CN106265638A - Linderolide H application in preparation treatment or preventing canker sore medicine - Google Patents

Linderolide H application in preparation treatment or preventing canker sore medicine Download PDF

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Publication number
CN106265638A
CN106265638A CN201610805945.XA CN201610805945A CN106265638A CN 106265638 A CN106265638 A CN 106265638A CN 201610805945 A CN201610805945 A CN 201610805945A CN 106265638 A CN106265638 A CN 106265638A
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CN
China
Prior art keywords
linderolide
preparation treatment
canker sore
day
application
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
CN201610805945.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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Publication date
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Priority to CN201610805945.XA priority Critical patent/CN106265638A/en
Publication of CN106265638A publication Critical patent/CN106265638A/en
Pending legal-status Critical Current

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    • 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
    • A61K31/365Lactones

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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)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The present invention relates to Linderolide H application in preparation treatment or preventing canker sore medicine.The Linderolide H that the present invention relates to purposes in preparation treatment stomatocace medicine belongs to first public, owing to framework types belongs to brand-new framework types, and its treatment oral ulcer activity is unexpectedly strong, there is not the possibility being provided any enlightenment by other compounds, possess prominent substantive distinguishing features, be simultaneously used for treating oral ulcer and obviously have the most progressive.

Description

Linderolide H application in preparation treatment or preventing canker sore medicine
Technical field
The present invention relates to the new application of compound L inderolide H, particularly relate to Linderolide H in preparation treatment Or the application in preventing canker sore medicine.
Background technology
Recurrent oral ulceration is modal disease in diseases of oral mucosa.The first place of prevalence office diseases of oral mucosa. Sircus (1975) investigates 1587 people, and prevalence is 20%.As can be seen here, oral ulcer patient is a group the hugest Body.The cause of disease of recurrent oral ulceration is complicated, the most indefinite, may infect with virus, in antibacterial infection and body The factor such as parasecretion, immune dysfunction is relevant.
The primary treatment measure of oral ulcer includes that local is treated and whole body therapeutic, due to local treatment toxic and side effects relatively Low, the people therefore having obtained people can.Although the buccal tablets that the local that occurs in recent years uses carries, easy to use, mouthfeel And compliance is preferable, such as lysozyme buccal tablet, watermelon crystal buccal tablet, cydiodine etc., but these medicines are in sterilization, antiinflammatory, pain relieving etc. just Face emphasizes particularly on different fields.
The compound L inderolide H that the present invention relates to be one within 2014, deliver (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, current purposes merely relates to parasite killing (Qing Liu, et al., Sesquiterpene lactones from the Roots of Lindera strychnifolia.Phytochemistry, 87 (2013) 112 118.), the present invention is related to And Linderolide H preparation treatment or preventing canker sore medicine in purposes belong to first public, complete owing to belonging to New structure type, and it is unexpectedly strong for treatment or preventing canker sore activity, does not exist by other compounds Provide the possibility of any enlightenment, possess prominent substantive distinguishing features, be simultaneously used for treatment or preventing canker sore obviously has aobvious The progress write.
Summary of the invention
Do not find in it is an object of the invention to study according to existing Linderolide H that it has treatment or prevention oral cavity The present situation of the report of ulcer, it is provided that Linderolide H application in preparation treatment or preventing canker sore medicine.
Described compound L inderolide H structure is as shown in formula I:
The Linderolide H that the present invention relates to purposes in preparation treatment or preventing canker sore medicine belongs to first Open, owing to framework types belongs to brand-new framework types, and its treatment or preventing canker sore activity are unexpectedly strong, There is not the possibility being provided any enlightenment by other compounds, possess prominent substantive distinguishing features, be simultaneously used for treatment or prevention Oral ulcer obviously has the most progressive.
Detailed description of the invention
The preparation method of compound L inderolide H involved in the present invention see 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 by concrete real Execute any restriction of example, but be defined in the claims.
