L-a-Cyclohexylglycine

CAS: 14328-51-9

Ref. 3D-FC43992

Produktinformation

• Name: L-a-Cyclohexylglycine
• Synonyme: (1-Ammoniocyclohexyl)Acetate, (2S)-2-Amino-2-cyclohexylacetic acid, (2S)-2-Amino-2-cyclohexylethanoic acid, (2S)-amino(cyclohexyl)ethanoic acid, (S)-2-Amino-2-cyclohexylacetic acid, (S)-2-Cyclohexylglycine, (αS)-α-Aminocyclohexaneacetic acid, <span class="text-smallcaps">L</span>-Cyclohexylglycine, <span class="text-smallcaps">L</span>-α-Cyclohexylglycine, Amino(Cyclohexyl)Acetic Acid, Cyclohexaneacetic acid, α-amino-, (S)-, Cyclohexaneacetic acid, α-amino-, (αS)-, Cyclohexaneacetic acid, α-amino-, <span class="text-smallcaps">L</span>-, H-Chg-OH, L-(+)-2-Cyclohexylglycine, L-Cyclohexyglycine, L-Cyclohexyl glycine, L-alpha-Cyclohexylglycine

Beschreibung

L-a-Cyclohexylglycine is an efficient, general method for the preparation of peptide aldehydes. It is a serine protease inhibitor that binds to thrombin and prevents it from converting fibrinogen into fibrin. L-a-Cyclohexylglycine has been shown to inhibit polymerization of fibrinogen and factor XIII, as well as the formation of thrombin, which is important for blood clotting. L-a-Cyclohexylglycine also inhibits hepatitis C virus (HCV) replication in vitro by binding to the HCV NS3 helicase protein. This compound has been shown to be able to inhibit HIV-1 protease activity and may have potential use as an antiviral agent.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 157.21 g/mol
• Formel: C₈H₁₅NO₂
• Reinheit: Min. 95%
• Farbe/Form: White Powder
• InChl: InChI=1S/C8H15NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h6-7H,1-5,9H2,(H,10,11)/t7-/m0/s1
• InChI Key: InChIKey=WAMWSIDTKSNDCU-ZETCQYMHSA-N
• SMILES: N[C@H](C(=O)O)C1CCCCC1