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Formula | C62H111N11O12 |
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Molecular Weight | 1202.61 | CAS No. | 59865-13-3 | ||||
Solubility (25°C)* | In vitro | DMSO | 100 mg/mL (83.15 mM) | ||||
Ethanol | 100 mg/mL (83.15 mM) | ||||||
Water | Insoluble | ||||||
In vivo (Add solvents to the product individually and in order) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Cyclosporin A, a non-polar cyclic oligopeptide, is an immunosuppressive agent that binds to cyclophilin and then inhibits calcineurin with IC50 of 7 nM in a cell-free assay. Cyclosporin A is generally given following transplant surgery to prevent rejection and has been used to test its toxic effect on a perfused 3D proximal tubule model. | ||
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Targets |
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In vitro | Cyclosporin A binds to the cyclophilin (immunophilin) in T cells[1] , forms a Cyclophilin-Cyclosporin A complex which the binds to and inhibits calcineurin. [2] Cyclosporin A inhibits calcineurin with IC50 of 7 nM[3], then blocks the nuclear translocation of NF-AT. [4] Cyclosporin A also affects mitochondria by preventing the MTP (mitochondrial permeability transition pore) from opening with an IC50 of 39 nM. [5] |
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In vivo | Cyclosporin A is an immunosuppressive agent that is effective following either parenteral or oral administration in mice, rat and guinea pigs. [6], is clinically used in organ transplantation to prevent rejection. [7] |
Kinase Assay: |
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Data from [Biochim Biophys Acta, 2013, 1833(3), 652-62]
Data from [Biochim Biophys Acta, 2013, 1833(3), 652-62]
Data from [Data independently produced by , , Pharm Res, 2016, 33(2):395-403]
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