17850

Ciprofloxacin

≥98% (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 85721-33-1

Synonym(S): 1-Cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid, Ciprobay

Select a Size

Pack Size SKU Availability Price
5 G 17850-5-G In Stock ₹ 3,563.10
25 G 17850-25-G In Stock ₹ 13,974.90

17850 - 5 G

₹ 3,563.10

In Stock

Quantity

1

Base Price: ₹ 3,563.10

GST (18%): ₹ 641.358

Total Price: ₹ 4,204.458

Agency

EPA 1694

Quality Level

200

Assay

≥98% (HPLC)

form

powder or crystals

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteria

application(s)

environmental

Mode of action

DNA synthesis | interferesenzyme | inhibits

SMILES string

OC(=O)C1=CN(C2CC2)c3cc(N4CCNCC4)c(F)cc3C1=O

InChI

1S/C17H18FN3O3/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24/h7-10,19H,1-6H2,(H,23,24)

InChI key

MYSWGUAQZAJSOK-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
PHR1167
Ciprofloxacin
Supelco ₹ 11,077.80
33434
Ciprofloxacin
Supelco ₹ 11,988.00
1134313
Ciprofloxacin
Sigma Aldrich ₹ 34,176.90

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Description

  • General description: Ciprofloxacin is a second-generation broad-spectrum fluoroquinolone antibiotic with extensive antimicrobial and pharmacokinetic properties that is widely used to combat bacterial infections. Its chemical name is 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid.[1][2]Chemical structure: fluoroquinolone
  • Application: Ciprofloxacin is widely used in clinical practices against Gram-positive and Gram-negative bacteria and the treatment of a broad range of infections, including those of the skin, eyes, urinary tract, lower respiratory tract, gastrointestinal tract, et cetera. It can also be combined with various antimicrobial agents to combat bacterial biofilms as well as multidrug-resistant microorganisms.[1] Its derivatives have been developed to synthesize novel antibacterials with enhanced potency and diverse antimicrobial effects including antibacterial, antifungal, anti-HIV, anti-tumor, and anti-TB properties.[2]
  • Biochem/physiol Actions: The mechanism of action of Ciprofloxacin is the inhibition of bacterial DNA synthesis by blocking the subunit A of DNA gyrase enzyme as well as by affecting the bacterial cell wall.[1]

SAFETY INFORMATION

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Sigma Aldrich

17850

≥98% (HPLC)...


Agency:
EPA 1694

Quality Level:
200

Assay:
≥98% (HPLC)

form:
powder or crystals

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteria

application(s):
environmental

Mode of action:
DNA synthesis | interferesenzyme | inhibits

SMILES string:
OC(=O)C1=CN(C2CC2)c3cc(N4CCNCC4)c(F)cc3C1=O

InChI:
1S/C17H18FN3O3/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24/h7-10,19H,1-6H2,(H,23,24)

InChI key:
MYSWGUAQZAJSOK-UHFFFAOYSA-N

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SMILES string:
CC1CCC(=O)C1=O

InChI:
1S/C6H8O2/c1-4-2-3-5(7)6(4)8/h4H,2-3H2,1H3

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OACYKCIZDVVNJL-UHFFFAOYSA-N

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SMILES string:
CC(=O)CCc1ccc(O)cc1

InChI:
1S/C10H12O2/c1-8(11)2-3-9-4-6-10(12)7-5-9/h4-7,12H,2-3H2,1H3

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NJGBTKGETPDVIK-UHFFFAOYSA-N

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CC(C)OC(OC(C)C)N(C)C

InChI:
1S/C9H21NO2/c1-7(2)11-9(10(5)6)12-8(3)4/h7-9H,1-6H3

InChI key:
XOZZATXWQMOVHL-UHFFFAOYSA-N