O0877

Oxolinic acid

Name: Oxolinic acid
Brand: SIGMA

quinolone antibiotic

Sinónimos:

5,8-Dihydro-5-ethyl-8-oxo-1,3-dioxolo[4,5-g]quinoline-7-carboxylic acid

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Fórmula empírica (notación de Hill):

C₁₃H₁₁NO₅

Número CAS:

14698-29-4

Peso molecular:

261.23

UNSPSC Code:

51282935

NACRES:

NA.85

PubChem Substance ID:

24278604

EC Number:

238-750-8

Beilstein/REAXYS Number:

620635

MDL number:

MFCD00056775

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Quality Level

200

antibiotic activity spectrum

Gram-negative bacteria

mode of action

DNA synthesis | interferes, enzyme | inhibits

storage temp.

2-8°C

SMILES string

CCN1C=C(C(O)=O)C(=O)c2cc3OCOc3cc12

InChI

1S/C13H11NO5/c1-2-14-5-8(13(16)17)12(15)7-3-10-11(4-9(7)14)19-6-18-10/h3-5H,2,6H2,1H3,(H,16,17)

InChI key

KYGZCKSPAKDVKC-UHFFFAOYSA-N

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Biochemicals

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Este artículo	67126	O0240000	C8645
Sigma-Aldrich O0877 Oxolinic acid	Supelco 67126 Oxolinic acid	O0240000 Oxolinic acid	Sigma-Aldrich C8645 Cinoxacin
antibiotic activity spectrum Gram-negative bacteria	antibiotic activity spectrum -	antibiotic activity spectrum -	antibiotic activity spectrum Gram-negative bacteria
mode of action DNA synthesis \| interferes, enzyme \| inhibits	mode of action -	mode of action -	mode of action DNA synthesis \| interferes, enzyme \| inhibits
Quality Level 200	Quality Level 100	Quality Level -	Quality Level 200
solubility 0.5 M NaOH: soluble 50 mg/mL	solubility -	solubility -	solubility -
storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C	storage temp. -

General description

Chemical structure: quinolone

Application

Oxolinic acid is used to study new transmissible resistance mechanisms qnrA, qnrB, qnrS, and aac(6′)Ib-cr, in Escherichia coli and Salmonella enterica. Oxolinic acid is added to culture medium for the isolation of Gardnerella vaginalis[1].

Biochem/physiol Actions

Oxolinic acid is a quinolone antibiotic. It is a DNA-gyrase (topoisomerase II) inhibitor used for studies on DNA winding and coiling and acts as a dopamine reuptake inhibitor for studies on dopaminergic neurotransmission processes.

Other Notes

5g,25g

Keep container tightly closed in a dry and well-ventilated place.

pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Clase de almacenamiento

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Colistin-oxolinic acid blood agar: a selective medium for the isolation of Gardnerella vaginalis.

J S Thompson

Journal of clinical microbiology, 21(5), 843-843 (1985-05-01)

Colistin-oxolinic acid medium is proposed as a selective isolation medium for Gardnerella vaginalis. The medium is effective in inhibiting staphylococci and gram-negative bacteria while allowing growth of G. vaginalis.

Behavioural and neurochemical evidence that the antimicrobial agent oxolinic acid is a dopamine uptake inhibitor.

J Garcia de Mateos-Verchere et al.

European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 8(4), 255-259 (1999-02-03)

The antimicrobial agent oxolinic acid, injected i.p. in mice, induced a dose dependent increase in locomotor activity. This stimulation culminated at the 32 mg/kg dose and became smaller for higher doses (64-128 mg/kg). When opposed to increasing doses (50-100-200 microg/kg

Suppression of pine wilt disease by an antibacterial agent, oxolinic acid.

Hyeok Ran Kwon et al.

Pest management science, 66(6), 634-639 (2010-02-13)

Pine wilt disease (PWD) is very complex and has been reported to be caused by pine wood nematode, Bursaphelenchus xylophilus (Steiner & Buhrer) Nickle, and its accompanying bacteria. However, there is no report on the control of PWD by antibacterial

Contribution of reactive oxygen species to pathways of quinolone-mediated bacterial cell death.

Xiuhong Wang et al.

The Journal of antimicrobial chemotherapy, 65(3), 520-524 (2010-01-14)

Quinolone-mediated death of Escherichia coli has been proposed to occur by two pathways. One is blocked by inhibitors of protein synthesis; the other is not. It is currently unknown how these two pathways fit with the recent observation that hydroxyl

Nickel-quinolones interaction. Part 5-Biological evaluation of nickel(II) complexes with first-, second- and third-generation quinolones.

Kalliopi C Skyrianou et al.

Journal of inorganic biochemistry, 105(10), 1273-1285 (2011-08-09)

The nickel(II) complexes with the quinolone antibacterial agents oxolinic acid, flumequine, enrofloxacin and sparfloxacin in the presence of the N,N'-donor heterocyclic ligand 2,2'-bipyridylamine have been synthesized and characterized. The quinolones act as bidentate ligands coordinated to Ni(II) ion through the

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Product Information Sheet - O0877

Product Information Sheet

Número de artículo de comercio global

SKU	GTIN
O0877-25G	04061834212652
O0877-5G	04061835507078

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