(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane

CAS : 98737-29-2

Ref. 3D-FB18916

Informations sur le produit

• Nom: (2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane
• Synonymes: N-[(1S)-1-[(2S)-2-Oxiranyl]-2-phenylethyl]-carbamic acid 1,1-dimethylethyl ester(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4- phenylbutane[(1S)-1-((2S)-Oxiranyl)-2-phenylethyl]carbamic acid tert-butyl ester, (1S,2S)-Boc epoxide, (1S,2S)1,2-Epoxy-3-(Boc Amino)-4-Phenylbutane, (2R)-[(1'S)-tert-butoxycarbonyl)amino-2'-phenyethyl]-oxirane, (2S)-[(1S)-1-[(tert-Butoxycarbonyl)amino]-2-phenylethyl]oxirane, (2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane, (2S,3S)-1,2-Epoxy-3-(Boc-Amino)-4-Phenylbutane, (2S,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane, (2S,3S)-N-t-Boc-3-amino-1,2-epoxy-4-phenylbutane, 1,2-Epoxy-(BOC amino)-4-phenyl butane, 1-Benzyl-2,3-Epoxypropyl-Carbamic Acid Tert-Butyl Ester, Boc-expoxide-4-phenylbutane, Carbamic acid, (1-oxiranyl-2-phenylethyl)-, 1,1-dimethylethyl ester, [S-(R*,R*)]-, Carbamic acid, N-[(1S)-1-[(2S)-2-oxiranyl]-2-phenylethyl]-, 1,1-dimethylethyl ester, Carbamic acid, [(1S)-1-(2S)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl este, Carbamic acid, [(1S)-1-(2S)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl ester, Tert-Butyl (1-Oxiran-2-Yl-2-Phenylethyl)Carbamate, Tert-Butyl{(S)-Α-[(S)-Oxiranyl]Phenethyl}Carbamate, [(1S)-1-((2S)-Oxiranyl)-2-phenylethyl]carbamic acid tert-butyl ester, tert-Butyl N-[(1S)-1-[(2S)-oxiran-2-yl]-2-phenylethyl]carbamate, tert-Butyl [(1S)-1-((2S)-oxiranyl)-2-phenylethyl]carbamate, tert-butyl {(1S)-1-[(2R)-oxiran-2-yl]-2-phenylethyl}carbamate, tert-butyl {(1S)-1-[(2S)-oxiran-2-yl]-2-phenylethyl}carbamate

Description

(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane is a potent and selective inhibitor of HIV protease. It binds to the active site of the enzyme and prevents the formation of an enzyme-substrate complex, which inhibits protein synthesis. (2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane has been shown to be a potent inhibitor for other serine proteases such as chymotrypsin and trypsin. This compound has also been shown to be effective in inhibiting a number of proteases from bacteria such as Bacillus subtilis and Pseudomonas aeruginosa. Inhibitors have also been found against nonenzymatic protein inhibitors such as bacitracin, polymyxin B, colistin sulfate, vancomycin, and daptomycin

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 263.33 g/mol
• Formule: C₁₅H₂₁NO₃
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C15H21NO3/c1-15(2,3)19-14(17)16-12(13-10-18-13)9-11-7-5-4-6-8-11/h4-8,12-13H,9-10H2,1-3H3,(H,16,17)/t12-,13+/m0/s1
• Code InChI: InChIKey=NVPOUMXZERMIJK-QWHCGFSZSA-N
• SMILES: CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H]1CO1