Table of Contents
- 1. Sultamicillin CAS 76497-13-7: Key Specifications & Comparative Analysis
- 2. Therapeutic Applications & Mechanism of Action
- 3. Clinical Usage Guidelines & Administration Protocols
- 4. Clinical Efficacy Case Studies
- 5. Verified Client Utilization Scenarios
- 6. Request Professional Consultation
1. Sultamicillin CAS 76497-13-7: Key Specifications & Comparative Analysis
Chemical Profile
| Parameter | Specification |
|---|---|
| CAS Number | 76497-13-7 |
| Molecular Formula | C25H30N4O9S2 |
| Molecular Weight | 627.66 g/mol |
| Appearance | White crystalline powder |
| Solubility | Freely soluble in water |
Comparative Analysis Table
| Feature | Sultamicillin | Standard Ampicillin |
|---|---|---|
| Beta-lactamase Inhibition | Yes (Sulbactam component) | No |
| Spectrum Coverage | Broad-spectrum (Gram+/Gram-) | Narrower spectrum |
| Dosage Frequency | BID-TID administration | QID required |
2. Therapeutic Applications & Mechanism of Action
Primary Clinical Indications
- Respiratory tract infections (Community-acquired pneumonia)
- Urinary tract infections (Complicated pyelonephritis)
- Skin/soft tissue infections (Diabetic foot infections)
- Intra-abdominal infections (Peritonitis)
Pharmacological Action
The 1:1 molecular combination of sulbactam (β-lactamase inhibitor) and ampicillin (β-lactam antibiotic) demonstrates synergistic bactericidal activity against β-lactamase-producing pathogens.
3. Clinical Usage Guidelines & Administration Protocols
Dosing Recommendations
| Patient Type | Dosage | Duration |
|---|---|---|
| Adult Patients | 750mg-1.5g every 8hrs | 7-14 days |
| Pediatric Patients | 25-50mg/kg/day divided doses | Minimum 5 days |
Contraindications
- Hypersensitivity to penicillin derivatives
- Severe renal impairment (CrCl <30ml/min)
4. Clinical Efficacy Case Studies
Case Study 1: MDR Respiratory Infection
A 2019 multicenter trial demonstrated 92.3% clinical cure rate in β-lactamase-positive Haemophilus influenzae pneumonia using sultamicillin 1g TID regimen.
Case Study 2: Complicated UTI Management
Phase III clinical data showed 87% microbiological eradication in extended-spectrum β-lactamase (ESBL) producing E. coli urinary infections.
5. Verified Client Utilization Scenarios
Client A: Southeast Asian Hospital Network
- Application: Post-surgical infection prophylaxis
- Outcome: 40% reduction in SSI rates
- Regimen: 750mg IV pre-op + 500mg PO BID post-op
Client B: European Infectious Disease Center
- Application: MDR abdominal sepsis protocol
- Outcome: 78% survival rate in ICU patients
- Regimen: 1.5g IV TID + targeted antifungals
6. Request Professional Consultation
Contact our antimicrobial specialists for formulation optimization, regulatory support, and clinical protocol development:
Email: info@vivalr.com
Tel: (86) 15866781826



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