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LTX-401 HCl

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Catalog No. T27859Cas No. 1398051-86-9
Alias LTX-401 dihydrochloride, LTX401 dihydrochloride, LTX 401 dihydrochloride

LTX-401 is an immunotherapeutic agent and an oncolytic amino acid derivative with potential immunogenic properties.

LTX-401 HCl
Other Forms of LTX-401 HCl:
LTX-401 dihydrochloride (1262851-70-6 free base)T13759
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LTX-401 HCl

😃Good
Catalog No. T27859Alias LTX-401 dihydrochloride, LTX401 dihydrochloride, LTX 401 dihydrochlorideCas No. 1398051-86-9
LTX-401 is an immunotherapeutic agent and an oncolytic amino acid derivative with potential immunogenic properties.
Pack SizePriceAvailabilityQuantity
25 mg$1,5206-8 weeks
50 mg$1,9806-8 weeks
100 mg$2,5006-8 weeks
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Product Introduction

Bioactivity
Description
LTX-401 is an immunotherapeutic agent and an oncolytic amino acid derivative with potential immunogenic properties.
AliasLTX-401 dihydrochloride, LTX401 dihydrochloride, LTX 401 dihydrochloride
Chemical Properties
Molecular Weight440.45
FormulaC23H35Cl2N3O
Cas No.1398051-86-9
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.

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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.
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Keywords

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