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?-(difluoromethyl)-DL-Arginine

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    ?-(difluoro<wbr/>methyl)-DL-<wbr/>Arginine
  • ?-(difluoro<wbr/>methyl)-DL-<wbr/>Arginine
Cat No: 16415
Cayman

Bacteria synthesize the cellular growth factor putrescine through a number of pathways. One pathway involves the decarboxylation of arginine by arginine decarboxylase to produce agmatine, which is then degraded to putrescine. While important for variou...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 2-(difluoromethyl)-arginine
Correlated keywords:
  • polyamines biosynthesis inhibitors plants growths regulators putrescines immunology infectious diseases arginines decarboxylases 77286-88-5 signals transductions cells biology biochemicals DL-?-(Difluoromethyl)arginine ?-Difluoromethylarginine ? enzymes activated enzyme-activated irreversible irreversibly inhibits E Escherichia coli Ecoli P Pseudomonas aeruginosa Paeruginosa K Klebsiella pneumonia Kpneumonia prevents prevention osmotic stress-induced stress induced increases activities activity synthesis oats leaf reduces reductions reduced T Trypanosoma cruzi Tcruzi mammalian mammals hosts C. Cryptosporidium parvum Cparvum T-cells Tcells receptors ?-deficient deficient mouse models polyamines analogs RMI 71897
Product Overview:
Bacteria synthesize the cellular growth factor putrescine through a number of pathways. One pathway involves the decarboxylation of arginine by arginine decarboxylase to produce agmatine, which is then degraded to putrescine. While important for various cellular processes (e.g., cell division, differentiation, environmental stress responses) in all living organisms, including plants, high levels of this polyamine can be toxic.{23742} α-(difluoromethyl)-DL-Arginine (DFMA) is an enzyme-activated, irreversible inhibitor of the arginine decarboxylases of E. coli (Ki = 800 µM), P. aeruginosa, and K. pneumoniae.{26879} At 0.01 mM, it has been shown to prevent the osmotic stress-induced increase in arginine decarboxylase activity and putrescine synthesis in oat leaf cells.{26875,26878} DFMA can also reduce the growth of T. cruzi in mammalian host cells at a minimal concentration of 10 mM and prevent the growth of C. parvum in a T cell receptor alpha-deficient mouse model when combined with various polyamine analogs.{26877,26876}
Size 1 mg
Shipping dry ice
CAS Number 69955-43-7
Molecular Formula C7H14F2N4O2
SMILES FC(F)C(C(O)=O)(N)CCCNC(N)=N
Molecular Weight 224,2
Formulation A crystalline solid
Purity ≥95%
Custom Code 2905.59
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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