ID: ALA4854210

Max Phase: Preclinical

Molecular Formula: C25H22F3N5O2

Molecular Weight: 481.48

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CN(C)c1ccc2c(Oc3ccc(NC(=O)NCc4ccc(C(F)(F)F)cc4)cc3)ncnc2c1

Standard InChI:  InChI=1S/C25H22F3N5O2/c1-33(2)19-9-12-21-22(13-19)30-15-31-23(21)35-20-10-7-18(8-11-20)32-24(34)29-14-16-3-5-17(6-4-16)25(26,27)28/h3-13,15H,14H2,1-2H3,(H2,29,32,34)

Standard InChI Key:  RGUIKCSKPKYQQL-UHFFFAOYSA-N

Associated Targets(Human)

Macrophage colony stimulating factor receptor 5179 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serine/threonine-protein kinase Aurora-A 10240 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serine/threonine-protein kinase Aurora-B 6805 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

BaF3 4657 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

NFS-60 160 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 481.48Molecular Weight (Monoisotopic): 481.1726AlogP: 5.83#Rotatable Bonds: 6
Polar Surface Area: 79.38Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.95CX Basic pKa: 4.23CX LogP: 5.36CX LogD: 5.36
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.36Np Likeness Score: -1.70

References

1. Lee KH, Yen WC, Lin WH, Wang PC, Lai YL, Su YC, Chang CY, Wu CS, Huang YC, Yang CM, Chou LH, Yeh TK, Chen CT, Shih C, Hsieh HP..  (2021)  Discovery of BPR1R024, an Orally Active and Selective CSF1R Inhibitor that Exhibits Antitumor and Immunomodulatory Activity in a Murine Colon Tumor Model.,  64  (19.0): [PMID:34606263] [10.1021/acs.jmedchem.1c01006]

Source