Patent Application
20230212179
The invention relates to chemistry and pharmacology, specifically to a synthetic biologically active substance -7,9-dibromo-2,4-dioxo-1,2,3,4-tetrahydrochromeno[2,3-d]-pyrimidinium-10 acetate, having antimicrobial activity, and the method of its synthesis.
The invention extends to all spatial isomers of the claimed substance, all its tautomeric and salt forms, as well as hydrated forms, solvates, complex compounds and adducts with organic substances.
The substance is intended for use in medical practice for the treatment of diseases caused by bacteria, as well as for similar purposes in veterinary medicine. The substance can be used both individually and in the form of their pharmacologically acceptable salts, complexes, as well as in combination with other drugs and complexes.
The range of diseases associated with bacteria is rapidly expanding, among which the most relevant are Staphylococcus spp, Streptococcus spp, Listeria spp, Rothia spp, various representatives of sporobiota and others (Clinical Pharmacist, September 2017, Vol 9, No 9, online | DOI: 10.1211/CP.2017.20203363 Tetz, G., & Tetz, V. (2017) Introducing the sporobiota and sporobiome Gut Pathogens, 9:38 DOI 10.1186/s13099-017-0187-8).
The high variability of bacteria, leading to the emergence and rapid spread of resistance to antibiotics, does not allow achieving a sufficient clinical effect in the treatment of a large number of diseases caused by them of various localization. A particular problem is the spread of multiple drug resistance. This problem is especially relevant for the treatment of infections caused by MRSA and VRSA strains of Staphylococcus spp and Streptococcus spp (J Glob Infect Dis. 2010 Sep.-Dec.; 2(3): 275-283. Methicillin and Vancomycin Resistant S. aureus in Hospitalized Patients Poonam Sood Loomba, Juhi Taneja, and Bibhabati Mishra Emerging Infectious Diseases•www.cdc.gov/eid•Vol. 11, No. 10, 2005 1539-1544 Jon P. Furuno*, Eli N. Perencevich*†‡, Judith A. Johnson*†, Marc-Oliver Wright‡2, Jessina C. McGregor*, J. Glenn Morris*†, Sandra M. Strauss*, Mary-Claire Roghman*†, Lucia L. Nemoy*†, Harold C. Standiford‡, Joan N. Hebden‡, and Anthony D. Harris Methicillin-resistant Staphylococcus aureus and Vancomycin-resistant Enterococci Co-colonization DOI: 10.3201/eid1110.050508
J Hosp Infect. 2018 February; 98(2):111-117. doi: 10.1016/j.jhin. 2017.11.008. Epub 2017 Nov. 22. Staphylococcus aureus and Staphylococcus epidermidis infections on implants. Oliveira WF1, Silva PMS1, Silva RCS2, Silva GMM2, Machado G2, Coelho LCBB1, Correia MTS3. The present invention is devoted to the solution of the problem of combating bacteria with multiple resistance to existing antimicrobial drugs.
The prototype of the invention, the closest in terms of the spectrum of antimicrobial activity, was the antibiotic lincomycin, which inhibits protein synthesis in a microbial cell (https://reference.medscape.com/drug/lincocin-lincomycin-342555) Lincomycin is a product of Streptomyces lincolnensis with the following structure:
Lincomycin is a narrow-spectrum antibiotic that is active primarily against firmicute bacteria. At the same time, it has no effect on methicillin- and vancomycin-resistant strains of Staphylococcus aureus and Streptococcus spp, (MRSA and VRSA) (Appl. Microbiol. Biotechnol. 2004 May; 64(4):455-64. Epub 2004 Feb. 5. Lincomycin, clindamycin and their applications Spizek J1, Rezanka T.).
The objective of the invention is to create a new chemical compound with high antibacterial activity and high efficiency in the treatment of diseases caused by bacteria, including bacteria with multiple resistance to existing antimicrobial drugs.
According to the invention, the problem is solved by synthesizing a new antimicrobial substance of the formula (1):
Examples of the invention include all spatial isomers of the claimed substance, all its tautomeric and salt forms, complex compounds, as well as hydrated forms and adducts with organic substances.
Also proposed is a pharmaceutical composition for the treatment of diseases caused by bacteria, containing an effective amount of a compound of formula 1 or its tautomeric, hydrated form, salt, solvate, complex compound and adduct, and a pharmaceutically acceptable carrier or adjuvant.
Also proposed is the use of a compound of formula 1 for the treatment of diseases caused by bacteria, including, but not limited to, bacterial infections of the oropharynx, skin, mucous membranes, urinary system, implants, respiratory system, gastrointestinal tract, osteomyelitis, sepsis, nosocomial and wound infections, as well as to suppress the viability of bacteria that are part of biofilms.
