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OTUB1/USP8-IN-1 HCl
OTUB1/USP8-IN-1 HCL is a potent dual inhibitor of OTUB1 and USP8 with potential antitumour activity, inhibiting both OTUB1 and USP8. OTUB1/USP8-IN-1 may be used in the study of leukaemia.
Catalog No. T72784L
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Purity:99.90%
ee:100%
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OTUB1/USP8-IN-1 HCl
Catalog No. T72784LAlias OTUB1/USP8-IN-1 HCl（2858800-98-1 Free base）
OTUB1/USP8-IN-1 HCL is a potent dual inhibitor of OTUB1 and USP8 with potential antitumour activity, inhibiting both OTUB1 and USP8. OTUB1/USP8-IN-1 may be used in the study of leukaemia.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose. | Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $162 | Backorder | |
| 5 mg | $357 | Backorder | |
| 10 mg | $429 | Backorder | |
| 25 mg | $987 | Backorder | |
| 50 mg | $1,520 | Backorder | |
| 100 mg | $1,980 | Backorder |
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Product Introduction
Bioactivity
Chemical Properties
| Description | OTUB1/USP8-IN-1 HCL is a potent dual inhibitor of OTUB1 and USP8 with potential antitumour activity, inhibiting both OTUB1 and USP8. OTUB1/USP8-IN-1 may be used in the study of leukaemia. |
| Targets&IC50 | USP8:0.28 nM, OTUB1:0.17 nM |
| In vitro | OTUB1/USP8-IN-1 (compound 61) exhibits antiproliferative effects in KRAS-WT (H1975, EBC-1, H1703) and KRAS-mutated (H23, A549) NSCLC cell lines when treated with concentrations ranging from 10 nM to 10 μM for 72 hours[1]. Additionally, treatment with OTUB1/USP8-IN-1 at 500 nM for 24 hours leads to a decrease in protein levels of both UBE2N and EGFR in H1975 cells[1]. |
| In vivo | In the H1975 xenograft mouse model, treatment with OTUB1/USP8-IN-1 (compound 61) at concentrations ranging from 10 nM to 10 μM for 72 hours results in a decrease in tumor burden[1]. |
| Alias | OTUB1/USP8-IN-1 HCl（2858800-98-1 Free base） |
| Molecular Weight | 463.29 |
| Formula | C22H17Cl2FN2O4 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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 DMSO (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.
(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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