
CAS 114014-15-2
:Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE
Description:
Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE, identified by its CAS number 114014-15-2, is a synthetic organic compound that belongs to the class of diazoketones. This compound features a diazo functional group, which is characterized by the presence of two nitrogen atoms connected by a double bond, and a ketone functional group, which is a carbonyl group (C=O) bonded to two carbon atoms. The presence of the Z-phenyl and tyrosine (Tyr) moieties suggests that it may have specific stereochemical configurations and functional properties that could be relevant in biochemical applications or as a building block in organic synthesis. The tert-butyl (TBU) group likely contributes to the compound's stability and solubility characteristics. Due to the reactive nature of diazoketones, this compound may be utilized in various chemical reactions, including cycloadditions and as intermediates in the synthesis of more complex molecules. However, handling such compounds requires caution due to their potential reactivity and toxicity.
Formula:C31H34N4O5
Synonyms:- Z-FY(T-BU)-DMK
- CBZ-PHE-TYR(O-T-BU)-CHN2;Z-PHE-TYR(TBU)-CHN2
- Cbz-Phe-Tyr(O-t-Bu)-CHN2
- CATHEPSIN L INHIBITOR III
- Z-Phe-Tyr(tBu)-CHN2
- Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE
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Found 4 products.
Z-Phe-Tyr(tBu)-diazomethylketone
CAS:Irreversible cathepsin L inhibitor which is ca 10’000 times more effective in inactivating cathepsin L than cathepsin S.Formula:C31H34N4O5Purity:> 98%Color and Shape:WhitishMolecular weight:542.63Z-Phe-Tyr(tBu)-diazomethylketone
CAS:<p>Irreversible cathepsin L inhibitor which is ca 10'000 times more effective in inactivating cathepsin L than cathepsin S.</p>Formula:C31H34N4O5Color and Shape:SolidMolecular weight:542.636Z-Phe-Tyr(tBu)-diazomethylketone
CAS:<p>Z-Phe-Tyr(tBu)-diazomethylketone is a compound that is used in the treatment of cancer and HIV. It was developed as an antiviral therapy for HIV, but it has been found to be ineffective against HIV. Z-Phe-Tyr(tBu)-diazomethylketone has been shown to produce attenuating effects on syncytial virus and may be a potential antiviral drug. This compound is not active against regulatory sequences or tissues, but it does inhibit endoproteolytic processing of n6-methyladenosine, which leads to modifications in rna binding.</p>Formula:C31H34N4O5Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:542.63 g/mol



