Patent Application
20080070942
The present invention relates to two kinds of derivatives of prazole compounds. The resulting compound products can be converted into pharmaceutically acceptable salts thereof by conventional process which are then used as active ingredients in medicament production.
European patent application EP150 586 disclosed 2-(pyridyl methylthio- or sulfinyl-)benzimidazole, wherein 4th position of the pyridine ring may be substituted by alkylthio or arylthio. This application revealed that the compound had a long-term and continuous inhibition against gastric acid secretion. An international application WO92/12967 recorded the compounds obtained by some specific substitutions of 2-(pyridyl methylthio- or sulfinyl-)benzimidazole which could effectively kill Helicobacter and these compounds could be used for preventing and curing gastric diseases. Another international application WO93/24480 also recorded other 2-(pyridyl methylthio- or sulfinyl-)benzimidazoles obtained by some specific substitutions which could effectively kill Helicobacter.
The purpose of the present invention is to provide two kinds of Prazole derivatives or salts thereof
To achieve the purpose of the invention, a derivative of the compound of formula (I) or (II) or a salt thereof is provided
Preferably, R1 is difluoromethyl and R3 is sodium in formula (I); and R2 is methyl and R3 is sodium in formula (II).
The compound or the salt thereof according to the present invention is also a compound or a salt thereof in the form of single (R) or (S) enantiomer, or rich in an enantiomer.
The present invention also provides a pharmaceutical composition comprising said compound and/or the pharmaceutically acceptable salt.
In addition, the present invention discloses the use of said compound and/or the pharmaceutically acceptable salt thereof in preparation of a medicament for killing Helicobacter pylori, and the use in preparation of a medicament for treating and/or preventing gastric and/or intestinal diseases.
The compounds of formula (I) or (II) of the present invention and their derivatives or pharmaceutically or pharmacologically acceptable salts can improve remarkably the effect against alimentary tract ulcer, and weakly inhibit gastric acid secretion, which reduces greatly the risk of stomach cancer, and additionally have more excellent in vivo pharmacokinetic characteristics such as the bio-availability, and the like.
The present invention will be illustrated detailedly by the following examples. The examples are provided for the purpose of illustration and are not meant to limit the scope of the present invention in any manner.
Compound (I) is taken as an example to indicate the synthetic route shown as follows;
Intermediate (2) is prepared by the substitution reaction of 2,3-dimethyl-4-Cl-pyridine N-oxide with sodium 3-methoxyl-1-propanoxide, and the latter is obtained by the reaction of 3-methoxyl-1-propanol with strong alkali. Said strong alkali includes sodium, sodium-hydride (60%-80%), sodamide, etc., which takes place in a solvent such as anhydrous tetrahydrofuran, N,N-dimethyl formamide, and dimethyl sulfoxide, and anhydrous tetrahydrofuran is preferred. The temperature for the reaction is between 50□ and 150□, and about 100□ is preferred.
Intermediate (3) is prepared by the reaction of 2,3-dimethyl-4-(3-methoxyl-propoxyl)-pyridine N-oxide with acid anhydride or acyl chloride, such as acetyl chloride, trichloroacetyl chloride, and trifluoroacetyl chloride, and acid anhydride is preferred. The reaction may take place in a solvent such as acetonitrile, benzene, chloroform, dichloromethane, dimethyl formamide, dimethyl sulfoxide, dioxane, tetrahydrofuran, and toluene, etc., and acetonitrile is preferred. The temperature for the reaction is from the ambient temperature to 150□, and 80-100□ is preferred. The reaction time is from 2 to 10 hours. After the reaction, the reaction solution is concentrated under vacuum to evaporate the solvent, and the resulting product is used in the next step.
Intermediate (4) is obtained from intermediate (3) by hydrolysis. The reaction may take place in a polar solvent containing hydroxyl such as water, methanol, ethanol, isopropanol or butanol, and water or methanol is preferred. The alkali used in this step is sodium hydroxide, potassium hydroxide, potassium carbonate, ammonia or sodium methoxide, etc., and sodium hydroxide is preferred. The reaction temperature may be controlled between 20-80□, and preferably between 30-50□. The reaction time may be controlled between 1-10 hours. After the reaction, the reaction solution is extracted by an organic solvent, such as dichloromethane, chloroform, ethyl ether, tert-butyl methyl ether, ethyl acetate, toluene, and isopropyl ether, and chloroform is preferred. After the organic layer is dried, the solvent is recovered under vacuum till the residue is dry, and the resulting product is then directly used in the next step.
