ID: ALA4877148

Max Phase: Preclinical

Molecular Formula: C24H22ClN5O3

Molecular Weight: 463.93

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccc(NC(=O)Nc2ccc(Oc3ncnc4cc(N(C)C)ccc34)cc2)cc1Cl

Standard InChI:  InChI=1S/C24H22ClN5O3/c1-30(2)17-7-10-19-21(13-17)26-14-27-23(19)33-18-8-4-15(5-9-18)28-24(31)29-16-6-11-22(32-3)20(25)12-16/h4-14H,1-3H3,(H2,28,29,31)

Standard InChI Key:  PYEYQQPNCFWLBM-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: 463.93Molecular Weight (Monoisotopic): 463.1411AlogP: 5.79#Rotatable Bonds: 6
Polar Surface Area: 88.61Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 11.74CX Basic pKa: 4.23CX LogP: 5.22CX LogD: 5.22
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.38Np Likeness Score: -1.51

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