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Ul/1677; Ccris 3400; 3-<3-Acetyl-4-(3-Tert-Butylamino-2-Hydroxy-Propoxy)-Phenyl>-1,1-Diethylharnstoff; Celectol; Einecs 260-497-7; Celiprololum [Inn-Latin]; Celiprolol; N'-(3-Acetyl-4-(3-((1,1-Dimethylethyl)-Amino)-2-Hydroxypropoxy)-Phenyl)-N,N-Diethylurea; N-[3-Acetyl-4-(3'-Tert-Butylamino-2'-Hydroxy)Propoxy]-Phenyl-N'-Diethylurea; Rhc-5320A; [14C]-Celiprolol; Selectol
Brief Introduction
Celiprolol hydrochloride, developed by Sanofi Aventis of France, was first listed in Austria in 1983. This product has a high degree of cardiac selectivity β 2-receptor excitability and weak α 2-receptor blocking activity, less and mild adverse reactions. There are many reports on the synthetic process, but the starting materials and synthetic routes are mostly the same, and the production cost and environmental pollution of the process need to be improved. Celiprolol is highly selectively bound to cardiomyocyte membrane β 1 receptor binding, and its affinity is higher than that of bronchial and vascular smooth muscle β 2 receptor was 20 ~ 30 times stronger. It can reduce the heart rate and cardiac output during rest and exercise, reduce the systolic blood pressure during exercise, and inhibit the tachycardia induced by isoproterenol.
CAS:57-41-0
Molecular Formula:C15H12N2O2
5,5-Diphenylhydantoin; 5,5-Diphenyl-2,4-Imidazolidinedione; 5,5-Diphenylimidazolidine-2,4-Dione
Brief Introduction
This product is a pharmaceutical intermediate used as an antiepileptic and antiarrhythmic drug.
CAS:57-47-6
Molecular Formula:C15H21N3O2
(3As,8Ar)-1,3A,8-Trimethyl-1,2,3,3A,8,8A-Hexahydropyrrolo[2,3-B]Indol-5-Yl Methylcarbamate; Pyrrolo[2,3-B]Indol-5-Ol, 1,2,3,3A,8,8A-Hexahydro-1,3A,8-Trimethyl-, Methylcarbamate (Ester), (3As-Cis)-; [(3Ar,8Bs)-3,4,8B-Trimethyl-2,3A-Dihydro-1H-Pyrrolo[2,3-B]Indol-7-Yl] N-Methylcarbamate; Eserine; Antilirium; Physostol
Brief Introduction
Physostigmine can inhibit the activity of cholinesterase in the body. It is a parasympathetic stimulant. It is mainly used to treat glaucoma. Its efficacy is stronger and longer than pilocarpine, and can last for several hours to several days. At present, it is also used as a wake-up medicine for traditional Chinese medicine anesthesia in China. Physostigmine is unstable. After being prepared into an aqueous solution, it must be stored in a closed non alkaline glass bottle protected from light and used within one week. This product is a biochemical agent.
CAS:57-66-9
Molecular Formula:C13H19NO4S
Proben; Benuryl; 4-(N,N-Dipropylaminosulphonyl)Benzoic Acid; Benzoic Acid, 4-[(Dipropylamino)Sulfonyl]-; Benacen; Apurina; Probenid; 4-Dipropylsulfamoyl-Benzoic Acid; 4-[(Di-N-Propylamino)Sulphonyl]Benzoic Acid; Benemid; Probalan; Benemide; Probexin; Probecid
Brief Introduction
Anti gout drugs. The product is an organic acid with strong fat solubility. It is secreted and excreted from renal tubules and is easy to be absorbed back. Therefore, in the presence of Propanesulfonate, the operation of some organic acids in renal tubules will be inhibited and the excretion of other organic acids will be reduced. Therefore, it is safe and effective for the treatment of chronic gout. It has no effect on pain and inflammation of acute gout and is not suitable for acute gout.
CAS:57-71-6
Molecular Formula:C4H7NO2
2,3-Butanedione Oxime; Diacetyl Monoxime; Butane-2,3-Dione Monooxime
Brief Introduction
2,3-butanedione monoxime was used to prepare sodium and potassium butanedione monoxime. Sodium dimethylglyoxime and potassium salt are the main active ingredients of a highly toxic chemical disinfectant. The skin disinfectant based on sodium dimethylglyoxime and potassium salt has the advantages of non toxicity, non irritation, easy storage, low corrosiveness and fast disinfection speed that traditional skin disinfectants do not have.
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