1. Anti-infection
  2. Antibiotic Bacterial
  3. Cefetamet pivoxyl

Cefetamet pivoxyl  (Synonyms: Ro 15-8075 free base)

Cat. No.: HY-B1894 Purity: 95.0%
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Cefetamet pivoxyl (Ro 15-8075 free base) is an orally active cephalosporin Antibiotic and a prodrug of Cefetamet (HY-A0111). After ingestion, Cefetamet pivoxyl is hydrolyzed by gastrointestinal esterases to form Cefetamet. Cefetamet pivoxyl is primarily active against aerobic Gram-negative bacteria (such as Enterobacteriaceae, *Neisseria*, *Haemophilus*) and some Gram-positive bacteria (such as non-enterococcal streptococci). Cefetamet pivoxyl exhibits potent in vivo antibacterial activity against strains of Gram-positive bacteria (S. pyogenes) and Gram-negative bacteria (E. coli, K. pneumoniae, S. marcescens, P. vulgaris, P. mirabilis, H. influenzae).

For research use only. We do not sell to patients.

Cefetamet pivoxyl

Cefetamet pivoxyl Chemical Structure

CAS No. : 65243-33-6

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Description

Cefetamet pivoxyl (Ro 15-8075 free base) is an orally active cephalosporin Antibiotic and a prodrug of Cefetamet (HY-A0111). After ingestion, Cefetamet pivoxyl is hydrolyzed by gastrointestinal esterases to form Cefetamet. Cefetamet pivoxyl is primarily active against aerobic Gram-negative bacteria (such as Enterobacteriaceae, *Neisseria*, *Haemophilus*) and some Gram-positive bacteria (such as non-enterococcal streptococci). Cefetamet pivoxyl exhibits potent in vivo antibacterial activity against strains of Gram-positive bacteria (S. pyogenes) and Gram-negative bacteria (E. coli, K. pneumoniae, S. marcescens, P. vulgaris, P. mirabilis, H. influenzae)[1][2].

In Vitro

Cefetamet pivoxyl is primarily active against aerobic Gram-negative bacteria (e.g., Enterobacteriaceae, *Neisseria*, *Haemophilus*) and some Gram-positive bacteria (e.g., non-enterococcal streptococci)[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Cefetamet pivoxyl (administered orally at 1 and 3 hours post-infection) exhibits potent in vivo antibacterial activity against Gram-positive (S. pyogenes) and Gram-negative (E. coli, K. pneumoniae, S. marcescens, P. vulgaris, P. mirabilis, H. influenzae) strains, but shows no significant activity against S. aureus[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: unspecified strain[2]
Dosage: ED50 0.11 mg/kg (S. pyogenes); ED50 0.73 mg/kg (E. coli); ED50 2.2 mg/kg (K. pneumoniae); ED50 1.8 mg/kg (S. marcescens); ED50 1.2 mg/kg (P. vulgaris); ED50 0.45 mg/kg (P. mirabilis); ED50 <2 mg/kg (H. influenzae); ED50 >25 mg/kg (S. aureus)
Administration: p.o.; at 1 and 3 hours post-challenge
Result: Achieved an ED50 of 0.11 mg/kg against S. pyogenes.
Achieved an ED50 of 0.73 mg/kg against E. coli.
Achieved an ED50 of 2.2 mg/kg against K. pneumoniae.
Achieved an ED50 of 1.8 mg/kg against S. marcescens.
Achieved an ED50 of 1.2 mg/kg against P. vulgaris.
Achieved an ED50 of 0.45 mg/kg against P. mirabilis.
Achieved an ED50 of <2 mg/kg against H. influenzae.
Showed no significant activity against S. aureus, with an ED50 >25 mg/kg.
Molecular Weight

511.57

Formula

C20H25N5O7S2

CAS No.
Appearance

Solid

Color

Off-white to light yellow

SMILES

O=C(C(N12)=C(C)CS[C@]2([H])[C@H](NC(/C(C3=CSC(N)=N3)=N\OC)=O)C1=O)OCOC(C(C)(C)C)=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

-20°C, protect from light, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)

Purity & Documentation
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Cefetamet pivoxyl
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HY-B1894
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