CAS 2096-10-8 | Adenosine, 2-amino- | CAS Number 2096-10-8

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2096-10-8 | Adenosine, 2-amino-

CAS No: 2096-10-8 Catalog No: AG002KBV MDL No:MFCD00053556

Product Description

Catalog Number:

AG002KBV

Chemical Name:

Adenosine, 2-amino-

CAS Number:

2096-10-8

Molecular Formula:

C10H14N6O4

Molecular Weight:

282.2560

MDL Number:

MFCD00053556

IUPAC Name:

(2R,3R,4S,5R)-2-(2,6-diaminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

InChI:

InChI=1S/C10H14N6O4/c11-7-4-8(15-10(12)14-7)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H4,11,12,14,15)/t3-,5-,6-,9-/m1/s1

InChI Key:

ZDTFMPXQUSBYRL-UUOKFMHZSA-N

SMILES:

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

Properties

Complexity:

363

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

282.108g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

282.26g/mol

Monoisotopic Mass:

282.108g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

166A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

-1.4

Literature

Title	Journal
S-Adenosylhomocysteine hydrolase of the protozoan parasite Trichomonas vaginalis: potent inhibitory activity of 9-(2-deoxy-2-fluoro-β,D-arabinofuranosyl)adenine.	Bioorganic & medicinal chemistry letters 20120615
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 of medicinal chemistry 20110825
An efficient and scalable synthesis of 2,6-diaminopurine riboside.	Nucleosides, nucleotides & nucleic acids 20080101
Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: synthesis, deamination and tautomerism.	Organic & biomolecular chemistry 20070921
Identification of an in vivo inhibitor of Bacillus anthracis spore germination.	The Journal of biological chemistry 20070420
An efficient process for synthesis of 2'-O-methyl and 3'-O-methyl guanosine from 2-aminoadenosine using diazomethane and the catalyst stannous chloride.	Nucleosides, nucleotides & nucleic acids 20060301
Quantitative assessment of the use of modified nucleoside triphosphates in expression profiling: differential effects on signal intensities and impacts on expression ratios.	BMC biotechnology 20020101
Chemical constituents of Typhonium giganteum Engl.	Journal of Asian natural products research 20010101
Acyclic nucleotide analogues: synthesis, antiviral activity and inhibitory effects on some cellular and virus-encoded enzymes in vitro.	Antiviral research 19900601
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 of medicinal chemistry 19841101