| Identification | Back Directory | [Name]
Pranoprofen Impurity 5 | [CAS]
145986-74-9 | [Synonyms]
Pranoprofen Impurity J
methyl 2-(5H-chromeno[2,3-b]pyridin-7-yl)propanoate
(2RS)-2-(10H-9-Oxa-1-azaanthracen-6-yl)propanoic acid methyl...
(2RS)-2-(10H-9-Oxa-1-azaanthracen-6-yl)propanoic acid methyl ester
5H-[1]Benzopyrano[2,3-b]pyridine-7-acetic acid, α-methyl-, methyl ester | [Molecular Formula]
C16H15NO3 | [MOL File]
145986-74-9.mol | [Molecular Weight]
269.3 |
| Chemical Properties | Back Directory | [Boiling point ]
414.3±33.0 °C(Predicted) | [density ]
1?+-.0.06 g/cm3(Predicted) | [solubility ]
PBS (pH 7.2): 10 mg/ml | [pka]
3.00±0.20(Predicted) | [InChI]
InChI=1S/C16H15NO3/c1-10(16(18)19-2)11-5-6-14-13(8-11)9-12-4-3-7-17-15(12)20-14/h3-8,10H,9H2,1-2H3 | [InChIKey]
OETZDTSQXPRXOB-UHFFFAOYSA-N | [SMILES]
C(C1C=CC2OC3=NC=CC=C3CC=2C=1)(C)C(=O)OC |
| Hazard Information | Back Directory | [Description]
UDP-N-acetyl-D-Glucosamine is a natural nucleotide sugar that is used by glycosyltransferases to transfer N-acetyl-D-glucosamine (Item No. 13136) residues to substrates.1 It is an important component of antibiotic biosynthesis pathways in fungi and lipopolysaccharide production in bacteria.2,3WARNING This product is not for human or veterinary use. | [References]
[1] ROSEMAN S. Reflections on Glycobiology* 1[J]. The Journal of Biological Chemistry, 2001, 38 1: 41527-41542. DOI: 10.1074/jbc.r100053200
[2] FUMITAKA KUDO Tadashi E. Biosynthetic genes for aminoglycoside antibiotics[J]. Journal of Antibiotics, 2009, 62 9: 471-481. DOI: 10.1038/ja.2009.76
[3] ERIN F MULROONEY. Biosynthesis of UDP-N-acetyl-L-fucosamine, a precursor to the biosynthesis of lipopolysaccharide in Pseudomonas aeruginosa serotype O11.[J]. The Journal of Biological Chemistry, 2005, 280 20: 19535-19542. DOI: 10.1074/jbc.m500612200 |
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TOSUN PHARM
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www.toref.cn/ |
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