CAS 51419-59-1
:cloruro di (4-metilfenil)metansolfonile
- P-Tolylmethanesulfonyl Chloride
- 4-Methylbenzylsulfonyl chloride
(4-Methylphenyl)methylsulphonyl chloride
CAS:(4-Methylphenyl)methylsulphonyl chlorideFormula:C8H9ClO2SPurezza:>97%Colore e forma:SolidPeso molecolare:204.67386p-Tolylmethanesulfonyl chloride
CAS:Formula:C8H9ClO2SPurezza:95%Colore e forma:SolidPeso molecolare:204.6739p-Tolylmethanesulfonyl chloride
CAS:p-Tolylmethanesulfonyl chlorideFormula:C8H9ClO2SPurezza:96%Peso molecolare:204.67p-Tolyl-methanesulfonyl chloride
CAS:Formula:C8H9ClO2SPurezza:95%Colore e forma:Chunks,Crystalline PowderPeso molecolare:204.674-Methylbenzylsulfonyl chloride
CAS:4-Methylbenzylsulfonyl chloride is a nontoxic chemical compound that inhibits the growth of breast cancer cells. It has been shown to react with and destroy RNA, proteins, and enzymes that are involved in cell division. 4-Methylbenzylsulfonyl chloride also has been shown to have antitumour activity in breast cancer cells. This compound is active against the MDA-MB-231 cell line, which is a human breast cancer cell line derived from metastatic mammary adenocarcinoma. The mechanisms of action of 4-methylbenzylsulfonyl chloride include interference with the synthesis of urokinase, an enzyme that plays an important role in tumour proliferation, as well as inhibition of the cyclooxygenase pathway and other biochemical pathways involved in urokinase production. 4-Methylbenzylsulfonyl chloride may also inhibit angiogenesis by inhibiting trypsin or
Formula:C8H9ClO2SPurezza:Min. 95%Peso molecolare:204.67 g/mol




