CN103462964B - Incarviatone A在制备治疗胆管癌药物中的应用 - Google Patents

Incarviatone A在制备治疗胆管癌药物中的应用 Download PDF

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CN103462964B
CN103462964B CN201310432528.1A CN201310432528A CN103462964B CN 103462964 B CN103462964 B CN 103462964B CN 201310432528 A CN201310432528 A CN 201310432528A CN 103462964 B CN103462964 B CN 103462964B
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incarviatone
medicine
bile duct
cancer
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CN103462964A (zh
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张红丽
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Anhui Bodhi biological medicine science and Technology Co Ltd
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Wenzhou Chengqiao Technology Co ltd
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Abstract

本发明公开了Incarviatone？A在制备治疗人胆管癌药物中的应用，属于药物新用途技术领域。本发明通过体外MTT抗肿瘤活性评价发现，Incarviatone？A对人胆管癌细胞株RBE的生长也具有显著的抑制作用。因此，Incarviatone？A能用于制备抗胆管癌药物，具有良好的开发应用前景。对于本发明涉及的Incarviatone？A在制备治疗人胆管癌药物中的用途属于首次公开，由于骨架类型属于全新的骨架类型，而且其对于人胆管癌细胞的抑制活性强得意想不到。

Description

Incarviatone A在制备治疗胆管癌药物中的应用
技术领域
本发明涉及化合物IncarviatoneA的新用途，尤其涉及IncarviatoneA在制备抗胆管癌药物中的应用。
技术背景
癌症是对人类生命健康危害最大的疾病之一，每年都有大量的人死于癌症。抗癌药物的研发一直是药学研究的热点。抗肿瘤药物中有74％是天然产物或其衍生物，如紫杉醇及其衍生物就是目前临床上应用效果比较好的抗肿瘤药物。因此，从天然产物中寻找抗癌化合物或先导化合物具有重要的意义。
本发明涉及的化合物IncarviatoneA是一个2012年发表(Shen,Y.H.etal.,2012.IncarviatoneA,astructurallyuniquenaturalproducthybridwithanewcarbonskeletonfromIncarvilleadelavayi,anditsabsoluteconfigurationviacalculatedelectroniccirculardichroicspectra.RSCAdvances2,4175–4180.)的新骨架化合物，该化合物拥有全新的骨架类型，目前没有关于该化合物活性方面的报道，对于本发明涉及的在制备治疗胆管癌药物中的用途属于首次公开，由于骨架类型属于全新的骨架类型，而且其对于胆管癌细胞的抑制活性强得意想不到，不存在由其他化合物给出任何启示的可能，具备突出的实质性特点，同时用于胆管癌的防治显然具有显著的进步。
发明内容
本发明提供化合物IncarviatoneA在制备抗肿瘤药物中的应用。
本发明采用如下技术方案：IncarviatoneA在制备抗胆管癌药物中的应用，IncarviatoneA的结构式如式(Ⅰ)所示：
本发明通过体外MTT抗肿瘤活性评价发现，IncarviatoneA对人胆管癌细胞株RBE的生长也具有显著的抑制作用，抑制这1株细胞生长的IC50值为1.19±0.12μM。因此，IncarviatoneA能用于制备抗胆管癌药物，具有良好的开发应用前景。
本发明涉及的IncarviatoneA在制备治疗胆管癌药物中的用途属于首次公开，由于骨架类型属于全新的骨架类型，而且其对于胆管癌细胞的抑制活性强得意想不到，不存在由其他化合物给出任何启示的可能，具备突出的实质性特点，同时用于胆管癌的防治显然具有显著的进步。
以下通过实施例对本发明作进一步详细的说明，但本发明的保护范围不受具体实施例的任何限制，而是由权利要求加以限定。
具体实施方式
本发明所涉及化合物IncarviatoneA的制备方法参见文献(Shen,Y.H.etal.,2012.IncarviatoneA,astructurallyuniquenaturalproducthybridwithanewcarbonskeletonfromIncarvilleadelavayi,anditsabsoluteconfigurationviacalculatedelectroniccirculardichroicspectra.RSCAdvances2,4175–4180.)。
以下通过实施例对本发明作进一步详细的说明，但本发明的保护范围不受具体实施例的任何限制，而是由权利要求加以限定。
实施例1：本发明所涉及化合物IncarviatoneA片剂的制备：
取20克化合物IncarviatoneA，加入制备片剂的常规辅料180克，混匀，常规压片机制成1000片。
实施例2：本发明所涉及化合物IncarviatoneA胶囊剂的制备：
取20克化合物IncarviatoneA，加入制备胶囊剂的常规辅料如淀粉180克，混匀，装胶囊制成1000片。
下面通过药效学实验来进一步说明其药物活性。
实验例：采用MTT法评价化合物IncarviatoneA对人胆管癌细胞株的生长抑制作用
1.方法：处于生长对数期的细胞：人胆管癌细胞株RBE(购买自中国科学院细胞库)以1.5×104浓度种于96孔板中。细胞培养24h贴壁后吸去原来的培养基。试验分为空白对照组、药物处理组。空白组更换含10％胎牛血清的1640培养基；药物处理组更换含浓度为100μM，50μM，10μM，1μM，0.1μM，0.01μM和0.001μM的IncarviatoneA的培养基。培养48h后，加入浓度5mg/mL的MTT，继续放于CO2培养箱培养4h，然后沿着培养液上部吸去100μL上清，加入100μLDMSO，暗处放置10min，利用酶标仪(Sunrise公司产品)测定吸光值(波长570nm)，并根据吸光值计算细胞存活情况，每个处理设6个重复孔。细胞存活率(％)＝ΔOD药物处理/ΔOD空白对照×100。
2.结果：IncarviatoneA对人胆管癌细胞株RBE的生长具有显著的抑制作用。该化合物抑制人胆管癌细胞株RBE生长的IC50值为：1.19±0.12μM。
由上述实施例表明，本发明的IncarviatoneA对人胆管癌细胞株RBE的生长具有很好的抑制作用。由此证明，本发明的IncarviatoneA具有抗胆管癌活性，能用于制备抗胆管癌药物。

Claims (1)

1.IncarviatoneA在制备治疗胆管癌药物中的应用，所述化合物IncarviatoneA结构如式（Ⅰ）所示：
式（Ⅰ）。
CN201310432528.1A 2013-09-22 2013-09-22 Incarviatone A在制备治疗胆管癌药物中的应用 Expired - Fee Related CN103462964B (zh)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005021496A2 (en) * 2003-08-27 2005-03-10 The Trustees Of Columbia University In The City Of New York Synthesis of derivatives of ginkgolide c
EP1939166A1 (en) * 2006-12-19 2008-07-02 InterMed Discovery GmbH Plants extracts for use in brain modulation

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005021496A2 (en) * 2003-08-27 2005-03-10 The Trustees Of Columbia University In The City Of New York Synthesis of derivatives of ginkgolide c
EP1939166A1 (en) * 2006-12-19 2008-07-02 InterMed Discovery GmbH Plants extracts for use in brain modulation

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ncarviatone A,a structurally unique natural product hybrid with a new carbon skeleton from Incarvillea delavayi,and its absolute configuration via calculated electronic circular dichroic spectra;Shen,Y.H.et al.,;《RSC ADVANCES》;20121231;4175-4180 *

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