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(4-(6,7-dimethoxyquinazolin-4-yl)piperidin-1-yl)(4-(2-hydroxyethoxy)phenyl)methanone ID: ALA4582719
PubChem CID: 155561898
Max Phase: Preclinical
Molecular Formula: C24H27N3O5
Molecular Weight: 437.50
Molecule Type: Unknown
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: COc1cc2ncnc(C3CCN(C(=O)c4ccc(OCCO)cc4)CC3)c2cc1OC
Standard InChI: InChI=1S/C24H27N3O5/c1-30-21-13-19-20(14-22(21)31-2)25-15-26-23(19)16-7-9-27(10-8-16)24(29)17-3-5-18(6-4-17)32-12-11-28/h3-6,13-16,28H,7-12H2,1-2H3
Standard InChI Key: OFWMJTJIACLWHG-UHFFFAOYSA-N
Molfile:
RDKit 2D
32 35 0 0 0 0 0 0 0 0999 V2000
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12.4906 -14.0844 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.1986 -14.4934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.9083 -14.0839 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.9054 -13.2613 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.1968 -12.8560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.7825 -14.4924 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.0751 -14.0833 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
11.7819 -15.3096 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
11.0722 -15.7129 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.0696 -16.5265 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.7752 -16.9395 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.4850 -16.5327 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.4893 -15.7129 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.7714 -17.7566 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.7627 -19.3881 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
12.4746 -18.9783 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.4752 -18.1632 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
11.0563 -18.9754 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.0624 -18.1600 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.3604 -17.7488 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6518 -18.1519 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6497 -18.9705 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.3523 -19.3780 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.9411 -19.3775 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.2343 -18.9673 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.9460 -17.7402 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.2364 -18.1456 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.6116 -12.8500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
14.6085 -12.0328 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.3147 -11.6216 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.3116 -10.8044 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0
2 3 1 0
3 4 2 0
4 5 1 0
5 6 2 0
6 1 1 0
2 7 1 0
7 8 2 0
7 9 1 0
9 10 1 0
9 14 1 0
10 11 1 0
11 12 1 0
12 13 1 0
13 14 1 0
12 15 1 0
15 20 2 0
19 16 2 0
16 17 1 0
17 18 2 0
18 15 1 0
19 20 1 0
20 21 1 0
21 22 2 0
22 23 1 0
23 24 2 0
24 19 1 0
23 25 1 0
25 26 1 0
22 27 1 0
27 28 1 0
5 29 1 0
29 30 1 0
30 31 1 0
31 32 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: 437.50Molecular Weight (Monoisotopic): 437.1951AlogP: 3.04#Rotatable Bonds: 7Polar Surface Area: 94.01Molecular Species: NEUTRALHBA: 7HBD: 1#RO5 Violations: ┄HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): ┄CX Acidic pKa: ┄CX Basic pKa: 2.56CX LogP: 1.96CX LogD: 1.96Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.61Np Likeness Score: -0.77
References 1. Nguyen D, Lemos C, Wortmann L, Eis K, Holton SJ, Boemer U, Moosmayer D, Eberspaecher U, Weiske J, Lechner C, Prechtl S, Suelzle D, Siegel F, Prinz F, Lesche R, Nicke B, Nowak-Reppel K, Himmel H, Mumberg D, von Nussbaum F, Nising CF, Bauser M, Haegebarth A.. (2019) Discovery and Characterization of the Potent and Highly Selective (Piperidin-4-yl)pyrido[3,2- d]pyrimidine Based in Vitro Probe BAY-885 for the Kinase ERK5., 62 (2): [PMID:30563338 ] [10.1021/acs.jmedchem.8b01606 ]