According to another aspect of the invention, the pharmaceutical composition contains an effective amount of a compound of formula 1 in combination with at least one other antimicrobial drug.
According to the invention the compound of formula 1 is used in compositions with at least one other antimicrobial drug for the treatment of diseases caused by antibiotic-resistant strains of MRSA, VISA, VRSA.
According to another aspect of the invention, a method of treating diseases caused by bacterial infections is provided, comprising administering to a subject in need of such treatment an effective amount of a compound of formula 1 or its tautomeric, hydrated form, salt, solvate, complex compound and adduct, or a pharmaceutical composition containing it.
In a further aspect of the invention, the disease is a disease caused by staphylococci or streptococci.
In yet another further aspect of the invention, said disease is a disease caused by Staphylococcus aureus.
In another additional aspect of the invention, said disease is selected from the group including bacterial infections of the oropharynx, skin, mucous membranes, urinary system, implants, respiratory system, gastrointestinal tract, osteomyelitis, sepsis, nosocomial and wound infections.
In another aspect of the invention, the compound of formula 1 or its tautomeric, hydrated form, salt, solvate, complex compound and adduct is administered at a dosage of 0.5 mg/kg to 2000 mg/kg.
In yet another aspect of the invention, the compound of formula 1 or its tautomeric, hydrated form, salt, solvate, complex compound and adduct is administered at a dosage of from 1 mg/kg to 1500 mg/kg, more preferably from 5 mg/kg to 1000 mg/kg, even more preferably 10 mg/kg to 500 mg/kg, even more preferably 10 mg/kg to 400 mg/kg, even more preferably 10 mg/kg to 350 mg/kg, even more preferably 10 mg/kg up to 300 mg/kg, even more preferably 10 mg/kg to 250 mg/kg, even more preferably 10 mg/kg to 200 mg/kg, even more preferably 10 mg/kg to 150 mg/kg, even more preferably 10 mg/kg to 100 mg/kg.
In another aspect of the invention, the compound of formula 1 or its tautomeric, hydrated form, salt, solvate, complex compound and adduct is administered at a dosage of 0.5 mg/kg to 2 mg/kg, 1 mg/kg to 10 mg/kg, 5 mg/kg to 30 mg/kg, preferably 10 mg/kg to 100 mg/kg, even more preferably 50 mg/kg to 150 mg/kg.
In a further aspect of the invention, said compound of formula 1 or its tautomeric, hydrated form, salt, solvate, complex compound and adduct, or a pharmaceutical composition containing it, is administered enterally to a subject.
The applicant is not aware of any sources of information that would contain information about identical technical solutions, which allows us to conclude that the claimed invention complies with the “Novelty” (N) criterion.
The applicant has not identified any sources of information containing information about the impact of the claimed distinctive features on the technical result achieved as a result of their implementation. This, according to the applicant, indicates the compliance of this technical solution with the criterion of “Inventive step” (IS).
In the following, the invention is explained by a detailed description of examples of its implementation without reference to the drawings.
The claimed substance is synthesized in accordance with scheme 1.
Where X−═CH3COO− or HOOCCH2CH2COO−
The synthesis of the claimed substance 1 according to scheme 1 is carried out in one stage.
The essence of the invention is illustrated by the following examples of the synthesis of the claimed substance and its characteristics, experiments to study the biological properties and tables of the results of experiments to determine the biological properties of the claimed substance, where:
example 1—a specific variant of the synthesis of the claimed substance (Compound 1a);
example 2—a specific variant of the synthesis of the claimed substance (Compound 1a);
example 3—a specific variant of the synthesis of the claimed substance (Compound 1b);
example 4—determination of the effectiveness of the test compounds on firmicutes bacteria;
example 5—determination of the effectiveness of the test compounds on gracilicutes and wall-less bacteria;
example 6—the effect of the claimed compounds on bacterial strains with multiple resistance to antibiotics;
example 7—the effect of the claimed compound on bacteria that are part of biofilms;
example 8—study of chemotherapeutic efficacy.
example 9—clinical data on the effectiveness of the claimed compound in the treatment of tonsillitis caused by staphylococcus or streptococcus;
example 10—use of the compound in the form of a composition with other antimicrobials.
Example 1. A variant of the synthesis of the claimed substance is the preparation of 7,9-dibromo-2,4-dioxo-1,2,3,4-tetrahydrochromeno[2,3-d]-pyrimidinium-10 acetate (Compound 1a).
