Balofloxacin structure, CAS 127294-70-6

Balofloxacin

CAS Number127294-70-6

Synonymsq35; MFCD00864925; baloxin; BALOFLOXACIN EXTRA PURE; Balofloxacin

Molecular FormulaC20H24FN3O4.2H2O

Molecular Weight389.42

Purity≥98 (HPLC)%

Density1.4±0.1 g/cm3

Boiling Point608.3±55.0 °C at 760 mmHg

Melting Point137ºC

Flash Point

Appearancepowder

EINECS

MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-9009297 Purity: ≥98 (HPLC)%
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Quality Control of [ 127294-70-6 ] Purity: ≥98 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number127294-70-6
Catalog No.2A-9009297
Chinese Name巴洛沙星
Synonymsq35; MFCD00864925; baloxin; BALOFLOXACIN EXTRA PURE; Balofloxacin
Molecular FormulaC20H24FN3O4.2H2O
Molecular Weight389.42
Purity≥98 (HPLC)
Density1.4±0.1 g/cm3
Boiling Point608.3±55.0 °C at 760 mmHg
Melting Point137ºC
Appearancepowder
Storage Condition2-8°C
Packaging25kg/drum
ApplicationBalofloxacin is a quinolone antibiotic that can inhibit bacterial DNA synthesis by interfering with DNA gyrase.
HTC2933990090
SMILESCNC1CCCN(C1)C2=C(C=C3C(=C2OC)N(C=C(C3=O)C(=O)O)C4CC4)F
InChI1S/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)
InChI KeyMGQLHRYJBWGORO-UHFFFAOYSA-N
NACRES CodeNA.41
UNSPSC51101500
MSDSmsds/9297_1_127294_70_6.pdf
BioactivityBalofloxacin is quinolone antibiotic, inhibiting the synthesis of bacterial DNA by interference with the enqyme DNA gyrase.Target: Antibacterial; DNA gyrase.Balofloxacin, an orally active fluoroquinolone antibiotic, has been developed by Choongwae Pharma in Korea, for the treatment of urinary tract infection (UTI). Chugai and Ciba were developing balofloxacin for respiratory tract infections (RTI) but discontinued development in 1995 due to changes in Chugai's R&D focus and a lack of efficacy of the drug. Following phase II trials, Choongwae bought the rights to develop balofloxacin in Korea from Chugai. Phase III trials for UTI were completed in early 2001. Balofloxacin was approved by the Korean FDA in December 2001 for UTI. In March 2002, phase II trials were underway for RTI. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Infection References [1]. Alksne L. Balofloxacin Choongwae. Curr Opin Investig Drugs. 2003 Feb;4(2):224-9. Chemical & Physical Properties Density 1.4±0.1 g/cm3 Boiling Point 608.3±55.0 °C at 760 mmHg Melting Point 137ºC Molecular Formula C20H24FN3O4 Molecular Weight 389.42 Flash Point 321.7±31.5 °C PSA 60.69000 LogP 1.24 Vapour Pressure 0.0±1.8 mmHg at 25°C Index of Refraction 1.639 InChIKey MGQLHRYJBWGORO-UHFFFAOYSA-N SMILES CNC1CCCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)C1 Storage condition 2-8°C
Use ofBalofloxacin is quinolone antibiotic, inhibiting the synthesis of bacterial DNA by interference with the enqyme DNA gyrase.Target: Antibacterial; DNA gyrase.Balofloxacin, an orally active fluoroquinolone antibiotic, has been developed by Choongwae Pharma in Korea, for the treatment of urinary tract infection (UTI). Chugai and Ciba were developing balofloxacin for respiratory tract infections (RTI) but discontinued development in 1995 due to changes in Chugai's R&D focus and a lack of efficacy of the drug. Following phase II trials, Choongwae bought the rights to develop balofloxacin in Korea from Chugai. Phase III trials for UTI were completed in early 2001. Balofloxacin was approved by the Korean FDA in December 2001 for UTI. In March 2002, phase II trials were underway for RTI. Properties Articles25 Name Balofloxacin Synonym More Synonyms Balofloxacin Biological Activity Description Balofloxacin is quinolone antibiotic, inhibiting the synthesis of bacterial DNA by interference with the enqyme DNA gyrase.Target: Antibacterial; DNA gyrase.Balofloxacin, an orally active fluoroquinolone antibiotic, has been developed by Choongwae Pharma in Korea, for the treatment of urinary tract infection (UTI). Chugai and Ciba were developing balofloxacin for respiratory tract infections (RTI) but discontinued development in 1995 due to changes in Chugai's R&D focus and a lack of efficacy of the drug. Following phase II trials, Choongwae bought the rights to develop balofloxacin in Korea from Chugai. Phase III trials for UTI were completed in early 2001. Balofloxacin was approved by the Korean FDA in December 2001 for UTI. In March 2002, phase II trials were underway for RTI. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Infection References [1]. Alksne L. Balofloxacin Choongwae. Curr Opin Investig Drugs. 2003 Feb;4(2):224-9. Chemical & Physical Properties Molecular Formula C20H24FN3O4 PSA 60.69000 Index of Refraction 1.639 InChIKey MGQLHRYJBWGORO-UHFFFAOYSA-N
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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