CN103393658A - Application of Sarcaboside A to medicament for treatment of bladder cancer - Google Patents

Application of Sarcaboside A to medicament for treatment of bladder cancer Download PDF

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Publication number
CN103393658A
CN103393658A CN2013102649591A CN201310264959A CN103393658A CN 103393658 A CN103393658 A CN 103393658A CN 2013102649591 A CN2013102649591 A CN 2013102649591A CN 201310264959 A CN201310264959 A CN 201310264959A CN 103393658 A CN103393658 A CN 103393658A
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sarcaboside
bladder cancer
application
medicaments
treatment
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丁圣雨
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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The invention discloses application of Sarcaboside A to preparation of medicaments for treatment of bladder cancer and belongs to the technical field of novel application of medicaments. Through in vitro MTT antineoplastic activity evaluation, it is discovered that Sarcaboside A has substantial inhibition effect on growth of a human bladder cancer cell strain T-24. Accordingly, the Sarcaboside A can be applied to preparation of medicaments for resisting bladder cancer and has good development and application prospects. The application of Sarcaboside A to preparation of medicaments for treatment of bladder cancer involved in the invention is disclosed for the first time. The Sarcaboside A has a novel skeleton type and unimaginably strong activity in inhibition of bladder cancer cells.

Description

The application of Sarcaboside A in treatment bladder cancer medicine
Technical field
The present invention relates to the new purposes of compound S arcaboside A, relate in particular to the application of Sarcaboside A in preparing the anti-bladder cancer medicine.
Technical background
Cancer is to one of disease of human life's health hazard maximum, and annual have a large amount of people to die from cancer.The research and development of cancer therapy drug are the focuses of study of pharmacy always.In antitumor drug, having 74% to be the natural product or derivatives thereof, is exactly the reasonable antitumor drug of effect clinically at present as paclitaxel and derivant thereof.Therefore, from searching anticancer compound or lead compound natural product, have great importance.
the compound S arcaboside A that the present invention relates to is one and delivered (Li in 2012, X. et al., 2012. Two New-Skeleton Compounds from Sarcandra glabra. Helvetica Chimica Acta 95 (6), 998-1002.) New skeleton compound, this compound has brand-new framework types, there is no at present the report about activity, for the purposes of the Sarcaboside A that the present invention relates in preparation treatment bladder cancer medicine, belong to open first, because framework types belongs to brand-new framework types, and its inhibition for transitional cell bladder carcinoma cell line is active unexpectedly strong, there do not is the possibility that is provided any enlightenment by other compounds, possesses outstanding substantive distinguishing features, control for bladder cancer simultaneously obviously has significant progress.
Summary of the invention
The invention provides the application of compound S arcaboside A in preparing antitumor drug.
The present invention adopts following technical scheme: the application of Sarcaboside A in preparing the anti-bladder cancer medicine, and the structural formula of Sarcaboside A is as shown in formula I:
Figure BDA0000341847511
Formula I
The present invention finds by external MTT anti-tumor activity evaluation, and Sarcaboside A also has significant inhibitory action to the growth of human bladder cancer cell's strain T-24, suppresses the IC of this 1 strain Growth of Cells 50Value is respectively 0.14 ± 0.03 μ M.Therefore, Sarcaboside A can, for the preparation of the anti-bladder cancer medicine, have good development prospect.
The purposes of the Sarcaboside A that the present invention relates in preparation treatment bladder cancer medicine belongs to open first, because framework types belongs to brand-new framework types, and its inhibition for transitional cell bladder carcinoma cell line is active unexpectedly strong, there do not is the possibility that is provided any enlightenment by other compounds, possess outstanding substantive distinguishing features, the control for bladder cancer 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 subjected to any restriction of specific embodiment, but be limited by claim.
The specific embodiment
The preparation method of compound S arcaboside A involved in the present invention is referring to document (Li, X. et al., 2012. Two New-Skeleton Compounds from Sarcandra glabra. Helvetica Chimica Acta 95 (6), 998-1002.).
The present invention is further detailed explanation by the following examples, but protection scope of the present invention is not subjected to any restriction of specific embodiment, but be limited by claim.
Embodiment 1: the preparation of compound S arcaboside A tablet involved in the present invention:
Get 20 and digest compound Sarcaboside A, add conventional adjuvant 180 grams that prepare tablet, mix, conventional tablet machine is made 1000.
Embodiment 2: the preparation of compound S arcaboside A capsule involved in the present invention:
Get 20 and digest compound Sarcaboside A, add the conventional adjuvant such as starch 180 grams that prepare capsule, 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 Sarcaboside A to human bladder cancer cell's strain
1. method: the cell that is in the growth logarithmic (log) phase: human bladder cancer cell's strain T-24(buys from Chinese Academy of Sciences's cell bank) with 1.5 * 10 4The concentration 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 that contain 10% hyclone; It is 100 μ M that the replacing of drug treating group contains concentration, 50 μ M, 10 μ M, 1 μ M, 0.1 μ M, 0.01 μ M, 0.001 μ M, the culture medium of the Sarcaboside A of 0.0001 μ M and 0.00001 μ M.After cultivating 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 the 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: Sarcaboside A has significant inhibitory action to the growth of human bladder cancer cell's strain T-24.This compound suppresses the IC of human bladder cancer cell's strain T-24 growth 50Value is: 0.14 ± 0.03 μ M.
By above-described embodiment, shown, Sarcaboside A of the present invention has good inhibitory action to the growth of human bladder cancer cell's strain T-24.Prove thus, Sarcaboside A of the present invention has the anti-bladder cancer activity, can be for the preparation of the anti-bladder cancer medicine.

Claims (1)

1.Sarcaboside the application of A in treatment bladder cancer medicine, described compound S arcaboside A structure as Formula IShown in:
Figure DEST_PATH_IMAGE001
Formula I.
CN2013102649591A 2013-06-27 2013-06-27 Application of Sarcaboside A to medicament for treatment of bladder cancer Pending CN103393658A (en)

Priority Applications (1)

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CN2013102649591A CN103393658A (en) 2013-06-27 2013-06-27 Application of Sarcaboside A to medicament for treatment of bladder cancer

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Application Number Priority Date Filing Date Title
CN2013102649591A CN103393658A (en) 2013-06-27 2013-06-27 Application of Sarcaboside A to medicament for treatment of bladder cancer

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CN103393658A true CN103393658A (en) 2013-11-20

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CN (1) CN103393658A (en)

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Application publication date: 20131120