0.1 mol (12.8 g) of barbituric acid (2) was dissolved with heating in 270 ml of glacial acetic acid. 0.105 mol (29.4 g) of 3,5-dibromo-2-hydroxybenzaldehyde (3) was added to this solution with stirring, and the resulting reaction mixture was left at room temperature for 40 h. The resulting crystalline product was filtered off, washed with cold acetic acid, then with ether, and dried on air. 30.7 g of product 1 (Compound 1a) was obtained in the form of yellow needle-like crystals with mp 255-260 oC (decomp.). Yield 71% of theory.
Elemental analysis data. Found, %: C, 36.31; H, 2.01; Br, 36.87; N, 6.44. C13H8Br2N205. Calculated, %: C, 36.14; H, 1.97; Br, 36.99; N, 6.48.
NMR spectrum in DMSO-d6. Chemical shift, ppm (J, Hz): 7.75 d (1H, J 8.2, ArH), 7.92 d (1H, J 8.2, ArH), 8.29 s (1H, ═CH), 11.18 s (1H, NH), 11.44 (1H, NH).
mass spectrum. MH+(I, %) 391 (24), 373 (100).
Example 2. A variant of the synthesis of the claimed substance is the preparation of 7,9-dibromo-2,4-dioxo-1,2,3,4-tetrahydrochromeno[2,3-d]-pyrimidinium-10 acetate (Compound 1a).
0.1 mol (12.8 g) of barbituric acid (2) was dissolved with heating in 300 ml of glacial acetic acid. To this solution was added with stirring 0.11 mol (30.8 g) of 3,5-dibromo-2-hydroxybenzaldehyde (3) and then 0.2 mol (20.4 g) of acetic anhydride. The resulting reaction mixture was left at room temperature for 24 h. The resulting crystalline product was filtered off, washed with cold acetic acid, then with ether, and dried in air. 36.6 g of product 1 were obtained in the form of yellow needle-shaped crystals with mp 255-260 o C (with decomposition). Yield 80% of theoretical. The characteristics of the product (Compound 1a) are the same as in Example 1.
Example 3. A variant of the synthesis of the claimed substance is the preparation of 7,9-dibromo-2,4-dioxo-1,2,3,4-tetrahydrochromeno[2,3-d]-pyrimidinium-10 succinate (Compound 1b).
0.1 mol (12.8 g) of barbituric acid (2) was dissolved with heating in 300 ml of glacial acetic acid. To this solution was added with stirring 0.105 mol (29.4 g) of 3,5-dibromo-2-hydroxybenzaldehyde (3) and then 0.2 mol (20.4 g) of succinic anhydride. The resulting reaction mixture was left at room temperature for 24 h. The resulting crystalline product was filtered off, washed with ether, and dried in air. 37.8 g of product 1b were obtained in the form of yellow needle-shaped crystals with mp 250-253 o C (with decomposition). Yield 73% of theoretical.
Elemental analysis data Compounds 1b. Found, %: C, 36.39; H, 2.09; Br, 32.54; N, 5.66. C15H10Br2N207. Calculated, %: C, 36.76; H, 2.06; Br, 32.61; N, 5.72.
Example 4 Determination of the effectiveness of the test compounds against firmicutes bacteria.
Determination of the antimicrobial activity of substances was carried out on dense and liquid nutrient media. To assess the minimum inhibitory concentration (MIC), the serial dilution method was used, according to the recommendations of CLSI (Clinical Laboratories and Standards Institute, formerly National Committee for Clinical Laboratory Standards) (Clinical Laboratories and Standards Institute. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically; Approved Standard—Seventh Edition Document M7-A7 CLSI, Wayne, Pa., 2006; Clinical Laboratories and Standards Institute).
The assessment of the antimicrobial activity of substances against firmicute bacteria was performed on fresh clinical isolates of strains of Streptococcus pyogenes, Streptococcus mitis, Bacillus subtilis, Bacillus cereus, Corynebacterium ulcerans, Micrococcus luteus.
S.
aureus
S
S.
B.
B.
L.
C.
M.
pyogenes
mitis
subtilis
cereus
monocytogenes
ulcerans
lutteus
As shown by the tests, Compound 1a and its salt have a high antimicrobial activity against firmicutes bacteria.
Example 5. Determination of the effectiveness of the test compounds on gracilicutes and wall-less bacteria.
The study of the effect on strains was performed on fresh clinical isolates of Haemophilus influenzae, Neisseria meningitides, Ureaplasma urealyticum strains, as well as on the Escherichia coli ATCC29592 strain.
