic resonance spectrum of the final product, and the structural formula of the final product is proved to be the compound (I).

The compound (I) of the invention introduces a methoxy group on the 6 th carbon atom of the critical indole ring on the basis of the molecular structure of melatonin, thereby leading to the increase of electronegativity of the whole indole ring, greatly enhancing the capacity of capturing free radicals, and supposing that the 6 th position of the indole ring is occupied by the methoxy group, the function of hydroxylase with strong specificity is blocked, thereby the metabolism is slowed down and the half-life period is prolonged. Meanwhile, due to the change of the structure of the key part, the affinity of the key part to the receptor is supposed to be reduced, and the side effect is correspondingly reduced. Thus, compound (I) has significant advantages over melatonin.

The present invention investigates the hydroxyl radical scavenging experiment and the animal experiment of protecting nervous system of the compound (I).

Experiment for scavenging free radicals of hydroxyl group of N-acetyl-5, 6-dimethoxytryptamine

Hydroxyl radical (OH) is the most violent and toxic oxidizing radical in organism. Many diseases such as nervous system degenerative diseases, senile dementia (Parkinson's disease), cardiovascular system diseasesDiseases, tumors, AIDS and aging are all directly and indirectly related to them. OH. has a very short half-life of about 10^-9About seconds, OH can not be directly measured at present, but an electron spin trapping agent, such as 5, 5-dimethylpyroline N-oxide (DMPO), can be used to trap OH to form a more stable adduct of DMPO and OH (DMPO-OH). Then, the amount of DMPO-OH can be measured by using a high-pressure liquid phase and an electro-chemical detector to estimate the generation amount of OH, and in order to measure the hydroxyl radical scavenging capacity of the N-acetyl-5, 6-dimethoxytryptamine, the following OH generation system is adopted, namely, hydrogen peroxide is photolyzed by short-wave violet light (with the wavelength of 254nm) to decompose one molecule of hydrogen peroxide into two molecules of OH, and the chemical expression is as follows:

the hydroxyl radical system was added with the same amount of DMPO and different concentrations of N-acetyl-5, 6-dimethyloxytetramine, and then the formation of DMPO-OH was measured, and the result showed that the formation of DMPO-OH was significantly inhibited by N-acetyl-5, 6-dimethoxytryptamine, i.e., significant hydroxyl radical scavenging effect was exhibited (FIG. 3), and the inhibition was dose-dependent (FIG. 4). Half inhibitory dose IC₅₀At a concentration of 17 micromolar, the free radical scavenger effect is superior to the currently accepted endogenous free radical scavenger melatonin (IC)₅₀21 micromolar).

Animal experiments for nervous system protection

Kainic Acid (KA) is a neurotoxin that can over-activate brain cell excitatory amino Acid receptors, producing free radicals, leading to neuronal damage and death. Therefore, KA is often used for inducing brain cell damage model, and in order to investigate the effect of N-acetyl-5, 6-dimethoxytryptamine (compound I) on protecting nerve cells, the following experiments were designed and completed:

the experimental method comprises the following steps: 40 CDs_2-F1The method comprises the following steps of feeding a male mouse with the weight of 26-28 g in a standard animal room, freely eating and drinking water at the room temperature of about 22 ℃, and controlling the room temperature and the illumination by a computer, wherein the illumination condition is 12 hours in the daytime and 12 hours in the night, namely, turning on the light at 7 morning and turning off the light at 19 afternoon.

Mice were randomly divided into 3 groups, 15 mice in group 1 (i.e., group KA), and subcutaneously injected with KA 40mg/kg body weight. In group 2 [ KA + Compound (I)]15 mice were pre-intraperitoneally injected with 5mg/kg body weight of compound (I) ethanol and aqueous solution (ethanol: water ratio 1: 500), and subcutaneously injected with 40mg/kg body weight of KA 10 minutes later, at the same dose as in group 1. Group 3 (i.e., blank control group) 10 mice were observed as normal controls by subcutaneous injection of an equal volume of saline only.

The observation indexes of each group of animals are as follows: spasticity, convulsions and death numbers, and the formation of Lipid Peroxides (LPO) in brain tissue was biochemically determined.

The experimental results are as follows: all 15 mice in group 1 developed spasticity and convulsions, of which 6 died. Only 3 animals in group 2 developed spasticity, 6 animals developed convulsions, but none died (fig. 5).

