[CAS NO. 23325-78-2]  Cephalexinmonohydrate

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PRODUCTS SPECIFICATIONS [23325-78-2]

Catalog
HY-B0200B
Brand
MCE
CAS
23325-78-2

DESCRIPTION [23325-78-2]

Overview

MDLMFCD00167148
Molecular Weight365.40
Molecular FormulaC16H19N3O5S
SMILESO=C(C(N12)=C(C)CS[C@]2([H])[C@H](NC([C@H](N)C3=CC=CC=C3)=O)C1=O)O.O

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


Summary

Cephalexin (Cefalexin) monohydrate is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) monohydrate has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) monohydrate targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) monohydrate is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2] .


In Vitro

Cephalexin (Cefalexin) monohydrate (10 μg/mL) disrupts polymer peptidoglycan (PG) biogenesis by inactivating enzymes called penicillin-binding proteins (PBPs) [1] .
Cephalexin (Cefalexin) monohydrate inhibits a broad spectrum of grampositive and gram-negative organisms with MIC values of 2, 2, 2, 2, 4, 4.4 and 5.7 μg/mL for Bacillus anthracis , Edwardsiella taFda , Vibrio cholera , Pasteurella multocida , Edwardsiella tarda , Alcaligenes sp and Proteus rettgeri , respectively [2] .

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


In Vivo

Cephalexin (Cefalexin) monohydrate (0-50 mg/kg; p.o.; for 3.5 hours) has antibacterial activity in male Swiss-Webster mice with infected bacterial [2] .

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

Animal Model: Male Swiss-Webster mice with infected bacterial [2]
Dosage: 0-50 mg/kg
Administration: Oral administration; for 3.5 hours
Result: Had antibacterial activity against Streptococcus pyogenes , Streptococcus pneumoniae , Staphylococcus aureus and several gram-negative species mice.

Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT01002911 Population Health Research Institute
Arrythmias
December 2009 Phase 3
NCT04876131 Murdoch Childrens Research Institute|Royal Children´s Hospital
Complicated Urinary Tract Infection|Infection|Pediatric Infectious Disease
May 30, 2022 Phase 4
NCT01073540 Bayer|Corporación Bonima S.A. de C.V.
Anti-Infective Agents
September 2009 Phase 1

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : 6.67 mg/mL ( 18.25 mM ; Need ultrasonic)

H 2 O : 2 mg/mL ( 5.47 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.7367 mL 13.6836 mL 27.3673 mL
5 mM 0.5473 mL 2.7367 mL 5.4735 mL
10 mM 0.2737 mL 1.3684 mL 2.7367 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: PBS

    Solubility: 8.33 mg/mL (22.80 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

  • 2.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 0.67 mg/mL (1.83 mM); Clear solution

  • 3.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 0.67 mg/mL (1.83 mM); Clear solution

  • 4.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 0.67 mg/mL (1.83 mM); Clear solution

* All of the co-solvents are available by MCE.


Synonyms

5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2R)-2-amino-2-phenylacetyl]amino]-3-methyl-8-oxo-, hydrate (1:1), (6R,7R)-
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-(2-amino-2-phenylacetamido)-3-methyl-8-oxo-, monohydrate, D-
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[(aminophenylacetyl)amino]-3-methyl-8-oxo-, monohydrate, [6R-[6α,7β(R*)]]-
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2R)-aminophenylacetyl]amino]-3-methyl-8-oxo-, monohydrate, (6R,7R)-
Cephalexin monohydrate
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