38198-98-0

Upstream product

• 124-09-4 1,6-Hexanediamine 
• 5843-59-4 6-chloropurine riboside 5'-monophosphate 

Downstream Products

• 81035-31-6 (3-{6-[9-((2R,3R,4S,5R)-3,4-Dihydroxy-5-phosphonooxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylamino]-hexylcarbamoyl}-propyl)-carbamic acid benzyl ester 
• 81035-30-5 ({6-[9-((2R,3R,4S,5R)-3,4-Dihydroxy-5-phosphonooxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylamino]-hexylcarbamoyl}-methyl)-carbamic acid benzyl ester 
• 81035-32-7 (5-{6-[9-((2R,3R,4S,5R)-3,4-Dihydroxy-5-phosphonooxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylamino]-hexylcarbamoyl}-pentyl)-carbamic acid benzyl ester 
• 81046-90-4 {6-[9-((2R,3R,4S,5R)-3,4-Dihydroxy-5-phosphonooxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylamino]-hexyl}-carbamic acid benzyl ester 
• 81035-24-7 C₁₆H₂₆N₆O₁₃P₃^(3-)*3Na⁽¹⁺⁾ 
• 81046-96-0 C₂₄H₃₁N₆O₁₅P₃^(4-)*4Na⁽¹⁺⁾ 

Relevant academic research and scientific papers

Affinity chromatography on immobilised adenosine 5' monophosphate. I. A new synthesis and some properties of an N6 immobilised 5' AMP

N6 (6 Aminohexyl) 5' AMP has been prepared by a single step reaction involving the nucleophylic displacement of the thiol group from 6 mercaptopurine riboside 5' phosphate by 1,6 hexane diamine. The structure of the product has been confirmed by physical, chemical and enzymic analyses. The 5' AMP derivative was coupled to Sepharose 4 B and used as an affinity adsorbent in the separation of dehydrogenases and kinases.