CN105198903A - Pharmaceutical composition for treating acute upper respiratory infection - Google Patents

Pharmaceutical composition for treating acute upper respiratory infection Download PDF

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Publication number
CN105198903A
CN105198903A CN201510755107.1A CN201510755107A CN105198903A CN 105198903 A CN105198903 A CN 105198903A CN 201510755107 A CN201510755107 A CN 201510755107A CN 105198903 A CN105198903 A CN 105198903A
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CN
China
Prior art keywords
pharmaceutical composition
compound
upper respiratory
acute upper
respiratory tract
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201510755107.1A
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Chinese (zh)
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CN105198903B (en
Inventor
魏芳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jiankangyuan Haibin Pharmaceutical Co.,Ltd.
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魏芳
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Priority to CN201510755107.1A priority Critical patent/CN105198903B/en
Publication of CN105198903A publication Critical patent/CN105198903A/en
Application granted granted Critical
Publication of CN105198903B publication Critical patent/CN105198903B/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems

Abstract

The invention relates to a pharmaceutical composition for treating acute upper respiratory infection. The pharmaceutical composition contains an effective quantity of a compound and a pharmaceutically acceptable vector, wherein the compound has a structure shown in the description. The compound provided by the invention has a significant effect on pathogenic bacteria causing the acute upper respiratory infection, and can be developed into a new clinically-effective pharmaceutical composition.

Description

A kind of pharmaceutical composition for the treatment of acute upper respiratory tract infection
Technical field
The present invention relates to field of medicaments, specifically, the present invention relates to a kind of pharmaceutical composition for the treatment of acute upper respiratory tract infection.
Background technology
Acute upper respiratory tract infection is current common clinical, and acute upper respiratory tract infection majority is caused by pathogenic bacterium, finds that in the recent period Klebsiella Pneumoniae ATCC700603 is also one of germ wherein.
Summary of the invention
The object of the present invention is to provide a kind of pharmaceutical composition for the treatment of acute upper respiratory tract infection.
In order to realize object of the present invention, the invention provides a kind of compound for the treatment of acute upper respiratory tract infection, this compound has having structure:
The present invention also provides a kind of pharmaceutical composition for the treatment of acute upper respiratory tract infection, and described pharmaceutical composition includes the compound of effective amount and pharmaceutically acceptable carrier, and described compound has having structure:
Preferably, described pharmaceutically acceptable carrier is thinner, disintegrating agent, tackiness agent, lubricant, stablizer or corrigent.
Preferably, described thinner is sugar derivatives, starch derivative or derivatived cellulose.
Preferably, described thinner is lactose.
Preferably, described pharmaceutical composition is powder, microgranules, granule, capsule or tablet.
The present invention also provides the purposes of compound in the medicine of preparation treatment acute upper respiratory tract infection, and this compound has having structure:
Preferably, described infection is caused by Klebsiella Pneumoniae ATCC700603.
The present invention also provides the purposes of compound in the medicine of preparation vitro inhibition Klebsiella Pneumoniae ATCC700603, and this compound has having structure:
Term used herein " pharmaceutically acceptable " refers to not eliminate the biologic activity of compound as herein described or the material of character, as carrier or thinner.This kind of material is applied to and individual does not cause undesirable biological action or not with harmful way and any component interaction comprised in its composition.
" pharmaceutically acceptable carrier " comprises any and all solvents as the term is employed herein, dispersion medium, coating material, tensio-active agent, antioxidant, sanitas (such as antiseptic-germicide, anti-mycotic agent), isotonic agent, absorption delay agent, salt, sanitas, drug stabilizing agent, tackiness agent, vehicle, disintegrating agent, lubricant, sweeting agent, correctives, dyestuff etc. and its combination, this is well-known to those skilled in the art (for example, see Remington ' sPharmaceuticalSciences, 18thEd.MackPrintingCompany, 1990, pp.1289-1329).Except with except the inconsistent carrier of activeconstituents, consider to use any conventional carrier in treatment or pharmaceutical composition.
Compound of the present invention, for the pathogenic bacteria Be very effective causing stomach and intestine, can be developed to pharmaceutical composition effectively new clinically.
Embodiment
Below by way of the description of embodiment, the invention will be further described, but this is not limitation of the present invention, those skilled in the art are according to basic thought of the present invention, various amendment or improvement can be made, but only otherwise depart from basic thought of the present invention, all within the scope of the present invention.
The research of the purposes of experimental example the compounds of this invention in the medicine of preparation vitro inhibition Klebsiella Pneumoniae ATCC700603
Bacteriostatic test
Use following compounds, adopt filter paper enzyme classical in this area to carry out bacteriostatic test, wherein:
The structural formula of target compound is:
For examination bacterial classification Klebsiella Pneumoniae ATCC700603 purchased from Bei Nuo bio tech ltd, Shanghai.
Nutrient solution
Nutrient agar medium and nutrient broth, purchased from Chen Yu experimental installation company limited of BeiJing ZhongKe.
Test method
Klebsiella Pneumoniae ATCC700603 is inoculated in agar plate nutritive medium plane, evenly gathers during inoculation.
Take target compound 0.01 gram, add 18000 ml sterile waters, ultrasonic 30 minutes, then the filtering with microporous membrane of 0.22 μm, obtained solution.The aseptic circular filter paper sheet of tweezer, sprays above-mentioned solution to complete wetting, is attached in the agar plate nutritive medium plane of inoculated bacteria.Agar plate is placed in the incubator of 37 DEG C, incubation 4 hours.Measure the diameter of bacterial restrain.Measure and average for 3 times.
1.4 result
The mean diameter of the bacterial restrain of Klebsiella Pneumoniae ATCC700603 is 13.66mm, and this shows that target compound has the effect of extremely strong vitro inhibition Klebsiella Pneumoniae ATCC700603.

