CN106389404A - Applications of Linderolide H in preparing medicines for treating rhinitis - Google Patents

Applications of Linderolide H in preparing medicines for treating rhinitis Download PDF

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Publication number
CN106389404A
CN106389404A CN201610803401.XA CN201610803401A CN106389404A CN 106389404 A CN106389404 A CN 106389404A CN 201610803401 A CN201610803401 A CN 201610803401A CN 106389404 A CN106389404 A CN 106389404A
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CN
China
Prior art keywords
linderolide
rhinitis
applications
treating rhinitis
treating
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.)
Pending
Application number
CN201610803401.XA
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Chinese (zh)
Inventor
田丽华
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Zibo Qidingli Patent Information Consulting Co Ltd
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Zibo Qidingli Patent Information Consulting Co Ltd
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Application filed by Zibo Qidingli Patent Information Consulting Co Ltd filed Critical Zibo Qidingli Patent Information Consulting Co Ltd
Priority to CN201610803401.XA priority Critical patent/CN106389404A/en
Publication of CN106389404A publication Critical patent/CN106389404A/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention relates to Linderolide H for treating immune inflammation, used for preparing medicines for treating immune inflammation, especially the medicines for treating rhinitis. According to the applications, terfenadine and diclofenac sodium are taken as contrasts, the curative effects of Linderolide H are definite, the applications of Linderolide H in preparing medicines for treating rhinitis are disclosed for the first time, the skeleton type belongs to the brand-new skeleton type, and Linderolide H has strong activity in treating rhinitis, has the outstanding substantive features, and obviously has the remarkable progress in preventing and treating rhinitis.

Description

Application in preparation treatment rhinitis medicine for the Linderolide H
Technical field
The present invention relates to the new application of compound L inderolide H, more particularly, to Linderolide H are in preparation treatment Application in rhinitis medicine.
Background technology
Rhinitis is common clinical and frequently-occurring disease, and the generation of rhinitis is mainly relevant with anaphylaxiss, belongs to immune inflammation Category.At present, treatment rhinitis mainly adopts the antiallergic agents such as antihistamine drug or tranilast, ketotifen such as teldane Thing, these medicines are poor or invalid to the chronicity of rhinitis and recurrent exerbation curative effect.Therefore, definite ingredients, quality controllable and peace Efficient micromolecular compound, in terms of developing treatment of rhinitis medicine, has potential value entirely.
Compound L inderolide H according to the present invention be one deliver within 2012 (Qing Liu, et al., Sesquiterpene lactones from the roots of Lindera Strychnifolia.Phytochemistry, 87 (2013) 112 118.) noval chemical compound, this compound has brand-new bone Frame type, is only capable of suppressing tumor cell proliferation (Qing Liu, et al., Sesquiterpene lactones from the Roots of Lindera strychnifol ia.Phytochemistry, 87 (2013) 112 118.), according to the present invention Purposes in preparation treatment rhinitis medicine for the Linderol ide H belongs to first public.
Content of the invention
It is an object of the invention to not finding in studying according to existing Linderolide H that it has the report of anti-rhinitis activity The present situation in road, there is provided application in preparing anti-rhinitis medicament thing for the Linderolide H.
Described compound L inderolide H, structure is as shown in formula I:
Linderolide H 10,20mg/kg oral administration, nose that rat caused by antigen (ovalbumin) and histamine is scratched Portion, sneeze reaction and the rising of nasal cavity vascular permeability are inhibited, therefore, can be used for preparing the medicine for the treatment of rhinitis.
Purposes in preparation treatment rhinitis medicine for the Linderolide H belongs to first public, because framework types belong to Brand-new framework types, and its treatment rhinitis activity is strong, possesses prominent substantive distinguishing features, the preventing and treating being simultaneously used for rhinitis shows So have and significantly improve.
The present invention is further detailed explanation by the following examples, but protection scope of the present invention is not subject to concrete reality Apply any restriction of example, but be defined in the claims.
Specific embodiment
The preparation method of compound L inderolide H involved in the present invention referring to document (Qing Liu, et al., Sesquiterpene lactones from the roots of Lindera strychnifolia.Phytochemistry,87(2013)112–118.)
The present invention is further detailed explanation by the following examples, but protection scope of the present invention is not subject to concrete reality Apply any restriction of example, but be defined in the claims.
Embodiment 1:The preparation of compound L inderol ide H tablet involved in the present invention:
Take 5 g of compound Linderolide H, add 195 grams of dextrin, mix, Conventional compression makes 1000.
Embodiment 2:The preparation of compound L inderol ide H capsule involved in the present invention:
Take 5 g of compound Linderolide H, add 180 grams of starch, mix, encapsulated make 1000.
To further illustrate its pharmaceutically active below by pharmacodynamic experiment.
Experimental example 1, Linderolide H of the present invention cause the impact of rat allergic rhinitises to ovalbumin
Male SD rat, body weight 180~220g, lumbar injection ovalbumin 1mg and gel aluminum hydroxide 10mg, thereafter every Day injection 1 time, totally 7 times.Began from the 14th day, instill 1mg/ml ovalbumin normal saline solution in rat both sides nasal cavity daily 10ul, totally 7 times.Last observes rat sneeze and the number of times wiping nose in 30 minutes at once after instiling, trial drug is in white of an egg egg White last instils and is orally administered to for first 1 hour.
Table 1 Linderolide H of the present invention causes the impact (x ± SD) of rat allergic rhinitises to ovalbumin
Compare with matched group, * * P<0.01*P<0.05
From table 1, Linderolide H (10,20mg/kg) substantially suppresses allergic rhinitises rat caused by ovalbumin Sneeze and scratch nose reaction.Teldane 10mg/kg also assumes significant inhibitory action.
The impact of the rat rhinitis that experimental example 2, Linderolide H of the present invention cause to histamine
Male SD rat, body weight 180~220g, it is orally administered to 1 hour after trial drug, both sides nasal cavity instills 1M histamine Normal saline solution 10ul, observes rat sneeze and the number of times wiping nose in 30 minutes.
Table 2 Linderolide H of the present invention causes the impact (x ± SD) of rat rhinitis to histamine
Compare with matched group, * * P<0.01*P<0.05
From table 2, Linderolide H (10,20mg/kg) of the present invention significantly reduces the spray of rhinitis rat caused by histamine Sneeze number of times, the nose reaction to scratching is in suppression trend.Teldane 10mg/kg is in then significant inhibitory action.
Conclusion:Linderolide H oral administration, nose that rat caused by antigen (ovalbumin) and histamine is scratched, beats Sneeze reaction is inhibited, therefore, can be used for preparing the medicine for the treatment of rhinitis.

Claims (1)

  1. Application in treatment rhinitis medicine for the 1.Linderolide H, described compound L inderolide H structure such as formula I Shown:
CN201610803401.XA 2016-09-05 2016-09-05 Applications of Linderolide H in preparing medicines for treating rhinitis Pending CN106389404A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610803401.XA CN106389404A (en) 2016-09-05 2016-09-05 Applications of Linderolide H in preparing medicines for treating rhinitis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610803401.XA CN106389404A (en) 2016-09-05 2016-09-05 Applications of Linderolide H in preparing medicines for treating rhinitis

Publications (1)

Publication Number Publication Date
CN106389404A true CN106389404A (en) 2017-02-15

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610803401.XA Pending CN106389404A (en) 2016-09-05 2016-09-05 Applications of Linderolide H in preparing medicines for treating rhinitis

Country Status (1)

Country Link
CN (1) CN106389404A (en)

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Application publication date: 20170215