Caroverine HCl rmofur Smiles: C[C@H](NC)C(=O)N[C@@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C1C=CC=CC=1)C1C=CC=CC=1)C(=O)NCCOCCOCCOCCNC(=O)C1=CC(=CC=C1)C1=CC(NC2C=CC(=CC=2)OC(F)(F)F)=NC=N1

Smiles: C[C@H](NC)C(=O)N[C@@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C1C=CC=CC=1)C1C=CC=CC=1)C(=O)NCCOCCOCCOCCNC(=O)C1=CC(=CC=C1)C1=CC(NC2C=CC(=CC=2)OC(F)(F)F)=NC=N1

Transforming growth factor beta receptor I inhibitor sensitizes drug-resistant pancreatic cancer cells to gemcitabine

In a modified Folts model in dog

8(19):31065-31078

The study was terminated early because of inadequate efficacy

Caroverine HCl rmofur Smiles: C[C@H](NC)C(=O)N[C@@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C1C=CC=CC=1)C1C=CC=CC=1)C(=O)NCCOCCOCCOCCNC(=O)C1=CC(=CC=C1)C1=CC(NC2C=CC(=CC=2)OC(F)(F)F)=NC=N1Caroverine HCl is a nonselective NMDA and AMPA glutamate receptor antagonist, also acting as a class B calcium channel blocker. Pharmacologically, it has been described as a nonspecific calcium channel blocker and as an antagonist of both non NMDA and NMDA glutamate receptors. It was discovered in Austria in the 1950s[3] Product information CAS Number: 55750 05 5 Molecular Weight: 401. 93 Formula: C22H28ClN3O2 Chemical Name: 1 (2 (diethylamino)ethyl)