1-(4-((7-Fluoroquinazolin-4-yl)oxy)phenyl)-3-phenylurea

ID: ALA4871510

PubChem CID: 68026871

Max Phase: Preclinical

Molecular Formula: C21H15FN4O2

Molecular Weight: 374.38

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccccc1)Nc1ccc(Oc2ncnc3cc(F)ccc23)cc1

Standard InChI:  InChI=1S/C21H15FN4O2/c22-14-6-11-18-19(12-14)23-13-24-20(18)28-17-9-7-16(8-10-17)26-21(27)25-15-4-2-1-3-5-15/h1-13H,(H2,25,26,27)

Standard InChI Key:  DDTPZGOVQRREQN-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

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   29.0738  -12.5821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   29.7841  -11.3496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.4969  -11.7548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.4976  -12.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.2062  -12.9892    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.9186  -12.5742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.9138  -11.7480    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.2006  -11.3446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.1963  -10.5233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.9059  -10.1068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.6153  -10.5192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.3245  -10.1034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.3206   -9.2812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.6017   -8.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   34.0297   -8.8679    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.7443   -9.2718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.4534   -8.8585    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   36.1638   -9.2624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.1654  -10.0839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.8791  -10.4918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.5892  -10.0744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.5812   -9.2489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.8669   -8.8487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.7497  -10.0890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.3654  -12.9895    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
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 19 27  2  0
  2 28  1  0
M  END

Alternative Forms

Associated Targets(Human)

CSF1R Tclin Macrophage colony stimulating factor receptor (5179 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AURKB Tchem Serine/threonine-protein kinase Aurora-B (6805 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

Calculated Properties

Molecular Weight: 374.38Molecular Weight (Monoisotopic): 374.1179AlogP: 5.21#Rotatable Bonds: 4
Polar Surface Area: 76.14Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 11.64CX Basic pKa: 1.89CX LogP: 4.81CX LogD: 4.81
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.51Np Likeness Score: -1.57

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