1. Anti-infection
  2. Antibiotic Beta-lactamase Bacterial Penicillin-binding protein (PBP)
  3. AM-112

AM-112 is a β-lactamase (β-lactamase) inhibitor and antibacterial agent, with IC50 values ranging from 0.0002 μg/mL to 0.67 μg/mL against class A, C, and D β-lactamase. By inhibiting PBP2, the penicillin-binding protein of E. coli, and protecting Ceftazidime (HY-B0593) from enzymatic hydrolysis, AM-112 significantly enhances the antibacterial efficacy of Ceftazidime against Gram-negative bacteria, enterococci, and staphylococci. AM-112 exhibits favorable pharmacokinetic properties and acid-base stability. AM-112 can be used for the research of bacterial infections.

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

AM-112

AM-112 Chemical Structure

CAS No. : 414858-51-8

Size Stock
50 mg   Get quote  
100 mg   Get quote  
250 mg   Get quote  

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Top Publications Citing Use of Products
  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

AM-112 is a β-lactamase (β-lactamase) inhibitor and antibacterial agent, with IC50 values ranging from 0.0002 μg/mL to 0.67 μg/mL against class A, C, and D β-lactamase. By inhibiting PBP2, the penicillin-binding protein of E. coli, and protecting Ceftazidime (HY-B0593) from enzymatic hydrolysis, AM-112 significantly enhances the antibacterial efficacy of Ceftazidime against Gram-negative bacteria, enterococci, and staphylococci. AM-112 exhibits favorable pharmacokinetic properties and acid-base stability. AM-112 can be used for the research of bacterial infections[1][2].

IC50 & Target

β-lactam

 

In Vitro

AM-112 (combined with Ceftazidime at a 2:1 ratio) synergistically reduces the MIC of Ceftazidime (HY-B0593) in all tested Enterococcus faecalis strains, with the greatest MIC reduction observed in E. faecalis SFZ (from 64 μg/mL to 8 μg/mL)[1].
AM-112 (0.5-32 μg/ml; 18-24 h) has an MIC of 2 μg/mL against Methicillin (HY-121544)-susceptible Staphylococcus aureus, an MIC range of 4-16 μg/mL against anaerobic bacteria of the genera Clostridium and Bacteroides, and an MIC of ≥32 μg/mL against Escherichia coli, Pseudomonas, Acinetobacter, Enterococcus and Methicillin-resistant Staphylococcus aureus[2].

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

Cell Viability AssayWestern Blot AnalysisCell Proliferation AssayApoptosis AnalysisCell Cytotoxicity AssayCell Cycle AnalysisRT-PCRCell Autophagy AssayImmunofluorescenceCell Differentiation AssayCell Invasion AssayCell Migration Assay Real Time qPCRELISA Assay[1]

Cell Line: Multiple bacterial strains including Escherichia coli, Enterobacter cloacae, Enterococcus faecalis, Pseudomonas aeruginosa ATCC 27853 producing Class A or Class C β-lactamases
Concentration: 10 μg of AM-112 per disk, combined with 30 μg Ceftazidime per disk
Incubation Time: overnight incubation at 37℃
Result: Enhanced the zone diameter of Ceftazidime against bacterial isolates producing Class A and Class C β-lactamases, while it showed no enhancing effect on the activity of Ceftazidime against Pseudomonas aeruginosa ATCC 27853.
Parmacokinetics
Species Dose Route Serum Concentration
Mice[1] 50 mg/kg s.c. 26 mg/L
Mice[1] 50 mg/kg p.o. 0 mg/L
In Vivo

AM-112 (administered subcutaneously at 1-2.6 mg/kg) exhibits potent inhibitory activity against Staphylococcus aureus-induced sepsis in mice, with an ED50 of 2.6 mg/kg, and enhances the efficacy of Ceftazidime (HY-B0593) when used in combination[1].
AM-112 (administered intravenously at 1.9-19 mg/kg) exhibits inhibitory effects against E. cloacae P99-induced sepsis in mice, with an ED50 of 19 mg/kg, and significantly enhances the efficacy of Ceftazidime when co-administered[1].
AM-112 (>40 mg/kg; s.c.) shows limited inhibitory effect on K. pneumoniae SHV-5-induced sepsis in mice, with an ED50 >40 mg/kg, but it can enhance the efficacy of Ceftazidime when administered in combination[1].

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

Animal Model: ICR mice (male, 20-22 g, intraperitoneal inoculation with S. aureus 3816)[1]
Dosage: 2.6 mg/kg (alone); 1.2 mg/kg (4:1 CAZ:AM-112 combination); 1 mg/kg (7:1 CAZ:AM-112 combination)
Administration: subcutaneous injection
Result: Had an ED50 of 2.6 mg/kg (95% CI: 2.2-3.1 mg/kg).
Had an ED50 of 1.2 mg/kg (95% CI for co-administered ceftazidime: 4.0-5.8 mg/kg) in 4:1 CAZ:AM-112 combination.
Had an ED50 of 1 mg/kg (95% CI for co-administered ceftazidime: 6.6-9.7 mg/kg) in 7:1 CAZ:AM-112 combination.
Animal Model: CD1 mice (male, 20-22 g, intraperitoneal inoculation with E. cloacae P99)[1]
Dosage: 19 mg/kg (alone); 2 mg/kg (1:1 CAZ:AM-112 combination); 1.9 mg/kg (2:1 CAZ:AM-112 combination); 2.9 mg/kg (4:1 CAZ:AM-112 combination)
Administration: intravenous injection
Result: Had an ED50 of 19 mg/kg (95% CI: 11.6-33.4 mg/kg).
Had an ED50 of 2 mg/kg (95% CI for co-administered ceftazidime: 1.0-5.5 mg/kg) in 1:1 CAZ:AM-112 combination.
Had an ED50 of 1.9 mg/kg (95% CI for co-administered ceftazidime: 2.3-5.9 mg/kg) in 2:1 CAZ:AM-112 combination.
Had an ED50 of 2.9 mg/kg (95% CI for co-administered ceftazidime: 7.2-17.4 mg/kg) in 4:1 CAZ:AM-112 combination.
Animal Model: ICR mice (female, 20-22 g, intraperitoneal inoculation with K. pneumoniae SHV-5)[1]
Dosage: >40 mg/kg (alone); 33.6 mg/kg (1:1 CAZ:AM-112 combination); 11.9 mg/kg (2:1 CAZ:AM-112 combination)
Administration: subcutaneous injection
Result: Had an ED50 of >40 mg/kg (no 95% CI determined).
Had an ED50 of 33.6 mg/kg (95% CI for co-administered ceftazidime: 25.1-45.1 mg/kg) in 1:1 CAZ:AM-112 combination.
Had an ED50 of 11.9 mg/kg (95% CI for co-administered ceftazidime: 18.8-30.1 mg/kg) in 2:1 CAZ:AM-112 combination.
Molecular Weight

298.34

Formula

C14H22N2O5

CAS No.
SMILES

[C@H](C)(O)[C@@]1([C@@]2(N(C(C(O)=O)=C(C(CCCN)(C)C)O2)C1=O)[H])[H]

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Your Recently Viewed Products:

Inquiry Online

Your information is safe with us. * Required Fields.

Product Name

 

Requested Quantity *

Applicant Name *

 

Salutation

Email Address *

 

Phone Number *

Department

 

Organization Name *

City

State

Country or Region *

     

Remarks

Bulk Inquiry

Inquiry Information

Product Name:
AM-112
Cat. No.:
HY-165460
Quantity:
MCE Japan Authorized Agent: