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ICSN3250 HCl is the salt form of ICSN3250.ICSN3250 is an mTOR inhibitor that specifically targets cancer cells, competing with and displacing phosphatidic acid in the FRB structural domain of mTOR, thereby preventing mTOR activation and leading to cytotoxicity.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
1 mg | $195 | In Stock | |
5 mg | $483 | In Stock | |
10 mg | $692 | In Stock |
Description | ICSN3250 HCl is the salt form of ICSN3250.ICSN3250 is an mTOR inhibitor that specifically targets cancer cells, competing with and displacing phosphatidic acid in the FRB structural domain of mTOR, thereby preventing mTOR activation and leading to cytotoxicity. |
In vitro | ICSN3250 HCl was tested on multiple cancer cell lines (HCT116, U2OS, U87, K562) and normal cells (HUVEC, NHDF, HFDPC) under standard culture conditions (10–100 nmol/L, 24–72 h). Western blot, autophagy markers, and viability assays were used to assess activity. Results showed ICSN3250 HCl selective mTORC1 inhibition and cytotoxicity in cancer cells with minimal toxicity to normal cells[1]. |
In vivo | Ex vivo: ICSN3250 HCl (100 nmol/L, 72 h) was applied to primary colorectal cancer cells and matched fibroblasts isolated from patient tumor tissue. Cell viability and morphology were assessed microscopically. ICSN3250 HCl selectively reduced cancer cell viability without affecting normal fibroblasts[1]. |
Alias | ICSN3250 HCl(1561902-73-5 Free base), ICSN 3250 HCl |
Molecular Weight | 633.13 |
Formula | C31H41ClN4O8 |
Cas No. | 1561902-79-1 |
Smiles | Cl.O=N(=O)C=1C=C(C=C(O)C1O)C2=CN(C=C2C=3C=C(O)C(O)=C(C3)N(=O)=O)CCCN4CCCCCCCCCCCC4 |
Relative Density. | no data available |
Storage | store at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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