CN102861099B - Application of Houttuynoid D in preparing medicine for treating endometrial cancer - Google Patents

Application of Houttuynoid D in preparing medicine for treating endometrial cancer Download PDF

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CN102861099B
CN102861099B CN201210419513.7A CN201210419513A CN102861099B CN 102861099 B CN102861099 B CN 102861099B CN 201210419513 A CN201210419513 A CN 201210419513A CN 102861099 B CN102861099 B CN 102861099B
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houttuynoid
endometrial cancer
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medicine
preparation
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CN102861099A (en
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黄蓉
蒋鹤松
吴俊华
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Qidong Tianfen Electric Tool Technology Innovation Center
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Abstract

The invention discloses application of Houttuynoid D in preparation of a medicine for treating endometrial cancer, belonging to the technical field of new application of medicine. The invention discovers that Houttuynoid D has the remarkable inhibitory effects on the growth of human endometrial cancer cell strains including ISK and RL95-2 through the evaluation of in vitro MTT antineoplastic activity. Therefore, Houttuynoid D can be used for preparing the anti-endometrial cancer medicine and has good development and application prospects. The application of Houttuynoid D in preparation of the medicine for treating endometrial cancer provided by the invention is disclosed firstly. The skeleton type belongs to new skeleton type, and the inhibitory activity of Houttuynoid D on endometrial cancer cells is unexpectedly strong.