E. coli
H. influenzae
N. meningitides
U. urealyticum
As can be seen from the table, the claimed Compounds 1a and 1b have antimicrobial activity against some gracilicutes and wall-less bacteria.
Example 6. The effect of the claimed compounds on bacterial strains with multiple resistance to antibiotics.
The study of the effect of Compound 1a on strains with multiple resistance to existing antibiotics was performed on fresh clinical isolates of strains: S.aureus VT-V-18, S.aureus VT-E-25 S.aureus VT-A-199 and S.aureus VT-P-82, as well as S.aureus strain American Type Culture Collection (Rockville, Md.) and strains S.aureus SA77 and S.aureus SA85,
Substance 1a is highly active at concentrations from 0.5 to 2.0 mg/kg. The efficacy of Compound 1a did not differ between methicillin/vancomycin-resistant and susceptible strains.
Example 7. The action of the claimed Compound on bacteria that are part of biofilms.
S. aureus ANCC29213 bacteria were grown in a 24-well plateau in LB medium for 24 hours at 37° C. After that, Compound 1a and lincomycin (8 wells for each preparation and control without preparations) were added to the wells at final concentrations of 10 μg/ml and incubated for 24 hours at 37° C. After incubation, the medium was removed, the biofilms were washed with a sterile solution of isotonic sodium chloride, the biofilms were removed from the bottom of the wells, resuspended in isotonic sodium chloride solution, and the number of colony forming units (CFU) was determined by the method of serial dilutions.
Substance 1a is highly active at concentrations from 0.5 to 2.0 mg/kg. The efficacy of Compound 1a did not differ between methicillin/vancomycin-resistant and susceptible strains.
Example 7. The action of the claimed Compound on bacteria that are part of biofilms. The data obtained show that Compound 1a penetrates into bacterial biofilms and reduces the number of bacteria capable of growth in them by 1000 times. The reference drug does not penetrate into bacterial biofilms and does not change the number of CFUs in them.
Example 8 Chemotherapeutic efficacy study.
To study the chemotherapeutic efficacy, a model of acute generalized infection in small animals was used. C57BL6 mice were intraperitoneally infected with Staphylococcus aureus ATCC 38591 at a dose of 1×108 microbial cells. The infectious dose was established in preliminary studies. Mice infected with the same dose of microbial culture but not treated served as controls.
The preparations were dissolved in an isotonic sodium chloride solution and substance 1a or Lincomycin was administered. 2 hours after infection, the drugs were administered
The results obtained indicate that the Compound according to the invention is highly effective in the treatment of diseases caused by staphylococcus, which in relation to human diseases means such diseases as inflammatory diseases of the oropharynx, including tonsillitis, purulent-inflammatory diseases of the skin and mucous membranes, cystitis, implant infections, osteomyelitis and sepsis, as well as pneumonia, and diseases of the gastrointestinal tract. The model used is also a reproduction of nosocomial infections resulting from diagnostic and surgical interventions.
Example 9. Clinical data on the effectiveness of the claimed compound in the treatment of tonsillitis caused by staphylococcus or streptococcus.
This pathology was chosen by us as one of the above lists to confirm the effectiveness and practical applicability of the claimed compound. The study was performed on two groups of patients, totaling 138 people, who received the drug enterally twice a day at doses from 500 mg to 2000 mg.
The compound was administered as a pharmaceutical composition containing Compound 1a in acetate form in an isotonic solution of a pharmaceutically acceptable sodium chloride carrier.
S. aureus
S. pyogenes
Thus, the effect of the claimed compound on the eradication of the pathogen is statistically significantly higher than at Phenoxymethylpenicillin, and the effect develops already on the 4th day of treatment.
The results obtained indicate that in the group of patients with tonsillitis, which is selected from the list of diseases of the possible use of the claimed compound, a high clinical efficacy of the claimed agent was registered, significantly exceeding that of the reference drug.
Example 10 Use of the Compound as a Composition with Other Antimicrobials.
The claimed compound can be used in the form of a composition with other antimicrobial drugs, and in this case it is possible to achieve a total antibacterial effect that is superior to that which can be obtained with the independent use of these drugs.
We used a strain of H. influenzae grown on a liquid nutrient medium. The minimum inhibitory concentration was determined by the method of serial dilutions.
The data obtained indicate that combinations of Compound 1a and an antibiotic taken in an amount less than its individual MIC (subinhibitory concentration) provide inhibition of growth of the test microbe.
Known materials and equipment are used to implement the invention, which, according to the applicant, determines the compliance of the invention with the criterion “Industrial applicability” (IA).
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020113508 | Apr 2020 | RU | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/RU2021/050101 | 4/14/2021 | WO |
