1058705-57-9

Basic information

• Product Name: (S)-N-FMoc-2-(6'-octenyl)glycine
• Synonyms: (S)-N-FMoc-2-(6'-octenyl)glycine;(2S)-2-{[(9H-Fluoren-9-ylmethoxy)-carbonyl]amino}non-8-enoic acid;(S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)non-8-enoic acid;(S)-N-Fmoc-2-(6'-heptenyl)glycine;Fmoc-S7H-OH
• CAS NO: 1058705-57-9
• Molecular Formula: C₂₄H₂₇NO₄
• Molecular Weight: 393.47548
• Mol File: 1058705-57-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 610.7±55.0 °C(Predicted)
• Appearance: /
• Density: 1.168±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.90±0.21(Predicted)
• CAS DataBase Reference: (S)-N-FMoc-2-(6'-octenyl)glycine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-FMoc-2-(6'-octenyl)glycine(1058705-57-9)
• EPA Substance Registry System: (S)-N-FMoc-2-(6'-octenyl)glycine(1058705-57-9)

Safety Data

• Hazardous Substances Data: 1058705-57-9(Hazardous Substances Data)

Downstream Products

• 1262886-65-6 (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}nonanoic acid 

Relevant articles and documents

Novel potent apoA-I peptide mimetics that stimulate cholesterol efflux and pre-β particle formation in vitro

Reverse cholesterol transport (RCT) is believed to be the primary mechanism by which HDL and its major protein apoA-I protect against atherosclerosis. Starting from the inactive 22-amino acid peptide representing the consensus sequence of the class A amphipathic helical repeats of apoA-I, we designed novel peptides able to mobilize cholesterol from macrophages in vitro, and to stimulate the formation of 'nascent HDL' particles, with potency comparable to the entire apoA-I protein.