共查询到20条相似文献,搜索用时 15 毫秒
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Nanyu Jiang Xiaomin Zhang Hong Hu Hongming Pan Da Li 《Clinical and experimental pharmacology & physiology》2017,44(11):1077-1082
Marine organisms are an important source of antitumour active substances. Thus, pharmaceutical research in recent years has focused on exploring new antitumour drugs derived from marine organisms, and, many peptide drugs with strong antitumour activities have been successfully extracted. Based on different mechanisms, this paper reviews the research on several typical antitumour bioactive peptides in marine drugs and the latest progress therein. Additionally, the development prospects for these antitumour bioactive peptide‐based drugs are discussed so as to provide a reference for future research in this field. 相似文献
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海洋生物活性肽及其生物活性研究进展 总被引:12,自引:0,他引:12
概述存在于海绵、海鞘等海洋低等生物和海洋鱼贝类中的生物活性肽,以及这些活性肽的抗肿瘤、抗菌、抗高血压及抗氧化等生物活性的研究进展。 相似文献
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Actinobacteria are quotidian microorganisms in the marine world, playing a crucial ecological role in the recycling of refractory biomaterials and producing novel secondary metabolites with pharmaceutical applications. Actinobacteria have been isolated from the huge area of marine organisms including sponges, tunicates, corals, mollusks, crabs, mangroves and seaweeds. Natural products investigation of the marine actinobacteria revealed that they can synthesize numerous natural products including alkaloids, polyketides, peptides, isoprenoids, phenazines, sterols, and others. These natural products have a potential to provide future drugs against crucial diseases like cancer, HIV, microbial and protozoal infections and severe inflammations. Therefore, marine actinobacteria portray as a pivotal resource for marine drugs. It is an upcoming field of research to probe a novel and pharmaceutically important secondary metabolites from marine actinobacteria. In this review, we attempt to summarize the present knowledge on the diversity, chemistry and mechanism of action of marine actinobacteria-derived secondary metabolites from 2007 to 2016. 相似文献
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海洋抗肿瘤活性蛋白与多肽的研究进展 总被引:9,自引:1,他引:9
海洋是人类赖以生存的资源宝库,海洋生物的多样性和特殊性,为人类提供了许多结构新颖、功能独特的生理活性物质。本文就具有抗肿瘤作用的海洋生物活性蛋白与多肽的研究现状作一概述。 相似文献
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Recent updates of marine antimicrobial peptides 总被引:1,自引:0,他引:1
Mohammad H. Semreen Mohammed I. El-Gamal Shifaa Abdin Hajar Alkhazraji Leena Kamal Saba Hammad Faten El-Awady Dima Waleed Layal Kourbaj 《Saudi Pharmaceutical Journal》2018,26(3):396-409
Antimicrobial peptides are group of proteins showing broad-spectrum antimicrobial activity that have been known to be powerful agents against a variety of pathogens. This class of compounds contributed to solving the microbial resistance dilemma that limited the use of many potent antimicrobial agents. The marine environment is known to be one of the richest sources for antimicrobial peptides, yet this environment is not fully explored. Hence, the scientific research attention should be directed toward the marine ecosystem as enormous amount of useful discoveries could be brought to the forefront. In the current article, the marine antimicrobial peptides reported from mid 2012 to 2017 have been reviewed. 相似文献
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Abstract: A number of peptide analogs derived from the N‐terminal α‐helical region of bovine lactoferrin (LFB 14–31), were designed in order to investigate how deviating numbers and positions of positively charged residues and numbers of aromatic residues affected their activity against prokaryotic, normal and transformed eukaryotic cells. Most of the LFB derivatives were highly active against both Escherichia coli and Staphylococcus aureus. The peptides were more active against the tumor cell lines MethA, HT‐29 and MT‐1 than normal eukaryotic cells. The peptides that were most active against the tumor cell lines had all cationic residues concentrated in one sector of the helical structure. These peptides were less selective against the tumor cell lines than against normal fibroblasts. Quantitative structure?activity relationship studies showed that certain structural parameters affected toxicity against the tumor cell lines more than against fibroblasts. Peptides encompassing these parameters were slightly less active against tumor cells, but gained significant selectivity. 相似文献
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海洋放线菌M326活性代谢产物的初步研究 总被引:8,自引:1,他引:8
目的对海洋放线菌M326活性代谢产物进行初步研究。方法以抑菌活性为指标,采用不同的培养基与培养时间研究代谢产物活性与培养条件的关系,用不同温度、pH处理了解活性产物的稳定性,用有机溶剂,大孔树脂对活性物质进行提取分离。结果人工海水、蒸馏水配制的GBP培养基产物活性较强。抗菌物质在pH 2~11时较稳定,强酸性条件下热稳定性好,难以用一般有机溶剂萃取,碱性条件下可被AB-8大孔树脂吸附。结论代谢产物对G 菌有较强的抑菌活性,对G-菌、耐药菌均有不同程度的抑菌活性,且抗菌物质的极性较强。 相似文献
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Jian-Wei Chen Qi-Hao Wu David C. Rowley Ammar M.Q. Al-Kareef 《Journal of Asian natural products research》2013,15(2):199-216
Marine natural products constitute a huge reservoir of anticancer agents. Consequently during the past decades, several marine anticancer compounds have been isolated, identified, and approved for anticancer treatment or are under trials. In this article the sources, structure, bioactivities, mode of actions, and analogs of some promising marine and derived anticancer compounds have been discussed. 相似文献
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几类重要的海洋抗肿瘤药物研究进展 总被引:7,自引:0,他引:7
目前对海洋抗肿瘤药物的研究已经成为全世界普遍关注的热点。近年来,苔藓抑素、ecteinascidin-743、海兔毒肽、膜海鞘素、psammaplin、软海绵素B等六类化合物的研究取得了较大进展。本文综述这几类海洋抗肿瘤药物及其衍生物的研究进展,并探讨海洋抗肿瘤药物发展的趋势。 相似文献
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SONG YUB SHIN MYUNG KYU LEE KIL LYONG KIM KYUNG-SOO HAHM 《Chemical biology & drug design》1997,50(4):279-285
The hybrid peptide (CA-ME) derived from cecropin A(1–8) and melittin(1–12) has potent antibacterial and antimalarial activities. Because the N-terminal sequence 1–12 of magainin 2 is similar to melittin(1–12), CA-MA with CA(1–8) and MA(1–12) and their analogues were designed and synthesized. Antitumor activities of these peptides were evaluated using three small cell lung cancer cell lines. Greater antitumor activity was observed when the residues 16, 18 and 19 of the peptide were hydrophobic (Leu or Val), basic (Lys) and basic (Lys), respectively. The IC50 values of the peptides with the residues were 2 to 4 μm . Residue 12 was related to hemolytic activity rather than antitumor activity. Increase in amphipathicity of P4 enhanced hemolytic activity without significant change in antitumor activity. The α-helicity of the peptides in a 30 mm sodium dodecyl sulfate solution was more closely correlated to hemolytic activity than antitumor activity. 相似文献