313983-92-5

Basic information

• Product Name: [4-({[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-phenoxy]-acetic acid allyl ester
• CAS NO: 313983-92-5
• Molecular Weight: 653.689
• Mol File: 313983-92-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [4-({[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-phenoxy]-acetic acid allyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [4-({[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-phenoxy]-acetic acid allyl ester(313983-92-5)
• EPA Substance Registry System: [4-({[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-phenoxy]-acetic acid allyl ester(313983-92-5)

Safety Data

• Hazardous Substances Data: 313983-92-5(Hazardous Substances Data)

Upstream product

• 155505-55-8 allyl (4-hydroxymethyl)phenoxyacetate 
• 226250-40-4 4-formylphenoxyallylacetate 
• 123-08-0 4-hydroxy-benzaldehyde 
• 22509-74-6 N-ethoxycarbonylphthalimide 
• 2916-14-5 allyl chloroacetate 
• 124-20-9 N-(3-aminopropyl)-1,4-diaminobutane 
• 104435-58-7 N¹,N¹⁰-bisphthaloylspermidine 
• 192064-31-6 4-nitrophenyl-4'-hydroxymethylphenyl-1'-oxyallylacetate carbonate 

Downstream Products

• 132194-39-9 N¹,N⁸-bis(dihydrocaffeoyl)spermidine 
• 313983-98-1 [4-({[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamoyloxy}-methyl)-phenoxy]-acetic acid 

Relevant articles and documents

Optimising inhibitors of trypanothione reductase using solid-phase chemistry

A series of inhibitors of the enzyme trypanothione reductase has been identified using directed solid-phase chemistry. The compounds were based on a series of polyamine scaffolds and used the natural product kukoamine A as the lead structure. A compound with a K(i) of 76 nM was identified, although somewhat surprisingly the compound appeared to be noncompetitive in nature. (C) 2000 Elsevier Science Ltd.