XL413

Chemical Information
XL413 is a benzofuropyrimidine that is 3,4-dihydro[1]benzofuro[3,2-d]pyrimidine substituted by (2S)-pyrrolidin-2-yl, oxo and chloro groups at positions 2, 4, and 8, respectively. It is a potent ATP competitive inhibitor of Cdc7 kinase (IC50 = 3.4 nM) and exhibits anticancer properties. It has a role as an antineoplastic agent and an EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor. It is a benzofuropyrimidine, an organochlorine compound and a member of pyrrolidines.
| CAS Number | 1169558-38-6 |
| PubChem CID | 135564632 |
| IUPAC Name | 8-chloro-2-[(2S)-pyrrolidin-2-yl]-3H-[1]benzofuro[3,2-d]pyrimidin-4-one |
| Molecular Formula | C14H12ClN3O2 |
| Molecular Weight | 289.71 |
| XLogP | 2.2 |
| Topological Polar Surface Area | 66.6 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 456 |
| Property | Value |
|---|---|
| Molecular Weight | 289.71 |
| XLogP3 | 2.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 289.0618043 |
| Monoisotopic Mass | 289.0618043 |
| Topological Polar Surface Area | 66.6 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 456 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Alternative Products
| Catalog | Name |
|---|---|
| T3352-01 | XL413 |
| B1015-5 | XL413 hydrochloride |
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