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8-(4-(2-(4-(3-(2-Morpholinoethyl)-5-(trifluoromethyl)phenyl)piperidin-1-yl)ethyl)-1H-pyrazol-1-yl)pyrido[3,4-d]pyrimidin-4(3H)-one ID: ALA4553540
PubChem CID: 155510449
Max Phase: Preclinical
Molecular Formula: C30H34F3N7O2
Molecular Weight: 581.64
Molecule Type: Unknown
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: O=c1[nH]cnc2c(-n3cc(CCN4CCC(c5cc(CCN6CCOCC6)cc(C(F)(F)F)c5)CC4)cn3)nccc12
Standard InChI: InChI=1S/C30H34F3N7O2/c31-30(32,33)25-16-21(2-7-39-11-13-42-14-12-39)15-24(17-25)23-4-9-38(10-5-23)8-3-22-18-37-40(19-22)28-27-26(1-6-34-28)29(41)36-20-35-27/h1,6,15-20,23H,2-5,7-14H2,(H,35,36,41)
Standard InChI Key: OFBASLHLTNSWOV-UHFFFAOYSA-N
Molfile:
RDKit 2D
42 47 0 0 0 0 0 0 0 0999 V2000
38.2704 -3.6938 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.2692 -4.5134 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
38.9773 -4.9223 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.9755 -3.2850 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
39.6841 -3.6902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
39.6849 -4.5092 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.3934 -4.9163 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
41.1017 -4.5055 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.0969 -3.6834 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
40.3878 -3.2800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.9797 -5.7371 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
38.3197 -6.2190 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
38.5740 -6.9956 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
39.3913 -6.9937 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
39.6419 -6.2159 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.3835 -2.4628 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
39.8732 -7.6537 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.6857 -7.5663 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.1676 -8.2263 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
40.8325 -8.9718 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.3108 -9.6300 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
42.1241 -9.5468 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
42.4568 -8.7994 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.9763 -8.1352 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
42.6010 -10.2053 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
42.2659 -10.9518 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
42.7446 -11.6132 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
43.5583 -11.5293 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
43.8911 -10.7782 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
43.4103 -10.1200 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
44.7036 -10.6911 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
45.1854 -11.3512 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
45.0344 -9.9438 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
45.4903 -10.4749 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
42.4108 -12.3591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.5979 -12.4430 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.2642 -13.1889 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
40.4528 -13.2706 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.1187 -14.0124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.5946 -14.6772 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
41.4086 -14.5952 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.7467 -13.8484 0.0000 C 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 1 0
10 5 1 0
11 12 1 0
12 13 2 0
13 14 1 0
14 15 2 0
15 11 1 0
3 11 1 0
10 16 2 0
14 17 1 0
17 18 1 0
18 19 1 0
19 20 1 0
19 24 1 0
20 21 1 0
21 22 1 0
22 23 1 0
23 24 1 0
25 26 2 0
26 27 1 0
27 28 2 0
28 29 1 0
29 30 2 0
30 25 1 0
22 25 1 0
29 31 1 0
31 32 1 0
31 33 1 0
31 34 1 0
27 35 1 0
35 36 1 0
36 37 1 0
37 38 1 0
37 42 1 0
38 39 1 0
39 40 1 0
40 41 1 0
41 42 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: 581.64Molecular Weight (Monoisotopic): 581.2726AlogP: 3.82#Rotatable Bonds: 8Polar Surface Area: 92.17Molecular Species: BASEHBA: 8HBD: 1#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 1CX Acidic pKa: 10.07CX Basic pKa: 9.01CX LogP: 3.29CX LogD: 1.79Aromatic Rings: 4Heavy Atoms: 42QED Weighted: 0.34Np Likeness Score: -1.22
References 1. Le Bihan YV, Lanigan RM, Atrash B, McLaughlin MG, Velupillai S, Malcolm AG, England KS, Ruda GF, Mok NY, Tumber A, Tomlin K, Saville H, Shehu E, McAndrew C, Carmichael L, Bennett JM, Jeganathan F, Eve P, Donovan A, Hayes A, Wood F, Raynaud FI, Fedorov O, Brennan PE, Burke R, van Montfort RLM, Rossanese OW, Blagg J, Bavetsias V.. (2019) C8-substituted pyrido[3,4-d]pyrimidin-4(3H)-ones: Studies towards the identification of potent, cell penetrant Jumonji C domain containing histone lysine demethylase 4 subfamily (KDM4) inhibitors, compound profiling in cell-based target engagement assays., 177 [PMID:31158747 ] [10.1016/j.ejmech.2019.05.041 ]