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189279-58-1

189279-58-1 | 3-Quinolinecarboxylic acid, 1-(6-amino-3,5-difluoro-2-pyridinyl)-8-chloro-6-fluoro-1,4-dihydro-7-(3-hydroxy-1-azetidinyl)-4-oxo-

CAS No: 189279-58-1 Catalog No: AG002I64 MDL No:

Product Description

Catalog Number:
AG002I64
Chemical Name:
3-Quinolinecarboxylic acid, 1-(6-amino-3,5-difluoro-2-pyridinyl)-8-chloro-6-fluoro-1,4-dihydro-7-(3-hydroxy-1-azetidinyl)-4-oxo-
CAS Number:
189279-58-1
Molecular Formula:
C18H12ClF3N4O4
Molecular Weight:
440.7605
IUPAC Name:
1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-hydroxyazetidin-1-yl)-4-oxoquinoline-3-carboxylic acid
InChI:
InChI=1S/C18H12ClF3N4O4/c19-12-13-7(1-9(20)14(12)25-3-6(27)4-25)15(28)8(18(29)30)5-26(13)17-11(22)2-10(21)16(23)24-17/h1-2,5-6,27H,3-4H2,(H2,23,24)(H,29,30)
InChI Key:
DYDCPNMLZGFQTM-UHFFFAOYSA-N
SMILES:
OC1CN(C1)c1c(F)cc2c(c1Cl)n(cc(c2=O)C(=O)O)c1nc(N)c(cc1F)F
UNII:
6315412YVF

Properties

Complexity:
755  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
440.05g/mol
Formal Charge:
0
Heavy Atom Count:
30  
Hydrogen Bond Acceptor Count:
11  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
440.763g/mol
Monoisotopic Mass:
440.05g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
120A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.7  

Literature

Title Journal
Managing community acquired pneumonia in the elderly - the next generation of pharmacotherapy on the horizon. Expert opinion on pharmacotherapy 20170801
The 2009 Nobel Prize in Chemistry: Thomas A. Steitz and the structure of the ribosome. The Yale journal of biology and medicine 20110601
Methicillin-resistant Staphylococcus aureus: a pervasive pathogen highlights the need for new antimicrobial development. The Yale journal of biology and medicine 20101201
New antibiotics for antibiotic-resistant bacteria. F1000 biology reports 20090101
Comparative pharmacodynamics of the new fluoroquinolone ABT492 and levofloxacin with Streptococcus pneumoniae in an in vitro dynamic model. International journal of antimicrobial agents 20050501
Comparative pharmacodynamics of the new fluoroquinolone ABT492 and ciprofloxacin with Escherichia coli and Pseudomonas aeruginosa in an in vitro dynamic model. International journal of antimicrobial agents 20040801
The in vitro activity of a new fluoroquinolone, ABT-492, against recent clinical isolates of Chlamydia pneumoniae. The Journal of antimicrobial chemotherapy 20040701
ABT492 and levofloxacin: comparison of their pharmacodynamics and their abilities to prevent the selection of resistant Staphylococcus aureus in an in vitro dynamic model. The Journal of antimicrobial chemotherapy 20040701
In vitro activity of ABT-492 against anaerobic bacteria. Journal of chemotherapy (Florence, Italy) 20040601
Comparative study of the in vitro activity of a new fluoroquinolone, ABT-492. The Journal of antimicrobial chemotherapy 20040501
Comparative antimicrobial activities of the newly synthesized quinolone WQ-3034, levofloxacin, sparfloxacin, and ciprofloxacin against Mycobacterium tuberculosis and Mycobacterium avium complex. Antimicrobial agents and chemotherapy 20000201

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