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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
28 31 0 0 0 0 0 0 0 0999 V2000
29.0749 -11.7584 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.0738 -12.5821 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.7859 -12.9952 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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
31.8954 -9.2905 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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
2 3 1 0
3 6 2 0
5 4 2 0
4 1 1 0
5 6 1 0
6 7 1 0
7 8 2 0
8 9 1 0
9 10 2 0
10 5 1 0
10 11 1 0
11 12 1 0
12 13 2 0
13 14 1 0
14 15 2 0
15 16 1 0
16 17 2 0
17 12 1 0
15 18 1 0
18 19 1 0
19 20 1 0
20 21 1 0
21 22 2 0
22 23 1 0
23 24 2 0
24 25 1 0
25 26 2 0
26 21 1 0
19 27 2 0
2 28 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 374.38Molecular Weight (Monoisotopic): 374.1179AlogP: 5.21#Rotatable Bonds: 4Polar Surface Area: 76.14Molecular Species: NEUTRALHBA: 4HBD: 2#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: 11.64CX Basic pKa: 1.89CX LogP: 4.81CX LogD: 4.81Aromatic 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 ]