Chemodex

Balofloxacin

Product Code:
 
CDX-B0302
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
Short term: +4°C. Long term: +4°C
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Chemical Structure
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Chemical Structure

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CodeSizePrice
CDX-B0302-M02525 mg£85.00
Quantity:
CDX-B0302-M100100 mg£213.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
(?)-1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[3-(methyl-amino)piperidino]-4-oxo-3-quinolinecarboxylic acid; Fluoroquinolone
Appearance:
White powder.
CAS:
127294-70-6
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C20H24FN3O4/c1-22-11-4-3-7-23(9-11)17-15(21)8-13-16(19(17)28-2)24(12-5-6-12)10-14(18(13)25)20(26)27/h8,10-12,22H,3-7,9H2,1-2H3,(H,26,27)
InChiKey:
MGQLHRYJBWGORO-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 127294-70-6. Formula: C20H24FN3O4. MW: 389.42. Synthetic. Fluoroquinolone antibiotic with potent bactericidal activity. Inhibits the synthesis of bacterial DNA by interfering with the the supercoiling activity of DNA gyrase.
MDL:
MFCD00864925
Molecular Formula:
C20H24FN3O4
Molecular Weight:
389.42
Package Type:
Vial
Product Description:
Fluoroquinolone antibiotic with potent bactericidal activity. Inhibits the synthesis of bacterial DNA by interfering with the the supercoiling activity of DNA gyrase.
Purity:
>98% (HPLC)
SMILES:
CNC(CCC1)CN1C2=C(F)C=C3C(N(C4CC4)C=C(C(O)=O)C3=O)=C2OC
Solubility Chemicals:
Soluble in DMSO (10mg/ml).
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.

References

(1) T. Ito, et al.; Antimicrob. Agents Chemother. 36, 1708 (1992) | (2) I. Takashima, et al.; Antimicrob. Agents Chemother. 37, 901 (1993) | (3) Y. Gohara, et al.; Antimicrob. Agents Chemother. 37, 1826 (1993) | (4) T. Ito, et al.; Biol. Pharm. Bull. 17, 927 (1994) | (5) N. Cho, et al.; Drugs 49, 391 (1995) | (6) H. Iwasaki, et al.; Chemotherapy 41, 100 (1995) | (7) T. Ito, et al.; Antimicrob. Agents Chemother. 39, 1522 (1995) | (8) L. Alksne; Curr. Opin. Investig. Drugs 4, 224 (2003) | (9) H. Jiang, et al.; J. Ocul. Pharmacol. Ther. 30, 482 (2014)