884498-64-0

Upstream product

• 853056-96-9 N-[(R)-α-methylbenzyl]-(2S)-aziridine-(N'-methoxy-N'-methyl)carboxamide 
• 68820-72-4 (2S)-1-[(R)-α-methylbenzyl]-2-aziridinecarboxylate ethyl ester 
• 884498-60-6 (R)-1-{(S)-1-[(R)-1-phenylethyl]aziridin-2-yl}hexadec-2-yn-1-ol 
• 884498-59-3 1-{(S)-1-[(R)-1-phenylethyl]aziridin-2-yl}hexadec-2-yn-1-one 
• 884498-61-7 (E,2S,3R)-2-[(R)-1-phenylethylamino]-3-(t-butyldimethylsilyloxy)octadec-4-enyl acetate 

Downstream Products

• 1345009-54-2 (S)-4-[(R,E)-1-hydroxyhexadec-2-enyl]-3-(2-phenylacetyl)oxazolidin-2-one 
• 884498-57-1 (S)-3-benzoyl-4-[(R,E)-1-hydroxyhexadec-2-enyl]oxazolidin-2-one 
• 1345009-56-4 (S)-4-[(R,E)-1-hydroxyhexadec-2-enyl]-3-(2-methoxybenzoyl)oxazolidin-2-one 
• 1345009-57-5 (S)-4-[(R,E)-1-hydroxyhexadec-2-enyl]-3-(4-nitrobenzoyl)-oxazolidin-2-one 

Relevant academic research and scientific papers

3,4-Disubstituted oxazolidin-2-ones as constrained ceramide analogs with anticancer activities

Heterocyclic analogs of ceramide as 3-alkanoyl or benzoyl-4-(1-hydroxy-2- enyl)-oxazolidin-2-ones were designed by binding of primary alcohol and amide in sphinogosine backbone as a carbamate. They were synthesized by addition of acyl halide to the common

Synthesis of constrained ceramide analogs and their potent antileukemic activities

Constrained ceramide analogs were designed and synthesized by binding terminal alcohol and amine of ceramide with additional carbonyl functional group as 3-acetyl (3), 3-propionyl (4), 3-benzoyl (5), and 3-hexadecanoyl-4-(1- hydroxyhexadec-2-enyl)-oxazoli