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CAS:51384-51-1
Molecular Formula:C15H25NO3
Medrol; Medrate; Metilbetasone; Methylprednisolone; Solomet; Dopomedrol; Promacortine; Urbason; Besonia; Medrone; (Rs)-Metoprolol; Spesicor; Beatrolol
Brief Introduction
Metoprolol, also known as metoprolol or metoprolol. In the United States, most of them are sold under the trade name Lopressor, which is selective β 1-receptor blocker. It is used to treat hypertension, angina pectoris and many symptoms related to tachycardia. The drug is also used to prevent cardiovascular disease after myocardial infarction and migraine related headache symptoms. Metoprolol can be administered orally or intravenously for several months. The general dosage is twice a day. It also has a long-term formula that can be used once a day. Metoprolol can also be mixed with hydrochlorothiazide to make a single compound tablet. Common side effects include insomnia, burnout, fainting and gastrointestinal discomfort. If the dose is too large, it may cause serious toxic reactions. At present, the possibility that the drug may cause harm during pregnancy has not been ruled out, and the current study has not shown the impact of drug use during lactation. If the patient has liver disease or asthma at the same time, close observation is required. After stopping taking, various side effects will be relieved, and any health crisis caused by this drug will disappear. The first metoprolol was made in 1969. It is not only a drug in the standard list of essential drugs of the World Health Organization, but also an extremely important drug in basic medical treatment, but also a common name drug. In 2013, metoprolol ranked 19th among the most frequently prescribed drugs in the United States.
(2S)-2-Amino-3-((((R)-2,3-Bis(Stearoyloxy)Propoxy)-(Hydroxy)Phosphoryl)Oxy)Propanoic Acid; Phosphatidylserine; Distearoyl Phosphatidylserine; 1,2-Dioctadecanoyl-Sn-Glycero-3-Phosphoserine
Brief Introduction
Derivatives of PHOSPHATIDIC ACIDS in which the phosphoric acid is bound in ester linkage to a SERINE moiety.
CAS:515-69-5
Molecular Formula:C15H26O
(+/-)-α-Bisabolol; α-Bisabolol; 6-Methyl-2-(4-Methyl-3-Cyclohexen-1-Yl)-5-Hepten-2-Ol; (R*, R*)-Alpha, 4-Dimethyl-Alpha-(4-Methyl-3-Pentyl)Cyclohex-3-En-1-Methanol; (R*,R*)-Alpha-4-Dimethyl-Alpha-(4-Methyl-3-Petenyl)-3-Cyclohexene-1-Methanol; α-Bisabolol,6-Methyl-2-(4-Methyl-3-Cyclohexen-1-Yl)-5-Hepten-2-Ol,Dragosantol; 6-Methyl-2-(4-Methyl-3-Cyclohexen-1-Yl)-5-Hepteno
Brief Introduction
This product is an oily sesquiterpenol from plants, with anti-inflammatory and antibacterial activities. It can be used as pharmaceutical and chemical raw materials.
CAS:5156-40-1
Molecular Formula:C6H11NO2
Nitrous Acid Cyclohexyl Ester; Unii-02Xu02Qrlx; 02Xu02Qrlx
Brief Introduction
The molecular formula of cyclohexyl nitrite is C6H11NO2.
CAS:5169-78-8
Molecular Formula:C15H17NS2
Bitiodin; 3-(Di-Thiophen-2-Yl-Methylene)-1-Methyl-Piperidine; (1-Methyl-3-Piperidyliden)Di-2-Thienylmethan-Embonat; 3-(Di-[2]Thienyl-Methylen)-1-Methyl-Piperidin; Tipepidinum [Inn-Latin]; Cr/662; Piperidine, 3-(Di-2-Thienylmethylene)-1-Methyl-; At 327; Tipepidine; Tipepidina [Inn-Spanish]; Asverin; (1-Methyl-3-Piperidylidene)Di(2-Thienyl)Methane; 3-(Di-[2]Thienyl-Methylene)-1-Methyl-Piperidine; Tipepidine [Inn:Dcf]; Tipedine
Brief Introduction
Tipepidine is a synthetic, non-opioid antitussive and expectorant of the thiambutene class. It acts as an inhibitor of G protein-coupled inwardly-rectifying potassium channels (GIRKs). The drug was discovered in the 1950s, and was developed in Japan in 1959. It is used as the hibenzate and citrate salts. The usual dose is 20mg every 4–6 hours. Possible side effects of tipepidine, especially in overdose, may include drowsiness, vertigo, delirium, disorientation, loss of consciousness, and confusion. Tipepidine has recently garnered interest as a potential psychiatric drug. It is being investigated in depression, obsessive-compulsive disorder, and attention-deficit hyperactivity disorder (ADHD). Through inhibition of GIRK channels, tipepidine increases dopamine levels in the nucleus accumbens, but without increasing locomotor activity or producing methamphetamine-like behavioral sensitization, and this action appears to be at least partly responsible for its antidepressant-like effects in rodents.
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