Satavaptan is under investigation in clinical trial NCT00359437 (Satavaptan in the Prevention of Ascites Recurrence in Patients With Ascites Due to Cirrhosis of the Liver).

3-Chlorocinnamic Acid

CAS:1866-38-2

Molecular Formula:C9H7ClO2

Alias

More Information

3-(3-Chlorophenyl)Acrylic Acid; 3-(3-Chlorophenyl)-2-Propenoic Acid; Cinnamic Acid,M-Chloro; (E)-3-Chlorocinnamic Acid; 3-(3-Chloro-Phenyl)-Acrylic Acid; M-Chlorocinnamic Acid; Trans-3-(3-Chlorophenyl)Propenoic Acid; Trans-3-(3-Chlorophenyl)Acrylic Acid; (E)-3-(3-Chlorophenyl)-2-Propenoate; (2E)-3-(3-Chlorophenyl)-2-Propenoic Acid; 2-Propenoic Acid, 3-(3-Chlorophenyl)-; Cinnamic Acid, M-Chlor

Brief Introduction

This product is used in organic synthesis. It is not only the raw material for the production of 5-chloroindenone, but also the intermediate of medicine and pesticide.

(1S,2R,4S,5S,7R)-7-[2-Hydroxy(Di-2-Thienyl)Acetoxy]-9,9-Dimethyl-3-Oxa-9-Azoniatricyclo[3.3.1.0<Sup>2,4</Sup>]Nonane Bromide

CAS:186691-13-4

Molecular Formula:C19H22BrNO4S2

Brief Introduction

Tiotropium bromide, a long-acting (24-hour) anticholinergic bronchodilator for the treatment of chronic obstructive pulmonary disease (COPD), Boehringer Ingelheim and Pfizer jointly launched an inhaled capsule called Spiriva.

N-(Diaminomethylidene)-2-Methyl-4,5-Bis(Methylsulfonyl)Benzamide

CAS:187870-78-6

Molecular Formula:C11H15N3O5S2

Brief Introduction

Rimeporide (EMD-87580) 是一种有效的选择性 Na+/H+ 交换泵 (NHE-1) 抑制剂。

5-[(1S,3S,4R)-7-Azabicyclo[2.2.1]Heptan-3-Yl]-3-Methyl-1,2-Oxazole

CAS:188895-96-7

Molecular Formula:C10H15ClN2O

Brief Introduction

Epiboxidine is a chemical compound which acts as a partial agonist at neural nicotinic acetylcholine receptors, binding to both the α3β4 and the α4β2 subtypes. It was developed as a less toxic analogue of the potent frog-derived alkaloid epibatidine, which is around 200 times stronger than morphine as an analgesic but produces extremely dangerous toxic side effects. Epiboxidine is around one-tenth as potent as epibatidine as an α4β2 agonist, but has around the same potency as an α3β4 agonist. It has only one-tenth of the analgesic power of epibatidine, but is also much less toxic.

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