Central Research Laboratory, Institute of Medical Sciences and Sum Hospital, Siksha 'O' Anusandhan University, Kalinga Nagar, Bhubaneswar 751003, Odisha, India.
Department of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Siksha 'O' Anusandhan University, Kalinga Nagar, Bhubaneswar 751003, Odisha, India.
Biomed Pharmacother. 2017 Jun;90:760-776. doi: 10.1016/j.biopha.2017.04.030. Epub 2017 Apr 15.
Infections from multidrug resistant (MDR) pathogenic bacteria, fungi and Mycobacterium tuberculosis remain progressively intractable. The search of effective antimicrobials from other possible non-conventional sources against MDR pathogenic bacteria, fungi and mycobacteria is call of the day. This review considers 121 cyanobacterial compounds or cyano-compounds with antimicrobial activities. Chemical structures of cyano-compounds were retrieved from ChemSpider and PubChem databases and were visualized by the software ChemDraw Ultra. Chemical information on cyano-compounds pertaining to Lipinski rules of five was assessed. The reviewed cyano-compounds belong to the following chemical classes (with examples): alkaloids (ambiguine isonitriles and 12-epi-hapalindole E isonitrile), aromatic compounds (benzoic acid and cyanobacterin), cyclic depsipeptides (cryptophycin 52 and lyngbyabellin A), cyclic peptides (calophycin and tenuecyclamides), cyclic undecapeptides (kawaguchipeptins and lyngbyazothrin A), cyclophane (carbamidocyclophane), extracellular pigment (nostocine A), fatty acids (alpha-dimorphecolic acid and majusculonic acid), linear peptides (muscoride A), lipopeptides (fischerellins and scytonemin A), nucleosides (tolytoxin and tubercidin), phenols (ambigols and 4-4'-hydroxybiphenyl), macrolides (scytophycin A and tolytoxin), polyketides (malyngolide and nostocyclyne), polyphenyl ethers (crossbyanol A), porphinoids (tolyporphin J) and terpenoids (noscomin and scytoscalarol). Cyanobacteria appear to be a diverse source of compounds with antimicrobial activity. Further attention is required to elucidate whether those could be applied as pharmaceuticals.
耐多药(MDR)病原菌、真菌和结核分枝杆菌的感染仍然越来越难以治疗。从其他可能的非常规来源寻找针对 MDR 病原菌、真菌和分枝杆菌的有效抗菌药物是当务之急。本综述考虑了 121 种具有抗菌活性的蓝藻化合物或蓝藻化合物。从 ChemSpider 和 PubChem 数据库中检索蓝藻化合物的化学结构,并使用 ChemDraw Ultra 软件进行可视化。评估了与 Lipinski 五规则相关的蓝藻化合物的化学信息。综述的蓝藻化合物属于以下化学类别(有示例):生物碱(ambiguine 异腈和 12-epi-hapalindole E 异腈)、芳香族化合物(苯甲酸和 cyanobacterin)、环状脱肽(cryptophycin 52 和 lyngbyabellin A)、环状肽(calophycin 和 tenuecyclamides)、环状十一肽(kawaguchipeptins 和 lyngbyazothrin A)、环芳烷(carbamidocyclophane)、细胞外色素(nostocine A)、脂肪酸(alpha-dimorphecolic acid 和 majusculonic acid)、线性肽(muscoride A)、脂肽(fischerellins 和 scytonemin A)、核苷(tolytoxin 和 tubercidin)、酚类(ambigols 和 4-4'-hydroxybiphenyl)、大环内酯(scytophycin A 和 tolytoxin)、聚酮(malyngolide 和 nostocyclyne)、多酚(crossbyanol A)、卟啉(tolyporphin J)和萜类(noscomin 和 scytoscalarol)。蓝藻似乎是具有抗菌活性的化合物的多样化来源。需要进一步关注的是,这些化合物是否可以用作药物。