Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Application of N-(5-bromo-2-methoxyphenyl)benzoimidazothiazole carboxamide

A technology of methoxyphenyl and methylbenzene, which is applied in the application field of thiazole compounds, can solve the serious problems of caries prevention, achieve the inhibition of the formation of streptococcus mutans planktonic cells and biofilms, and have broad application prospects. strong inhibitory effect

Inactive Publication Date: 2018-10-23
SHANDONG UNIV
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, with the large and long-term use of fluoride, Streptococcus mutans has begun to develop fluoride resistance (Hoelscher and Hudson, 1996), which makes the situation of caries prevention more severe

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Application of N-(5-bromo-2-methoxyphenyl)benzoimidazothiazole carboxamide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0015] Example 1: Preparation of N-(5-bromo-2-methoxyphenyl)-3-methylbenzo[4,5]imidazo[2,1-b]thiazole-2-carboxamide

[0016] (1) Preparation of 2-mercaptobenzimidazole

[0017] Place o-phenylenediamine (21.61g, 0.20mol), carbon disulfide (18.24g, 0.24mol), sodium carbonate (14.84g, 0.14mol) and 300mL of water in a 500mL eggplant-shaped bottle, and heat to reflux for 7 hours. Cool to room temperature, suction filter, and dry to obtain 29.4 g of white solid, yield 98.0%.

[0018] m.p.290-292℃(lit.:303-305℃), ESI-MS(m / z):151.1([M+H]+);

[0019] IR(KBr):υ3441,3153,3114,2979,2877,1618,1513,1467,1215;

[0020] 1 H-NMR (400MHz, DMSO): δ7.10~7.15 (m, 4H), 12.51 (s, 2H).

[0021] (2) Preparation of ethyl 2-((1H-benzo[d]imidazol-2-yl)mercapto)-3-oxybutanoate

[0022] Put 2-mercaptobenzimidazole (18.00g, 0.12mol), sodium bicarbonate (30.24g, 0.36mol), ethyl 2-chloroacetoacetate (22.96g, 0.14mol) and 200mL of ethanol in a 1000mL eggplant-shaped flask , after stirring at room tempera...

Embodiment 2

[0048] Embodiment 2: the cultivation of Streptococcus mutans

[0049] (1) The medium for cultivating Streptococcus mutans is Brain Heart Infusion medium (brand OXOID, product number CM1135). The main components of the medium are Brain infusion solids 12.5g / L, Beef heartinfusion solids 5.0g / L , Proteose peptone 10.0g / L, Glucose 2.0g / L, Sodiumchloride 5.0g / L, Di-sodium phosphate 2.5g / L, pH 7.4±0.2. If it needs to be configured into a solid, 15g / L of agar powder needs to be added. Sterilize at 115°C for 30 minutes and cool down for use.

[0050] (2) The medium for cultivating Streptococcus mutans biofilm is brain heart infusion-sucrose medium, that is, sucrose with a final concentration of 1% is added to the brain heart infusion medium. Sucrose needs to be made into 20% stock solution in advance and sterilized by filtering with a 0.22 μm sterile filter.

[0051] (3) Streptococcus mutans type strain UA159 and Streptococcus mutans strain UA246 isolated from the oral cavity of de...

Embodiment 3

[0054] Example 3: N-(5-bromo-2-methoxyphenyl)-3-methylbenzo[4,5]imidazo[2,1-b]thiazole-2-carboxamide compound on deformed chain Viability detection of cocci planktonic cells

[0055] (1) According to the method described in Example 1, N-(5-bromo-2-methoxyphenyl)-3-methylbenzo[4,5]imidazo[2,1-b]thiazole- 2-formamide, accurately weigh the compound with an analytical balance, and add DMSO to dissolve it, then filter and sterilize it with a sterile filter with a pore size of 0.22 μm, and make a stock solution with a final concentration of 1024 mg / L, and store it in - 20°C for use;

[0056] Prepare Streptococcus mutans UA159 and UA246 bacterium liquid according to the method described in embodiment 2, it is cultivated to logarithmic phase and makes Streptococcus mutans bacterium liquid OD 600 nm=0.8~1.0, diluted with brain heart infusion medium to a final concentration of 5×10 5 cfu / ml for use.

[0057] (2) Detection of N-(5-bromo-2-methoxyphenyl)-3-methylbenzo[4,5]imidazo[2,1-...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
concentrationaaaaaaaaaa
Login to View More

Abstract

The invention discloses an application of N-(5-bromo-2-methoxyphenyl)benzoimidazothiazole carboxamide in preparation of drugs for inhibiting and killing streptococcus mutans type strains or in preparation of drugs for inhibiting formation of a streptococcus mutans type strain biofilm. Experiments prove that the compound shows good bacteriostatic and bactericidal activities against the streptococcus mutans type strains in a floating state, and the inhibition rate of the compound to the streptococcus mutans biofilm reaches 99% or more when the final concentration of the compound in a culture medium reaches 4 mg / L. The compound can be used as a novel lead compound for preventing dental caries, and has broad application prospects in preparation of oral streptococcus mutans biofilm inhibitors.

Description

technical field [0001] The present invention relates to the application of a thiazole compound, in particular to a kind of N-(5-bromo-2-methoxyphenyl)-3-methylbenzo[4,5]imidazo[2,1-b ] Application of thiazole-2-carboxamide in the preparation of drugs for inhibiting and killing Streptococcus mutans (Streptococcus mutans). Background technique [0002] Dental caries, commonly known as caries and tooth decay, is characterized by the demineralization of enamel and dentin and the decomposition of organic matter. It is a worldwide chronic disease induced by bacteria and is especially common in adolescents and children. Due to its high incidence and wide prevalence, dental caries has become one of the major oral diseases that seriously endanger human health (Pitts, 2004). Under normal circumstances, the microorganisms in the oral cavity are in a relatively stable physiological balance on the tooth surface, once this balance is broken, dental caries will be induced (Selwitz et al.,...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A61K31/429A61P31/04
CPCA61K31/429A61P31/04
Inventor 张尚立宋超马剑峰
Owner SHANDONG UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products