P0106

Pefloxacin mesylate dihydrate

Manufacturer: Sigma Aldrich

CAS Number: 149676-40-4

Synonym(S): 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-, monomethanesulfonate, dihydrate, Pefloxacine monomethanesulfonate dihydrate, Pefloxacinium methanesulfonate dihydrate

Select a Size

Pack Size SKU Availability Price
10 G P0106-10-G In Stock ₹ 8,424.90

P0106 - 10 G

₹ 8,424.90

In Stock

Quantity

1

Base Price: ₹ 8,424.90

GST (18%): ₹ 1,516.482

Total Price: ₹ 9,941.382

form

powder

Quality Level

100

solubility

H2O: 50 mg/mL

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteria

Mode of action

DNA synthesis | interferesenzyme | inhibits

storage temp.

2-8°C

SMILES string

O.O.CS(O)(=O)=O.CCN1C=C(C(O)=O)C(=O)c2cc(F)c(cc12)N3CCN(C)CC3

InChI

1S/C17H20FN3O3.CH4O3S.2H2O/c1-3-20-10-12(17(23)24)16(22)11-8-13(18)15(9-14(11)20)21-6-4-19(2)5-7-21;1-5(2,3)4;;/h8-10H,3-7H2,1-2H3,(H,23,24);1H3,(H,2,3,4);2*1H2

InChI key

LEULAXMUNMRLPW-UHFFFAOYSA-N

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Description

  • General description: Chemical structure: fluoroquinolone
  • Application: Pefloxacin is a synthetic broad-spectrum fluoroquinolone antibiotic that is effective against most gram-negative and gram-positive bacteria. It is used to treat gonococcal urethritis and for gram-negative-bacterial infections in the gastrointestinal system and the genitourinary tract. Pefloxacin mesylate dihydrate has been used to induce achilles tendon toxicity in rodents[1]. It′s cytotoxicity and uptake have been studied in primary cultures of rat hepatocytes[2].
  • Biochem/physiol Actions: Pefloxacin inhibits the bacterial enzymes DNA gyrase and topoisomerase IV, which are needed for the transcription and replication of bacterial DNA. DNA gyrase is thought to be the primary quinolone target for gram-negative bacteria. Topoisomerase IV is thought to be the primary target in gram-positive organisms. The inhibition of the topoisomerases results in strand breakage of the bacterial chromosome, supercoiling, and resealing. Therefore, DNA replication and transcription is inhibited . Pefloxacin is an analog of norfloxacin.
  • Other Notes: Keep container tightly closed in a dry and well-ventilated place.

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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100

solubility:
H2O: 50 mg/mL

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteria

Mode of action:
DNA synthesis | interferesenzyme | inhibits

storage temp.:
2-8°C

SMILES string:
O.O.CS(O)(=O)=O.CCN1C=C(C(O)=O)C(=O)c2cc(F)c(cc12)N3CCN(C)CC3

InChI:
1S/C17H20FN3O3.CH4O3S.2H2O/c1-3-20-10-12(17(23)24)16(22)11-8-13(18)15(9-14(11)20)21-6-4-19(2)5-7-21;1-5(2,3)4;;/h8-10H,3-7H2,1-2H3,(H,23,24);1H3,(H,2,3,4);2*1H2

InChI key:
LEULAXMUNMRLPW-UHFFFAOYSA-N

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