| Stereochemistry | ABSOLUTE |
| Molecular Formula | C30H38ClN7O3 |
| Molecular Weight | 580.121 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)C1=CC=CC=C1NC2=NC(NC3=C(OC)C4=C(C[C@H](CCC4)N5CCN(CCO)CC5)C=C3)=NC=C2Cl
InChI
InChIKey=BCSHRERPHLTPEE-NRFANRHFSA-N
InChI=1S/C30H38ClN7O3/c1-32-29(40)23-7-3-4-9-25(23)34-28-24(31)19-33-30(36-28)35-26-11-10-20-18-21(6-5-8-22(20)27(26)41-2)38-14-12-37(13-15-38)16-17-39/h3-4,7,9-11,19,21,39H,5-6,8,12-18H2,1-2H3,(H,32,40)(H2,33,34,35,36)/t21-/m0/s1
CEP-37440 is a potent ATP-competitive, highly kinase selective, and orally active inhibitor of FAK1 and anaplastic lymphoma kinase (ALK). In addition to a favorable metabolic stability and pharmacokinetic profile preclinically, CEP-37440 is also a brain penetrant. CEP-37440 was able to inhibit the proliferation of certain IBC cells by decreasing the levels of phospho-FAK1 (Tyr 397); none of the cells expressed ALK. Studies using IBC xenograft models showed that CEP-37440 also effectively reduces the growth of the primary tumor xenografts and inhibits the development of brain metastases in mice.
Originator
Approval Year
Sourcing
PubMed
Patents
Sample Use Guides
CEP-37440 supplied as 25 mg and 100 mg capsules and orally administered daily.
Route of Administration:
Oral
ACTIVE MOIETY
SALT/SOLVATE (PARENT)