Embodiment 1: the preparation of compound L inderolide H tablet involved in the present invention:
Take 20 g of compound Linderolide H additions and prepare the customary adjuvant 180 grams of tablet, mixing, conventional tablet presses Make 1000.
Embodiment 2: the preparation of compound L inderolide H capsule involved in the present invention:
Take 20 g of compound Linderolide H additions and prepare the customary adjuvant such as starch 180 grams of capsule, mixing, dress Capsule makes 1000.
Its pharmaceutically active is further illustrated below by pharmacodynamic experiment.
The H anti-oral ulcer experimental study of test example 1:Linderolide
1, test objective: manufacture Oral ulcer model with phenol, gives Oral ulcer model rat certain number of times every day Linderolide H, observes whether Linderolide H is reduced the effect of ulcer.
2, test medicine and reagent
Cydiodine (Beijing Sihuan Medicine Science and Technology Co., Ltd);Phenol
Animal: Wistar rat, male, body weight 240~280g
3, test method
Take rat 50, male, body weight 240~280g, 10% chloral hydrate anesthesia, dosage: 0.35ml/100g, anesthesia After plastic dropper (internal diameter: the 3mm) lower end of 90% phenol cotton balls is flat on the cheek film at rats with left bicker about 1mm, burn Burn 30min, i.e. see the white infringement of about 3mm at this.It is grouped immediately after 24 hours, often group 10, divides 5 groups, i.e. model group (adjuvant 4 times/day, not drug containing);Linderolide H high dose group (4 times/day, 0.5mg/ time);Dosage (4 in Linderolide H Times/day, 0.1mg/ time);Linderolide H low dose group (4 times/day, 0.02mg/ time);Positive controls: cydiodine group (4 Times/day, 0.5mg/ time).Linderolide H and cydiodine buccal tablet are ground into powder before use, are administered with flap coverage for degree. Successive administration 5 days, after before being administered and being administered, next day observes ulcer area size (in terms of the diameter of ulcer) and ulcer healing every time Situation (ulcer being visible by naked eyes is considered as healing), first administration to last is administered and is recorded as 1,2,3,4,5,6 days respectively.Ulcer Size t checks, and ulcer healing rate X2 checks.
4, result of the test
Ulcer area compares (table 1): Linderolide H high dose group compares with model group, within the 3rd day, plays examination from being administered Testing end, corresponding every day compares significant difference;Cydiodine group compares with model group, within the 3rd day, plays off-test from being administered, Corresponding every day compares significant difference;In Linderolide H, dosage group compares with model group, within the 3rd day, plays examination from being administered Testing end, corresponding every day compares significant difference;Linderolide H low dose group compares with model group, from being administered the 5th day Playing off-test, corresponding every day compares significant difference;In Linderolide H, dosage group compares with cydiodine group, from Being administered the 1st day and play off-test, corresponding every day compares significant difference.
The table 1 impact on rat ulcer area
Note: compare with model group, * p < 0.05, * p < 0.01.
Healing rate (table 2): model group and Linderolide H low dose group play off-test, ulcer on the 1st day from administration Not healing;And Linderolide H high dose group is from being administered the 4th day, just there is ulcer healing, to off-test, reach 90%; Cydiodine group, from being administered the 4th day, has ulcer healing, to off-test, reaches 60%;In Linderolide H, dosage group is from giving Medicine rises on the 5th day, has ulcer healing, to off-test, reaches 40%.
The table 2 impact on rat ulcer healing time
Note: compare with model group, * p < 0.05, * p < 0.01.
5, conclusion
Linderolide H has the effect being obviously promoted oral ulcer healing.

Claims (1)

1.Linderolide H application in treatment or preventing canker sore medicine, described compound L inderolide H ties Structure is as shown in formula I:
CN201610805945.XA 2016-09-07 2016-09-07 Linderolide H application in preparation treatment or preventing canker sore medicine Pending CN106265638A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610805945.XA CN106265638A (en) 2016-09-07 2016-09-07 Linderolide H application in preparation treatment or preventing canker sore medicine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610805945.XA CN106265638A (en) 2016-09-07 2016-09-07 Linderolide H application in preparation treatment or preventing canker sore medicine

Publications (1)

Publication Number Publication Date
CN106265638A true CN106265638A (en) 2017-01-04

Family

ID=57710917

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610805945.XA Pending CN106265638A (en) 2016-09-07 2016-09-07 Linderolide H application in preparation treatment or preventing canker sore medicine

Country Status (1)

Country Link
CN (1) CN106265638A (en)

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Application publication date: 20170104

WD01 Invention patent application deemed withdrawn after publication