Antibioticcgp9000; Cgp9000; 7-(D-2-Amino-2-(1,4-Cyclohexadienyl)Acetamide)-3-Methoxy-3-Cephem-4-Carboxyl; (6R)-7T-((R)-2-Amino-2-Cyclohexa-1,4-Dienyl-Acetylamino)-3-Methoxy-8-Oxo-(6Rh)-5-Thia-1-Aza-Bicyclo[4.2.0]Oct-2-Ene-2-Carboxylic Acid; Cefroxadin

Brief Introduction

Cefroxadine is a semisynthetic first-generation cephalosporin with antibacterial activity. Cefroxadine binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis.

(2-Phenoxy)Methylsulfonylaniline

MSDS

CAS:51765-51-6

Molecular Formula:C13H13NO3S

Alias

More Information

2-((Phenoxymethyl)Sulfonyl)Aniline; N-(2-Phenoxyphenyl)Methanesulfonamide; 2-Phenoxymethanesulfonanilide; N-(2-Phenoxyphenyl)Methanesulphonamide; Mls000113923

Brief Introduction

The molecular formula of 2-phenoxymethanesulfonanilide is C13H13NO3S.

3,4-Dimethoxythiophene

MSDS

CAS:51792-34-8

Molecular Formula:C6H8O2S

Alias

More Information

2,3-Dimethoxythiophene; 3,4-Dimethoxythiophen; 3,4-Dimethoxytiophene; 3,4-Dimethoxy Thiophene; 3,4-Dimethoxythiophene 98%; ,4-Dimethoxythiophene; 3,4-Dimethoxy Thiophene (Dmot); 3,4- Twomethoxythiophene; Dmot; Akos Bbs-00006359

Thiotepa

MSDS

CAS:52-24-4

Molecular Formula:C6H12N3PS

Alias

More Information

N,N‘,N’‘-Triethylenethiophosphoramide; Phosphine, Tris(1-Aziridinyl)-, Sulfide; Tris(Aziridinyl)Phosphine Sulfide; Tri(Aziridin-1-Yl)Phosphine Sulfide; Tri(1-Aziridinyl)Phosphine Sulfide; 1,1',1''-Phosphorothioyltriaziridine; 1,1’,1″-Phosphinothioylidynetris[Aziridine]; 1,1’,1″-Phosphorothioyltris(Aziridine); Phosphorothioic Tri(Ethyleneamide); N,N',N''-Triethylenethiophosphoramide; Tris(1-Aziridinyl)Phosphine Sulfide; Triethylenethiophosphoramide

Brief Introduction

The ethylimine group in the chemical structure of the product can combine with the DNA nuclear base in the cell, such as guanine, so as to denature the DNA and affect the division of cancer cells. This product is a non-specific cell cycle drug, and has a good effect on breast cancer and ovarian cancer. It also has a certain effect on gastrointestinal adenocarcinoma, cervical cancer, thyroid cancer, lung cancer and sub melanoma.

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