Ampicillin (trihydrate)

• Description :

  Ampicillin trihydrate (D- (-) -α-Aminobenzylpenicillin trihydrate) is a broad-spectrum beta-lactam antibiotic against a variety of gram-positive and gram-negative bacteria.

• Product Name Alternative :

  D- (-) -α-Aminobenzylpenicillin (trihydrate)

• UNSPSC :

  12352005

• Hazard Statement :

  H302, H315, H319, H335

• Target :

  Antibiotic; Bacterial

• Type :

  Reference compound

• Related Pathways :

  Anti-infection

• Applications :

  COVID-19-immunoregulation

• Field of Research :

  Infection

• Assay Protocol :

  https://www.medchemexpress.com/ampicillin-trihydrate.html

• Purity :

  99.92

• Solubility :

  H2O : 4.55 mg/mL (ultrasonic; warming; heat to 60°C)

• Smiles :

  OC([C@@H]1N(C2=O)[C@]([C@@H]2NC([C@@H](C3=CC=CC=C3)N)=O)([H])SC1(C)C)=O.[3H2O]

• Molecular Formula :

  C16H25N3O7S

• Molecular Weight :

  403.45

• Precautions :

  H302, H315, H319, H335

• References & Citations :

  [1]Chopra SL, et al. Effect of Ampicillin on E. Coli of Swine Origin. Can J Comp Med Vet Sci. 1963 Sep;27 (9) :223-7.|[2]Lund B, et al. Ampicillin in portal and peripheral blood and bile after oral administration of ampicillin andpivampicillin. Eur J Clin Pharmacol. 1974;7 (2) :133-5.|[3]Lee KE, et al. The neuroprotective mechanism of ampicillin in a mouse model of transient forebrain ischemia. Korean J Physiol Pharmacol. 2016 Mar;20 (2) :185-92.

• Shipping Conditions :

  Room Temperature

• Storage Conditions :

  4°C (Powder, sealed storage, away from moisture and light)

• Scientific Category :

  Reference compound1

• Clinical Information :

  Launched

• Isoform :

  β-lactam

• CAS Number :

  [7177-48-2]