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. 2021 Oct 14;10(10):1041. doi: 10.3390/biology10101041

Table 2.

New chemical classes of NO donors.

No Donor Class Effect Species Tolerance References
(Z)-ethyl 12-nitrooxy-octadec-9-enoate (NCOE) Organic nitrate -Short-lasting hypotension and bradycardia
-Vasorelaxation
Rat Does not cause in vitro tolerance [126]
2-nitrate-1,3-dibuthoxypropan (NDBP) Organic nitrate -Hypotension, bradycardia, and bradypnea
-Prevention of the progression of angiotensin II-mediated hypertension
Rat Does not cause in vitro tolerance [228,229,231]
Cyclohexane Nitrate (HEX) Organic nitrate -Reduction in blood pressure and heart rate
-Antihypertensive effect in renovascular hypertension
-Vasorelaxation in cranial artery
Rat - [235]
1,3-bis (hexyloxy) propan-2-yl nitrate (NDHP) Organic nitrate - Reduction in blood pressure in hypertensive animals
-Vasorelaxation
-Prevention of the progression of hypertension and endothelial dysfunction
Rat Does not cause in vitro tolerance [236]
[Ru(terpy)(bdq)NO+]3+ (TERPY) Metal-based drugs -Vasorelaxation in aorta and mesenteric resistance arteries from Sham and two-kidney-one-clip hypertensive (2K1C)
-Long-lasting hypotensive effect in 2K-1C, but not in normotensive
-Similar vasorelaxation and released NO in aortas from Wistar and Spontaneously Hypertensive Rats (SHR)
- Does not induce vasorelaxation in basilar arteries
-Hypotensive effect in SHR
Rat - [231,232,233,234,245,251,252,254]
[Ru(bpy)2(py)(NO2)](PF6) (RuBPY) Metal-based drugs -Induced relaxation in aorta, mesenteric resistance arteries; coronary arteries between normotensive and 2K1C rats
-Did not induce hypotensive effect in normotensive rats
-Induced coronary artery relaxation (which may be useful for angina) and a minor effect in basilar artery (which may indicate that it does not induce headache).
-NO· release that activates K+ channels in cultured VCMC aorta
Rat Does not cause in vitro tolerance (self- or cross-tolerance) [42,125,255,256,257]
trans-[Ru(Cl)NO(cyclam)2+ Metal-based drugs -Long-lasting hypotensive effect (20 times greater than SNP) in normotensive and hypertensive animals Mouse - [249]
trans-[RuCl([15]aneN4)NO]2+ Metal-based drugs -Vasorelaxation in aorta (due to the release of NO· and NO-species) Rat - [243,244]
Ru(NO)(salenCO2H)Cl Metal-based drugs -Vasorelaxation in aorta Rat - [258]
Rut-bpy (Cis-[Ru(bpy)2(SO3)(NO)]PF6 Metal-based drugs -Stabilization of BP in anesthetized hypotensive animals Rat - [260]
cis-[Ru(bpy)2(SO3)(NO)]PF-6-9 (FONO1) Metal-based drugs -Vasodilation in corpus cavernosum Rabbit - [261]
trans-[Ru(NH3)4(caffeine)(NO)]C13 (LLNO1) Metal-based drugs -Vasodilation in corpus cavernosum Rabbit - [261]
cis-[Ru(bpy)2(2-MIM)(NO)](PF6)3 (FOR811A) Metal-based drugs -Decrease in alveolar collapse and prevention of bronchoconstriction during asthma Mouse - [262]
cis-[Ru(bpy)2(ImN)(NO)]3+ (FOR0811) Metal-based drugs -Decrease in BP (long-lasting) with no reflex tachycardia in L-NG-Nitro arginine methyl ester (L-NAME) hypertensive rats
-Reduction in the low (LF) and very low (VLF) frequency bands in rats
-Vasorelaxation in rat aorta
-Vasorelaxation of human corpus cavernosum
Rat and human - [248]