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Home Aminos D-Glucose, 3-amino-3-deoxy-

D-Glucose, 3-amino-3-deoxy-

CAS No.:
576-44-3
Catalog Number:
AG00EBFR
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00EBFR
Chemical Name:
D-Glucose, 3-amino-3-deoxy-
CAS Number:
576-44-3
MDL Number:
MFCD00672150
IUPAC Name:
(2R,3S,4S,5R)-3-amino-2,4,5,6-tetrahydroxyhexanal
InChI:
InChI=1S/C6H13NO5/c7-5(3(10)1-8)6(12)4(11)2-9/h1,3-6,9-12H,2,7H2/t3-,4+,5+,6+/m0/s1
InChI Key:
FOEXHEVNPRRHDY-SLPGGIOYSA-N
UNII:
8EB87VF7OH
Properties
Complexity:
142  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0
Exact Mass:
179.079g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
5  
Isotope Atom Count:
0
Molecular Weight:
179.172g/mol
Monoisotopic Mass:
179.079g/mol
Rotatable Bond Count:
5  
Topological Polar Surface Area:
124A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-3.7  
Literature
Title Journal
Synthesis and antibacterial activity of aminodeoxyglucose derivatives against Listeria innocua and Salmonella typhimurium. Journal of agricultural and food chemistry 20091014
Characterization of the complete zwittermicin A biosynthesis gene cluster from Bacillus cereus. Applied and environmental microbiology 20090201
Kanosamine biosynthesis: a likely source of the aminoshikimate pathway's nitrogen atom. Journal of the American Chemical Society 20020911
Characterization of the early stage aminoshikimate pathway in the formation of 3-amino-5-hydroxybenzoic acid: the RifN protein specifically converts kanosamine into kanosamine 6-phosphate. Journal of the American Chemical Society 20020911
Mechanism of antifungal action of kanosamine. Medical mycology 20011001
Trehalose-containing lipooligosaccharides from mycobacteria: structures of the oligosaccharide segments and recognition of a unique N-acylkanosamine-containing epitope. Biochemistry 19850521
Properties