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Eravacycline dihydrochloride

🥰Excellent
Catalog No. T11227LCas No. 1334714-66-7
Alias TP-434-046, TP-434 dihydrochloride

Eravacycline dihydrochloride (TP-434-046) is a potent and broad-spectrum antibacterial agent against six E. coli (MICs: 0.125-0.25 mg/L).

Eravacycline dihydrochloride

Eravacycline dihydrochloride

🥰Excellent
Purity: 100%
Catalog No. T11227LAlias TP-434-046, TP-434 dihydrochlorideCas No. 1334714-66-7
Eravacycline dihydrochloride (TP-434-046) is a potent and broad-spectrum antibacterial agent against six E. coli (MICs: 0.125-0.25 mg/L).
Pack SizePriceAvailabilityQuantity
1 mg$123In Stock
5 mg$372In Stock
10 mg$619In Stock
25 mg$1,090In Stock
50 mg$1,930In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
Eravacycline dihydrochloride (TP-434-046) is a potent and broad-spectrum antibacterial agent against six E. coli (MICs: 0.125-0.25 mg/L).
In vitro
Eravacycline shows inhibitory activity against A. baumannii, including isolates that are resistant to sulbactam, SM 7338, and BAY 41-6551(MIC50/90 = 0.5/1 mg/L)[1]. Eravacycline shows potent broad-spectrum activity against 90% of the isolates for all species panels (MIC90 0.008-2 μg/mL) except those of Pseudomonas aeruginosa and Burkholderia cenocepacia (MIC90 = 32 μg/mL). Eravacycline is active against multidrug-resistant bacteria including β-lactamases and antibiotics, including carbapenem resistance[4].
In vivo
Eravacycline(3.125-50 mg/kg) shows mean fAUC/MIC magnitude associated with net stasis and 1-log kill endpoint of 27.97 and 32.60[2]. In mouse septicemia models, Eravacycline is efficacious against Staphylococcus aureus and demonstrates 50% protective dose values of ≤1 mg/kg. The PD50s are 1.2-4.4 mg/kg against Escherichia coli isolates[5].
AliasTP-434-046, TP-434 dihydrochloride
Chemical Properties
Molecular Weight631.48
FormulaC27H33Cl2FN4O8
Cas No.1334714-66-7
SmilesCl.Cl.[H][C@@]12Cc3c(F)cc(NC(=O)CN4CCCC4)c(O)c3C(=O)C1=C(O)[C@]1(O)C(=O)C(C(N)=O)=C(O)[C@@H](N(C)C)[C@]1([H])C2
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 135.0 mg/mL (213.8 mM), Sonication is recommended.
H2O: 45.0 mg/mL (71.3 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM1.5836 mL7.9179 mL15.8358 mL79.1791 mL
5 mM0.3167 mL1.5836 mL3.1672 mL15.8358 mL
10 mM0.1584 mL0.7918 mL1.5836 mL7.9179 mL
20 mM0.0792 mL0.3959 mL0.7918 mL3.9590 mL
50 mM0.0317 mL0.1584 mL0.3167 mL1.5836 mL
DMSO
1mg5mg10mg50mg
100 mM0.0158 mL0.0792 mL0.1584 mL0.7918 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
1 Enter information below:
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2 Enter the in vivo formulation:
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