Physicochemical Properties
Molecular Formula | C43H50CL2N8O9 |
Molecular Weight | 893.81 |
CAS # | 2935587-90-7 |
Appearance | Typically exists as solid at room temperature |
HS Tariff Code | 2934.99.9001 |
Storage |
Powder-20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
Shipping Condition | Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs) |
Biological Activity
ln Vitro | In Molm-13 cells, PROTAC CDK9 degrader-7 (compound 15f) degrades CDK9 with an IC50 of 40 nM, demonstrating maximal efficacy [1]. |
Cell Assay |
Western Blot Analysis[1] Cell Types: MV411 cells Tested Concentrations: 0.01 μM, 0.05 μM, 0.1 μM, 0.5 μM, 1 μM, 5 μM Incubation Duration: 6 h Experimental Results: Dramatically diminished the protein level of MCL2, and almostly and competely degraded CKD9 at low concentration as 0.1 μM. |
References | [1]. Tokarski RJ 2nd, et al. Bifunctional degraders of cyclin dependent kinase 9 (CDK9): Probing the relationship between linker length, properties, and selective protein degradation. Eur J Med Chem. 2023 Jun 5;254:115342. |
Solubility Data
Solubility (In Vitro) | DMSO : ~100 mg/mL (~111.88 mM) |
Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (2.80 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.  (Please use freshly prepared in vivo formulations for optimal results.) |
Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
1 mM | 1.1188 mL | 5.5940 mL | 11.1881 mL | |
5 mM | 0.2238 mL | 1.1188 mL | 2.2376 mL | |
10 mM | 0.1119 mL | 0.5594 mL | 1.1188 mL |