Novel primary amine diazeniumdiolatesChemical and biological characterization

被引:8
作者
Puglisi, Melany P. [1 ]
Bradaric, Michael J. [1 ,4 ]
Pontikis, John [2 ]
Cabai, Jonathan [2 ]
Weyna, Theodore [2 ]
Tednes, Patrick [2 ]
Schretzman, Robert [2 ]
Rickert, Karl [2 ]
Cao, Zhao [3 ]
Andrei, Daniela [2 ]
机构
[1] Chicago State Univ, Dept Pharmaceut Sci, Chicago, IL USA
[2] Dominican Univ, Dept Chem, River Forest, IL 60305 USA
[3] Leidos Biomed Res Inc, Basic Res Program, Frederick Natl Lab Canc Res, Frederick, MD USA
[4] Rush Univ, Dept Cell & Mol Med, Coll Med, Chicago, IL 60612 USA
关键词
primary amine diazeniumdiolates; HNO; NO donors; Fusarium; ovarian cancer; synthesis; DETERRENT AGENT CYANAMIDE; FUSARIUM HEAD BLIGHT; NITRIC-OXIDE; NITROXYL HNO; OVARIAN-CANCER; ANGELIS SALT; ALDEHYDE DEHYDROGENASE; SODIUM TRIOXODINITRATE; DONATING PROPERTIES; FUNCTIONAL-GROUP;
D O I
10.1002/ddr.21428
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diazeniumdiolates, also known as NONOates, are extensively used in biochemical, physiological, and pharmacological studies due to their ability to release nitric oxide (NO.) and/or their congeneric nitroxyl (HNO). The purpose of this work was to synthesize a series of primary amine-based diazeniumdiolates as HNO/NO donors and to determine their efficacy as anticancer and antifungal agents in vivo. The seven compounds (3a-3g) were successfully synthesized and characterized, one of which had been previously reported in the literature (3g). Two compounds showed anti-proliferative effects against ovarian (ES2 and SKOV3) and AML monocyte-derived cancer cells (THP-1) when tested with standard MTT assays. Compounds 3a and 3g demonstrated reduced ovarian cancer cell proliferation when treated at doses from 0.033 to 1.0 mg/mL at the 24 hr time point. These compounds also exhibited moderate and selective antifungal activity against Fusarium oxysporum f.sp. lycopersici, one cause of opportunistic infections of immunocompromised patients, inhibiting the growth of the fungi at LD50 at 10 mg/mL. A third compound (3e) did not exhibit similar activities, possibly due to the alkyl chain. Our results suggest that the primary amine diazeniumdiolates may offer a versatile platform for the development of HNO/NO donors for biomedical applications.
引用
收藏
页码:136 / 143
页数:8
相关论文
共 46 条
[1]   Dual Mechanisms of HNO Generation by a Nitroxyl Prodrug of the Diazeniumdiolate (NONOate) Class [J].
Andrei, Daniela ;
Salmon, Debra J. ;
Donzelli, Sonia ;
Wahab, Azadeh ;
Klose, John R. ;
Citro, Michael L. ;
Saavedra, Joseph E. ;
Wink, David A. ;
Miranda, Katrina M. ;
Keefer, Larry K. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (46) :16526-16532
[2]  
Angeli A., 1903, GAZZ CHIM ITAL, V33, P245
[3]  
[Anonymous], 2018, NCI SEER DATABASE
[4]   In vitro synergy of caspofungin and amphotericin B against Aspergillus and Fusarium spp. [J].
Arikan, S ;
Lozano-Chiu, M ;
Paetznick, V ;
Rex, JH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :245-247
[5]   Analysis of the HNO and NO donating properties of alicyclic amine diazeniumdiolates [J].
Bharadwaj, Gaurav ;
Benini, Patricia G. Z. ;
Basudhar, Debashree ;
Ramos-Colon, Cyf N. ;
Johnson, Gail M. ;
Larriva, Marti M. ;
Keefer, Larry K. ;
Andrei, Daniela ;
Miranda, Katrina M. .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2014, 42 :70-78
[6]   Fusarium, a significant emerging pathogen in patients with hematologic malignancy: Ten years' experience at a cancer center and implications for management [J].
Boutati, EI ;
Anaissie, EJ .
BLOOD, 1997, 90 (03) :999-1008
[7]  
Cabanes FJ, 1997, J CLIN MICROBIOL, V35, P3343
[8]   Mechanisms of inhibition of aldehyde dehydrogenase by nitroxyl, the active metabolite of the alcohol deterrent agent cyanamide [J].
DeMaster, EG ;
Redfern, B ;
Nagasawa, HT .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (12) :2007-2015
[9]   Mechanisms of HNO and NO production from Angeli's salt: Density functional and CBS-QB3 theory predictions [J].
Dutton, AS ;
Fukuto, JM ;
Houk, KN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (12) :3795-3800
[10]   The nitroxyl anion (HNO) is a potent dilator of rat coronary vasculature [J].
Favaloro, Joanne L. ;
Kemp-Harper, Barbara K. .
CARDIOVASCULAR RESEARCH, 2007, 73 (03) :587-596