Intermediate (5) is prepared by the reaction of the intermediate obtained from the preceding step with a halide reagent, such as sulfoxide halide or phosphorus trihalide, and sulfoxide chloride is preferred. The reaction takes place in an inert solvent, such as acetonitrile, benzene, chloroform, dichloromethane, dimethyl formamide, dimethyl sulfoxide and tetrahydro furan, etc., and dichloromethane or chloroform is preferred. The reaction temperature may be controlled between −10□ and the temperature of solvent reflux, and the temperature between 0-25□ is preferred. After the reaction, the reaction solution is neutralized by alkali, such as sodium hydroxide, potassium hydroxide, sodium carbonate, and potassium carbonate, etc., and sodium carbonate is preferred. The pH value is adjusted to 7-8. The solution is extracted by an organic solvent such as dichloromethane, chloroform, ethyl ether and ethyl acetate, and chloroform or dichloromethane is preferred. The organic phase is dried and then concentrated under vacuum. The resulting product is directly used in the next step.
Intermediate (6) is obtained by the condensation reaction of 2-chloromethyl-3-methyl-4-(3-methoxyl-propoxyl)-pyridine with 5-difluoromethoxyl-2-mercapto benzimidazole. The reaction can take place under the condition of liquid-liquid phase transfer. The inorganic alkali used includes sodium hydroxide or potassium hydroxide, etc. The phase transfer catalyst may be R4NX, R4PX or crown ether, etc., and R4NX is preferred. R4NX includes tetrabutyl ammonium, tetraethyl ammonium, and triethyl phenyl ammonium, etc., and X represents chlorine, bromine or iodine, etc., and triethyl phenyl ammonium chloride is preferred. The temperature for the reaction is 0-100° C., and 15-30° C. is preferred. The reaction time is between 1-10 hours. The reaction may also take place in a homogeneous phase with polar solvent such as water, methanol, ethanol, iso-propanol and n-butanol, etc. Under these conditions, 5-difluoromethoxy-2-mercapto-benzimidazole salt is firstly formed, and then reacts with intermediate (5) to produce intermediate (6).
Intermediate (7) is prepared by the reaction of the intermediate obtained from the preceding step with an oxidant, such as m-chloro-peroxybenzoic acid, peracetic acid, and hydrogen peroxide, etc., and m-cloro-peroxybenzoic acid is preferred. The reaction temperature is from −80□to 0□, and −50□-40□is preferred.
The derivative rich in (R) or (S) enantiomer can be obtained by asymmetry oxidation of Intermediate (6). The asymmetry oxidation is carried out by known processes, such as the process mentioned in Patent WO96/02535. Alternatively, the derivative can be separated from the compound of formula (I) or (II) by chiral resolution or chiral column.
The present invention will be described in detail by following examples:
7.8 g sodium was suspended in 90 ml 3-methoxy-1-propanol, and then the suspension was heated up to 100□ by oil bath until it turned clear completely. After cooled, 120 ml THF and 30 g 2,3-dimethyl-4-chloro-pyridine N-oxide were added and then the reflux reaction took place for 12 hours and was cooled again. 200 ml water was added and pH value was adjusted to 7. The reaction solution was extracted with chloroform, dried with anhydrous magnesium sulfate and filtered. The filtrate was concentrated under vacuum to recover chloroform and 3-methoxy-1-propanol, the obtained product was used in the next step.
50 g 4-(3-methoxy-propoxy)-2,3-dimethyl-pyridine N-oxide, 150 ml acetic anhydride and 8 drops of concentrated sulfuric acid were put into a reaction flask and reacted at 90° C. for 3 hours in oil bath. The acetic anhydride was vaporized under vacuum. 100 ml water and 20 g sodium hydroxide at ambient temperature were added to the flask and reacted at 50° C. for 1 hour in water bath. And then the reaction solution was cooled, extracted by chloroform, dried, filtered and concentrated till dry. 200 ml fresh chloroform and 30 ml thionyl chloride were added to the residue and the reaction took place at ambient temperature for 5 hours and the reaction solution was concentrated under vacuum. After that, 400 ml water was added to the residue and the pH value was adjusted to 8 with sodium carbonate solution. Finally, the expected product (brown semi-solid) was produced after the procedures of extracting the reaction solution by chloroform, drying and concentration.
