106881-92-9

Upstream product

• 17677-16-6 3-dodecyloxy-1-triphenylmethoxy-2-propanol 
• 100-39-0 benzyl bromide 
• 117089-03-9 2,2-dimethyl-4-dodecyloxymethyl-1,3-dioxolane 
• 143-15-7 1-dodecylbromide 
• 76-83-5 trityl chloride 
• 100165-14-8 3-dodecyloxypropane-1,2-diol 
• 100-44-7 benzyl chloride 
• 96093-52-6 3-O-Dodecyl-1-O-trityl-sn-glycerin 
• 112-53-8 1-dodecyl alcohol 
• 90904-23-7 3-O-dodecyl-sn-glycerol 
• 51323-71-8 dodecyl mesylate 

Downstream Products

• 70641-54-2 C₂₇H₅₀NO₆P 
• 106881-97-4 Phosphoric acid 2-benzyloxy-3-dodecyloxy-propyl ester 2-bromo-ethyl ester 
• 73073-46-8 3-(dodecyloxy)-2-hydroxypropyl 2-(trimethylammonio)ethyl phosphate 
• 96022-69-4 2-O-Benzyl-3-O-dodecyl-1-O-<2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranosyl>-sn-glycerin 
• 96022-95-6 2-O-Benzyl-3-O-dodecyl-sn-glycerin 
• 125001-94-7 2-(benzyloxy)-3-(dodecyloxy)propan-1-ol 

Relevant academic research and scientific papers

Design, synthesis and cytotoxicity of chimeric erlotinib-alkylphospholipid hybrids

Two series of erlotinib-alkylphospholipid hybrids were prepared and evaluated for their antiproliferative activities against a panel of four cell lines representing lung, breast, liver and skin cancers using erlotinib and miltefosine as reference standards. Amide analogs elicited more enhanced cytotoxic activity than analogous esters. Amide derivatives 8d and 8e exhibited promising broad-spectrum antiproliferative activity and higher efficacy than reference erlotinib and miltefosine. Their cellular GI50 values was in the ranges of 24.7–46.9 μM and 26.8–43.1 μM for 8e and 8d respectively. Assay results of the inhibitory activity of the prepared compounds on EGFR kinase reaction and Akt phosphorylation in conjugation with statistical correlation analysis indicated that other mechanisms might contribute to their elicited cytotoxicities. In addition, statistical correlation analysis revealed that mechanisms of elicited cytotoxicities for amide series might be different from ester series. In addition, correlation analysis indicated variations in the mechanisms according to the types of cell line.

Structure-Activity Relationship in PAF-acether. 3. Hydrophobic Contribution to Agonistic Activity

The synthesis of some selected PAF-acether homologues with an alkoxy-chain length from C1 to C20 in position 1 is described.All agonist activities are closely correlated among themselves and with the calculated fatty-chain hydrophobicity.After a discussio

Stereoselective Synthesis of Long-chain 1-O-(β-D-Maltosyl)-3-O-alkyl-sn-glycerols (Alkyl Glyceryl Ether Lysoglycolipids)

The synthesis of long-chain 2-O-benzyl-3-O-alkyl-sn-glycerols 5 was improved, making these compounds easily accessible for glycosylation experiments.Glycosylation with α-acetobromomaltose following a modified Koenings-Knorr procedure after removal of the protective groups yielded the title compound 9 in good yields.These compounds represent examples of alkyl glyceryl ether lysoglycolipids.Some properties of these amphiphilic compounds with a nonionic carbohydrate head-group differ not much (critical micell concentration, hemolytic activity), other properties differ very much (antitumor efficiency) from the properties of the analogous compounds with a zwitterionic phosphorylcholine head-group.