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Home Other Building Blocks 2',3',5'-Triacetylguanosine

2',3',5'-Triacetylguanosine

CAS No.:
6979-94-8
Catalog Number:
AG003FFJ
Molecular Formula:
C16H19N5O8
Molecular Weight:
409.3508
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$14
- +
5g
95%
In Stock USA
United States
$32
- +
25g
95%
In Stock USA
United States
$88
- +
100g
95%
In Stock USA
United States
$313
- +
Product Description
Catalog Number:
AG003FFJ
Chemical Name:
2',3',5'-Triacetylguanosine
CAS Number:
6979-94-8
Molecular Formula:
C16H19N5O8
Molecular Weight:
409.3508
MDL Number:
MFCD00057054
IUPAC Name:
[(2R,3R,4R,5R)-3,4-diacetyloxy-5-(2-amino-6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl acetate
InChI:
InChI=1S/C16H19N5O8/c1-6(22)26-4-9-11(27-7(2)23)12(28-8(3)24)15(29-9)21-5-18-10-13(21)19-16(17)20-14(10)25/h5,9,11-12,15H,4H2,1-3H3,(H3,17,19,20,25)/t9-,11-,12-,15-/m1/s1
InChI Key:
ULXDFYDZZFYGIY-SDBHATRESA-N
SMILES:
CC(=O)O[C@@H]1[C@H](OC(=O)C)[C@H](O[C@H]1n1cnc2c1nc(N)[nH]c2=O)COC(=O)C
EC Number:
230-242-4
Properties
Complexity:
743  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0
Exact Mass:
409.123g/mol
Formal Charge:
0
Heavy Atom Count:
29  
Hydrogen Bond Acceptor Count:
10  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
409.355g/mol
Monoisotopic Mass:
409.123g/mol
Rotatable Bond Count:
8  
Topological Polar Surface Area:
173A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.7  
Literature
Title Journal
Structure and gelation mechanism of tunable guanosine-based supramolecular hydrogels. Langmuir : the ACS journal of surfaces and colloids 20100615
Oxidative modification of guanine bases initiated by oxyl radicals derived from photolysis of azo compounds. The journal of physical chemistry. B 20100520
Tailoring the properties of guanosine-based supramolecular hydrogels. Langmuir : the ACS journal of surfaces and colloids 20090804
Pathways of arachidonic acid peroxyl radical reactions and product formation with guanine radicals. Chemical research in toxicology 20080201
Oxidative generation of guanine radicals by carbonate radicals and their reactions with nitrogen dioxide to form site specific 5-guanidino-4-nitroimidazole lesions in oligodeoxynucleotides. Chemical research in toxicology 20030801
Peroxynitrite-induced reactions of synthetic oligo 2'-deoxynucleotides and DNA containing guanine: formation and stability of a 5-guanidino-4-nitroimidazole lesion. Biochemistry 20020611
A novel nitroimidazole compound formed during the reaction of peroxynitrite with 2',3',5'-tri-O-acetyl-guanosine. Journal of the American Chemical Society 20011212
Properties