Wu, Xia published the artcileApplication of urapidil in prevention and treatment of adverse reactions caused by carboprost tromethamine in cesarean section, Recommanded Product: 2-Amino-2-(hydroxymethyl)propane-1,3-diol (Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((S,E)-3-hydroxy-3-methyloct-1-en-1-yl)cyclopentyl)hept-5-enoic acid, the publication is Nanjing Yike Daxue Xuebao, Ziran Kexueban (2015), 35(9), 1305-1307, database is CAplus.
The application effect of urapidil on prevention and treatment of adverse reactions caused by carboprost tromethamine in cesarean section was observed A total of 60 full-term pregnant patients who needed cesarean section of lower uterine segment were randomly divided into urapidil group (U group) and normal saline group (N group), 30 cases in each group. After fetal childbirth, based on injection of carboprost tromethamine 250 μg, urapidil of 12.5 mg was i.v. injected in U group, and 20 mL normal saline was injected in N group. The mean arterial blood pressure (MAP), heart rate (HR) and pulse oxygen saturation (SPO2) were recorded in both groups before anesthesia (T0), at fetal childbirth (T1), 10 min after injection of carboprost tromethamine (T2) and 30 min after injection of carboprost tromethamine (T3). And the adverse reactions in both groups were observed There were no statistically significant differences in MAP, HR and SPO2 at T0 between both two groups (P>0.05). Compared with T0, MAP and HR in N group were increased at T2 (P<0.05), while SPO2 was decreased (P<0.05). Compared with N group, MAP and HR in U group were decreased at T2 (P<0.05), while SPO2 was increased (P<0.05). The incidences of headache and chest tightness were higher in N group than in U group (P<0.05). Urapidil can be effectively used in the prevention and treatment of adverse reactions caused by carboprost tromethamine in cesarean section, which is conducive to the stability of circular breathing.
Nanjing Yike Daxue Xuebao, Ziran Kexueban published new progress about 58551-69-2. 58551-69-2 belongs to alcohols-buliding-blocks, auxiliary class Chiral,Alkenyl,Amine,Aliphatic cyclic hydrocarbon,Ester,Alcohol,Inhibitor,, name is 2-Amino-2-(hydroxymethyl)propane-1,3-diol (Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((S,E)-3-hydroxy-3-methyloct-1-en-1-yl)cyclopentyl)hept-5-enoic acid, and the molecular formula is C11H8O3, Recommanded Product: 2-Amino-2-(hydroxymethyl)propane-1,3-diol (Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((S,E)-3-hydroxy-3-methyloct-1-en-1-yl)cyclopentyl)hept-5-enoic acid.
Referemce:
https://en.wikipedia.org/wiki/Alcohol,
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