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1-(3-((4-amino-3-(6-ethoxynaphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)azetidin-1-yl)ethanone ID: ALA4582694
PubChem CID: 155558144
Max Phase: Preclinical
Molecular Formula: C23H24N6O2
Molecular Weight: 416.49
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: CCOc1ccc2cc(-c3nn(CC4CN(C(C)=O)C4)c4ncnc(N)c34)ccc2c1
Standard InChI: InChI=1S/C23H24N6O2/c1-3-31-19-7-6-16-8-18(5-4-17(16)9-19)21-20-22(24)25-13-26-23(20)29(27-21)12-15-10-28(11-15)14(2)30/h4-9,13,15H,3,10-12H2,1-2H3,(H2,24,25,26)
Standard InChI Key: YEVFGVGSJHZJGK-UHFFFAOYSA-N
Molfile:
RDKit 2D
31 35 0 0 0 0 0 0 0 0999 V2000
9.7558 -9.6586 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
9.7441 -10.4757 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.4452 -10.8938 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.4377 -11.7109 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.2099 -11.9723 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
11.4495 -12.7502 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.2369 -12.9744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.9496 -12.5754 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.3486 -13.2882 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
14.1360 -13.5083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.7213 -12.9371 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.3379 -14.2997 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
12.6359 -13.6872 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.6987 -11.3143 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
11.2272 -10.6501 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.4886 -9.8737 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.9485 -9.2608 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.2099 -8.4886 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.0114 -8.3250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.2770 -7.5528 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.0785 -7.3934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.3400 -6.6211 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
14.1415 -6.4617 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.3617 -5.6744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.6146 -8.0103 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.3532 -8.7826 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.5516 -8.9420 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.2902 -9.7143 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.7208 -12.1099 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
9.0197 -11.6918 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.0313 -10.8747 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 2 0
3 4 1 0
4 5 1 0
5 6 1 0
6 7 1 0
7 8 1 0
8 9 1 0
9 10 1 0
10 11 1 0
10 12 2 0
9 13 1 0
7 13 1 0
5 14 1 0
14 15 2 0
3 15 1 0
15 16 1 0
16 17 2 0
17 18 1 0
18 19 2 0
19 20 1 0
20 21 2 0
21 22 1 0
22 23 1 0
23 24 1 0
21 25 1 0
25 26 2 0
19 27 1 0
26 27 1 0
27 28 2 0
16 28 1 0
4 29 2 0
29 30 1 0
30 31 2 0
2 31 1 0
M END Associated Targets(Human) Associated Targets(non-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: 416.49Molecular Weight (Monoisotopic): 416.1961AlogP: 3.11#Rotatable Bonds: 5Polar Surface Area: 99.16Molecular Species: NEUTRALHBA: 7HBD: 1#RO5 Violations: ┄HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: ┄CX Basic pKa: 4.08CX LogP: 1.98CX LogD: 1.98Aromatic Rings: 4Heavy Atoms: 31QED Weighted: 0.54Np Likeness Score: -0.98
References 1. Vidadala RS, Rivas KL, Ojo KK, Hulverson MA, Zambriski JA, Bruzual I, Schultz TL, Huang W, Zhang Z, Scheele S, DeRocher AE, Choi R, Barrett LK, Siddaramaiah LK, Hol WG, Fan E, Merritt EA, Parsons M, Freiberg G, Marsh K, Kempf DJ, Carruthers VB, Isoherranen N, Doggett JS, Van Voorhis WC, Maly DJ.. (2016) Development of an Orally Available and Central Nervous System (CNS) Penetrant Toxoplasma gondii Calcium-Dependent Protein Kinase 1 (TgCDPK1) Inhibitor with Minimal Human Ether-a-go-go-Related Gene (hERG) Activity for the Treatment of Toxoplasmosis., 59 (13): [PMID:27309760 ] [10.1021/acs.jmedchem.6b00760 ]