Proparacaine is a benzoic acid derivative anesthetic agent, with local anesthetic activity. Upon administration, proparacaine stabilizes the neuronal membrane by binding to and inhibiting voltage-gated sodium channels. This inhibits the sodium ion influx required for the initiation and conduction of impulses within the neuronal cell, increases the threshold for electrical stimulation and results in a loss of sensation.

Thalidomide

MSDS

CAS:50-35-1

Molecular Formula:C13H10N2O4

Alias

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Thalomid; 2-(2,6-Dioxopiperidin-3-Yl)Isoindoline-1,3-Dione; Sedoval; (+/-)-Thalidomide; N-Phthalylglutamic Acid Imide; 3-Phthalimidoglutarimide; Alpha-Phthalimidoglutarimide; (+-)-Thalidomide; 2,6-Dioxo-3-Phthalimidopiperidine; Thalidomide Celgene; Alpha-N-Phthalylglutaramide; N-(2,6-Dioxo-3-Piperidyl)Phthalimide; Glutarimide, 2-Phthalimido-; N-Phthalyl-Glutaminsaeure-Imid; Alpha-(N-Phthalimido)Glutarimide; 1H-Isoindole-1,3(2H)-Dione, 2-(2,6-Dioxo-3-Piperidinyl)-; 1,3-Dioxo-2-(2,6-Dioxopiperidin-3-Yl)Isoindoline; .Alpha.-N-Phthalylglutaramide; Phthalimide, N-(2,6-Dioxo-3-Piperidyl)-; 2-(2,6-Dioxopiperidin-3-Yl)-1H-Isoindole-1,3(2H)-Dione; 2-(2,6-Dioxopiperidin-3-Yl)-2,3-Dihydro-1H-Isoindole-1,3-Dione; .Alpha.-Phthalimidoglutarimide; 2-(2,6-Dioxo-3-Piperidinyl)-1H-Isoindole-1,3(2H)-Dione

Brief Introduction

Thalidomide is a synthetic glutamate derivative, which is mainly used to treat epilepsy. However, due to its lack of effectiveness, thalidomide was subsequently used as a sleep adjuvant and widely used to stop vomiting during pregnancy. In the early 1960s, thalidomide was reported to cause a large number of infant malformations, which was banned by many countries and withdrawn from the pharmaceutical market. However, scientists did not completely deny thalidomide and continued to conduct in-depth research on it, especially in immunization, anti-inflammatory Gratifying and encouraging results have been obtained in the pharmacology of anti angiogenesis and the clinical treatment of some difficult diseases, so that people have a new understanding of thalidomide.

Clomiphene Citrate

MSDS

CAS:50-41-9

Molecular Formula:C32H36ClNO8

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Clomiphene Citrate Salt; Diethylethanamine,Clomiphene Citrate Salt; {2-[4-(2-Chloro-1,2-Diphenylvinyl)Phenoxy]Ethyl}Diethylamine 2-Hydroxy-1,2,3-Propanetricarboxylate (Salt); 2-(4-(2-Chloro-1,2-Diphenylvinyl)Phenoxy)-N,N-Diethylethanamine 2-Hydroxypropane-1,2,3-Tricarboxylate; 2-[4-(2-Chloro-1,2-Diphenylethenyl)Phenoxy]-N,N-Diethyl-Ethanamine, 2-Hydroxy-1,2,3-Propanetricarboxylate; Clomifene Citrate

Brief Introduction

This product is an anti estrogen (fertility inducer), which is suitable for functional uterine bleeding, polycystic ovary, menstrual disorder, drug-induced amenorrhea and other gynecological diseases.

Amitriptyline

MSDS

CAS:50-48-6

Molecular Formula:C20H24ClN###C20H23N

Alias

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3-(10,11-Dihydro-5H-Dibenzo[A,D][7]Annulen-5-Ylidene)-N,N-Dimethyl-1-Propanamine; 3-(5,6-Dihydrodibenzo[2,1-B:2',1'-F][7]Annulen-11-Ylidene)-N,N-Dimethylpropan-1-Amine; N,N-Dimethyl-3-(2-Tricyclo[9.4.0.03,8]Pentadeca-1(15),3,5,7,11,13-Hexaenylidene)Propan-1-Amine; Amitriptylin; Elavil; Damitriptyline

Brief Introduction

Amitriptyline is a tricyclic antidepressant with analgesic effect. It is widely used in the treatment of depression and neuropathic pain. Amitriptyline is an inhibitor of serotonintransporter (SERT) and norepine phenetransporter (net), with Ki values of 3.45 nm and 13.3 nm, respectively. Amitriptyline also inhibited histamine receptor H1, histamine receptor H4, 5-HT2 and sigma 1 receptor, and the corresponding Ki values were 0.5 nm, 7.31 nm, 235 nm and 287 nm, respectively. The product is colloidal.

Imipramine

MSDS

CAS:50-49-7

Molecular Formula:C19H24N2

Alias

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Berkomine; Melipramine; Melipramin; [14C]-Imipramine; Antideprin; 3-(5,6-Dihydrobenzo[B][1]Benzazepin-11-Yl)-N,N-Dimethylpropan-1-Amine; Nelipramin; [3H]-Imipramine; Tofranil; 3-(10,11-Dihydro-5H-Dibenzo[B,F]Azepin-5-Yl)-N,N-Dimethylpropan-1-Amine; Intalpram; Imidobenzyle; Dimipressin

Brief Introduction

It has strong antidepressant effect, but the excitatory effect is not obvious and the sedative effect is weak. It is almost ineffective or ineffective for the depression associated with schizophrenia. It can also be used for pediatric enuresis.

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