90015-82-0

Basic information

• Product Name: ((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate
• Synonyms: ((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate;((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H) -yl)-3-hydroxytetrahydrofur;((2R,3S,5R)-5-(5-(3-AMinoprop-1-en-1-yl)-2,4-dioxo-3,4-dihydropyriMidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)Methyl tetrahydrogen triphosphate;((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrof;5-(3-Amino-1-propenyl)-2'-deoxyuridine 5'-(tetrahydrogen triphosphate)
• CAS NO: 90015-82-0
• Molecular Formula: C₁₂H₂₀N₃O₁₄P₃
• Molecular Weight: 525.235
• Mol File: 90015-82-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Density: 1.819 g/cm³
• Refractive Index: 1.602
• CAS DataBase Reference: ((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate(CAS DataBase Reference)
• NIST Chemistry Reference: ((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate(90015-82-0)
• EPA Substance Registry System: ((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate(90015-82-0)

Safety Data

• Hazardous Substances Data: 90015-82-0(Hazardous Substances Data)

Usage

General Description

The chemical named ((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dinoxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate, also known as hATP, is a complex organic molecule. It has elements of carbon, hydrogen, nitrogen, oxygen, and phosphorus in its structure. ((2R,3S,5R)-5-(5-(3-Aminopropyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate can be classified under the Nucleoside Triphosphates chemical category, hence, is likely to be involved in biological reactions pertaining to nucleic acids synthesis, such as DNA replication and repair or RNA synthesis. The chemical structure contains a dihydropyrimidinyl group which is linked to a hydroxytetrahydrofuran. The 'amino-propyl' extension likely increases its molecular flexibility, whereas the triphosphate group provides the potential for high-energy bonds, making it a possible part of ATP-related biochemical processes. Further studies are needed for its comprehensive understanding.

InChI:InChI=1/C12H22N3O14P3/c13-3-1-2-7-5-15(12(18)14-11(7)17)10-4-8(16)9(27-10)6-26-31(22,23)29-32(24,25)28-30(19,20)21/h5,8-10,16H,1-4,6,13H2,(H,22,23)(H,24,25)(H,14,17,18)(H2,19,20,21)/t8-,9-,10-/m1/s1

Upstream product

• 96102-22-6 5-(3'-trifluoroacetamidoallyl)-2'-deoxyuridine 
• 102-82-9 tributyl-amine 
• 15715-58-9 triethylamine carbonate 
• 5975-18-8 tri(n-butyl)ammonium pyrophosphate 

Downstream Products

• 1383917-01-8 SITC-dUTP 

Relevant articles and documents

A SYSTEM FOR DELIVERING THERAPEUTIC AGENTS INTO LIVING CELLS AND CELL NUCLEI

A novel class of oligomeric compounds designed for forming conjugates with biologically active substances and delivering these substances to a desired bodily target are disclosed. Nove1 conjugates of biologically active moities and such oligomeric compounds, pharmaceutical compositions containing such conjugates, and uses thereof as delivery systems for delivering the biologically active substances to a desired target are further disclosed. Processes of preparing the conjugates and the oligomeric compounds and novel intermediates designed for and used in these processes are also disclosed.