Name: Name:2-Aminoadenosine
Brand: AABLOCKS
SKU: AA002K93
Rating: 90 (10 reviews)

Catalog No.: AA002K93

2096-10-8 | 2-Aminoadenosine

Pack Size： 5g

Purity： 98%(HPLC)

in stock

$24.00 $17.00

Pack Size： 25g

Purity： 98%

in stock

$43.00 $30.00

Pack Size： 100g

Purity： 98%

in stock

$107.00 $75.00

Pack Size： 500g

Purity： 98%

in stock

$486.00 $340.00

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Technical Information

Catalog Number: AA002K93

Chemical Name: 2-Aminoadenosine

CAS Number: 2096-10-8

Molecular Formula: C10H14N6O4

Molecular Weight: 282.2560

MDL Number: MFCD00053556

SMILES: OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1nc(N)nc2N

Properties

BP: 798.5°C at 760 mmHg

Form: Solid

MP: 241-243°C (dec.)

Storage: Keep in dry area;Room Temperature;Light sensitive;

Complexity: 363

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 4

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 20

Hydrogen Bond Acceptor Count: 9

Hydrogen Bond Donor Count: 5

Isotope Atom Count: 0

Rotatable Bond Count: 2

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: -1.4

Upstream Synthesis Route

2096-10-8

146-78-1

1818-71-9

[1]NucleosidesandNucleotides,1994,vol.13,#1-3,p.673-678

2096-10-8

1818-71-9

[1]JournaloftheAmericanChemicalSociety,1951,vol.73,p.3174

[2]PLoSONE,2018,vol.13,#5,

67-56-1

3387-63-1

2004-07-1

7803-88-5

2096-10-8

[1]JournalofOrganicChemistry,2007,vol.72,#1,p.173-179

2096-10-8

2140-71-8

[1]CanadianJournalofChemistry,1981,vol.59,p.3360-3364

6482-24-2

2096-10-8

473278-54-5

[1]Nucleosides,NucleotidesandNucleicAcids,2008,vol.27,#9,p.1024-1033

Downstream Synthesis Route

2096-10-8

146-78-1

[1]Montgomery;Hewson[JournaloftheAmericanChemicalSociety,1957,vol.79,p.4559]

[2]CurrentPatentAssignee:BAYERAG-US5696255,1997,A

[3]CurrentPatentAssignee:LANTHEUSMIHOLDINGSINC-US2005/106101,2005,A1Locationinpatent:Page/Pagecolumn9

2096-10-8

1818-71-9

[1]JournalofMedicinalChemistry,2020,vol.63,p.2941-2957

[2]JournaloftheAmericanChemicalSociety,1951,vol.73,p.3174

[3]PLoSONE,2018,vol.13

2',3',5'-tri-O-acetyl-2-chloroadenosine

2096-10-8

[1]Muraoka[ChemicalandPharmaceuticalBulletin,1981,vol.29,#12,p.3449-3454]

118-00-3

2096-10-8

[1]Ross,BruceS.;Springer,RobertH.;Ravikumar,VasulingaT.[Nucleosides,nucleotidesandnucleicacids,2008,vol.27,#1,p.67-69]

[2]Robins,MorrisJ.;Hansske,Fritz;Bernier,SalwaE.[CanadianJournalofChemistry,1981,vol.59,p.3360-3364]

[3]Ozola;Persson;Gronowitz;Hornfeldt[JournalofHeterocyclicChemistry,1995,vol.32,#3,p.863-866]

[4]CurrentPatentAssignee:LANTHEUSMIHOLDINGSINC-US2005/106101,2005,A1Locationinpatent:Page/Pagecolumn9

[5]Volpini,Rosaria;Marucci,Gabriella;Buccioni,Michela;DalBen,Diego;Lambertucci,Catia;Lammi,Carmen;Mishra,RamC.;Thomas,Ajiroghene;Cristalli,Gloria[ChemMedChem,2011,vol.6,#6,p.1074-1080]

[6]Bhattarai,Sanjay;Pippel,Jan;Scaletti,Emma;Idris,Riham;Freundlieb,Marianne;Rolshoven,Georg;Renn,Christian;Lee,Sang-Yong;Abdelrahman,Aliaa;Zimmermann,Herbert;El-Tayeb,Ali;Müller,ChristaE.;Sträter,Norbert[JournalofMedicinalChemistry,2020,vol.63,#6,p.2941-2957]

622-34-4

23192-64-5

53296-10-9

2096-10-8

[1]Omura;Marumoto;Furukawa[ChemicalandPharmaceuticalBulletin,1981,vol.29,#7,p.1870-1875]

Literature fold

Title: S-Adenosylhomocysteine hydrolase of the protozoan parasite Trichomonas vaginalis: potent inhibitory activity of 9-(2-deoxy-2-fluoro-β,D-arabinofuranosyl)adenine.

Journal: Bioorganic & medicinal chemistry letters20120615

Title: Adenosine deaminase-like protein 1 (ADAL1): characterization and substrate specificity in the hydrolysis of N(6)- or O(6)-substituted purine or 2-aminopurine nucleoside monophosphates.

Journal: Journal of medicinal chemistry20110825

Title: An efficient and scalable synthesis of 2,6-diaminopurine riboside.

Journal: Nucleosides, nucleotides & nucleic acids20080101

Title: Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: synthesis, deamination and tautomerism.

Journal: Organic & biomolecular chemistry20070921

Title: Identification of an in vivo inhibitor of Bacillus anthracis spore germination.

Journal: The Journal of biological chemistry20070420

Title: An efficient process for synthesis of 2'-O-methyl and 3'-O-methyl guanosine from 2-aminoadenosine using diazomethane and the catalyst stannous chloride.

Journal: Nucleosides, nucleotides & nucleic acids20060301

Title: Quantitative assessment of the use of modified nucleoside triphosphates in expression profiling: differential effects on signal intensities and impacts on expression ratios.

Journal: BMC biotechnology20020101

Title: Chemical constituents of Typhonium giganteum Engl.

Journal: Journal of Asian natural products research20010101

Title: Acyclic nucleotide analogues: synthesis, antiviral activity and inhibitory effects on some cellular and virus-encoded enzymes in vitro.

Journal: Antiviral research19900601

Title: Synthesis and antiviral activity of carbocyclic analogues of 2'-deoxyribofuranosides of 2-amino-6-substituted-purines and of 2-amino-6-substituted-8-azapurines.

Journal: Journal of medicinal chemistry19841101