Taking 6 mice from each group, killing after 3 days, taking out the whole brain tissue immediately after killing, freezing and storing at-80 deg.C, homogenizing the whole brain tissue, and detecting the generation amount of lipid peroxide in the brain tissue by conventional method. As a result: the brain tissue lipid peroxide content of the animals in group 1 (group KA) was significantly increased, and the increase was statistically significant (P<0.05) compared to the control group. While the animals of group 2 were previously injected with compound (I), the brain tissue lipid peroxide content was maintained at the same level as that of the control group (fig. 6). The experimental results show once more: the subcutaneous injection of KA (40 mg/kg body weight) can ensure that the hippocampus cerebri CA of an experimental mouse₃The neural cells of the vertebral body (cells related to short-term memory) in the area are completely necrosed, and the compound (I) is intraperitoneally injected for 10 minutes in advance for 5mg/kg of body weight, so that 95% of the neural cells of the vertebral body in the CA3 area can be preserved. N-acetyl-5, 6-dimethoxytryptamine [ Compound (I)]The compound (I) achieves strong protection effect on nerve cells through antioxidation, and also has great potential clinical application value.

Through the chemical method and the preliminary experiment result, the compound (I) has strong hydroxyl free radical scavenging effect, so that the compound (I) is presumed to have good curative effect and no obvious toxic or side effect and long half-life period on diseases related to free radicals in clinic, such as delaying senility, preventing and treating degenerative changes of the central nervous system, including senile dementia, Parkinson's disease, heart disease, auxiliary treatment of tumors, auxiliary treatment of AIDS and the like.

Description of the drawings:

FIG. 3 is a high pressure liquid phase (HPLC) chart illustrating the effect of N-acetyl-5, 6-dimethoxytryptamine on the formation of DMPO-OH adduct. Peaks 1, 2 are solvent fronts and peak 3 is the DMPO-OH. signal.

A: is an HPLC (high performance liquid chromatography) spectrum after hydrogen peroxide is photolyzed under short-wave ultraviolet radiation to form OH&and then reacts with DMPO to form an addition product.

B: is HPLC chromatogram after adding 60 micromolar N-acetyl-5, 6-dimethoxytryptamine under the same conditions as A. DMPO-OH. formation was significantly inhibited.

FIG. 4 is a graph showing the effect of N-acetyl-5, 6-dimethoxytryptamine on the formation of DMPO-OH. the data are obtained from the measurement of DMPO-OH. by HPLC-electrochemical detector, and the data are expressed as mean. + -. standard error and the number of samples is 6.

FIG. 5 shows the test results of N-acetyl-5, 6-dimethoxytryptamine for the neuroprotective effect of KA mice.

FIG. 6 is a graph of the effect of N-acetyl-5, 6-dimethyltryptamine on KA-induced brain lipid peroxide formation, data expressed as mean. + -. standard error for 6 samples.

The compound (I) can be processed into oral dosage forms, including tablets, sustained-release tablets, capsules, granules and oral liquid, injection dosage forms, including powder injections and injections, and external dosage forms, such as transdermal absorption films, ointments and creams. The above dosage forms are prepared by techniques well known to those of ordinary skill in the art. The result of animal experiments estimates that the effective dose of human body is 2-10 mg/person/day, 1-4 times per day.

The compound (I) of the present invention can also be processed into a radical scavenger for external use, and added to cosmetics as a sunscreen agent.

The present invention will be further described with reference to the following examples.

Example 1, synthesis of compound (I):

the first step is as follows: synthesis of 3-diethylaminomethyl 5, 6-dimethoxyindole

1 g of 5, 6-dimethoxyindole, dissolved in 2ml of EtOH and cooled to 15 ℃ until use. 1.4ml of 60% acetic acid and 0.48 g Et were prepared₂NH solution, cooled to 5 ℃ and then 0.51ml of 37% formalin was added, stirred at 5 ℃ for 10 minutes and poured into the prepared 5, 6-dimethoxyindole EtOH solution. When the temperature is raised to about 23 ℃ at room temperature, stirring is carried out for one hour, the mixture is poured into 20ml of a cooled one-equivalent NaOH solution and then 3 parts of Et are added₂And O extraction. The extract was eluted three times with saturated NaCl solution and Na₂SO₄Drying, Et₂O is volatilized to leave 3-diethylaminomethyl, 5, 6-dimethoxyindole as an oil.

The second step is that: synthesis of 3-acetonitrile, 5, 6-dimethoxyindole

The first step of the composition is dissolved in 20ml MeOH, 1ml DMF, 1ml water and 1.4 g NaCN mixture, slowly drop into 2.1ml MeI, standing for 1 hours, and stirring for 1 hour. This mixture was poured into a large volume of cooled double distilled water (400m 1). Reuse of CH₂Cl₂Extracting, washing the extract with water for 3 times, and Na₂SO₄Drying, removal of the solvent under vacuum and recrystallization from benzene-hexane (1: 1 benzene-hexane). The yield was 0.5g (about 50% based on synthetic starting material).

