[CAS NO. 104376-79-6]  Ceftriaxone sodium hydrate

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PRODUCTS SPECIFICATIONS [104376-79-6]

Catalog
HY-B0712A
Brand
MCE
CAS
104376-79-6

DESCRIPTION [104376-79-6]

Overview

MDL-
Molecular Weight661.60
Molecular FormulaC18H23N8Na2O10.5S3
SMILESO=C(O[Na])C(N12)=C(CSC(N(C)N=C3O[Na])=NC3=O)CS[C@]2([H])[C@H](NC(/C(C4=CSC(N)=N4)=N\OC)=O)C1=O.[3.5H2O]

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


Summary

Ceftriaxone sodium hydrate (Ro 13-9904 sodium hydrate) is a broad spectrum β-lactam third-generation cephalosporin antibiotic , which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone sodium hydrate is a covalent inhibitor of GSK3β with IC 50 value of 0.78 μM. Ceftriaxone sodium hydrate is an inhibitor of Aurora B . Ceftriaxone sodium hydrate has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone sodium hydrate can be used in the study of bacterial infections and meningitis [1] [2] [3] [4] [5] [6] [7] .


IC50 & Target

β-lactam


In Vitro

Ceftriaxone sodium hydrate (100 μM, 24 h) protects MPP + treated astrocytes by inhibiting the NF-κB/JNK/c-Jun signaling pathway [3].
Ceftriaxone sodium hydrate (500 μM, 24-48 h) effectively inhibits unanchored cell growth in A549, H520 and H1650 lung cancer cells by inhibiting Aurora B [4] .

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

Cell Viability Assay [3]

Cell Line: Astrocyte
Concentration: 100 μM
Incubation Time: 24 h
Result: Improved cell viability and increased glutamate uptake after MPP + expose.

Western Blot Analysis [3]

Cell Line: Astrocyte
Concentration: 100 μM
Incubation Time: 24 h
Result: Enhanced GLT-1 and GFAP expression.
Decreased the expression of p-p50、p-IKKα、p-Relb.
Decreased the number of TUNEL-positive cells.

In Vivo

Ceftriaxone sodium hydrate (200 mg/kg Intraperitoneal injection for 6 weeks) improves functional markers and oxidative stress and inflammation parameters in a rat model of D-galactose (DGL) -induced liver and kidney injury [5] .
Ceftriaxone sodium hydrate (200, 400 mg/kg, Intraperitoneal injection) has a protective effect on convulsion induced by Pentylenetetrazol (PTZ) and PTZ-related oxidative damage in rats [6] .
Ceftriaxone sodium hydrate (100, 200 mg/kg, Intraperitoneal injection) reduces mechanical dysodynia and hyperalgesia by activating GLT-1 in Streptozocin ( HY-13753 )-induced diabetic rat models [7] .

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

Animal Model: DGL-induced rat model [5]
Dosage: 200 mg/kg
Administration: i.p.
Result: Reduced the BUN、Cr 、AST and ALT levels.
Attenuated the MDA levels and enhanced GPx and CAT activities.
Reduced the levels of IL-1β and TNF-α mRNA.
Animal Model: PTZ-induced rat model [6]
Dosage: 200, 400 mg/kg
Administration: i.p. 60 min before to PTZ (70 mg/kg)
Result: Both of the two ceftriaxone groups had lower spike percentages than the saline group.
Significantly lower MDA levels and higher SOD activity in 200 and 400 mg/kg.

Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT03012360 University Hospital, Lille|Ministry of Health, France
Mechanical Ventilation Complication|Critical Illness
February 8, 2018 Phase 4
NCT01645735 Forest Laboratories|AstraZeneca
Infections
October 2012 Phase 4
NCT01421693 Oxford University Clinical Research Unit, Vietnam|University of Oxford|Patan Academy of Health Sciences, Nepal|Patan Hospital, Nepal|Civil Hospital, Nepal
Enteric Fever|Typhoid Fever
September 2011 Phase 4

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

4°C, stored under nitrogen, away from moisture

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