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N6-(2,4-difluorobenzyl)-N4-(5-methylthiazol-2-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine ID: ALA5200812
PubChem CID: 168290381
Max Phase: Preclinical
Molecular Formula: C21H21F2N7OS
Molecular Weight: 457.51
Associated Items:
Names and Identifiers Canonical SMILES: Cc1cnc(Nc2nc(NCc3ccc(F)cc3F)nc3c2cnn3C2CCOCC2)s1
Standard InChI: InChI=1S/C21H21F2N7OS/c1-12-9-25-21(32-12)28-18-16-11-26-30(15-4-6-31-7-5-15)19(16)29-20(27-18)24-10-13-2-3-14(22)8-17(13)23/h2-3,8-9,11,15H,4-7,10H2,1H3,(H2,24,25,27,28,29)
Standard InChI Key: QNXGZWQGLLPXFL-UHFFFAOYSA-N
Molfile:
RDKit 2D
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-1.0761 0.8760 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3642 0.4641 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.3642 -0.3610 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.0743 -0.7728 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.7907 -0.3647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5981 -0.6158 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-3.0708 0.0403 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-2.5768 0.7106 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.8116 -1.4129 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.2282 -1.9964 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4417 -2.7935 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.2388 -3.0071 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.8223 -2.4236 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6087 -1.6265 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.3503 -0.7736 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
1.0650 -0.3610 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7796 -0.7736 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4944 -0.3612 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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3.2065 -1.5986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4962 -2.0105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7796 -1.6023 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9211 -2.0112 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
2.4944 0.4639 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
-1.0761 1.7012 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.7907 2.1138 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5054 1.7012 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
-3.1241 2.2725 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9692 2.9147 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-3.9211 2.0590 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.7934 3.0071 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
3 2 1 0
4 3 2 0
5 4 1 0
1 6 1 0
6 5 2 0
6 7 1 0
7 8 1 0
1 9 1 0
9 8 2 0
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11 10 1 0
12 11 1 0
13 12 1 0
14 13 1 0
10 15 1 0
15 14 1 0
4 16 1 0
16 17 1 0
17 18 1 0
19 18 2 0
20 19 1 0
21 20 2 0
22 21 1 0
18 23 1 0
23 22 2 0
21 24 1 0
19 25 1 0
2 26 1 0
26 27 1 0
28 27 1 0
28 29 1 0
27 30 2 0
29 31 1 0
29 32 2 0
30 32 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: 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: 457.51Molecular Weight (Monoisotopic): 457.1496AlogP: 4.58#Rotatable Bonds: 6Polar Surface Area: 89.78Molecular Species: NEUTRALHBA: 9HBD: 2#RO5 Violations: ┄HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 9.29CX Basic pKa: 2.50CX LogP: 4.01CX LogD: 4.00Aromatic Rings: 4Heavy Atoms: 32QED Weighted: 0.44Np Likeness Score: -2.20
References 1. Sun Y, Sun Y, Wang L, Wu T, Yin W, Wang J, Xue Y, Qin Q, Sun Y, Yang H, Zhao D, Cheng M.. (2022) Design, synthesis, and biological evaluation of novel pyrazolo [3,4-d]pyrimidine derivatives as potent PLK4 inhibitors for the treatment of TRIM37-amplified breast cancer., 238 [PMID:35576702 ] [10.1016/j.ejmech.2022.114424 ]