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  3. Ceftriaxone sodium hydrate

Ceftriaxone sodium hydrate  (Synonyms: Ro 13-9904 sodium hydrate)

Cat. No.: HY-B0712A Purity: 99.25%
COA Handling Instructions

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 IC50 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.

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

Ceftriaxone sodium hydrate Chemical Structure

Ceftriaxone sodium hydrate Chemical Structure

CAS No. : 104376-79-6

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Customer Review

Based on 5 publication(s) in Google Scholar

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  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

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 IC50 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
Molecular Weight

661.60

Formula

C18H23N8Na2O10.5S3

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=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]

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)

Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (151.15 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.5115 mL 7.5574 mL 15.1149 mL
5 mM 0.3023 mL 1.5115 mL 3.0230 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (stored under nitrogen, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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

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

This equation is commonly abbreviated as: C1V1 = C2V2

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In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (stored under nitrogen, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.5115 mL 7.5574 mL 15.1149 mL 37.7872 mL
5 mM 0.3023 mL 1.5115 mL 3.0230 mL 7.5574 mL
10 mM 0.1511 mL 0.7557 mL 1.5115 mL 3.7787 mL
15 mM 0.1008 mL 0.5038 mL 1.0077 mL 2.5191 mL
20 mM 0.0756 mL 0.3779 mL 0.7557 mL 1.8894 mL
25 mM 0.0605 mL 0.3023 mL 0.6046 mL 1.5115 mL
30 mM 0.0504 mL 0.2519 mL 0.5038 mL 1.2596 mL
40 mM 0.0378 mL 0.1889 mL 0.3779 mL 0.9447 mL
50 mM 0.0302 mL 0.1511 mL 0.3023 mL 0.7557 mL
60 mM 0.0252 mL 0.1260 mL 0.2519 mL 0.6298 mL
80 mM 0.0189 mL 0.0945 mL 0.1889 mL 0.4723 mL
100 mM 0.0151 mL 0.0756 mL 0.1511 mL 0.3779 mL
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  • 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.

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Ceftriaxone sodium hydrate
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