T1052 |
Proglumide |
Proglumide is a cholecystokinin antagonist, which blocks both the CCKA and CCKB subtypes. Proglumide is a drug that exerts an inhibitory effect on gastric secretion and reduces gas |
T2312 |
Loxiglumide |
Loxiglumide is a cholecystokinin (CCK-1) receptor antagonist. |
T6940 |
PHA767491 HCl |
PHA-767491 is an effective ATP-competitive dual Cdc7/CDK9 inhibitor (IC50: 10/34 nM). It has ~20-fold selectivity against GSK3-β and CDK1/2, 50-fold selectivity against CDK5 and M |
TQ0062 |
Nastorazepide |
Nastorazepide (Z-360) is a selective, orally available antagonist of gastrin/cholecystokinin 2 (CCK-2) receptor with potential antineoplastic activity. |
T3352 |
XL413 |
XL-413 is an orally bioavailable cell division cycle 7 homolog (CDC7) kinase inhibitor with potential antineoplastic activity. XL-413 binds to and inhibits the activity of CDC7, wh |
T6735 |
XL413 hydrochloride |
XL-413 is an orally bioavailable cell division cycle 7 homolog (CDC7) kinase inhibitor with potential antineoplastic activity. CDC7 kinase inhibitor BMS-863233 binds to and inhibit |
T6206 |
PHA767491 |
PHA-767491 is a potent ATP-competitive dual Cdc7/CDK9 inhibitor with IC50 of 10 nM and 34 nM, respectively. |
T15759 |
Lintitript |
Lintitript is a highly potent, selective, orally active, competitive, and non-peptide cholecystokinin (CCK1) receptor antagonist (EC50: 6 nM and a Ki: 0.2 nM). Lintitript enhances |
T11868 |
Lorglumide sodium salt |
Lorglumide sodium salt is a potent cholecystokinin (CCK) receptor antagonist. |