School of Chemistry, University of KwaZulu-Natal, Durban 4000, South Africa.
Chem Biol Drug Des. 2011 Apr;77(4):295-9. doi: 10.1111/j.1747-0285.2011.01055.x. Epub 2011 Feb 22.
The antifungal and antimicrobial activities of three pentacycloundecane (PCU) tetra-amine derivatives are reported herein. The in vitro activity of these PCU derivatives against yeasts (Candida albicans and non-albicans species) and filamentous fungi was evaluated using the Clinical and Laboratory Standards Institute (CLSI) M27-A2 and M38-A2 guidelines and the 2H-tetrazolium salt, (MTS) colorimetric method. The minimum inhibitory concentration against most of the tested clinical fungal strains for GKM8 and GKM9 derivatives ranges from 15.6 to 62.5 μg/mL while GKM11 ranged from 3.9 to 7.8 μg/mL. The GKM11 derivative was also active against fluconazole-resistant strains of fungi. The GKM11 derivative also exhibited promising activity against filamentous fungi in that it was 2.5 times more active than amphotericin B against Sporothrix schenckii. Antibacterial activity was determined using the broth microdilution method (BMM) and the iodonitrotetrazolium chloride (INT) colorimetric method. The GKM11 derivative was mainly active against Gram-positive bacteria with MIC ranging from 3.9 to 7.8 μg/mL. Activity against Gram-negative bacteria tested was limited to Escherichia coli and Elizabethkingia meningoseptica (MIC of 31 μg/mL).
本文报道了三种五环十一烷(PCU)四胺衍生物的抗真菌和抗菌活性。根据临床和实验室标准协会(CLSI)M27-A2 和 M38-A2 指南以及 2H-四唑盐(MTS)比色法,评估了这些 PCU 衍生物对酵母菌(白色念珠菌和非白色念珠菌属)和丝状真菌的体外活性。GKM8 和 GKM9 衍生物对大多数测试的临床真菌菌株的最小抑制浓度范围为 15.6 至 62.5μg/mL,而 GKM11 范围为 3.9 至 7.8μg/mL。GKM11 衍生物对真菌的氟康唑耐药株也具有活性。GKM11 衍生物对丝状真菌也表现出有希望的活性,因为它对申克孢子丝菌的活性比两性霉素 B 高 2.5 倍。使用肉汤微量稀释法(BMM)和碘硝基四唑氯化物(INT)比色法测定了抗菌活性。GKM11 衍生物主要对革兰氏阳性菌具有活性,MIC 范围为 3.9 至 7.8μg/mL。对测试的革兰氏阴性菌的活性仅限于大肠杆菌和伊丽莎白菌脑膜炎(MIC 为 31μg/mL)。