Description

The application of Houttuynoid D in preparation treatment endometrium cancer drug
Technical field
The present invention relates to the new purposes of compound H outtuynoid D, relate in particular to the application of Houttuynoid D in the anti-endometrium cancer drug of preparation.
Technical background
Cancer is to one of disease of human life's health hazard maximum, has a large amount of people to die from cancer every year.The research and development of cancer therapy drug are the focuses of study of pharmacy always.In antitumor drug, have 74% to be natural product or derivatives thereof, if paclitaxel and derivant thereof are exactly the reasonable antitumor drug of effect clinically at present.Therefore, from natural product, find anticancer compound or lead compound has great importance.
The compound H outtuynoid D the present invention relates to is one and within 2012, delivers (Chen, S. D. et al., 2012. Houttuynoid D_E, Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata. Organic Letters 14 (7), 1772 – 1775.) New skeleton compound, this compound has brand-new framework types, current purposes only relates to anti-herpes simplex virus activity (Chen, S. D. et al., 2012. Houttuynoid D_E, Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata. Organic Letters 14 (7), 1772 – 1775.), purposes for the Houttuynoid D the present invention relates in preparation treatment endometrium cancer drug belongs to open first, because framework types belongs to brand-new framework types, and its inhibition for endometrial carcinoma cell is active unexpectedly strong, there is not the possibility that is provided any enlightenment by other compounds, possesses outstanding substantive distinguishing features, control for carcinoma of endometrium simultaneously obviously has significant progress.
Summary of the invention
The invention provides the application of compound H outtuynoid D in preparing antitumor drug.
The present invention adopts following technical scheme: the application of Houttuynoid D in the anti-endometrium cancer drug of preparation, and the structural formula of Houttuynoid D is as shown in formula I:
Figure BDA0000231838081
Formula I
The present invention finds by the evaluation of external MTT anti-tumor activity, and Houttuynoid D also has significant inhibitory action to the growth of people's Endometrial carcinoma cell line ISK and RL95-2, suppresses the IC of this 2 strain Growth of Cells 50value is respectively 0.19 ± 0.09 μ M and 0.23 ± 0.06 μ M.Therefore, Houttuynoid D can, for the preparation of anti-endometrium cancer drug, have good development prospect.
The purposes of the Houttuynoid D the present invention relates in preparation treatment endometrium cancer drug belongs to open first, because framework types belongs to brand-new framework types, and its inhibition for endometrial carcinoma cell is active unexpectedly strong, there is not the possibility that is provided any enlightenment by other compounds, possess outstanding substantive distinguishing features, the control for carcinoma of endometrium simultaneously obviously has significant progress.
The present invention is further detailed explanation by the following examples, but protection scope of the present invention is not subject to any restriction of specific embodiment, but be limited by claim.
The specific embodiment
The preparation method of compound H outtuynoid D involved in the present invention is referring to document (Chen, S. D. et al., 2012. Houttuynoid D_E, Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata. Organic Letters 14 (7), 1772 – 1775.).
The present invention is further detailed explanation by the following examples, but protection scope of the present invention is not subject to any restriction of specific embodiment, but be limited by claim.
Embodiment 1: the preparation of compound H outtuynoid D tablet involved in the present invention:
Get 20 and digest compound Houttuynoid D, add 180 grams of conventional adjuvants preparing tablet, mix, conventional tablet machine is made 1000.
Embodiment 2: the preparation of compound H outtuynoid D capsule involved in the present invention:
Get 20 and digest compound Houttuynoid D, add the conventional adjuvant of preparing capsule as 180 grams of starch, mix, encapsulatedly make 1000.
Below by pharmacodynamic experiment, further illustrate its pharmaceutically active.
Experimental example: adopt the growth inhibited effect of mtt assay assessing compound Houttuynoid D to people's Endometrial carcinoma cell line
1. method: the cell in growth logarithmic (log) phase: people's Endometrial carcinoma cell line ISK and RL95-2(buy from Chinese Academy of Sciences's cell bank) with 1.5 * 10 4concentration kind is in 96 orifice plates.After cell culture 24 h are adherent, suck original culture medium.Test is divided into blank group, drug treating group.Blank group is changed 1640 culture medium containing 10% hyclone; It is 100 μ M that drug treating group is changed containing concentration, 50 μ M, 10 μ M, 1 μ M, 0.1 μ M, the culture medium of the Houttuynoid D of 0.01 μ M and 0.001 μ M.Cultivate after 48 h, add the MTT of concentration 5mg/mL, continue to be put in CO 2incubator is cultivated 4 h, then along culture fluid top, suck 100 μ L supernatants, add 100 μ L DMSO, 10 min are placed in dark place, utilize microplate reader (Sunrise company product) to measure light absorption value (wavelength 570nm), and calculating cell survival situation according to light absorption value, 6 repeating holes are established in each processing.Cell survival rate (%)=Δ OD drug treating/ Δ OD blank* 100.
2. result: Houttuynoid D has significant inhibitory action to the growth of people's Endometrial carcinoma cell line ISK and RL95-2.This compound suppresses the IC of people Endometrial carcinoma cell line ISK and RL95-2 growth 50value is respectively: 0.19 ± 0.09 μ M and 0.23 ± 0.06 μ M.
By above-described embodiment, shown, Houttuynoid D of the present invention has good inhibitory action to the growth of people's Endometrial carcinoma cell line ISK and RL95-2.Prove thus, it is active that Houttuynoid D of the present invention has anti-carcinoma of endometrium, can be for the preparation of anti-endometrium cancer drug.

Claims (1)

  1. The application of 1.Houttuynoid D in preparation treatment endometrium cancer drug, described compound H outtuynoid D structure as formula Ishown in:
    Figure 565757DEST_PATH_IMAGE001
    formula I.
CN201210419513.7A 2012-10-27 2012-10-27 Application of Houttuynoid D in preparing medicine for treating endometrial cancer Active CN102861099B (en)

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Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105287521A (en) * 2015-11-05 2016-02-03 淄博齐鼎立专利信息咨询有限公司 Application of Nagelamides Y in preparation of endometrial cancer treating medicine

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata;Shao-Dan Chen et al.;《Organic Letters》;20120313;第14卷(第7期);第1772-1775页 *
Shao-Dan Chen et al..Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata.《Organic Letters》.2012,第14卷(第7期),第1772-1775页.

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