86669-32-1

Basic information

• Product Name: (S)-2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-pentanedioic acid dioctadecyl ester
• Synonyms: (S)-2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-pentanedioic acid dioctadecyl ester
• CAS NO: 86669-32-1
• Molecular Weight: 959.413
• Mol File: 86669-32-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-pentanedioic acid dioctadecyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-pentanedioic acid dioctadecyl ester(86669-32-1)
• EPA Substance Registry System: (S)-2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-pentanedioic acid dioctadecyl ester(86669-32-1)

Safety Data

• Hazardous Substances Data: 86669-32-1(Hazardous Substances Data)

Upstream product

• 3386-33-2 1-chlorooctadecane 
• 59-05-2 N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamic acid 

Relevant articles and documents

Methotrexate Analogues. 18. Enhancement of the Antitumor Effect of Methotrexate and 3',5'-Dichloromethotrexate by the Use of Lipid-Soluble Diesters

Lipophilic methotrexate (MTX) and 3',5'-dichloromethotrexate (DCM) diesters were prepared by HCl-catalyzed esterification or by neutral esterification using cesium carbonate and an alkyl or aralkyl halide in Me2SO.The products were tested for in vivo antitumor activity against L1210 leukemia in mice to test whether all MTX and DCM diesters are therapeutically equivalent in this species.Contrary to what has been found with simple primary dialkyl esters, ortho-substituted dibenzyl esters of MTX produce longer survival on a q3d*3 schedule than does MTX itself and show a dose-sparing effect comparable to that of MTX at shorter treatment intervals.Thus, MTX bis(6-chloropiperonyl) ester at an MTX-equivalent dose of 5.5 mg/kg gave a +88percent increase in median life span (ILS), whereas for MTX a +88percent ILS required 30 mg/kg.When the MTX-equivalent dose of MTX bis(6-chloropiperonyl) ester was increased to 40 mg/kg, a +167percent ILS was observed, as compared with a +100percent ILS with 60 mg/kg of the parent drug.High activity (>100percent ILS) was likewise shown by the bis(2,5-dimethylbenzyl), bis(2,6-dichlorobenzyl), and di-3-picolyl esters of MTX and by the bis(1-methylbutyl) ester of DCM.The results of this study indicate that MTX and DCM esters are not therapeutically equivalent in mice, despite the high serum esterase activity in this species, and that an up to 10-fold reduction in total administered dose on the q3d*3 schedule is feasible by this approach.