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Vipivotide tetraxetan Linker

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Catalog No. T17233Cas No. 1703768-74-4
Alias PSMA-617 Linker

Vipivotide tetraxetan Linker (PSMA-617 Linker) is a noncleavable peptide linker utilized in the synthesis of Vipivotide tetraxetan (PSMA-617), a ligand instrumental in producing 177Lu-PSMA-617. This radioactive molecule is applied in the treatment of prostate cancer[1].

Vipivotide tetraxetan Linker

Vipivotide tetraxetan Linker

😃Good
Catalog No. T17233Alias PSMA-617 LinkerCas No. 1703768-74-4
Vipivotide tetraxetan Linker (PSMA-617 Linker) is a noncleavable peptide linker utilized in the synthesis of Vipivotide tetraxetan (PSMA-617), a ligand instrumental in producing 177Lu-PSMA-617. This radioactive molecule is applied in the treatment of prostate cancer[1].
Pack SizePriceAvailabilityQuantity
5 mg361 €7-10 days
10 mg541 €7-10 days
25 mg921 €7-10 days
50 mg1.387 €7-10 days
100 mg2.079 €7-10 days
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Product Introduction

Bioactivity
Description
Vipivotide tetraxetan Linker (PSMA-617 Linker) is a noncleavable peptide linker utilized in the synthesis of Vipivotide tetraxetan (PSMA-617), a ligand instrumental in producing 177Lu-PSMA-617. This radioactive molecule is applied in the treatment of prostate cancer[1].
AliasPSMA-617 Linker
Chemical Properties
Molecular Weight655.74
FormulaC33H45N5O9
Cas No.1703768-74-4
Relative Density.1.303 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 270 mg/mL (411.75 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.5250 mL7.6250 mL15.2499 mL76.2497 mL
5 mM0.3050 mL1.5250 mL3.0500 mL15.2499 mL
10 mM0.1525 mL0.7625 mL1.5250 mL7.6250 mL
20 mM0.0762 mL0.3812 mL0.7625 mL3.8125 mL
50 mM0.0305 mL0.1525 mL0.3050 mL1.5250 mL
100 mM0.0152 mL0.0762 mL0.1525 mL0.7625 mL

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In Vivo Formulation Calculator (Clear solution)

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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