2. Anti-infection Cell Cycle/DNA Damage
  3. Bacterial Antibiotic DNA/RNA Synthesis
  4. Cinoxacin

Cinoxacin  (Synonyms: Compound 64716)

Cat. No.: HY-B1085 Purity: 99.99%
SDS COA Handling Instructions

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Cinoxacin (Compound 64716), a synthetic antimicrobial related to the quinolone class of orally active antibacterial agent. Cinoxacin has antibacterial activity against many gram-negative aerobic bacteria and inhibits bacterial DNA synthesis. Cinoxacin can be used for the research of urinary tract infections and bacterial prostatitis.

For research use only. We do not sell to patients.

Cinoxacin Chemical Structure

Cinoxacin Chemical Structure

CAS No. : 28657-80-9

Size Price Stock Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
 USD 35 In-stock
Solution
10 mM * 1 mL in DMSO USD 35 In-stock
Solid
25 mg USD 32 In-stock
50 mg USD 50 In-stock
100 mg USD 80 In-stock
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500 mg   Get quote  

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Based on 1 publication(s) in Google Scholar

Other Forms of Cinoxacin:

Cinoxacin Related Antibodies

Top Publications Citing Use of Products

1 Publications Citing Use of MCE Cinoxacin

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  • Biological Activity

  • Purity & Documentation

  • References

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Description

Cinoxacin (Compound 64716), a synthetic antimicrobial related to the quinolone class of orally active antibacterial agent. Cinoxacin has antibacterial activity against many gram-negative aerobic bacteria and inhibits bacterial DNA synthesis. Cinoxacin can be used for the research of urinary tract infections and bacterial prostatitis[1][2].

IC50 & Target

Quinolone

 

In Vitro

Cinoxacin (0-200μg/mL approximately, 3-24 h) inhibits many gram-negative aerobic bacteria with MIC values ranging from 4 to 64 μg/mL[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cinoxacin Related Antibodies

Cell Proliferation Assay[2]

Cell Line: Gram-negative aerobic bacteria (Escherichia coli, Proteus sp. etc.)
Concentration: 0-200μg/mL approximately
Incubation Time: 3-24 h
Result: Inhibited basal cell proliferation (40% in FB-2 and 35% in WRO) at 10 μM, inhibited cell number (by 68% to 73%) at 40 and 60 μM).
In Vivo

Cinoxacin (Oral administration, 1.7 g/kg, treated at 1 and 5 h postinfection) is effective in experimental bacterial infections in mice, with ED50 values ranging from 8.1 to 58.6 mg/kg[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Indicated bacterial infected mice model[2]
Dosage: 1.7 g/kg, treated at 1 and 5 h postinfection
Administration: Oral administration
Result: Displayed antibacterial activity with ED50 values ranging from 8.1 to 58.6 mg/kg.
Molecular Weight

262.22

Formula

C12H10N2O5
CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C(C1=NN(CC)C2=C(C=C3C(OCO3)=C2)C1=O)O
Shipping

Room temperature in continental US; may vary elsewhere.
Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
Solvent & Solubility
In Vitro: 

DMSO : 8.33 mg/mL (31.77 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.8136 mL 19.0680 mL 38.1359 mL
5 mM 0.7627 mL 3.8136 mL 7.6272 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Purity & Documentation

Purity: 99.99%

SDS (393 KB)

COA (250 KB) LCMS (264 KB)

Handling Instructions (2659 KB)
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.8136 mL 19.0680 mL 38.1359 mL 95.3398 mL
5 mM 0.7627 mL 3.8136 mL 7.6272 mL 19.0680 mL
10 mM 0.3814 mL 1.9068 mL 3.8136 mL 9.5340 mL
15 mM 0.2542 mL 1.2712 mL 2.5424 mL 6.3560 mL
20 mM 0.1907 mL 0.9534 mL 1.9068 mL 4.7670 mL
25 mM 0.1525 mL 0.7627 mL 1.5254 mL 3.8136 mL
30 mM 0.1271 mL 0.6356 mL 1.2712 mL 3.1780 mL
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Cinoxacin Related Classifications

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Cinoxacin28657-80-9Compound 64716Compound64716Compound-64716BacterialAntibioticDNA/RNA SynthesisGram-negative aerobic bacteriaantibioticsantibacterial agenturinary tract infectionsInhibitorinhibitorinhibit

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