74089
1-Amino-1-deoxy-scyllo-inositol
≥95.0% (TLC)
Synonym(s):
scyllo-Inosamine
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About This Item
Empirical Formula (Hill Notation):
C6H13NO5
CAS Number:
Molecular Weight:
179.17
UNSPSC Code:
12352201
PubChem Substance ID:
Beilstein/REAXYS Number:
2802457
InChI
1S/C6H13NO5/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6,8-12H,7H2/t1-,2-,3+,4+,5-,6-
SMILES string
O[C@@H]1[C@@H](N)[C@H](O)[C@@H](O)[C@H](O)[C@H]1O
InChI key
JXAOTICXQLILTC-CDRYSYESSA-N
assay
≥95.0% (TLC)
form
powder
storage temp.
2-8°C
Quality Level
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Lucía Díaz et al.
Journal of medicinal chemistry, 54(7), 2069-2079 (2011-03-05)
A library of aminocyclitols derived from CuAAC reaction between N-propargylaminocyclitol 4 and a series of azides [1-25] is described and tested against GCase. Azides have been chosen from a large collection of potential candidates that has been filtered according to
Christopher P Phenix et al.
Chembiochem : a European journal of chemical biology, 9(10), 1591-1602 (2008-06-07)
MosA is an enzyme from Sinorhizobium meliloti L5-30, a beneficial soil bacterium that forms a symbiotic relationship with leguminous plants. MosA was proposed to catalyze the conversion of scyllo-inosamine to 3-O-methyl-scyllo-inosamine (compounds known as rhizopines), despite the MosA sequence showing
Meritxell Egido-Gabás et al.
Organic & biomolecular chemistry, 3(7), 1195-1201 (2005-03-24)
A series of 13 aminocyclitol derivatives belonging to two different families is described. Their configuration is governed by the regio- and stereocontrolled epoxide opening of a suitably protected conduritol-B epoxide. Studies on several glycosyl processing enzymes indicate that some of
Stereochemical recognition of doubly functional aminotransferase in 2-deoxystreptamine biosynthesis.
Kenichi Yokoyama et al.
Journal of the American Chemical Society, 127(16), 5869-5874 (2005-04-21)
The doubly functional aminotransferase BtrS in the 2-deoxystreptamine (DOS) biosynthesis, in which two transaminations are involved, was characterized by a genetic as well as a chemical approach with the heterologously expressed enzyme. The gene disruption study clearly showed that BtrS
C P Saint et al.
Journal of bacteriology, 175(16), 5205-5215 (1993-08-01)
Rhizopines are selective growth substrates synthesized in nodules only by strains of rhizobia capable of their catabolism. We report the isolation and study of genes for the synthesis and catabolism of a new rhizopine, scyllo-inosamine (sIa), from alfalfa nodules induced
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