42 g 2-chloromethyl-4-(3-methoxy-propoxy)-3-methyl pyridine, 29 g 5-difluoromethoxyl-2-mercapto benzimidazole, 0.3 g tetrabutyl ammonium bromide, 35 g potassium carbonate and 200 ml anhydrous ethanol were put into a reaction flask and reacted at 70° C. for one hour. After filtration and concentration, the residue was mixed with 300 ml dichloromethane, water-washed, dried, filtered, concentrated till dry, and then mixed with 100 ml ethyl acetate for recrystallization, thereby a solid product was obtained.
42 g 2-chloromethyl-4-(3-methoxy-propoxy)-3-methyl pyridine, 27 g 6-methoxyl-2-mercapto pyridoimidazole, 0.3 g tetrabutyl ammonium bromide, 35 g potassium carbonate and 200 ml anhydrous ethanol were put into a reaction flask and reacted at 70° C. for 1 hour. After filtration and concentration, the residue was mixed with 300 ml dichloromethane and then water-washed, dried, filtered and then concentrated till dry, and recrystallized in 100 ml ethyl acetate to obtain a solid product.
4.4 g (10.65 mmol) 2-{[4-3-methoxy-propoxy)-3-methyl pyridine-2-yl]-methyl-sulfinyl]-1H-5-difluoromethoxyl-benzimidazole was added to a solution prepared with 0.412 g (10.3 mmol) sodium hydroxide and 100 ml water. After dissolving, 200 ml ethanol was put into the solution which was then concentrated till dry under vacuum. The resulting residue was mixed with tert-butyl methyl ether and then filtered, dried and finally the expected product was obtained.
4.4 g (10.65 mmol) 2-{[4-(3-methoxy-propoxy)-3-methylpyridine-2-yl]-methyl-sulfonyl]-1H-5-difluoromethoxyl-benzimidazole was added to the solution prepared with 0.25 g (10.3 mmol) lithium hydroxide and 100 ml water. After dissolving, 200 ml ethanol was put into the solution which was then concentrated till dry under vacuum. The residue was mixed with tert-butyl methyl ether and then filtered and dried to obtain the product.
0.735 g (0.005 mol) calcium chloride dihydrate was dissolved in 6 ml water, then the solution was dropped slowly into 4.35 g (0.01 mol) of 2-{[4-(3-methoxy-propoxy)-3-methylpyridine-2-yl]-methyl-sulfinyl}-1H-5-difluoromethoxy benzimidazole sodium salt (prepared in Example 5) in 25 ml water. Then stirred magnetically for 1 hour, and then the reaction solution was filtered, the obtained filter cake was washed by water and vacuum dried at 40□ for 10 hours to obtain the title product.
The preparation method is similar to that used in Example 5 except that 4.4 g (10.65mmol) 2-{[4-(3-methoxy-propoxy)-3-methylpyridine-2-YL]-methyl-sulfinyl}-1H-5-difluoromethoxyl-benzimidazole was replaced by 4.0 g (10.65 mmol) 2-{[4-(3-methoxy-propoxy)-3-methyl pyridine-2-yl]-methyl sulfinyl}-1H-6-methoxy-pyridoimidazole.
The preparation method is similar to that used in Example 7 except that 4.35 g (0.01 mol) 2-{[4-(3-methoxy-propoxy)-3-methyl pyridine-2-YL]-methyl-sulfonyl}-1H-5-difluoromethoxyl-benzimidazole sodium salt prepared in Example 5 was replaced by 4.0 g (0.01 mol) 2-{[4-(-methoxy-propox)-3-methylpyridine-2-yl]-methyl-sulfonyl}-1H-6-methoxy pyridoimidazole sodium salt prepared in Example 8.
10.1 g (0.05 mol) magnesium chloride hexahydrate was dissolved in 100 ml water, and 10 ml of the obtained solution was dropped slowly into 4.0 g (0.01 mol) 2-{[4-(3-methoxy-propoxy)-3-methyl pyridine-2-yl]-methyl-sulfonyl}-1H-6-methoxy pyridoimidazole sodium salt prepared in Example 8 in 15 ml water. After stirring, filtration and vacuum drying, the expected product was thus obtained.
