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# Aladdin ID Assay Type Description Organism Compounds Reference BAO Format Source 1. ALA2026240 B Inhibition of Des1 in human A549 cells assessed as formation of CerC6NBD from dhCerC6NBD at =>100 uM after 4 hrs by HPLC-FD analysis Homo sapiens 2 ALA2021903 cell-based format Scientific Literature 2. ALA2026241 B Inhibition of Des1 in human HCT116 cells assessed as formation of CerC6NBD from dhCerC6NBD at =>100 uM after 4 hrs by HPLC-FD analysis Homo sapiens 2 ALA2021903 cell-based format Scientific Literature 3. ALA2026163 B Inhibition of Des1 in human A549 cells assessed as formation of CerC6NBD from dhCerC6NBD after 4 hrs by HPLC-FD analysis Homo sapiens 1 ALA2021903 cell-based format Scientific Literature 4. ALA2026164 B Inhibition of Des1 in human HCT116 cells assessed as formation of CerC6NBD from dhCerC6NBD after 4 hrs by HPLC-FD analysis Homo sapiens 1 ALA2021903 cell-based format Scientific Literature 5. ALA3767201 B Inhibition of Des1 activity in human Jurkat cells using fluorescence labeled DhCer-C6-NBD as substrate at 0.1 to 10 uM after 3 hrs by HPLC method Homo sapiens 4 ALA3763012 cell-based format Scientific Literature 6. ALA3767202 B Inhibition of Des1 activity in human Jurkat cells using fluorescence labeled DhCer-C6-NBD as substrate at 10 uM after 3 hrs by HPLC method Homo sapiens 1 ALA3763012 cell-based format Scientific Literature 7. ALA3767203 B Inhibition of Des1 activity in human Jurkat cells using fluorescence labeled DhCer-C6-NBD as substrate at 1 and 10 uM after 3 hrs by HPLC method Homo sapiens 1 ALA3763012 cell-based format Scientific Literature 8. ALA3767358 B Irreversible inhibition of Des1 activity in human Jurkat cells treated with parent compound treated with fenretinide using fluorescence labeled DhCer-C6-NBD as substrate by HPLC method Homo sapiens 1 ALA3763012 cell-based format Scientific Literature 9. ALA3767367 B Inhibition of Des1 (unknown origin) at 30 uM Homo sapiens 1 ALA3763012 single protein format Scientific Literature 10. ALA3767373 A Drug metabolism in human Jurkat cells assessed as DES1-mediated (2E,4E,6E,8E)-3,7-dimethyl-N-(4-oxocyclohexa-2,5-dienylidene)-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetraenamide formation Homo sapiens 1 ALA3763012 cell-based format Scientific Literature 11. ALA3767374 A Drug level in human Jurkat cells assessed as DES1-mediated compound oxidation treated with fenretinide Homo sapiens 1 ALA3763012 cell-based format Scientific Literature 12. ALA4310700 B Inhibition of dihydroceramide desaturase in human MCF7 cells assessed as decrease in remaining activity at 5 to 10 uM after 24 hrs Homo sapiens 1 ALA4308872 cell-based format Scientific Literature 13. ALA5226556 B Noncompetitive inhibition of DES1 in human HGC-27 cell lysates assessed as inhibition constant Homo sapiens 1 ALA5226284 subcellular format Scientific Literature 14. ALA5226562 B Inhibition of DES1 in human HGC-27 cell lysates Homo sapiens 2 ALA5226284 subcellular format Scientific Literature 15. ALA5226563 B Binding affinity to DES1 in human HGC-27 cell lysates assessed as inhibition constant Homo sapiens 1 ALA5226284 subcellular format Scientific Literature 16. ALA5226566 B Inhibition of DES1 (unknown origin) Homo sapiens 5 ALA5226284 single protein format Scientific Literature