54608-35-4

Basic information

• Product Name: Glycine, N-(2-phenylethyl)-, ethyl ester
• CAS NO: 54608-35-4
• Molecular Formula: C12H17NO2
• Molecular Weight: 207.272
• Mol File: 54608-35-4.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Glycine, N-(2-phenylethyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-(2-phenylethyl)-, ethyl ester(54608-35-4)
• EPA Substance Registry System: Glycine, N-(2-phenylethyl)-, ethyl ester(54608-35-4)

Safety Data

• Hazardous Substances Data: 54608-35-4(Hazardous Substances Data)

Upstream product

• 623-73-4 diazoacetic acid ethyl ester 
• 64-04-0 phenethylamine 
• 103-63-9 1-phenyl-2-bromoethane 
• 459-73-4 GlyOEt*HCl 
• 623-33-6 glycine ethyl ester hydrochloride 
• 924-44-7 glyoxylic acid ethyl ester 
• 122-78-1 phenylacetaldehyde 
• 105-36-2 ethyl bromoacetate 

Downstream Products

• 7738-38-7 2-(phenethylamino)acetic acid 
• 102181-59-9 1,4-bis(phenethyl)piperazine-2,5-dione 
• 1027093-01-1 {[2-(Adamantan-2-yloxycarbonylamino)-2-methyl-3-phenyl-propionyl]-phenethyl-amino}-acetic acid ethyl ester 
• 1026160-29-1 {[2-(Adamantan-2-yloxycarbonylamino)-3-(4-bromo-phenyl)-2-methyl-propionyl]-phenethyl-amino}-acetic acid ethyl ester 
• 1025903-95-0 {[2-(Adamantan-2-yloxycarbonylamino)-2-methyl-3-naphthalen-2-yl-propionyl]-phenethyl-amino}-acetic acid ethyl ester 
• 1223389-60-3 ethyl (allyloxycarbonyl-(2-phenethyl)amino)acetate 
• 1332713-38-8 ethyl 2-(N-phenethylformamido)acetate 
• 1332457-48-3 ethyl 2-(N-phenethylacetamido)acetate 
• 1375092-49-1 C₁₈H₂₅NO₂ 
• 949902-88-9 (2-hydroxyethyl)phenethylcarbamic acid t-butyl ester 
• 182921-00-2 (2-oxoethyl)phenethylcarbamic acid t-butyl ester 
• 193818-10-9 (t-butoxycarbonylphenethylamino)acetic acid ethyl ester 

Relevant articles and documents

Psammocindoles A-C: Isolation, Synthesis, and Bioactivity of Indole-γ-lactams from the Sponge Psammocinia vermis

Psammocindoles A-C (1-3), a new class of indole alkaloids, were isolated from a Psammocinia vermis sponge. By combined spectroscopic analyses, the structures of these compounds were determined to be the indole-γ-lactams derived from three amino acid residues. In addition, an enantiomer psammocindole D (4), and the N-lactam isomers isopsammocindoles A-D (5-8) were also synthesized. These natural products and synthetic analogues were found to significantly stimulate adiponectin secretion in human bone marrow mesenchymal stem cells.

EIF4E INHIBITORS AND USES THEREOF

The present invention provides compounds inhibiting elF4E activity and compositions and methods of using thereof.

The discovery of new human coagulation factor XIa (FXIa) inhibitors by synthesis, biological evaluation, and structure-based modeling

Factor XIa (FXIa) is an enzyme that is activated during the earliest stage of initiation of the intrinsic pathway of the blood coagulation mechanism. In this study, we attempted to discover a new FXIa inhibitor based on structure-based molecular modeling. We found that compound 16 exhibits satisfactory predicted properties while maintaining important binding interactions with FX1a.