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Golotimod hydrochloride

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Catalog No. T11449Cas No. 1029401-59-9
Alias SCV07 hydrochloride, SCV 07 hydrochloride, Golotimod hydrochloride (229305-39-9 free base), Gamma-D-glutamyl-L-tryptophan hydrochloride

Golotimod hydrochloride (SCV 07 hydrochloride) is an immunomodulatory peptide with antibacterial activity that inhibits the homodimerization of STAT3 in the cytoplasm, thereby inhibiting STAT3 signaling. It can be used for studying immune-sensitive diseases and HCV infections.

Golotimod hydrochloride

Golotimod hydrochloride

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Purity: 99.86%
Catalog No. T11449Alias SCV07 hydrochloride, SCV 07 hydrochloride, Golotimod hydrochloride (229305-39-9 free base), Gamma-D-glutamyl-L-tryptophan hydrochlorideCas No. 1029401-59-9
Golotimod hydrochloride (SCV 07 hydrochloride) is an immunomodulatory peptide with antibacterial activity that inhibits the homodimerization of STAT3 in the cytoplasm, thereby inhibiting STAT3 signaling. It can be used for studying immune-sensitive diseases and HCV infections.
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5 mg$98In Stock
10 mg$159In Stock
50 mg$398Backorder
100 mg$534Backorder
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Purity:99.86%
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Product Introduction

Bioactivity
Description
Golotimod hydrochloride (SCV 07 hydrochloride) is an immunomodulatory peptide with antibacterial activity that inhibits the homodimerization of STAT3 in the cytoplasm, thereby inhibiting STAT3 signaling. It can be used for studying immune-sensitive diseases and HCV infections.
In vitro
Golotimod hydrochloride can stimulate T helper cells to shift to TH1-like immune response.
Golotimod hydrochloride can stimulate macrophage function decreased by TB infection and isoniazid treatment, and improve phagocytosis activity of peritoneal macrophages.
It can be used as a prospective immunomodulator for the complex treatment of tuberculosis (TB). [1]
In vivo
Oral administration of Golotimod hydrochloride at a dose of 5μg/kg after fasting overnight significantly reduced infectional recurrent lesions in recurrent genital HSV-2 guinea pigs. [2]
Golotimod hydrochloride is able to alter the duration and severity of oral mucositis and depends on time and dose.
AliasSCV07 hydrochloride, SCV 07 hydrochloride, Golotimod hydrochloride (229305-39-9 free base), Gamma-D-glutamyl-L-tryptophan hydrochloride
Chemical Properties
Molecular Weight369.8
FormulaC16H20ClN3O5
Cas No.1029401-59-9
SmilesC([C@@H](NC(CC[C@H](C(O)=O)N)=O)C(O)=O)C=1C=2C(NC1)=CC=CC2.Cl
Relative Density.1.31g/cm3
Storage & Solubility Information
Storagekeep away from moisture,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 120 mg/mL (324.5 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM2.7042 mL13.5208 mL27.0416 mL135.2082 mL
5 mM0.5408 mL2.7042 mL5.4083 mL27.0416 mL
10 mM0.2704 mL1.3521 mL2.7042 mL13.5208 mL
20 mM0.1352 mL0.6760 mL1.3521 mL6.7604 mL
50 mM0.0541 mL0.2704 mL0.5408 mL2.7042 mL
100 mM0.0270 mL0.1352 mL0.2704 mL1.3521 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
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