7.8 g 2-{[4-(3-methoxy-propoxy)-3-methyl pyridine-2-yl]-methylthio}-1H-5-difluoromethoxy benzimidazole and 32 ml toluene were put into a reaction flask and heated to 54° C. with agitation, and then added with 2.8 ml (−)-diisopropyl-D-tartaric acid, 2.2 ml isopropyl-titanium peroxide and 56 μl distilled water. After that, the reaction took place for 50 minutes at a constant temperature. 1.25 ml N,N-isopropyl ethamine was added to the reaction when the temperature dropped to 30° C. and then added with 4.6ml cumene hydroperoxide in drops, and the reaction took place at 30° C. for 1 hour. The reaction solution was extracted with 12.5% ammonia (3×25 ml), collecting all three extraction solutions, adjusted to pH=7 with acetic acid, and finally extracted with 4-methyl-2-pentanone (3×12 ml). The extraction solution was dried, filtered, concentrated till dry, and recrystallized with ethyl acetate and n-hexane to obtained the title compound (5.2 g).
Note: In Compound (II) of the invention, R2 is methyl and R3 is hydrogen.
1. Purpose of the Experiment
To compare effects of prazole compounds on gastric acid secretion
2. Materials
2.1 Animal
Wistar rat, weight 180-220 g, male, obtained from Institute of Zoology, Chinese Academy of Medical Sciences.
2.2 Drugs for Administration
Sodium rabeprazole, compound (II) of the present invention and tenatoprazole, provided by Jiangsu Hansen Pharmaceutical Co., Ltd.
2.3 Preparation of the Drug
Added 1 drop of Tween-80 as a solubilizing assistant and prepared the required concentrations with distilled water.
3. Methods and Results
Methods: 48-hour fasting rats were divided into groups randomly. Pylon ligation was carried out under ether anaesthesia. During the operation, different doses of the drugs were administered respectively through the duodenum and the volume for administration is 5 ml/kg. The rats were sacrificed at 5 hours after the operation and the gastric juice was collected and measured. The content of HCl in gastric juice is determined by titration with 0.1 mol/L NaOH and the significance test was made by t-programme.
Results: See the table below. It has been reported in a number of literatures that over strong effect of inhibition of a prazole drug on gastric acid secretion may induce a feed-back mechanism of gastric sinus, resulting in a high level of gastric secretin in plasma and the formation of gastric cancer due to proliferation of secretory cell. In contrast, if this drug has a weak effect of inhibition on gastric acid secretion, there will be no a feed-back mechanism of gastric sinus induced, or a high gastric secretion in plasma thus caused and accordingly, it is impossible to make a proliferation of secretory cell hyperplasia and the risk of gastric cancer will be greatly decreased. The effect of inhibition of compound (II) of the present invention on gastric acid secretion is weak and thus may reduce the risk of gastric cancer.
Compared with the control group:
*p < 0.05,
**p < 0.01,
***p < 0.001.
Note: In compound (I), R1 is difluoromethyl and R3 is sodium. In compound (II), R2 is methyl and R3 is sodium.
1. Purpose of the Experiment
To understand the effects of Compound (I), Compound (II) and Sodium Rabeprazole on anti-ulcer.
2. Materials
2.1 Animal
Wistar rat, weight: 180-220 g, male, obtained from Institute of Zoology, Chinese Academy of Medical Sciences.
2.2 Drug
Compound (I) and Compound (II) of the present invention and sodium rabeprazole, provided by Jiangsu Hansen Pharmaceutical Co., Ltd.
2.3 Preparation of the Drug
The required concentration is prepared with distilled water and the volume for administration of drug is 10 ml/kg.
3. Methods and Results
Methods: 40-hour fasting rats were randomly divided into groups and treated with different doses of sodium rabeprazole, compound (I), compound (II) and distilled water (as control) by gastric perfusion, respectively. After 0.5 hour, each rat was administered with 1 ml anhydrous ethanol and then rats were sacrificed 1 hour later. The stomachs were taken out and injected with 10 ml fix solution. After fixed in 3% formaldehyde solution, the stomachs were dissected and the ulcer areas were measured. The significance test was made by t-programme.
Results: The ulcer areas of rats administered with sodium rabeprazole were reduced. Compounds (I) & (II) have same function and even have a more significant effect. See Table 1 for details.
In this example, compound (II) of the present invention was used, wherein, R2 is methyl and R3 is hydrogen.
