O8757

Ofloxacin

fluoroquinolone antibiotic

Manufacturer: Sigma Aldrich

CAS Number: 82419-36-1

Synonym(S): Dextrofloxacin

Select a Size

Pack Size SKU Availability Price
1 G O8757-1-G In Stock ₹ 7,794.00
10 G O8757-10-G In Stock ₹ 20,545.85

O8757 - 1 G

₹ 7,794.00

In Stock

Quantity

1

Base Price: ₹ 7,794.00

GST (18%): ₹ 1,402.92

Total Price: ₹ 9,196.92

biological source

synthetic

Quality Level

200

Assay

≥99% (HPLC)

form

powder

solubility

1 M NaOH: soluble 50 mg/mL

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteriamycobacteria

Mode of action

DNA synthesis | interferesenzyme | inhibits

storage temp.

2-8°C

InChI

1S/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)

InChI key

GSDSWSVVBLHKDQ-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
PHR1168
Ofloxacin
Supelco ₹ 10,900.78
33703
Ofloxacin
Supelco ₹ 8,768.25
1478108
Ofloxacin
Sigma Aldrich ₹ 40,756.13

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Description

  • General description: Chemical structure: fluoroquinolone
  • Application: Ofloxacin is a synthetic fluoroquinolone with broad-spectrum antibacterial activity. It is a nalidixic acid analog. It is given to patients before undergoing retinal reattachment surgery[1].
  • Biochem/physiol Actions: Ofloxacin inhibits bacterial DNA gyrase and topoisomerase IV, which haults DNA replication and cell division. Ofloxacin has been shown to convert LytA from the inactive E-form to the active C-form[2]. It is a chiral molecule that inhibits pneumococcal cell wall-degrading virulence factors[2].
  • Other Notes: Keep container tightly closed in a dry and well-ventilated place.

SAFETY INFORMATION

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Show Difference

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Sigma Aldrich

O8757

fluoroquinolone antibiotic...


biological source:
synthetic

Quality Level:
200

Assay:
≥99% (HPLC)

form:
powder

solubility:
1 M NaOH: soluble 50 mg/mL

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteriamycobacteria

Mode of action:
DNA synthesis | interferesenzyme | inhibits

storage temp.:
2-8°C

InChI:
1S/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)

InChI key:
GSDSWSVVBLHKDQ-UHFFFAOYSA-N

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__

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≥98% (TLC)

form:
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__

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__

Mode of action:
__

storage temp.:
−20°C

InChI:
1S/C14H23NO4/c1-2-3-4-5-6-7-11(16)10-13(17)15-12-8-9-19-14(12)18/h12H,2-10H2,1H3,(H,15,17)/t12-/m0/s1

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KYGIKEQVUKTKRR-LBPRGKRZSA-N

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InChI:
1S/C16H27NO4/c1-2-3-4-5-6-7-8-9-13(18)12-15(19)17-14-10-11-21-16(14)20/h14H,2-12H2,1H3,(H,17,19)/t14-/m0/s1

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PHSRRHGYXQCRPU-AWEZNQCLSA-N

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InChI:
1S/C18H31NO4/c1-2-3-4-5-6-7-8-9-10-11-15(20)14-17(21)19-16-12-13-23-18(16)22/h16H,2-14H2,1H3,(H,19,21)/t16-/m0/s1

InChI key:
YQFJJDSGBAAUPW-INIZCTEOSA-N