10-494322 - fmoc-lysn3-oh | 159610-89-6

L-Isoleucine, FMOC protected

<p>L-Leucine, FMOC protected</p>

<p>Stability Moisture Sensitive<br>Applications Used in conjunction with Isothiocyanate to conduct partial Edman Degradation on biologically active peptides.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Heidenreich, O., et al.: J. Biol. Chem., 269, 2131 (1994), Kothe, U., et al.: Anal. Biochem., 356, 148 (2006), Thakkar, A., et al.: Anal. Chem., 78, 5935 (2006),<br></p>

Fmoc morpholino uridine monomer is a novel anticancer drug. It can inhibit the proliferation of cancer cells and induce cell apoptosis by interfering with the synthesis of DNA, RNA and protein. Fmoc morpholino uridine monomer has been shown to be active against viruses, such as human immunodeficiency virus (HIV), herpes simplex virus (HSV) and influenza A virus. This compound is also reported to have antiviral activity against HIV-1 in vitro and HSV-2 in vivo.

<p>Fmoc morpholino cytidine monomer is a novel nucleoside that can be used as an anticancer, antiviral, and antiretroviral agent. The monophosphate form of this compound is inhibitory to DNA polymerase, while the diphosphate form inhibits viral replication by blocking the activity of reverse transcriptase. This product is highly pure and has been modified with a Fmoc group to enhance its stability in biological systems. The CAS number for this product is 611-87-7.</p>

<p>Fmoc-morpholino adenosine monomer is a synthetic nucleoside that is used in the synthesis of oligonucleotides for use as antiviral and anticancer agents. Fmoc-morpholino adenosine monomer has been synthesized by modifying the deoxyribonucleosides, which are then phosphoramidite derivatives of ribonucleosides. This novel chemical compound has shown high activity against DNA-dependent RNA polymerase, suggesting that it may be an effective antiviral agent.</p>

Fmoc Morpholino Guanosine Monomer is a novel and modified nucleoside with antiviral and anticancer activities. It is synthesized from the ribonucleotide, deoxyribonucleotide, and phosphoramidite. Fmoc Morpholino Guanosine Monomer is an activator of RNA polymerase and inhibits cell proliferation in vitro. This compound has been shown to be a potential candidate for treatment of viral infections such as HIV-1, herpes simplex virus type 1, or influenza A virus.

Fmoc L-aspartic acid is a cyclic peptide with growth factor activity. It has been shown to promote the replication of human immunodeficiency virus in vitro. Fmoc L-aspartic acid is synthesized by solid-phase synthesis and contains a hydroxyl group that may be necessary for its antiviral properties. Fmoc L-aspartic acid inhibits apoptotic cell death. It also has chemoenzymatic and endoglycosidase activities, which can degrade glycopeptides.

<p>2-Acetamido-3-O-benzoyl-2-deoxy-a-D-galactopyranosyl Fmoc serine phenacyl ester is a complex carbohydrate. It is an oligosaccharide with a molecular weight of 902 Da that is synthesized from 2,4,6,-trihydroxybenzoic acid and 2,3,4,6,-tetraacetylphenylserine. The carbohydrate has been modified by methylation, glycosylation and fluorination. The synthesis of this compound has been carried out using the click chemistry reaction. This product has a purity of 99+% and can be used in the modification of other carbohydrates.</p>

Please enquire for more information about Fmoc Gly TentaGel® S RAM resin (particle size: 90 µm capacity: 0.2 - 0.25 mmol/g) including the price, delivery time and more detailed product information at the technical inquiry form on this page