Methods: Abdominal cavities of fasting rats were cut under the anaesthesia of sodium pentobarbital and gently stretched the stomachs. The glandular stomachs near pylons were injected with 20 μl 30% acetic acid and then the abdominal cavities were re-closed. At the day the operation finished, rats were randomly divided into groups and started to be administered with drugs of 10 ml/kg once a day for 10 continuous days. Rats were then sacrificed in the following day when the last drug was administered, and stomachs were taken out and were injected with 10 ml water, and then were put into 3% formaldehyde solution to be fixed for 30 minutes. The stomachs were dissected along their greater curvatures and stretched on a glass plate and the ulcer areas were measured. The significance test was made by t-programme.
Results: Rats with the treatment of prazole compounds showed smaller ulcer areas than those of the control group. Specifically, a significant difference was indicated between the following groups and control group: large dosage group of sodium rabeprazole, large dosage group and small dosage group of Compound (II), and large dosage group of tenatoprazole. See the table below for details.
Compared with the control group:
*p < 0.05,
**p < 0.01.
**Compound (II) 2 of the present invention.
Note: In compound (II) of the present invention, R2 is methyl and R3 is hydrogen.
1. Purpose of the Experiment
To learn the effects on ulcer rat models induced by indomethacin, pylon ligation, cold water restraint stress and acetic acid, and to observe effects of compound (II) on gastric acid secretion and pepsin activity as well as the effect of Prazole B on H+—K+-ATPase in gastric parietal cell in rats.
2. Experiment Materials
2.1 Animal
Wistar rats, weight: 180-220 g, same number of male and female, provided by Institute of Zoology, Chinese Academy of Medical Sciences. (Certification of Qualification of Animal: scxk Beijing 2000-0006)
2.2 Drugs
Compound (II): provided by Jiangsu Hansen Pharmaceutical Co., Ltd
Sodium Rabeprazole: provided by Jiangsu Hansen Pharmaceutical Co., Ltd
2.3 Preparation of the Drugs
0.5% methylcellulose sodium: 2 g/L NaHCO3 is contained and pH value is adjusted to 9.0 with NaOH.
Preparation: The drug was porphyrized and diluted with 0.5% methylcellulose sodium to the required concentration. It must be used up in 30 minutes.
3. Effects on Gastric Ulcer Model Induced by Indomethacin in Rats
Methods: Sixty 48-hour fasting rats were divided into six groups and gastric-perfused with different doses of compound (II), sodium rabeprazole and 0.5% methylcellulose sodium (as control), respectively. After 0.5 hour, 20 mg/kg indomethacin was injected into the abdominal cavities. Six hours later, rats were sacrificed by cervical dislocation and the stomachs were taken out. After injected with 10 ml water, stomachs were then fixed in 3% formaldehyde solution. The hemorrhagic spots were counted. A significance test was carried out by t-programme.
Results: see Table 5 for details. It was indicated that after the treatment of compound (II) by gastric perfusion, the hemorrhagic spots on gastric mucosal induced by indomethacin in rats were remarkably reduced. It also showed a dose dependent effect. Ulcer inhibition of ED50 was 14.1 μmol/kg. It thus proved that compound (II) has an obvious function of protection of gastric mucosal hemorrhage induce by indomethacin. Sodium Rabeprazole has the same function but the effect is lower than that of compound (II).
Ulcer inhibition ED50 = 14.1 μmol/kg (95% confidence limit: 12.9-15.5).
Compared with the control group
**p < 0.01,
***p < 0.001.
In Compound (II) used in this example, R2 is methyl and R3 is hydrogen.
Methods: Sixty 40 hour-fasting rats were divided into 6 groups according to Table 2. A pylori ligation operation was carried out under the anaesthesia of ether. Different doses of compound (II), sodium rabeprazole and 0.5% methylcellulose sodium (as control) were administered through duodenum during the operation, respectively. Rats were sacrificed at 18 hours after the operation and the stomachs were taken out and then fixed in 3% formaldehyde solution after injecting 10 ml water. The stomachs were dissected and the number of gastric ulcers was counted. The result was tested by a significance test of t-programme.
Results: see the table below for details. It was shown that after treated with compound (II), ulcers in the rats were obviously mitigated and the inhibition rate was 41.4˜96.7%. It also showed a dose dependent effect. The ulcer inhibition of ED50 was 16 μmol/kg. It is thus obvious that compound (II) has a significant function of protection of gastric ulcer model induced by pylori ligation. Sodium rabeprazole has an essentially same function.