Claims (9)

1. treat a compound for acute upper respiratory tract infection, it is characterized in that, this compound has having structure:
2. treat a pharmaceutical composition for acute upper respiratory tract infection, it is characterized in that, described pharmaceutical composition includes the compound of effective amount and pharmaceutically acceptable carrier, and described compound has having structure:
3. the pharmaceutical composition for the treatment of acute upper respiratory tract infection according to claim 2, is characterized in that, described pharmaceutically acceptable carrier is thinner, disintegrating agent, tackiness agent, lubricant, stablizer or corrigent.
4. the pharmaceutical composition for the treatment of acute upper respiratory tract infection according to claim 3, is characterized in that, described thinner is sugar derivatives, starch derivative or derivatived cellulose.
5. the pharmaceutical composition for the treatment of acute upper respiratory tract infection according to claim 4, is characterized in that, described thinner is lactose.
6. the pharmaceutical composition for the treatment of acute upper respiratory tract infection according to claim 3, is characterized in that, described pharmaceutical composition is powder, microgranules, granule, capsule or tablet.
7. the purposes of compound in the medicine of preparation treatment acute upper respiratory tract infection, it is characterized in that, this compound has having structure:
8. purposes according to claim 7, is characterized in that, described infection is caused by Klebsiella Pneumoniae ATCC700603.
9. the purposes of compound in the medicine of preparation vitro inhibition Klebsiella Pneumoniae ATCC700603, it is characterized in that, this compound has having structure:
CN201510755107.1A 2015-11-09 2015-11-09 A kind of pharmaceutical composition treating acute upper respiratory tract infection Active CN105198903B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510755107.1A CN105198903B (en) 2015-11-09 2015-11-09 A kind of pharmaceutical composition treating acute upper respiratory tract infection

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510755107.1A CN105198903B (en) 2015-11-09 2015-11-09 A kind of pharmaceutical composition treating acute upper respiratory tract infection

Publications (2)

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CN105198903A true CN105198903A (en) 2015-12-30
CN105198903B CN105198903B (en) 2016-08-24

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105409962A (en) * 2015-11-09 2016-03-23 胡昱 Environment-friendly disinfectant
TWI818967B (en) * 2018-03-22 2023-10-21 瑞士商赫孚孟拉羅股份公司 New heterocyclic compounds

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5350196A (en) * 1976-10-15 1978-05-08 Hisamitsu Pharmaceut Co Inc Novel 4hhpyrido *2*33d**1*3* oxazinee44one derivatives
CN103694255A (en) * 2014-01-09 2014-04-02 华中师范大学 Pyridinooxazone-pyridinopyrimidone compounds and preparation method and application thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5350196B2 (en) * 2009-11-26 2013-11-27 アルプス電気株式会社 Switch device

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5350196A (en) * 1976-10-15 1978-05-08 Hisamitsu Pharmaceut Co Inc Novel 4hhpyrido *2*33d**1*3* oxazinee44one derivatives
CN103694255A (en) * 2014-01-09 2014-04-02 华中师范大学 Pyridinooxazone-pyridinopyrimidone compounds and preparation method and application thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
高建宏: "吡啶并噁嗪酮和吡啶并嘧啶酮类化合物的合成与生物活性研究", 《中国优秀硕士学位论文全文数据库工程科技Ⅰ辑》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105409962A (en) * 2015-11-09 2016-03-23 胡昱 Environment-friendly disinfectant
TWI818967B (en) * 2018-03-22 2023-10-21 瑞士商赫孚孟拉羅股份公司 New heterocyclic compounds

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Inventor after: Dai Xianhui

Inventor after: Zhang Xuwei

Inventor before: Wei Fang

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TA01 Transfer of patent application right

Effective date of registration: 20160718

Address after: 266109 Chengyang District Qingdao people's Hospital, 600 the Great Wall Road, Chengyang District, Shandong, Qingdao

Applicant after: Dai Xianhui

Address before: 071003 Hebei Province, Baoding City area Yonghua No. 19 North Street

Applicant before: Wei Fang

C14 Grant of patent or utility model
GR01 Patent grant
CB03 Change of inventor or designer information
CB03 Change of inventor or designer information

Inventor after: Ma Anshun

Inventor before: Dai Xianhui

Inventor before: Zhang Xuwei

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Effective date of registration: 20170912

Address after: 466224, Henan, Zhoukou province Xiangcheng city government will be the town of Yang Village No. 1 hospital

Patentee after: Ma Anshun

Address before: 266109 Chengyang District Qingdao people's Hospital, 600 the Great Wall Road, Chengyang District, Shandong, Qingdao

Patentee before: Dai Xianhui

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TR01 Transfer of patent right

Effective date of registration: 20180328

Address after: 226100 Fuxing Road, yuimen Town, Haimen City, Nantong, Jiangsu Province, No. 20

Patentee after: Nantong excellent art design Co., Ltd.

Address before: 466224, Henan, Zhoukou province Xiangcheng city government will be the town of Yang Village No. 1 hospital

Patentee before: Ma Anshun

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20210526

Address after: No. 11, Jinhui Road, Kengzi street, Pingshan District, Shenzhen City, Guangdong Province

Patentee after: Jiankangyuan Haibin Pharmaceutical Co.,Ltd.

Address before: 226100 Fuxing Road, Yuet Lai Town, Haimen, Nantong, Jiangsu, 20

Patentee before: NANTONG YOUYUAN ART PATTERN DESIGN Co.,Ltd.