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About This Item
Empirical Formula (Hill Notation):
C13H9F2NO4
CAS Number:
Molecular Weight:
281.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
mp
320-322 °C (lit.)
functional group
carboxylic acid
fluoro
ketone
SMILES string
CC1COc2c(F)c(F)cc3C(=O)C(=CN1c23)C(O)=O
InChI
1S/C13H9F2NO4/c1-5-4-20-12-9(15)8(14)2-6-10(12)16(5)3-7(11(6)17)13(18)19/h2-3,5H,4H2,1H3,(H,18,19)
InChI key
NVKWWNNJFKZNJO-UHFFFAOYSA-N
Gene Information
human ... CSNK2A1(1457)
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General description
(S)-(-)-9,10-Difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid may be used in the preparation of the following:
- kynurenine aminotransferase II (KAT II) inhibitor, [(S)-(-)-9-(4-aminopiperazine-1-yl)-8-fluoro-3-methyl-6-oxo-2,3,5,6-tetrahydro-4H-1-oxa-3a-aza-phenalene-5-carboxylic acid]
- fused-ring derivatives
- N-desmethyllevofloxacin
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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7-Piperazinylquinolones with methylene-bridged nitrofuran scaffold as new antibacterial agents.
Emami S, et al.
Medicinal Chemistry Research, 22(12), 5940-5947 (2013)
On the relationship between the two branches of the kynurenine pathway in the rat brain in vivo.
Amori L, et al.
Journal of Neurochemistry, 109(2), 316-325 (2009)
Andriy G Golub et al.
Journal of medicinal chemistry, 49(22), 6443-6450 (2006-10-27)
Due to the emerging role of protein kinase CK2 as a molecule that participates not only in the development of some cancers but also in viral infections and inflammatory failures, small organic inhibitors of CK2, besides application in scientific research
Muhammad Malik et al.
Antimicrobial agents and chemotherapy, 54(12), 5214-5221 (2010-09-22)
Quinolones rapidly kill bacteria by two mechanisms, one that requires protein synthesis and one that does not. The latter, which is measured as lethal action in the presence of the protein synthesis inhibitor chloramphenicol, is enhanced by N-1 cyclopropyl and
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