Ulcer inhibition of ED50 = 16.0 μmol/kg (95% confidence limit: 12.9-18.9)
Compared with the control group
*p < 0.05,
**p < 0.01,
***p < 0.001
This example used compound (II) of the present invention, wherein R2 is methyl and R3 is hydrogen.
Methods: Six healthy male beagle dogs with weight 5.5˜6.7 kg were randomly divided into three groups for triple cross over administration. They were perfused with rabeprazole, tenatoprazole and compound (II) respectively after one-night fasting. The dose of each drug was 5 mg/kg. Each dog was fed with 50 ml water by gastric perfusion after administration of the drug. 2 ml blood was taken respectively from forelimb saphenous vein at 0.25, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12 hours after tenatoprazole was administered, at 5, 10, 20, 30, 40, 50, 60, 75, 90, 120, 180 minutes after rabeprazole was administered, and at 1, 2, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 10, 12 hours after compound (II) was administered, and then put each blood sample in each test tube treated with EDTA, then centrifuging for 10 min at 3500 rpm. The upper plasma was removed from the test tube into another test tube containing 50 μl 2% NaOH solution and reserved at −20□. The plasma drug concentration was determined by HPLC. Cross-over administration to dogs was performed one week later.
The calculation method for pharmacokinetic parameters: compartment model is estimated by software DAS1.0. The calculation of the related pharmacokinetic parameters by moment method, i.e., area under the curve (AUC), mean residence time (MRT) and clearance (Cl/F), can be carried out respectively according to each of the following equations:
AUC24=Σ(Ci+Ci−1)(ti−ti−1)/2
AUC=AUC24+C24/λZ
AUMC24=Σ(Ci.t1+Ci−1·ti−1)(ti−ti−1)/2
AUMC=AUMC24+C24(24/λz+1/λ2Z)
MRT=AUMC/AUC
Cl/F=D/AUC
Wherein C24 is the blood drug concentration at 12 hours after administration, λz is the terminal phase rate constant, obtained by linear regression of terminal phase In C˜t. T½=0.693/λz, Tmax and Cmax are are measured values.
Results: Data of blood drug concentration-time: Concentrations of rabeprazole, tenatoprazole and compound (II) in plasma after 6 dogs were administrated with 5 mg/kg each of them respectively can be seen in Tables 1-2 and
a, If the concentration is lower than the minimum detection concentration, it can be considered as “0’.
It can be seen from the above data that concentrations of rabeprazole are mostly below the detectable limit, i.e., the plasma concentrations of rabeprazole in dogs are low (also see FIGS. 1A-F and
Pharmacokinetic parameters: The pharmacokinetic parameters after administrating 5 mg/kg of each of tenatoprazole and compound (II) to Beagle dogs were estimated by Moment method as shown in Table 5 and Table 6:
The Comparison of Pharmacokinetic Parameters Between Tenatoprazole and Compound (II) in Beagle Dogs
Table 7 shows results of the main pharmacokinetic parameters after orally administrating 5 mg/kg of tenatoprazole and compound (II) respectively in Beagle dogs
It can be seen from the above results that after administrating 5 mg/kg of tenatoprazole and compound (II) to Beagle dogs respectively, the pharmacokinetic parameters are: Cmax: tenatoprazole is 4.28+1.18, compound (II) is 5.95+3.11; Tmax: tenatoprazole is 2.17+1.33, compound (II) is 3.1+1.0; T½: tenatoprazole is 3.74+0.37, compound (II) is 3.34+0.36; MRT: tenatoprazole is 5.40+0.53, compound (II) is 4.83+0.52; AUC12: tenatoprazole is 16.87+4.11, compound (II) is 25.67+13.52; AUC: tenatoprazole is 18.02+3.71, compound (II) is 26.44+13.46.
Conclusion: It can be concluded that the pharmacokinetic behaviors of compound (II) are remarkably improved compared with those of rabeprazole. In particular, compound (II) shows a better absorption and longer elimination half-life. As for the half life, tenatoprazole and compound (II) are similar, but compound (II) shows an increase with respect to Cmax and AUC, which indicates a much better absorption for compound (II).
The grain-making by conventional wet process, tablet pressing and enteric coating are carried out.
| Number | Date | Country | Kind |
|---|---|---|---|
| 200410081026.X | Sep 2004 | CN | national |
| 200510059391.5 | Mar 2005 | CN | national |
| 200510077315.7 | Jun 2005 | CN | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CN05/01545 | 9/23/2005 | WO | 3/30/2007 |