The third step: synthesis of 5, 6-dimethoxytryptamine

4ml of a solution containing 0.52ml of 100% H₂SO₄The THF solution of (1) was added dropwise to a previously prepared LiALH solution (0.76 g)₄In a mixture with 20ml of THF without removing precipitated Li₂SO4, 4ml of 3-acetonitrile containing 0.5g of 5, 6-dimethoxyindole (addition completed in 30 minutes) was slowly added dropwise, stirred for 1 hour, and ice was added to destroy excess hydride. Is poured offMost of the THF supernatant (aimed at reducing the formation of emulsions during extraction) and the precipitated aluminum salts reacted with 20% NaOH to form a cloudy solution from CHCl₃Extracting, eluting with saturated NaCl solution 3 times, and collecting the extract containing part of THF solution₂SO₄Drying and removing the solvent by vacuumizing. The residue was extracted with Et₂O-Pentane (1: 1 ether: n-Pentane) crystallized, then washed with water and dried to obtain 0.4g of pure 5, 6-dimethoxytryptamine (yield about 80%).

The fourth step: synthesis of N-acetyl-5, 6-dimethoxytryptamine

3.2ml of C containing 0.4g of 5, 6-dimethoxytryptamine₆H₆And 0.8ml pyridine was added to the mixture in an ice bath, followed by 0.4ml Ac₂And O, removing the ice bath, stirring for 3 hours, and vacuumizing to volatilize the organic solvent. With 1: 1 CHCl₃And EtOAc redissolved the residue, then 5% NaHCO₃Alternately cleaning with saturated NaCl solution for 3 times, vacuum-pumping to volatilize organic solvent, and adding boiled C₆H₆Purification gave 0.35g of Compound (I) (yield about 87%).

Preparation of the preparation: collecting compound (I), filtering at 1mg/ml concentration, dissolving in water for injection, packaging, sterilizing, and making into injection.

Example 2, synthesis of compound (I):

the first step and the second step are the same as those of example 1.

The third step: synthesis of 5, 6-dimethoxytryptamine

Dissolving 3-acetonitrile and 5, 6-dimethoxy indole in ethanol, adding metal sodium, reacting for 1 hr, adding water, removing excessive sodium, extracting with chloroform (chloroform), eluting with saturated NaCl solution, drying with anhydrous sodium sulfate, removing solvent, and recrystallizing.

The fourth step: synthesis of Compound (I)

By using

(acetyl chloride) instead of acetic anhydride, the rest is as in example 1.

Preparation of the preparation:

taking the compound (I), adding starch or dextrin or powdered sugar or microcrystalline cellulose as a diluent, taking water or starch slurry or gums or hydroxymethyl cellulose as a wetting agent, taking dry starch or sodium carboxymethyl starch or low-substituted hydroxypropyl cellulose as a disintegrant, taking magnesium stearate and talcum powder as a lubricant and a glidant, granulating by a wet method, drying, adding the lubricant and the glidant, and tabletting to obtain the tablet. The dosage was 1mg of compound (I) per tablet.

Example 3, synthesis of compound (I).

The first step and the second step are the same as those of example 1.

The third step: 5, 6-Dimethoxyindole

Taking 3-acetonitrile and 5, 6-dimethoxy indole, carrying out catalytic addition by adopting a nickel-hydrogen catalyst under the conditions of 130 atmospheric pressure and 120-130 ℃, extracting and purifying to obtain the 5, 6-dimethoxy tryptamine.

The fourth step: the same as in example 1.

Preparation of the preparation:

adding polyvinyl alcohol into a proper amount of the compound (I), heating, uniformly mixing, adding azone as a transdermal absorption enhancer, andpreparing into a transdermal absorption paste.

Each step of the synthesis of the compound (I) is independent from each other, for example, the third step can adopt a catalytic hydrogenation method, a sodium-alcohol addition method or a lithium aluminum hydride reduction method, and the fourth step can adopt an acylation reaction of acetyl anhydride or acyl chloride. And is not limited to the above-described embodiments.

The preparation of the compound (I) formulations of the present invention can be prepared into various dosage forms using techniques well known to those of ordinary skill in the art, and is not limited to the examples described above.

Claims (2)

1. N-acetyl-5, 6-dimethoxytryptamine is used for preparing the anti-oxidation free radical medicine.

2. Use of N-acetyl-5, 6-dimethoxytryptamine according to claim 1 for the preparation of a medicament against oxidative free radicals, characterized in that it is added to cosmetics as a sunscreen.

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