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Minocycline hydrochloride

Catalog No. T1101Cas No. 13614-98-7
Alias Minocycline HCl

Minocycline hydrochloride (Minocycline HCl) is a tetracycline antibiotic with excellent absorption and tissue penetration that is used for several bacterial infections as well as treatment of acne. Minocycline hydrochloride can cause both an acute hepatitis-like syndrome occurring within 1 to 3 months of starting therapy or a more insidious chronic hepatitis with autoimmune features typically after long-term treatment.

Minocycline hydrochloride

Minocycline hydrochloride

Purity: 100%
Catalog No. T1101Alias Minocycline HClCas No. 13614-98-7
Minocycline hydrochloride (Minocycline HCl) is a tetracycline antibiotic with excellent absorption and tissue penetration that is used for several bacterial infections as well as treatment of acne. Minocycline hydrochloride can cause both an acute hepatitis-like syndrome occurring within 1 to 3 months of starting therapy or a more insidious chronic hepatitis with autoimmune features typically after long-term treatment.
Pack SizePriceAvailabilityQuantity
25 mg$38In Stock
50 mg$50In Stock
100 mg$62In Stock
200 mg$92In Stock
1 mL x 10 mM (in DMSO)$50In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
Minocycline hydrochloride (Minocycline HCl) is a tetracycline antibiotic with excellent absorption and tissue penetration that is used for several bacterial infections as well as treatment of acne. Minocycline hydrochloride can cause both an acute hepatitis-like syndrome occurring within 1 to 3 months of starting therapy or a more insidious chronic hepatitis with autoimmune features typically after long-term treatment.
In vitro
Minocycline exhibits significant neuroprotective effects in models of cerebral ischemia, traumatic brain injury, Huntington's disease, and Parkinson's disease. Its neuroprotective properties may involve the inhibition of 5-lipoxygenase (an inflammatory enzyme associated with brain aging). Additionally, Minocycline's activity is linked to the inhibition of protein synthesis.
In vivo
Minocycline inhibits the release of cytochrome c mediated by the permeability transition in mitochondria. This inhibition by minocycline on cytochrome c release has been demonstrated in vivo, in cells, and isolated mitochondria. Additionally, minocycline suppresses the activity of inducible caspase-1 and caspase-3, inducible nitric oxide synthase (iNOS), and p38 mitogen-activated protein kinase (MAPK). Following experimental focal ischemia, minocycline reduces the upregulation of caspase-1 and iNOS, thereby decreasing infarct size.
AliasMinocycline HCl
Chemical Properties
Molecular Weight493.94
FormulaC23H28ClN3O7
Cas No.13614-98-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 12.4 mg/mL (25 mM)
DMSO: 60 mg/mL (121.47 mM)
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.0245 mL10.1227 mL20.2454 mL101.2269 mL
5 mM0.4049 mL2.0245 mL4.0491 mL20.2454 mL
10 mM0.2025 mL1.0123 mL2.0245 mL10.1227 mL
20 mM0.1012 mL0.5061 mL1.0123 mL5.0613 mL
DMSO
1mg5mg10mg50mg
50 mM0.0405 mL0.2025 mL0.4049 mL2.0245 mL
100 mM0.0202 mL0.1012 mL0.2025 mL1.0123 mL

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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
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