14365-45-8,MFCD02683610
Catalog No.:AA007JME

14365-45-8 | 2'-Deoxy-l-adenosine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
98%
in stock  
$107.00   $75.00
- +
250mg
98%
in stock  
$193.00   $135.00
- +
1g
98%
in stock  
$512.00 $358.00
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA007JME
Chemical Name:
2'-Deoxy-l-adenosine
CAS Number:
14365-45-8
Molecular Formula:
C10H13N5O3
Molecular Weight:
251.2419
MDL Number:
MFCD02683610
SMILES:
OC[C@@H]1O[C@H](C[C@H]1O)n1cnc2c1ncnc2N
Properties
Computed Properties
 
Complexity:
307  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.5  

Downstream Synthesis Route
14365-45-8    23107-12-2   
Phosphoricacidmono-{(2S,3R,5S)-3-hydroxy-5-6-(7-hydroxymethyl-2,3-dihydro-1H-pyrrolizin-1-ylamino)-purin-9-yl-tetrahydro-furan-2-ylmethyl}ester 

[1]Wickramanayake,PalithaP.;Arbogast,BrianL.;Buhler,DonaldR.;Deinzer,MaxL.;Burlingame,AlmaL.[JournaloftheAmericanChemicalSociety,1985,vol.107,#8,p.2485-2488]

14365-45-8    40615-36-9   
(2S,3R,5S)-5-(6-Amino-purin-9-yl)-2-bis-(4-methoxy-phenyl)-phenyl-methoxymethyl-tetrahydro-furan-3-ol 

[1]Hashimoto,Yuichi;Iwanami,Naoko;Fujimori,Shizuyoshi;Shudo,Koichi[JournaloftheAmericanChemicalSociety,1993,vol.115,#22,p.9883-9887]

[1]Spadari;Maga;Focher;Ciarrocchi;Manservigi;Arcamone;Capobianco;Carcuro;Colonna;Iotti;Garbesi[JournalofMedicinalChemistry,1992,vol.35,#22,p.4214-4220]

[1]Boudou[NucleosidesandNucleotides,1999,vol.18,#4-5,p.607-609]

Literature

Title: Inhibition of severe acute respiratory syndrome-associated coronavirus (SARSCoV) by calpain inhibitors and beta-D-N4-hydroxycytidine.

Journal: Antiviral chemistry & chemotherapy 20040101

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SDS
Historical Records
Tags:14365-45-8 Molecular Formula|14365-45-8 MDL|14365-45-8 SMILES|14365-45-8 2'-Deoxy-l-adenosine
Catalog No.: AA007JME
14365-45-8,MFCD02683610
14365-45-8 | 2'-Deoxy-l-adenosine
Pack Size: 100mg
Purity: 98%
in stock
$107.00 $75.00
Pack Size: 250mg
Purity: 98%
in stock
$193.00 $135.00
Pack Size: 1g
Purity: 98%
in stock
$512.00 $358.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA007JME
Chemical Name: 2'-Deoxy-l-adenosine
CAS Number: 14365-45-8
Molecular Formula: C10H13N5O3
Molecular Weight: 251.2419
MDL Number: MFCD02683610
SMILES: OC[C@@H]1O[C@H](C[C@H]1O)n1cnc2c1ncnc2N
Properties
Complexity: 307  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 3  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.5  
Downstream Synthesis Route
14365-45-8    23107-12-2   
Phosphoricacidmono-{(2S,3R,5S)-3-hydroxy-5-6-(7-hydroxymethyl-2,3-dihydro-1H-pyrrolizin-1-ylamino)-purin-9-yl-tetrahydro-furan-2-ylmethyl}ester 

[1]Wickramanayake,PalithaP.;Arbogast,BrianL.;Buhler,DonaldR.;Deinzer,MaxL.;Burlingame,AlmaL.[JournaloftheAmericanChemicalSociety,1985,vol.107,#8,p.2485-2488]

14365-45-8    40615-36-9   
(2S,3R,5S)-5-(6-Amino-purin-9-yl)-2-bis-(4-methoxy-phenyl)-phenyl-methoxymethyl-tetrahydro-furan-3-ol 

[1]Hashimoto,Yuichi;Iwanami,Naoko;Fujimori,Shizuyoshi;Shudo,Koichi[JournaloftheAmericanChemicalSociety,1993,vol.115,#22,p.9883-9887]

137157-38-1    14365-45-8 

[1]Spadari;Maga;Focher;Ciarrocchi;Manservigi;Arcamone;Capobianco;Carcuro;Colonna;Iotti;Garbesi[JournalofMedicinalChemistry,1992,vol.35,#22,p.4214-4220]

258529-64-5    14365-45-8 

[1]Boudou[NucleosidesandNucleotides,1999,vol.18,#4-5,p.607-609]

Literature fold

Title: Inhibition of severe acute respiratory syndrome-associated coronavirus (SARSCoV) by calpain inhibitors and beta-D-N4-hydroxycytidine.

Journal: Antiviral chemistry & chemotherapy20040101

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